Title Authors Journal Year
Preclinical studies for a phase 1 clinical trial of autologous hematopoietic stem cell gene therapy for sickle cell disease.Urbinati F, Wherley J, Geiger S, Fernandez BC, Kaufman ML, Cooper A, Romero Z, Marchioni F, Reeves L, Read E, Nowicki B, Grassman E, Viswanathan S, Wang X, Hollis RP, Kohn DB Cytotherapy2017
Diminished ovarian reserve in women with transfusion-dependent beta-thalassemia major: Is iron gonadotoxic?Uysal A, Alkan G, Kurtoğlu A, Erol O, Kurtoğlu E Eur. J. Obstet. Gynecol. Reprod. Biol.2017
Human leukocyte antigen distribution and genomic ancestry in Brazilian patients with sickle cell disease.da Silva-Malta MCF, Rodrigues PS, Zuccherato LW, de Souza FCB, Domingues EMFL, Souza VR, Tarazona-Santos E, Martins ML HLA2017
To learn more about sickle cell ulcers.Aractingi S Br. J. Dermatol.2017
Transcranial color Doppler in stroke-free adult patients with sickle cell disease.Graziadei G, Casoni FM, Annoni F, Cortinovis I, Ridolfi P, Gandolfi I, Marcon A, Di Pierro E, Cappellini MD Ann. Hematol.2017
Proponent or collaborative: Physician perspectives and approaches to disease modifying therapies in sickle cell disease.Bakshi N, Sinha CB, Ross D, Khemani K, Loewenstein G, Krishnamurti L PLoS ONE2017
Sickle Cell Disease.Milunsky A N. Engl. J. Med.2017
Sickle Cell Disease.Smith ER, Heeney M, Scott RM N. Engl. J. Med.2017
Sickle Cell Disease.Piel FB, Steinberg MH, Rees DC N. Engl. J. Med.2017
Sickle Cell Disease.Lionnet F, Haymann JP, Bachmeyer C N. Engl. J. Med.2017
Sickle Cell Disease.Bibas M N. Engl. J. Med.2017
Sickle Cell Disease.Inusa B, Popoola J, Wonkam A N. Engl. J. Med.2017
Sickle cell disease deserves a place in nurse education.Eboh WO Nurs Stand2017
Lived experiences of Iranian parents of beta-thalassemia children.Shahraki-Vahed A, Firouzkouhi M, Abdollahimohammad A, Ghalgaie J J Multidiscip Healthc2017
Is there a standard-of-care for transfusion therapy in thalassemia?Franchini M, Forni GL, Liumbruno GM Curr. Opin. Hematol.2017
Thalidomide has a significant effect in patients with thalassemia intermedia.Li Y, Ren Q, Zhou Y, Li P, Lin W, Yin X Hematology2017
Patient Perspectives on Gene Transfer Therapy for Sickle Cell Disease.Strong H, Mitchell MJ, Goldstein-Leever A, Shook L, Malik P, Crosby LE Adv Ther2017
Cell-free methemoglobin drives platelets to apoptosis via mitochondrial ROS-mediated activation of JNK and p38 MAP kinase.NaveenKumar SK, Hemshekhar M, Sundaram MS, Kemparaju K, Girish KS Biochem. Biophys. Res. Commun.2017
Pneumococcal vaccination for splenectomized patients with thalassemia major in Indonesia.Sari TT, Akib AAP, Gatot D, Roswita Harahap A, Bardosono S, Hadinegoro SRS Vaccine2017
Association of pancreatic MRI R2* with blood glucose and cardiac MRI R2* among thalassemia major patients in Indonesia.Wahidiyat PA, Sekarsari D, Adnani NB, Putriasih SA, Berdoukas V Am. J. Hematol.2017
Individuals with sickle cell disease have a significantly greater vasoconstriction response to thermal pain than controls and have significant vasoconstriction in response to anticipation of pain.Khaleel M, Puliyel M, Shah P, Sunwoo J, Kato RM, Chalacheva P, Thuptimdang W, Detterich J, Wood JC, Tsao J, Zeltzer L, Sposto R, Khoo MCK, Coates TD Am. J. Hematol.2017
Soluble form of transferrin receptor-1 level is associated with the age at first diagnosis and the risk of therapeutic intervention and iron overloading in patients with non-transfusion-dependent thalassemia.Ricchi P, Meloni A, Costantini S, Spasiano A, Di Matola T, Pepe A, Cinque P, Filosa A Ann. Hematol.2017
Advances in iron chelation therapy: transitioning to a new oral formulation.Shah NR Drugs Context2017
The role of discriminant functions in screening beta thalassemia trait and iron deficiency anemia among laboratory samples.Kumar A, Saha D, Kini J, Murali N, Chakraborti S, Adiga D J Lab Physicians2017
[Impact of sickle cell trait on arterial stiffness in African subjects].Ouédraogo V, Soleti R, Signolet I, Diaw M, Hallab M, Samb A, Andriantsitohaina R, Ba A, Lefthériotis G J Med Vasc2017
[Blood transfusion : optimizing the use of a scarce and expensive resource].Kherad O Rev Med Suisse2017
Extracorporeal Lung Support in Acute Chest Syndrome Associated With Sickle Cell Disease: A Rare Report of a Common Case.Mashhour A, Easo J, Horst M, Weyland A, Zundel J, Eichstaedt HC, Book M, Dohmen PM, Weymann A Artif Organs2017
Olfactory dysfunction and quality of life in patients with transfusion-dependent thalassemia.Yilmaz Y, Karakas Z, Uzun B, Sen C, Comoglu S, Orhan KS, Aydogdu S, Karagenc AO, Tugcu D, Karaman S, Wylie C, Doty RL Eur Arch Otorhinolaryngol2017
Mesoscopic Adaptive Resolution Scheme toward Understanding of Interactions between Sickle Cell Fibers.Lu L, Li H, Bian X, Li X, Karniadakis GE Biophys. J.2017
The super sickling haemoglobin HbS-Oman: a study of red cell sickling, K(+) permeability and associations with disease severity in patients heterozygous for HbA and HbS-Oman (HbA/S-Oman genotype).Al Balushi HWM, Wali Y, Al Awadi M, Al-Subhi T, Rees DC, Brewin JN, Hannemann A, Gibson JS Br. J. Haematol.2017
A proposed treatment algorithm for adults with Haemoglobin SC disease.Naessens V, Ward R, Kuo KHM Br. J. Haematol.2017
Roles of APOL1 G1 and G2 variants in sickle cell disease patients: kidney is the main target.Kormann R, Jannot AS, Narjoz C, Ribeil JA, Manceau S, Delville M, Joste V, Prié D, Pouchot J, Thervet E, Courbebaisse M, Arlet JB Br. J. Haematol.2017
A monocyte-TNF-endothelial activation axis in sickle transgenic mice: Therapeutic benefit from TNF blockade.Solovey A, Somani A, Belcher JD, Milbauer L, Vincent L, Pawlinski R, Nath KA, Kelm RJ, Mackman N, O'Sullivan MG, Gupta K, Vercellotti GM, Hebbel RP Am. J. Hematol.2017
Prospective evaluation of chronic organ damage in adult sickle cell patients: A seven-year follow-up study.van Tuijn CFJ, Schimmel M, van Beers EJ, Nur E, Biemond BJ Am. J. Hematol.2017
Comparison of the characteristics of two hemoglobin variants, Hb D-Iran and Hb E, eluting in the Hb A2 window.Dass J, Gupta A, Mittal S, Saraf A, Langer S, Bhargava M Blood Res2017
Prevalence and Etiology of Bacteremia in Febrile Children with Sickle Cell Disease at a Nigeria Tertiary Hospital.Brown B, Dada-Adegbola H, Trippe C, Olopade O Mediterr J Hematol Infect Dis2017
Liver Iron Content (LIC) in Adults with Sickle Cell Disease (SCD): Correlation with Serum Ferritin and Liver Enzymes Concentrations in Trasfusion Dependent (TD-SCD) and Non-Transfusion Dependent (NT-SCD) Patients.Yassin M, Soliman A, De Sanctis V, Nashwan A, Abusamaan S, Moustafa A, Kohla S, Soliman D Mediterr J Hematol Infect Dis2017
Subdissociative intranasal ketamine plus standard pain therapy versus standard pain therapy in the treatment of paediatric sickle cell disease vaso-occlusive crises in resource-limited settings: study protocol for a randomised controlled trial.Young JR, Sawe HR, Mfinanga JA, Nshom E, Helm E, Moore CG, Runyon MS, Reynolds SL BMJ Open2017
The protective role of TET2 in erythroid iron homeostasis against oxidative stress and erythropoiesis.Guo S, Jiang X, Wang Y, Chen L, Li H, Li X, Jia Y Cell. Signal.2017
Revisiting the Structure of Hemoglobin and Myoglobin with Cryo-Electron Microscopy.Khoshouei M, Danev R, Plitzko JM, Baumeister W J. Mol. Biol.2017
Renal Medullary Carcinoma: The Kidney Cancer That Affects Individuals With Sickle Cell Trait and Disease.Alvarez OA J Oncol Pract2017
Sciatic (Popliteal Fossa) Catheter for Pediatric Pain Management of Sickle Cell Crisis: A Case Report.Weber G, Liao S, Burns MA A A Case Rep2017
Decompensated Cirrhosis and Sickle Cell Disease: Case Reports and Review of the Literature.D'Ambrosio R, Maggioni M, Donato MF, Lampertico P, Cappellini MD, Graziadei G Hemoglobin2017
Comparison of MicroRNAs Mediated in Reactivation of the γ-Globin in β-Thalassemia Patients, Responders and Non-Responders to Hydroxyurea.Hojjati MT, Azarkeivan A, Pourfathollah AA, Amirizadeh N Hemoglobin2017
Hb Amsterdam-A1 [α32(B13)Met→Ile; HBA1: c.99G>A]: A Hyperunstable Variant Due to a New Mutation on the α1 Gene.Brennan SO, Wang D, Horridge M, Sheen CR Hemoglobin2017
The role of diffusion-weighted imaging in prediction liver iron concentration in beta-thalassaemia patients.Akpinar S, Yilmaz G, Bulakbasi N, Kocaoglu M J Med Imaging Radiat Oncol2017
Use of anti-inflammatory analgesics in sickle-cell disease.Han J, Saraf SL, Lash JP, Gordeuk VR J Clin Pharm Ther2017
First study on iron complexes in blood and organ samples from thalassaemic and normal laboratory mice using Mössbauer spectroscopy.Charitou G, Petousis V, Tsertos C, Parpottas Y, Kleanthous M, Phylactides M, Christou S Eur. Biophys. J.2017
Extensive Bone Marrow Necrosis: Initial Presentation in Sickle Cell Anemia-A Case Report and Review of the Literature.Alsafwani SA, Al-Saeed A, Bukhamsin R Case Rep Hematol2017
Evaluation of staff performance and interpretation of the screening program for prevention of thalassemia.Prommetta S, Sanchaisuriya K, Fucharoen G, Yamsri S, Chaiboonroeng A, Fucharoen S Biochem Med (Zagreb)2017
Variability of homozygous sickle cell disease: The role of alpha and beta globin chain variation and other factors.Serjeant GR, Vichinsky E Blood Cells Mol. Dis.2017
Inflammatory targets of therapy in sickle cell disease.Owusu-Ansah A, Ihunnah CA, Walker AL, Ofori-Acquah SF Transl Res2016
The Prevalence of Sickle Cell Disease and Its Implication for Newborn Screening in Germany (Hamburg Metropolitan Area).Grosse R, Lukacs Z, Cobos PN, Oyen F, Ehmen C, Muntau B, Timmann C, Noack B Pediatr Blood Cancer2016
Hydroxyurea Therapy for Children With Sickle Cell Anemia in Sub-Saharan Africa: Rationale and Design of the REACH Trial.McGann PT, Tshilolo L, Santos B, Tomlinson GA, Stuber S, Latham T, Aygun B, Obaro SK, Olupot-Olupot P, Williams TN, Odame I, Ware RE, Pediatr Blood Cancer2016
Phenotype and Genotype in a Cohort of 312 Adult Patients with Nontransfusion-Dependent Thalassemia in Northeast Thailand.Prayalaw P, Teawtrakul N, Jetsrisuparb A, Pongudom S, Fucharoen G, Fucharoen S Acta Haematol.2016
Effect of antiretroviral therapy on hemoglobin A2 values can have implications in antenatal beta-thalassemia screening programs.Bhagat P, Kaur Sachdeva R, Sharma P, Updesh Singh Sachdeva M, Chhabra S, Sharma A, Das R Infect Dis (Lond)2016
Molecular Heterogeneity of Thalassemia among Pregnant Laotian Women.Wongprachum K, Sanchaisuriya K, Dethvongphanh M, Norcharoen B, Htalongsengchan B, Vidamaly V, Sanchaisuriya P, Fucharoen S, Fucharoen G, Schelp FP Acta Haematol.2016
Cognitive and behavior deficits in sickle cell mice are associated with profound neuropathologic changes in hippocampus and cerebellum.Wang L, Almeida LE, de Souza Batista CM, Khaibullina A, Xu N, Albani S, Guth KA, Seo JS, Quezado M, Quezado ZM Neurobiol. Dis.2016
Preoperative screening for sickle cell disease in children: a pragmatic solution in a UK district hospital.Jemmett K, Williams A Paediatr Anaesth2016
Tissue Doppler Imaging-derived Diastolic Function Assessment in Children With Sickle Cell Disease and Its Relation With Ferritin.Olson M, Hebson C, Ehrlich A, New T, Sachdeva R J. Pediatr. Hematol. Oncol.2016
Higher Serum Ferritin Levels Correlate with an Increased Risk of Cutaneous Morbidity in Adult Patients with β-Thalassemia: A Single-Center Retrospective Study.Skandalis K, Vlachos C, Pliakou X, Gaitanis G, Kapsali E, Bassukas ID Acta Haematol.2016
Point mutations which should not be overlooked in Hb H disease.Farashi S, Bayat N, Vakili S, Faramarzi Garous N, Ashki M, Imanian H, Najmabadi H, Azarkeivan A Expert Rev Hematol2016
Hemoglobin F Only Syndrome at Birth: A Case of Maternal HbA2' Complicating the Diagnosis of β-Thalassemia.Yee ME, Quarmyne MO, Segbefia C, Young AN, Zhuang L, Kutlar F J. Pediatr. Hematol. Oncol.2016
Early Cardiac Involvement and Risk Factors for the Development of Arrhythmia in Patients With β-Thalassemia Major.Hamed AA, Elguindy W, Elhenawy YI, Ibrahim RH J. Pediatr. Hematol. Oncol.2016
Characterization of Deletions of the HBA and HBB Loci by Array Comparative Genomic Hybridization.Sabath DE, Bender MA, Sankaran VG, Vamos E, Kentsis A, Yi HS, Greisman HA J Mol Diagn2016
Therapeutic fetal-globin inducers reduce transcriptional repression in hemoglobinopathy erythroid progenitors through distinct mechanisms.Dai Y, Sangerman J, Luo HY, Fucharoen S, Chui DH, Faller DV, Perrine SP Blood Cells Mol. Dis.2016
Which side of the balance determines the frequency of vaso-occlusive crises in children with sickle cell anemia: Blood viscosity or microvascular dysfunction?Charlot K, Romana M, Moeckesch B, Jumet S, Waltz X, Divialle-Doumdo L, Hardy-Dessources MD, Petras M, Tressières B, Tarer V, Hue O, Etienne-Julan M, Antoine-Jonville S, Connes P Blood Cells Mol. Dis.2016
Serum YKL-40 in young patients with β-thalassemia major: Relation to hepatitis C virus infection, liver stiffness by transient elastography and cardiovascular complications.El-Asrar MA, Elbarbary NS, Ismail EA, Elshenity AM Blood Cells Mol. Dis.2016
Pentraxin-3 Levels in Beta Thalassemia Major and Minor Patients and Its Relationship With Antioxidant Capacity and Total Oxidant Stress.Isik Balci Y, Nuray E, Polat A, Enli Y, Ozgurler F, Akin M J. Pediatr. Hematol. Oncol.2016
Radical scavenging activities of Tyr-, Trp-, Cys- and Met-Gly and their protective effects against AAPH-induced oxidative damage in human erythrocytes.Zheng L, Dong H, Su G, Zhao Q, Zhao M Food Chem2016
The molecular spectrum and distribution of haemoglobinopathies in Cyprus: a 20-year retrospective study.Kountouris P, Kousiappa I, Papasavva T, Christopoulos G, Pavlou E, Petrou M, Feleki X, Karitzie E, Phylactides M, Fanis P, Lederer CW, Kyrri AR, Kalogerou E, Makariou C, Ioannou C, Kythreotis L, Hadjilambi G, Andreou N, Pangalou E, Savvidou I, Angastiniotis M, Hadjigavriel M, Sitarou M, Kolnagou A, Kleanthous M, Christou S Sci Rep2016
Erythroid differentiation of human induced pluripotent stem cells is independent of donor cell type of origin.Dorn I, Klich K, Arauzo-Bravo MJ, Radstaak M, Santourlidis S, Ghanjati F, Radke TF, Psathaki OE, Hargus G, Kramer J, Einhaus M, Kim JB, Kögler G, Wernet P, Schöler HR, Schlenke P, Zaehres H Haematologica2015
Antioxidant activity evaluation involving hemoglobin-related free radical reactivity.Mot AC, Bischin C, Damian G, Silaghi-Dumitrescu R Methods Mol. Biol.2015
Complications of ERCP for choledocholithiasis in a sickle cell cohort.Cawich SO, Arthurs M, Murphy T, Bonadie KO, Roberts HA, Naraynsingh V Trop Doct2015
Advances in detection of hemoglobinopathies.Greene DN, Vaughn CP, Crews BO, Agarwal AM Clin. Chim. Acta2015
A novel type of electrochemical sensor based on ferromagnetic carbon-encapsulated iron nanoparticles for direct determination of hemoglobin in blood samples.Matysiak E, Donten M, Kowalczyk A, Bystrzejewski M, Grudzinski IP, Nowicka AM Biosens Bioelectron2015
Next Generation Sequencing Identifies a Novel Rearrangement in the HBB Cluster Permitting to-the-Base Characterization.Shooter C, Rooks H, Thein SL, Clark B Hum. Mutat.2015
Depression in children suffering from sickle cell anemia.Lukoo RN, Ngiyulu RM, Mananga GL, Gini-Ehungu JL, Ekulu PM, Tshibassu PM, Aloni MN J. Pediatr. Hematol. Oncol.2015
Challenges and resilience in the lives of adults with sickle cell disease.Williams-Gray B, Senreich E Soc Work Public Health2015
Is testosterone deficiency a possible risk factor for priapism associated with sickle-cell disease?Morrison BF, Anele UA, Reid ME, Madden WA, Feng Z, Burnett AL Int Urol Nephrol2015
Evaluating the Capacity to Generate and Preserve Nitric Oxide Bioactivity in Highly Purified Earthworm Erythrocruorin: A GIANT POLYMERIC HEMOGLOBIN WITH POTENTIAL BLOOD SUBSTITUTE PROPERTIES.Roche CJ, Talwar A, Palmer AF, Cabrales P, Gerfen G, Friedman JM J. Biol. Chem.2015
Peptide nucleic acids targeting β-globin mRNAs selectively inhibit hemoglobin production in murine erythroleukemia cells.Montagner G, Gemmo C, Fabbri E, Manicardi A, Accardo I, Bianchi N, Finotti A, Breveglieri G, Salvatori F, Borgatti M, Lampronti I, Bresciani A, Altamura S, Corradini R, Gambari R Int. J. Mol. Med.2015
Preclinical Evaluation of Efficacy and Safety of an Improved Lentiviral Vector for the Treatment of β-Thalassemia and Sickle Cell Disease.Negre O, Bartholomae C, Beuzard Y, Cavazzana M, Christiansen L, Courne C, Deichmann A, Denaro M, Dreuzy Ed, Finer M, Fronza R, Gillet-Legrand B, Joubert C, Kutner R, Leboulch P, Maouche L, Paulard A, Pierciey FJ, Rothe M, Ryu B, Schmidt M, Kalle Cv, Payen E, Veres G Curr Gene Ther2015
How people in Benin assess a couple's risk of having a baby with sickle cell disease.Zounon O, Sorum PC, Mullet E J Community Genet2015
High impact of uranyl ions on carrying-releasing oxygen capability of hemoglobin-based blood substitutes.Duan L, Du L, Jia Y, Liu W, Liu Z, Li J Chemistry2015
Mechanisms of human erythrocytic bioactivation of nitrite.Liu C, Wajih N, Liu X, Basu S, Janes J, Marvel M, Keggi C, Helms CC, Lee AN, Belanger AM, Diz DI, Laurienti PJ, Caudell DL, Wang J, Gladwin MT, Kim-Shapiro DB J. Biol. Chem.2015
[Hb Burgos (α1 CD64(E13)(Asp→Asn)): A new hemoglobin variant detected during follow-up of diabetic patients].de la Fuente-Gonzalo F, Martínez Nieto J, Torrejón MJ, Mayor LA, Velasco D, González Fernández FA, Ropero Gradilla P Med Clin (Barc)2015
Genetic variant in the BCL11A (rs1427407), but not HBS1-MYB (rs6934903) loci associate with fetal hemoglobin levels in Indian sickle cell disease patients.Bhanushali AA, Patra PK, Nair D, Verma H, Das BR Blood Cells Mol. Dis.2015
Platelet hyperactivity in thalassemia patients with elevated tricuspid regurgitant velocity and the association with hemolysis.Srihirun S, Tanjararak N, Chuncharunee S, Sritara P, Kaewvichit R, Fucharoen S, Pattanapanyasat K, Sibmooh N Thromb. Res.2015
Prasugrel in Children With Sickle Cell Disease: Pharmacokinetic and Pharmacodynamic Data From an Open-label, Adaptive-design, Dose-ranging Study.Styles L, Heiselman D, Heath LE, Moser BA, Small DS, Jakubowski JA, Zhou C, Redding-Lallinger R, Heeney MM, Quinn CT, Rana SR, Kanter J, Winters KJ J. Pediatr. Hematol. Oncol.2015
Fast generation of T2(⁎) maps in the entire range of clinical interest: Application to thalassemia major patients.Positano V, Meloni A, Santarelli MF, Gerardi C, Bitti PP, Cirotto C, De Marchi D, Salvatori C, Landini L, Pepe A Comput. Biol. Med.2015
Direct mail does not improve screening in sickle cell disease.Fisher PG J. Pediatr.2015
Sickle cell disease clinical phenotypes in children from South-Western, Nigeria.Adegoke SA, Adeodu OO, Adekile AD Niger J Clin Pract2015
Chronic and acute anemia and extracranial internal carotid stenosis are risk factors for silent cerebral infarcts in sickle cell anemia.Bernaudin F, Verlhac S, Arnaud C, Kamdem A, Vasile M, Kasbi F, Hau I, Madhi F, Fourmaux C, Biscardi S, Epaud R, Pondarré C Blood2015
Thalassemia and heart surgery: aortic valve repair after endocarditis.Raffa GM, Mularoni A, Di Gesaro G, Vizzini G, Cipolla T, Pilato M Ann. Thorac. Surg.2015
Left ventricular rotational mechanics in Tanzanian children with sickle cell disease.Di Maria MV, Hsu HH, Al-Naami G, Gruenwald J, Kirby KS, Kirkham FJ, Cox SE, Younoszai AK J Am Soc Echocardiogr2015
Distribution of alpha-thalassemia mutations in Iranian population.Dehbozorgian J, Moghadam M, Daryanoush S, Haghpanah S, Imani Fard J, Aramesh A, Shahsavani A, Karimi M Hematology2015
Effect of coping strategies training on its use by thalassemia major adolescents: a randomized controlled clinical trial.Hashemi F, Naderi Darshori A, Sharif F, Karimi M, Zare N Int J Community Based Nurs Midwifery2015
Clinicoinvestigational and demographic profile of children with thalassemia major.Trehan A, Sharma N, Das R, Bansal D, Marwaha RK Indian J Hematol Blood Transfus2015
HPLC in characterization of hemoglobin profile in thalassemia syndromes and hemoglobinopathies: a clinicohematological correlation.Khera R, Singh T, Khuana N, Gupta N, Dubey AP Indian J Hematol Blood Transfus2015
The screening and morbidity pattern of sickle cell anemia in chhattisgarh.Panigrahi S, Patra PK, Khodiar PK Indian J Hematol Blood Transfus2015
Spectrum of Hemoglobinopathies in West Bengal, India: A CE-HPLC Study on 10407 Subjects.Mukhopadhyay D, Saha K, Sengupta M, Mitra S, Datta C, Mitra PK Indian J Hematol Blood Transfus2015
Unrelated Umbilical Cord Blood Transplant for Children with β-Thalassemia Major.Shah SA, Shah KM, Patel KA, Anand AS, Talati SS, Panchal HP, Patel AA, Parikh SK, Parekh BB, Shukla SN, Raut SS Indian J Hematol Blood Transfus2015
Primer-introduced restriction analysis polymerase chain reaction method for non-invasive prenatal testing of β-thalassemia.Liu S, Chen L, Zhang X, Li J, Lin H, Liu L, Xie J, Ge H, Ye M, Chen C, Ji X, Zhang C, Xu F, Jiang H, Zhen H, Chen S, Wang W Hemoglobin2015
Denaturant effects on HbGp hemoglobin as monitored by 8-anilino-1-naphtalene-sulfonic acid (ANS) probe.Barros AE, Carvalho FA, Alves FR, Carvalho JW, Tabak M Int. J. Biol. Macromol.2015
Low and fixed dose of hydroxyurea is effective and safe in patients with HbSβ(+) thalassemia with IVS1-5(G→C) mutation.Dehury S, Purohit P, Patel S, Meher S, Kullu BK, Sahoo LK, Patel NK, Mohapatra AK, Das K, Patel DK Pediatr Blood Cancer2015
Improvement in influenza vaccination rates in a pediatric sickle cell disease clinic.Sobota AE, Kavanagh PL, Adams WG, McClure E, Farrell D, Sprinz PG Pediatr Blood Cancer2015
Potential utility of melatonin as an antioxidant therapy in the management of sickle cell anemia.da Silva DG, Ricci O, de Almeida EA, Bonini-Domingos CR J. Pineal Res.2015
The association between dental and periodontal diseases and sickle cell disease. A pilot case-control study.Al-Alawi H, Al-Jawad A, Al-Shayeb M, Al-Ali A, Al-Khalifa K Saudi Dent J2015
Evaluation of two methods to measure hemoglobin concentration among women with genetic hemoglobin disorders in Cambodia: a method-comparison study.Karakochuk CD, Janmohamed A, Whitfield KC, Barr SI, Vercauteren SM, Kroeun H, Talukder A, McLean J, Green TJ Clin. Chim. Acta2015
Serum IL-6, IL-10, and TNFα levels in pediatric sickle cell disease patients during vasoocclusive crisis and steady state condition.Sarray S, Saleh LR, Lisa Saldanha F, Al-Habboubi HH, Mahdi N, Almawi WY Cytokine2015
Angioid streaks in association with sickle thalassemia trait.Ketner S, Moradi IE, Rosenbaum PS JAMA Ophthalmol2015
Integrative proteome and transcriptome analysis of extramedullary erythropoiesis and its reversal by transferrin treatment in a mouse model of beta-thalassemia.Vallelian F, Gelderman-Fuhrmann MP, Schaer CA, Puglia M, Opitz L, Baek JH, Vostal J, Buehler PW, Schaer DJ J. Proteome Res.2015
Development, Content Validity, and User Review of a Web-based Multidimensional Pain Diary for Adolescent and Young Adults With Sickle Cell Disease.Bakshi N, Stinson JN, Ross D, Lukombo I, Mittal N, Joshi SV, Belfer I, Krishnamurti L Clin J Pain2015
A new Aγ-globin chain variant: Hb F-Sykesville MD [Aγ113(G15)Val → Ile; HBG1: c.340G>A] detected in a Caucasian baby.Patel N, Fixler J, Unguru Y, Kutlar A, Kutlar F Hemoglobin2015
The effects of economic sanctions on disease specific clinical outcomes of patients with thalassemia and hemophilia in Iran.Karimi M, Haghpanah S Health Policy2015
Thalassemia major patients using iron chelators showed a reduced plasma thioredoxin level and reduced thioredoxin reductase activity, despite elevated oxidative stress.Ozturk Z, Genc GE, Kupesiz A, Kurtoglu E, Gumuslu S Free Radic. Res.2015
A 5-year follow-up in deferasirox treatment: improvement of cardiac and hepatic iron overload and amelioration in cardiac function in thalassemia major patients.Cassinerio E, Roghi A, Orofino N, Pedrotti P, Zanaboni L, Poggiali E, Giuditta M, Consonni D, Cappellini MD Ann. Hematol.2015
Blood cell exchange in the treatment of exercise-induced rhabdomyolysis in a patient with sickle cell trait.Papacostas MF, McLean M Mil Med2015
Clinical relevance of erythrocyte ferritin in microcytic anemias.Vagace JM, Peças A, Groiss J, Bento C, Ribeiro ML, Gervasini G Clin. Chim. Acta2015
Management of patients with sickle cell disease--reply.Yawn BP, Buchanan G, Hassell K JAMA2015
Management of patients with sickle cell disease.Klings ES, Kato GJ, Gladwin MT JAMA2015
Management of patients with sickle cell disease.Pollack S JAMA2015
Clinical biomarkers in sickle cell disease.Damanhouri GA, Jarullah J, Marouf S, Hindawi SI, Mushtaq G, Kamal MA Saudi J Biol Sci2015
The perception of biological experience in patients with major Thalassemia: a qualitative research.Arbabisarjou A, Karimzaei T, Jamalzaei A Glob J Health Sci2015
Health-related quality of life after allogeneic hematopoietic stem cell transplantation for sickle cell disease.Bhatia M, Kolva E, Cimini L, Jin Z, Satwani P, Savone M, George D, Garvin J, Paz ML, Briamonte C, Cruz-Arrieta E, Sands S Biol. Blood Marrow Transplant.2015
Combination therapy with a Tmprss6 RNAi-therapeutic and the oral iron chelator deferiprone additively diminishes secondary iron overload in a mouse model of β-thalassemia intermedia.Schmidt PJ, Racie T, Westerman M, Fitzgerald K, Butler JS, Fleming MD Am. J. Hematol.2015
New insights into the pharmacokinetics of intravenous busulfan in children with sickle cell anemia undergoing bone marrow transplantation.Gaziev J, Isgrò A, Mozzi AF, Petain A, Nguyen L, Ialongo C, Dinallo V, Sodani P, Marziali M, Andreani M, Testi M, Paciaroni K, Gallucci C, De Angelis G, Alfieri C, Ribersani M, Lucarelli G Pediatr Blood Cancer2015
Phenylbutyric Acid: simple structure - multiple effects.Kusaczuk M, Bartoszewicz M, Cechowska-Pasko M Curr. Pharm. Des.2015
A controlled study of internalizing symptoms in older adolescents with sickle cell disease.Kelly AD, Egan AM, Reiter-Purtill J, Gerhardt CA, Vannatta K, Noll RB Pediatr Blood Cancer2015
Longitudinal differences in aerobic capacity between children with sickle cell anemia and matched controls.Watson AM, Liem RI, Lu Z, Saville B, Acra S, Shankar S, Buchowski M Pediatr Blood Cancer2015
Elevated hypercoagulability markers in hemoglobin SC disease.Colella MP, de Paula EV, Machado-Neto JA, Conran N, Annichino-Bizzacchi JM, Costa FF, Olalla Saad ST, Traina F Haematologica2015
Differences in the erythropoiesis-hepcidin-iron store axis between hemoglobin H disease and β-thalassemia intermedia.Origa R, Cazzola M, Mereu E, Danjou F, Barella S, Giagu N, Galanello R, Swinkels DW Haematologica2015
Interleukin-1β and interleukin-6 gene polymorphisms are associated with manifestations of sickle cell anemia.Vicari P, Adegoke SA, Mazzotti DR, Cançado RD, Nogutti MA, Figueiredo MS Blood Cells Mol. Dis.2015
Spectral domain optical coherence tomography in patients with sickle cell disease.Mathew R, Bafiq R, Ramu J, Pearce E, Richardson M, Drasar E, Thein SL, Sivaprasad S Br J Ophthalmol2015
Frequency of Gγ-globin promoter -158 (C>T) XmnI polymorphism in patients with homozygous/compound heterozygous beta thalassaemia.Ali N, Ayyub M, Khan SA, Ahmed S, Abbas K, Malik HS, Tashfeen S Hematol Oncol Stem Cell Ther2015
Enrichment of human hematopoietic stem/progenitor cells facilitates transduction for stem cell gene therapy.Baldwin K, Urbinati F, Romero Z, Campo-Fernandez B, Kaufman ML, Cooper AR, Masiuk K, Hollis RP, Kohn DB Stem Cells2015
Compound heterozygosity for KLF1 mutations is associated with microcytic hypochromic anemia and increased fetal hemoglobin.Huang J, Zhang X, Liu D, Wei X, Shang X, Xiong F, Yu L, Yin X, Xu X Eur. J. Hum. Genet.2015
Deafness and sickle cell disease: three case reports and review of the literature.Desai P, Dejoie-Brewer M, Ballas SK J Clin Med Res2015
Cerebral microhaemorrhages secondary to fat embolus syndrome in sickle cell disease.Alobeidi F, Inusa BP, Singh RR, U-King-Im JM Postgrad Med J2015
Mutation screening of the Krüppel-like factor 1 gene using single-strand conformational polymorphism in a cohort of Iranian β-thalassemia patients.Zaker-Kandjani B, Namdar-Aligoodarzi P, Azarkeivan A, Najmabadi H, Banan M Hemoglobin2015
Haptoglobin attenuates hemoglobin-induced heme oxygenase-1 in renal proximal tubule cells and kidneys of a mouse model of sickle cell disease.Chintagari NR, Nguyen J, Belcher JD, Vercellotti GM, Alayash AI Blood Cells Mol. Dis.2015
Efficacy of hepatic T2* MRI values and serum ferritin concentration in predicting thalassemia major classification for hematopoietic stem cell transplantation.Hamidieh AA, Moeininia F, Tayebi S, Shamshiri AR, Behfar M, Jalili M, Alimoghaddam K, Ghavamzadeh A Pediatr Transplant2015
Safety and Utility of Quantitative Sensory Testing among Adults with Sickle Cell Disease: Indicators of Neuropathic Pain?Ezenwa MO, Molokie RE, Wang ZJ, Yao Y, Suarez ML, Pullum C, Schlaeger JM, Fillingim RB, Wilkie DJ Pain Pract2015
N-terminal pro-B-type natriuretic peptide, tricuspid jet flow velocity, and death in adults with sickle cell disease.Schimmel M, van Beers EJ, van Tuijn CF, Nur E, Rijneveld AW, Mac Gillavry MR, Brandjes DP, Schnog JJ, Biemond BJ, Am. J. Hematol.2015
[Delta⁰-thalassemia by insertion of 27 base pairs in δ-globin gene with decreased hemoglobin A₂ levels].González Borrachero ML, de la Fuente-Gonzalo F, González FA, Nieto JM, Villegas A, Ropero P Med Clin (Barc)2015
Diagnosis of a novel hemoglobinopathy of compound heterozygosity of hemoglobin S/hemoglobin Q India.Parab S, Sakhare S, Sengupta C, Velumani A Clin. Chim. Acta2015
Periapical cytokine expression in sickle cell disease.Ferreira SB, de Brito LC, Oliveira MP, Maciel KF, Martelli Júnior H, Vieira LQ, Sobrinho AP J Endod2015
A Comparison of Pain Assessment Measures in Pediatric Sickle Cell Disease: Visual Analog Scale Versus Numeric Rating Scale.Myrvik MP, Drendel AL, Brandow AM, Yan K, Hoffmann RG, Panepinto JA J. Pediatr. Hematol. Oncol.2015
Invasive pulmonary aspergillosis in a haematopoietic stem cell transplant recipient with sickle cell disease: a successful treatment.Paciaroni K, De Angelis G, Gallucci C, Alfieri C, Ribersani M, Roveda A, Isgrò A, Marziali M, Aloi IP, Inserra A, Gaziev J, Sodani P, Lucarelli G Mediterr J Hematol Infect Dis2015
The Frequency of Adrenal Insufficiency in Adolescents and Young Adults with Thalassemia Major versus Thalassemia Intermedia in Iran.Matin S, Jahromi MG, Karemizadeh Z, Haghpanah S, De Sanctis V, Soliman A, Dehbozorgian J, Majd Z, Rezaei N, Karimi M Mediterr J Hematol Infect Dis2015
Prevalence of alpha thalassemia in microcytic anemia: a tertiary care experience from north India.Sharma M, Pandey S, Ranjan R, Seth T, Saxena R Mediterr J Hematol Infect Dis2015
Higher-than-expected prevalence of silent cerebral infarcts in children with hemoglobin SC disease.Guilliams KP, Fields ME, Hulbert ML Blood2015
Changing practice: red blood cell typing by molecular methods for patients with sickle cell disease.Casas J, Friedman DF, Jackson T, Vege S, Westhoff CM, Chou ST Transfusion2015
Rare hemoglobin variants: Hb G-Szuhu (HBB: c.243C>G), Hb G-Coushatta (HBB: c.68A>C) and Hb Mizuho (HBB: c.206T>C) in Sri Lankan families.Perera PS, Silva I, Hapugoda M, Wickramarathne MN, Wijesiriwardena I, Efremov DG, Fisher CA, Weatherall DJ, Premawardhena A Hemoglobin2015
Identification of a novel mutation in the β-globin gene 3' untranslated region (HBB: c.*+118A > G) in Spain.Herrera MA, De La Fuente-Gonzalo F, González FA, Nieto JM, Dominguez AB, Villegas A, Ropero P Hemoglobin2015
Hb Feilding [β12(A9)Thr → Pro; HBB: c.37A>C]: a novel unstable β-globin chain variant.Ghallyan N, Donald T, Broad D, Johnson S, Browett P, Van de Water N Hemoglobin2015
Insulin resistance and β cell function in patients with β-thalassemia major.Ghergherehchi R, Habibzadeh A Hemoglobin2015
The first report of a homozygous codons 9/10 (+T) β-thalassemia mutation in a Turkish patient.Unal S, Chui DH, Luo HY, Okur H, Oymak Y, Gumruk F Hemoglobin2015
Erectile dysfunction after sickle cell disease-associated recurrent ischemic priapism: profile and risk factors.Anele UA, Burnett AL J Sex Med2015
Single-dose intravenous gammaglobulin can stabilize neutrophil Mac-1 activation in sickle cell pain crisis.Manwani D, Chen G, Carullo V, Serban S, Olowokure O, Jang J, Huggins M, Cohen HW, Billett H, Atweh GF, Frenette PS, Shi PA Am. J. Hematol.2015
Allogeneic Hematopoietic Cell Transplantation for Children with Sickle Cell Disease Is Beneficial and Cost-Effective: A Single-Center Analysis.Arnold SD, Jin Z, Sands S, Bhatia M, Kung AL, Satwani P Biol. Blood Marrow Transplant.2015
Sonographic markers of fetal α-thalassemia major.Li X, Zhou Q, Zhang M, Tian X, Zhao Y J Ultrasound Med2015
A mouse model to study thrombotic complications of thalassemia.Kalish Y, Malyutin Z, Shai E, Dana M, Avraham L, Jahshan N, Rachmilewitz E, Fibach E, Varon D Thromb. Res.2015
Premarital screening for hemoglobinopathies: experience of a single center in Kurdistan, Iraq.Al-Allawi NA, Al-Doski AA, Markous RS, Mohamad Amin KA, Eissa AA, Badi AI, Asmaro RR, Hamamy H Public Health Genomics2015
Therapeutic phlebotomy is safe in children with sickle cell anaemia and can be effective treatment for transfusional iron overload.Aygun B, Mortier NA, Kesler K, Lockhart A, Schultz WH, Cohen AR, Alvarez O, Rogers ZR, Kwiatkowski JL, Miller ST, Sylvestre P, Iyer R, Lane PA, Ware RE, Br. J. Haematol.2015
α-Hemoglobin-stabilizing Protein: An Effective Marker for Erythroid Precursors in Bone Marrow Biopsy Specimens.Yu H, Pinkus JL, Pinkus GS Appl. Immunohistochem. Mol. Morphol.2015
Six-day stability of erythrocyte and reticulocyte parameters in-vitro: a comparison of blood samples from healthy, iron-deficient, and thalassemic individuals.Sudmann-Day ÅA, Piehler A, Klingenberg O, Urdal P Scand. J. Clin. Lab. Invest.2015
In vitro culture of stress erythroid progenitors identifies distinct progenitor populations and analogous human progenitors.Xiang J, Wu DC, Chen Y, Paulson RF Blood2015
New look at hemoglobin allostery.Yuan Y, Tam MF, Simplaceanu V, Ho C Chem. Rev.2015
Comparison of DNA methylation profiles in human fetal and adult red blood cell progenitors.Lessard S, Beaudoin M, Benkirane K, Lettre G Genome Med2015
Kinetics of sickle cell biorheology and implications for painful vasoocclusive crisis.Du E, Diez-Silva M, Kato GJ, Dao M, Suresh S Proc. Natl. Acad. Sci. U.S.A.2015
α-Thalassaemia trait is associated with antibody prevalence against malaria antigens AMA-1 and MSP-1.Daou M, Kituma E, Kavishe R, Chilongola J, Mosha F, van der Ven A, Kouriba B, Bousema T, Sauerwein R, Doumbo O J. Trop. Pediatr.2015
Modulation of Sickle Red Blood Cell Adhesion and its Associated Changes in Biomarkers by Sulfated Nonanticoagulant Heparin Derivative.Alshaiban A, Muralidharan-Chari V, Nepo A, Mousa SA Clin. Appl. Thromb. Hemost.2015
Genetic modifiers of secondary iron overload in beta thalassemia major.Athiyarath R, George B, Abraham A, Viswabandya A, Srivastava A, Edison ES Blood Cells Mol. Dis.2015
Efficacy and safety of a novel combination of two oral chelators deferasirox/deferiprone over deferoxamine/deferiprone in severely iron overloaded young beta thalassemia major patients.Elalfy MS, Adly AM, Wali Y, Tony S, Samir A, Elhenawy YI Eur. J. Haematol.2015
The invisibility of sickle cell disease in Brazil: lessons from a study in Maranhão.Viana MB Rev Bras Hematol Hemoter2015
Mechanisms and pathophysiological significance of eryptosis, the suicidal erythrocyte death.Lang E, Lang F Semin. Cell Dev. Biol.2015
[Screening of cerebral vasculopathy in sickle cell anemia children using transcranial Doppler].Dorie A, Guindo A, Saro YS, Touré BA, Fané B, Dembelé AK, Diallo DA Arch Pediatr2015
Discrimination of various thalassemia syndromes and iron deficiency and utilization of reticulocyte measurements in monitoring response to iron therapy.Winichagoon P, Kumbunlue R, Sirankapracha P, Boonmongkol P, Fucharoen S Blood Cells Mol. Dis.2015
Accelerated telomere shortening in β-thalassemia/HbE patients.Chaichompoo P, Pattanapanyasat K, Winichagoon P, Fucharoen S, Svasti S Blood Cells Mol. Dis.2015
Red cell exchange transfusion halts progressive proliferative sickle cell retinopathy in a teenaged patient with hemoglobin SC disease.McKinney CM, Siringo F, Olson JL, Capocelli KE, Ambruso DR, Nuss R Pediatr Blood Cancer2015
Sensitization of nociceptive spinal neurons contributes to pain in a transgenic model of sickle cell disease.Cataldo G, Rajput S, Gupta K, Simone DA Pain2015
A comparison of chronic manual and automated red blood cell exchange transfusion in sickle cell disease patients.Kuo KH, Ward R, Kaya B, Howard J, Telfer P Br. J. Haematol.2015
Is sickle cell anemia a risk factor for severe dental malocclusion?Costa CP, Carvalho HL, Souza Sde F, Thomaz EB Braz Oral Res2015
Successful implantation and live birth of a healthy boy after triple biopsy and double vitrification of oocyte-embryo-blastocyst.Greco E, Biricik A, Cotarelo RP, Iammarone E, Rubino P, Tesarik J, Fiorentino F, Minasi MG Springerplus2015
Spontaneous central retinal artery occlusion in a teenager with sickle cell trait.Pai SA, Hebri SP, Dekhain MA Middle East Afr J Ophthalmol2015
Bayesian analyses demonstrate tissue blood volume is not decreased during acute sickle cell pain episodes: A preliminary study.Perry M, Simon J, Gareau D, Glassberg J Clin. Hemorheol. Microcirc.2015
[Neonatal screening for hemoglobinopathies in São Carlos, São Paulo, Brazil: analysis of a series of cases].Silva Cde A, Baldim LB, Nhoncanse GC, Estevão Ida F, Melo DG Rev Paul Pediatr2015
'Who's the guy in the room?' Involving fathers in antenatal care screening for sickle cell disorders.Atkin K, Berghs M, Dyson S Soc Sci Med2015
Increased risk of severe vaso-occlusive episodes after initial acute chest syndrome in children with sickle cell anemia less than 4 years old: Sleep and asthma cohort.Vance LD, Rodeghier M, Cohen RT, Rosen CL, Kirkham FJ, Strunk RC, DeBaun MR Am. J. Hematol.2015
Using fludarabine to reduce exposure to alkylating agents in children with sickle cell disease receiving busulfan, cyclophosphamide, and antithymocyte globulin transplant conditioning: results of a dose de-escalation trial.Horan JT, Haight A, Dioguardi JL, Brown C, Grizzle A, Shelman C, Kanter J, Hale G, Nieder M, Benton M, Kasow KA, Abraham A, Chiang KY Biol. Blood Marrow Transplant.2015
β-Globin Mutations in Egyptian Patients With β-Thalassemia.Elmezayen AD, Kotb SM, Sadek NA, Abdalla EM Lab Med2015
[HSP70 regulates ineffective erythropoiesis in beta-thalassaemia].Arlet JB, Ribeil JA, Guillem F, Hermine O, Courtois G Med Sci (Paris)2015
Bee sting envenomation resulting in gross haematuria in an eight-year-old Nigerian male with sickle cell anaemia: A case report.Odinaka KK, Achigbu K, Ike I, Iregbu F Niger Med J2015
A novel promoter mutation (HBB: c.-75G>T) was identified as a cause of β(+)-thalassemia.Li Z, Li L, Yao Y, Li N, Li Y, Zhang Z, Yan F, Qiu H, Wu C, Zhang Z Hemoglobin2015
Morphine for the treatment of pain in sickle cell disease.Gupta M, Msambichaka L, Ballas SK, Gupta K ScientificWorldJournal2015
Sickle cell trait as a contributory cause of death in natural disease.Podduturi V, Guileyardo JM J. Forensic Sci.2015
Genetics of fetal hemoglobin in tribal Indian patients with sickle cell anemia.Bhanushali AA, Patra PK, Pradhan S, Khanka SS, Singh S, Das BR Transl Res2015
Review: Beta-thalassemia and molecular chaperones.Sumera A, Radhakrishnan A, Baba AA, George E Blood Cells Mol. Dis.2015
Infectious complications following allogeneic stem cell transplantation by using anti-thymocyte globulin-based myeloablative conditioning regimens in children with hemoglobinopathies.Goussetis E, Efstathiou E, Paisiou A, Avgerinou G, Zisaki K, Giamouris VJ, Peristeri I, Kitra V, Vessalas G, Gamaletsou MN, Sipsas NV, Graphakos S Transpl Infect Dis2015
The delay time in sickle cell disease after 40 years: A paradigm assessed.Ferrone FA Am. J. Hematol.2015
Evaluating the safety and efficacy of silymarin in β-thalassemia patients: a review.Moayedi Esfahani BA, Reisi N, Mirmoghtadaei M Hemoglobin2015
Comparing segmented ASL perfusion of vascular territories using manual versus semiautomated techniques in children with sickle cell anemia.Helton KJ, Glass JO, Reddick WE, Paydar A, Zandieh AR, Dave R, Smeltzer MP, Wu S, Hankins J, Aygun B, Ogg RJ J Magn Reson Imaging2015
Vitamin D deficiency and acute vaso-occlusive complications in children with sickle cell disease.Lee MT, Licursi M, McMahon DJ Pediatr Blood Cancer2015
Single-tube nonaplex microsatellite PCR panel for preimplantation genetic diagnosis of Hb Bart's hydrops fetalis syndrome.Chen M, Chan JK, Nadarajah S, Tan AS, Chan ML, Mathew J, Saw EE, Lim C, Wong W, Cheah FS, Law HY, Wong PC, Chong SS Prenat. Diagn.2015
Preemptive Genotyping of CYP2C8 and CYP2C9 Allelic Variants Involved in NSAIDs Metabolism for Sickle Cell Disease Pain Management.Jaja C, Bowman L, Wells L, Patel N, Xu H, Lyon M, Kutlar A Clin Transl Sci2015
Impact of a dedicated infusion clinic for acute management of adults with sickle cell pain crisis.Lanzkron S, Carroll CP, Hill P, David M, Paul N, Haywood C Am. J. Hematol.2015
Evidence gaps in the management of sickle cell disease: A summary of needed research.Savage WJ, Buchanan GR, Yawn BP, Afenyi-Annan AN, Ballas SK, Goldsmith JC, Hassell KL, James AH, John-Sowah J, Jordan L, Lottenberg R, Murad MH, Ortiz E, Tanabe PJ, Ware RE, Lanzkron SM Am. J. Hematol.2015
Heme oxygenase-1 deficiency alters erythroblastic island formation, steady-state erythropoiesis and red blood cell lifespan in mice.Fraser ST, Midwinter RG, Coupland LA, Kong S, Berger BS, Yeo JH, Andrade OC, Cromer D, Suarna C, Lam M, Maghzal GJ, Chong BH, Parish CR, Stocker R Haematologica2015
Hb S/β+-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the β locus control region.Amid A, Cheong M, Eng B, Hanna M, Hohenadel BA, Nakamura LM, Walker L, Odame I, Kirby-Allen M, Waye JS Haematologica2015
Potentially therapeutic levels of anti-sickling globin gene expression following lentivirus-mediated gene transfer in sickle cell disease bone marrow CD34(+) cells.Urbinati F, Hargrove PW, Geiger S, Romero Z, Wherley J, Kaufman ML, Hollis RP, Chambers CB, Persons DA, Kohn DB, Wilber A Exp. Hematol.2015
Carotid endarterectomy in a young symptomatic patient with B-thalassemia major.Kotsis T, Pappas E, Sarmas G, Basilopoulou S, Hatzioannou A, Theodoraki K, Mylonas S, Speggos K Ann Vasc Surg2015
Hemoglobinopathies and sleep - The road less traveled.Gileles-Hillel A, Kheirandish-Gozal L, Gozal D Sleep Med Rev2015
Broader spectrum of β-thalassemia mutations in Oman: regional distribution and comparison with neighboring countries.Hassan SM, Harteveld CL, Bakker E, Giordano PC Hemoglobin2015
Coronary artery ectasia in atherosclerotic coronary artery disease, inflammatory disorders, and sickle cell disease.Dahhan A Cardiovasc Ther2015
Hyperhemolysis syndrome in patients with sickle cell anemia: report of three cases.Santos B, Portugal R, Nogueira C, Loureiro M Transfusion2015
Salmonella osteomyelitis of the hand in an infant with sickle cell disease.Sinkin JC, Wood BC, Sauerhammer TM, Boyajian MJ, Rogers GF, Oh AK Plast Reconstr Surg Glob Open2015
A novel hemoglobin variant found on the α1 chain: Hb KSVGH (HBA1: p.Lys57_Gly58insSerHisGlySerAlaGlnValLys).Wang MC, Tsai KW, Chu CH, Yu MS, Lam HC Hemoglobin2015
Sickle cell disease: renal manifestations and mechanisms.Nath KA, Hebbel RP Nat Rev Nephrol2015
Management of sickle cell disease: a review for physician education in Nigeria (sub-saharan Africa).Adewoyin AS Anemia2015
Timing of opioid administration as a quality indicator for pain crises in sickle cell disease.Mathias MD, McCavit TL Pediatrics2015
Newborn screening for sickle cell disease: necessary but not sufficient.Wang WC J Pediatr (Rio J)2015
Coinheritance of Hb D-Punjab and β-thalassemia: diagnosis and implications in prenatal diagnosis.Das S, Mashon RS Hemoglobin2015
Attenuating a sickle cell crisis with annexin V.Kennedy JR Med. Hypotheses2015
A unified sensor architecture for isothermal detection of double-stranded DNA, oligonucleotides, and small molecules.Brown CW, Lakin MR, Fabry-Wood A, Horwitz EK, Baker NA, Stefanovic D, Graves SW Chembiochem2015
Allogeneic donor availability for hematopoietic stem cell transplantation in children with sickle cell disease.Justus D, Perez-Albuerne E, Dioguardi J, Jacobsohn D, Abraham A Pediatr Blood Cancer2015
[Muscle involvement in sickle cell disease.]Rubio MÁ, Díez L, Álvarez N, Munteis E Med Clin (Barc)2015
Left atrial volume is not an index of left ventricular diastolic dysfunction in patients with sickle cell anaemia.Hammoudi N, Charbonnier M, Levy P, Djebbar M, Stankovic Stojanovic K, Ederhy S, Girot R, Cohen A, Isnard R, Lionnet F Arch Cardiovasc Dis2015
[Breastfeeding and the anthropometric profile of children with sickle cell anemia receiving follow-up in a newborn screening reference service].Nogueira ZD, Boa-Sorte N, Leite ME, Kiya MM, Amorim T, Fonseca SF Rev Paul Pediatr2015
Hemoglobin C in a patient with sickle cell anemia: transfusion-acquired SC disease.Estey MP, Capote KR, Barakauskas VE, Clarke G, Higgins T Clin. Biochem.2015
Paracentral acute middle maculopathy in sickle cell disease.Ilginis T, Keane PA, Tufail A JAMA Ophthalmol2015
Mass spectrometric analysis of unknown haemoglobin fractions identified by high-performance liquid chromatography in an antenatal screening programme.Griffin M, Eyre J, Dack S, Wright J J. Clin. Pathol.2015
Krüppel-like factor 1 mutations and expression of hemoglobins F and A2 in homozygous hemoglobin E syndrome.Tepakhan W, Yamsri S, Fucharoen G, Sanchaisuriya K, Fucharoen S Ann. Hematol.2015
Macrophages and regulation of erythropoiesis.Jacobsen RN, Perkins AC, Levesque JP Curr. Opin. Hematol.2015
Utility of labile plasma iron and transferrin saturation in addition to serum ferritin as iron overload markers in different underlying anemias before and after deferasirox treatment.Porter JB, El-Alfy M, Viprakasit V, Giraudier S, Chan LL, Lai Y, El-Ali A, Han J, Cappellini MD Eur. J. Haematol.2015
Association of an α-globin gene cluster duplication and heterozygous β-thalassemia in a patient with a severe thalassemia syndrome.Jiang H, Liu S, Zhang YL, Wan JH, Li R, Li DZ Hemoglobin2015
A new Krüppel-like factor 1 mutation (c.947G > A or p.C316Y) in humans causes β-thalassemia minor.Nitta T, Kawano F, Yamashiro Y, Takagi F, Murata T, Tanaka T, Ferania M, Adhiyanto C, Hattori Y Hemoglobin2015
A rapid paper-based test for quantifying sickle hemoglobin in blood samples from patients with sickle cell disease.Piety NZ, Yang X, Lezzar D, George A, Shevkoplyas SS Am. J. Hematol.2015
Polychlorinated biphenyls (PCBs) inhibit hepcidin expression through an estrogen-like effect associated with disordered systemic iron homeostasis.Qian Y, Zhang S, Guo W, Ma J, Chen Y, Wang L, Zhao M, Liu S Chem. Res. Toxicol.2015
Does Sickle Cell Disease Protect Against Diabetes Mellitus?: Cross-sectional study.Mohamed AA, Al-Qurashi F, Whitford DL Sultan Qaboos Univ Med J2015
Point-of-care end-tidal carbon monoxide reflects severity of hemolysis in sickle cell anemia.Lal A, Patterson L, Goldrich A, Marsh A Pediatr Blood Cancer2015
Age-dependent pathophysiology of acute chest syndrome in children with sickle cell disease.Renella R Am. J. Hematol.2015
The accuracy of using ICD-9-CM codes to determine genotype and fever status of patients with sickle cell disease.Eisenbrown K, Nimmer M, Brousseau DC Pediatr Blood Cancer2015
Deep venous thrombosis in children with sickle cell disease.Boechat Tde O, do Nascimento EM, Lobo CL, Ballas SK Pediatr Blood Cancer2015
Prospects for early investigational therapies for sickle cell disease.Conran N Expert Opin Investig Drugs2015
Type I allergic hypersensitivity reactions due to ethylene oxide sterilised leucocyte filters in patients with thalassaemia: report of four cases.Belen B, Polat M BMJ Case Rep2015
Defining the morphology and mechanism of the hemoglobin transport pathway in Plasmodium falciparum-infected erythrocytes.Milani KJ, Schneider TG, Taraschi TF Eukaryotic Cell2015
Dexmedetomidine ameliorates nocifensive behavior in humanized sickle cell mice.Calhoun G, Wang L, Almeida LE, Kenyon N, Afsar N, Nouraie M, Finkel JC, Quezado ZM Eur. J. Pharmacol.2015
KLF1-null neonates display hydrops fetalis and a deranged erythroid transcriptome.Magor GW, Tallack MR, Gillinder KR, Bell CC, McCallum N, Williams B, Perkins AC Blood2015
[Role of alpha-hemoglobin molecular chaperone in the hemoglobin formation and clinical expression of some hemoglobinopathies].Vasseur C, Baudin-Creuza V Transfus Clin Biol2015
Insulin resistance, impaired glucose tolerance and alpha-thalassemia carrier state.Bahar A, Shekarriz R, Janbabai G, Shirzad R, Aarabi M, Kashi Z J Diabetes Metab Disord2015
Alloimmunization in patients with sickle cell disease in French Guiana.Elenga N, Niel L J Blood Transfus2015
Hematopoietic stem-cell transplantation in the developing world: experience from a center in Western India.Shah CA, Karanwal A, Desai M, Pandya M, Shah R, Shah R J Oncol2015
Study of red blood cell alloimmunization in multitransfused thalassemic children of Jammu region.Dogra A, Sidhu M, Kapoor R, Kumar D Asian J Transfus Sci2015
A cost effective model for appropriate administration of red cell units and salvaging un-transfused red cell units by using temperature sensitive indicators for blood component transportation in a hospital setting.Tiwari AK, Sharma P, Pandey PK, Rawat GS, Dixit S, Raina V, Bhargava R Asian J Transfus Sci2015
Embryo genome profiling by single-cell sequencing for preimplantation genetic diagnosis in a β-thalassemia family.Xu Y, Chen S, Yin X, Shen X, Pan X, Chen F, Jiang H, Liang Y, Wang W, Xu X, Wang J, Zhang X, Zhou C, Wang J Clin. Chem.2015
Hemoglobinopathy in India.Iyer S, Sakhare S, Sengupta C, Velumani A Clin. Chim. Acta2015
Erroneous HbA1c measurements in the presence of β-thalassemia and common Chinese hemoglobin variants.Ji L, Yu J, Zhou Y, Xia Y, Xu A, Li W, Li L Clin. Chem. Lab. Med.2015
Transcriptional activity of erythroid Kruppel-like factor (EKLF/KLF1) modulated by PIAS3 (protein inhibitor of activated STAT3).Siatecka M, Soni S, Planutis A, Bieker JJ J. Biol. Chem.2015
Novel Insights Into the Protective Role of Hemoglobin S and C Against Plasmodium falciparum Parasitemia.Mangano VD, Kabore Y, Bougouma EC, Verra F, Sepulveda N, Bisseye C, Santolamazza F, Avellino P, Tiono AB, Diarra A, Nebie I, Rockett KA, Sirima SB, Modiano D, J. Infect. Dis.2015
Interference of Hemoglobin N-Baltimore on Measurement of HbA1c Using the HA-8160 and HA-8180 HPLC Methods.Lorenzo-Medina M, Nogueira-Salgueiro P, Martin-Aguila A, Ruiz-Garcia L J Diabetes Sci Technol2015
Cochlear implantation in children with sickle cell disease.Ashfield T, Pai I, Wilson K, Britz A, Connor S, Fitzgerald-O'Connor A, Jiang D Pediatr Int2015
Membranous nephropathy presenting with nephrotic syndrome in a child with thalassemia major.Yavuz S, Anarat A, Bayazıt AK, Karagun BŞ, Yılmaz S, Kılınc Y, Gonlusen G, Kuyucu Y Pediatr Int2015
New insights into iron regulation and erythropoiesis.Kim A, Nemeth E Curr. Opin. Hematol.2015
Unruptured intracranial aneurysms in children with sickle cell disease: analysis of 18 aneurysms in 5 patients.Saini S, Speller-Brown B, Wyse E, Meier ER, Carpenter J, Fasano RM, Pearl MS Neurosurgery2015
Biochemical storage lesions occurring in nonirradiated and irradiated red blood cells: a brief review.Adams F, Bellairs G, Bird AR, Oguntibeju OO Biomed Res Int2015
Genetic determinants of β-thalassemia intermedia in Pakistan.Khan J, Ahmad N, Siraj S, Hoti N Hemoglobin2015
Prevalence of Hb S (HHB: c.20A > T) in a Honduran population of African descent.Erazo BM, Ramírez GA, Cerrato LE, Pinto LJ, Castro EJ, Yanez NJ, Montoya B, Fontecha GA Hemoglobin2015
First report of acute lymphoblastic leukemia in an Egyptian child with β-thalassemia major.Sherief LM, Kamal NM, Abdelrahman HM, Hassan BA, Zakaria MM Hemoglobin2015
The fucosylation inhibitor, 2-fluorofucose, inhibits vaso-occlusion, leukocyte-endothelium interactions and NF-ĸB activation in transgenic sickle mice.Belcher JD, Chen C, Nguyen J, Abdulla F, Nguyen P, Nguyen M, Okeley NM, Benjamin DR, Senter PD, Vercellotti GM PLoS ONE2015
Hemoglobin to Hematocrit Ratio: The Strongest Predictor of Femoral Head Osteonecrosis in Children With Sickle Cell Disease.Worrall D, Smith-Whitley K, Wells L J Pediatr Orthop2015
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Production of Gene-Corrected Adult Beta Globin Protein in Human Erythrocytes Differentiated from Patient iPSCs After Genome Editing of the Sickle Point Mutation.Huang X, Wang Y, Yan W, Smith C, Ye Z, Wang J, Gao Y, Mendelsohn L, Cheng L Stem Cells2015
Survival of children with sickle cell disease in the comprehensive newborn screening programme in Minas Gerais, Brazil.Sabarense AP, Lima GO, Silva LM, Viana MB Paediatr Int Child Health2015
Hydroxyurea for sickle-cell anaemia in Africa: mind the gap.Obaro SK Lancet Glob Health2015
A Randomized Trial to Compare the Safety, Tolerability, and Effectiveness of 3 Antimalarial Regimens for the Prevention of Malaria in Nigerian Patients With Sickle Cell Disease.Olaosebikan R, Ernest K, Bojang K, Mokuolu O, Rehman AM, Affara M, Nwakanma D, Kiechel JR, Ogunkunle T, Olagunju T, Murtala R, Omefe P, Lambe T, Bello S, Ibrahim O, Olorunsola B, Ojuawo A, Greenwood B, Milligan P J. Infect. Dis.2015
Platelet Aggregation Study in Patients With Hemoglobin Eβ Thalassemia in India.Ghosal T, Dolai TK, Mandal PK, Karthik S, Bandyopadhyay A Clin. Appl. Thromb. Hemost.2015
Erythroid differentiation ability of butyric acid analogues: identification of basal chemical structures of new inducers of foetal haemoglobin.Bianchi N, Chiarabelli C, Zuccato C, Lampronti I, Borgatti M, Amari G, Delcanale M, Chiavilli F, Prus E, Fibach E, Gambari R Eur. J. Pharmacol.2015
Hemoglobin S and C affect protein export in Plasmodium falciparum-infected erythrocytes.Kilian N, Srismith S, Dittmer M, Ouermi D, Bisseye C, Simpore J, Cyrklaff M, Sanchez CP, Lanzer M Biol Open2015
Endothelial nitric oxide synthase gene intron 4 variable number tandem repeat polymorphism in β-thalassemia major: relation to cardiovascular complications.Tantawy AA, Adly AA, Ismail EA, Aly SH Blood Coagul. Fibrinolysis2015
The Role of the Carotid Doppler Examination in the Evaluation of Atherosclerotic Changes in β-Thalassemia Patients.Abdelsamei HA, El-Sherif AM, Ismail AM, Abdel Hakeem GL Mediterr J Hematol Infect Dis2015
Reliability of Different RBC Indices and Formulas in Discriminating between β-Thalassemia Minor and other Microcytic Hypochromic Cases.Bordbar E, Taghipour M, Zucconi BE Mediterr J Hematol Infect Dis2015
Study of serum haptoglobin level and its relation to erythropoietic activity in Beta thalassemia children.Ragab SM, Safan MA, Badr EA Mediterr J Hematol Infect Dis2015
Liver Iron Concentration and Liver Impairment in Relation to Serum IGF-1 Levels in Thalassaemia Major Patients: A Retrospective Study.De Sanctis V, Soliman AT, Candini G, Kattamis C, Raiola G, Elsedfy H Mediterr J Hematol Infect Dis2015
Acute chest syndrome following adenotonsillectomy in a pediatric patient with Hemoglobin SC disease.Plum AW, Mortelliti AJ Int. J. Pediatr. Otorhinolaryngol.2015
Obstructive sleep apnea and sickle cell disease: Towards hemorheological abnormalities and vascular dysfunction worsening.Connes P Sleep Med Rev2015
Anemia: progress in molecular mechanisms and therapies.Sankaran VG, Weiss MJ Nat. Med.2015
Validation of noninvasive hemoglobin measurement by pulse co-oximeter in newborn infants.Nicholas C, George R, Sardesai S, Durand M, Ramanathan R, Cayabyab R J Perinatol2015
Thrombocytosis in a patient with alpha thalassemia trait.Taylor S, Strauch S, Lewis S Lab Med2015
Biochemical markers of glucose metabolism may be used to estimate the degree and progression of iron overload in the liver and pancreas of patients with β-thalassemia major.Bas M, Gumruk F, Gonc N, Cetin M, Tuncer M, Hazırolan T, Yildirim G, Karabulut E, Unal S Ann. Hematol.2015
Recent trends in the gene therapy of β-thalassemia.Finotti A, Breda L, Lederer CW, Bianchi N, Zuccato C, Kleanthous M, Rivella S, Gambari R J Blood Med2015
Ferric Citrate Reduces Intravenous Iron and Erythropoiesis-Stimulating Agent Use in ESRD.Umanath K, Jalal DI, Greco BA, Umeukeje EM, Reisin E, Manley J, Zeig S, Negoi DG, Hiremath AN, Blumenthal SS, Sika M, Niecestro R, Koury MJ, Ma KN, Greene T, Lewis JB, Dwyer JP, J. Am. Soc. Nephrol.2015
Exercise-induced cardiac arrest in a sickle cell trait-positive Air Force recruit: a case report.Fajardo KA, Tchandja J Mil Med2015
Prevalence of vitamin D deficiency in sickle cell disease: a systematic review.Nolan VG, Nottage KA, Cole EW, Hankins JS, Gurney JG PLoS ONE2015
Correction of the sickle cell disease mutation in human hematopoietic stem/progenitor cells.Hoban MD, Cost GJ, Mendel MC, Romero Z, Kaufman ML, Joglekar AV, Ho M, Lumaquin D, Gray D, Lill GR, Cooper AR, Urbinati F, Senadheera S, Zhu A, Liu PQ, Paschon DE, Zhang L, Rebar EJ, Wilber A, Wang X, Gregory PD, Holmes MC, Reik A, Hollis RP, Kohn DB Blood2015
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α-Thalassemia associated with hb instability: a tale of two features. the case of Hb Rogliano or α1 Cod 108(G15)Thr→Asn and Hb Policoro or α2 Cod 124(H7)Ser→Pro.Bisconte MG, Caldora M, Musollino G, Cardiero G, Flagiello A, La Porta G, Lagona L, Prezioso R, Qualtieri G, Gaudiano C, Medulla E, Merlino A, Pucci P, Lacerra G PLoS ONE2015
The recommendation of the International Network of Clinicians for Endocrinopathies in Thalassemia and Adolescent Medicine for the assessment of growth hormone secretion in thalassemia.De Sanctis V, Soliman AT, Candini G, Elsedfy H Indian J Endocrinol Metab2015
Insulin-like growth factor- I and factors affecting it in thalassemia major.Soliman AT, De Sanctis V, Elalaily R, Yassin M Indian J Endocrinol Metab2015
Transcranial Doppler screening in sickle cell disease: The implications of using peak systolic criteria.Naffaa LN, Tandon YK, Irani N World J Radiol2015
Incidence of haemoglobinopathies in Sicily: the impact of screening and prenatal diagnosis.Giambona A, Damiani G, Vinciguerra M, Jakil C, Cannata M, Cassarà F, Picciotto F, Schillaci G, Cigna V, Renda D, Leto F, Passarello C, Maggio A Int. J. Clin. Pract.2015
[Pitfalls in hemoglobin oxygen saturation measurement: a case of chronic desaturation].Eguienta S, Martigne L, Dulucq S, Fayon M Arch Pediatr2015
Altered left ventricular twist is associated with clinical severity in adults and adolescents with homozygous sickle cell anemia.Braga JC, Assef JE, Waib PH, de Sousa AG, de Mattos Barretto RB, Guimarães Filho FV, Rodrigues A, Vilela FD, de Castro Bienert IR, Tan DM, Peluccio DC J Am Soc Echocardiogr2015
Key endothelial cell angiogenic mechanisms are stimulated by the circulating milieu in sickle cell disease and attenuated by hydroxyurea.Lopes FC, Traina F, Almeida CB, Leonardo FC, Franco-Penteado CF, Garrido VT, Colella MP, Soares R, Olalla-Saad ST, Costa FF, Conran N Haematologica2015
Interventions for treating intrahepatic cholestasis in people with sickle cell disease.Martí-Carvajal AJ, Simancas-Racines D Cochrane Database Syst Rev2015
Update of hematopoietic cell transplantation for sickle cell disease.Walters MC Curr. Opin. Hematol.2015
Thalassemia major is a major risk factor for pediatric melioidosis in Kota Kinabalu, Sabah, Malaysia.Fong SM, Wong KJ, Fukushima M, Yeo TW Clin. Infect. Dis.2015
Cerebral lesions on 7 tesla MRI in patients with sickle cell anemia.van der Land V, Zwanenburg JJ, Fijnvandraat K, Biemond BJ, Hendrikse J, Mutsaerts HJ, Visser F, Wardlaw JM, Nederveen AJ, Majoie CB, Nederkoorn PJ Cerebrovasc. Dis.2015
[Two novel potential markers for iron metabolism: hepcidin and non-transferrin-bound iron (NTBI)].Ikuta K Rinsho Ketsueki2015
[Update on the biology of heme synthesis in erythroid cells].Fujiwara T, Harigae H Rinsho Ketsueki2015
Fluid replacement therapy for acute episodes of pain in people with sickle cell disease.Okomo U, Meremikwu MM Cochrane Database Syst Rev2015
Phenotypic differences of CD4(+) T cells in response to red blood cell immunization in transfused sickle cell disease patients.Vingert B, Tamagne M, Habibi A, Pakdaman S, Ripa J, Elayeb R, Galacteros F, Bierling P, Ansart-Pirenne H, Bartolucci P, Noizat-Pirenne F Eur. J. Immunol.2015
EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.Traeger-Synodinos J, Harteveld CL, Old JM, Petrou M, Galanello R, Giordano P, Angastioniotis M, De la Salle B, Henderson S, May A Eur. J. Hum. Genet.2015
Air pollution and children's health: sickle cell disease.Barbosa SM, Farhat SC, Martins LC, Pereira LA, Saldiva PH, Zanobetti A, Braga AL Cad Saude Publica2015
Refractory cardiogenic shock in a patient with β-thalassemia major requiring mechanical circulatory support: Case report and literature review.Horne D, Conway J, Kantor PF, AlAklabi MM, Anand V, Bruce A, Garcia Guerra G, Rebeyka IM, Ross DB, Buchholz H Pediatr Transplant2015
Exercise collapse associated with sickle cell trait (ECAST): case report and literature review.Quattrone RD, Eichner ER, Beutler A, Adams WB, O'Connor FG Curr Sports Med Rep2015
Interethnic diversity of the CD209 (rs4804803) gene promoter polymorphism in African but not American sickle cell disease.Noble JA, Duru KC, Guindo A, Yi L, Imumorin IG, Diallo DA, Thomas BN PeerJ2015
Is low dose hydroxyurea the solution to the global epidemic of sickle cell disease?Strouse JJ Pediatr Blood Cancer2015
Two new β+ -thalassemia mutation [β -56 (G → C); HBBc. -106 G → C] and [β -83 (G → A); HBBc. -133 G → A] described among the Tunisian population.Douzi K, Moumni I, Zorai A, Ben Mustapha M, Ben Mansour IM, Dorra C, Salem A Am. J. Hum. Biol.2015
Negative health implications of sickle cell trait in high income countries: from the football field to the laboratory.Key NS, Connes P, Derebail VK Br. J. Haematol.2015
Delayed haemolytic transfusion reaction in adults with sickle cell disease: a 5-year experience.Vidler JB, Gardner K, Amenyah K, Mijovic A, Thein SL Br. J. Haematol.2015
The effects of an overnight holding of whole blood at room temperature on haemoglobin modification and in vitro markers of red blood cell aging.Eckstein M, Zimmermann R, Roth T, Hauck-Dlimi B, Strasser EF, Xiang W Vox Sang.2015
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Cough and wheeze events are temporally associated with increased pain in individuals with sickle cell disease without asthma.Diep RT, Busani S, Simon J, Punzalan A, Skloot GS, Glassberg JA Br. J. Haematol.2015
Identification of hemoglobin variants by top-down mass spectrometry using selected diagnostic product ions.Coelho Graça D, Hartmer R, Jabs W, Beris P, Clerici L, Stoermer C, Samii K, Hochstrasser D, Tsybin YO, Scherl A, Lescuyer P Anal Bioanal Chem2015
Genetic Modifiers in β-Thalassemia Intermedia: A Study on 102 Iraqi Arab Patients.Al-Allawi NA, Puehringer H, Raheem RA, Oberkanins C Genet Test Mol Biomarkers2015
The clinical significance of K-Cl cotransport activity in red cells of patients with HbSC disease.Rees DC, Thein SL, Osei A, Drasar E, Tewari S, Hannemann A, Gibson JS Haematologica2015
Antibiotics for treating acute chest syndrome in people with sickle cell disease.Martí-Carvajal AJ, Conterno LO, Knight-Madden JM Cochrane Database Syst Rev2015
Beta-globin gene haplotypes among cameroonians and review of the global distribution: is there a case for a single sickle mutation origin in Africa?Bitoungui VJ, Pule GD, Hanchard N, Ngogang J, Wonkam A OMICS2015
2014 William Allan Award: A hematologist's pursuit of hemoglobin genetics.Orkin SH Am. J. Hum. Genet.2015
[Acute painful crisis in a female Nigerian patient with sickle cell disease].Nin S, Seki M, Maie K, Kuroda A, Miyamoto K, Ogawa S, Ito Y, Kurita N, Yokoyama Y, Sakata Yanagimoto M, Obara N, Hasegawa Y, Ogino Y, Ito T, Chiba S Rinsho Ketsueki2015
Factor-induced Reprogramming and Zinc Finger Nuclease-aided Gene Targeting Cause Different Genome Instability in β-Thalassemia Induced Pluripotent Stem Cells (iPSCs).Ma N, Shan Y, Liao B, Kong G, Wang C, Huang K, Zhang H, Cai X, Chen S, Pei D, Chen N, Pan G J. Biol. Chem.2015
Attitudes toward Management of Sickle Cell Disease and Its Complications: A National Survey of Academic Family Physicians.Mainous AG, Tanner RJ, Harle CA, Baker R, Shokar NK, Hulihan MM Anemia2015
Intracranial aneurysms in sickle cell anemia: clinical and imaging findings.Nabavizadeh SA, Vossough A, Ichord RN, Kwiatkowski J, Pukenas BA, Smith MJ, Storm PB, Zager EL, Hurst RW J Neurointerv Surg2015
Molecular characterization of Hb Hamilton Hill (HBA2: c.388delC), a novel HBA2 variant generating a premature termination codon and truncated HBA2 chain.Qadah T, Finlayson J, North E, Ghassemifar R Hemoglobin2015
Use of a dual lumen port for automated red cell exchange in adults with sickle cell disease.Shrestha A, Jawa Z, Koch KL, Rankin AB, Xiang Q, Padmanabhan A, Karafin MS, Field JJ J Clin Apher2015
Acute Sickle Hepatic Crisis after Liver Transplantation in a Patient with Hb SC Disease.Gillis JH, Satapathy SK, Parsa L, Sylvestre PB, Dbouk N Case Rep Transplant2015
Extensive genomic variability of knops blood group polymorphisms is associated with sickle cell disease in Africa.Duru KC, Noble JA, Guindo A, Yi L, Imumorin IG, Diallo DA, Thomas BN Evol. Bioinform. Online2015
Curing sickle cell disease: Mission accomplished?Lipton JM Pediatr Blood Cancer2015
Gross hematuria in sickle cell disease at Tokoin teaching hospital in Lomé (Togo).Guedenon KM, Gbadoe AD, Nouwakpo NB Med Sante Trop2015
Two novel α2 gene mutations causing altered amino acid sequences produce a mild (Hb Kinshasa, HBA2: c.428A > T) and severe (HBA2: c.342-345insCC) α-thalassemia phenotype.Saller E, Dutly F, Frischknecht H Hemoglobin2015
Hemoglobin Valme HBB:c.124T>G: a new hemoglobin variant with diminished oxygen affinity causes interference in hemoglobin A1c measurement in an automated ion-exchange HPLC method.Benítez IC, Lameiro PC, Ropero P, De la Osa JJ, Fernández FG, Ortiz AM Clin. Chem. Lab. Med.2015
Parvovirus B19 infection presenting with severe erythroid aplastic crisis during pregnancy in a woman with autoimmune hemolytic anemia and alpha-thalassemia trait: a case report.Chen CC, Chen CS, Wang WY, Ma JS, Shu HF, Fan FS J Med Case Rep2015
Variation in pediatric emergency department care of sickle cell disease and fever.Ellison AM, Thurm C, Alessandrini E, Jain S, Cheng J, Black K, Schroeder L, Stone K, Alpern ER Acad Emerg Med2015
Aspirin resistance in children and young adults with splenectomized thalassemia diseases.Sirachainan N, Wijarn P, Chuansumrit A, Kadegasem P, Wongwerawattanakoon P, Soisamrong A Thromb. Res.2015
Traffic Light: prognosis-based eligibility for clinical trials of hematopoietic SCT in adults with sickle cell anemia.Rotz SJ, O'Riordan MA, Kim C, de Lima M, Gladwin MT, Little JA Bone Marrow Transplant.2015
Evidence for a profound remodeling of skeletal muscle and its microvasculature in sickle cell anemia.Ravelojaona M, Féasson L, Oyono-Enguéllé S, Vincent L, Djoubairou B, Ewa'Sama Essoue C, Messonnier LA Am. J. Pathol.2015
The Daily Experiences of Adolescents in Lebanon With Sickle Cell Disease.Atoui M, Badr LK, Brand TD, Khoury R, Shahine R, Abboud M J Pediatr Health Care2015
Fetal cardiac Doppler indices in fetuses with hemoglobin Bart's disease at 12-14weeks of gestation.Luewan S, Tongprasert F, Srisupundit K, Tongsong T Int. J. Cardiol.2015
Cultural preferences and limited public resources influence the spectrum of thalassemia in Egypt.Adly AA, Ebeid FS J. Pediatr. Hematol. Oncol.2015
Metal accumulation in the renal cortex of a pediatric patient with sickle cell disease: a case report and review of the literature.Maximova N, Zanon D, Pascolo L, Zennaro F, Gregori M, Grosso D, Sonzogni A J. Pediatr. Hematol. Oncol.2015
How I treat priapism.Anele UA, Le BV, Resar LM, Burnett AL Blood2015
Health related quality of life and perception of stigmatisation in adolescents living with sickle cell disease in Nigeria: A cross sectional study.Adeyemo TA, Ojewunmi OO, Diaku-Akinwumi IN, Ayinde OC, Akanmu AS Pediatr Blood Cancer2015
Hemoglobin βCys93 is essential for cardiovascular function and integrated response to hypoxia.Zhang R, Hess DT, Qian Z, Hausladen A, Fonseca F, Chaube R, Reynolds JD, Stamler JS Proc. Natl. Acad. Sci. U.S.A.2015
Late complications of mixed chimerism following allogeneic bone marrow transplantation for thalassemia major.Spitzer B, Giardina PJ, O'Reilly RJ, Boulad F Pediatr Blood Cancer2015
Safety and efficacy of blood exchange transfusion for priapism complicating sickle cell disease.Ballas SK, Lyon D J Clin Apher2015
Current attitudes of parents and patients toward hematopoietic stem cell transplantation for sickle cell anemia.Meier ER, Dioguardi JV, Kamani N Pediatr Blood Cancer2015
Deferiprone versus deferoxamine in thalassemia intermedia: Results from a 5-year long-term Italian multicenter randomized clinical trial.Calvaruso G, Vitrano A, Di Maggio R, Lai E, Colletta G, Quota A, Gerardi C, Rigoli LC, Sacco M, Pitrolo L, Maggio A Am. J. Hematol.2015
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Survival and mortality among users and non-users of hydroxyurea with sickle cell Araujo OM, Ivo ML, Ferreira Júnior MA, Pontes ER, Bispo IM, de Oliveira EC Rev Lat Am Enfermagem2015
Is the medical home for adult patients with sickle cell disease a reality or an illusion?Ballas SK, Vichinsky EP Hemoglobin2015
Genetic Modifiers of Sickle Cell Disease: A Genotype-Phenotype Relationship Study in a Cohort of 82 Children on Mayotte Island.Muszlak M, Pissard S, Badens C, Chamouine A, Maillard O, Thuret I Hemoglobin2015
Screening for thalassemia carriers in populations with a high rate of iron deficiency: revisiting the applicability of the Mentzer Index and the effect of iron deficiency on Hb A2 levels.Amid A, Haghi-Ashtiani B, Kirby-Allen M, Haghi-Ashtiani MT Hemoglobin2015
Sickle cell disease: time for a targeted neonatal screening programme.Gibbons C, Geoghegan R, Conroy H, Lippacott S, O'Brien D, Lynam P, Langabeer L, Cotter M, Smith O, McMahon C Ir Med J2015
Molecular mechanisms of erythrocyte aging.Hoehn RS, Jernigan PL, Chang AL, Edwards MJ, Pritts TA Biol. Chem.2015
Erythrocyte indices in Pre-school Nigerian Children with Sickle Cell Anaemia in Steady State.Akodu SO, Njokanma OF, AdeoluKehinde O Int J Hematol Oncol Stem Cell Res2015
Myelodysplastic syndrome with clonal cytogenetic abnormalities followed by fatal erythroid leukemia after 14 years of exposure to hydroxyurea for sickle cell anemia.Aumont C, Driss F, Lazure T, Picard V, Creidy R, De Botton S, Saada V, Lambotte O, Bilhou-Nabera C, Tertian G, Michot JM Am. J. Hematol.2015
Combination therapy - deferasirox and deferoxamine - in thalassemia major patients in emerging countries with limited resources.Arandi N, Haghpanah S, Safaei S, Zahedi Z, Ashrafi A, Eatemadfar P, Zarei T, Radwan AH, Taher AT, Karimi M Transfus Med2015
Adverse maternal and perinatal outcomes in pregnant women with sickle cell disease: systematic review and meta-analysis.Oteng-Ntim E, Meeks D, Seed PT, Webster L, Howard J, Doyle P, Chappell LC Blood2015
Hemoglobin Constant Spring exhibits prolonged ex vivo stability when assessed by HPLC.Estey MP, Belletrutti M, Rodriguez-Capote K, Higgins T Clin. Biochem.2015
[Diagnosis and prenatal diagnosis to a family of hemoglobin variant with α-thalassemia].Du L, Wu J, Qin D, Wang J, Luo M, Guo H, Yuan T, Zhang Y, Wang Y, Yin A Zhonghua Yi Xue Yi Chuan Xue Za Zhi2015
Cirrhosis: an unusual presentation of sickle cell disease.Dosi R, Patell R, Jariwala P, Shah P, Jasdanwala S J Clin Diagn Res2015
Fortuitous description of haemoglobin A2' [δ16 (A13) Gly→Arg (GGC→CGC)] in a Tunisian family: study of the molecular defect and its origin.Sahli CA, Gritli S, Dabboubi R, Omar S, Siala H, Kaabachi N, Bibi A, Messaoud T Ann. Biol. Clin. (Paris)2015
Imaging flow cytometry for the study of erythroid cell biology and pathology.Samsel L, McCoy JP J. Immunol. Methods2015
First Detection of a Splice Site β-Thalassemia Mutation, IVS-I-6 (T > C) (HBB: c.92 + 6T > C) in a Chinese Family.Chen B, Huang P, Yi S, Chen Q, Tang Y, Zhang Q, He S Hemoglobin2015
Estimated pulmonary artery systolic pressure and sickle cell disease: a meta-analysis and systematic review.Caughey MC, Poole C, Ataga KI, Hinderliter AL Br. J. Haematol.2015
Distinctive patterns of evolution of the δ-globin gene (HBD) in primates.Moleirinho A, Lopes AM, Seixas S, Morales-Hojas R, Prata MJ, Amorim A PLoS ONE2015
Response to hydroxyurea among Kuwaiti patients with sickle cell disease and elevated baseline HbF levels.Adekile A, Menzel S, Gupta R, Al-Sharida S, Farag A, Haider M, Akbulut N, Mustafa N, Thein SL Am. J. Hematol.2015
Dramatic erythroid response to low-dose thalidomide in two patients with transfusion independent thalassemia and severe post-transfusional alloimmune hemolysis.Fozza C, Pardini S, Giannico DB, Targhetta C, Di Tucci AA, Dessalvi P, Angelucci E, Dore F Am. J. Hematol.2015
Increase of microRNA-210, decrease of raptor gene expression and alteration of mammalian target of rapamycin regulated proteins following mithramycin treatment of human erythroid cells.Bianchi N, Finotti A, Ferracin M, Lampronti I, Zuccato C, Breveglieri G, Brognara E, Fabbri E, Borgatti M, Negrini M, Gambari R PLoS ONE2015
Genetic heterogeneity of the β-globin gene in various geographic populations of Yunnan in southwestern China.Zhang J, He J, Zeng XH, Ge SJ, Huang Y, Su J, Ding XM, Yang JQ, Cao YJ, Chen H, Zhang YH, Zhu BS PLoS ONE2015
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Reduced fitness and abnormal cardiopulmonary responses to maximal exercise testing in children and young adults with sickle cell anemia.Liem RI, Reddy M, Pelligra SA, Savant AP, Fernhall B, Rodeghier M, Thompson AA Physiol Rep2015
Hydroxyurea lowers transcranial Doppler flow velocities in children with sickle cell anaemia in a Nigerian cohort.Lagunju I, Brown BJ, Sodeinde O Pediatr Blood Cancer2015
Phytomedicines (medicines derived from plants) for sickle cell disease.Oniyangi O, Cohall DH Cochrane Database Syst Rev2015
The sickle cell mouse lung: proinflammatory and primed for allergic inflammation.Andemariam B, Adami AJ, Singh A, McNamara JT, Secor ER, Guernsey LA, Thrall RS Transl Res2015
Assessing Parental Knowledge About Thalassemia in a Thalassemia Center of Karachi, Pakistan.Maheen H, Malik F, Siddique B, Qidwai A J Genet Couns2015
Cognitive behavioral therapy in patients with sickle cell disease.Daniels S Creat Nurs2015
Polymorphic variations influencing fetal hemoglobin levels: association study in beta-thalassemia carriers and in normal individuals of Portuguese origin.Pereira C, Relvas L, Bento C, Abade A, Ribeiro ML, Manco L Blood Cells Mol. Dis.2015
The effect of sleep continuity on pain in adults with sickle cell disease.Moscou-Jackson G, Finan PH, Campbell CM, Smyth JM, Haythornthwaite JA J Pain2015
[Information for parents of children with sickle cell trait detected by neonatal screening: A 10-year experience].Joly P, Badens C, Fekih S, Philippe N, Merono F, Thuret I, Pondarré C Arch Pediatr2015
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Molecular Basis of β-Thalassemia Intermedia in Erbil Province of Iraqi Kurdistan.Shamoon RP, Al-Allawi NA, Cappellini MD, Di Pierro E, Brancaleoni V, Granata F Hemoglobin2015
Simultaneous anterior and posterior segment fluorescein angiography in sickle cell disease.Kourti P, Pournaras JA Klin Monbl Augenheilkd2015
Compensation of CD55 Underexpression on Red Blood Cells of β-Thalassemia Major Patients.Obaid JM, Abo El-Nazar SY, Ghanem AM, El-Hadidi AS, Mersal BH Hemoglobin2015
α(+)-Thalassemia Due to a Frameshift Mutation of the α2-Globin Gene [codons 55/56 (+T) or HBA2: c.168dup].Waye JS, Eng B, Hanna M, Hohenadel BA, Nakamura LM, Walker L Hemoglobin2015
Hb H Hydrops Fetalis Syndrome Caused by Association of the - -(SEA) Deletion and Hb Constant Spring (HBA2: c.427T > C) Mutation in a Chinese Family.He S, Zheng C, Meng D, Chen R, Zhang Q, Tian X, Chen S Hemoglobin2015
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Multi-allele DNA biosensor for the rapid genotyping of 'nondeletion' alpha thalassaemia mutations in HBA1 and HBA2 genes by means of multiplex primer extension reaction.Petropoulou M, Poula A, Traeger-Synodinos J, Kanavakis E, Christopoulos TK, Ioannou PC Clin. Chim. Acta2015
Gout and sickle cell disease: not all pain is sickle cell pain.Gupta S, Yui JC, Xu D, Fitzhugh CD, Clark C, Siddiqui S, Conrey AK, Kato GJ, Minniti CP Br. J. Haematol.2015
Differential gene expression analysis in early and late erythroid progenitor cells in β-thalassaemia.Forster L, McCooke J, Bellgard M, Joske D, Finlayson J, Ghassemifar R Br. J. Haematol.2015
Red blood cell transfusions are associated with HLA class I but not H-Y alloantibodies in children with sickle cell disease.Nickel RS, Hendrickson JE, Yee MM, Bray RA, Gebel HM, Kean LS, Miklos DB, Horan JT Br. J. Haematol.2015
Effect of iron chelator desferrioxamine on serum zinc levels in patients with beta thalassemia major.Sultan S, Irfan SM, Kakar J, Zeeshan R Malays J Pathol2015
Nanoscale Surface Characterization of Human Erythrocytes by Atomic Force Microscopy: A Critical Review.Mukherjee R, Saha M, Routray A, Chakraborty C IEEE Trans Nanobioscience2015
Dietary ω-3 fatty acids protect against vasculopathy in a transgenic mouse model of sickle cell disease.Kalish BT, Matte A, Andolfo I, Iolascon A, Weinberg O, Ghigo A, Cimino J, Siciliano A, Hirsch E, Federti E, Puder M, Brugnara C, De Franceschi L Haematologica2015
Hb M-Iwate in an Indian family.Kumar GV, Sharma P, Chhabra S, Hira JK, Trehan A, Das R Clin. Chim. Acta2015
RN-1, a potent and selective lysine-specific demethylase 1 inhibitor, increases γ-globin expression, F reticulocytes, and F cells in a sickle cell disease mouse model.Rivers A, Vaitkus K, Ruiz MA, Ibanez V, Jagadeeswaran R, Kouznetsova T, DeSimone J, Lavelle D Exp. Hematol.2015
Hydroxyurea use in prevention of stroke recurrence in children with sickle cell disease in a developing country: A cost effectiveness analysis.Cunningham-Myrie C, Abdulkadri A, Waugh A, Bortolusso Ali S, King LG, Knight-Madden J, Reid M Pediatr Blood Cancer2015
Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer.Mtatiro SN, Mgaya J, Singh T, Mariki H, Rooks H, Soka D, Mmbando B, Thein SL, Barrett JC, Makani J, Cox SE, Menzel S BMC Med. Genet.2015
Serologic evaluation of celiac disease in patients with beta thalassemia major and control.Shahramian I, Dehghani SM, Haghighat M, Noori NM, Teimouri AR, Sharafi E, Kalili M Gastroenterol Hepatol Bed Bench2015
Examining the usefulness of a Family Empowerment Program guided by the Illness Beliefs Model for families caring for a child with thalassemia.Wacharasin C, Phaktoop M, Sananreangsak S J Fam Nurs2015
Pregnancy outcomes among women with hemoglobin E trait.Kemthong W, Jatavan P, Traisrisilp K, Tongsong T J. Matern. Fetal. Neonatal. Med.2015
Correlation of hepcidin level with insulin resistance and endocrine glands function in major thalassemia.Al-Hakeim HK, Al-Khakani MM, Al-Kindi MA Adv Clin Exp Med2015
Magnetic resonance comparison of left-right heart volumetric and functional parameters in thalassemia major and thalassemia intermedia patients.Liguori C, Pitocco F, Di Giampietro I, De Vivo AE, Schena E, Giurazza F, Sorrentino F, Zobel BB Biomed Res Int2015
Study of Adrenal Functions using ACTH stimulation test in Egyptian children with Sickle Cell Anemia: Correlation with Iron Overload.A Hagag A, S El-Farargy M, M Abo El-Enein A Int J Hematol Oncol Stem Cell Res2015
Hepatic iron overload and fibrosis in patients with beta thalassemia major after hematopoietic stem cell transplantation: A pilot study.Ghavamzadeh A, Mirzania M, Kamalian N, Sedighi N, Azimi P Int J Hematol Oncol Stem Cell Res2015
Thalassaemia and risk of cancer: a population-based cohort study.Chung WS, Lin CL, Lin CL, Kao CH J Epidemiol Community Health2015
Molecular identification of rare FY*Null and FY*X alleles in Caucasian thalassemic family from Sardinia.Manfroi S, Scarcello A, Pagliaro P Transfus. Apher. Sci.2015
[Molecular bases of α-thalassemia in Argentina].Scheps KG, Francipane L, Nash A, Cerrone GE, Copelli SB, Varela V Medicina (B Aires)2015
50 Years Ago in The Journal of Pediatrics: Normal Response of Sickle Cell Anemia Patients to Immunization with Salmonella Vaccines.Forster CS J. Pediatr.2015
Safety of deep sedation in young children with sickle cell disease: a retrospective cohort study.Belmont AP, Nossair F, Brambilla D, Friedman M, Boswinkel J, Bradford AB, Kwiatkowski JL J. Pediatr.2015
Proportion of adults with sickle cell anemia and pain crises receiving hydroxyurea.Stettler N, McKiernan CM, Melin CQ, Adejoro OO, Walczak NB JAMA2015
Satisfied or not satisfied: pain experiences of patients with sickle cell disease.Ezenwa MO, Molokie RE, Wang ZJ, Suarez ML, Yao Y, Wilkie DJ J Adv Nurs2015
Erythropoietin in the general population: reference ranges and clinical, biochemical and genetic correlates.Grote Beverborg N, Verweij N, Klip IT, van der Wal HH, Voors AA, van Veldhuisen DJ, Gansevoort RT, Bakker SJ, van der Harst P, van der Meer P PLoS ONE2015
G6PD Deficiency and Hemoglobinopathies: Molecular Epidemiological Characteristics and Healthy Effects on Malaria Endemic Bioko Island, Equatorial Guinea.Lin M, Yang LY, Xie DD, Chen JT, Nguba SM, Ehapo CS, Zhan XF, Eyi JU, Matesa RA, Obono MM, Yang H, Yang HT, Cheng JD PLoS ONE2015
The Effectiveness of self management program on quality of life in patients with sickle cell disease.Ahmadi M, Jahani S, Poormansouri S, Shariati A, Tabesh H Iran J Ped Hematol Oncol2015
The Correlation between Serum Level of Leptin and Troponin in Children with Major Beta-Thalassemia.Shahramian I, Noori NM, Teimouri A, Akhlaghi E, Sharafi E Iran J Ped Hematol Oncol2015
Red blood cell parameters in antenatal nonsickling hemoglobinopathy screening.Bencaiova G, Dapoto K, Zimmermann R, Krafft A Int J Womens Health2015
[Infectious complications after surgical splenectomy in children with sickle cell anemia disease].Monaco Junior CP, Fonseca PB, Braga JA Rev Paul Pediatr2015
Apolipoproteins A1, B, and other prognostic biochemical cardiovascular risk factors in patients with beta-thalassemia major.Ghorban K, Shanaki M, Mobarra N, Azad M, Asadi J, Pakzad R, Ehteram H Hematology2015
Hematopoietic Stem Cell Transplantation in Adult Sickle Cell Disease: Problems and Solutions.Özdoğu H, Boğa C Turk J Haematol2015
Effects of nitric oxide and its congeners on sickle red blood cell deformability.Belanger AM, Keggi C, Kanias T, Gladwin MT, Kim-Shapiro DB Transfusion2015
Microarchitectural and mechanical characterization of the sickle bone.Green M, Akinsami I, Lin A, Banton S, Ghosh S, Chen B, Platt M, Osunkwo I, Ofori-Acquah S, Guldberg R, Barabino G J Mech Behav Biomed Mater2015
Pseudo-Gaucher Cells in Thalassemia Intermedia.Gajendra S, Sachdev R Int. J. Surg. Pathol.2015
Biological parameters predictive of percent dense red blood cell decrease under hydroxyurea.Rakotoson MG, Di Liberto G, Audureau E, Habibi A, Fauroux C, Khorgami S, Hulin A, Loric S, Noizat-Pirenne F, Galacteros F, Bartolucci P Orphanet J Rare Dis2015
Neonatal screening for α-thalassemia by cord hemoglobin Barts: how effective is it?Wu MY, Xie XM, Li J, Li DZ Int J Lab Hematol2015
Positron Emission Tomography With 18F-Fluorodeoxyglucose in Patients With Sickle Cell Acute Chest Prost N, Sasanelli M, Deux JF, Habibi A, Razazi K, Galactéros F, Meignan M, Maître B, Brun-Buisson C, Itti E, Mekontso Dessap A Medicine (Baltimore)2015
Single-cell evaluation of red blood cell bio-mechanical and nano-structural alterations upon chemically induced oxidative stress.Sinha A, Chu TT, Dao M, Chandramohanadas R Sci Rep2015
Efficiency assessment of immunochromatographic strip test for the diagnosis of alpha-thalassemia-1 carriers.Sudjaroen Y J Lab Physicians2015
[Effect of astaxanthin on oxidative stress of red blood cells and peroxidation damage of membrane].Wang SL, He LJ, He TB, Han W, Wang Q Zhongguo Shi Yan Xue Ye Xue Za Zhi2015
[Correlation between the Expression of microRNA 451 in Red Blood Cells and Chronic Mountain Sickness].Wang ZY, Yang FM, Liu J, Li R, Li XP, Jing ZH Zhongguo Shi Yan Xue Ye Xue Za Zhi2015
Correlation between the Lactate Dehydrogenase Levels with Laboratory Variables in the Clinical Severity of Sickle Cell Anemia in Congolese Patients.Mikobi TM, Lukusa Tshilobo P, Aloni MN, Mvumbi Lelo G, Akilimali PZ, Muyembe-Tamfum JJ, Race V, Matthijs G, Mbuyi Mwamba JM PLoS ONE2015
Non-transfusion-dependent thalassemia: a complex mix of genetic entities yet to be fully discovered.Ricchi P, Filosa A, Maggio A, Fucharoen S Biomed Res Int2015
How I manage cerebral vasculopathy in children with sickle cell disease.Brousse V, Kossorotoff M, de Montalembert M Br. J. Haematol.2015
Hb Cervantes, Hb Marañón, Hb La Mancha and Hb Goya: Description of 4 new la Fuente-Gonzalo F, Nieto JM, Ricard P, Anguita J, Martínez R, Cervera A, Villegas A, González FA, Ropero P Clin. Biochem.2015
Extracellular hemoglobin: the case of a friend turned foe.Quaye IK Front Physiol2015
Malaria continues to select for sickle cell trait in Central Africa.Elguero E, Délicat-Loembet LM, Rougeron V, Arnathau C, Roche B, Becquart P, Gonzalez JP, Nkoghe D, Sica L, Leroy EM, Durand P, Ayala FJ, Ollomo B, Renaud F, Prugnolle F Proc. Natl. Acad. Sci. U.S.A.2015
Molecular spectrum of α-globin gene mutations in the Aegean region of Turkey: first observation of three α-globin gene mutations in the Turkish population.Onay H, Aykut A, Karaca E, Durmaz A, Solmaz AE, Çoğulu Ö, Aydınok Y, Vergin C, Özkınay F Int. J. Hematol.2015
Restrictive and liberal red cell transfusion strategies in adult patients: reconciling clinical data with best practice.Mirski MA, Frank SM, Kor DJ, Vincent JL, Holmes DR Crit Care2015
BCL11A deletions result in fetal hemoglobin persistence and neurodevelopmental alterations.Basak A, Hancarova M, Ulirsch JC, Balci TB, Trkova M, Pelisek M, Vlckova M, Muzikova K, Cermak J, Trka J, Dyment DA, Orkin SH, Daly MJ, Sedlacek Z, Sankaran VG J. Clin. Invest.2015
Histone H3.3 is required for endogenous retroviral element silencing in embryonic stem cells.Elsässer SJ, Noh KM, Diaz N, Allis CD, Banaszynski LA Nature2015
Alpha-thalassemia X-linked intellectual disability syndrome identified by whole exome sequencing in two boys with white matter changes and developmental retardation.Lee JS, Lee S, Lim BC, Kim KJ, Hwang YS, Choi M, Chae JH Gene2015
Improving survival for children with sickle cell disease: newborn screening is only the first step.McGann PT Paediatr Int Child Health2015
Fanconi's Anemia Effect or Sickle Cell Anemia Effect: That is the Question.Unal S, Chui DH, Gumruk F Hemoglobin2015
Evaluation of Mental Health and Physical Pain in Patients with β-Thalassemia Major in Northern Greece.Vlachaki E, Neokleous N, Paspali D, Vetsiou E, Onoufriadis E, Sousos N, Hissan S, Vakalopoulou S, Garypidou V, Boura P Hemoglobin2015
A 21 Nucleotide Duplication on the α1- and α2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease.Farashi S, Faramarzi Garous N, Zeinali F, Vakili S, Ashki M, Imanian H, Najmabadi H, Azarkeivan A, Tamaddoni A Hemoglobin2015
Thalassemia major between liver and heart: Where we are now.Dessì C, Leoni G, Moi P, Danjou F, Follesa I, Foschini ML, Morittu M, Zappu A, Defraia E, Bina P, Cunico A, Civolani A, Podda RA, Origa R Blood Cells Mol. Dis.2015
Development of a capillary zone electrophoresis method for rapid determination of human globin chains in α and β-thalassemia subjects.Lin L, Chen DN, Guo J, Zhou WJ, Xu XM Blood Cells Mol. Dis.2015
The effects of hydroxyurea and bone marrow transplant on Anti-Müllerian hormone (AMH) levels in females with sickle cell anemia.Elchuri SV, Williamson RS, Clark Brown R, Haight AE, Spencer JB, Buchanan I, Hassen-Schilling L, Brown MR, Mertens AC, Meacham LR Blood Cells Mol. Dis.2015
Omega 3 (n-3) fatty acids down-regulate nuclear factor-kappa B (NF-κB) gene and blood cell adhesion molecule expression in patients with homozygous sickle cell disease.Daak AA, Elderdery AY, Elbashir LM, Mariniello K, Mills J, Scarlett G, Elbashir MI, Ghebremeskel K Blood Cells Mol. Dis.2015
Co-inheritance of novel ATRX gene mutation and globin (α & β) gene mutations in transfusion dependent beta-thalassemia patients.Al-Nafie AN, Borgio JF, AbdulAzeez S, Al-Suliman AM, Qaw FS, Naserullah ZA, Al-Jarrash S, Al-Madan MS, Al-Ali RA, AlKhalifah MA, Al-Muhanna F, Steinberg MH, Al-Ali AK Blood Cells Mol. Dis.2015
Genotype-phenotype correlation and report of novel mutations in β-globin gene in thalassemia patients.Nagar R, Sinha S, Raman R Blood Cells Mol. Dis.2015
Early insights into the neurobiology of pain in sickle cell disease: A systematic review of the literature.Brandow AM, Farley RA, Panepinto JA Pediatr Blood Cancer2015
Quantitative microfluidic fluorescence microscopy to study vaso-occlusion in sickle cell disease.Jimenez MA, Tutuncuoglu E, Barge S, Novelli EM, Sundd P Haematologica2015
The effect of thalassemia on erythrocyte reference intervals in a representative Han Chinese adult population.Xu JH, Hao XK, Mu RQ, Pan BS, Zhang J, Peng MT, Wang LL, Huang XZ, Ma YY, Zhao M, Guo W, Qiao R, Chen WX, Jiang H, Shang H Clin. Lab.2015
Identification of a novel class of covalent modifiers of hemoglobin as potential antisickling agents.Omar AM, Mahran MA, Ghatge MS, Chowdhury N, Bamane FH, El-Araby ME, Abdulmalik O, Safo MK Org. Biomol. Chem.2015
Noninvasive Assessment of Excessive Erythrocytosis as a Screening Method for Chronic Mountain Sickness at High Altitude.Vyas KJ, Danz D, Gilman RH, Wise RA, León-Velarde F, Miranda JJ, Checkley W High Alt. Med. Biol.2015
Hip Dysfunction and Quality of Life in Patients With Sickle Cell Disease.Malheiros CD, Lisle L, Castelar M, Sá KN, Matos MA Clin Pediatr (Phila)2015
Higher nocturnal and awake oxygen saturations in children with sickle cell disease receiving hydroxyurea therapy.Narang I, Kadmon G, Lai D, Dhanju S, Kirby-Allen M, Odame I, Amin R, Lu Z, Al-Saleh S Ann Am Thorac Soc2015
Association of HLA class II alleles with hepatitis C virus clearance and persistence in thalassemia patients from Iran.Samimi-Rad K, Sadeghi F, Amirzargar A, Eshraghian MR, Alavian SM, Rahimnia R J. Med. Virol.2015
Effectiveness of Prenatal Screening for Hemoglobinopathies in a Developing Country.Choudhuri S, Sen A, Ghosh MK, Misra S, Bhattacharyya M Hemoglobin2015
Hypersensitivity reaction with deferasirox.Sharma A, Arora E, Singh H J Pharmacol Pharmacother2015
The Association Between Thalassemia Major and Periodontal Health.Akcalı A, Kahraman Çeneli S, Gümüş P, Buduneli N, Lappin DF, Özçaka Ö J. Periodontol.2015
How we treat delayed haemolytic transfusion reactions in patients with sickle cell disease.Gardner K, Hoppe C, Mijovic A, Thein SL Br. J. Haematol.2015
White Matter Damage Relates to Oxygen Saturation in Children With Sickle Cell Anemia Without Silent Cerebral Infarcts.Kawadler JM, Kirkham FJ, Clayden JD, Hollocks MJ, Seymour EL, Edey R, Telfer P, Robins A, Wilkey O, Barker S, Cox TC, Clark CA Stroke2015
Iron overload in transfusion-dependent thalassemia.Saliba A, Taher A Hematology2015
Increased false positive Down syndrome screening in women with sickle cell anemia.Kneitel AW, Rhee-Morris L, Obadia R, Towner D Prenat. Diagn.2015
Red cell alloimmunization in multi-transfused patients with sickle cell anemia in Benin City, Nigeria.Ugwu NI, Awodu OA, Bazuaye GN, Okoye AE Niger J Clin Pract2015
Psychological therapies for sickle cell disease and pain.Anie KA, Green J Cochrane Database Syst Rev2015
Negative Epistasis between Sickle and Foetal Haemoglobin Suggests a Reduction in Protection against Malaria.Mmbando BP, Mgaya J, Cox SE, Mtatiro SN, Soka D, Rwezaula S, Meda E, Msaki E, Snow RW, Jeffries N, Geller NL, Makani J PLoS ONE2015
GFR in Patients with β-Thalassemia Major.Milo G, Feige Gross Nevo R, Pazgal I, Gafter-Gvili A, Shpilberg O, Gafter U, Erman A, Stark P Clin J Am Soc Nephrol2015
Pulmonary hypertension in non-transfusion-dependent thalassemia: Correlation with clinical parameters, liver iron concentration, and non-transferrin-bound iron.Inthawong K, Charoenkwan P, Silvilairat S, Tantiworawit A, Phrommintikul A, Choeyprasert W, Natesirinilkul R, Siwasomboon C, Visrutaratna P, Srichairatanakool S, Chattipakorn N, Sanguansermsri T Hematology2015
Alloimmunization is associated with older age of transfused red blood cells in sickle cell disease.Desai PC, Deal AM, Pfaff ER, Qaqish B, Hebden LM, Park YA, Ataga KI Am. J. Hematol.2015
Sickle cell disease and H3Africa: enhancing genomic research on cardiovascular diseases in African patients.Wonkam A, Makani J, Ofori-Aquah S, Nnodu OE, Treadwell M, Royal C, Ohene-Frempong K, Cardiovasc J Afr2015
Selected highlights of the VIII International Symposium of Clinicians for Endocrinopathies in Thalassemia and Adolescent Medicine (ICET-A) on Growth, Puberty and Endocrine Complications in Thalassaemia. Auditorium of the Sultan Qaboos University (SQU) Muscat (Sultanate of Oman), 20th of December 2014.De Sanctis V, Soliman AT, Wali Y, Elsedfy H, Daar S, Al-Yaarubi SA, Mevada ST, Tony S, Elshinawy M, Fawzy H, Al-Subhi T, Al-Rawas A, Al-Muslehi M, El Kholy M Pediatr Endocrinol Rev2015
Community healthcare workers' perception of an educational intervention in the care of patients with sickle cell disease in Brazil.Gomes LM, de Andrade Barbosa TL, Vieira ED, Vieira LJ, Castro KP, Pereira IA, Caldeira AP, de Carvalho Torres H, Viana MB Mediterr J Hematol Infect Dis2015
MALDI-ISD Mass Spectrometry Analysis of Hemoglobin Variants: a Top-Down Approach to the Characterization of Hemoglobinopathies.Théberge R, Dikler S, Heckendorf C, Chui DH, Costello CE, McComb ME J. Am. Soc. Mass Spectrom.2015
Brain venular pattern by 7T MRI correlates with memory and haemoglobin in sickle cell anaemia.Novelli EM, Elizabeth Sarles C, Jay Aizenstein H, Ibrahim TS, Butters MA, Connelly Ritter A, Erickson KI, Rosano C Psychiatry Res2015
Survival analysis and its associated factors of Beta thalassemia major in hamadan province.Zamani R, Khazaei S, Rezaeian S Iran J Med Sci2015
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Development of hemoglobin typing control materials for laboratory investigation of thalassemia and hemoglobinopathies.Pornprasert S, Tookjai M, Punyamung M, Pongpunyayuen P, Jaiping K Clin. Chem. Lab. Med.2015
Sickle-cell disease: a call to action.Piel FB, Weatherall DJ Trans. R. Soc. Trop. Med. Hyg.2015
Sickle-cell Anemia and Latent Diastolic Dysfunction: Echocardiographic Alterations.Fattori A, Oliveira DC, Castilho RF, Coelho OR Arq. Bras. Cardiol.2015
Correction: prevalence of vitamin d deficiency in sickle cell disease: a systematic review. PLoS ONE2015
Physical activity level is not a determinant of autonomic nervous system activity and clinical severity in children/adolescents with sickle cell anemia: A pilot study.Charlot K, Moeckesch B, Jumet S, Romana M, Waltz X, Divialle-Doumdo L, Hardy-Dessources MD, Petras M, Tressières B, Pichon A, Tarer V, Hue O, Etienne-Julan M, Antoine-Jonville S, Connes P Pediatr Blood Cancer2015
Life-threatening delayed hyperhemolytic transfusion reaction in a patient with sickle cell disease: effective treatment with eculizumab followed by rituximab.Boonyasampant M, Weitz IC, Kay B, Boonchalermvichian C, Liebman HA, Shulman IA Transfusion2015
Hemoglobin H identification by high-performance liquid chromatography in confirmed hemoglobin H disease.Turley E, McFarlane A, Halchuk L, Verhovsek M Int J Lab Hematol2015
Hemoglobin detection using carbon dots as a fluorescence probe.Barati A, Shamsipur M, Abdollahi H Biosens Bioelectron2015
Correlation between liver iron concentration determined by magnetic resonance imaging and serum ferritin in adolescents with thalassaemia disease.Chuansumrit A, Laothamathat J, Sirachainan N, Sungkarat W, Wongwerawattanakoon P, Kumkrua P Paediatr Int Child Health2015
Predictors of abnormal bone mass density in adult patients with homozygous sickle-cell disease.Garadah TS, Hassan AB, Jaradat AA, Diab DE, Kalafalla HO, Kalifa AK, Sequeira RP, Alawadi AH Clin Med Insights Endocrinol Diabetes2015
[Diagnosis and management of priapism].Kaminsky A, Sperling H Urologe A2015
Sickle cell disease is associated with iron mediated hypercoagulability.Shah N, Welsby IJ, Fielder MA, Jacobsen WK, Nielsen VG J. Thromb. Thrombolysis2015
Pharmacological Induction of Human Fetal Globin Gene in Hydroxyurea-Resistant Primary Adult Erythroid Cells.Chou YC, Chen RL, Lai ZS, Song JS, Chao YS, Shen CK Mol. Cell. Biol.2015
Daily home opioid use in adults with sickle cell disease: The PiSCES project.Smith WR, McClish DK, Dahman BA, Levenson JL, Aisiku IP, de A Citero V, Bovbjerg VE, Roberts JD, Penberthy LT, Roseff SD J Opioid Manag2015
Safety and Efficacy of High-dose Daily Vitamin D3 Supplementation in Children and Young Adults With Sickle Cell Disease.Dougherty KA, Bertolaso C, Schall JI, Smith-Whitley K, Stallings VA J. Pediatr. Hematol. Oncol.2015
High rate of sickle cell anaemia in Sub-Saharan Africa underlines the need to screen all children with severe anaemia for the disease.Kadima BT, Gini Ehungu JL, Ngiyulu RM, Ekulu PM, Aloni MN Acta Paediatr.2015
Nurses' attitudes toward patients with sickle cell disease: a worksite comparison.Jenerette CM, Pierre-Louis BJ, Matthie N, Girardeau Y Pain Manag Nurs2015
Genetic polymorphism of APOB is associated with diabetes mellitus in sickle cell disease.Zhang X, Zhang W, Saraf SL, Nouraie M, Han J, Gowhari M, Hassan J, Miasnikova G, Sergueeva A, Nekhai S, Kittles R, Machado RF, Garcia JG, Gladwin MT, Steinberg MH, Sebastiani P, McClain DA, Gordeuk VR Hum. Genet.2015
Mechanism of testosterone deficiency in the transgenic sickle cell mouse.Musicki B, Zhang Y, Chen H, Brown TR, Zirkin BR, Burnett AL PLoS ONE2015
Serum Ferritin Levels Correlation With Heart and Liver MRI and LIC in Patients With Transfusion-Dependent Thalassemia.Majd Z, Haghpanah S, Ajami GH, Matin S, Namazi H, Bardestani M, Karimi M Iran Red Crescent Med J2015
MR imaging of spleen in beta-thalassemia major.Papakonstantinou O, Drakonaki EE, Maris T, Vasiliadou A, Papadakis A, Gourtsoyiannis N Abdom Imaging2015
Thalassemia Major: Who Is Afraid of Serum Ferritin below 500 μg/l?Pinna F, Carta R, Morittu M, Dessì C, Moi P, Leoni G, Foschini ML, Defraia E, Zappu A, Origa R Acta Haematol.2015
Uncommon Posterior Reversible Encephalopathy Syndrome in a Sickle-Cell Patient.Landais A, Lemonne N, Etienne-Julan M J Clin Neurol2015
Coexistence of sickle cell nephropathy and lupus nephritis in a Sudanese child.Idris AB, Abdulgayoom A, Mudawi E, El Hassan AM, Elamin EM, El Hassan LA Saudi J Kidney Dis Transpl2015
Efficacy of autologous stem cell-based therapy for osteonecrosis of the femoral head in sickle cell disease: a five-year follow-up study.Daltro GC, Fortuna V, de Souza ES, Salles MM, Carreira AC, Meyer R, Freire SM, Borojevic R Stem Cell Res Ther2015
Enhanced suicidal erythrocyte death contributing to anemia in the elderly.Lupescu A, Bissinger R, Goebel T, Salker MS, Alzoubi K, Liu G, Chirigiu L, Mack AF, Qadri SM, Lang F Cell. Physiol. Biochem.2015
Evaluation of cardiac sequelae in patients with sickle cell anemia.Amoozgar H, Dastgheib L, Seifi V, Karimi M Hellenic J Cardiol2015
[Dysregulation of microRNA in thalassemia].Umemura T, Svasti S Fukuoka Igaku Zasshi2015
Whole genome prediction for preimplantation genetic diagnosis.Kumar A, Ryan A, Kitzman JO, Wemmer N, Snyder MW, Sigurjonsson S, Lee C, Banjevic M, Zarutskie PW, Lewis AP, Shendure J, Rabinowitz M Genome Med2015
Hemoglobin C Trait Provides Protection From Clinical Falciparum Malaria in Malian Children.Travassos MA, Coulibaly D, Laurens MB, Dembélé A, Tolo Y, Koné AK, Traoré K, Niangaly A, Guindo A, Wu Y, Berry AA, Jacob CG, Takala-Harrison S, Adams M, Shrestha B, Mu AZ, Kouriba B, Lyke KE, Diallo DA, Doumbo OK, Plowe CV, Thera MA J. Infect. Dis.2015
Acute hemolytic vascular inflammatory processes are prevented by nitric oxide replacement or a single dose of hydroxyurea.Almeida CB, Souza LE, Leonardo FC, Costa FT, Werneck CC, Covas DT, Costa FF, Conran N Blood2015
2p15-p16.1 microdeletions encompassing and proximal to BCL11A are associated with elevated HbF in addition to neurologic impairment.Funnell AP, Prontera P, Ottaviani V, Piccione M, Giambona A, Maggio A, Ciaffoni F, Stehling-Sun S, Marra M, Masiello F, Varricchio L, Stamatoyannopoulos JA, Migliaccio AR, Papayannopoulou T Blood2015
How we prevent and manage infection in sickle cell disease.Sobota A, Sabharwal V, Fonebi G, Steinberg M Br. J. Haematol.2015
Role of vitamin C as an adjuvant therapy to different iron chelators in young β-thalassemia major patients: efficacy and safety in relation to tissue iron overload.Elalfy MS, Saber MM, Adly AA, Ismail EA, Tarif M, Ibrahim F, Elalfy OM Eur. J. Haematol.2015
Multiplex Minisequencing of the HBB Gene: A Rapid Strategy to Confirm the Most Frequent β-Thalassemia Mutations in the Tunisian Population.Ben Charfeddine I, Ben Lazreg T, M'sakni A, Amara A, Mlika A, Chaïeb A, Hlel K, Zouari N, Zbidi F, Bouguila J, Soyah N, Ayedi A, Ben Hamouda H, Abroug S, Boughamoura L, Saad A, Gribaa M Hemoglobin2015
Compound Heterozygosity for HKαα and an in Cis Deletion of Double α Genes Presents as α-Thalassemia Trait.Wu MY, Li J, Li SC, Li R, Liao C, Li DZ Hemoglobin2015
Identification of Hb Constant Spring (HBA2: c.427T > C) by an Automated High Performance Liquid Chromatography Method.Wisedpanichkij R, Jindadamrongwech S, Butthep P Hemoglobin2015
Efficacy of Rapamycin as Inducer of Hb F in Primary Erythroid Cultures from Sickle Cell Disease and β-Thalassemia Patients.Pecoraro A, Troia A, Calzolari R, Scazzone C, Rigano P, Martorana A, Sacco M, Maggio A, Di Marzo R Hemoglobin2015
Molecular Diagnosis of α⁰-Thalassemia Through Urine DNA: A Novel DNA Source to Facilitate Prevention Programs in Remote Geographical Areas.Suwannakhon N, Seeratanachot T, Mahingsa K, Sanguansermsri T Hemoglobin2015
A qualitative study to explore how professionals in the United Kingdom make decisions to test children for a sickle cell carrier status.Noke M, Peters S, Wearden A, Ulph F Eur. J. Hum. Genet.2015
Hemophagocytic lymphohistiocytosis following dengue hemorrhagic fever in Hb H/Hb Constant Spring patient.Phuakpet K, Sanpakit K, Vathana N, Takpradit C, Chokephaibulkit K, Viprakasit V Pediatr Int2015
Effects of blood transfusion on exercise capacity in thalassemia major patients.Benedetto D, Rao CM, Cefalù C, Aguglia DO, Cattadori G, D'Ascola DG, Benedetto FA, Agostoni P, Sciomer S PLoS ONE2015
Fentanyl Buccal Tablet: A New Breakthrough Pain Medication in Early Management of Severe Vaso-Occlusive Crisis in Sickle Cell Disease.De Franceschi L, Mura P, Schweiger V, Vencato E, Quaglia FM, Delmonte L, Evangelista M, Polati E, Olivieri O, Finco G Pain Pract2015
[French guidelines for the management of adult sickle cell disease: 2015 update].Habibi A, Arlet JB, Stankovic K, Gellen-Dautremer J, Ribeil JA, Bartolucci P, Lionnet F, Rev Med Interne2015
Gαs proteins activate p72(Syk) and p60-c-Src tyrosine kinases to mediate sickle red blood cell adhesion to endothelium via LW-αvβ3 and CD44-CD44 interactions.Chiou E, Zennadi R Int. J. Biochem. Cell Biol.2015
Phase 1/2 trial of vorinostat in patients with sickle cell disease who have not benefitted from hydroxyurea.Okam MM, Esrick EB, Mandell E, Campigotto F, Neuberg DS, Ebert BL Blood2015
Lack of association between the Duffy antigen receptor for chemokines (DARC) expression and clinical outcome of children with sickle cell anemia.Araujo NB, Domingos IF, Medeiros FS, Hatzlhofer BL, Mendonça TF, Vasconcelos LR, Cavalcanti Mdo S, Araujo AS, Oliveira Mdo C, Lucena-Araujo AR, Bezerra MA Immunol. Lett.2015
Exploring the Effectiveness of Mandatory Premarital Screening and Genetic Counselling Programmes for β-Thalassaemia in the Middle East: A Scoping Review.Saffi M, Howard N Public Health Genomics2015
Occurrence of the Codon 24 (A > T) Mutation in the Mauritanian Population.Veten F, Ghaber S, Habti N, Houmeida A Hemoglobin2015
Perspectives in Genetics and Sickle Cell Disease Prevention in Africa: Beyond the Preliminary Data from Cameroon.Wonkam A, Ngo Bitoungui VJ, Ngogang J Public Health Genomics2015
Fertility in transfusion-dependent thalassemia men: effects of iron burden on the reproductive axis.Singer ST, Killilea D, Suh JH, Wang ZJ, Yuan Q, Ivani K, Evans P, Vichinsky E, Fischer R, Smith JF Am. J. Hematol.2015
Pancreatic iron overload by T2* MRI in a large cohort of well treated thalassemia major patients: can it tell us heart iron distribution and function?Meloni A, Restaino G, Missere M, De Marchi D, Positano V, Valeri G, Giuseppe D'Ascola D, Peluso A, Caterina Putti M, Lendini M, Giovanna Neri M, Midiri M, Sallustio G, Pepe A Am. J. Hematol.2015
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Vaccines for preventing invasive salmonella infections in people with sickle cell disease.Odey F, Okomo U, Oyo-Ita A Cochrane Database Syst Rev2015
Zinc status affects glucose homeostasis and insulin secretion in patients with thalassemia.Fung EB, Gildengorin G, Talwar S, Hagar L, Lal A Nutrients2015
Why the DNA self-depurination mechanism operates in HB-β but not in β-globin paralogs HB-δ, HB-ɛ1, HB-γ1 and HB-γ2.Amosova O, Alvarez-Dominguez JR, Fresco JR Mutat. Res.2015
Label-free and depth resolved optical sectioning of iron-complex deposits in sickle cell disease splenic tissue by multiphoton microscopy.Vigil GD, Adami AJ, Ahmed T, Khan A, Chapman S, Andemariam B, Thrall RS, Howard SS J Biomed Opt2015
Compound heterozygous state of β-thalassemia with IVS1-5 (G→C) mutation and Indian deletion-inversion Gγ(Aγδβ)(0)-thalassemia in eastern India.Dehury S, Purohit P, Meher S, Das K, Patel S Rev Bras Hematol Hemoter2015
Very mild forms of Hb S/beta(+)-thalassemia in Brazilian children.Belisário AR, Sales RR, Viana MB Rev Bras Hematol Hemoter2015
Socioeconomic and demographic characteristics of sickle cell disease patients from a low-income region of northeastern Brazil.Fernandes TA, Medeiros TM, Alves JJ, Bezerra CM, Fernandes JV, Serafim ÉS, Fernandes MZ, Sonati Mde F Rev Bras Hematol Hemoter2015
Pattern of hemolysis parameters and association with fetal hemoglobin in sickle cell anemia patients in steady state.Moreira JA, Laurentino MR, Machado RP, Barbosa MC, Gonçalves RP, Mota Ade M, Rocha LB, Martins AM, de Lima Arruda AB, de Souza IP, Gonçalves RP Rev Bras Hematol Hemoter2015
The compound state: Hb S/beta-thalassemia.Figueiredo MS Rev Bras Hematol Hemoter2015
Fetal hemoglobin and hemolysis markers in sickle cell anemia.Colella MP, Traina F Rev Bras Hematol Hemoter2015
Angiotensin-converting enzyme (ACE) inhibitors for proteinuria and microalbuminuria in people with sickle cell disease.Sasongko TH, Nagalla S, Ballas SK Cochrane Database Syst Rev2015
Sickle Cell Trait Screening of Collegiate Athletes: Ethical Reasons for Program Reform.Ferrari R, Parker LS, Grubs RE, Krishnamurti L J Genet Couns2015
The role of donor-derived veto cells in nonmyeloablative haploidentical HSCT.Or-Geva N, Reisner Y Bone Marrow Transplant.2015
Microfluidic study of enhanced deposition of sickle cells at acute corners.Loiseau E, Massiera G, Mendez S, Martinez PA, Abkarian M Biophys. J.2015
The Incidence Rate of Acute Transfusion Reactions in Thalassemia Patients Referred to the Shiraz Thalassemia Centre, Shiraz, Iran, Before and After the Establishment of the Hemovigilance System.Kasraian L, Karimi MH Hemoglobin2015
A novel double heterozygous Hb Fontainebleau/HbD Punjab hemoglobinopathy.Rodríguez-Capote K, Estey MP, Barakauskas V, Bordeleau P, Christensen CL, Zuberbuhler P, Higgins TN Clin. Biochem.2015
Chronic transfusion therapy improves but does not normalize systemic and pulmonary vasculopathy in sickle cell disease.Detterich JA, Kato RM, Rabai M, Meiselman HJ, Coates TD, Wood JC Blood2015
A family empowerment program for families having children with thalassemia, Thailand.Wacharasin C, Phaktoop M, Sananreangsak S Nurs Health Sci2015
Screening non-deletion α-thalassaemia mutations in the HBA1 and HBA2 genes by high-resolution melting analysis.Petropoulou M, Poula A, Traeger-Synodinos J, Vrettou C, Kanavakis E, Christopoulos TK, Ioannou PC Clin. Chem. Lab. Med.2015
Two novel haemoglobin variants that affect haemoglobin A1c measurement by ion-exchange chromatography.Bots M, Stroobants AK, Delzenne B, Soeters MR, de Vries JE, Weykamp CW, Norg RJ, Veldthuis M, Zwieten Rv Clin. Chem. Lab. Med.2015
Red blood cell storage duration is not associated with clinical outcomes for acute chest syndrome in children with sickle cell disease.Fields ME, Hulbert ML, Chen L, Berlin AN, Jackups R, Spinella PC Transfusion2015
The LSD1 inhibitor RN-1 induces fetal hemoglobin synthesis and reduces disease pathology in sickle cell mice.Cui S, Lim KC, Shi L, Lee M, Jearawiriyapaisarn N, Myers G, Campbell A, Harro D, Iwase S, Trievel RC, Rivers A, DeSimone J, Lavelle D, Saunthararajah Y, Engel JD Blood2015
Heart Rate Variability for Early Detection of Iron Overload Cardiomyopathy in β-Thalassemia Patients.Koonrungsesomboon N, Tantiworawit A, Phrommintikul A, Saekho S, Srichairattanakool S, Chattipakorn N Hemoglobin2015
Elevated Hb A₂ Levels in a Patient with a Compound Heterozygosity for the (β⁺) -31 (A > G) and (β⁰) Codon 17 (A > T) Mutations Together with a Single α-Globin Gene.Panyasai S, Jaiping K, Pornprasert S Hemoglobin2015
The human ankyrin 1 promoter insulator sustains gene expression in a β-globin lentiviral vector in hematopoietic stem cells.Romero Z, Campo-Fernandez B, Wherley J, Kaufman ML, Urbinati F, Cooper AR, Hoban MD, Baldwin KM, Lumaquin D, Wang X, Senadheera S, Hollis RP, Kohn DB Mol Ther Methods Clin Dev2015
Clinical Utility of Lactate Dehydrogenase in Determining the Severity of Hemolysis in Sickle Cell Anemia.Ballas SK Am. J. Clin. Pathol.2015
Lactate dehydrogenase isoenzyme 3 and hemolysis in sickle cell anemia: a possible correlation?Mecabo G, Yamamoto M, Biassi TP, Figueiredo MS Blood2015
Mechanical differences of sickle cell trait (SCT) and normal red blood cells.Zheng Y, Cachia MA, Ge J, Xu Z, Wang C, Sun Y Lab Chip2015
Influence of Genetic Variants in EGF and Other Genes on Hematological Traits in Korean Populations by a Genome-Wide Approach.Kim YK, Oh JH, Kim YJ, Hwang MY, Moon S, Low SK, Takahashi A, Matsuda K, Kubo M, Lee J, Kim BJ Biomed Res Int2015
Tonsilectomy in sickle cell diseases.Helvaci MR, Gokce C, Davran R, Acipayam C, Akkucuk S, Ugur M Int J Clin Exp Med2015
Can the ductus venosus doppler predict the hemoglobinopathies?Karateke A, Silfeler DB, Güngören A, Kurt RK, Okyay AG, Dokuyucu R, Ulutas T, Un B, Paksoy H, Hakverdi AU Int J Clin Exp Med2015
The Role of Inspiratory Muscle Training in Sickle Cell Anemia Related Pulmonary Damage due to Recurrent Acute Chest Syndrome Attacks.Camcıoğlu B, Boşnak-Güçlü M, Karadallı MN, Akı ŞZ, Türköz-Sucak G Case Rep Hematol2015
Thalassaemia major and infectious risk: High Mobility Group Box-1 represents a novel diagnostic and prognostic biomarker.Chirico V, Lacquaniti A, Piraino B, Cutrupi M, Cuppari C, Grasso L, Rigoli L, David A, Arrigo T, Salpietro C Br. J. Haematol.2015
The Interplay Between Peroxiredoxin-2 and Nuclear Factor-Erythroid 2 Is Important in Limiting Oxidative Mediated Dysfunction in β-Thalassemic Erythropoiesis.Matte A, De Falco L, Iolascon A, Mohandas N, An X, Siciliano A, Leboeuf C, Janin A, Bruno M, Choi SY, Kim DW, De Franceschi L Antioxid. Redox Signal.2015
Silent cerebral infarcts in very young children with sickle cell anaemia are associated with a higher risk of stroke.Cancio MI, Helton KJ, Schreiber JE, Smeltzer MP, Kang G, Wang WC Br. J. Haematol.2015
Impact of sickle cell trait on the thrombotic risk associated with non-O blood groups in northern Nigeria.Ahmed SG, Kagu MB, Ibrahim UA, Bukar AA Blood Transfus2015
Cyclic headaches in β-thalassemia intermedia case presenting as moyamoya syndrome.Akpınar S, Yılmaz G, Çelebioğlu E Iran J Neurol2015
Mechanisms of sickle cell alloimmunization.Yazdanbakhsh K Transfus Clin Biol2015
Renal medullary carcinoma and sickle cell trait: A systematic review.Alvarez O, Rodriguez MM, Jordan L, Sarnaik S Pediatr Blood Cancer2015
Variation in Gamma-Globin Expression before and after Induction with Hydroxyurea Associated with BCL11A, KLF1 and TAL1.Grieco AJ, Billett HH, Green NS, Driscoll MC, Bouhassira EE PLoS ONE2015
Safety profile of a liquid formulation of deferiprone in young children with transfusion-induced iron overload: a 1-year experience.Chuansumrit A, Songdej D, Sirachainan N, Wongwerawattanakoon P, Kadegasem P, Sasanakul W Paediatr Int Child Health2015
Efficient genome editing in hematopoietic stem cells with helper-dependent Ad5/35 vectors expressing site-specific endonucleases under microRNA regulation.Saydaminova K, Ye X, Wang H, Richter M, Ho M, Chen H, Xu N, Kim JS, Papapetrou E, Holmes MC, Gregory PD, Palmer D, Ng P, Ehrhardt A, Lieber A Mol Ther Methods Clin Dev2015
Leukocytes apoptosis and adipocytokines in children with beta thalassemia major.Elsayh KI, Mohammed WS, Zahran AM, Saad K Clin. Exp. Med.2015
Thalassemia and risk of dementia: a nationwide population-based retrospective cohort study.Chen YG, Lin TY, Chen HJ, Dai MS, Ho CL, Kao CH Eur. J. Intern. Med.2015
l-Arginine supplementation enhances antioxidant activity and erythrocyte integrity in sickle cell anaemia subjects.Kehinde MO, Ogungbemi SI, Anigbogu CN, Jaja SI Pathophysiology2015
Simultaneous Determination of Plasma Deferasirox and Deferasirox-Iron Complex Using an HPLC-UV System and Pharmacokinetics of Deferasirox in Patients With β-Thalassemia Major: Once-daily Versus Twice-daily Administration.Lu MY, Wang N, Wu WH, Lai CW, Kuo PH, Chiang PH, Lin KH, Wu TH Clin Ther2015
Myocardial fibrosis by late gadolinium enhancement cardiac magnetic resonance and hepatitis C virus infection in thalassemia major patients.Pepe A, Meloni A, Borsellino Z, Cuccia L, Borgna-Pignatti C, Maggio A, Restaino G, Gagliardotto F, Caruso V, Spasiano A, Filosa A, Centra M, D'Ascola D, Quarta A, Peluso A, Midiri M, Rossi G, Positano V, Capra M J Cardiovasc Med (Hagerstown)2015
Sickle cell trait, exertional rhabdomyolysis, and compartment syndrome.Connes P Lancet2015
Body composition and grip strength are improved in transgenic sickle mice fed a high-protein diet.Capers PL, Hyacinth HI, Cue S, Chappa P, Vikulina T, Roser-Page S, Weitzmann MN, Archer DR, Newman GW, Quarshie A, Stiles JK, Hibbert JM J Nutr Sci2015
Plerixafor+G-CSF-mobilized CD34+ cells represent an optimal graft source for thalassemia gene therapy.Karponi G, Psatha N, Lederer CW, Adair JE, Zervou F, Zogas N, Kleanthous M, Tsatalas C, Anagnostopoulos A, Sadelain M, Rivière I, Stamatoyannopoulos G, Yannaki E Blood2015
A case of acute chest syndrome complicated by diffuse cerebral infarcts in an adult with HbSβ-thalassemia(.).Chandran R, Moran A, Barash M, Hopper B, Rankin A, Field JJ Am. J. Hematol.2015
Thalassemia Phenotypes and Genotypes in Taiwan: A Retrospective Study Based on Thalassemia Screening of Young Men for Military Conscription.Lee HW, Han SM, Yang Y, Lin TH, Tzeng HE, Chang KH, Hwang WL, Teng CL Hemoglobin2015
Liver iron concentration measurements by MRI in chronically transfused children with sickle cell anemia: baseline results from the TWiTCH trial.Wood JC, Pressel S, Rogers ZR, Odame I, Kwiatkowski JL, Lee MT, Owen WC, Cohen AR, St Pierre T, Heeney MM, Schultz WH, Davis BR, Ware RE, Am. J. Hematol.2015
Thalassemia Intermedia Caused by 16p13.3 Sectional Duplication in a β-Thalassemia Heterozygous Child.Liu S, Jiang H, Wu MY, Zhang YL, Li DZ Pediatr Hematol Oncol2015
Thalassemia Modular Stratification System for Personalized Therapy of Beta-Thalassemia (THALAMOSS). Hum Gene Ther Clin Dev2015
Health-Related Quality of Life in Adolescents with Thalassemia.Boonchooduang N, Louthrenoo O, Choeyprasert W, Charoenkwan P Pediatr Hematol Oncol2015
Systematic review of interventional sickle cell trials registered in JD, Hilliard LM, Pair LE, Oster R, Howard TH, Cutter GR Clin Trials2015
Role of Purinergic Receptors of Erythrocytes in the Regulation of Conformation and Oxygen- and NO-Transporting Capacity of Hemoglobin.Kovalenko SS, Yusipovich AI, Parshina EY, Maksimov GV Bull. Exp. Biol. Med.2015
Caries prevalence and impact on oral health-related quality of life in children with sickle cell disease: cross-sectional study.Fernandes ML, Kawachi I, Corrêa-Faria P, Pattusi MP, Paiva SM, Pordeus IA BMC Oral Health2015
Bacteraemia in sickle cell anaemia is associated with low haemoglobin: a report of 890 admissions to a tertiary hospital in Tanzania.Makani J, Mgaya J, Balandya E, Msami K, Soka D, Cox SE, Komba AN, Rwezaula S, Meda E, Muturi D, Kitundu J, Fegan G, Kirkham FJ, Newton CR, Snow RW, Lowe B Br. J. Haematol.2015
[Hemoglobin disorders].Dickerhoff R Internist (Berl)2015
Interaction of an α-Globin Gene Triplication with β-Globin Gene Mutations in Iranian Patients with β-Thalassemia Intermedia.Farashi S, Bayat N, Faramarzi Garous N, Ashki M, Montajabi Niat M, Vakili S, Imanian H, Zeinali S, Najmabadi H, Azarkeivan A Hemoglobin2015
Heart Rate Variability as an Alternative Indicator for Identifying Cardiac Iron Status in Non-Transfusion Dependent Thalassemia Patients.Wijarnpreecha K, Siri-Angkul N, Shinlapawittayatorn K, Charoenkwan P, Silvilairat S, Siwasomboon C, Visarutratna P, Srichairatanakool S, Tantiworawit A, Phrommintikul A, Chattipakorn SC, Chattipakorn N PLoS ONE2015
Precision of SPECT/CT Allows the Diagnosis of a Hidden Brodie's Abscess of the Talus in a Patient with Sickle Cell Disease.Al-Jafar H, Al-Shemmeri E, Al-Shemmeri J, Aytglu L, Afzal U, Al-Enizi S Nucl Med Mol Imaging2015
miRNA-embedded shRNAs for Lineage-specific BCL11A Knockdown and Hemoglobin F Induction.Guda S, Brendel C, Renella R, Du P, Bauer DE, Canver MC, Grenier JK, Grimson AW, Kamran SC, Thornton J, de Boer H, Root DE, Milsom MD, Orkin SH, Gregory RI, Williams DA Mol. Ther.2015
Hematologic Disorders: Sickle Cell Disease.Baltierra D, Harper T, Jones MP, Nau KC FP Essent2015
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Spectrum of α-thalassemia and β-thalassemia mutations in the Guilin Region of southern China.Tang W, Zhang C, Lu F, Tang J, Lu Y, Cui X, Qin X, Li S Clin. Biochem.2015
Treatment of β-Thalassemia/Hemoglobin E with Antioxidant Cocktails Results in Decreased Oxidative Stress, Increased Hemoglobin Concentration, and Improvement of the Hypercoagulable State.Yanpanitch OU, Hatairaktham S, Charoensakdi R, Panichkul N, Fucharoen S, Srichairatanakool S, Siritanaratkul N, Kalpravidh RW Oxid Med Cell Longev2015
Family caregiving for adults with sickle cell disease and extremely high hospital use.Brown SE, Weisberg DF, Sledge WH J Health Psychol2015
Clinical and Molecular Characteristics of Non-Transfusion-Dependent Thalassemia in Kuwait.Adekile AD, Azab AF, Al-Sharida SI, Al-Nafisi BA, Akbulut N, Marouf RA, Mustafa NY Hemoglobin2015
Molecular Basis of β-Thalassemia in the Population of the Aegean Region of Turkey: Identification of A Novel Deletion Mutation.Ozkinay F, Onay H, Karaca E, Arslan E, Erturk B, Ece Solmaz A, Tekin IM, Cogulu O, Aydinok Y, Vergin C Hemoglobin2015
Red Cell Indices and Formulas Used in Differentiation of β-Thalassemia Trait from Iron Deficiency in Thai Adults.Plengsuree S, Punyamung M, Yanola J, Nanta S, Jaiping K, Maneewong K, Wongwiwatthananukit S, Pornprasert S Hemoglobin2015
Clinical to Molecular Screening Paradigm for β-Thalassemia Carriers.Abdel-Messih IY, Youssef SR, Mokhtar GM, Elmogy MI, Mahmoud HM, Ayoub M, Pessar SA Hemoglobin2015
Does Insulin Like Growth Factor-1 (IGF-1) Deficiency Have a De Sanctis V, Incorvaia C, Soliman AT, Candini G, Pepe A, Kattamis C, Soliman NA, Elsedfy H, Kholy ME Mediterr J Hematol Infect Dis2015
Perception of young adults with sickle cell disease or sickle cell trait about participation in the CHOICES randomized controlled trial.Hershberger PE, Gallo AM, Molokie R, Thompson AA, Suarez ML, Yao Y, Wilkie DJ J Adv Nurs2015
G6PD deficiency and absence of α-thalassemia increase the risk for cerebral vasculopathy in children with sickle cell anemia.Joly P, Garnier N, Kebaili K, Renoux C, Dony A, Cheikh N, Renard C, Ceraulo A, Cuzzubbo D, Pondarré C, Martin C, Pialoux V, Francina A, Bertrand Y, Connes P Eur. J. Haematol.2015
Novel 31.2 kb α0 Deletion in a Palestinian Family with α-Thalassemia.Brieghel C, Birgens H, Frederiksen H, Hertz JM, Steenhof M, Petersen J Hemoglobin2015
Optimal Manual Exchange Transfusion Protocol for Sickle Cell Disease: A Retrospective Comparison of Two Comprehensive Care Centers in the United Kingdom and Canada.Mian HS, Ward R, Telfer P, Kaya B, Kuo KH Hemoglobin2015
A Mixed-Methods Study of Pain-related Quality of Life in Sickle Cell Vaso-Occlusive Crises.Lin RJ, Evans AT, Wakeman K, Unterbrink M Hemoglobin2015
Efficacy of Deferasirox (Exjade®) in Modulation of Iron Overload in Patients with β-Thalassemia Intermedia.Karimi M, Arandi N, Haghpanah S, Ansari S, Azarkeyvan A, Bordbar M, Safaei S Hemoglobin2015
Efficacy of Interferon A-2b monotherapy in Β-thalassemics with chronic hepatitis C.Kalafateli M, Kourakli A, Gatselis N, Lambropoulou P, Thomopoulos K, Tsamandas A, Christofidou M, Zachou K, Jelastopoulou E, Nikolopoulou V, Symeonidis A, Dalekos GN, Lambropoulou-Karatza C, Triantos C J Gastrointestin Liver Dis2015
Status of Superoxide Dismutase in Transfusion Dependent Thalassaemia.Rujito L, Mulatsih S, Sofro AS N Am J Med Sci2015
Implications of radiologic-pathologic correlation for gallbladder disease in children and young adults with sickle cell disease.Gale HI, Setty BN, Sprinz PG, Doros G, Williams DD, Morrison TC, Kalajian TA, Tu P, Mundluru SN, Mehta MN, Castro-Aragon I Emerg Radiol2015
Red Blood Cells Store and Release Interleukin-33.Wei J, Zhao J, Schrott V, Zhang Y, Gladwin M, Bullock G, Zhao Y J. Investig. Med.2015
HbA2 : biology, clinical relevance and a possible target for ameliorating sickle cell disease.Steinberg MH, Rodgers GP Br. J. Haematol.2015
Marked Direct Hyperbilirubinemia due to Ceftriaxone in an Adult with Sickle Cell Disease.Khurram D, Shamban L, Kornas R, Paul M Case Rep Gastrointest Med2015
Post Splenectomy Outcome in β-Thalassemia.Merchant RH, Shah AR, Ahmad J, Karnik A, Rai N Indian J Pediatr2015
Generation and Characterization of a Transgenic Mouse Carrying a Functional Human β -Globin Gene with the IVSI-6 Thalassemia Mutation.Breveglieri G, Mancini I, Bianchi N, Lampronti I, Salvatori F, Fabbri E, Zuccato C, Cosenza LC, Montagner G, Borgatti M, Altruda F, Fagoonee S, Carandina G, Rubini M, Aiello V, Breda L, Rivella S, Gambari R, Finotti A Biomed Res Int2015
Heterozygous β-thalassemia with complete absence of hemoglobin A2 in a Chinese adult.Yan JM, Wu MY, Xie XM, Li DZ Int J Lab Hematol2015
Identification of Two Novel β-Thalassemia Mutations (HBB: c.335-346del and HBB: c.108 C > G) in Han Chinese.Wang W, Wang Q, Tao T, Sun A, Ruan C, Chen S Hemoglobin2015
Important clinical and laboratory correlates of glomerular filtration rate in sickle cell anemia.Madu AJ, Ubesie A, Ocheni S, Chinawa J, Madu KA, Ibegbulam OG, Nlemadim C, Eze A Niger J Clin Pract2015
Adverse Reactions to Pneumococcal Vaccine in Pediatric and Adolescent Patients with Sickle Cell Disease.Han J, Kemiki O, Hsu LL, Rivers AE Pharmacotherapy2015
Routine non-ABO blood group antigen genotyping in sickle cell disease: the new frontier in pretransfusion testing?Tormey CA, Hendrickson JE Transfusion2015
The Influence of Polymorphisms in Disease Severity in β-Thalassemia.Mohammdai-Asl J, Ramezani A, Norozi F, Alghasi A, Asnafi AA, Jaseb K, Saki N Biochem. Genet.2015
An international effort to cure a global health problem: A report on the 19th Hemoglobin Switching Conference.Blobel GA, Bodine D, Brand M, Crispino J, de Bruijn MF, Nathan D, Papayannopoulou T, Porcher C, Strouboulis J, Zon L, Higgs DR, Stamatoyannopoulos G, Engel JD Exp. Hematol.2015
Sickle Cell Disease in Priapism: Disparity in Care?Joice GA, Kates M, Sopko NA, Hannan JL, Bivalacqua TJ Urology2015
Intermediaries of branched chain amino acid metabolism induce fetal hemoglobin, and repress SOX6 and BCL11A, in definitive erythroid cells.Karkashon S, Raghupathy R, Bhatia H, Dutta A, Hess S, Higgs J, Tifft CJ, Little JA Blood Cells Mol. Dis.2015
Impact of eNOS polymorphisms on red blood cell aggregation in sickle cell disease.Ferdinand S, Connes P, Brudey L, Cita KC, Tressières B, Lemonne N, Hardy-Dessources MD, Lamarre Y, Waltz X, Etienne-Julan M, Romana M Blood Cells Mol. Dis.2015
Growth differentiation factor-15 in children and adolescents with thalassemia intermedia: Relation to subclinical atherosclerosis and pulmonary vasculopathy.Tantawy AA, Adly AA, Ismail EA, Youssef OI, Ali ME Blood Cells Mol. Dis.2015
Hemoglobin level and morbidity in non-transfusion-dependent thalassemia.Taher AT, Musallam KM, Saliba AN, Garziadei G, Cappellini MD Blood Cells Mol. Dis.2015
Alpha hemoglobin stabilizing protein: Its causal relationship with the severity of beta thalassemia.Sagar CS, Kumar R, Sharma DC, Kishor P Blood Cells Mol. Dis.2015
Impact of epigenetic mechanisms on therapeutic approaches of hemoglobinopathies.Costa D, Capuano M, Sommese L, Napoli C Blood Cells Mol. Dis.2015
[Vitamin D in children and adolescents with sickle cell disease: an integrative review].de Oliveira JF, Vicente NG, Santos JP, Weffort VR Rev Paul Pediatr2015
Intravenous infusion of haptoglobin for the prevention of adverse clinical outcome in Sickle Cell Disease.Quimby KR, Hambleton IR, Landis RC Med. Hypotheses2015
Effect of gamma radiation on the growth, survival, hematology and histological parameters of rainbow trout (Oncorhynchus mykiss) larvae.Oujifard A, Amiri R, Shahhosseini G, Davoodi R, Moghaddam JA Aquat. Toxicol.2015
Hemoglobin interacting proteins and implications of spectrin hemoglobin interaction.Basu A, Chakrabarti A J Proteomics2015
Oral contraceptive use and incident stroke in women with sickle cell disease.Qureshi AI, Malik AA, Adil MM, Suri MF Thromb. Res.2015
Sickle cell disease in tribal populations in India.Colah RB, Mukherjee MB, Martin S, Ghosh K Indian J. Med. Res.2015
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Heart valve surgery in patients with homozygous sickle cell disease: A management strategy.Moutaouekkil el M, Najib A, Ajaja R, Arji M, Slaoui A Ann Card Anaesth2015
Iron overload and fragmented QRS in patients with Thalassemia major: Mechanisms, therapies, and new horizons.Karakulak UN, Tutkun E, Yılmaz ÖH Anatol J Cardiol2015
Hydroxyurea treatment does not increase blood viscosity and improves red blood cell rheology in sickle cell anemia.Lemonne N, Charlot K, Waltz X, Ballas SK, Lamarre Y, Lee K, Hierso R, Connes C, Etienne-Julan M, Romana M, Connes P Haematologica2015
High Foetal Haemoglobin in Sickle Cell Disease: Not so Protective?Conran N EBioMedicine2015
Erythroid Adhesion Molecules in Sickle Cell Anaemia Infants: Insights Into Early Pathophysiology.Brousse V, Colin Y, Pereira C, Arnaud C, Odièvre MH, Boutemy A, Guitton C, de Montalembert M, Lapouméroulie C, Picot J, Le Van Kim C, El Nemer W EBioMedicine2015
Measurement of hair iron concentration as a marker of body iron content.Sahin C, Pala C, Kaynar L, Torun YA, Cetin A, Kurnaz F, Sivgin S, Sahin FS Biomed Rep2015
Lessons Learned From a Randomized Controlled Trial of a Family-Based Intervention to Promote School Functioning for School-Age Children With Sickle Cell Disease.Daniel LC, Li Y, Smith K, Tarazi R, Robinson MR, Patterson CA, Smith-Whitley K, Stuart M, Barakat LP J Pediatr Psychol2015
Improving Clinician Attitudes of Respect and Trust for Persons With Sickle Cell Disease.Haywood C, Williams-Reade J, Rushton C, Beach MC, Geller G Hosp Pediatr2015
Contribution of Reduced Interleukin-10 Levels to the Pathogenesis of Osteomyelitis in Children with Sickle Cell Disease.Sarray S, Almawi WY Clin. Vaccine Immunol.2015
Acute on chronic liver failure in a patient with sickle cell anaemia (HbSS).Im DD, Essien U, DePasse JW, Chiappa V BMJ Case Rep2015
Splenic infarction associated with sickle cell trait at low altitude.Seegars MB, Brett AS Hematology2015
Non-transfusion Dependent Thalassemias: A Developing Country Perspective.Mukherjee S, Das RR, Raghuwanshi B Curr Pediatr Rev2015
Allogeneic bone marrow transplant in a child with thalassaemia.Gooneratne LV, Dissanayake R, Jayawardena A, Jayaweera G, Abayadeera A, Samarasinghe M, Chandrasiri P, Dissanayake VH, Weerasinghe T, Brambilla CZ, Manna N, Faulkner LB Ceylon Med J2015
Prevalence and specificities of red cell alloantibodies in transfusion-dependent beta thalassemia patients in Yazd.Vaziri M, JavadzadehShahshahani H, Moghaddam M, Taghvaee N Iran J Ped Hematol Oncol2015
Association between serum ferritin level and diastolic cardiac function in patients with major β-thalassemia.Eghbali A, Taherahmadi H, Bagheri B, Nikanjam S, Ebrahimi L Iran J Ped Hematol Oncol2015
Evaluation of Intracranial Cerebral Blood Flow Velocities in Splenectomised and Non-Splenectomised Patients with β-Thalassemia Intermedia Using Transcranial Doppler Sonography.Kanavaki A, Kattamis A, Delaporta P, Papassotiriou I, Spengos K In Vivo2015
Extracorporeal membrane oxygenation for the treatment of adult sickle cell acute chest syndrome.Parhar K, Parizkova B, Jones N, Valchanov K, Fowles JA, Besser M, Telfer P, Kaya B, Vuylsteke A, Rubino A Perfusion2015
Increased circulating fibrocytes are associated with higher reticulocyte percent in children with sickle cell anemia.Karafin MS, Dogra S, Rodeghier M, Burdick M, Mehrad B, Rose CE, Strieter RM, DeBaun MR, Strunk RC, Field JJ Pediatr. Pulmonol.2015
Blood transfusion and 30-day readmission rate in adult patients hospitalized with sickle cell disease crisis.Nouraie M, Gordeuk VR Transfusion2015
Rs 11886868 and rs 4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients.Chaouch L, Moumni I, Ouragini H, Darragi I, Kalai M, Chaouachi D, Boudrigua I, Hafsia R, Abbes S Hematology2015
Alpha thalassemia among sickle cell anaemia patients in Kampala, Uganda.Lubega I, Ndugwa CM, Mworozi EA, Tumwine JK Afr Health Sci2015
Iron chelation therapy in transfusion-dependent thalassemia patients: current strategies and future directions.Saliba AN, Harb AR, Taher AT J Blood Med2015
Correction of murine hemoglobinopathies by prenatal tolerance induction and postnatal nonmyeloablative allogeneic BM transplants.Peranteau WH, Hayashi S, Abdulmalik O, Chen Q, Merchant A, Asakura T, Flake AW Blood2015
The trials and hopes for drug development in sickle cell disease.Ataga KI, Stocker J Br. J. Haematol.2015
Haemoglobin Variant Screening in Jamaica: Meeting Student's Request.Mason K, Gibson F, Higgs D, Fisher C, Thein SL, Clark B, Kulozik A, Happich M, Serjeant B, Serjeant G Br. J. Haematol.2015
Abnormal Regulation of Microvascular Tone in a Murine Model of Sickle Cell Disease Assessed by Contrast Ultrasound.Wu MD, Belcik JT, Qi Y, Zhao Y, Benner C, Pei H, Linden J, Lindner JR J Am Soc Echocardiogr2015
Left ventricular remodeling in patients with sickle cell disease: determinants factors and impact on outcome.Vasconcelos MC, Nunes MC, Barbosa MM, Fernandes BM, Passaglia LG, Silva CM, Ferrari TC Ann. Hematol.2015
Transition Needs of Adolescents With Sickle Cell Disease.Abel RA, Cho E, Chadwick-Mansker KR, D'Souza N, Housten AJ, King AA Am J Occup Ther2015
The Prevalence of Hemoglobinopathies in Young Adolescents in the Province of Muğla in Turkey: Results of a Screening Program.Topal Y, Topal H, Ceyhan MN, Azik F, Çapanoğlu M, Kocabaş CN Hemoglobin2015
β-Globin gene cluster haplotypes of Hb D-Los Angeles in Mazandaran Province, Iran.Mahdavi MR, Jalali H, Kosaryan M, Roshan P, Mahdavi M Genes Genet. Syst.2015
A successful twin pregnancy in a patient with HbE-β-thalassemia in western India.Merchant R, Italia K, Ahmed J, Ghosh K, Colah RB J Postgrad Med2015
Interaction of Hb Grey Lynn (Vientiane) [α91(FG3)Leu>Phe (α1)] with Hb E [β26(B8) Glu>Lys] and α(+)-thalassemia: Molecular and Hematological Analysis.Singha K, Fucharoen G, Fucharoen S Clin. Lab.2015
Sickle Cell Hemoglobin with Mutation at αHis-50 Has Improved Solubility.Tam MF, Tam TC, Simplaceanu V, Ho NT, Zou M, Ho C J. Biol. Chem.2015
Late-onset Male Hypogonadism and Fertility Potential in Thalassemia Major Patients: Two Emerging Issues.De Sanctis V, Soliman AT, Elsedfy H, Soliman NA, Elalaily R Mediterr J Hematol Infect Dis2015
Association of DNA Damage Repair Gene Polymorphisms hOGG1, XRCC1and p53 with Sickle Cell Disease Patients in India.Nishank SS Mediterr J Hematol Infect Dis2015
Red blood cell transfusion is associated with increased hemolysis and an acute phase response in a subset of critically ill children.L'Acqua C, Bandyopadhyay S, Francis RO, McMahon DJ, Nellis M, Sheth S, Kernie SG, Brittenham GM, Spitalnik SL, Hod EA Am. J. Hematol.2015
First Detection of a Splice Acceptor Site β-Thalassemia Mutation: IVS-I-130 (HBB: c.93-1G > C) in a Chinese Patient.He S, Zhang Q, Zheng C, Wei Y, Tang Y, Chen Q, Chen S Hemoglobin2015
Α-Thalassemia: Genotypic Profile Associated with Ethnicity and Hematological Differentiation of Iron Deficiency Anemia in the Region of Uberaba, Minas Gerais, Souza RA, Carlos AM, de Souza BM, Rodrigues CV, Pereira Gde A, Moraes-Souza H Hemoglobin2015
Aging in Sickle Cell Disease: Co-morbidities and New Issues in Management.Sandhu MK, Cohen A Hemoglobin2015
Hemoglobinopathy Screening in a 15-Year-old Patient With Anemia.Honarpisheh H, Staba Hogan MJ, Rinder HM, Siddon AJ J. Pediatr. Hematol. Oncol.2015
Screening for common β-globin gene cluster deletions in Chinese individuals with increased hemoglobin F.Cai WJ, Li J, Xie XM, Li DZ Int J Lab Hematol2015
A Rare Case of Variant Hemoglobin (Hb Yahata) Suspected Based on Inconsistent Plasma Glucose and HbA1c Levels.Iizuka K, Mizuno M, Niwa H, Takeda J Intern. Med.2015
Adherence to prompt fever evaluation in children with sickle cell disease and the health belief model.Schultz CL, Tchume-Johnson T, Schapira MM, Bellamy S, Smith-Whitley K, Ellison A Pediatr Blood Cancer2015
2015 Clinical trials update in sickle cell anemia.Archer N, Galacteros F, Brugnara C Am. J. Hematol.2015
Transfusion service management of sickle-cell disease patients.Yazer MH, Lozano M, Crighton G, Greenway A, Comande M, Savoia H, Wood E, Gilli S, Castilho L, Saad ST, Galactéros F, Noizat-Pirenne F, Pazgal I, Stark P, Orlin Y, Perseghin P, Masera N, Cela E, Anguita J, Wikman A, Delaney M Vox Sang.2015
Autonomic responses to cold face stimulation in sickle cell disease: a time-varying model analysis.Chalacheva P, Kato RM, Sangkatumvong S, Detterich J, Bush A, Wood JC, Meiselman H, Coates TD, Khoo MC Physiol Rep2015
The impact of noninvasive, capillary, and venous hemoglobin screening on donor deferrals and the hemoglobin content of red blood cells concentrates: a prospective study.Sümnig A, Hron G, Westphal A, Petersmann A, Kohlmann T, Greinacher A, Thiele T Transfusion2015
Five Years of Deferasirox Therapy for Cardiac Iron in β-Thalassemia Major.Vlachaki E, Agapidou A, Spanos G, Klonizakis P, Vetsiou E, Mavroudi M, Boura P Hemoglobin2015
Pulmonary hypertension in sickle cell disease.Fonseca G, Souza R Curr Opin Pulm Med2015
Management of the Dialysis Patient with Sickle Cell Disease.Boyle SM, Jacobs B, Sayani FA, Hoffman B Semin Dial2015
Coexistence of Malaria and Thalassemia in Malaria Endemic Areas of Thailand.Kuesap J, Chaijaroenkul W, Rungsihirunrat K, Pongjantharasatien K, Na-Bangchang K Korean J. Parasitol.2015
Contribution of Sickle Cell Disease to the Pediatric Stroke Burden Among Hospital Discharges of African-Americans-United States, 1997-2012.Baker C, Grant AM, George MG, Grosse SD, Adamkiewicz TV Pediatr Blood Cancer2015
Sickle cell comes out of the shadows.Trueland J Nurs Stand2015
Effects of teriparatide retreatment in a patient with β-thalassemia major.Tournis S, Dede AD, Savvidis C, Triantafyllopoulos IK, Kattamis A, Papaioannou N Transfusion2015
Hemoglobin assay for validation and quality control of medical device reprocessing.Frey J, Guan A, Li Z, Turtil S, Phillips KS Anal Bioanal Chem2015
Survival among children and adults with sickle cell disease in Belgium: Benefit from hydroxyurea treatment.Lê PQ, Gulbis B, Dedeken L, Dupont S, Vanderfaeillie A, Heijmans C, Huybrechts S, Devalck C, Efira A, Dresse MF, Rozen L, Benghiat FS, Ferster A Pediatr Blood Cancer2015
First Ischemic Stroke in Sickle-Cell Disease: Are There Any Adult Specificities?Calvet D, Bernaudin F, Gueguen A, Hosseini H, Habibi A, Galactéros F, Bartolucci P Stroke2015
Extramedullary hematopoiesis of the liver in a child with sickle cell disease: A rare complication.Barrier A, Willy S, Slone JS Pediatr Int2015
Neurological Complications and Cataract in a Child With Thalassemia Major Treated With Deferiprone.Parakh N, Sharma R, Prakash O, Mahto D, Dhingra B, Sharma S, Chandra J J. Pediatr. Hematol. Oncol.2015
Comparative study of the effect of BPA and its selected analogues on hemoglobin oxidation, morphological alterations and hemolytic changes in human erythrocytes.Maćczak A, Bukowska B, Michałowicz J Comp. Biochem. Physiol. C Toxicol. Pharmacol.2015
A multicenter randomized controlled trial of intravenous magnesium for sickle cell pain crisis in children.Brousseau DC, Scott JP, Badaki-Makun O, Darbari DS, Chumpitazi CE, Airewele GE, Ellison AM, Smith-Whitley K, Mahajan P, Sarnaik SA, Casper TC, Cook LJ, Dean JM, Leonard J, Hulbert ML, Powell EC, Liem RI, Hickey R, Krishnamurti L, Hillery CA, Nimmer M, Panepinto JA, Blood2015
Sodium nitrite-induced oxidative stress causes membrane damage, protein oxidation, lipid peroxidation and alters major metabolic pathways in human erythrocytes.Ansari FA, Ali SN, Mahmood R Toxicol In Vitro2015
Metabolically programmed iron chelators.Bergeron RJ, Bharti N, McManis JS, Wiegand J Bioorg. Med. Chem.2015
Clinical and Geographic Characterization of 30-Day Readmissions in Pediatric Sickle Cell Crisis Patients.McMillan JE, Meier ER, Winer JC, Coco M, Daymont M, Long S, Jacobs BR Hosp Pediatr2015
Curcumin Attenuates Iron Accumulation and Oxidative Stress in the Liver and Spleen of Chronic Iron-Overloaded Rats.Badria FA, Ibrahim AS, Badria AF, Elmarakby AA PLoS ONE2015
Heterozygosis deficit of polymorphic markers linked to the β-globin gene cluster region in the Iranian population.Moradi T, Vallian R, Fazeli Z, Haghighatnia A, Vallian S Iran J Basic Med Sci2015
Adolescents with sickle cell anaemia: Experience in a private tertiary hospital serving a tertiary institution.John-Olabode S, Awodele I, Oni O Niger Med J2015
Haematopoietic stem cell transplantation in Nigerian sickle cell anaemia children patients.Isgrò A, Paciaroni K, Gaziev J, Sodani P, Gallucci C, Marziali M, Angelis GD, Alfieri C, Ribersani M, Roveda A, Akinyanju OO, Wakama TT, Olowoselu FO, Adediran A, Lucarelli G Niger Med J2015
Short term results of cementless total hip arthroplasty in sicklers.Gulati Y, Sharma M, Bharti B, Bahl V, Bohra I, Goswani A Indian J Orthop2015
Extramedullary hematopoiesis is associated with lower cardiac iron loading in chronically transfused thalassemia patients.Ricchi P, Meloni A, Spasiano A, Neri MG, Gamberini MR, Cuccia L, Caruso V, Gerardi C, D'Ascola DG, Rosso R, Campisi S, Rizzo M, Terrazzino F, Vangosa AB, Chiodi E, Missere M, Mangione M, Positano V, Pepe A Am. J. Hematol.2015
Status of oxidant, antioxidantand serum enzymes in thalassaemic children receiving multiple blood transfusions.Asif M, Manzoor Z, Farooq MS, Munawar SH, Aziz A, Khan IA J Pak Med Assoc2015
Fluorescence assay of the interaction between hemoglobin and the cytoplasmic domain of erythrocyte membrane band 3.Sega MF, Chu H, Christian JA, Low PS Blood Cells Mol. Dis.2015
Molecular understanding of Indian untransfused thalassemia intermedia.Nadkarni A, Dabke P, Colah R, Ghosh K Int J Lab Hematol2015
Sickle Cell Trait Complicated by Acute Rhabdomyolysis in Military Personnel: A Case Report.Harrison JM, Wuerdeman MF Mil Med2015
Sickle Cell Trait-Related Exertional Deaths: Observations at Autopsy and Review of the Literature.Hughes RL, Feig J Mil Med2015
O2 and Water Migration Pathways between the Solvent and Heme Pockets of Hemoglobin with Open and Closed Conformations of the Distal HisE7.Shadrina MS, Peslherbe GH, English AM Biochemistry2015
Self-efficacy and readiness for transition from pediatric to adult care in sickle cell disease.Treadwell M, Johnson S, Sisler I, Bitsko M, Gildengorin G, Medina R, Barreda F, Major K, Telfair J, Smith WR Int J Adolesc Med Health2015
Development of a sickle cell disease readiness for transition assessment.Treadwell M, Johnson S, Sisler I, Bitsko M, Gildengorin G, Medina R, Barreda F, Major K, Telfair J, Smith WR Int J Adolesc Med Health2015
Sickle Cell Trait Causing Splanchnic Venous Thrombosis.Saxena P, Dhiman P, Bihari C, Rastogi A Case Reports Hepatol2015
Influence of splenectomy on immunoglobulins and complement components in major thalassemia.Darzi AA, Kamali S, Khakzad M Caspian J Intern Med2015
Pulmonary function indices in children with sickle cell anemia in Enugu, south-east Nigeria.Achigbu KI, Odetunde OI, Chinawa JM, Achigbu EO, Ikefuna AN, Emodi IJ, Ibe BC Saudi Med J2015
Oro-facial characteristics and the surgical correction of patients affected by beta-thalassaemia: a review of the literature and report of a case.Tehranchi A, Behnia H, Ghochani MS, Younessian F Aust Orthod J2015
Fetal anaemia from red blood cell membrane defect and co-inherited haemoglobin Constant Spring.Srisupundit K, Charoenkwan P, Traisrisilp K, Tongsong T BMJ Case Rep2015
Iron and oxidative stress in cardiomyopathy in thalassemia.Berdoukas V, Coates TD, Cabantchik ZI Free Radic. Biol. Med.2015
Genomic approaches to identifying targets for treating β hemoglobinopathies.Ngo DA, Steinberg MH BMC Med Genomics2015
[Evaluation of tolerance and efficacy of the treatment of chronic viral hepatitis C in homozygous sickle cell patients].El Agheb MO, Grange JD Pan Afr Med J2015
Prevention of Hb Bart's (γ4) Disease Associated with the - -(THAI) α(0)-Thalassemia Deletion in Mainland China.Li DZ, Li Y, Li J, Li SC, Li R Hemoglobin2015
Prevalence of Depression in Patients with β-Thalassemia as Assessed by the Beck's Depression Inventory [Hemoglobin. 2014;38(4):289-291].Cakir U, Demircioglu F Hemoglobin2015
Hb G-Waimanalo [A1] or α64(E13)Asp→Asn (α1) (HBA1: c.193G>A) Observed in a Bulgarian Family.Petkov G, Dimishkovska M, Tsoneva Ivanova V, Yordanov G, Zdraveski A, Plaseska-Karanfilska D Hemoglobin2015
Analysis of survival data in thalassemia patients in Shiraz, Iran.Rajaeefard A, Hajipour M, Tabatabaee HR, Hassanzadeh J, Rezaeian S, Moradi Z, Sharafi M, Shafiee M, Semati A, Safaei S, Soltani M Epidemiol Health2015
Sickle cell anemia induces changes in peripheral lymphocytes E-NTPDase/E-ADA activities and cytokines secretion in patients under treatment.Castilhos LG, Doleski PH, Bertoldo TM, Passos DF, Bertoncheli Cde M, Rezer JF, Schlemmer JB, Leal DB Biomed. Pharmacother.2015
Erythroferrone contributes to hepcidin suppression and iron overload in a mouse model of β-thalassemia.Kautz L, Jung G, Du X, Gabayan V, Chapman J, Nasoff M, Nemeth E, Ganz T Blood2015
Psychometric Properties of the Psychosocial Assessment Tool-General in Adolescents and Young Adults With Sickle Cell Disease.Crosby LE, Joffe NE, Reynolds N, Peugh JL, Manegold E, Pai AL J Pediatr Psychol2015
A 2-year prospective densitometric study on the influence of Fok-I gene polymorphism in young patients with thalassaemia major.Dimitriadou M, Christoforidis A, Fidani L, Economou M, Vlachaki E, Athanassiou-Metaxa M, Katzos G Osteoporos Int2015
Sehgal index: A new index and its comparison with other complete blood count-based indices for screening of beta thalassemia trait in a tertiary care hospital.Sehgal K, Mansukhani P, Dadu T, Irani M, Khodaiji S Indian J Pathol Microbiol2015
Immunity to tetanus in major beta thalassemia patients.Jahromi AS, Rahmanian K Clin Exp Vaccine Res2015
Immunogenicity of pneumococcal vaccination in a patient with sickle hemoglobinopathy: a case report.Clay EL, Burrell T, Belhorn T, Redding-Lallinger R Clin Case Rep2015
Coagulopathy and functional hyposplenism during an episode of thrombotic thrombocytopenic purpura in a HgbS/β (+)-thalassemia patient.Gangemi AJ, Pickens PV Clin Case Rep2015
Poor graft function can be durably and safely improved by CD34(+)-selected stem cell boosts after allogeneic unrelated matched or mismatched hematopoietic cell transplantation.Haen SP, Schumm M, Faul C, Kanz L, Bethge WA, Vogel W J. Cancer Res. Clin. Oncol.2015
The time scale of the quaternary structural changes in hemoglobin revealed using the transient grating technique.Yang C, Choi J, Ihee H Phys Chem Chem Phys2015
First Description of a β-Thalassemia Mutation, -86 (C > G) (HBB: c.-136C > G), in a Chinese Family.He S, Qin Q, Yi S, Zhou W, Deng J, Zheng C, Chen B Hemoglobin2015
A Novel Heme Pocket Hemoglobin Variant Associated with Normal Hematology: Hb Zara or α91(FG3)Leu→Ile (α2) (HBA2: c.274C > A).Trova S, Mereu P, Decandia L, Cocco E, Masala B, Manca L, Pirastru M Hemoglobin2015
β-Thalassemia Intermedia Caused by Compound Heterozygosity for Hb Lepore-Hollandia and β-Thalassemia is Rare in the Indian Population.Sreedharanunni S, Chhabra S, Hira JK, Bansal D, Sharma P, Das R Hemoglobin2015
Pulmonary Haemodynamics in Sickle Cell Disease Are Driven Predominantly by a High-Output State Rather Than Elevated Pulmonary Vascular Resistance: A Prospective 3-Dimensional Echocardiography/Doppler Study.Mushemi-Blake S, Melikian N, Drasar E, Bhan A, Lunt A, Desai SR, Greenough A, Monaghan MJ, Thein SL, Shah AM PLoS ONE2015
Antioxidant status in haemoglobin E carriers after acute and chronic strenuous exercises.Palasuwan A, Soogarun S, Suksom D, Pitaksathienkul C, Rousseau AS Res Sports Med2015
Is MRI Necessary for Skeletal Evaluation in Sickle Cell Disease.Sachan AA, Lakhkar BN, Lakhkar BB, Sachan S J Clin Diagn Res2015
A case of transfusion related acute lung injury in a thalassemic child.Agrawal A, Kumar D, Verma T, Gupta R Med J Armed Forces India2015
Hydroxyurea with AKT2 inhibition decreases vaso-occlusive events in sickle cell disease mice.Barazia A, Li J, Kim K, Shabrani N, Cho J Blood2015
Reticulocyte parameters of delta beta thalassaemia trait, beta thalassaemia trait and iron deficiency anaemia.Velasco-Rodríguez D, Alonso-Domínguez JM, González-Fernández FA, Villarrubia J, Sopeña M, Abalo L, Ropero P, Martínez-Nieto J, de la Fuente Gonzalo F, Cava F J. Clin. Pathol.2015
Burden of Hemoglobinopathies (Thalassemia, Sickle Cell Disorders and G6PD Deficiency) in Iran, 1990-2010: findings from the Global Burden of Disease Study 2010.Rezaei N, Naderimagham S, Ghasemian A, Saeedi Moghaddam S, Gohari K, Zareiy S, Sobhani S, Modirian M, Kompani F Arch Iran Med2015
Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease.Hussein N, Weng SF, Kai J, Kleijnen J, Qureshi N Cochrane Database Syst Rev2015
Non-invasive prenatal detection of haemoglobin Bart's disease by cardiothoracic ratio during the first trimester.Zhen L, Pan M, Han J, Yang X, Ou YM, Liao C, Li DZ Eur. J. Obstet. Gynecol. Reprod. Biol.2015
Exploring the Challenges and Opportunities of eHealth Tools for Patients with Sickle Cell Disease.Issom DZ, Zosso A, Ehrler F, Wipfli R, Lovis C, Koch S Stud Health Technol Inform2015
Spectrum of alpha-globin gene mutations among premarital Baluch couples in southeastern Iran.Miri-Moghaddam E, Nikravesh A, Gasemzadeh N, Badaksh M, Rakhshi N Int J Hematol Oncol Stem Cell Res2015
A case of severe rhabdomyolysis with minor trauma: Is sickle cell trait to blame?Krieger P, Zapolsky N, Lowery SJ Am J Emerg Med2015
Critical Reviews: How we treat sickle cell patients with leg ulcers.Minniti CP, Kato GJ Am. J. Hematol.2015
Cohort study of adult patients with haemoglobin SC disease: clinical characteristics and predictors of mortality.Gualandro SF, Fonseca GH, Yokomizo IK, Gualandro DM, Suganuma LM Br. J. Haematol.2015
Effectiveness of β-thalassemia prenatal diagnosis in Southern Iran: a cohort study.Moghadam M, Karimi M, Dehghani SJ, Dehbozorgian J, Montazeri S, Javanmardi E, Asadzade R, Amiri A, Saghatoleslam Z, Sotodegan F, Morshedi N, Imanifard J, Afrasiabi A Prenat. Diagn.2015
[Beta thalassemia intermedia: clinical characteristics and molecular analysis. Case series].Eandi Eberle S, Pepe C, Aguirre F, Milanesio B, Fernández D, Mansini A, Chávez A, Sciuccati G, Díaz L, Candás A, Avalos Gómez V, Bonduel M, Feliú Torres A Arch Argent Pediatr2015
Hemoglobinopathies and Leg Ulcers.Alavi A, Kirsner RS Int J Low Extrem Wounds2015
Prevalence of hemoglobin E in Yunnan Province of Southwest China.He J, Zeng X, Zhang Y, Su J, Ding X, Li S, Xu Y, Pu J, Jin C, Zhu B Hematology2015
First Description of a β-Thalassemia Mutation, -86 (C > G) (HBB: c.-136C > G), in a Chinese Family.He S, Qin Q, Yi S, Zhou W, Deng J, Zheng C, Chen B Hemoglobin2015
A Novel Heme Pocket Hemoglobin Variant Associated with Normal Hematology: Hb Zara or α91(FG3)Leu→Ile (α2) (HBA2: c.274C > A).Trova S, Mereu P, Decandia L, Cocco E, Masala B, Manca L, Pirastru M Hemoglobin2015
β-Thalassemia Intermedia Caused by Compound Heterozygosity for Hb Lepore-Hollandia and β-Thalassemia is Rare in the Indian Population.Sreedharanunni S, Chhabra S, Hira JK, Bansal D, Sharma P, Das R Hemoglobin2015
Hb G-Waimanalo [A1] [α64(E13)Asp→Asn; HBA1: c.193 G > A] with Decreased Oxygen Affinity.Karow A, Eekels JJ, Zurbriggen K, Schmid M, Schmugge M, Speer O Hemoglobin2015
Molecular Scanning of β-Thalassemia in the Southern Region of Central Java, Indonesia; a Step Towards a Local Prevention Program.Rujito L, Basalamah M, Mulatsih S, Sofro AS Hemoglobin2015
Frequency of Hospitalizations for Pain and Association With Altered Brain Network Connectivity in Sickle Cell Disease.Darbari DS, Hampson JP, Ichesco E, Kadom N, Vezina G, Evangelou I, Clauw DJ, Taylor Vi JG, Harris RE J Pain2015
Brodie's Abscess in a Patient Presenting with Sickle Cell Vasoocclusive Crisis.Ogbonna OH, Paul Y, Nabhani H, Medina A Case Rep Med2015
Evidence of Selection for the α-Globin Gene Deletions and Triplications in a Southern Chinese Population.Xie XM, Wu MY, Li DZ Hemoglobin2015
Identification of a Rare β(0)-Thalassemia Mutation, Codon 54 (-T) (HBB: c.165delT) in an Iranian Family.Ghasemian Dastjerdy N, Banihashemi A, Azizi M, Akhavan-Niaki H Hemoglobin2015
Molecular Epidemiological Investigation of Thalassemia in the Chengdu Region, Sichuan Province, Southwest China.Yu X, Yang LY, Yang HT, Liu CG, Cao DC, Shen W, Yang H, Zhan XF, Li J, Xue BR, Lin M Hemoglobin2015
Adults with sickle cell disease may perform cognitive tests as well as controls when processing speed is taken into account: a preliminary case-control study.Crawford RD, Jonassaint CR J Adv Nurs2015
Thalassaemia in children: from quality of care to quality of life.Amid A, Saliba AN, Taher AT, Klaassen RJ Arch. Dis. Child.2015
Acute Splenic Sequestration Crisis in Adult Sickle Cell Disease: A Report of 16 Cases.Naymagon L, Pendurti G, Billett HH Hemoglobin2015
Frequencies of HKαα and anti-HKαα Alleles in Chinese Carriers of Silent Deletional α-Thalassemia.Wu MY, Li J, Li SC, Li Y, Li DZ Hemoglobin2015
The Spectrum of α-Thalassemia Mutations in Kermanshah Province, West Iran.Alibakhshi R, Mehrabi M, Omidniakan L, Shafieenia S Hemoglobin2015
Genetic diminution of circulating prothrombin ameliorates multiorgan pathologies in sickle cell disease mice.Arumugam PI, Mullins ES, Shanmukhappa SK, Monia BP, Loberg A, Shaw MA, Rizvi T, Wansapura J, Degen JL, Malik P Blood2015
Oxidative stress in β-thalassaemia and sickle cell disease.Voskou S, Aslan M, Fanis P, Phylactides M, Kleanthous M Redox Biol2015
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Cell signaling pathways involved in drug-mediated fetal hemoglobin induction: Strategies to treat sickle cell disease.Pace BS, Liu L, Li B, Makala LH Exp. Biol. Med. (Maywood)2015
Prophylactic laparoscopic cholecystectomy in adult sickle cell disease patients with cholelithiasis: A prospective cohort study.Muroni M, Loi V, Lionnet F, Girot R, Houry S Int J Surg2015
Changes in Conjunctival Hemodynamics Predict Albuminuria in Sickle Cell Nephropathy.Kord Valeshabad A, Wanek J, Saraf SL, Gaynes BI, Gordeuk VR, Molokie RE, Shahidi M Am. J. Nephrol.2015
Do the Eyes Reveal More Than Scleral Icterus in Sickle Cell Disease?Pittman CA, Fitzhugh CD Am. J. Nephrol.2015
Macular Vascular Abnormalities Identified by Optical Coherence Tomographic Angiography in Patients With Sickle Cell Disease.Han IC, Tadarati M, Scott AW JAMA Ophthalmol2015
The relationship between genotype, psychiatric symptoms and quality of life in adult patients with sickle cell disease in São Paulo, Brazil: a cross-sectional study.Mastandréa ÉB, Lucchesi F, Kitayama MM, Figueiredo MS, Citero VA Sao Paulo Med J2015
[Comparison of the effect of three β-thalassemia prenatal screening strategies using in Guangdong province].Li B, Yin A, Luo M, Wu L, Ma Y, Wang X, Zhang X, Zhao Q Zhonghua Fu Chan Ke Za Zhi2015
Breathing Exercises for Inpatients with Sickle Cell Disease.Matthie N, Brewer CA, Moura VL, Jenerette CM Medsurg Nurs2015
Does Profile of Hemoglobin Eβ-thalassemia Patients Change After Splenectomy? Experience of a Tertiary Thalassemia Care Centre in Eastern India.Mandal PK, Ghosh MK, Bhattacharyya M Indian J Hematol Blood Transfus2015
[Hemolytic anemias and vitamin B12 deficieny].Dietzfelbinger H, Hubmann M Dtsch. Med. Wochenschr.2015
Effect of Chronic Blood Transfusion on Biomarkers of Coagulation Activation and Thrombin Generation in Sickle Cell Patients at Risk for Stroke.Hyacinth HI, Adams RJ, Greenberg CS, Voeks JH, Hill A, Hibbert JM, Gee BE PLoS ONE2015
Low Oxygen Affinity Variant Haemoglobin in an elderly woman presenting with low oxygen saturation.Igbineweka NE, Horne GA, Jackson MB, Chevassut TJ Acute Med2015
Prevention of Morbidity in sickle cell disease--qualitative outcomes, pain and quality of life in a randomised cross-over pilot trial of overnight supplementary oxygen and auto-adjusting continuous positive airways pressure (POMS2a): study protocol for a randomised controlled trial.Howard J, Inusa B, Liossi C, Jacob E, Murphy PB, Hart N, Gavlak J, Sahota S, Chorozoglou M, Nwosu C, Gwam M, Gupta A, Rees DC, Thein SL, Reading IC, Kirkham FJ, Cheng MY Trials2015
Hydroxyurea therapy for children with sickle cell disease: describing how caregivers make this decision.Creary S, Zickmund S, Ross D, Krishnamurti L, Bogen DL BMC Res Notes2015
Prophylactic transfusion for pregnant women with sickle cell disease: a systematic review and meta-analysis.Malinowski AK, Shehata N, D'Souza R, Kuo KH, Ward R, Shah PS, Murphy K Blood2015
Pathophysiology and perioperative management of sickle cell disease.Paradowski K J Perioper Pract2015
Electrocardiographic abnormalities and dyslipidaemic syndrome in children with sickle cell anaemia.Adegoke SA, Okeniyi JA, Akintunde AA Cardiovasc J Afr2015
Updated Mechanisms of Sickle Cell Disease-Associated Chronic pain.Lutz B, Meiler SE, Bekker A, Tao YX Transl Perioper Pain Med2015
Systematic and Meta-Analytic Review: Medication Adherence Among Pediatric Patients With Sickle Cell Disease.Loiselle K, Lee JL, Szulczewski L, Drake S, Crosby LE, Pai AL J Pediatr Psychol2015
Development and Validation of a Multidimensional Expectation Questionnaire for Thalassaemia Major Patients.Koutelekos IG, Kyritsi H, Makis A, Vassalos CM, Ktenas E, Polikandrioti M, Tzoumaka-Bakoula C, Chaliasos N Glob J Health Sci2015
Mortal quintet of sickle cell diseases.Helvaci MR, Gokce C, Davran R, Akkucuk S, Ugur M, Oruc C Int J Clin Exp Med2015
Oral and Dental Considerations in Management of Sickle Cell Anemia.Acharya S Int J Clin Pediatr Dent2015
Psychosocial and Functional Outcomes in Youth with Chronic Sickle Cell Pain.Sil S, Cohen LL, Dampier C Clin J Pain2015
Validation of a novel point of care testing device for sickle cell disease.Kanter J, Telen MJ, Hoppe C, Roberts CL, Kim JS, Yang X BMC Med2015
Gap-PCR Screening for Common Large Deletional Mutations of β-Globin Gene Cluster Revealed a Higher Prevalence of the Turkish inv/del (δβ)o Mutation in Antalya.Bilgen T, Altiok Clark O, Öztürk Z, Yesilipek MA, Keser İ Turk J Haematol2015
Evaluation of Alpha-Thalassemia Mutations in Cases with Hypochromic Microcytic Anemia: The İstanbul Perspective.Karakaş Z, Koç B, Temurhan S, Elgün T, Karaman S, Asker G, Gencay G, Timur Ç, Yıldırmak ZY, Celkan T, Devicioğlu Ö, Aydın F Turk J Haematol2015
First Observation of Hemoglobin Kansas [β102(G4)Asn→Thr, AAC>ACC] in Turkish Population.Keser İ, Öztaş A, Bilgen T, Canatan D Turk J Haematol2015
Correlation of BACH1 and HbE/Beta-Thalassemia Globin Expression.Lee TY, Muniandy L, Teh LK, Abdullah M, George E, Sathar J, Lai MI Turk J Haematol2015
Serum Lipids in Turkish Patients with β-Thalassemia Major and β-Thalassemia Minor.Balcı YI, Unal S, Gumruk F Turk J Haematol2015
Hemoglobin H Dısease In Turkey: Experıence From Eıght Center.Ünal S, Oktay G, Acıpayam C, Ilhan G, Gali E, Celkan T, Bay A, Malbora B, Akar N, Oymak Y, Toptaş T Turk J Haematol2015
Hemoglobin switching's surprise: the versatile transcription factor BCL11A is a master repressor of fetal hemoglobin.Bauer DE, Orkin SH Curr. Opin. Genet. Dev.2015
Gilbert syndrome acts as a risk factor of developing gallstone among β hemoglobinopathy Tunisian patients.Chaouch L, Kalai M, Chaouachi D, Mallouli F, Hafsia R, Ben Ammar S, Abbes S Tunis Med2015
Iron restriction in sickle cell anemia: Time for controlled clinical studies.Castro O, Kato GJ Am. J. Hematol.2015
BCL11A enhancer dissection by Cas9-mediated in situ saturating mutagenesis.Canver MC, Smith EC, Sher F, Pinello L, Sanjana NE, Shalem O, Chen DD, Schupp PG, Vinjamur DS, Garcia SP, Luc S, Kurita R, Nakamura Y, Fujiwara Y, Maeda T, Yuan GC, Zhang F, Orkin SH, Bauer DE Nature2015
A review of spontaneous intracranial extradural hematoma in sickle-cell disease.Hettige S, Sofela A, Bassi S, Chandler C Acta Neurochir (Wien)2015
The Spectrum of β-Thalassemia Mutations in a Population from the Brazilian Amazon.Silva AN, Cardoso GL, Cunha DA, Diniz IG, Santos SE, Andrade GB, Trindade SM, Cardoso MD, Francês LT, Guerreiro JF Hemoglobin2015
Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease.Akinbami AO, Campbell AD, Han ZJ, Luo HY, Chui DH, Steinberg MH Hemoglobin2015
Distance from an Urban Sickle Cell Center and its Effects on Routine Healthcare Management and Rates of Hospitalization.Smeltzer MP, Nolan VG, Yu X, Nottage KA, Wang WC, Hankins JS, Gurney JG Hemoglobin2015
ICSH recommendations for assessing automated high-performance liquid chromatography and capillary electrophoresis equipment for the quantitation of HbA2.Stephens AD, Colah R, Fucharoen S, Hoyer J, Keren D, McFarlane A, Perrett D, Wild BJ, Int J Lab Hematol2015
Sleep Quality, Pain and Self-Efficacy among Community-Dwelling Adults with Sickle Cell Disease.Adegbola M J Natl Black Nurses Assoc2015
Amelioration of inflammation and tissue damage in sickle cell model mice by Nrf2 activation.Keleku-Lukwete N, Suzuki M, Otsuki A, Tsuchida K, Katayama S, Hayashi M, Naganuma E, Moriguchi T, Tanabe O, Engel JD, Imaizumi M, Yamamoto M Proc. Natl. Acad. Sci. U.S.A.2015
A Japanese Family with Congenital Erythrocytosis Caused by Haemoglobin Bethesda.Tamura S, Tamura T, Gima H, Nishikawa A, Okamoto Y, Kanazawa N, Relvas L, Cunha E, Frances McMullin M, Bento C Intern. Med.2015
Pulmonary Endarterectomy as Treatment for Chronic Thromboembolic Pulmonary Hypertension in Sickle Cell Disease.Freeman AT, Ataga KI Am. J. Hematol.2015
Barriers to care and quality of primary care services in children with sickle cell disease.Jacob E, Childress C, Nathanson JD J Adv Nurs2015
Prevalence and incidence of erythrovirus B19 infection in children with sickle cell disease: The impact of viral infection in acute clinical events.Dos Santos Brito Silva Furtado M, Borato Viana M, Silqueira Hickson Rrios J, Laís Lima Gontijo R, Maria Silva C, do Val Rezende P, de Figueiredo RM, Martins ML J. Med. Virol.2015
Considerations of red blood cell molecular testing in transfusion medicine.Svensson AM, Delaney M Expert Rev. Mol. Diagn.2015
Hydroxyurea therapy for sickle cell anemia.McGann PT, Ware RE Expert Opin Drug Saf2015
Absolute Reticulocyte Count Acts as a Surrogate for Fetal Hemoglobin in Infants and Children with Sickle Cell Anemia.Meier ER, Byrnes C, Weissman M, Lee YT, Miller JL PLoS ONE2015
Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels.Danjou F, Zoledziewska M, Sidore C, Steri M, Busonero F, Maschio A, Mulas A, Perseu L, Barella S, Porcu E, Pistis G, Pitzalis M, Pala M, Menzel S, Metrustry S, Spector TD, Leoni L, Angius A, Uda M, Moi P, Thein SL, Galanello R, Abecasis GR, Schlessinger D, Sanna S, Cucca F Nat. Genet.2015
Glomerular and tubular functions in children with different forms of beta thalassemia.Uzun E, Balcı YI, Yüksel S, Aral YZ, Aybek H, Akdağ B Ren Fail2015
A novel gap-PCR with high resolution melting analysis for the detection of α-thalassaemia Southeast Asian and Filipino β°-thalassaemia deletion.Kho SL, Chua KH, George E, Tan JA Sci Rep2015
Characterization of Clinical and Laboratory Profiles of the Deletional α2-Globin Gene Polyadenylation Signal Sequence (AATAAA > AATA- -) in an Indian Population.Deshpande P, Kamalanathan N, Sampath E, George B, Shaji RV, Edison ES Hemoglobin2015
Correlation between blood rheological properties and red blood cell Indices(MCH, MCV, MCHC) in healthy women.Tempelhoff GV, Schelkunov O, Demirhan A, Tsikouras P, Rath W, Velten E, Maka E, Csorba R Clin. Hemorheol. Microcirc.2015
[Symptomatic extramedullary haematopoiesis in β-thalassemia: A retrospective single centre study].Maazoun F, Gellen Dautremer J, Boutekadjirt A, Pissard S, Habibi A, Bachir D, Rahmouni A, Bartolucci P, Debbache K, Lagrange JL, Michel M, Galacteros F Rev Med Interne2015
Haptoglobin gene polymorphisms and interleukin-6 and -8 levels in patients with sickle cell anemia.Pierrot-Gallo BS, Vicari P, Matsuda SS, Adegoke SA, Mecabo G, Figueiredo MS Rev Bras Hematol Hemoter2015
Left ventricular hypertrophy in children, adolescents and young adults with sickle cell anemia.Faro GB, Menezes-Neto OA, Batista GS, Silva-Neto AP, Cipolotti R Rev Bras Hematol Hemoter2015
Hemoglobin A2 values in sickle cell disease patients quantified by high performance liquid chromatography and the influence of alpha thalassemia.da Fonseca SF, Amorim T, Purificação A, Gonçalves M, Boa-Sorte N Rev Bras Hematol Hemoter2015
The importance of hemoglobin A2 determination.Figueiredo MS Rev Bras Hematol Hemoter2015
Tissue Iron Distribution Assessed by MRI in Patients with Iron Loading Anemias.Gutiérrez L, House MJ, Vasavda N, Drašar E, Gonzalez-Gascon Y Marin I, Kulasekararaj AG, St Pierre TG, Thein SL PLoS ONE2015
Combination of Tmprss6-ASO and the iron chelator deferiprone improves erythropoiesis and reduces iron overload in a mouse model of beta-thalassemia intermedia.Casu C, Aghajan M, Oikonomidou PR, Guo S, Monia BP, Rivella S Haematologica2015
The long-term efficacy and tolerability of oral deferasirox for patients with transfusion-dependent β-thalassemia in Taiwan.Chang HH, Lu MY, Peng SS, Yang YL, Lin DT, Jou ST, Lin KH Ann. Hematol.2015
Differentiation Between Sickle Cell Anemia and S/β0 Thalassemia.Fanestil V, Van Siclen C Lab Med2015
How I Diagnose Non-thalassemic Microcytic Anemias.Bruno M, De Falco L, Iolascon A Semin. Hematol.2015
Mutation Spectrum of β-Thalassemia and Other Hemoglobinopathies in Chittagong, Southeast Bangladesh.Chatterjee T, Chakravarty A, Chakravarty S, Chowdhury MA, Sultana R Hemoglobin2015
Design of the DOVE (Determining Effects of Platelet Inhibition on Vaso-Occlusive Events) Trial: A Global Phase 3 Double-Blind, Randomized, Placebo-Controlled, Multicenter Study of the Efficacy and Safety of Prasugrel in Pediatric Patients With Sickle Cell Anemia Utilizing a Dose Titration Strategy.Hoppe CC, Styles L, Heath LE, Zhou C, Jakubowski JA, Winters KJ, Brown PB, Rees DC, Heeney MM Pediatr Blood Cancer2015
The Diagnostic Value of Pulsed Wave Tissue Doppler Imaging in Asymptomatic Beta- Thalassemia Major Children and Young Adults; Relation to Chemical Biomarkers of Left Ventricular Function and Iron Overload.Ragab SM, Fathy WM, El-Aziz WF, Helal RT Mediterr J Hematol Infect Dis2015
Influence of Sickle Cell Gene on the Allelic Diversity at the msp-1 locus of Plasmodium falciparum in Adult Patients with Severe Malaria.Patel DK, Mashon RS, Purohit P, Meher S, Dehury S, Marndi C, Das K, Kullu BK, Patel S, Das P Mediterr J Hematol Infect Dis2015
Caregiver Burden, Spirituality, and Psychological Well-Being of Parents Having Children with Thalassemia.Anum J, Dasti R J Relig Health2015
An accurate and affordable test for the rapid diagnosis of sickle cell disease could revolutionize the outlook for affected children born in resource-limited settings.Williams TN BMC Med2015
Too much technology--or just enough? Identifying hemoglobin variants through routine and advanced laboratory techniques.Burgess TE, Miller WM MLO Med Lab Obs2015
Rana et al. Hydroxyurea and Growth in Young Children With Sickle Cell Disease. Pediatrics. 2014;134(3):465-472. Pediatrics2015
Multiple Diaphyseal Bone Infarcts in a Patient With Sickle Cell Trait.Liao S, Solanki K, Doube A J Clin Rheumatol2015
Sickle Cell Hemoglobin in the Ferryl State Promotes βCys-93 Oxidation and Mitochondrial Dysfunction in Epithelial Lung Cells (E10).Kassa T, Jana S, Strader MB, Meng F, Jia Y, Wilson MT, Alayash AI J. Biol. Chem.2015
Understanding the contrasting spatial haplotype patterns of malaria-protective β-globin polymorphisms.Hockham C, Piel FB, Gupta S, Penman BS Infect. Genet. Evol.2015
Control materials for immunochromatographic strip used for α-thalassemia screening.Pornprasert S Clin. Chem. Lab. Med.2015
Association between Variants at BCL11A Erythroid-Specific Enhancer and Fetal Hemoglobin Levels among Sickle Cell Disease Patients in Cameroon: Implications for Future Therapeutic Interventions.Pule GD, Ngo Bitoungui VJ, Chetcha Chemegni B, Kengne AP, Antonarakis S, Wonkam A OMICS2015
Serendipity: A Rare Discovery of Haemoglobin D-Iran in An Indian Female During Routine Antenatal Screening for β-Thalassemia.Chandel RS, Roy A, Abichandani LG J Clin Diagn Res2015
The Acute Chest Syndrome in Cameroonian children living with sickle cell disease.Nansseu JR, Alima Yanda AN, Chelo D, Tatah SA, Mbassi Awa HD, Seungue J, Koki PO BMC Pediatr2015
Serendipitous detection of Hemoglobin G-Ferrara variant with Sysmex DIFF channel.Rosetti M, Poletti G, Ivaldi G, Rondoni M, Baldrati L, Dorizzi RM Clin. Biochem.2015
The frequency of silent cerebral ischemia in patients with transfusion-dependent β-thalassemia major.Karimi M, Toosi F, Haghpanah S, Pishdad P, Avazpour A, Rachmilewitz EA Ann. Hematol.2015
Prevalence of Pulmonary Hypertension in Patients with Thalassemia Intermedia in 2009: a single center's experience.Moghaddam HM, Badiei Z, Eftekhari K, Shakeri R, Farhangi H Electron Physician2015
[Epileptic seizures and hematemesis in a young patient with sickle cell disease].Chevalier J, Villeneuve J, Lecapitaine AL, Gros H, Bakir R, Delaval A, Bouldouyre MA Rev Med Interne2015
Generation of iPSC line MU011.A-hiPS from homozygous α-thalassemia fetal skin fibroblasts.Tangprasittipap A, Satirapod C, Jittorntrum B, Lertritanan S, Anurathaphan U, Phanthong P, Borwornpinyo S, Kitiyanant N, Hongeng S Stem Cell Res2015
Prevention of Ischemic Priapism in Sickle Cell Disease: Sildenafil: Commentary on: Randomized Controlled Trial of Sildenafil for Preventing Recurrent Ischemic Priapism in Sickle Cell Disease.Shakeri A, Van Asseldonk B, Elterman DS Urology2015
Adjunctive therapy with inhaled nitric oxide for severe acute chest syndrome in patients with sickle cell disease.Wrigge H, Costa EL, Busch T Intensive Care Med2015
Inhaled nitric oxide for acute chest syndrome in adult sickle cell patients: a randomized controlled study.Maitre B, Djibre M, Katsahian S, Habibi A, Stankovic Stojanovic K, Khellaf M, Bourgeon I, Lionnet F, Charles-Nelson A, Brochard L, Lemaire F, Galacteros F, Brun-Buisson C, Fartoukh M, Mekontso Dessap A Intensive Care Med2015
Investigating the mental health and coping strategies of parents with major thalassemic children in Bandar Abbas.Dadipoor S, Haghighi H, Madani A, Ghanbarnejad A, Shojaei F, Hesam A, Moradabadi AS J Educ Health Promot2015
Juvenile fibromyalgia in an adolescent patient with sickle cell disease presenting with chronic pain.Ramprakash S, Fishman D BMJ Case Rep2015
Population Screening and Prevention Strategies for Thalassemias and other Hemoglobinopathies of Eastern India: Experience of 18,166 cases.Chatterjee T, Chakravarty A, Chakravarty S Hemoglobin2015
Hemoglobin oxidation at functional amino acid residues during routine storage of red blood cells.Wither M, Dzieciatkowska M, Nemkov T, Strop P, D'Alessandro A, Hansen KC Transfusion2015
Priapism in Homozygous Sickle Cell Disease: A 40-year Study of the Natural History.Serjeant G, Hambleton ID West Indian Med J2015
Erratum to Opi DH, Ochola LB, Tendwa M, Siddondo BR, Ocholla H, Fanjo H, Ghumra A, Ferguson DJ, Rowe JA, Williams TN EBioMedicine2015
A Retrospective Analysis of the Significance of Haemoglobin SS and SC in Disease Outcome in Patients With Sickle Cell Disease and Dengue Fever.Rankine-Mullings A, Reid ME, Moo Sang M, Richards-Dawson MA, Knight-Madden JM EBioMedicine2015
Hemoglobin E disease and glycosylated hemoglobin.Yedla N, Kuchay MS, Mithal A Indian J Endocrinol Metab2015
Frequency of Red Cell Alloimmunization and Autoimmunization in Thalassemia Patients: A Report from Eastern India.Datta SS, Mukherjee S, Talukder B, Bhattacharya P, Mukherjee K Adv Hematol2015
A predictable but life-threatening complication of hydroxyurea in a patient with sickle cell anaemia: an experience learned from a Jehovah's Witness.Tun AM, Naing EE, Tun NM, Guevara E BMJ Case Rep2015
A Sickle Cell Disease Patient with Severe Tricuspid Regurgitation and Early Developed Pulmonary Hypertension.Vaidya G, Sarwar M, Sun Z, Wei T, Liu K Intern. Med.2015
Management of Maxillary Deformity with Segmental Osteotomy followed by Implant Insertion in β-Thalassemia Major Patient.Pektas ZO, Cubuk S, Kircelli B, Uckan S J Contemp Dent Pract2015
Pulmonary Functions in Children With Thalassemia Major.Ozyoruk D, Misirlioglu ED J. Pediatr. Hematol. Oncol.2015
The Changing Epidemiology of Pediatric Hemoglobinopathy Patients in Northern Alberta, Canada.Corriveau-Bourque C, Bruce AA J. Pediatr. Hematol. Oncol.2015
Application of an Asthma Screening Questionnaire in Children with Sickle Cell Disease.Yadav A, Corrales-Medina FF, Stark JM, Hashmi SS, Carroll MP, Smith KG, Meulmester KM, Brown DL, Jon C, Mosquera RA Pediatr Allergy Immunol Pulmonol2015
Relationship Between Serum Hepcidin and Ferritin Levels in Patients With Thalassemia Major and Intermedia in Southern Iran.Haghpanah S, Esmaeilzadeh M, Honar N, Hassani F, Dehbozorgian J, Rezaei N, Abdollahi M, Bardestani M, Safaei S, Karimi M Iran Red Crescent Med J2015
[Sickle cell disease and biliary lithiasis - about two observations in Lubumbashi (DR Congo)].Ngombe LK, Mukanya PK, Kanteng GW, Mulangu AM, Numbi OL Pan Afr Med J2015
Safety Profile of Oral Iron Chelator Deferiprone in Chinese Children with Transfusion-dependent Thalassaemia.Botzenhardt S, Sing CW, Wong IC, Chan GC, Wong LY, Felisi M, Rascher W, Ceci A, Neubert A Curr Drug Saf2015
[Application of multiplex ligation-dependent probe amplification technique in prenatal diagnosis of α-thalassemia].Hao Y, Xu X, Xu Z, Jiang N, Wu W, Jin Q, Yin S, Cai Y, Xie J Zhonghua Yi Xue Yi Chuan Xue Za Zhi2015
Co-heredity of silent CAP + 1570 T>C (HBB:c*96T>C) defect and severe β-thal mutation: a cause of mild β-thalassemia intermedia.Vinciguerra M, Passarello C, Cassarà F, Leto F, Cannata M, Calvaruso G, Di Maggio R, Renda D, Maggio A, Giambona A Int J Lab Hematol2015
Transfusion-acquired Hemoglobinopathies: A Report of Two Cases.Somasundaram V, Purohit A, Manivannan P, Saxena R J Lab Physicians2015
Anaesthetic management of beta thalassemia major with hypersplenism for splenectomy in pediatric age group: Report of four cases.Jyothi B, Sushma KS, Syeda S, Raza SO Anesth Essays Res2015
Nocturnal enuresis: prevalence and risk factors among school-aged children with sickle-cell anaemia in a South-east Nigerian city.Eneh CI, Okafor HU, Ikefuna AN, Uwaezuoke SN Ital J Pediatr2015
Prevention of conversion to abnormal tcd with hydroxyurea in sickle cell anemia: A phase III international randomized clinical trial.Hankins JS, McCarville MB, Rankine-Mullings A, Reid ME, Lobo CL, Moura PG, Ali S, Soares D, Aldred K, Jay DW, Aygun B, Bennett J, Kang G, Goldsmith JC, Smeltzer MP, Boyett JM, Ware RE Am. J. Hematol.2015
Recent patents and technology transfer for molecular diagnosis of β-thalassemia and other hemoglobinopathies.Breveglieri G, Finotti A, Borgatti M, Gambari R Expert Opin Ther Pat2015
Distinctive Acellular Lipid Emboli in Hemoglobin SC Disease following Bone Marrow Infarction with Parvovirus Infection.Graff DM, Owen E, Bendon R, Bertolone S, Raj A Case Rep Hematol2015
Hydroxyurea and Zileuton Differentially Modulate Cell Proliferation and Interleukin-2 Secretion by Murine Spleen Cells: Possible Implication on the Immune Function and Risk of Pain Crisis in Patients with Sickle Cell Disease.Kuvibidila S, Warrier RP, Haynes J, Baliga SB Ochsner J2015
[Genotypes and clinical features of 595 children with HbH disease in Guangxi, China].He S, Zhang Q, Chen BY, Huang P, Tang YQ, Wei Y, Chen QL, Zheng CG Zhongguo Dang Dai Er Ke Za Zhi2015
Sea-level haemoglobin concentration is associated with greater exercise capacity in Tibetan males at 4200 m.Wagner PD, Simonson TS, Wei G, Wagner HE, Wuren T, Qin G, Yan M, Ge RL Exp. Physiol.2015
Infection, Immune Disorders, Hemoglobinopathies, and Lower Extremity Wounds: Are We Doing Enough?Rerkasem K, Mani R Int J Low Extrem Wounds2015
Hematopoietic stem cell transplantation in the Eastern Mediterranean Region (EMRO) 2011-2012: A comprehensive report on behalf of the Eastern Mediterranean Blood and Marrow Transplantation group (EMBMT).Aljurf M, Nassar A, Hamidieh AA, Elhaddad A, Hamladji RM, Bazarbachi A, Ibrahim A, Ben Othman T, Abdel-Rahman F, Alseraihy A, Fahmy O, Hussein AA, Alabdulaaly A, Adil S, Alkindi SS, Bayoumy M, Dennison D, Bekadja MA, Redhouane AN, Rasheed W, AlSagheir A, Alsudairy R, Ladeb S, Benchekroun S, Ramzi M, Ahmed P, ElSolh H, Ahmed SO, Hussain F, Ghavamzadeh A Hematol Oncol Stem Cell Ther2015
Laser therapy for retinopathy in sickle cell disease.Myint KT, Sahoo S, Thein AW, Moe S, Ni H Cochrane Database Syst Rev2015
Activation of the erythroid K-Cl cotransporter Kcc1 enhances sickle cell disease pathology in a humanized mouse model.Brown FC, Conway AJ, Cerruti L, Collinge JE, McLean C, Wiley JS, Kile BT, Jane SM, Curtis DJ Blood2015
Youth with Sickle Cell Disease: Genetic and Sexual Health Education Needs.Housten AJ, Abel RA, Dadekian J, Schwieterman K, Jason D, King AA Am J Health Behav2015
Exploring Transition to Self-Management Within the Culture of Sickle Cell Disease.Labore N, Mawn B, Dixon J, Andemariam B J Transcult Nurs2015
Quantitative trait locus analysis of parasite density reveals that HbS gene carriage protects severe malaria patients against Plasmodium falciparum Sambo MR, Penha-Gonçalves C, Trovoada MJ, Costa J, Lardoeyt R, Coutinho A Malar. J.2015
Trend in Prevalence of Hepatitis C Virus Infection among β-thalassemia Major Patients: 10 Years of Experience in Iran.Jafroodi M, Davoudi-Kiakalayeh A, Mohtasham-Amiri Z, Pourfathollah AA, Haghbin A Int J Prev Med2015
Importance of methodological standardization for the ektacytometric measures of red blood cell deformability in sickle cell anemia.Renoux C, Parrow N, Faes C, Joly P, Hardeman M, Tisdale J, Levine M, Garnier N, Bertrand Y, Kebaili K, Cuzzubbo D, Cannas G, Martin C, Connes P Clin. Hemorheol. Microcirc.2015
Conjunctival microvascular hemodynamics following vaso-occlusive crisis in sickle cell disease.Valeshabad AK, Wanek J, Gaynes B, Saraf SL, Molokie R, Shahidi M Clin. Hemorheol. Microcirc.2015
Pfaffia Paniculata extract improves red blood cell deformability in sickle cell patients.Mozar A, Charlot K, Sandor B, Rabaï M, Lemonne N, Billaud M, Hardy-Dessources MD, Beltan E, Pandey RC, Connes P, Ballas SK Clin. Hemorheol. Microcirc.2015
Musculoskeletal complications of haematological disease.Morais SA, du Preez HE, Akhtar MR, Cross S, Isenberg DA Rheumatology (Oxford)2015
Premarital genetic screening for beta thalassemia carrier status of indexed families using HbA2 electrophoresis.Nosheen A, , Ahmad H, Qayum I, Siddiqui N, Abbasi FM, , Iqbal MS J Pak Med Assoc2015
Changes in the skeletal system and extramedullary hematopoiesis in a patient with thalassemia.Cullu N, Deveer M, Yeniceri O, Kalemci S Quant Imaging Med Surg2015
Protective effect of HLA-DQB1 alleles against alloimmunization in patients with sickle cell disease.Tatari-Calderone Z, Gordish-Dressman H, Fasano R, Riggs M, Fortier C, Campbell AD, Charron D, Gordeuk VR, Luban NL, Vukmanovic S, Tamouza R Hum. Immunol.2015
Coexistence of rare variant HbD Punjab [α2β2121(Glu→Gln)] and alpha 3.7 kb deletion in a young boy of Hindu family in West Bengal, India.Ghosh A, Basak J, Mukhopadhyay A Cell. Mol. Biol. Lett.2015
Generation of Human Induced Pluripotent Stem Cells from Extraembryonic Tissues of Fetuses Affected by Monogenic Diseases.Spitalieri P, Talarico RV, Botta A, Murdocca M, D'Apice MR, Orlandi A, Giardina E, Santoro M, Brancati F, Novelli G, Sangiuolo F Cell Reprogram2015
Association between Hospital Volume and Within-Hospital Intensive Care Unit Transfer for Sickle Cell Disease in Children's Hospitals.Raphael JL, Richardson T, Hall M, Oyeku SO, Bundy DG, Kalpatthi RV, Shah SS, Ellison AM J. Pediatr.2015
The factors influencing utilization of hospital services by adult sickle cell disease patients: a systematic review protocol.Benenson I, Jadotte YT, Echevarria M JBI Database System Rev Implement Rep2015
A complicated disease: what can be done to manage thalassemia major more effectively?Origa R, Baldan A, Marsella M, Borgna-Pignatti C Expert Rev Hematol2015
Genitourinary manifestations of sickle cell disease.Gebreselassie S, Simmons MN, Montague DK Cleve Clin J Med2015
First Documented Transmission of Trypanosoma cruzi Infection through Blood Transfusion in a Child with Sickle-Cell Disease in Belgium.Blumental S, Lambermont M, Heijmans C, Rodenbach MP, El Kenz H, Sondag D, Bottieau E, Truyens C PLoS Negl Trop Dis2015
Pattern and prevelence of alloimmunization in multiply transfused patients with sickle cell disease in Nigeria.Kangiwa U, Ibegbulam O, Ocheni S, Madu A, Mohammed N Biomark Res2015
APHON/ASPHO Policy Statement for the Transition of Patients With Sickle Cell Disease From Pediatric to Adult Health Care.Bryant R, Porter JS, Sobota A J Pediatr Oncol Nurs2015
The free heme concentration in healthy human erythrocytes.Aich A, Freundlich M, Vekilov PG Blood Cells Mol. Dis.2015
Klotho, a new marker for osteoporosis and muscle strength in β-thalassemia major.Baldan A, Giusti A, Bosi C, Malaventura C, Musso M, Forni GL, Volpato S, Zuliani G, Borgna-Pignatti C Blood Cells Mol. Dis.2015
Effect of deferasirox on iron overload in patients with transfusion-dependent haemoglobinopathies.Fragomeno C, Roccabruna E, D'Ascola DG Blood Cells Mol. Dis.2015
Rapamycin increases fetal hemoglobin and ameliorates the nociception phenotype in sickle cell mice.Khaibullina A, Almeida LE, Wang L, Kamimura S, Wong EC, Nouraie M, Maric I, Albani S, Finkel J, Quezado ZM Blood Cells Mol. Dis.2015
Study of alpha hemoglobin stabilizing protein expression in patients with β thalassemia and sickle cell anemia and its impact on clinical severity.Mahmoud HM, Shoeib AA, Abd El Ghany SM, Reda MM, Ragab IA Blood Cells Mol. Dis.2015
Filterability of freshly-collected sickle erythrocytes under venous oxygen pressure without exposure to air.Shah S, Acholonu RG, Ohene-Frempong K, Asakura T Blood Cells Mol. Dis.2015
TR2/TR4 overexpression in a humanized sickle cell disease mouse model decreases RBC adhesion to VCAM-1.White JC, Pawar A, Fu G, Cui S, Tavernier F, Hamid M, Harro D, Giacherio D, Campbell AD, Hines PC Blood Cells Mol. Dis.2015
Erythropoietic drive is the strongest predictor of hepcidin level in adults with sickle cell disease.Karafin MS, Koch KL, Rankin AB, Nischik D, Rahhal G, Simpson P, Field JJ Blood Cells Mol. Dis.2015
Peroxisome proliferator-activated receptor-α-mediated transcription of miR-301a and miR-454 and their host gene SKA2 regulates endothelin-1 and PAI-1 expression in sickle cell disease.Gonsalves CS, Li C, Malik P, Tahara SM, Kalra VK Biosci. Rep.2015
Hemoglobin C after a red blood cell transfusion for sickle cell disease.DeSimone RA, Mitsios JV, Kucine N, Goss CA, Chadburn A, Cushing MM Transfusion2015
[Iron dysregulation and anemias].Ikuta K Rinsho Ketsueki2015
The Challenges and Opportunities Associated with Sickle Cell Disease Prevention, Education, and Management.Smith M, Praetorius RT Soc Work Public Health2015
Challenges in Prenatal Diagnosis of Beta Thalassaemia: Couples with Normal HbA2 in One Partner.Gorivale M, Sawant P, Mehta P, Nadkarni A, Ghosh K, Colah R Prenat. Diagn.2015
Establishing sickle cell diagnostics and characterizing a paediatric sickle cell disease cohort in Malawi.Heimlich JB, Chipoka G, Kamthunzi P, Krysiak R, Majawa Y, Mafunga P, Fedoriw Y, Phiri A, Key NS, Ataga KI, Gopal S Br. J. Haematol.2015
Spinal versus general anesthesia for Cesarean section in patients with sickle cell anemia.Bakri MH, Ismail EA, Ghanem G, Shokry M Korean J Anesthesiol2015
Erythroferrone: the missing link in β-thalassemia?Moura IC, Hermine O Blood2015
HbM methaemoglobinaemia as a rare case of early neonatal benign cyanosis.Elboraee MS, Clarke G, Belletrutti MJ, Escoredo S BMJ Case Rep2015
Hematopoietic stem cell transplantation from non-sibling matched family donors for patients with thalassemia major in Jordan.Hussein AA, Al-Zaben A, Khattab E, Haroun A, Frangoul H Pediatr Transplant2015
Hydroxyurea: Clinical and Hematological Effects in Patients With Sickle Cell Anemia.Keikhaei B, Yousefi H, Bahadoram M Glob J Health Sci2015
β-thalassemia patients and gynecological approach: review and clinical experience.Ambroggio S, Peris C, Picardo E, Mitidieri M, Minniti E, Benedetto C, Gregori G, Baù MG Gynecol. Endocrinol.2015
Autologous bone marrow stromal cells are promising candidates for cell therapy approaches to treat bone degeneration in sickle cell disease.Lebouvier A, Poignard A, Coquelin-Salsac L, Léotot J, Homma Y, Jullien N, Bierling P, Galactéros F, Hernigou P, Chevallier N, Rouard H Stem Cell Res2015
Risk factor analysis of cerebral white matter hyperintensities in children with sickle cell disease.van der Land V, Mutsaerts HJ, Engelen M, Heijboer H, Roest M, Hollestelle MJ, Kuijpers TW, Nederkoorn PJ, Cnossen MH, Majoie CB, Nederveen AJ, Fijnvandraat K Br. J. Haematol.2015
Transitioning Adolescents and Young Adults With Sickle Cell Disease From Pediatric to Adult Health Care: Provider Perspectives.Stollon NB, Paine CW, Lucas MS, Brumley LD, Poole ES, Peyton T, Grant AW, Jan S, Trachtenberg S, Zander M, Bonafide CP, Schwartz LA J. Pediatr. Hematol. Oncol.2015
Pulmonary Platelet Thrombi and Vascular Pathology in Acute Chest Syndrome in Patients with Sickle Cell Disease.Anea CB, Lyon M, Lee I, Gonzales JN, Adeyemi A, Falls G, Kutlar A, Brittain JE Am. J. Hematol.2015
Sickle cell detection using a smartphone.Knowlton SM, Sencan I, Aytar Y, Khoory J, Heeney MM, Ghiran IC, Tasoglu S Sci Rep2015
Airway and alveolar nitric oxide production, lung function, and pulmonary blood flow in sickle cell disease.Lunt A, Ahmed N, Rafferty GF, Dick M, Rees D, Height S, Thein SL, Greenough A Pediatr. Res.2015
Ineffective erythropoiesis and regulation of iron status in iron loading anaemias.Camaschella C, Nai A Br. J. Haematol.2015
The Homozygous Hemoglobin EE Genotype and Chronic Inflammation Are Associated with High Serum Ferritin and Soluble Transferrin Receptor Concentrations among Women in Rural Cambodia.Karakochuk CD, Whitfield KC, Rappaport AI, Barr SI, Vercauteren SM, McLean J, Prak S, Hou K, Talukder A, Devenish R, Green TJ J. Nutr.2015
Venous thromboembolism in adults with sickle cell disease: experience of a single centre in the UK.van Hamel Parsons V, Gardner K, Patel R, Thein SL Ann. Hematol.2015
Pitfalls in the biological diagnosis of common hemoglobin disorders.Wajcman H, Moradkhani K Ann. Biol. Clin. (Paris)2015
Anaplastic Ependymoma in a Child With Sickle Cell Anemia: A Case Report Highlighting Treatment Challenges for Young Children With Central Nervous System Tumors and Underlying Vasculopathy.Crotty EE, Meier ER, Wells EM, Hwang EI, Packer RJ Pediatr Blood Cancer2015
Bone microstructural defects and osteopenia in hemizygous βIVSII-654 knockin thalassemic mice: sex-dependent changes in bone density and osteoclast function.Thongchote K, Svasti S, Teerapornpuntakit J, Suntornsaratoon P, Krishnamra N, Charoenphandhu N Am. J. Physiol. Endocrinol. Metab.2015
HB Puerta del Sol [HBA1:c.148A>C], HB Valdecilla [HBA2:c.3G>T], HB Gran Vía [HBA2:c.98T>G], HB Macarena [HBA2:c.358C>T], and HB El Retiro [HBA2:c.364_366dupGTG]: description of five new la Fuente-Gonzalo F, Nieto JM, Velasco D, Cela E, Pérez G, Fernández-Teijeiro A, Escudero A, Villegas A, González-Fernández FA, Ropero P Clin. Chem. Lab. Med.2015
The paradox of the serrated sickle erythrocyte: The importance of the red blood cell membrane topography.Ballas SK, Connes P Clin. Hemorheol. Microcirc.2015
Thalidomide can promote erythropoiesis by induction of STAT5 and repression of external pathway of apoptosis resulting in increased expression of GATA-1 transcription factor.Grzasko N, Chocholska S, Goracy A, Hus M, Dmoszynska A Pharmacol Rep2015
Prevalence of hemoglobin S trait among blood donors: a cross-sectional study.Antwi-Baffour S, Asare RO, Adjei JK, Kyeremeh R, Adjei DN BMC Res Notes2015
Hemoglobin-Based Nanoarchitectonic Assemblies as Oxygen Carriers.Jia Y, Duan L, Li J Adv. Mater. Weinheim2015
Diagnosis of a Family with the Novel -α(21.9) Thalassemia Deletion.Long J, Pang W, Sun L, Lao K, Weng X, Ye X, Wu S, Song C, Wei X, Yan S Hemoglobin2015
Health-related Quality of Life in Infants With Sickle Cell Disease.Beverung LM, Bemrich-Stolz C, Torres S, Panepinto JA J. Pediatr. Hematol. Oncol.2015
Fatigue in Children With Sickle Cell Disease: Association With Neurocognitive and Social-Emotional Functioning and Quality of Life.Anderson LM, Allen TM, Thornburg CD, Bonner MJ J. Pediatr. Hematol. Oncol.2015
Red Blood Cell Membrane-Facilitated Release of Nitrite-Derived Nitric Oxide Bioactivity.Salgado MT, Cao Z, Nagababu E, Mohanty JG, Rifkind JM Biochemistry2015
Re: Safety and Efficacy of Blood Exchange Transfusion for Priapism Complicating Sickle Cell Disease.Seftel AD J. Urol.2015
Successful Management of a Chronic Refractory Leg Ulcer in an Adolescent with Sickle Cell Anemia.Paolino G, Santopietro M, Palumbo G, Onesti MG, Micozzi A, Venosi S, Laurino M, Ferrazza G, Fino P, Foà R, Giona F Acta Dermatovenerol Croat2015
Pregnancy outcomes among women with beta-thalassemia trait.Charoenboon C, Jatavan P, Traisrisilp K, Tongsong T Arch. Gynecol. Obstet.2015
TIGIT-positive circulating follicular helper T cells and sickle cell alloimmunization.Pirenne F Haematologica2015
The association between glycated hemoglobin levels and mortality in non-diabetic elderly subjects.Grossman A, Beloosesky Y, Schlesinger A, Gafter-Gvili A, Koren-Morag N, Meyerovitch J, Weiss A Eur. J. Intern. Med.2015
Hb Taybe: clinical and morphological findings in 43 patients.Koren A, Levin C, Zalman L, Palmor H, Filon D, Chubar E, Resnitzky P, Bennett M Eur. J. Haematol.2015
Screening for Thalassemia Carrier Status in Pregnancy and Pre-Natal Diagnosis.Gupta V, Sharma P, Jora R, Amandeep M, Kumar A Indian Pediatr2015
Iron Chelation in Thalassemia Major.Borgna-Pignatti C, Marsella M Clin Ther2015
Pharmacotherapy of Sickle Cell Disease in Children.Neville KA, Panepinto JA Curr. Pharm. Des.2015
How to Use SNP_TATA_Comparator to Find a Significant Change in Gene Expression Caused by the Regulatory SNP of This Gene's Promoter via a Change in Affinity of the TATA-Binding Protein for This Promoter.Ponomarenko M, Rasskazov D, Arkova O, Ponomarenko P, Suslov V, Savinkova L, Kolchanov N Biomed Res Int2015
DETECTION OF DELETION α(+)-THALASSEMIA MUTATION [-α (3.7), -α (4.2)] BY QUANTITATIVE PCR ASSAY.Seeratanachot T, Shimbhu D, Charoenkwan P, Sanguansermsri T Southeast Asian J. Trop. Med. Public Health2015
Coagulation activation in sickle cell trait: an exploratory study.Amin C, Adam S, Mooberry MJ, Kutlar A, Kutlar F, Esserman D, Brittain JE, Ataga KI, Chang JY, Wolberg AS, Key NS Br. J. Haematol.2015
Impact of red blood cell alloimmunization on sickle cell disease mortality: a case series.Nickel RS, Hendrickson JE, Fasano RM, Meyer EK, Winkler AM, Yee MM, Lane PA, Jones YA, Pashankar FD, New T, Josephson CD, Stowell SR Transfusion2015
A Novel High-Content Immunofluorescence Assay as a Tool to Identify at the Single Cell Level γ-Globin Inducing Compounds.Durlak M, Fugazza C, Elangovan S, Marini MG, Marongiu MF, Moi P, Fraietta I, Cappella P, Barbarani G, Font-Monclus I, Mauri M, Ottolenghi S, Gasparri F, Ronchi A PLoS ONE2015
Urinary Transforming Growth Factor β-1 as a Marker of Renal Dysfunction in Sickle Cell Disease.Ghobrial EE, Abdel-Aziz HA, Kaddah AM, Mubarak NA Pediatr Neonatol2015
Mechanism of two-photon excited hemoglobin fluorescence emission.Sun Q, Zheng W, Wang J, Luo Y, Qu JY J Biomed Opt2015
Photophysical characterization of sickle cell disease hemoglobin by multi-photon microscopy.Vigil GD, Howard SS Biomed Opt Express2015
Haemoglobin content modulated deformation dynamics of red blood cells on a compact disc.Kar S, Ghosh U, Maiti TK, Chakraborty S Lab Chip2015
Inheritance of Hereditary Persistence of Fetal Haemoglobin (HPFH) in a Family of Western Odisha, India.Patel S, Dehury S, Purohit P, Meher S, Das K J Clin Diagn Res2015
Prevalence of β(S)-globin gene haplotypes, α-thalassemia (3.7 kb deletion) and redox status in patients with sickle cell anemia in the state of Paraná, Brazil.Shimauti EL, Silva DG, de Souza EM, de Almeida EA, Leal FP, Bonini-Domingos CR Genet. Mol. Biol.2015
Indications and Results of HLA-Identical Sibling Hematopoietic Cell Transplantation for Sickle Cell Disease.Walters MC, De Castro LM, Sullivan KM, Krishnamurti L, Kamani N, Bredeson C, Neuberg D, Hassell KL, Farnia S, Campbell A, Petersdorf E Biol. Blood Marrow Transplant.2015
Challenges of vascular access in red cell exchange in sickle cell patients.Putensen D Br J Nurs2015
Hemoglobin A2-Leuven (α2δ2 143(H21) His>Asp): a novel delta-chain variant potentially interfering in hemoglobin A1c measurement using cation exchange HPLC.Kieffer DM, Harteveld CL, Lee DH, Schiemsky T, Desmet KJ, Gillard P Clin. Chem. Lab. Med.2015
Evolution of Sickle Cell Disease from a life-threatening disease of children to a chronic disease of adults: The last 40 years.Chaturvedi S, DeBaun MR Am. J. Hematol.2015
Spinal glial activation and oxidative stress are alleviated by treatment with curcumin or coenzyme Q in sickle mice.Valverde Y, Benson B, Gupta M, Gupta K Haematologica2015
Medullary Microvascular Thrombosis and Injury in Sickle Hemoglobin C Disease.Bissonnette ML, Henriksen KJ, Delaney K, Stankus N, Chang A J. Am. Soc. Nephrol.2015
Hemoglobin Variants in Northern Thailand: Prevalence, Heterogeneity and Molecular Characteristics.Panyasai S, Fucharoen G, Fucharoen S Genet Test Mol Biomarkers2015
Serum Total Bilirubin, not Cholelithiasis, is Influenced by UGT1A1 Polymorphism, Alpha Thalassemia and β(s) Haplotype: First Report on Comparison between Arab-Indian and African β(s) Genes.Alkindi SY, Pathare A, Al Zadjali S, Panjwani V, Wasim F, Khan H, Chopra P, Krishnamoorthy R, Alkindi S Mediterr J Hematol Infect Dis2015
Screening of Transcription Factors Involved in Fetal Hemoglobin Regulation Using Phylogenetic Souza Carrocini GC, Venancio LP, Bonini-Domingos CR Evol. Bioinform. Online2015
Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 14: Sickle Cell Trait: A Scientific Statement From the American Heart Association and American College of Cardiology.Maron BJ, Harris KM, Thompson PD, Eichner ER, Steinberg MH J. Am. Coll. Cardiol.2015
Extramedullary Hematopoiesis in β-Thalassemia.Kalchiem-Dekel O, Greenbaum U Mayo Clin. Proc.2015
Increasing prevalence of thalassemia in America: Implications for primary care.Sayani FA, Kwiatkowski JL Ann. Med.2015
Sickle cell disease in the ICU.Cecchini J, Fartoukh M Curr Opin Crit Care2015
Missed Opportunities for Transcranial Doppler Screening Among Children With Sickle Cell Disease.Reeves SL, Fullerton HJ, Cohn LM, Dombkowski KJ, Boulton ML, Braun TM, Lisabeth LD Clin Pediatr (Phila)2015
A treatment algorithm to identify therapeutic approaches for leg ulcers in patients with sickle cell disease.Altman IA, Kleinfelder RE, Quigley JG, Ennis WJ, Minniti CP Int Wound J2015
Characteristics of a rapid, point-of-care lateral flow immunoassay for the diagnosis of sickle cell disease.McGann PT, Schaefer BA, Paniagua M, Howard TA, Ware RE Am. J. Hematol.2015
Thalassemia 2016: Modern Medicine Battles an Ancient Disease.Rund D Am. J. Hematol.2015
[Therapy for thalassemia and sickle-cell disease].Dickerhoff R Dtsch. Med. Wochenschr.2015
Caregiver Perspectives of Stigma Associated With Sickle Cell Disease in Adolescents.Wesley KM, Zhao M, Carroll Y, Porter JS J Pediatr Nurs2015
Cognitive Testing of A Modified Version of The Faces Pain Scale-Revised In Children With Sickle-Cell Disease.Naegeli AN, Heath L, Turner-Bowker DM, Flood E, Dampier C Value Health2015
Identification of Mutations Causing Aberrant Termination and Deficient Splice Donor Site on the HBA1 Gene.Farashi S, Vakili S, Garous NF, Ashki M, Forouzesh Pour F, Zeinali F, Rad F, Imanian H, Azarkeivan A, Najmabadi H Hemoglobin2015
Improved R2* liver iron concentration assessment using a novel fuzzy c-mean clustering scheme.Saiviroonporn P, Viprakasit V, Krittayaphong R BMC Med Imaging2015
Contrast-optimized composite image derived from multigradient echo cardiac magnetic resonance imaging improves reproducibility of myocardial contours and T2* measurement.Triadyaksa P, Handayani A, Dijkstra H, Aryanto KY, Pelgrim GJ, Xie X, Willems TP, Prakken NH, Oudkerk M, Sijens PE MAGMA2015
Erythrocyte Catalase Activity in More Frequent Microcytic Hypochromic Anemia: Beta-Thalassemia Trait and Iron Deficiency Anemia.Lazarte SS, Mónaco ME, Jimenez CL, Ledesma Achem ME, Terán MM, Issé BA Adv Hematol2015
Characterization of the HBB: c.*233G > C Variant: No Evidence of a β-Thalassemic Phenotype.Smith DL, Mitui M, Park JY, Luu HS, Timmons CF Hemoglobin2015
[Testicular Tumor in a Patient with Delta Thalassemia Complicated with Hereditary Persistence of Fetal Hemoglobin].Inaba T, Shimomoto B, Hirose Y, Shimotsuma M, Nanbu A, Komori T, Nakamura T, Yamashiro Y, Fujita N Rinsho Byori2015
[Application of Next Generation Sequencing to Screen the Neonatal Thalassemia Genes].Tan M, Lu S, Wu LS, Jin DW, Peng ZY, Chen Y Zhongguo Shi Yan Xue Ye Xue Za Zhi2015
Organ iron accumulation in chronically transfused children with sickle cell anaemia: baseline results from the TWiTCH trial.Wood JC, Cohen AR, Pressel SL, Aygun B, Imran H, Luchtman-Jones L, Thompson AA, Fuh B, Schultz WH, Davis BR, Ware RE, Br. J. Haematol.2015
ARare Haemoglobin Variant Identified as K Woolwich in a Pakistani Male.Ali SA, Ali N J Coll Physicians Surg Pak2015
Elevated Transpulmonary Gradient and Cardiac Magnetic Resonance-Derived Right Ventricular Remodeling Predict Poor Outcomes in Sickle Cell Disease.Nguyen KL, Alam S, Tian X, Mehari A, Leung SW, Seamon C, Allen D, Minniti CP, Sachdev V, Arai AE, Kato GJ Haematologica2015
Modified mRNA as a new therapeutic option for pediatric respiratory diseases and hemoglobinopathies.Antony JS, Dewerth A, Haque A, Handgretinger R, Kormann MS Mol Cell Pediatr2015
Frataxin expression in reticulocytes of non-splenectomized and splenectomized patients with HbE-β-thalassaemia.Suebpeng Y, Jetsrisuparb A, Fucharoen S, Tripatara A Clin. Biochem.2015
Hospitalization Events among Children and Adolescents with Sickle Cell Disease in Basra, Iraq.Salman ZA, Hassan MK Anemia2015
[Hematological and nutritional profile of homozygous sickle cell SS aged 6 to 59 months in Lubumbashi, Democratic Republic of Congo].Shongo MY, Mukuku O, Mutombo AM, Lubala TK, Ilunga PM, Sombodi WU, Wembonyama SO, Luboya O Pan Afr Med J2015
Six Months of Hydroxyurea Reduces Albuminuria in Patients with Sickle Cell Disease.Bartolucci P, Habibi A, Stehlé T, Di Liberto G, Rakotoson MG, Gellen-Dautremer J, Loric S, Moutereau S, Sahali D, Wagner-Ballon O, Remy P, Lang P, Grimbert P, Audureau E, Godeau B, Galacteros F, Audard V J. Am. Soc. Nephrol.2015
Lactate dehydrogenase as a biomarker for early renal damage in patients with sickle cell disease.Alzahri MS, Mousa SA, Almomen AM, Hasanato RM, Polimeni JM, Racz MJ Saudi J Kidney Dis Transpl2015
Transfusion for sickle cell disease in pregnancy. Blood2015
Licochalcone A Induced Suicidal Death of Human Erythrocytes.Egler J, Lang F Cell. Physiol. Biochem.2015
Correlation between criteria of diagnosis of low bone mineral density in adult and pediatric thalassemic patients: a prospective study.Mohseni F, Mohajeri-Tehrani MR, Larijani B, Hamidi Z Minerva Pediatr.2015
ABO incompatibility and bone marrow transplantation in children with thalassemia major.Naithani R, Sachdev M, Uttam R, Dayal N, Rai R Pediatr Transplant2015
[Susceptibility of induced sickle in samples of heterozygous hemoglobin S patients (sickle cell trait) suffering diabetes mellitus type 2].Díaz-Piedra P, Cervantes-Villagrana AR, Ramos-Jiménez R, Presno-Bernal JM, Cervantes-Villagrana RD Gac Med Mex2015
When diagnostics meets translational research: detection of hemoglobin fractions in cellular lysates from in vitro erythroid cultures by Capillarys 2 Flex Piercing analyzer (Sebia).Aprile A, Passerini G, Cappellini MD, Marktel S, Ciceri F, Ferrari G, Ceriotti F Transl Res2015
Analysis of Fetal Blood: Is There Still a Role for Prenatal Diagnosis of Thalassemia?Yang Y, He P, Li DZ Hemoglobin2015
HbSC Disease and Spontaneous Epidural Hematoma with Kernohan's Notch Phenomena.Yogarajah M, Agu CC, Sivasambu B, Mittler MA Case Rep Hematol2015
Profiling β Thalassemia Mutations in Consanguinity and Nonconsanguinity for Prenatal Screening and Awareness Programme.Kumar R, Arya V, Agarwal S Adv Hematol2015
Hydroxyurea-Increased Fetal Hemoglobin Is Associated with Less Organ Damage and Longer Survival in Adults with Sickle Cell Anemia.Fitzhugh CD, Hsieh MM, Allen D, Coles WA, Seamon C, Ring M, Zhao X, Minniti CP, Rodgers GP, Schechter AN, Tisdale JF, Taylor JG PLoS ONE2015
The Prevalence of α-Thalassemia and Its Relation to Plasmodium falciparum Infection in Patients Presenting to Clinics in Two Distinct Ecological Zones in Ghana.Ghartey-Kwansah G, Boampong JN, Aboagye B, Afoakwah R, Ameyaw EO, Quashie NB Hemoglobin2015
Prevalence of Developmental Delay and Contributing Factors Among Children With Sickle Cell Disease.Drazen CH, Abel R, Gabir M, Farmer G, King AA Pediatr Blood Cancer2015
Functional Analysis of an (A)γ-Globin Gene Promoter Variant (HBG1: g.-225_-222delAGCA) Underlines Its Role in Increasing Fetal Hemoglobin Levels Under Erythropoietic Stress.Ugrin M, Stojiljkovic M, Zukic B, Klaassen K, Katsila T, Vasiljevic J, Dokmanovic L, Janic D, Patrinos GP, Pavlovic S Hemoglobin2015
Curative Stem Cell Transplantation for Severe Hb H Disease Manifesting From Early Infancy: Phenotypic and Genotypic Analyses.Surapolchai P, Sirachainan N, So CC, Hongeng S, Pakakasama S, Anurathapan U, Chuansumrit A Hemoglobin2015
A Further Note on the Thalassemia Screening Program in the Muğla Region of Turkey.Akar N Hemoglobin2015
A Fetus with Hb Bart's Disease Due to Maternal Uniparental Disomy for Chromosome 16.Au PK, Kan AS, Tang MH, Leung KY, Chan KY, Tang TW, Lau ET Hemoglobin2015
Characterization of Homozygous Hb Setif (HBA2: c.283G>T) in the Iranian Population.Farashi S, Garous NF, Vakili S, Ashki M, Imanian H, Azarkeivan A, Najmabadi H Hemoglobin2015
Interaction of cationic dodecyl-trimethyl-ammonium bromide with oxy-HbGp by isothermal titration and differential scanning calorimetric studies: Effect of proximity of isoelectric point.Alves FR, Carvalho FA, Carvalho JW, Tabak M Biopolymers2015
Health-related quality of life in patients with sickle cell disease in Saudi Arabia.Ahmed AE, Alaskar AS, Al-Suliman AM, Jazieh AR, McClish DK, Al Salamah M, Ali YZ, Malhan H, Mendoza MA, Gorashi AO, El-Toum ME, El-Toum WE Health Qual Life Outcomes2015
PHEDRE trial protocol - observational study of the prevalence of problematic use of Equimolar Mixture of Oxygen and Nitrous Oxide (EMONO) and analgesics in the French sickle-cell disease population.Gérardin M, Couec ML, Grall-Bronnec M, Feuillet F, Wainstein L, Rousselet M, Pinot ML, Perrouin F, Bonnot O, Drouineau MH, Jolliet P, Victorri-Vigneau C BMC Psychiatry2015
Hb F-Avellino [(G)γ41(C7)Phe → Leu; HBG2: c.124 T > C]: A New Hemoglobin Variant Observed In A Healthy Newborn.Pirastru M, Mereu P, Trova S, Masala B, Manca L Hemoglobin2015
Estimation of Hepatitis B Virus, Hepatitis C Virus, and Different Clinical Parameters in the Thalassemic Population of Capital Twin Cities of Pakistan.Saeed U, Waheed Y, Ashraf M, Waheed U, Anjum S, Afzal MS Virology (Auckl)2015
Association of social-environmental factors with cognitive function in children with sickle cell disease.Yarboi J, Compas BE, Brody GH, White D, Rees Patterson J, Ziara K, King A Child Neuropsychol2015
Development of a Pharmacokinetic-Guided Dose Individualization Strategy for Hydroxyurea Treatment in Children with Sickle Cell Anaemia.Dong M, McGann PT, Mizuno T, Ware RE, Vinks AA Br J Clin Pharmacol2015
Rare but Lethal Hepatopathy-Sickle Cell Intrahepatic Cholestasis and Management Strategies.Malik A, Merchant C, Rao M, Fiore RP Am J Case Rep2015
Clinical monitoring and management of complications related to chelation therapy in patients with β-thalassemia.Saliba AN, Rassi FE, Taher AT Expert Rev Hematol2015
Common gynecological challenges in adolescents with sickle cell disease.Stimpson SJ, Rebele EC, DeBaun MR Expert Rev Hematol2015
Sickle cell anaemia: The need for new approaches in management.Ghosh K Natl Med J India2015
Pain management trend of vaso-occulsive crisis (VOC) at a community hospital emergency department (ED) for patients with sickle cell disease.Inoue S, Khan I, Mushtaq R, Sanikommu SR, Mbeumo C, LaChance J, Roebuck M Ann. Hematol.2015
Hydroxyurea in Pediatric Patients With Sickle Cell Disease: What Nurses Need to Know.Rees AL J Pediatr Oncol Nurs2015
Accelerated apoptotic death and in vivo turnover of erythrocytes in mice lacking functional mitogen- and stress-activated kinase MSK1/2.Lang E, Bissinger R, Fajol A, Salker MS, Singh Y, Zelenak C, Ghashghaeinia M, Gu S, Jilani K, Lupescu A, Reyskens KM, Ackermann TF, Föller M, Schleicher E, Sheffield WP, Arthur JS, Lang F, Qadri SM Sci Rep2015
High cost effectiveness of newborn screening for sickle cell disease in resource-limited Angola.Long SS J. Pediatr.2015
Erythrocyte & platelet proteomics in haematological disorders.Chakrabarti A, Halder S, Karmakar S Proteomics Clin Appl2015
Phytochelators Intended for Clinical Use in Iron Overload, Other Diseases of Iron Imbalance and Free Radical Pathology.Kontoghiorghe CN, Kolnagou A, Kontoghiorghes GJ Molecules2015
Circulating microparticles, protein C, free protein S and endothelial vascular markers in children with sickle cell anaemia.Piccin A, Murphy C, Eakins E, Kunde J, Corvetta D, Di Pierro A, Negri G, Guido M, Sainati L, Mc Mahon C, Smith OP, Murphy W J Extracell Vesicles2015
Vitamin B12 Deficiency and Hemoglobin H Disease Early Misdiagnosed as Thrombotic Thrombocytopenic Purpura: A Series of Unfortunate Events.Andreadis P, Theodoridou S, Pasakiotou M, Arapoglou S, Gigi E, Vetsiou E, Vlachaki E Case Rep Hematol2015
Serum Paraoxonase Activity and Malondialdehyde Serum Levels Remain Unaffected in Response to Hydroxyurea Therapy in β-Thalassemia Patients.Zohaib M, Ansari SH, Hashim Z, Shamsi TS, Zarina S J Clin Pharmacol2015
Outcome results of self-efficacy in children with sickle disease pain who were trained to use guided imagery.Dobson C Appl Nurs Res2015
2,3,7,8-tetrachlorodibenzo-p-dioxin decrease expression of aryl hydrocarbon receptor in peripheral lymphocyte of β-thalassemia major patients.Ghatrehsamani M, Soleimani M, Esfahani BA, Hakemi MG, Shirzad H, Eskandari N, Adib M Adv Biomed Res2015
Frequency distribution of sickle cell anemia, sickle cell trait and sickle/beta-thalassemia among anemic patients in Saudi Arabia.Elsayid M, Al-Shehri MJ, Alkulaibi YA, Alanazi A, Qureshi S J Nat Sci Biol Med2015
T1 at 1.5T and 3T compared with conventional T2* at 1.5T for cardiac siderosis.Alam MH, Auger D, Smith GC, He T, Vassiliou V, Baksi AJ, Wage R, Drivas P, Feng Y, Firmin DN, Pennell DJ J Cardiovasc Magn Reson2015
Surgical management of osteonecrosis of the femoral head in patients with sickle cell disease.Kamath AF, McGraw MH, Israelite CL World J Orthop2015
High-resolution melting analysis for noninvasive prenatal diagnosis of IVS-II-I (G-A) fetal DNA in minor beta-thalassemia mothers.Zafari M, Gill P, Kowsaryan M, Alipour A, Banihashemi A J. Matern. Fetal. Neonatal. Med.2015
Documentation of renal glomerular and tubular impairment and glomerular hyperfiltration in multitransfused patients with beta thalassemia.Deveci B, Kurtoglu A, Kurtoglu E, Salim O, Toptas T Ann. Hematol.2015
Improving Emergency Providers' Attitudes Towards Sickle Cell Patients in Pain.Puri A, Haywood C, Beach MC, Guidera M, Lanzkron S, Valenzuela-Araujo D, Rothman RE, Dugas AF J Pain Symptom Manage2015
Sickle Cell Disease: A Review of Non-Pharmacological Approaches for Pain.Williams H, Tanabe P J Pain Symptom Manage2015
Facile synthesis of copper(II)-decorated magnetic particles for selective removal of hemoglobin from blood samples.Ding C, Ma X, Yao X, Jia L J Chromatogr A2015
Sample acceptance time criteria, electronic issue and alloimmunisation in thalassaemia.Trompeter S, Baxter L, McBrearty M, Zatkya E, Porter J Transfus Med2015
Molecular nature of alpha-globin genes in the Saudi population.Borgio JF Saudi Med J2015
Early Reticulocytosis and Anemia Are Associated with Abnormal and Conditional Transcranial Doppler Velocities in Children with Sickle Cell Anemia.Meier ER, Fasano RM, Estrada M, He J, Luban NL, McCarter R J. Pediatr.2015
Sickle cell trait is not associated with chronic kidney disease in adult Congolese patients: a clinic-based, cross-sectional study.Mukendi K, Lepira FB, Makulo JR, Sumaili KE, Kayembe PK, Nseka MN Cardiovasc J Afr2015
Characterization of iron metabolism and erythropoiesis in erythrocyte membrane defects and thalassemia traits.Sulovska L, Holub D, Zidova Z, Divoka M, Hajduch M, Mihal V, Vrbkova J, Horvathova M, Pospisilova D Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub2015
Transfusion strategy in hematological intensive care unit: study protocol for a randomized controlled trial.Chantepie SP, Mear JB, Guittet L, Dervaux B, Marolleau JP, Jardin F, Dutheil JJ, Parienti JJ, Vilque JP, Reman O Trials2015
Lung function, transfusion, pulmonary capillary blood volume and sickle cell disease.Lunt A, McGhee E, Robinson P, Rees D, Height S, Greenough A Respir Physiol Neurobiol2015
[Newborn screening : the point of view of the paediatrician].De Laet C, Laeremans H, Ferster A, Gulbis B, Mansbach AL, Jonniaux E, Regal L, Goyens P Rev Med Brux2015
Hemoglobin screening using noninvasive methods.Dos Santos CF MLO Med Lab Obs2015
Complex preimplantation genetic diagnosis for beta-thalassaemia, sideroblastic anaemia, and human leukocyte antigen (HLA)-typing.Kakourou G, Vrettou C, Kattamis A, Destouni A, Poulou M, Moutafi M, Kokkali G, Pantos K, Davies S, Kitsiou-Tzeli S, Kanavakis E, Traeger-Synodinos J Syst Biol Reprod Med2015
Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.Henderson SJ, Timbs AT, McCarthy J, Gallienne AE, Proven M, Rugless MJ, Lopez H, Eglinton J, Dziedzic D, Beardsall M, Khalil MS, Old JM Hemoglobin2015
Increased hepcidin in transferrin-treated thalassemic mice correlates with increased liver BMP2 expression and decreased hepatocyte ERK activation.Chen H, Choesang T, Li H, Sun S, Pham P, Bao W, Feola M, Westerman M, Li G, Follenzi A, Blanc L, Rivella S, Fleming R, Ginzburg Y Haematologica2015
Observed and expected frequencies of structural hemoglobin variants in newborn screening surveys in Africa and the Middle East: deviations from Hardy-Weinberg equilibrium.Piel FB, Adamkiewicz TV, Amendah D, Williams TN, Gupta S, Grosse SD Genet. Med.2015
[Hemoglobin variants in Colombian patients referred to discard hemoglobinopathies].Romero-Sánchez C, Gómez Gutiérrez A, Duarte Y, Amazo C, Manosalva C, Chila M L, Casas-Gómez MC, Briceño Balcázar I Rev Med Chil2015
[CD4⁻ CD8⁻ TCRγδ⁺T cell large granular lymphocyte leukemia associated with β- thalassemia minor: one case report and literature review].Yu Y, Song P, Mei J, An Z, Wang L, Zhou X, Li F, Tang Y, Zhai Y Zhonghua Xue Ye Xue Za Zhi2015
Relating oxygen partial pressure, saturation and content: the haemoglobin-oxygen dissociation curve.Collins JA, Rudenski A, Gibson J, Howard L, O'Driscoll R Breathe (Sheff)2015
Unusual presentation of ocular trauma in sickle cell trait.Pandey N Indian J Ophthalmol2015
Ocular abnormalities in multi-transfused beta-thalassemia patients.Jafari R, Heydarian S, Karami H, Shektaei MM, Dailami KN, Amiri AA, Rezaee MR, Far AA Indian J Ophthalmol2015
MEK1/2 inhibitors reverse acute vascular occlusion in mouse models of sickle cell disease.Zhao Y, Schwartz EA, Palmer GM, Zennadi R FASEB J.2015
Which pamidronate protocol is the best for treating osteoporosis in beta-thalassemia major?Kowsaryan M, Zafari M Ann. Hematol.2015
Prevention of sickle cell disease: observations on females with the sickle cell trait from the Manchester project, Jamaica.Mason K, Gibson F, Gardner RA, Serjeant B, Serjeant GR J Community Genet2015
Comment on: negative health implications of sickle cell trait in high income countries: from the football field to the laboratory.Ballas SK Br. J. Haematol.2015
Transfusion according to haemoglobin levels or therapeutic objectives.Colomina MJ, Guilabert P Rev Esp Anestesiol Reanim2015
The illness of women and men with sickle cell disease: a Grounded Theory study.Cordeiro RC, Ferreira SL, Santos AC Rev Lat Am Enfermagem2015
Musculoskeletal Manifestations of Sickle Cell Disease: A Review.Vaishya R, Agarwal AK, Edomwonyi EO, Vijay V Cureus2015
Intrathoracic extramedullary hematopoiesis presenting as tumor-simulating lesions of the mediastinum in α-thalassemia: A case report.An J, Weng Y, He J, Li Y, Huang S, Cai S, Zhang J Oncol Lett2015
The financial burden of sickle cell disease on households in Ekiti, Southwest Nigeria.Olatunya OS, Ogundare EO, Fadare JO, Oluwayemi IO, Agaja OT, Adeyefa BS, Aderiye O Clinicoecon Outcomes Res2015
The use of cell-free fetal DNA in maternal plasma for noninvasive prenatal linkage analysis in beta globin gene cluster.Khordadpoor-Deilamani F, Akbari MT Bratisl Lek Listy2015
The Role of Spirituality and Religiosity in Persons Living With Sickle Cell Disease: A Review of the Literature.Clayton-Jones D, Haglund K J Holist Nurs2015
Use of Iron Chelating Agents in Transfusion Dependent Thalassaemia Major Patients.Santra S, Bhattacharya A, Mukhopadhyay T, Agrawal D, Kumar S, Das P, Chakrabarty P Mymensingh Med J2015
Adenylyl Cyclase 9 Polymorphisms Reveal Potential Link to HDL Function and Cardiovascular Events in Multiple Pathologies: Potential Implications in Sickle Cell Disease.Niesor EJ, Benghozi R, Amouyel P, Ferdinand KC, Schwartz GG Cardiovasc Drugs Ther2015
Adherence to iron chelation therapy and associated healthcare resource utilization and costs in Medicaid patients with sickle cell disease and thalassemia.Vekeman F, Sasane M, Cheng WY, Ramanakumar AV, Fortier J, Qiu Y, Duh MS, Paley C, Adams-Graves P J Med Econ2015
[Issues and difficulties in the relationship between patients and caregivers in painful sickle cell vaso-occlusive crisis].Dzierzynski N, Stankovic Stojanovic K, Georgin-Lavialle S, Lionnet F Rev Med Interne2015
Hemoglobin Hirose: A rare beta chain variant causing falsely low HbA1c by HPLC.Estey MP, Rodriguez-Capote K, Adelowokan T, Higgins T Clin. Biochem.2015
Effects of hydroxyurea treatment for patients with hemoglobin SC disease.Luchtman-Jones L, Pressel S, Hilliard L, Brown RC, Smith MG, Thompson AA, Lee MT, Rothman J, Rogers ZR, Owen W, Imran H, Thornburg C, Kwiatkowski JL, Aygun B, Nelson S, Roberts C, Gauger C, Piccone C, Kalfa T, Alvarez O, Hassell K, Davis BR, Ware RE Am. J. Hematol.2015
Abdominal pain in children with sickle cell disease.Rhodes MM, Bates DG, Andrews T, Adkins L, Thornton J, Denham JM J. Clin. Gastroenterol.2014
Dark blood versus bright blood T2* acquisition in cardiovascular magnetic resonance (CMR) for thalassaemia major (TM) patients: Evaluation of feasibility, reproducibility and image quality.Liguori C, Di Giampietro I, Pitocco F, De Vivo AE, Schena E, Mortato L, Pirro F, Cianciulli P, Zobel BB Eur J Radiol2014
TNF-α, IFN-γ, IL-10, and IL-4 levels were elevated in a murine model of human sickle cell anemia maintained on a high protein/calorie diet.Hyacinth HI, Capers PL, Archer DR, Hibbert JM Exp. Biol. Med. (Maywood)2014
EXAMINER Executive Function Battery and Neurologic Morbidity in Pediatric Sickle Cell Disease.Schatz J, Stancil M, Katz T, Sanchez CE J Int Neuropsychol Soc2014
A simple and highly sensitive ELISA for screening of the α-thalassemia-1 Southeast Asian-type deletion.Pata S, Khummuang S, Pornprasert S, Tatu T, Kasinrerk W J Immunoassay Immunochem2014
Chronic inflammatory state in sickle cell anemia patients is associated with HBB(*)S haplotype.Bandeira IC, Rocha LB, Barbosa MC, Elias DB, Querioz JA, Freitas MV, Gonçalves RP Cytokine2014
Asymptomatic bacteriuria among pregnant women with sickle cell trait in Enugu, South Eastern Nigeria.Obiora CC, Dim CC, Ezegwui HU, Nwogu-Ikojo EE, Okeudo C Niger J Clin Pract2014
Avascular necrosis in sickle cell (homozygous S) patients: predictive clinical and laboratory indices.Madu AJ, Madu AK, Umar GK, Ibekwe K, Duru A, Ugwu AO Niger J Clin Pract2014
Advances in technologies for screening and diagnosis of hemoglobinopathies.Traeger-Synodinos J, Harteveld CL Biomark Med2014
European association of urology guidelines on priapism.Salonia A, Eardley I, Giuliano F, Hatzichristou D, Moncada I, Vardi Y, Wespes E, Hatzimouratidis K Eur. Urol.2014
Identification of risk factors for an unsuccessful transition from pediatric to adult sickle cell disease care.Andemariam B, Owarish-Gross J, Grady J, Boruchov D, Thrall RS, Hagstrom JN Pediatr Blood Cancer2014
Comprehensive integrated care for patients with sickle cell disease in a remote aboriginal tribal population in southern India.Nimgaonkar V, Krishnamurti L, Prabhakar H, Menon N Pediatr Blood Cancer2014
Wheezing in children with sickle cell disease.Glassberg JA, Strunk R, Debaun MR Curr. Opin. Pediatr.2014
Priapism in children and adolescents homozygous sickle cell disease in Brazzaville.Okoko AR, Odzébé AS, Moyen E, Ekouya Bowassa G, Oko AP, Mbika-Cardorelle A, Bozock P, Atanda HL, Moyen GM Prog. Urol.2014
Neurologic complications of sickle cell disease.Venkataraman A, Adams RJ Handb Clin Neurol2014
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Hydroxycarbamide reduces eosinophil adhesion and degranulation in sickle cell anaemia patients.Pallis FR, Conran N, Fertrin KY, Olalla Saad ST, Costa FF, Franco-Penteado CF Br. J. Haematol.2014
Efficacy and Safety of Deferasirox in β-Thalassemia Major Patients in Iran: A Prospective Study from a Single referral Center in Iran.Alavi S, Ebadi M, Ghazizadeh F, Arzanian MT, Shamsian B, Abdollah Gorji F Pediatr Hematol Oncol2014
Molecular diagnosis of α-thalassemias by the colorimetric nanogold.Chomean S, Wangmaung N, Sritongkham P, Promptmas C, Mas-Oodi S, Tanyong D, Ittarat W Analyst2014
Pial synangiosis for moyamoya syndrome in children with sickle cell anemia: a comprehensive review of reported cases.Kennedy BC, McDowell MM, Yang PH, Wilson CM, Li S, Hankinson TC, Feldstein NA, Anderson RC Neurosurg Focus2014
Fatigue in adolescents and young adults with sickle cell disease: biological and behavioral correlates and health-related quality of life.Ameringer S, Elswick RK, Smith W J Pediatr Oncol Nurs2014
Evaluation of Th17 related cytokines associated with clinical and laboratorial parameters in sickle cell anemia patients with leg ulcers.da Silva RR, Pereira MC, Melo Rêgo MJ, Domingues Hatzlhofer BL, da Silva Araújo A, Cavalcanti Bezerra MA, da Rocha Pitta I, da Rocha Pitta MG Cytokine2014
Response to low bone mineral areal density in patients with sickle cell anaemia (SCA) and short stature should be interpreted with caution.Gurgel RQ, Cipolotti R, Meeuwes M, Souza de Carvalho TF, Ferrão TO, Peters M, Agyemang C Trop. Med. Int. Health2014
Identification of three new nucleotide substitutions in the β globin gene: laboratoristic approach and impact on genetic counseling for beta thalassaemia.Vinciguerra M, Passarello C, Leto F, Cassarà F, Cannata M, Maggio A, Giambona A Eur. J. Haematol.2014
Effect of genotype on pulmonary hypertension risk in patients with thalassemia.Teawtrakul N, Ungprasert P, Pussadhamma B, Prayalaw P, Fucharoen S, Jetsrisuparb A, Pongudom S, Sirijerachai C, Chansung K, Wanitpongpun C, Chuncharunee S Eur. J. Haematol.2014
Regular long-term red blood cell transfusions for managing chronic chest complications in sickle cell disease.Cho G, Hambleton IR Cochrane Database Syst Rev2014
Phenotypic Effect of α-Globin Gene Numbers on Indian Sickle β-Thalassemia Patients.Pandey SK, Pandey S, Ranjan R, Shah V, Mishra RM, Sharma M, Saxena R J. Clin. Lab. Anal.2014
The case for and against initiating either hydroxyurea therapy, blood transfusion therapy or hematopoietic stem cell transplant in asymptomatic children with sickle cell disease.Kassim AA, Debaun MR Expert Opin Pharmacother2014
Spinal epidural extramedullary haematopoiesis in β-thalassaemia intermedia.Wong KH, Li A, Lui TH, Sit YK BMJ Case Rep2014
Access to Patient-Centered Medical Homes in Children with Sickle Cell Disease.Liem RI, O'Suoji C, Kingsberry PS, Pelligra SA, Kwon S, Mason M, Thompson AA Matern Child Health J2014
Current level of information about sickle cell disease among medical students at Brussels, Belgium.Aloni MN, Kumumangi JM, Malemba-Ilunga JJ, Usungo FU, Nzuka SK, Lapu BS, Ekila MB, Kittel F Rev Epidemiol Sante Publique2014
A Centralized Recipient Database Enhances the Serologic Safety of RBC Transfusions for Patients With Sickle Cell Disease.Harm SK, Yazer MH, Monis GF, Triulzi DJ, Aubuchon JP, Delaney M Am. J. Clin. Pathol.2014
A pilot study of electronic directly observed therapy to improve hydroxyurea adherence in pediatric patients with sickle-cell disease.Creary SE, Gladwin MT, Byrne M, Hildesheim M, Krishnamurti L Pediatr Blood Cancer2014
Laboratory Investigation of Platelet Function in Patients with Thalassaemia.Theodoridou S, Economou M, Vyzantiadis TA, Teli A, Vlachaki E, Neokleous N, Kargioti A, Vakalopoulou S, Garypidou V, Gombakis N, Papachristou F Acta Haematol.2014
Haematopoietic stem cell transplantation for severe sickle cell disease in childhood: a single centre experience of 50 patients.Dedeken L, Lê PQ, Azzi N, Brachet C, Heijmans C, Huybrechts S, Devalck C, Rozen L, Ngalula M, Ferster A Br. J. Haematol.2014
Hb Memphis [HBA2: c.70G>C (or HBA1)] in a Turkish Child: A Case Report and Comparison to Hb Q-Thailand (HBA1: c.223G>C).Lubrano L, Donnelly MJ, Sandler G, Hoyer JD, Swanson KC, Dawson DB, Oliveira JL Hemoglobin2014
Social Skills and Executive Function Among Youth With Sickle Cell Disease: A Preliminary Investigation.Hensler M, Wolfe K, Lebensburger J, Nieman J, Barnes M, Nolan W, King A, Madan-Swain A J Pediatr Psychol2014
Molecular mechanisms underlying synergistic adhesion of sickle red blood cells by hypoxia and low nitric oxide bioavailability.Gutsaeva DR, Montero-Huerta P, Parkerson JB, Yerigenahally SD, Ikuta T, Head CA Blood2014
Safe mobilization of CD34+ cells in adults with beta-thalassemia and validation of effective globin gene transfer for clinical investigation.Boulad F, Wang X, Qu J, Taylor C, Ferro L, Karponi G, Bartido S, Giardina P, Heller G, Prockop SE, Maggio A, Sadelain M, Rivière I Blood2014
First North American case of Hemoglobin Shepherds Bush (β 74[E18] Gly → Asp) in a central Pennsylvania family.Paradise SL, Estep L, Olson J, Donaldson K BMC Clin Pathol2014
Tricuspid regurgitant jet velocity and hospitalization in Tanzanian children with sickle cell anemia.Cox SE, Soka D, Kirkham FJ, Newton CR, Prentice AM, Makani J, Younoszai AK Haematologica2014
Blood pressure abnormalities in children with sickle cell anemia.Becker AM, Goldberg JH, Henson M, Ahn C, Tong L, Baum M, Buchanan GR Pediatr Blood Cancer2014
Maternal and Perinatal Outcome of Women With Sickle Cell Disease of a Tribal Population in Central India.Natu N, Khandelwal S, Kumar R, Dave A Hemoglobin2014
Low bone mineral density in patients with Sickle Cell Anaemia (SCA) and short stature should be interpreted with caution.Spinola-Castro AM, Siviero-Miachon AA Trop. Med. Int. Health2014
How early can myocardial iron overload occur in Beta thalassemia major?Yang G, Liu R, Peng P, Long L, Zhang X, Yang W, Tan S, Pan H, Long X, He T, Anderson L, Lai Y PLoS ONE2014
50 years ago in the journal of pediatrics: treatment of painful crises of sickle cell disease.Cuello-Garcia CA J. Pediatr.2014
Approaching low liver iron burden in chelated patients with non-transfusion-dependent thalassemia: The safety profile of deferasirox.Taher AT, Porter JB, Viprakasit V, Kattamis A, Chuncharunee S, Sutcharitchan P, Siritanaratkul N, Origa R, Karakas Z, Habr D, Zhu Z, Cappellini MD Eur. J. Haematol.2014
Differential structural status of the RNA counterpart of an undecamer quasi-palindromic DNA sequence present in LCR of human β-globin gene cluster.Kaushik M, Kukreti S J. Biomol. Struct. Dyn.2014
Myocardial iron overload in thalassaemia major. How early to check?Borgna-Pignatti C, Meloni A, Guerrini G, Gulino L, Filosa A, Ruffo GB, Casini T, Chiodi E, Lombardi M, Pepe A Br. J. Haematol.2014
Sickle Trait in African-American Hemodialysis Patients and Higher Erythropoiesis-Stimulating Agent Dose.Derebail VK, Lacson EK, Kshirsagar AV, Key NS, Hogan SL, Hakim RM, Mooney A, Jani CM, Johnson C, Hu Y, Falk RJ, Lazarus JM J. Am. Soc. Nephrol.2014
"Packaging" of fetal hemoglobin in sickle cell anemia.Buchanan GR Blood2014
Prevalence and Correlates of Metabolic Acidosis among Patients with Homozygous Sickle Cell Disease.Maurel S, Stankovic Stojanovic K, Avellino V, Girshovich A, Letavernier E, Grateau G, Baud L, Girot R, Lionnet F, Haymann JP Clin J Am Soc Nephrol2014
Rapid and reliable detection of α-globin copy number variations by quantitative real-time PCR.Grimholt RM, Urdal P, Klingenberg O, Piehler AP BMC Hematol2014
Hypothyroidism in β-Thalassemia Intermedia Patients with and without Hydroxyurea.Zekavat OR, Makarem AR, Haghpanah S, Karamizadeh Z, Javad P, Karimi M Iran J Med Sci2014
Burden of diagnostic radiation exposure in children with sickle cell disease.Vetter CL, Buchanan GR, Quinn CT Pediatr Blood Cancer2014
Differential contribution of FXa and thrombin to vascular inflammation in a mouse model of sickle cell disease.Sparkenbaugh EM, Chantrathammachart P, Mickelson J, van Ryn J, Hebbel RP, Monroe DM, Mackman N, Key NS, Pawlinski R Blood2014
Non-traumatic spontaneous acute epidural hematoma in a patient with sickle cell disease.Serarslan Y, Aras M, Altaş M, Kaya H, Urfalı B Neurocirugia (Astur)2014
Effectiveness of biofield therapy for individuals with sickle cell disease in Africa.Minga TM, Kule Koto FK, Egboki H, Suzuki K Altern Ther Health Med2014
Mutations in Kruppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression.Viprakasit V, Ekwattanakit S, Riolueang S, Chalaow N, Fisher C, Lower K, Kanno H, Tachavanich K, Bejrachandra S, Saipin J, Juntharaniyom M, Sanpakit K, Tanphaichitr VS, Songdej D, Babbs C, Gibbons RJ, Philipsen S, Higgs DR Blood2014
An in vivo model for analysis of developmental erythropoiesis and globin gene regulation.McColl B, Kao BR, Lourthai P, Chan K, Wardan H, Roosjen M, Delagneau O, Gearing LJ, Blewitt ME, Svasti S, Fucharoen S, Vadolas J FASEB J.2014
Intravenous magnesium for pediatric sickle cell vaso-occlusive crisis: Methodological issues of a randomized controlled trial.Badaki-Makun O, Scott JP, Panepinto JA, Casper TC, Hillery CA, Dean JM, Brousseau DC, Pediatr Blood Cancer2014
Conditioning regimens in allo-SCT for thalassemia major.Mathews V, Savani BN Bone Marrow Transplant.2014
Compound heterozygotes and beta-thalassemia: Top-down mass spectrometry for detection of haemoglobinopathies.Edwards RL, Griffiths P, Bunch J, Cooper HJ Proteomics2014
Respiratory syncytial virus and seasonal influenza cause similar illnesses in children with sickle cell disease.Sadreameli SC, Reller ME, Bundy DG, Casella JF, Strouse JJ Pediatr Blood Cancer2014
Epistasis between the haptoglobin common variant and α+thalassemia influences risk of severe malaria in Kenyan children.Atkinson SH, Uyoga SM, Nyatichi E, Macharia AW, Nyutu G, Ndila C, Kwiatkowski DP, Rockett KA, Williams TN Blood2014
Factors Associated with Survival in a Contemporary Adult Sickle Cell Disease Cohort.Elmariah H, Garrett ME, De Castro LM, Jonassaint J, Ataga KI, Eckman J, Ashley-Koch AE, Telen MJ Am. J. Hematol.2014
Effective Iron Chelation Practice for Patients With β-Thalassemia Major.Carson SM, Martin MB Clin J Oncol Nurs2014
Plasma concentration of platelet-derived microparticles is related to painful vaso-occlusive phenotype severity in sickle cell anemia.Nebor D, Bowers A, Connes P, Hardy-Dessources MD, Knight-Madden J, Cumming V, Reid M, Romana M PLoS ONE2014
Spatial repolarization heterogeneity detected by magnetocardiography correlates with cardiac iron overload and adverse cardiac events in Beta-thalassemia major.Chen CA, Lu MY, Peng SF, Lin KH, Chang HH, Yang YL, Jou ST, Lin DT, Liu YB, Horng HE, Yang HC, Wang JK, Wu MH, Wu CC PLoS ONE2014
Effect of Swiss-type heterocellular HPFH from XmnI-(G)γ and HBBP1 polymorphisms on HbF, HbE, MCV and MCH levels in Thai HbE carriers.Kerdpoo S, Limweeraprajak E, Tatu T Int. J. Hematol.2014
Identification of rare and novel deletions that cause (δβ)(0) - thalassaemia and HPFH in Indian population.Mayuranathan T, Rayabaram J, Das R, Arora N, Edison ES, Chandy M, Srivastava A, Velayudhan SR Eur. J. Haematol.2014
Two New Hemoglobin Variants: Hb Tallahassee [α3(A1)Ser→Tyr; HBA2: c.11C>A] and Hb Madison-NC [β119(GH2)Gly→Ser; HBB: c.358G>A].Kutlar F, Unguru Y, Dixon N, Patel N, Bailey L, Zhuang L, Carmichael H, Kutlar A Hemoglobin2014
Case Report: Prenatal Diagnosis of Hb Hammersmith [β42(CD1)Phe→Ser; HBB: c.128T > C] in a Family with an Adult Male Patient.Li R, Wang T, Xie XM, Li DZ Hemoglobin2014
Hb A2-Konz [δ50(D1)Ser → Thr; HBD: c.151T > A]: a New δ Chain Hemoglobin Variant Characterized by Mass Spectrometry and High Performance Liquid Chromatography.Alayi TD, Van Dorsselaer A, Epting T, Bissé E, Schaeffer-Reiss C Hemoglobin2014
A New Hemoglobin Variant: Hb Henan [β90(F6)Glu → Gln; HBB: c.271G < C].Cai WJ, Xie XM, Zhang YL, Li R, Liao C, Li DZ Hemoglobin2014
Hb Ashburton [β12(A9)Thr → Pro; HBB: c.37A > C], a Novel, Mildly Unstable Variant and the First Substitution Identified at Codon 12.Brennan SO, Povall A, Lankes U Hemoglobin2014
Detection of Hb Anti-Lepore Hong Kong (NG_000007.3: g.63154_70565dup) in Chinese Individuals.Lou JW, He Y, Liu YH, Zhong BM, Zhao Y, He XX, Li DZ Hemoglobin2014
Leg Amputation for an Extensive, Severe and Intractable Sickle Cell Anemia Ulcer in a Brazilian Patient.Queiroz AM, Campos J, Lobo C, Bonini-Domingos CR, Cardoso G, Ballas SK Hemoglobin2014
A New δ Chain Variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], Observed in a Tunisian Family in Association with a Compound Heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β(0)-Thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A].Moumni I, Zorai A, Mahjoub S, Mosbahi I, Chaouechi D, Benromdhane N, Abbes S Hemoglobin2014
Report on Patients with Non Transfusion-Dependent β-Thalassemia Major Being Treated with Hydroxyurea Attending the Thalassemia Research Center, Sari, Mazandaran Province, Islamic Republic of Iran in 2013.Kosaryan M, Karami H, Zafari M, Yaghobi N Hemoglobin2014
Bone marrow necrosis and fat embolism syndrome in sickle cell disease: Increased susceptibility of patients with non-SS genotypes and a possible association with human parvovirus B19 infection.Tsitsikas DA, Gallinella G, Patel S, Seligman H, Greaves P, Amos RJ Blood Rev.2014
High School Knowledge and Attitudes towards Thalassemia in Southeastern Iran.Miri-Moghaddam E, Motaharitabar E, Erfannia L, Dashipour A, Houshvar M Int J Hematol Oncol Stem Cell Res2014
The role of epigenetics in the induction of fetal hemoglobin: a combination therapy approach.Ahmadvand M, Noruzinia M, Fard AD, Zohour MM, Tabatabaiefar MA, Soleimani M, Kaviani S, Abroun S, Beiranvand S, Saki N Int J Hematol Oncol Stem Cell Res2014
Renal Tubular Dysfunction in Sickle Cell Disease.Silva Junior GB, Vieira AP, Couto Bem AX, Alves MP, Meneses GC, Martins AM, Sanches TR, Andrade LC, Seguro AC, Libório AB, Daher EF Kidney Blood Press. Res.2014
Assessment of Iron Overload in Very Young Children with Limited Thalassemia Care Resources in South China.Au WY, Li CF, Fang JP, Chen GF, Sun X, Li CG, Zhang XH, Wu XD, Gao HY, Hao WG, Rasalkar D, Deng M, Mok SP, Tricta F, Chu WC Hemoglobin2014
A New (G)γ-Globin Variant Causing Low Oxygen Affinity: Hb F-Brugine/Feldkirch [(G)γ105(G7)Leu→His; HBG2: c.317T>A].Saller E, Kohne E, Dutly F, Frischknecht H Hemoglobin2014
Genotyping of BCL11A and HBS1L-MYB SNPs associated with fetal haemoglobin levels: a SNaPshot minisequencing approach.Fanis P, Kousiappa I, Phylactides M, Kleanthous M BMC Genomics2014
A commentary on molecular basis of transfusion dependent beta-thalassemia major patients in Sabah.Teh LK, Elizabeth G, Lai MI, Jin Ai MA, Wong L, Ismail P, Setianingsih I J. Hum. Genet.2014
Development and feasibility of a home-based education model for families of children with sickle cell disease.Hoyt Drazen C, Abel R, Lindsey T, King AA BMC Public Health2014
Efficacy and safety of sildenafil for the treatment of severe pulmonary hypertension in patients with hemoglobinopathies: results from a long-term follow up.Derchi G, Balocco M, Bina P, Caruso V, D'Ascola DG, Littera R, Origa R, Cappellini MD, Forni GL Haematologica2014
Influence of the β(s) haplotype and α-thalassemia on stroke development in a Brazilian population with sickle cell anaemia.Domingos IF, Falcão DA, Hatzlhofer BL, Cunha AF, Santos MN, Albuquerque DM, Fertrin KY, Costa FF, Azevedo RC, Machado CG, Araújo AS, Lucena-Araujo AR, Bezerra MA Ann. Hematol.2014
The sex difference in haemoglobin levels in adults - Mechanisms, causes, and consequences.Murphy WG Blood Rev.2014
Descriptive profile of β-thalassemia mutations in West Bengal population: a hospital-based study.Bhattacharyya DM, Mukhopadhyay A, Basak J Int. J. Hematol.2014
Association of Xmn1 -158 γ(G) variant with severity and HbF levels in β-thalassemia major and sickle cell anaemia.Dadheech S, Jain S, Madhulatha D, Sharma V, Joseph J, Jyothy A, Munshi A Mol. Biol. Rep.2014
Red cell alloimmunization in thalassemia patients in a developing country - What can be done?Moiz B Transfus. Apher. Sci.2014
Serum angiogenin level in sickle cell disease and Beta thalassemia patients.Matter RM, Abdelmaksoud AA, Shams MA, Bebawy EK Pediatr Hematol Oncol2014
A new unstable variant of the fetal hemoglobin HBG2 gene: Hb F-Turritana [(G) γ64(E8)Gly→Asp, HBG2:c.194G>A] found in cis to the Hb F-Sardinia gene [(A) γ(E19)Ile→Thr, HBG1:c.227T>C].Pirastru M, Mereu P, Trova S, Manca L, Masala B Eur. J. Haematol.2014
Intravascular Hemolysis, Vascular Endothelial Cell Activation and Thrombophilia in Splenectomized Patients with Hemoglobin E/β-Thalassemia Disease.Atichartakarn V, Chuncharunee S, Archararit N, Udomsubpayakul U, Aryurachai K Acta Haematol.2014
Pain control in sickle cell disease patients: use of complementary and alternative medicine.Thompson WE, Eriator I Pain Med2014
Evaluation of the Effect of miR-26b Up-Regulation on HbF Expression in Erythroleukemic K-562 Cell Line.Alijani S, Alizadeh S, Kazemi A, Khatib ZK, Soleimani M, Rezvani M, Minayi N, Karami F, Tayebi B Avicenna J Med Biotechnol2014
Neuroimaging abnormalities in adults with sickle cell anemia: Associations with cognition.Mackin RS, Insel P, Truran D, Vichinsky EP, Neumayr LD, Armstrong FD, Gold JI, Kesler K, Brewer J, Weiner MW, Neurology2014
Efficiency of recombinant erythropoietin administration in hemoglobinopathy h.Hasanova M, Asadov Ch, Alimirzoyeva Z, Mammadova T, Shirinova A Georgian Med News2014
Reduced forced expiratory flow but not increased exhaled nitric oxide or airway responsiveness to methacholine characterises paediatric sickle cell airway disease.Chaudry RA, Rosenthal M, Bush A, Crowley S Thorax2014
Risk and resilience factors for grade retention in youth with sickle cell disease.Ladd RJ, Valrie CR, Walcott CM Pediatr Blood Cancer2014
The Proportion of Potentially Preventable Emergency Department Visits by Patients With Sickle Cell Disease.Nimmer M, Hoffmann RG, Dasgupta M, Panepinto J, Brousseau DC J. Pediatr. Hematol. Oncol.2014
Renal Medullary Carcinoma in a White Adolescent With Sickle Cell Trait.Daher P, Bourgi A, Riachy E, Khoury A, Rehayem C, Sader-Ghorra C J. Pediatr. Hematol. Oncol.2014
Self-reported Transition Readiness Among Young Adults With Sickle Cell Disease.Sobota A, Akinlonu A, Champigny M, Eldridge M, McMahon L, Telfair J, Sprinz P J. Pediatr. Hematol. Oncol.2014
Frequency of glomerular dysfunction in children with Beta thalassaemia major.Ali BA, Mahmoud AM Sultan Qaboos Univ Med J2014
The Hypoxic Response Contributes to Altered Gene Expression and Pre-Capillary Pulmonary Hypertension in Patients with Sickle Cell Disease.Zhang X, Zhang W, Ma SF, Desai AA, Saraf S, Miasnikova G, Sergueeva A, Ammosova T, Xu M, Nekhai S, Abbasi T, Casanova NG, Steinberg MH, Baldwin CT, Sebastiani P, Prchal JT, Kittles R, Garcia JG, Machado RF, Gordeuk VR Circulation2014
Patients Welcome the Sickle Cell Disease Mobile Application to Record Symptoms via Technology (SMART).Shah N, Jonassaint J, De Castro L Hemoglobin2014
Evidence-based focused review of the status of hematopoietic stem cell transplantation as treatment for sickle cell disease and thalassemia.King A, Shenoy S Blood2014
Oxidant-antioxidant status in Egyptian children with sickle cell anemia: a single center study.El-Ghamrawy MK, Hanna WM, Abdel-Salam A, El-Sonbaty MM, Youness ER, Adel A J Pediatr (Rio J)2014
Anemia and hemoglobin diseases in patients with migration background.Eber S, Dickerhoff R Dtsch. Med. Wochenschr.2014
Psychosocial Stressors of Sickle Cell Disease on Adult Patients in Cameroon.Wonkam A, Mba CZ, Mbanya D, Ngogang J, Ramesar R, Angwafo FF J Genet Couns2014
Prevalence of iron deficiency in thalassemia minor.Madan N, Sikka M, Sharma S, Rusia U Indian J Hematol Blood Transfus2014
Sickle cell anemia with malaria: a rare case report.Gupta NK, Gupta M Indian J Hematol Blood Transfus2014
Ferritin and LIC: Predicting Liver Injury in Children With Sickle Cell.Smith E, Lebensburger J, Hilliard L, Kelly D, Fineberg N, Bai S, Howard T J. Pediatr. Gastroenterol. Nutr.2014
Effectiveness of imatinib therapy for sickle cell anemia and chronic myeloid leukemia.Murphy M, Close J, Lottenberg R, Rajasekhar A Am. J. Med. Sci.2014
Endothelial activation by platelets from sickle cell anemia patients.Proença-Ferreira R, Brugnerotto AF, Garrido VT, Dominical VM, Vital DM, Ribeiro Mde F, Dos Santos ME, Traina F, Olalla-Saad ST, Costa FF, Conran N PLoS ONE2014
Fluorescence spectral classification of iron deficiency anemia and thalassemia.Devanesan S, Mohamad Saleh A, Ravikumar M, Perinbam K, Prasad S, Abbas HA, Palled SR, Jeyaprakash K, Masilamani V J Biomed Opt2014
Attitudes toward clinical trials among patients with sickle cell disease.Haywood C, Lanzkron S, Diener-West M, Haythornthwaite J, Strouse JJ, Bediako S, Onojobi G, Beach MC, Clin Trials2014
Headache and Migraine in Children with Sickle Cell Disease Are Associated with Lower Hemoglobin and Higher Pain Event Rates But Not Silent Cerebral Infarction.Dowling MM, Noetzel MJ, Rodeghier MJ, Quinn CT, Hirtz DG, Ichord RN, Kwiatkowski JL, Roach ES, Kirkham FJ, Casella JF, Debaun MR J. Pediatr.2014
Harvesting autologous stem cells from a patient with red blood cell abnormalities of β-thalassemia intermedia.Sanford K, Roseff SD, Anderson J, Chung HM, McPherson RA Transfusion2014
Detection of hemoglobinopathies and thalassemias using automated separation systems.Brants A MLO Med Lab Obs2014
Translocation Renal Cell Carcinoma t(6;11)(p21;q12) and Sickle Cell Anemia: First Report and Review of the Literature.Chaste D, Vian E, Verhoest G, Blanchet P Korean J Urol2014
MR Quantitative Susceptibility Imaging for the Evaluation of Iron Loading in the Brains of Patients with β-Thalassemia.Qiu D, Chan GC, Chu J, Chan Q, Ha SY, Moseley ME, Khong PL AJNR Am J Neuroradiol2014
Metabolic Pathways Related to Oxidative Stress in Patients With Hemoglobin H Disease and Iron Overload.Chiou SS, Tsao CJ, Tsai SM, Wu YR, Liao YM, Lin PC, Tsai LY J. Clin. Lab. Anal.2014
Splenectomy for Children With Thalassemia: Total or Partial Splenectomy, Open or Laparoscopic Splenectomy.Al-Salem AH J. Pediatr. Hematol. Oncol.2014
Elevated tricuspid regurgitant jet velocity in subgroups of thalassemia patients: insight into pathophysiology and the effect of splenectomy.Singer ST, Kuypers F, Fineman J, Gildengorin G, Larkin S, Sweeters N, Rosenfeld H, Kurio G, Higa A, Jeng M, Huang J, Vichinsky EP Ann. Hematol.2014
Echocardiography-Derived Tricuspid Regurgitant Jet Velocity Is an Important Marker for the Progression of Sickle-Cell Disease.Upadhya B, Stacey RB, Ntim W, Knovich MA, Pu M Acta Haematol.2014
Ivy Sign in Mildly Symptomatic β-Thalassemia Intermedia, with Development of Moyamoya Disease.El Beltagi AH, El-Sheikh A, El-Saif R, Norbash A Neuroradiol J2014
Treatment of the acute sickle cell vaso-occlusive crisis in the Emergency Department: A Brazilian method of switching from intravenous to oral morphine.Campos J, Lobo C, Queiroz AM, do Nascimento EM, Lima CB, Cardoso G, Ballas SK Eur. J. Haematol.2014
Renal cell carcinoma in adult patients with thalassaemia major: a description of three cases.Ricchi P, Ammirabile M, Spasiano A, Costantini S, Di Matola T, Cartenì G, Filosa A, Cinque P Br. J. Haematol.2014
Adipocytokine concentrations in children with different types of Beta-thalassemia.Enli Y, Balc YI, Gönen C, Uzun E, Polat A Scand. J. Clin. Lab. Invest.2014
The 6-min walk test: an independent correlate of elevated tricuspid regurgitant jet velocity in children and young adult sickle cell patients.Agha H, El Tagui M, El Ghamrawy M, Hady MA Ann. Hematol.2014
Clinical findings associated with homozygous sickle cell disease in the Barbadian population - do we need a national SCD registry?Quimby KR, Moe S, Sealy I, Nicholls C, Hambleton IR, Landis RC BMC Res Notes2014
Psychological therapies for thalassaemia.Anie KA, Massaglia P Cochrane Database Syst Rev2014
Sickle Cell Trait-Neglected Opportunities in the Era of Genomic Medicine.Taylor C, Kavanagh P, Zuckerman B JAMA2014
A narrative review of peri-operative management of patients with thalassaemia.Staikou C, Stavroulakis E, Karmaniolou I Anaesthesia2014
α-Thalassemia Does Not Seem to Influence Erythrocyte Deformability in Sickle Cell Trait Carriers.Vayá A, Collado S, Alis R, Vera B, Romagnoli M, Barragán E Hemoglobin2014
A Study of δ-Globin Gene Mutations in the UK Population: Identification of Three Novel Variants and Development of a Novel DNA Test for Hb A'2.Khalil MS, Marouf S, Element D, Timbs A, Gallienne A, Schuh A, Old JM, Henderson S Hemoglobin2014
A decisional algorithm to start iron chelation in patients with beta thalassemia.Danjou F, Cabantchik ZI, Origa R, Moi P, Marcias M, Barella S, Defraia E, Dessì C, Foschini ML, Giagu N, Leoni GB, Morittu M, Galanello R Haematologica2014
Globin Gene Induction Therapy for β-Thalassemia.Lu ZM Zhongguo Shi Yan Xue Ye Xue Za Zhi2014
Extracranial carotid arteriopathy in stroke-free children with sickle cell anemia: detection by submandibular Doppler sonography.Verlhac S, Balandra S, Cussenot I, Kasbi F, Vasile M, Kheniche A, Elmaleh-Bergès M, Ithier G, Benkerrou M, Bernaudin F, Sebag G Pediatr Radiol2014
Effects of o-vanillin on K(+) transport of red blood cells from patients with sickle cell disease.Hannemann A, Cytlak UM, Gbotosho OT, Rees DC, Tewari S, Gibson JS Blood Cells Mol. Dis.2014
Craniofacial features of patients with sickle cell anemia and sickle cell trait.Pithon MM, Palmeira LM, Barbosa AA, Pereira R, de Andrade AC, Coqueiro RD Angle Orthod2014
Genomic architecture of sickle cell disease in West African children.Quinlan J, Idaghdour Y, Goulet JP, Gbeha E, de Malliard T, Bruat V, Grenier JC, Gomez S, Sanni A, Rahimy MC, Awadalla P Front Genet2014
Emerging therapy in hemoglobinopathies: lessons from the past and optimism for the future.Vichinsky EP Hematol. Oncol. Clin. North Am.2014
Modulators of Erythropoiesis: Emerging Therapies for Hemoglobinopathies and Disorders of Red Cell Production.Breda L, Rivella S Hematol. Oncol. Clin. North Am.2014
Role of the Hemostatic System on Sickle Cell Disease Pathophysiology and Potential Therapeutics.Pakbaz Z, Wun T Hematol. Oncol. Clin. North Am.2014
Alterations of the Arginine Metabolome in Sickle Cell Disease: A Growing Rationale for Arginine Therapy.Morris CR Hematol. Oncol. Clin. North Am.2014
The Role of Adenosine Signaling in Sickle Cell Therapeutics.Field JJ, Nathan DG, Linden J Hematol. Oncol. Clin. North Am.2014
Inflammatory Mediators of Endothelial Injury in Sickle Cell Disease.Hoppe CC Hematol. Oncol. Clin. North Am.2014
Does Erythropoietin Have a Role in the Treatment of β-Hemoglobinopathies?Fibach E, Rachmilewitz EA Hematol. Oncol. Clin. North Am.2014
Targeted Fetal Hemoglobin Induction for Treatment of Beta Hemoglobinopathies.Perrine SP, Pace BS, Faller DV Hematol. Oncol. Clin. North Am.2014
Therapeutic Strategies to Alter the Oxygen Affinity of Sickle Hemoglobin.Safo MK, Kato GJ Hematol. Oncol. Clin. North Am.2014
Gene Therapy for Hemoglobinopathies: The State of the Field and the Future.Chandrakasan S, Malik P Hematol. Oncol. Clin. North Am.2014
Ischemia-reperfusion Injury in Sickle Cell Anemia: Relationship to Acute Chest Syndrome, Endothelial Dysfunction, Arterial Vasculopathy, and Inflammatory Pain.Hebbel RP Hematol. Oncol. Clin. North Am.2014
Hemoglobin S Polymerization and Red Cell Membrane Changes.Kuypers FA Hematol. Oncol. Clin. North Am.2014
The Prevalence and Molecular Spectrum of α- and β-Globin Gene Mutations in 14,332 Families of Guangdong Province, China.Yin A, Li B, Luo M, Xu L, Wu L, Zhang L, Ma Y, Chen T, Gao S, Liang J, Guo H, Qin D, Wang J, Yuan T, Wang Y, Huang WW, He WF, Zhang Y, Liu C, Xia S, Chen Q, Zhao Q, Zhang X PLoS ONE2014
Imaging flow cytometry for automated detection of hypoxia-induced erythrocyte shape change in sickle cell disease.van Beers EJ, Samsel L, Mendelsohn L, Saiyed R, Fertrin K, Brantner CA, Daniels MP, Nichols J, McCoy JP, Kato GJ Am. J. Hematol.2014
Partial splenectomy in sickle cell disease.Gutiérrez Díaz AI, Svarch E, Arencibia Núñez A, Sabournin Ferrier V, Machín García S, Menendez Veitía A, Ramón Rodriguez L, Serrano Mirabal J, García Peralta T, López Martin LG An Pediatr (Barc)2014
Variability of hemoglobin F expression in hemoglobin EE disease: Hematological and molecular analysis.Pakdee N, Yamsri S, Fucharoen G, Sanchaisuriya K, Pissard S, Fucharoen S Blood Cells Mol. Dis.2014
Interaction of hemoglobin Grey Lynn (Vientiane) with a non-deletional α(+)-thalassemia in an adult Thai proband.Singha K, Fucharoen G, Fucharoen S Biochem Med (Zagreb)2014
An update on sickle cell nephropathy.Alhwiesh A Saudi J Kidney Dis Transpl2014
Scope and efficiency of the newborn screening program in identifying hemoglobin S.Ivo ML, de Araujo OM, Barbieri AR, Corrêa Filho RA, Pontes ER, Botelho CA Rev Bras Hematol Hemoter2014
Values of mean cell volume and mean sphered cell volume can differentiate hereditary spherocytosis and thalassemia.Liao L, Deng ZF, Qiu YL, Chen P, Chen WQ, Lin FQ Hematology2014
Erythrocytic phosphatidylserine exposure and hemostatic alterations in β-thalassemia intermediate patients.Zahedpanah M, Azarkeivan A, Aghaieepour M, Nikogoftar M, Ahmadinegad M, Hajibeigi B, Tabatabaiee MR, Maghsudlu M Hematology2014
Heme-induced neutrophil extracellular traps contribute to the pathogenesis of sickle cell disease.Chen G, Zhang D, Fuchs TA, Wagner DD, Frenette PS Blood2014
Refractory sickle cell leg ulcer: is heparan sulphate a new hope?Hayek S, Dibo S, Baroud J, Ibrahim A, Barritault D Int Wound J2014
Nocturnal enuresis in sickle cell disease.Wolf RB, Kassim AA, Goodpaster RL, Debaun MR Expert Rev Hematol2014
Red blood cell oxidative stress impairs oxygen delivery and induces red blood cell aging.Mohanty JG, Nagababu E, Rifkind JM Front Physiol2014
Hydroxycarbamide Decreases Sickle Reticulocyte Adhesion to Resting Endothelium by Inhibiting Endothelial Lutheran/Basal Cell Adhesion Molecule (Lu/BCAM) through Phosphodiesterase 4A Activation.Chaar V, Laurance S, Lapoumeroulie C, Cochet S, De Grandis M, Colin Y, Elion J, Le Van Kim C, El Nemer W J. Biol. Chem.2014
The effect of hydroxyurea on compound heterozygotes for sickle cell-hemoglobin D-Punjab-A single centre experience in eastern India.Patel S, Purohit P, Mashon RS, Dehury S, Meher S, Sahoo S, Dash SS, Das K, Das P, Patel DK Pediatr Blood Cancer2014
Second BMT for thalassemia major using CY post transplant.Yaqub N, Khalid S, Itrat F, Khan A, Gilani SK, Missiry ME, Hussain MH, Uderzo C, Faulkner L Bone Marrow Transplant.2014
HBS1L-MYB intergenic variants modulate fetal hemoglobin via long-range MYB enhancers.Stadhouders R, Aktuna S, Thongjuea S, Aghajanirefah A, Pourfarzad F, van Ijcken W, Lenhard B, Rooks H, Best S, Menzel S, Grosveld F, Thein SL, Soler E J. Clin. Invest.2014
Sickle cell disease in sub-Saharan Africa: stakes and strategies for control of the disease.Diallo DA, Guindo A Curr. Opin. Hematol.2014
Management of sickle cell disease in the community.Brousse V, Makani J, Rees DC BMJ2014
Efficacy of deferasirox in children with beta-thalassemia: a single-center 3-year experience.Aycicek A, Koc A, Abuhandan M Pediatr Int2014
Haemolysis and abnormal haemorheology in sickle cell anaemia.Connes P, Lamarre Y, Waltz X, Ballas SK, Lemonne N, Etienne-Julan M, Hue O, Hardy-Dessources MD, Romana M Br. J. Haematol.2014
Red blood cell transfusions for thalassemia: results of a survey assessing current practice and proposal of evidence-based guidelines.Goss C, Giardina P, Degtyaryova D, Kleinert D, Sheth S, Cushing M Transfusion2014
Hb Manukau [β67(E11)Val → Gly; HBB: c.203T>G]: The Role of Genetic Testing in the Diagnosis of Idiopathic Hemolytic Anemia.Kumar MK, Judd C, Hoyer JD, Swanson KC, Nelson L, Oliveira JL Hemoglobin2014
Oxidation Status of β-Thalassemia Minor and Hb H Disease, and Its Association with Glycerol Lysis Time (GLT50).Adhiyanto C, Hattori Y, Yamashiro Y, Mella F, Nitta T, Iihoshi M, Araki S, Matar M, Takagi F Hemoglobin2014
Outcome of overt stroke in sickle cell anaemia, a single institution's experience.Majumdar S, Miller M, Khan M, Gordon C, Forsythe A, Smith MG, Megason G, Iyer R Br. J. Haematol.2014
Essential role of hemoglobin beta-93-cysteine in post-hypoxia facilitation of breathing in conscious mice.Gaston B, May WJ, Sullivan S, Yemen S, Marozkina NV, Palmer LA, Bates JN, Lewis SJ J. Appl. Physiol.2014
Inferior vena cava Doppler indices in fetuses with hemoglobin Bart's hydrops fetalis.Luewan S, Tongprasert F, Srisupundit K, Tongsong T Prenat. Diagn.2014
Laboratory tests for coagulation system monitoring in a patient with β-thalassemia.Seregina EA, Nikulina OF, Tsvetaeva NV, Rodionova MN, Gribkova IV, Orel EB, Zapariy AP, Erasov AV, Balandina AN, Ananyeva NM, Ataullakhanov FI Int. J. Hematol.2014
Thromboelastometry profile in children with beta-thalassemia.Turhan AB, Bör O, Akay OM, Akgün NA Int. J. Hematol.2014
Modulation of gamma globin genes expression by histone deacetylase Inhibitors: an in vitro study.Ronzoni L, Sonzogni L, Fossati G, Modena D, Trombetta E, Porretti L, Cappellini MD Br. J. Haematol.2014
Can a polymorphism in the thalassemia gene and a heterozygote CFTR mutation cause acute pancreatitis?Löhr JM, Haas S World J Clin Cases2014
Increased stroke size following MCA occlusion in a mouse model of sickle cell disease.Luo W, Su EJ, Wang J, Wang H, Guo C, Pawar A, Campbell AD, Lawrence DA, Eitzman DT Blood2014
A phase 2 trial of HQK-1001 in HbE-β thalassemia demonstrates HbF induction and reduced anemia.Patthamalai P, Fuchareon S, Chaneiam N, Ghalie RG, Chui DH, Boosalis MS, Perrine SP Blood2014
MRI guided iron assessment and oral chelator use improve iron status in thalassemia major patients.Nichols-Vinueza DX, White MT, Powell AJ, Banka P, Neufeld EJ Am. J. Hematol.2014
Brucella Sacroiliitis in Thalassemia Major.Topal Y, Topal H, Senel S Indian J Pediatr2014
Ex-Vivo Cytoadherence Phenotypes of Plasmodium falciparum Strains from Malian Children with Hemoglobins A, S, and C.Beaudry JT, Krause MA, Diakite SA, Fay MP, Joshi G, Diakite M, White NJ, Fairhurst RM PLoS ONE2014
Children with sickle cell disease need more effective therapies, not more X-rays.Hulbert ML Pediatr Blood Cancer2014
Not simply misshapen red cells: multimolecular and cellular events in sickle vaso-occlusion.Vercellotti GM, Belcher JD J. Clin. Invest.2014
Coinheritance of sickle cell anemia and α-thalassemia delays disease onset and could improve survival in cameroonian's patients (Sub-Saharan Africa).Wonkam A, Rumaney MB, Ngo Bitoungui VJ, Vorster AA, Ramesar R, Ngogang J Am. J. Hematol.2014
Outpatient Pain Predicts Subsequent One-Year Acute Health Care Utilization Among Adults With Sickle Cell Disease.Ezenwa MO, Molokie RE, Wang ZJ, Yao Y, Suarez ML, Angulo V, Wilkie DJ J Pain Symptom Manage2014
Ocular findings in children with thalassemia major in Eastern Mediterranean.Aksoy A, Aslankurt M, Aslan L, Gül O, Garipardıç M, Celik O, Okumuş S, Ozdemir M, Ozdemir G Int J Ophthalmol2014
Impaired blood rheology plays a role in the chronic disorders associated with sickle cell-hemoglobin C disease.Lemonne N, Lamarre Y, Romana M, Hardy-Dessources MD, Lionnet F, Waltz X, Tarer V, Mougenel D, Tressières B, Lalanne-Mistrih ML, Etienne-Julan M, Connes P Haematologica2014
Prodromal Illness Before Acute Chest Syndrome in Pediatric Patients With Sickle Cell Disease.Creary SE, Krishnamurti L J. Pediatr. Hematol. Oncol.2014
Pediatric Hematology Providers on Referral for Transplant Evaluation for Sickle Cell Disease: A Regional Perspective.Mikles B, Bhatia M, Oyeku SO, Jin Z, Green NS J. Pediatr. Hematol. Oncol.2014
Original research: using guided imagery to manage pain in young children with sickle cell disease.Dobson CE, Byrne MW Am J Nurs2014
Sickle cell disease: is hydroxyurea the final answer?Ramzan M, Yadav SP Indian Pediatr2014
[Cerebral vasculopathy in pediatric sickle-cell anemia].Kossorotoff M, Grevent D, de Montalembert M Arch Pediatr2014
Blood substitutes: why haven't we been more successful?Alayash AI Trends Biotechnol.2014
Sickle Cell Anemia: An Underappreciated and Unaddressed Contributor to Global Childhood Mortality.McGann PT J. Pediatr.2014
High index of suspicion for early diagnosis of alendronate-induced stage zero osteonecrosis of jaw in thalassaemia major.Chatterjee R, Bajoria R, Shah FT, Porter JB, Fedele S Br. J. Haematol.2014
An official american thoracic society clinical practice guideline: diagnosis, risk stratification, and management of pulmonary hypertension of sickle cell disease.Klings ES, Machado RF, Barst RJ, Morris CR, Mubarak KK, Gordeuk VR, Kato GJ, Ataga KI, Gibbs JS, Castro O, Rosenzweig EB, Sood N, Hsu L, Wilson KC, Telen MJ, Decastro LM, Krishnamurti L, Steinberg MH, Badesch DB, Gladwin MT, Am. J. Respir. Crit. Care Med.2014
The Price of Mercy: Comment to the Paper Entitled Giordano PC, Rachmilewitz E Mediterr J Hematol Infect Dis2014
Procalcitonin as a biomarker of bacterial infection in sickle cell vaso-occlusive crisis.Patel DK, Mohapatra MK, Thomas AG, Patel S, Purohit P Mediterr J Hematol Infect Dis2014
Prevention of β Thalassemia in Northern Israel - a Cost-Benefit Analysis.Koren A, Profeta L, Zalman L, Palmor H, Levin C, Zamir RB, Shalev S, Blondheim O Mediterr J Hematol Infect Dis2014
Associated factors of acute chest syndrome in children with sickle cell disease in French Guiana.Elenga N, Cuadro E, Martin E, Cohen-Addad N, Basset T Int J Pediatr2014
A double-blind, placebo-controlled phase II study of the efficacy and safety of 2,2-dimethylbutyrate (HQK-1001), an oral fetal globin inducer, in sickle cell disease.Reid ME, El Beshlawy A, Inati A, Kutlar A, Abboud MR, Haynes J, Ward R, Sharon B, Taher AT, Smith W, Manwani D, Ghalie RG Am. J. Hematol.2014
Mechanistic Insights and Characterization of Sickle Cell Disease Associated Cardiomyopathy.Desai AA, Patel AR, Ahmad H, Groth JV, Thiruvoipati T, Turner K, Yodwut C, Czobor P, Artz N, Machado RF, Garcia JG, Lang RM Circ Cardiovasc Imaging2014
Lung function and six-minute walk test performance in individuals with sickle cell disease.Ohara DG, Ruas G, Walsh IA, Castro SS, Jamami M Braz J Phys Ther2014
Outcomes of Adult Patients With Sickle-Cell Disease Admitted to the ICU: A Case Series.Cecchini J, Lionnet F, Djibré M, Parrot A, Stojanovic KS, Girot R, Fartoukh M Crit. Care Med.2014
Relation of Myocardial Systolic Mechanics to Serum Ferritin Level as a Prognosticator in Thalassemia Patients Undergoing Repeated Transfusion.Chen MR, Ko HS, Chao TF, Liu HC, Kuo JY, Bulwer BE, Yeh HI, Hung CL Echocardiography2014
Proteasome Inhibition Induces Both Antioxidant and Hb F Responses in Sickle Cell Disease Via the Nrf2 Pathway.Pullarkat V, Meng Z, Tahara SM, Johnson CS, Kalra VK Hemoglobin2014
Challenge of Managing Sickle Cell Disease in a Pediatric Population Living in Kinshasa, Democratic Republic of Congo: A Sickle Cell Center Experience.Aloni MN, Nkee L Hemoglobin2014
Evaluation of the National Prevention Program in Iran, 2007-2009: the Accomplishments and Challenges with Reflections on the Path Ahead.Hadipour Dehshal M, Tabrizi Namini M, Ahmadvand A, Manshadi M, Sadeghian Varnosfaderani F, Abolghasemi H Hemoglobin2014
Plastic bronchitis in beta thalassemia minor.Zaki SA Lung India2014
Cerebral reorganization of language and motor control secondary to chronic hemispheric vasculopathy in a patient with homozygous sickle-cell disease.Mellerio C, Farhat WH, Calvet D, Oppenheim C, Lefaucheur JP, Bartolucci P Am. J. Hematol.2014
Association between relative systemic hypertension and otologic disorders in patients with sickle cell-hemoglobin C disorder.Lemonne N, Romana M, Lamarre Y, Hardy-Dessources MD, Lionnet F, Waltz X, Tarer V, Mougenel D, Tressières B, Lalanne-Mistrih ML, Etienne-Julan M, Connes P Am. J. Hematol.2014
Association of Variants at BCL11A and HBS1L-MYB with Hemoglobin F and Hospitalization Rates among Sickle Cell Patients in Cameroon.Wonkam A, Ngo Bitoungui VJ, Vorster AA, Ramesar R, Cooper RS, Tayo B, Lettre G, Ngogang J PLoS ONE2014
Haptoglobin, alpha-thalassaemia and glucose-6-phosphate dehydrogenase polymorphisms and risk of abnormal transcranial Doppler among patients with sickle cell anaemia in Tanzania.Cox SE, Makani J, Soka D, L'esperence VS, Kija E, Dominguez-Salas P, Newton CR, Birch AA, Prentice AM, Kirkham FJ Br. J. Haematol.2014
Leucocyte telomere length in patients with sickle cell disease.Drašar ER, Jiang J, Gardner K, Howard J, Vulliamy T, Vasavda N, Thein SL Br. J. Haematol.2014
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Microvascular oxygen consumption during sickle cell pain crisis.Rowley CA, Ikeda AK, Seidel M, Anaebere TC, Antalek MD, Seamon C, Conrey AK, Mendelsohn L, Nichols J, Gorbach AM, Kato GJ, Ackerman H Blood2014
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Successful Outcome of Chronic Intrahepatic Cholestasis in an Adult Patient with Sickle Cell/ β (+) Thalassemia.Vlachaki E, Andreadis P, Neokleous N, Agapidou A, Vetsiou E, Katsinelos P, Boura P Case Rep Hematol2014
An activin receptor IIA ligand trap corrects ineffective erythropoiesis in β-thalassemia.Dussiot M, Maciel TT, Fricot A, Chartier C, Negre O, Veiga J, Grapton D, Paubelle E, Payen E, Beuzard Y, Leboulch P, Ribeil JA, Arlet JB, Coté F, Courtois G, Ginzburg YZ, Daniel TO, Chopra R, Sung V, Hermine O, Moura IC Nat. Med.2014
An Uncommon Cause of Abdominal Pain in a Patient with Thalassemia Intermedia.McDonald K, Kermalli H, Majumder S, Naut E Am. J. Med.2014
Sickle cell disease and posterior reversible leukoencephalopathy.Geevasinga N, Cole C, Herkes GK, Barnett Y, Lin J, Needham M J Clin Neurosci2014
Prevalence of Hypoparathyroidism (HPT) in Beta Thalassemia Major.Basha N KP, Shetty B, Shenoy UV J Clin Diagn Res2014
Growth hormone - insulin-like growth factor-I axis and bone mineral density in adults with thalassemia major.Soliman A, De Sanctis V, Yassin M, Abdelrahman MO Indian J Endocrinol Metab2014
Progression and Prognostic Indicators of Bronchial Disease in Children with Sickle Cell Disease.Williams SN, Nussbaum E, Yoonessi L, Morphew T, Randhawa I Lung2014
VCL-ALK Renal Cell Carcinoma in Children With Sickle-cell Trait: The Eighth Sickle-cell Nephropathy?Smith NE, Deyrup AT, Mariño-Enriquez A, Fletcher JA, Bridge JA, Illei PB, Netto GJ, Argani P Am. J. Surg. Pathol.2014
Hydroxycarbamide modulates components involved in the regulation of adenosine levels in blood cells from sickle-cell anemia patients.Silva-Pinto AC, Dias-Carlos C, Saldanha-Araujo F, Ferreira FI, Palma PV, Araujo AG, Queiroz RH, Elion J, Covas DT, Zago MA, Panepucci RA Ann. Hematol.2014
Evaluation of infectious disease markers in multitransfused egyptian children with thalassemia.Hussein E Ann. Clin. Lab. Sci.2014
Induction of Fetal Hemoglobin as a Novel Therapeutic Strategy for β-Hemoglobinopathy.Fard AD, Kaviani S, Noruzinia M, Saki N, Mortaz E Lab Hematol2014
Hemoglobinopathic erythrocytes affect the intraerythrocytic multiplication of Plasmodium falciparum in vitro.Glushakova S, Balaban A, McQueen PG, Coutinho R, Miller JL, Nossal R, Fairhurst RM, Zimmerberg J J. Infect. Dis.2014
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Performances of Capillary Electrophoresis and HPLC Methods in HbA1c Determination: Diagnostic Accuracy in HbS and HbD-Iran Variants' Presence.Dessi M, Pieri M, Pignalosa S, Martino FG, Zenobi R J. Clin. Lab. Anal.2014
Leg ulcers in patients with sickle-cell disease in Libreville (Gabon): clinical aspects and management.Mouba JF, Mengue C, Eko L, Ondo A Med Sante Trop2014
Psychosocial and pharmacological management of pain in pediatric sickle cell disease.Hildenbrand AK, Nicholls EG, Daly BP, Marsac ML, Tarazi R, Deepti R Postgrad Med2014
Priapism in Homozygous Sickle Cell Patients: Important Clinical and Laboratory Associations.Madu AJ, Ubesie A, Ocheni S, Chinawa J, Madu KA, Ibegbulam OG, Nonyelu C, Eze A Med Princ Pract2014
Discordance between Self-Report and Genetic Confirmation of Sickle Cell Disease Status in African-American Adults.Bean CJ, Hooper WC, Ellingsen D, Debaun MR, Sonderman J, Blot WJ Public Health Genomics2014
Comparison of Tissue Doppler Imaging with MRI T2* and 24-Hour Rhythm Holter Heart Rate Variability for Diagnosing Early Cardiac Impairment in Thalassemia Major Patients.Yetimakman AF, Oztarhan K, Aydogan G Pediatr Hematol Oncol2014
Relationship among chelator adherence, change in chelators, and quality of life in Thalassemia.Trachtenberg FL, Gerstenberger E, Xu Y, Mednick L, Sobota A, Ware H, Thompson AA, Neufeld EJ, Yamashita R Qual Life Res2014
Pulmonary function, CT and echocardiographic abnormalities in sickle cell disease.Lunt A, Desai SR, Wells AU, Hansell DM, Mushemi S, Melikian N, Shah AM, Thein SL, Greenough A Thorax2014
CE Test 2.6 Hours: Using Guided Imagery to Manage Pain in Young Children with Sickle Cell Disease.Contrada E Am J Nurs2014
Association between morphometric variables and nocturnal desaturation in sickle-cell anemia.Salles C, Bispo M, Trindade-Ramos RT J Pediatr (Rio J)2014
Randomized Controlled Trial of Sildenafil for Preventing Recurrent Ischemic Priapism in Sickle Cell Disease.Burnett AL, Anele UA, Trueheart IN, Strouse JJ, Casella JF Am. J. Med.2014
Spectral detection of thalassemia: a preliminary study.Alsalhi MS, Algahtani FH, Devanesan S, Vijmasi VT, Jeyaprakash K, Alsaeed AH, Masilamani V J. Biomed. Sci.2014
Efficacy and safety of combined oral iron chelation therapy with deferasirox and deferiprone in a patient with beta-thalassemia major and persistent iron overload.Alavi S, Sadeghi E, Ashenagar A Blood Res2014
Reduction in serum IL-10 levels is a surrogate marker for predicting vasocclusive crisis in sickle cell disease.Sarray S, Mahdi N, Saleh LR, Almaoui WY Am. J. Hematol.2014
β -Thalassemia Intermedia in Northern Iraq: A Single Center Experience.Al-Allawi NA, Jalal SD, Mohammad AM, Omer SQ, Markous RS Biomed Res Int2014
Cardiac T2* MRI assessment in patients with thalassaemia major and its effect on the preference of chelation therapy.Akcay A, Salcioglu Z, Oztarhan K, Tugcu D, Aydogan G, Ayaz NA, Bornaun H, Sen HS, Akici F, Akdana B Int. J. Hematol.2014
Rapid screening for sickle cell disease by polymerase chain reaction-high resolution melting analysis.Yue L, Lin M, Chen JT, Zhan XF, Zhong DS, Monte-Nguba SM, Liu PF, Pan XF, Huang JH, Wang X, Salas Ehapo JC, Eyi UM, Yang HT, Yang LY Mol Med Rep2014
The Impact of Sickle Cell Disease on Oral Health-related Quality of Life.Ralstrom E, da Fonseca MA, Rhodes M, Amini H Pediatr Dent2014
Hydroxyurea as a first-line treatment of extramedullary hematopoiesis in patients with beta thalassemia: Four case reports.Karimi M, Cohan N, Pishdad P Hematology2014
A combination of two novel alpha globin variants Hb Bridlington (HBA1) and Hb Taybe (HBA2) resulting in severe hemolysis, pulmonary hypertension, and death.Hill QA, Farrar L, Lordan J, Gallienne A, Henderson S Hematology2014
Sickle cell disease in India.Colah R, Mukherjee M, Ghosh K Curr. Opin. Hematol.2014
Practice Patterns of Stroke Screening and Hydroxyurea Use in Children With Sickle Cell Disease: A Survey of Health Care Providers.Madden NA, Jones GL, Kalpatthi R, Woods G J. Pediatr. Hematol. Oncol.2014
The Role of ROS in Hydroquinone-induced Inhibition of K562 Cell Erythroid Differentiation.Yu CH, Suriguga , Li Y, Li YR, Tang KY, Jiang L, Yi ZC Biomed. Environ. Sci.2014
Sustained ventricular tachycardia in a patient with thalassemia major.Bayar N, Arslan S, Erkal Z, Küçükseymen S Ann Noninvasive Electrocardiol2014
Complications of HbH disease in adulthood.Sheeran C, Weekes K, Shaw J, Pasricha SR Br. J. Haematol.2014
Predictors of splenic function preservation in children with sickle cell anemia treated with hydroxyurea.Nottage KA, Ware RE, Winter B, Smeltzer M, Wang WC, Hankins JS, Dertinger SD, Shulkin B, Aygun B Eur. J. Haematol.2014
Hypoxia and inflammation in children with sickle cell disease: implications for hippocampal functioning and episodic memory.Iampietro M, Giovannetti T, Tarazi R Neuropsychol Rev2014
Perceived Discrimination in Health Care is Associated With a Greater Burden of Pain in Sickle Cell Disease.Haywood C, Diener-West M, Strouse J, Carroll CP, Bediako S, Lanzkron S, Haythornthwaite J, Onojobi G, Beach MC, J Pain Symptom Manage2014
Outcomes of matched sibling donor hematopoietic stem cell transplantation for severe sickle cell disease with myeloablative conditioning and intermediate-dose of rabbit anti-thymocyte globulin.Soni S, Gross TG, Rangarajan H, Baker KS, Sturm M, Rhodes M Pediatr Blood Cancer2014
Activation of STAT3 stimulates AHSP expression in K562 cells.Cao C, Zhao G, Yu W, Xie X, Wang W, Yang R, Lv X, Liu D Sci China Life Sci2014
What regulates hepcidin in poly-transfused β-Thalassemia Major: Erythroid drive or store drive?Chauhan R, Sharma S, Chandra J Indian J Pathol Microbiol2014
[Liver and heart iron deposition status in patients with β thalassemia major: a multicenter study].Li C, Liu S, Wang Y, Wen F, Gao H, Chen G, Li C, Wu X, Fang J, Hao W, Liu R, Zhang X, Chu CW, Au W Zhonghua Er Ke Za Zhi2014
Thinking beyond sickling to better understand pain in sickle cell disease.Darbari DS, Ballas SK, Clauw DJ Eur. J. Haematol.2014
Association between serum ferritin level, cardiac and hepatic T2-star MRI in patients with major β-thalassemia.Eghbali A, Taherahmadi H, Shahbazi M, Bagheri B, Ebrahimi L Iran J Ped Hematol Oncol2014
Population Pharmacokinetics of Hydroxyurea for Children and Adolescents with Sickle Cell Disease.Wiczling P, Liem RI, Panepinto JA, Garg U, Abdel-Rahman SM, Kearns GL, Neville KA J Clin Pharmacol2014
Prevalence of the Sickle Cell Trait in Gabon: A nationwide study.Délicat-Loembet LM, Elguero E, Arnathau C, Durand P, Ollomo B, Ossari S, Mezui-Me-Ndong J, Mbang Mboro T, Becquart P, Nkoghe D, Leroy E, Sica L, Gonzalez JP, Prugnolle F, Renaud F Infect. Genet. Evol.2014
The use of Taqman genotyping assays for rapid confirmation of β-thalassaemia mutations in the Malays: accurate diagnosis with low DNA concentrations.Teh LK, Lee TY, Tan JA, Lai MI, George E Int J Lab Hematol2014
Left ventricular torsional mechanics and myocardial iron load in beta-thalassaemia major: a potential role of titin degradation.Chen MP, Li SN, Lam WW, Ho YC, Ha SY, Chan GC, Cheung YF BMC Cardiovasc Disord2014
β-Thalassemia Intermedia: A Bird's-Eye View.Haddad A, Tyan P, Radwan A, Mallat N, Taher A Turk J Haematol2014
How I treat renal complications in sickle cell disease.Sharpe CC, Thein SL Blood2014
Physical activity limits pulmonary endothelial activation in sickle cell SAD mice.Aufradet E, Douillard A, Charrin E, Romdhani A, De Souza G, Bessaad A, Faes C, Bourgeaux V, Chirico EN, Canet-Soulas E, Pialoux V, Martin C Blood2014
Thalassemia Bone Disease: A 19 Year Longitudinal Analysis.Wong P, Fuller PJ, Gillespie MT, Kartsogiannis V, Kerr PG, Doery JC, Paul E, Bowden DK, Strauss BJ, Milat F J. Bone Miner. Res.2014
Molecular characteristic of alpha thalassaemia among patients diagnosed in UKM Medical Centre.Azma RZ, Ainoon O, Azlin I, Noor Farisah NA, Nor Hidayati S, Noor Hamidah H Malays J Pathol2014
Prevalence of Low Bone Mass and Vitamin D Deficiency in β-Thalassemia Major.Tzoulis P, Ang AL, Shah FT, Berovic M, Prescott E, Jones R, Barnard M Hemoglobin2014
The influence of decreased levels of high density lipoprotein cholesterol on hematological indices in sickle cell disease patients.Emokpae A, Kuliya-Gwarzo A Ann Med Health Sci Res2014
Red blood cells and thrombin generation in sickle cell disease.Whelihan MF, Lim MY, Key NS Thromb. Res.2014
Assessing the quality of life of children with sickle cell anaemia using self-, parent-proxy, and health care professional-proxy reports.Constantinou C, Payne N, Inusa B Br J Health Psychol2014
Decitabine.Hackanson B, Daskalakis M Recent Results Cancer Res.2014
Verbal autopsy as a tool for identifying children dying of sickle cell disease: a validation study conducted in Kilifi district, Kenya.Ndila C, Bauni E, Nyirongo V, Mochamah G, Makazi A, Kosgei P, Nyutu G, Macharia A, Kapesa S, Byass P, Williams TN BMC Med2014
Impact of iron deficiency on hemoglobin A2% in obligate β-thalassemia heterozygotes.Sharma P, Das R, Trehan A, Bansal D, Chhabra S, Kaur J, Marwaha RK, Varma N, Garewal G Int J Lab Hematol2014
Effects of oxidative stress on red blood cell rheology in sickle cell patients.Hierso R, Waltz X, Mora P, Romana M, Lemonne N, Connes P, Hardy-Dessources MD Br. J. Haematol.2014
Complete recovery from paraparesis in spinal cord compression due to extramedullary haemopoiesis in beta-thalassaemia by emergency radiation therapy.Ruo Redda MG, Allis S, Reali A, Bartoncini S, Roggero S, Anglesio SM, Piga A Intern Med J2014
Asymmetric dimethylarginine levels in children with β-thalassemia and their correlations to tricuspid regurgitant jet velocity.Mohamed ES, Ibrahim B, Amr D, Noha EK, Mokhtar M Pediatr Blood Cancer2014
Do difficulties in swallowing medication impede the use of hydroxyurea in children?Bekele E, Thornburg CD, Brandow AM, Sharma M, Smaldone AM, Jin Z, Green NS Pediatr Blood Cancer2014
Randomization is not associated with socio-economic and demographic factors in a multi-center clinical trial of children with sickle cell anemia.Roberts DO, Covert B, Rodeghier MJ, Parmar N, Debaun MR, Thompson AA, Liem RI Pediatr Blood Cancer2014
Transthoracic echocardiography and 6-minute walk test in kuwaiti sickle cell disease patients.Marouf R, Behbehani N, Zubaid M, Al Wazzan H, El Muzaini H, Abdulla R, Mojiminiyi OA, Adekile AD Med Princ Pract2014
Degrees of kidney disease in nigerian adults with sickle-cell disease.Aneke JC, Adegoke AO, Oyekunle AA, Osho PO, Sanusi AA, Okocha EC, Ibeh NC, Akinola NO, Durosinmi MA Med Princ Pract2014
Structural determinants of human ζ-globin mRNA stability.He Z, Song D, van Zalen S, Russell JE J Hematol Oncol2014
Management of the acute painful crisis in sickle cell disease- a re-evaluation of the use of opioids in adult patients.Telfer P, Bahal N, Lo A, Challands J Br. J. Haematol.2014
Bisphosphonates in the management of thalassemia-associated osteoporosis: a systematic review of randomised controlled trials.Giusti A J. Bone Miner. Metab.2014
High multi-cytokine levels are not a predictive marker of alloimmunization in transfused sickle cell disease patients.Tatari-Calderone Z, Fasano RM, Miles MR, Pinto LA, Luban NL, Vukmanovic S Cytokine2014
Secondary haemochromatosis in a patient with thalassemia intermedia.Rotaru I, Gaman A, Gaman G Curr Health Sci J2014
Influence of βS-globin haplotypes and hydroxyurea on tumor necrosis factor-alpha levels in sickle cell anemia.Laurentino MR, Maia PA, Barbosa MC, Bandeira IC, Rocha LB, Gonçalves RP Rev Bras Hematol Hemoter2014
Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: indications and management recommendations from an international expert panel.Angelucci E, Matthes-Martin S, Baronciani D, Bernaudin F, Bonanomi S, Cappellini MD, Dalle JH, Di Bartolomeo P, de Heredia CD, Dickerhoff R, Giardini C, Gluckman E, Hussein AA, Kamani N, Minkov M, Locatelli F, Rocha V, Sedlacek P, Smiers F, Thuret I, Yaniv I, Cavazzana M, Peters C, Haematologica2014
Rare form of autosomal dominant thalassemia-Hemoglobin Hakkari.Nair S, Eldjerou LK, Harris NS, Dunbar LN Pediatr Blood Cancer2014
Sickle Cell Disease and Stroke.Talahma M, Strbian D, Sundararajan S Stroke2014
PIPKIIα is widely expressed in hematopoietic-derived cells and may play a role in the expression of alpha- and gamma-globins in K562 cells.Peretti de Albuquerque Wobeto V, Machado-Neto JA, Zaccariotto TR, Ribeiro DM, da Silva Santos Duarte A, Saad ST, Costa FF, de Fatima Sonati M Mol. Cell. Biochem.2014
Client Views and Attitudes to Non-Invasive Prenatal Diagnosis for Sickle Cell Disease, Thalassaemia and Cystic Fibrosis.Hill M, Compton C, Karunaratna M, Lewis C, Chitty L J Genet Couns2014
Management of pulmonary arterial hypertension associated to thalassemia: when pulmonary endarterectomy is the best therapeutical option? A case report.Roggero S, Vullo S, Volpe G, Piga A, Albera C J. Thromb. Thrombolysis2014
Predictors of Red Cell Alloimmunization in Multitransfused Egyptian Patients With β-Thalassemia.Hussein E, Desooky N, Rihan A, Kamal A Arch. Pathol. Lab. Med.2014
Circulating cell-free DNA in sickle cell disease: is it a potentially useful biomarker?Al-Humood S, Zueriq R, Al-Faris L, Marouf R, Al-Mulla F Arch. Pathol. Lab. Med.2014
Splenomegaly in adult sickle cell disease patients.Achanta L, Bhaskar N, Ledoux S J Ark Med Soc2014
Thalassemia diagnosis in a blood donor from a unique trimorphic red blood cell population observed in the recipient.Vagace JM, de la Maya MD, Gervasini G Clin. Chem. Lab. Med.2014
Prevalence and Progression of Chronic Kidney Disease in Adult Patients With Sickle Cell Disease.Gosmanova EO, Zaidi S, Wan JY, Adams-Graves PE J. Investig. Med.2014
Running exercise alleviates trabecular bone loss and osteopenia in hemizygous β-globin knockout thalassemic mice.Thongchote K, Svasti S, Teerapornpuntakit J, Krishnamra N, Charoenphandhu N Am. J. Physiol. Endocrinol. Metab.2014
First evidence of subclinical renal tubular injury during sickle-cell crisis.Audard V, Moutereau S, Vandemelebrouck G, Habibi A, Khellaf M, Grimbert P, Levy Y, Loric S, Renaud B, Lang P, Godeau B, Galactéros F, Bartolucci P Orphanet J Rare Dis2014
Sickle-cell disease stroke throughout life: A retrospective study in an adult referral center.Gueguen A, Mahevas M, Nzouakou R, Hosseini H, Habibi A, Bachir D, Brugière P, Lionnet F, Ribei JA, Godeau B, Girot R, Ibrahima V, Calvet D, Galactéros F, Bartolucci P Am. J. Hematol.2014
Partial dysfunction of Treg activation in sickle cell disease.Vingert B, Tamagne M, Desmarets M, Pakdaman S, Elayeb R, Habibi A, Bernaudin F, Galacteros F, Bierling P, Noizat-Pirenne F, Cohen J Am. J. Hematol.2014
Ambulatory quality indicators to prevent infection in sickle cell disease.Beverung LM, Brousseau D, Hoffmann RG, Yan K, Panepinto JA Am. J. Hematol.2014
Homozygous hemoglobin S with concomitant hemoglobin G-Philadelphia: A diagnostic challenge.Racsa L, Rogers ZR, Mitui M, Park JY, Timmons C, Luu H Pediatr Blood Cancer2014
Epidemiology and screening of sickle cell anemia in the Mediterranean area and in developing countries.Amato A, Grisanti P, Mastropietro F, Lerone M, Cappabianca MP, Ponzini D, Piscitelli R Ig Sanita Pubbl2014
Prenatal control of Hb Bart's hydrops fetalis: a two-year experience at a mainland Chinese hospital.Liao C, Pan M, Han J, Yang X, Zhen L, Li J, Li R, Li DZ J. Matern. Fetal. Neonatal. Med.2014
Nutritional biomarkers in children and adolescents with Beta-thalassemia-major: an egyptian center experience.Sherief LM, Abd El-Salam SM, Kamal NM, El Safy O, Almalky MA, Azab SF, Morsy HM, Gharieb AF Biomed Res Int2014
[Transfusion and sickle cell disease: Axes of transfusion safety optimization].Noizat-Pirenne F Transfus Clin Biol2014
Maxillofacial extramedullary hematopoiesis in a child with sickle cell presenting as bilateral periorbital cellulitis.Reiersen DA, Mandava M, Jeroudi M, Gungor A Int. J. Pediatr. Otorhinolaryngol.2014
Prevalence of deletional alpha thalassemia and sickle gene in a tribal dominated malaria endemic area of eastern India.Purohit P, Dehury S, Patel S, Patel DK ISRN Hematol2014
The injection of air/oxygen bubble into the anterior chamber of rabbits as a treatment for hyphema in patients with sickle cell disease.Ayintap E, Keskin U, Sadigov F, Coskun M, Ilhan N, Motor S, Semiz H, Parlakfikirer N J Ophthalmol2014
Serum YKL-40 levels and chitotriosidase activity in patients with beta-thalassemia major.Musumeci M, Caruso V, Medulla E, Torrisi V, Migale R, Angeletti S, Musumeci S Dis. Markers2014
Sickle Cell Trait and Renal Papillary Necrosis.Li EJ, Carroll VG Clin Pediatr (Phila)2014
Patient-centered Approach to Designing Sickle Cell Transition Education.Williams CP, Smith CH, Osborn K, Bemrich-Stolz CJ, Hilliard LM, Howard TH, Lebensburger JD J. Pediatr. Hematol. Oncol.2014
Alpha-thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation - c.109C>T (p.R37X).Basehore MJ, Michaelson-Cohen R, Levy-Lahad E, Sismani C, Bird LM, Friez MJ, Walsh T, Abidi F, Holloway L, Skinner C, McGee S, Alexandrou A, Syrrou M, Patsalis PC, Raymond G, Wang T, Schwartz CE, King MC, Stevenson RE Clin. Genet.2014
Variance of pain prevalence and associated severity during the transfusion cycle of adult thalassaemia patients.Green ST, Martin MB, Haines D, Carson S, Coates T, Oliveros O, Gerstenberger E, Trachtenberg F, Kwiatkowski JL, Br. J. Haematol.2014
Longitudinal Study on Liver Functions in Patients with Thalassemia Major before and after Deferasirox (DFX) Therapy.Soliman A, Yassin M, Al Yafei F, Al-Naimi L, Almarri N, Sabt A, De Sanctis V Mediterr J Hematol Infect Dis2014
Hypoxia-inducible factor-1α (HIF-1α) expression in placentae of women with iron deficiency anemia and β-thalassemia trait.Michalitsi V, Dafopoulos K, Gourounti K, Messini C, Ioannou M, Christodoulaki C, Panagopoulos P, Messinis I J. Matern. Fetal. Neonatal. Med.2014
Fannin-Lubbock-I [α2β 2 (119(GLY>ASP))], a rare mutation in the β-globin gene, has been detected for the first time in a Hindu Brahmin family in West Bengal, India.Basak J, Bhattacharyya DM, Mukhopadhyay A Cell. Mol. Biol. Lett.2014
Improved non-invasive total haemoglobin measurements after in-vivo adjustment.Miyashita R, Hirata N, Sugino S, Mimura M, Yamakage M Anaesthesia2014
The prevalence of anemia and hemoglobinopathies in the hematologic clinics of the kermanshah province, Western iran.Payandeh M, Rahimi Z, Zare ME, Kansestani AN, Gohardehi F, Hashemian AH Int J Hematol Oncol Stem Cell Res2014
Cut off Determination of Discrimination Indices in Differential Diagnosis between Iron Deficiency Anemia and β- Thalassemia Minor.Miri-Moghaddam E, Sargolzaie N Int J Hematol Oncol Stem Cell Res2014
Doctors urge disclosure of sickle cell trait.Shuchman M CMAJ2014
Exercise tolerance, lung function abnormalities, anemia, and cardiothoracic ratio in sickle cell patients.van Beers EJ, van der Plas MN, Nur E, Bogaard HJ, van Steenwijk RP, Biemond BJ, Bresser P Am. J. Hematol.2014
Splenectomy for haematological disorders.Jankulovski N, Antovic S, Kuzmanovska B, Mitevski A Prilozi2014
Priapism in a patient with sickle cell trait using marijuana.Matta A, Tandra PK, Berim L BMJ Case Rep2014
Diagnosis of diabetes in anaemias and haemoglobinopathies: salutary lessons for improved reporting and patient empowerment.Campbell B, Burnett L Pathology2014
Sickle cell anemia: Intracranial stenosis and silent cerebral infarcts in children with low risk of stroke.Arkuszewski M, Krejza J, Chen R, Ichord R, Kwiatkowski JL, Bilello M, Zimmerman R, Ohene-Frempong K, Melhem ER Adv Med Sci2014
Improving Outcomes in Children with Sickle Cell Disease: Treatment Considerations and Strategies.Amid A, Odame I Paediatr Drugs2014
Immunologic characterization suggests reduced alloimmunization in a murine model of thalassemia intermedia.Bao W, Zhong H, Yazdanbakhsh K Transfusion2014
Reduced toxicity, myeloablative conditioning with BU, fludarabine, alemtuzumab and SCT from sibling donors in children with sickle cell disease.Bhatia M, Jin Z, Baker C, Geyer MB, Radhakrishnan K, Morris E, Satwani P, George D, Garvin J, Del Toro G, Zuckerman W, Lee MT, Licursi M, Hawks R, Smilow E, Baxter-Lowe LA, Schwartz J, Cairo MS Bone Marrow Transplant.2014
A retrospective analysis of the cost of hospitalizations for sickle cell disease with crisis in England, 2010/11.Pizzo E, Laverty AA, Phekoo KJ, Aljuburi G, Green SA, Bell D, Majeed A J Public Health (Oxf)2014
Modified activin receptor IIB ligand trap mitigates ineffective erythropoiesis and disease complications in murine β-thalassemia.Suragani RN, Cawley SM, Li R, Wallner S, Alexander MJ, Mulivor AW, Gardenghi S, Rivella S, Grinberg AV, Pearsall RS, Kumar R Blood2014
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First successful allogeneic hematopoietic stem cell transplantation for a sickle cell disease patient in a low resource country (Nigeria): a case report.Bazuaye N, Nwogoh B, Ikponmwen D, Irowa O, Okugbo S, Isa I, Ighodaro E, Aina YI, Osaguona A, Idemudia O, Iyoha O, Ighosewe O, Osaghae D, Bucher C Ann. Transplant.2014
Prevention and control of Hb Bart's Disease in Guangxi Zhuang Autonomous Region, China.He S, Zhang Q, Li D, Chen S, Tang Y, Chen Q, Zheng C Eur. J. Obstet. Gynecol. Reprod. Biol.2014
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Hemoglobin α in the blood vessel wall.Butcher JT, Johnson T, Beers J, Columbus L, Isakson BE Free Radic. Biol. Med.2014
Genomic analyses of pneumococci from children with sickle cell disease expose host-specific bacterial adaptations and deficits in current interventions.Carter R, Wolf J, van Opijnen T, Muller M, Obert C, Burnham C, Mann B, Li Y, Hayden RT, Pestina T, Persons D, Camilli A, Flynn PM, Tuomanen EI, Rosch JW Cell Host Microbe2014
Pneumococcus adapts to the sickle cell host.Mitchell TJ, Mitchell AM Cell Host Microbe2014
Erythroid Krüppel-like factor mutations are relatively more common in a thalassemia endemic region and ameliorate the clinical and hematological severity of β-thalassemia.Liu D, Zhang X, Yu L, Cai R, Ma X, Zheng C, Zhou Y, Liu Q, Wei X, Lin L, Yan T, Huang J, Mohandas N, An X, Xu X Blood2014
A Case Series of α-Thalassemia Intermedia Due to Compound Heterozygosity for Hb Adana [HBA2: c179G>A (or HBA1); p.Gly60Asp] With Other α-Thalassemias in Malay Families.Alauddin H, Jaapar NA, Azma RZ, Ithnin A, Razak NF, Loh CK, Alias H, Abdul-Latiff Z, Othman A Hemoglobin2014
Molecular Update of β-Thalassemia Mutations in the Syrian Population: Identification of Rare β-Thalassemia Mutations.Jarjour RA, Murad H, Moasses F, Al-Achkar W Hemoglobin2014
Autologous Platelet Gel: Five Cases Illustrating Use on Sickle Cell Disease Ulcers.Gilli SC, Oliveira SA, Saad ST Int J Low Extrem Wounds2014
Hb Fontainebleau (HBA2: c.64G > C) in the United Arab Emirates.Turner A, Sasse J, Varadi A Hemoglobin2014
Novel Point Mutation of the α2-Globin Gene (HBA2) and a Rare 2.4 kb Deletion of the α1-Globin Gene (HBA1), Identified in Two Chinese Patients with Hb H Disease.So CC, Chan AY, Ma ES Hemoglobin2014
α-Globin Gene Mutations in Isfahan Province, Iran.Karamzade A, Mirzapour H, Hoseinzade M, Asadi S, Gholamrezapour T, Tavakoli P, Selebi M Hemoglobin2014
Screening and Diagnosis of Hb Quong Sze [HBA2: c.377T > C (or HBA1)] in a Prenatal Control Program for Thalassemia.Yang Y, Lou JW, Liu YH, He Y, Li DZ Hemoglobin2014
Characterizing a Cohort of α-Thalassemia Couples Collected During Screening for Hemoglobinopathies: 14 Years of an Iranian Experience.Hafezi-Nejad N, Khosravi M, Bayat N, Kariminejad A, Hadavi V, Oberkanins C, Azarkeivan A, Najmabadi H Hemoglobin2014
Fetal outcomes in pregnant women with sickle cell disease.Al-Farsi SH, Al-Khabori MK, Al-Hunieni MN, Al-Riyami NM Saudi Med J2014
Surgical treatment of thoraco-lumbar fractures in sickle cell disease: a case report.Terzi S, Griffoni C, Babbi L, Barbanti Brodano G Eur Rev Med Pharmacol Sci2014
Hydroxyurea therapy for priapism prevention and erectile function recovery in sickle cell disease: a case report and review of the literature.Anele UA, Kyle Mack A, Resar LM, Burnett AL Int Urol Nephrol2014
Sickle cell trait and safe athletic participation: the way forward.Abkowitz JL, O'Connor FG, Deuster PA, Thompson AA Curr Sports Med Rep2014
Hematological indices for differential diagnosis of Beta thalassemia trait and iron deficiency anemia.Vehapoglu A, Ozgurhan G, Demir AD, Uzuner S, Nursoy MA, Turkmen S, Kacan A Anemia2014
Transfusion therapy and alloimmunization in Thalassemia Intermedia: A 10 year experience at a tertiary care university hospital.Al-Riyami AZ, Al-Mahrooqi S, Al-Hinai S, Al-Hosni S, Al-Madhani A, Daar S Transfus. Apher. Sci.2014
Therapeutic effects of induced pluripotent stem cells in chimeric mice with beta-thalassemia.Yang G, Shi W, Hu X, Zhang J, Gong Z, Guo X, Ren Z, Zeng F Haematologica2014
The dual effects of nitrite on hemoglobin-dependent redox reactions.Lu N, Chen C, He Y, Tian R, Xiao Q, Peng YY Nitric Oxide2014
Haemoglobin sickle d punjab: - a case report.Rahimah A, Syahira Lazira O, Siti Hida HM, Faidatul Syazlin AH, Nur Aisyah A, Nik Hafidzah NM, Zubaidah Z Med. J. Malaysia2014
The Prevalence of Sensorineural Hearing Loss in β-thalassaemia patient treated with Desferrioxamine.Kong MH, Goh BS, Hamidah A, Zarina AL Med. J. Malaysia2014
Deferiprone versus Deferoxamine in Sickle Cell Disease: Results from a 5-year long-term Italian multi-center randomized clinical trial.Calvaruso G, Vitrano A, Di Maggio R, Ballas S, Steinberg MH, Rigano P, Sacco M, Telfer P, Renda D, Barone R, Maggio A, Blood Cells Mol. Dis.2014
Repeated Evolution of Chimeric Fusion Genes in the β-Globin Gene Family of Laurasiatherian Mammals.Gaudry MJ, Storz JF, Butts GT, Campbell KL, Hoffmann FG Genome Biol Evol2014
Back pain: the sole of presentation of sickle cell disease.Osman S, Khan S, Hendaus MA J Blood Med2014
Endocrinopathies in Turkish Children with Beta Thalassemia Major: Results from a Single Center Study.Isik P, Yarali N, Tavil B, Demirel F, Karacam GB, Sac RU, Fettah A, Ozkasap S, Kara A, Tunc B Pediatr Hematol Oncol2014
Evaluating the Patients with Thalassemia Major for Long-Term Endocrinological Complications After Bone Marrow Transplantation.Aldemir-Kocabaş B, Tezcan-Karasu G, Bircan I, Bircan O, Aktaş-Samur A, Yeşilipek MA Pediatr Hematol Oncol2014
Fetal blood sampling in prenatal diagnosis of thalassemia at late pregnancy.Karnpean R J Med Assoc Thai2014
Neuroimaging findings in sickle cell disease.Thust SC, Burke C, Siddiqui A Br J Radiol2014
Gangrene of the digits of the right lower limb in a patient with homozygous sickle cell disease and ulcerative colitis.Rankine-Mullings AE, Knight-Madden JM, Reid M, Ferguson TS Clin Pract2014
High protein diet attenuates histopathologic organ damage and vascular leakage in transgenic murine model of sickle cell anemia.Manci EA, Hyacinth HI, Capers PL, Archer DR, Pitts S, Ghosh S, Patrickson J, Titford ME, Ofori-Acquah SF, Hibbert JM Exp. Biol. Med. (Maywood)2014
Fever in sickle cell disease patients in the Kingdom of Bahrain.Al Salman J, Al Agha RA, Al Taitoon S, Al Arrayed A J Infect Public Health2014
The glomerulopathy of sickle cell disease.Ataga KI, Derebail VK, Archer DR Am. J. Hematol.2014
[Primary care follow-up of newborns with sickle cell disease detected in neonatal screening in the Community of Madrid.]Rodríguez-Moldes B, Carbajo AJ, Sánchez B, Fernández M, Garí M, Fernández MC, Alvarez J, García A, Cela E An Pediatr (Barc)2014
Glutathione S-Transferase Gene Polymorphisms (GSTM1, GSTT1 and GSTP1) in Egyptian Pediatric Patients with Sickle Cell Disease.Shiba HF, El-Ghamrawy MK, Shaheen IA, Ali RA, Mousa SM Pediatr. Dev. Pathol.2014
Bradykinin stimulation of nitric oxide production is not sufficient for gamma-globin induction.Cokić VP, Suboticki T, Beleslin-Cokić B, Diklić M, Milenković P, Jovcić G Srp Arh Celok Lek2014
Hydroxyurea in sickle cell disease: drug review.Agrawal RK, Patel RK, Shah V, Nainiwal L, Trivedi B Indian J Hematol Blood Transfus2014
[Evaluation of bone mineral density in children with sickle cell disease.]Garrido Colino C, Beléndez Bieler C, Pérez Díaz M, Cela de Julián E An Pediatr (Barc)2014
Elevated sphingosine-1-phosphate promotes sickling and sickle cell disease progression.Zhang Y, Berka V, Song A, Sun K, Wang W, Zhang W, Ning C, Li C, Zhang Q, Bogdanov M, Alexander DC, Milburn MV, Ahmed MH, Lin H, Idowu M, Zhang J, Kato GJ, Abdulmalik OY, Zhang W, Dowhan W, Kellems RE, Zhang P, Jin J, Safo M, Tsai AL, Juneja HS, Xia Y J. Clin. Invest.2014
Human induced pluripotent stem cell derived erythroblasts can undergo definitive erythropoiesis and co-express gamma and beta globins.Yang CT, French A, Goh PA, Pagnamenta A, Mettananda S, Taylor J, Knight S, Nathwani A, Roberts DJ, Watt SM, Carpenter L Br. J. Haematol.2014
Quantitative Magnetic Resonance Imaging Analysis of the Lacrimal Gland in Sickle Cell Disease.Buch K, Watanabe M, Elias EJ, Liao JH, Jara H, Nadgir RN, Saito N, Steinberg MH, Sakai O J Comput Assist Tomogr2014
Heme and erythropoieis: more than a structural role.Chiabrando D, Mercurio S, Tolosano E Haematologica2014
Molecular diagnostics of the HBB gene in an Omani cohort using bench-top DNA Ion Torrent PGM technology.Hassan SM, Vossen RH, Chessa R, den Dunnen JT, Bakker E, Giordano PC, Harteveld CL Blood Cells Mol. Dis.2014
Epigenetic regulation of fetal globin gene expression in adult erythroid cells.Ginder GD Transl Res2014
Hemin controls T cell polarization in sickle cell alloimmunization.Zhong H, Bao W, Friedman D, Yazdanbakhsh K J. Immunol.2014
Severe nocturnal and postexercise hypoxia in children and adolescents with sickle cell disease.Halphen I, Elie C, Brousse V, Le Bourgeois M, Allali S, Bonnet D, de Montalembert M PLoS ONE2014
β-Globin gene sequencing of hemoglobin Austin revises the historically reported electrophoretic migration pattern.Racsa LD, Luu HS, Park JY, Mitui M, Timmons CF Arch. Pathol. Lab. Med.2014
Multicolor staining of globin subtypes reveals impaired globin switching during erythropoiesis in human pluripotent stem cells.Ochi K, Takayama N, Hirose S, Nakahata T, Nakauchi H, Eto K Stem Cells Transl Med2014
The molecular biology of human iron metabolism.Winter WE, Bazydlo LA, Harris NS Lab Med2014
Evaluation of the new red cell parameters on Beckman Coulter DxH800 in distinguishing iron deficiency anaemia from thalassaemia trait.Ng EH, Leung JH, Lau YS, Ma ES Int J Lab Hematol2014
Pregnancy in patients with sickle cell disease: maternal and perinatal outcomes.Costa VM, Viana MB, Aguiar RA J. Matern. Fetal. Neonatal. Med.2014
Cormic index profile of children with sickle cell anaemia in lagos, Nigeria.Akodu SO, Njokanma OF, Kehinde OA Anemia2014
Automated interventricular septum segmentation for black-blood myocardial T2* measurement in thalassemia.Zheng Q, Feng Y, Wei X, Feng M, Chen W, Lu Z, Xu Y, Chen H, He T J Magn Reson Imaging2014
The spleen and sickle cell disease: the sick(led) spleen.Brousse V, Buffet P, Rees D Br. J. Haematol.2014
H-ferritin ferroxidase induces cytoprotective pathways and inhibits microvascular stasis in transgenic sickle mice.Vercellotti GM, Khan FB, Nguyen J, Chen C, Bruzzone CM, Bechtel H, Brown G, Nath KA, Steer CJ, Hebbel RP, Belcher JD Front Pharmacol2014
Trends in family planning and counselling for women with sickle cell disease in the UK over two decades.Eissa AA, Tuck SM, Rantell K, Stott D J Fam Plann Reprod Health Care2014
Towards an optimization of the management of endocrine complications of thalassemia.El Kholy M, Elsedfy H, Soliman A, Anastasi S, Raiola G, De Sanctis V J. Pediatr. Endocrinol. Metab.2014
Prevalence of HBV and HCV among the multi-transfused beta thalassemic major patients in a day care centre of blood transfusion department of Mymensingh Medical College Hospital.Chakrabarty P, Rudra S, Hossain MA Mymensingh Med J2014
Molecular characterization of α- and β-thalassaemia among Malay patients.Yatim NF, Rahim MA, Menon K, Al-Hassan FM, Ahmad R, Manocha AB, Saleem M, Yahaya BH Int J Mol Sci2014
Percutaneous excretion of iron and ferritin (through Al-hijamah) as a novel treatment for iron overload in beta-thalassemia major, hemochromatosis and sideroblastic anemia.El Sayed SM, Abou-Taleb A, Mahmoud HS, Baghdadi H, Maria RA, Ahmed NS, Nabo MM Med. Hypotheses2014
[Prevalence and molecular analysis of α-thalassemia in preschool children in Chongqing city].Yu J, Xian Y, Yao X, Xiao J, Liu H, Chen S, Zhang L, Zhang Y, Qin Z, Fan R, Zhong X Zhonghua Xue Ye Xue Za Zhi2014
Serial assessment of laser Doppler flow during acute pain crises in sickle cell disease.Shi PA, Manwani D, Olowokure O, Nandi V Blood Cells Mol. Dis.2014
Routine screening for α-thalassaemia using an immunochromatographic strip assay for haemoglobin Bart's.Prayalaw P, Fucharoen G, Fucharoen S J Med Screen2014
Iron distribution and histopathological characterization of the liver and heart of β-thalassemic mice with parenteral iron overload: Effects of deferoxamine and deferiprone.Yatmark P, Morales NP, Chaisri U, Wichaiyo S, Hemstapat W, Srichairatanakool S, Svasti S, Fucharoen S Exp. Toxicol. Pathol.2014
Moderate endurance exercise in patients with sickle cell anaemia: effects on oxidative stress and endothelial activation.Faes C, Balayssac-Siransy E, Connes P, Hivert L, Danho C, Bogui P, Martin C, Pialoux V Br. J. Haematol.2014
Deformability analysis of sickle blood using ektacytometry.Rabai M, Detterich JA, Wenby RB, Hernandez TM, Toth K, Meiselman HJ, Wood JC Biorheology2014
Risk factors of portal vein thrombosis in patients with beta thalassemia major after splenectomy: laparoscopic versus open procedure.Wang M, Zhang M, Li J, Zhou J, Wu Z, Peng B Hepatogastroenterology2014
Cochlear implant for bilateral profound sensorineural hearing loss in an adolescent with sickle cell anemia.Almuhawas FA, Hagr AA Ann Saudi Med2014
Overproduction of CXC chemokines CXCL1, CXCL9, CXCL10 and CXCL12 in β-thalassemia major or patients.Najmaddini H, Hassanshahi G, Ostadebrahimi H, Barkhordari H, Mashayekhi H, Nazari M, Moogooei M, Arababadi YS, Peighambari F, Karimabad MN Ann Saudi Med2014
Deferasirox for managing transfusional iron overload in people with sickle cell disease.Meerpohl JJ, Schell LK, Rücker G, Motschall E, Fleeman N, Niemeyer CM, Bassler D Cochrane Database Syst Rev2014
Reticulocytosis and anemia are associated with an increased risk of death and stroke in the newborn cohort of the Cooperative Study of Sickle Cell Disease.Meier ER, Wright EC, Miller JL Am. J. Hematol.2014
Pregnancy in beta-thalassemia intermedia: 20-year experience of a Greek thalassemia center.Voskaridou E, Balassopoulou A, Boutou E, Komninaka V, Christoulas D, Dimopoulou M, Delaki EE, Loukopoulos D, Terpos E Eur. J. Haematol.2014
CYP2C9 Allelic Variants and Frequencies in a Pediatric Sickle Cell Disease Cohort: Implications for NSAIDs Pharmacotherapy.Jaja C, Patel N, Scott SA, Gibson R, Kutlar A Clin Transl Sci2014
Impact of psychosocial status and disease knowledge on deferoxamine adherence among thalassaemia major adolescents.Al-Kloub MI, Salameh TN, Froelicher ES Int J Nurs Pract2014
Overlapping biological mechanisms underlying sickle cell disease, stress, and depression: a stress-vulnerability framework.Katz T, Schatz JC Harv Rev Psychiatry2014
Sickle cell disease in areas of immigration of high-risk populations: a low cost and reproducible method of screening in northern Italy.Venturelli D, Lodi M, Palazzi G, Bergonzini G, Doretto G, Zini A, Monica C, Cano MC, Ilaria M, Montagnani G, Paolucci P Blood Transfus2014
Erythropoietic potential of CD34+ hematopoietic stem cells from human cord blood and G-CSF-mobilized peripheral blood.Jin H, Kim HS, Kim S, Kim HO Biomed Res Int2014
Identifying Sickle Cell Disease Cases Using Administrative Claims.Reeves S, Garcia E, Kleyn M, Housey M, Stottlemyer R, Lyon-Callo S, Dombkowski K Acad Pediatr2014
Extramedullary hemopoiesis.Orphanidou-Vlachou E, Tziakouri-Shiakalli C, Georgiades CS Semin. Ultrasound CT MR2014
Lactose intolerance is not the cause of gastrointestinal adverse effects in beta thalassemia patients treated with deferasirox.Pazgal I, Brown M, Perets TT, Niv Y, Rachmilewitz E, Stark P Am. J. Hematol.2014
Genetic epidemiology and preventive healthcare in multiethnic societies: the hemoglobinopathies.Giordano PC, Harteveld CL, Bakker E Int J Environ Res Public Health2014
Deferasirox: a review of its use for chronic iron overload in patients with non-transfusion-dependent thalassaemia.Shirley M, Plosker GL Drugs2014
Cost-utility of chelators in transfusion-dependent β-thalassemia major patients: a review of the pharmacoeconomic literature.Lee TA, von Riedemann S, Tricta F Expert Rev Pharmacoecon Outcomes Res2014
Magnetic resonance imaging/angiography and transcranial Doppler velocities in sickle cell anemia: results from the SWiTCH trial.Helton KJ, Adams RJ, Kesler KL, Lockhart A, Aygun B, Driscoll C, Heeney MM, Jackson SM, Krishnamurti L, Miller ST, Sarnaik SA, Schultz WH, Ware RE, Blood2014
Hydroxyurea-inducible SAR1 gene acts through the Giα/JNK/Jun pathway to regulate γ-globin expression.Zhu J, Chin K, Aerbajinai W, Kumkhaek C, Li H, Rodgers GP Blood2014
Live birth following double-factor pre-implantation genetic diagnosis for both reciprocal translocation and alpha-thalassaemia.Lee VC, Chow JF, Lau EY, Yeung WS, Ng EH Hong Kong Med J2014
[Sickle cell disease patients, sickness and medical accompanying questioning related to specific adolescent period].De Pauw S, Maccioni J, Efira A Rev Med Brux2014
A thalassaemia intermedia case with concomitant left atrial thrombus.Sahin C, Basaran O, Topal Y, Akin F BMJ Case Rep2014
Pulmonary hypertension of sickle cell disease: new guidelines.Furlow B Lancet Respir Med2014
Can STOP Trial Velocity Criteria Be Applied to Iranian Children with Sickle Cell Disease?Bavarsad Shahripour R, Mortazavi MM, Barlinn K, Keikhaei B, Mousakhani H, Azarpazhooh MR, Oghbaee M, Sajedi SA, Kepplinger J, Tubbs RS, Albright KC, Alexandrov AV J Stroke2014
Atrial Fibrillation and Beta Thalassemia Major: The Predictive Role of the 12-lead Electrocardiogram Analysis.Russo V, Rago A, Pannone B, Papa AA, Mayer MC, Spasiano A, Calabro R, Russo MG, Gerardo N Indian Pacing Electrophysiol J2014
Travelers With Sickle Cell Disease.Willen SM, Thornburg CD, Lantos PM J Travel Med2014
Investigation of sensitivity, specificity and accuracy of Tetra primer ARMS PCR method in comparison with conventional ARMS PCR, based on sequencing technique outcomes in IVS-II-I genotyping of beta thalassemia patients.Honardoost MA, Tabatabaeian H, Akbari M, Salehi M Gene2014
Serum levels of TGFβ, IL-10, IL-17, and IL-23 cytokines in β-thalassemia major patients: the impact of silymarin therapy.Balouchi S, Gharagozloo M, Esmaeil N, Mirmoghtadaei M, Moayedi B Immunopharmacol Immunotoxicol2014
Elevation of Plasma Cell Free Hemoglobin in Pulmonary Arterial Hypertension.Brittain EL, Janz DR, Austin ED, Bastarache JA, Wheeler LA, Ware LB, Hemnes AR Chest2014
Glucose homeostasis in Egyptian children and adolescents with β-Thalassemia major: Relationship to oxidative stress.Metwalley KA, El-Saied AR Indian J Endocrinol Metab2014
Pattern of hemoglobinopathies and thalassemias in upper Assam region of North Eastern India: high performance liquid chromatography studies in 9000 patients.Baruah MK, Saikia M, Baruah A Indian J Pathol Microbiol2014
A Significant Proportion of Thalassemia Major Patients Have Adrenal Insufficiency Detectable on Provocative Testing.Huang KE, Mittelman SD, Coates TD, Geffner ME, Wood JC J. Pediatr. Hematol. Oncol.2014
Elevated Tricuspid Regurgitant Velocity as a Marker for Pulmonary Hypertension in Children With Sickle Cell Disease: Less Prevalent and Predictive Than Previously Thought?Hebson C, New T, Record E, Oster M, Ehrlich A, Border W, James-Herry A, Kanaan U J. Pediatr. Hematol. Oncol.2014
Clinically Meaningful Interpretation of Pediatric Health-related Quality of Life in Sickle Cell Disease.Beverung LM, Varni JW, Panepinto JA J. Pediatr. Hematol. Oncol.2014
Assessment of sleep-related disorders in children with sickle cell disease.Hankins JS, Verevkina NI, Smeltzer MP, Wu S, Aygun B, Clarke DF Hemoglobin2014
Comparison of patients from Nigeria and the USA highlights modifiable risk factors for sickle cell anemia complications.Akingbola TS, Tayo BO, Salako B, Layden JE, Hsu LL, Cooper RS, Gordeuk VR, Saraf SL Hemoglobin2014
Epidemiology of hemoglobinopathies and thalassemias in individuals referred to the haematology research centre, shiraz university of medical sciences, shiraz, iran from 2006 to 2011.Haghpanah S, Ramzi M, Zakerinia M, Nourani Khojasteh H, Haghshenas M, Rezaei N, Moayed V, Rezaei A, Karimi M Hemoglobin2014
Blood Transfusion from a Hb E Trait Donor Can Affect β-Thalassemia Diagnosis.Pornprasert S, Jaiping K Hemoglobin2014
Community genetics approaches in the prevention of beta-thalassemia: towards achieving 'Zero beta-thalassemia' status in India.Rao VR Mol Cytogenet2014
Autoimmune thyroid disease following alemtuzumab therapy and hematopoietic cell transplantation in pediatric patients with sickle cell disease.Williams KM, Dietzen D, Hassoun AA, Fennoy I, Bhatia M Pediatr Blood Cancer2014
An unequal burden: Poor patient-provider communication and sickle cell disease.Jr CH, Bediako S, Lanzkron S, Diener-West M, Strouse J, Haythornthwaite J, Onojobi G, Beach MC, Patient Educ Couns2014
Recent trends for novel options in experimental biological therapy of β-thalassemia.Finotti A, Gambari R Expert Opin Biol Ther2014
Proteinuria in adults with sickle-cell disease: the role of hydroxycarbamide(hydroxyurea) as a protective agent.Silva Junior GB, Vieira AP, Couto Bem AX, Alves MP, Meneses GC, Martins AM, Araújo SM, Libório AV, Daher EF Int J Clin Pharm2014
Pain, coping, and sleep in children and adolescents with sickle cell disease.Graves JK, Jacob E J Child Adolesc Psychiatr Nurs2014
Sickle cell patients face death in the ICU*.Rice L, Teruya M Crit. Care Med.2014
Endothelin-1 but not Endothelial Nitric Oxide Synthase Gene Polymorphism is Associated with Sickle Cell Disease in Africa.Thakur TJ, Guindo A, Cullifer LR, Li Y, Imumorin IG, Diallo DA, Thomas BN Gene Regul Syst Bio2014
Changes in hematological parameters in α-thalassemia individuals co-inherited with erythroid Krüppel-like factor mutations.Yu LH, Liu D, Cai R, Shang X, Zhang XH, Ma XX, Yan SH, Fang P, Zheng CG, Wei XF, Liu YH, Zhou TB, Xu XM Clin. Genet.2014
Successful pregnancy outcome after in vitro fertilisation following Pre-implantation Genetic Diagnosis/Polymerase Chain Reaction screening for single gene disorder (sickle cell anaemia) before embryo transfer: The clinical experience of an in vitro fertilisation clinic in Nigeria.Okeke C, Ailoje-Ibru K, Olukoya K, Ogbeche R, Adewusi A, Iloabachie E, Ashiru O Niger Med J2014
Association of Iron Overload with Oxidative Stress, Hepatic Damage and Dyslipidemia in Transfusion-Dependent β-Thalassemia/HbE Patients.Sengsuk C, Tangvarasittichai O, Chantanaskulwong P, Pimanprom A, Wantaneeyawong S, Choowet A, Tangvarasittichai S Indian J Clin Biochem2014
A 65 bp deletion in band 3 gene of beta-thalassemia patients in Indonesia.Dewajanthi AM, Lubis VK, Wanandi SI, Gatot D, Soegianto RR, Freisleben SK, Wahidiyat I, Freisleben HJ Southeast Asian J. Trop. Med. Public Health2014
New mathematical formula for differentiating thalassemia trait and iron deficiency anemia in thalassemia prevalent area: a study in healthy school-age children.Sirachainan N, Iamsirirak P, Charoenkwan P, Kadegasem P, Wongwerawattanakoon P, Sasanakul W, Chansatitporn N, Chuansumrit A Southeast Asian J. Trop. Med. Public Health2014
Evaluation of Arm Span and Sitting Height as Proxy for Height in Children with Sickle Cell Anemia in Lagos, Nigeria.Akodu SO, Diaku-Akinwumi IN, Kehinde OA, Njokanma OF J Am Coll Nutr2014
The ethics of a proposed study of hematopoietic stem cell transplant for children with Nickel RS, Hendrickson JE, Haight AE Blood2014
A rare disorder in an orphan disease: Kikuchi-Fujimoto disease in a young-adult patient with sickle cell anemia.Vencato E, Manfredi R, Zamò A, Chilosi M, Beccari S, De Franceschi L Am. J. Hematol.2014
Impact of individualized pain plan on the emergency management of children with sickle cell disease.Krishnamurti L, Smith-Packard B, Gupta A, Campbell M, Gunawardena S, Saladino R Pediatr Blood Cancer2014
Blood viscosity is lower in trained than in sedentary sickle cell trait carriers.Diaw M, Diop S, Soubaiga FY, Seck M, Faye BF, Niang MN, Samb A, Connes P Clin. Hemorheol. Microcirc.2014
Splenectomy improves anaemia but does not reduce iron burden in patients with haemoglobin H Constant Spring disease.Zhou YL, Zhang XH, Liu TN, Wang L, Yin XL Blood Transfus2014
Variant RH alleles and Rh immunisation in patients with sickle cell disease.Sippert E, Fujita CR, Machado D, Guelsin G, Gaspardi AC, Pellegrino Jr J, Gilli S, Saad SS, Castilho L Blood Transfus2014
Facial swelling in a sickle cell patient.DeBlieux TK, Jackson N, Jeyakumar A, Townsend JA, Naik BV Pediatr Dent2014
ß-thalassemia and alkaptonuria.Yasri S, Wiwanitkit V Indian J Hum Genet2014
Detection of sickle cell hemoglobin in haiti by genotyping and hemoglobin solubility tests.Carter TE, von Fricken M, Romain JR, Memnon G, St Victor Y, Schick L, Okech BA, Mulligan CJ Am. J. Trop. Med. Hyg.2014
Development of interactive algorithm for clinical management of acute events related to sickle cell disease in emergency department.Forni GL, Finco G, Graziadei G, Balocco M, Rigano P, Perrotta S, Olivieri O, Cappellini MD, De Franceschi L Orphanet J Rare Dis2014
Emotional reactions to pain predict psychological distress in adult patients with Sickle Cell Disease (SCD).Edwards CL, Killough A, Wood M, Doyle T, Feliu M, Barker CS, Uppal P, DeCastro L, Wellington C, Whitfield KE, O'Garo KG, Morgan K, Edwards Alesii LY, Byrd GS, McCabe M, Goli V, Keys A, Hill L, Collins-McNeil J, Trambadia J, Guinyard D, Muhammad M, McDonald P, Schmechel DE, Robinson E Int J Psychiatry Med2014
A systematic review of effectiveness of daily oral penicillin v prophylaxis in the prevention of pneumococcal infection in children with sickle cell anaemia.Gwaram HA, Gwaram BA Niger J Med2014
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Cold hypersensitivity increases with age in mice with sickle cell disease.Zappia KJ, Garrison SR, Hillery CA, Stucky CL Pain2014
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Subclinical left ventricular systolic impairment in steady state young adult patients with sickle-cell anemia.Hammoudi N, Arangalage D, Djebbar M, Stojanovic KS, Charbonnier M, Isnard R, Girot R, Michel PL, Lionnet F Int J Cardiovasc Imaging2014
The Measure of Sickle Cell Stigma: Initial findings from the Improving Patient Outcomes through Respect and Trust study.Bediako SM, Lanzkron S, Diener-West M, Onojobi G, Beach MC, Haywood C J Health Psychol2014
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Hepatocellular carcinoma in thalassaemia. An update of the Italian Registry.Borgna-Pignatti C, Garani MC, Forni GL, Cappellini MD, Cassinerio E, Fidone C, Spadola V, Maggio A, Restivo Pantalone G, Piga A, Longo F, Gamberini MR, Ricchi P, Costantini S, D'Ascola D, Cianciulli P, Lai ME, Carta MP, Ciancio A, Cavalli P, Putti MC, Barella S, Amendola G, Campisi S, Capra M, Caruso V, Colletta G, Volpato S Br. J. Haematol.2014
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Vascular Dysfunction in Patients With Young β-Thalassemia: Relation to Cardiovascular Complications and Subclinical Atherosclerosis.Adly AA, El-Sherif NH, Ismail EA, El-Zaher YA, Farouk A, El-Refaey AM, Wahba MS Clin. Appl. Thromb. Hemost.2014
What dentists should know about sickle cell disease.Devine BP J Mich Dent Assoc2014
Phase 1 study of the E-selectin inhibitor GMI 1070 in patients with sickle cell anemia.Wun T, Styles L, DeCastro L, Telen MJ, Kuypers F, Cheung A, Kramer W, Flanner H, Rhee S, Magnani JL, Thackray H PLoS ONE2014
Risk factors for death in 632 patients with sickle cell disease in the United States and United Kingdom.Gladwin MT, Barst RJ, Gibbs JS, Hildesheim M, Sachdev V, Nouraie M, Hassell KL, Little JA, Schraufnagel DE, Krishnamurti L, Novelli E, Girgis RE, Morris CR, Berman Rosenzweig E, Badesch DB, Lanzkron S, Castro OL, Taylor JG, Goldsmith JC, Kato GJ, Gordeuk VR, Machado RF, PLoS ONE2014
[Thoracic extramedullary hematopoiesis secondary to beta-thalassemia.]Ben Amar J, Berrais M, El Gharbi L, Dhahri B, Aouina H, Bouacha H Presse Med2014
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Prevalence of Depression in Patients with β-Thalassemia as Assessed by the Beck's Depression Inventory.Shafiee A, Nazari S, Jorjani S, Bahraminia E, Sadeghi-Koupaei M Hemoglobin2014
β-Thalassemia Major Resulting from Compound Heterozygosity for HBB: c.92+2T>C [formerly known as IVS-I-2 (T>C)] and a Novel β(0)-Thalassemia Frameshift Mutation: HBB: c.209delG; p.Gly70Valfs*20.Kluge ML, Hoyer JD, Swanson KC, Oliveira JL Hemoglobin2014
Known and New δ-Globin Gene Mutations and Other Factors Influencing Hb A2 Measurement in the Omani Population.Hassan SM, Harteveld CL, Bakker E, Giordano PC Hemoglobin2014
Red Cell Indices and Formulas Used in Differentiation of β-Thalassemia Trait from Iron Deficiency in Thai School Children.Pornprasert S, Panya A, Punyamung M, Yanola J, Kongpan C Hemoglobin2014
Prevalence and molecular characterization of structural hemoglobin variants in the dongguan region of guangdong province, southern china.Lou JW, Wang T, Liu YH, He Y, Zhong BM, Liu JX, Zhao Y, Ye WL, Li DZ Hemoglobin2014
[Clinical signifcance of soluble E-selectin and tissue factor in β-Thalassemia].Yin F, Deng D, Lai Y, Liu R, Cheng P Zhonghua Xue Ye Xue Za Zhi2014
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Sickle cell trait and diving: review and recommendations.Vigilante JA, DiGeorge NW Undersea Hyperb Med2014
Combined versus monotherapy or concurrent therapy for treatment of thalassaemia.Song TS, Hsieh YW, Peng CT, Chen TL, Lee HZ, Chung JG, Hour MJ In Vivo2014
Vitamin D deficiency and its correction in children with sickle cell anaemia.Wykes C, Arasaretnam A, O'Driscoll S, Farnham L, Moniz C, Rees DC Ann. Hematol.2014
Negative predictive value of the chorionic villous sampling (CVS) in diagnosis of thalassemia in genetic laboratory of Dastgheib Hospital, Shiraz, Iran, 2012.Ghahramani F, Alimohamadi Y, Mahboubi M, Afrasiabi A Arch Iran Med2014
A novel alpha-thalassemia nonsense mutation in HBA2: C.382 A > T globin gene.Hamid M, Bokharaei Merci H, Galehdari H, Saberi AH, Kaikhaei B, Mohammadi-Anaei M, Ahmadzadeh A, Shariati G Arch Iran Med2014
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The co-inheritance of alpha-thalassemia and sickle cell anemia is associated with better hematological indices and lower consultations rate in Cameroonian patients and could improve their survival.Rumaney MB, Ngo Bitoungui VJ, Vorster AA, Ramesar R, Kengne AP, Ngogang J, Wonkam A PLoS ONE2014
Deferasirox for cardiac siderosis in β-thalassaemia major: a multicentre, open label, prospective study.Piga A, Longo F, Origa R, Roggero S, Pinna F, Zappu A, Castiglioni C, Cappellini MD Br. J. Haematol.2014
Associations among emergency room visits, parenting styles, and psychopathology among pediatric patients with sickle cell.Latzman RD, Shishido Y, Latzman NE, Elkin TD, Majumdar S Pediatr Blood Cancer2014
[Hemostasis alterations in sickle cell syndrome].Higuera D, Bravo M, Guerrero B Invest Clin2014
Effects of 5-hydroxymethyl-2-furfural on the volume and membrane permeability of red blood cells from patients with sickle cell disease.Hannemann A, Cytlak UM, Rees DC, Tewari S, Gibson JS J. Physiol. (Lond.)2014
Imbalanced coagulation profile as a biomarker of migraine in children with sickle cell: Is this a link with cerebral ischemia?Kossorotoff M, Lasne D, Brousse V, Desguerre I, de Montalembert M, Gaussem P J. Pediatr.2014
Sensory and Thermal Quantitative Testing in Children With Sickle Cell Disease.Jacob E, Chan VW, Hodge C, Zeltzer L, Zurakowski D, Sethna NF J. Pediatr. Hematol. Oncol.2014
Treatment for avascular necrosis of bone in people with sickle cell disease.Martí-Carvajal AJ, Solà I, Agreda-Pérez LH Cochrane Database Syst Rev2014
[Advances in pathogenesis and correlated clinical research of hypercoagulability in β thalassemia].Lv RY, Wen FQ, Yu J Zhongguo Dang Dai Er Ke Za Zhi2014
Coexisting iron deficiency anemia and Beta thalassemia trait: effect of iron therapy on red cell parameters and hemoglobin subtypes.Verma S, Gupta R, Kudesia M, Mathur A, Krishan G, Singh S ISRN Hematol2014
Computed tomography correlates with cardiopulmonary hemodynamics in pulmonary hypertension in adults with sickle cell disease.Linguraru MG, Pura JA, Gladwin MT, Koroulakis AI, Minniti C, Machado RF, Kato GJ, Wood BJ Pulm Circ2014
Parents' responses to receiving sickle cell or cystic fibrosis carrier results for their child following newborn screening.Ulph F, Cullinan T, Qureshi N, Kai J Eur. J. Hum. Genet.2014
Bone density in transfusion dependent thalassemia patients in Urmia, Iran.Valizadeh N, Farrokhi F, Alinejad V, Said Mardani S, Valizadeh N, Hejazi S, Noroozi M Iran J Ped Hematol Oncol2014
Seroprovalence of herpes simplex1, 2 IgG antibodies in patients with beta thalassemia in a major tertiary care hospital located in Yazd, Iran.Atefi A, Binesh F, Hashemi A, Atefi A, Aminorroaya M Iran J Ped Hematol Oncol2014
Quality of life in patients with thalassemia major.Ansari Sh, Baghersalimi A, Azarkeivan A, Nojomi M, Hassanzadeh Rad A Iran J Ped Hematol Oncol2014
Frequency of Celiac Disease in Children with Beta Thalassemia major.Honar N, Kamali S, Karimi M Iran J Ped Hematol Oncol2014
Addressing the global health burden of sickle cell disease.Carey PJ Int Health2014
Underestimation of the coexistence of iron deficiencies and thalassemia minors: a single institution experience in Taiwan.Lin CK, Chen LP, Chang HL, Sung YC Kaohsiung J. Med. Sci.2014
MRI monitoring of myocardial iron overload: Use of cardiac MRI combined with hepatic MRI in a cohort of multi-transfused patients with thalassaemia.Quatre A, Jacquier A, Petit P, Giorgi R, Thuret I Diagn Interv Imaging2014
Erythrocyte phosphatidylserine exposure in β-thalassemia.Ibrahim HA, Fouda MI, Yahya RS, Abousamra NK, Abd Elazim RA Lab Hematol2014
Update on the diagnosis and management of thalassemia.Weiss MJ Clin Adv Hematol Oncol2014
T2(∗) MRI changes in the heart and liver of ex-thalassemic patients after hematopoietic stem cell transplantation.Hamidieh AA, Tayebi S, Moeininia F, Shamshiri AR, Behfar M, Alimoghaddam K, Ghavamzadeh A Hematol Oncol Stem Cell Ther2014
Response to hydroxycarbamide in pediatric β-thalassemia intermedia: 8 years' follow-up in Egypt.El-Beshlawy A, El-Ghamrawy M, El-Ela MA, Said F, Adolf S, Abdel-Razek AR, Magdy RI, Abdel-Salam A Ann. Hematol.2014
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Understanding sickle cell anemia in the perianesthesia arena.Cartwright SM J. Perianesth. Nurs.2014
Identification of a Small Molecule that Increases Hemoglobin Oxygen Affinity and Reduces SS Erythrocyte Sickling.Nakagawa A, Lui FE, Wassaf D, Yefidoff-Freedman R, Casalena D, Palmer MA, Meadows J, Mozzarelli A, Ronda L, Abdulmalik O, Bloch KD, Safo MK, Zapol WM ACS Chem. Biol.2014
Sickle Cell Disease in the Emergency Department.Lovett PB, Sule HP, Lopez BL Emerg. Med. Clin. North Am.2014
Personalized Medicine and Human Genetic Diversity.Lu YF, Goldstein DB, Angrist M, Cavalleri G Cold Spring Harb Perspect Med2014
Haemoglobinopathies in eastern Indian states: a demographic evaluation.Nagar R, Sinha S, Raman R J Community Genet2014
[Stroke in paediatric patients with sickle-cell anaemia].Diaz-Diaz J, Camacho-Salas A, Nunez-Enamorado N, Carro-Rodriguez MA, Sanchez-Galan V, Martinez de Aragon A, Simon-De Las Heras R Rev Neurol2014
IthaGenes: An Interactive Database for Haemoglobin Variations and Epidemiology.Kountouris P, Lederer CW, Fanis P, Feleki X, Old J, Kleanthous M PLoS ONE2014
Nonmyeloablative HLA-matched sibling allogeneic hematopoietic stem cell transplantation for severe sickle cell phenotype.Hsieh MM, Fitzhugh CD, Weitzel RP, Link ME, Coles WA, Zhao X, Rodgers GP, Powell JD, Tisdale JF JAMA2014
Reconsideration of age as a contraindication for curative therapy of sickle cell disease.King AA, DiPersio JF JAMA2014
Sickle Cell Disease Patients With and Without Extremely High Hospital Use: Pain, Opioids, and Coping.Brown SE, Weisberg D, Balf-Soran G, Sledge W J Pain Symptom Manage2014
Lipoprotein-associated phospholipase A2 (Lp-PLA2) and tumor necrosis factor-alpha (TNF-α) and their relation to premature atherosclerosis in β-thalassemia children.Ragab SM, Safan MA, Obeid OM, Sherief AS Hematology2014
Quality of life in patients with thalassemia major in a developing country.Siddiqui SH, Ishtiaq R, Sajid F, Sajid R J Coll Physicians Surg Pak2014
Immunological Evaluation of β-Thalassemia Major Patients Receiving Oral Iron Chelator Deferasirox.Aleem A, Shakoor Z, Alsaleh K, Algahtani F, Iqbal Z, Al-Momen A J Coll Physicians Surg Pak2014
Rising to the sickle cell challenge.Trueland J Nurs Stand2014
[Haemoglobinopathy in the 21st century: incidence, diagnosis and heel prick screening].Suijker MH, Roovers EA, Fijnvandraat CJ, Dors N, Rodrigues Pereira R, Giordano PC, Verkerk PH, Peters M Ned Tijdschr Geneeskd2014
EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.Traeger-Synodinos J, Harteveld CL, Old JM, Petrou M, Galanello R, Giordano P, Angastioniotis M, De la Salle B, Henderson S, May A Eur. J. Hum. Genet.2014
Incidence of Ototoxicity in Pediatric Patients with Transfusion-Dependent Thalassemia Who Are Less Well-Chelated by Mono- and Combined Therapy of Iron Chelating Agents.Tanphaichitr A, Kusuwan T, Limviriyakul S, Atipas S, Pooliam J, Sangpraypan T, Tanphaichitr VS, Viprakasit V Hemoglobin2014
Measurement of HbA2 by Capillary Electrophoresis for Diagnosing β-thalassemia/HbE Disease in Patients With Low HbF.Prasing W, Pornprasert S Lab Med2014
Thalassemia and hemoglobin e in southern thai blood donors.Nuinoon M, Kruachan K, Sengking W, Horpet D, Sungyuan U Adv Hematol2014
Self-Efficacy, Transition, and Patient Outcomes in the Sickle Cell Disease Population.Molter BL, Abrahamson K Pain Manag Nurs2014
Sleep disturbance, depression and pain in adults with sickle cell disease.Wallen GR, Minniti CP, Krumlauf M, Eckes E, Allen D, Oguhebe A, Seamon C, Darbari DS, Hildesheim M, Yang L, Schulden JD, Kato GJ, Taylor JG BMC Psychiatry2014
Reduction of intramedullary apoptosis after stem cell transplantation in black african variant of pediatric sickle cell anemia.Isgrò A, Sodani P, Marziali M, Gaziev J, Fraboni D, Paciaroni K, Gallucci C, De Angelis G, Alfieri C, Ribersani M, Armiento D, Roveda A, Andreani M, Testi M, Lucarelli G Mediterr J Hematol Infect Dis2014
A Case of Iron Deficiency Anemia with Co-existing Hb Fontainebleau.Purohit A, Aggarwal M, Colah RB, Nadkarni AH, Pati HP Mediterr J Hematol Infect Dis2014
Clinical significance of assessment of thrombospondin and placenta growth factor levels in patients with sickle cell anemia: two centers egyptian studies.Hagag AA, Elmashad G, Abd El-Lateef AE Mediterr J Hematol Infect Dis2014
Sleep pathology characterization in sickle cell disease: Case-control study.Mascarenhas MI, Loureiro HC, Ferreira T, Dias A Pediatr. Pulmonol.2014
First report of the spectrum of δ-globin gene mutations in Omani subjects - identification of novel mutations.Alkindi S, AlZadjali S, Daar S, Ambusaidi R, Gravell D, Al Haddabi H, Krishnamoorthy R, Pathare A Int J Lab Hematol2014
When a blood donor has sickle cell trait: incidental findings and public health.Lee LM, Marks P Hastings Cent Rep2014
The genetics of hemoglobin A2 regulation in sickle cell anemia.Griffin PJ, Sebastiani P, Edward H, Baldwin CT, Gladwin MT, Gordeuk VR, Chui DH, Steinberg MH Am. J. Hematol.2014
Silent cerebral infarction, income, and grade retention among students with sickle cell anemia.King AA, Rodeghier MJ, Panepinto JA, Strouse JJ, Casella JF, Quinn CT, Dowling MM, Sarnaik SA, Thompson AA, Woods GM, Minniti CP, Redding-Lallinger RC, Kirby-Allen M, Kirkham FJ, McKinstry R, Noetzel MJ, White DA, Kwiatkowski JK, Howard TH, Kalinyak KA, Inusa B, Rhodes MM, Heiny ME, Fuh B, Fixler JM, Gordon MO, DeBaun MR Am. J. Hematol.2014
Regular automated red cell exchange transfusion in the management of pulmonary hypertension in sickle cell disease.Tsitsikas DA, Seligman H, Sirigireddy B, Odeh L, Nzouakou R, Amos RJ Br. J. Haematol.2014
Red blood cells of sickle cell disease patients exhibit abnormally high abundance of N-methyl D-aspartate receptors mediating excessive calcium uptake.Hänggi P, Makhro A, Gassmann M, Schmugge M, Goede JS, Speer O, Bogdanova A Br. J. Haematol.2014
Successful pulmonary thromboendarterectomy in a patient with sickle cell disease treated with a single preoperative red blood cell exchange.Marques MB, Wille KM, Ren Z, Sheth M, McGiffin DC Transfusion2014
Treating pain in sickle cell disease with opioids: clinical advances, ethical pitfalls.Smith WR J Law Med Ethics2014
Prevention of stroke in sickle cell anemia.Adams RJ J Law Med Ethics2014
Sickle cell disease in children: chronic complications and search of predictive factors for adverse outcomes.Silva IV, Reis AF, Palaré MJ, Ferrão A, Rodrigues T, Morais A Eur. J. Haematol.2014
Inhaled bronchodilators for acute chest syndrome in people with sickle cell disease.Knight-Madden JM, Hambleton IR Cochrane Database Syst Rev2014
Genotyping of α-thalassemias by the colorimetric nanogold probes.Chomean S, Wangmaung N, Sritongkham P, Promptmas C, Ittarat W Clin. Chim. Acta2014
DNA polymorphisms at BCL11A, HBS1L-MYB and Xmn1-HBG2 site loci associated with fetal hemoglobin levels in sickle cell anemia patients from Northern Brazil.Cardoso GL, Diniz IG, Martins da Silva AN, Cunha DA, da Silva Junior JS, Carvalho Uchôa CT, Dos Santos SE, Trindade SM, Cardoso MD, Guerreiro JF Blood Cells Mol. Dis.2014
Determination of deferasirox plasma concentrations: do gender, physical and genetic differences affect chelation efficacy?Mattioli F, Puntoni M, Marini V, Fucile C, Milano G, Robbiano L, Perrotta S, Pinto V, Martelli A, Forni GL Eur. J. Haematol.2014
Hypothermic cardiopulmonary bypass without exchange transfusion in sickle-cell patients: a matched-pair analysis.Edwin F, Aniteye E, Tettey M, Tamatey M, Entsua-Mensah K, Ofosu-Appiah E, Sereboe L, Gyan B, Adzamli I, Frimpong-Boateng K Interact Cardiovasc Thorac Surg2014
The Case | Microhematuria in a patient with beta-thalassemia major: a casual or a causal association?Piccoli GB, Roggero S, De Pascale A, Vigotti FN, Piga A, Veltri A Kidney Int.2014
Massive splenic infarction leading to sickle cell disease.Mengual-Ballester M, Pellicer-Franco E, De Andrés-García B, Aguayo-Albasini JL Rev Esp Enferm Dig2014
Acid sphingomyelinase is activated in sickle cell erythrocytes and contributes to inflammatory microparticle generation in sickle cell disease.Awojoodu AO, Keegan PM, Lane AR, Zhang Y, Lynch KR, Platt MO, Botchwey EA Blood2014
Correlation of Iron Overload and Glomerular Filtration Rate Estimated by Cystatin C in Patients with β-Thalassemia Major.Al-Khabori M, Bhandari S, Al-Rasadi K, Mevada S, Al-Dhuhli H, Al-Kemyani N, Daar S Hemoglobin2014
Clinical Trial Decision-making in Pediatric Sickle Cell Disease: A Qualitative Study of Perceived Benefits and Barriers to Participation.Patterson CA, Chavez V, Mondestin V, Deatrick J, Li Y, Barakat LP J. Pediatr. Hematol. Oncol.2014
Understanding and Improving Health Education Among First-time Parents of Infants With Sickle Cell Anemia in Alabama: A Mixed Methods Approach.Lebensburger JD, Grosse SD, Altice JL, Thierry JM, Ivankova NV J. Pediatr. Hematol. Oncol.2014
Sickle cell disease in mice is associated with sensitization of sensory nerve fibers.Kenyon N, Wang L, Spornick N, Khaibullina A, Almeida LE, Cheng Y, Wang J, Guptill V, Finkel JC, Quezado ZM Exp. Biol. Med. (Maywood)2014
Prophylactic red blood cell exchange may be beneficial in the management of sickle cell disease in pregnancy.Asma S, Kozanoglu I, Tarım E, Sarıturk C, Gereklioglu C, Akdeniz A, Kasar M, Turgut NH, Yeral M, Kandemir F, Boga C, Ozdogu H Transfusion2014
Global Genetic Architecture of an Erythroid Quantitative Trait Locus, HMIP-2.Menzel S, Rooks H, Zelenika D, Mtatiro SN, Gnanakulasekaran A, Drasar E, Cox S, Liu L, Masood M, Silver N, Garner C, Vasavda N, Howard J, Makani J, Adekile A, Pace B, Spector T, Farrall M, Lathrop M, Thein SL Ann. Hum. Genet.2014
Effects Of Blood Transfusion On Cytokine Profile and Pulmonary Function In Patients with Thalassemia Major.Gülhan B, Yalçın E, Unal S, Oğuz B, Ozçelik U, Ersöz DD, Gümrük F, Kiper N Clin Respir J2014
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What are the most promising emerging therapies for sickle cell disease?Ferreira de Melo TR, Chin CM, Dos Santos JL Future Med Chem2014
Hematopoietic SCT for the Black African and non-Black African variants of sickle cell anemia.Lucarelli G, Isgrò A, Sodani P, Marziali M, Gaziev J, Paciaroni K, Gallucci C, Cardarelli L, Ribersani M, Alfieri C, De Angelis G, Armiento D, Andreani M, Testi M, Amato A, Akinyanju OO, Wakama TT Bone Marrow Transplant.2014
Hydroxyurea Treatment in Transfusion-Dependent β-Thalassemia Patients.Bordbar MR, Silavizadeh S, Haghpanah S, Kamfiroozi R, Bardestani M, Karimi M Iran Red Crescent Med J2014
Growth differentiation factor-15 in young sickle cell disease patients: Relation to hemolysis, iron overload and vascular complications.Tantawy AA, Adly AA, Ismail EA, Darwish YW, Zedan MA Blood Cells Mol. Dis.2014
A novel HBA2 gene conversion in cis or trans: Borgio JF, AbdulAzeez S, Al-Nafie AN, Naserullah ZA, Al-Jarrash S, Al-Madan MS, Al-Muhanna F, Steinberg MH, Al-Ali AK Blood Cells Mol. Dis.2014
Transfusional Iron Overload and Iron Chelation Therapy in Thalassemia Major and Sickle Cell Disease.Marsella M, Borgna-Pignatti C Hematol. Oncol. Clin. North Am.2014
The Pathophysiology of Transfusional Iron Overload.Porter JB, Garbowski M Hematol. Oncol. Clin. North Am.2014
Dopamine D3 Receptor Ser9Gly and Catechol-O-Methyltransferase Val158Met Polymorphisms and Acute Pain in Sickle Cell Disease.Jhun E, He Y, Yao Y, Molokie RE, Wilkie DJ, Wang ZJ Anesth. Analg.2014
Erythrocyte membrane model with explicit description of the lipid bilayer and the spectrin network.Li H, Lykotrafitis G Biophys. J.2014
Pregnancy Outcomes in Women with Homozygous Beta Thalassaemia: A single-centre experience from Oman.Al-Riyami N, Al-Khaduri M, Daar S Sultan Qaboos Univ Med J2014
β-Thalassemia hijacking ineffective erythropoietin and iron overload: Two case reports and a review of literature.Byatnal A, Byatnal AA, Parvathi Devi MK, Badriramkrishna B J Nat Sci Biol Med2014
Seamless gene correction of β-thalassemia mutations in patient-specific iPSCs using CRISPR/Cas9 and piggyBac.Xie F, Ye L, Chang JC, Beyer AI, Wang J, Muench MO, Kan YW Genome Res.2014
Inflammatory bowel disease in a child with sickle cell anemia.Alqoaer K, Ahmed MM, Alhowaiti ES Case Rep Pediatr2014
High Resolution Melting Analysis: A Rapid Screening and Typing Tool for Common β-Thalassemia Mutation in Chinese Population.Lin M, Jiao JW, Zhan XH, Zhan XF, Pan MC, Wang JL, Wang CF, Zhong TY, Zhang Q, Yu X, Wu JR, Yang HT, Lin F, Tong X, Yang H, Zha GC, Wang Q, Zheng L, Wen YF, Yang LY PLoS ONE2014
Severe Anemia in an Adolescent Male With Sickle Cell Trait: A Case Report.Chapa-Rodriguez A, Dighe D, Giordano L J. Pediatr. Hematol. Oncol.2014
Genetic Education and Sickle Cell Disease: Feasibility and Efficacy of a Program Tailored to Adolescents.Porter JS, Matthews CS, Carroll YM, Anderson SM, Smeltzer MP, Hankins JS J. Pediatr. Hematol. Oncol.2014
Factors predicting future ACS episodes in children with sickle cell anemia.DeBaun MR, Rodeghier M, Cohen R, Kirkham FJ, Rosen CL, Roberts I, Cooper B, Stocks J, Wilkey O, Inusa B, Warner JO, Strunk RC Am. J. Hematol.2014
Ultrasonographic spleen size and haematological parameters in children with sickle cell anaemia in Kano, Nigeria.Abdullahi SU, Hassan-Hanga F, Ibrahim M Niger Postgrad Med J2014
Thoracic cord compression by extramedullary hematopoiesis in thalassemia.Hashmi MA, Guha S, Sengupta P, Basu D, Baboo S, Neha Asian J Neurosurg2014
Poor health related quality of life among patients of sickle cell disease.Bhagat VM, Baviskar SR, Mudey AB, Goyal RC Indian J Palliat Care2014
The associations of SEA-alpha thalassemia 1, XmnI-Ggamma polymorphism and beta-globin gene mutations with the clinical severity of beta-thalassemia syndrome in northern Thailand.Tatu T, Sritong W, Sa-Nguansermsri T J Med Assoc Thai2014
Novel approach to reactive oxygen species in nontransfusion-dependent thalassemia.Tyan PI, Radwan AH, Eid A, Haddad AG, Wehbe D, Taher AT Biomed Res Int2014
Intrathoracic extramedullary hematopoiesis in E-beta thalassemia.Mandal PK, Dolai TK Indian J Pathol Microbiol2014
Co-inheritance of α-thalassaemia and β-thalassaemia in a prenatal screening population in mainland China.Li J, Xie XM, Liao C, Li DZ J Med Screen2014
Development of Bead-Based Suspension Array Technology for the Diagnosis of Thalassemia.Yin A, Zhang L, Luo M, He T, Zhang Y, Liu C, Du L, Qin D, Liang J, Li B, Wu L, Ma Y, Guo H, Wang J, Yuan T, Wang Y, Zhang Y, Zhang X Am. J. Hematol.2014
Predictors of Health-Related Quality of Life over Time Among Adolescents and Young Adults with Sickle Cell Disease.Jackson JL, Lemanek KL, Clough-Paabo E, Rhodes M J Clin Psychol Med Settings2014
Influence of iron regulating genes mutations on iron status in Egyptian patients with sickle cell disease.Abdel Rahman HA, Abou-Elew HH, El-Shorbagy RM, Fawzy R, Youssry I Ann. Clin. Lab. Sci.2014
Higher sensitivity of capillary electrophoresis in detecting hemoglobin A2'compared to traditional gel electrophoresis.Oleske DA, Huang RS, Dasgupta A, Nguyen A, Wahed A Ann. Clin. Lab. Sci.2014
Predictors of Non-Adherence to Follow-up Visits and Deferasirox Chelation Therapy Among Jordanian Adolescents with Thalassemia Major.Al-Kloub MI, A Bed MA, Al Khawaldeh OA, Al Tawarah YM, Froelicher ES Pediatr Hematol Oncol2014
Treatment of alpha(0)-thalassemia (--(SEA)/--(SEA)) via serial fetal and post-natal transfusions: Can early fetal intervention improve outcomes?Chmait RH, Baskin JL, Carson S, Randolph LM, Hamilton A Hematology2014
Educational Intervention to Improve the Health Outcomes of Children With Sickle Cell Disease.Shahine R, Badr LK, Karam D, Abboud M J Pediatr Health Care2014
Reassessing the approach to informed consent: the case of unrelated hematopoietic stem cell transplantation in adult thalassemia patients.Pisu S, Caocci G, d'Aloja E, Efficace F, Vacca A, Piras E, Orofino MG, Addari C, Pintor M, Demontis R, Demuru F, Pittau MR, Collins GS, La Nasa G Philos Ethics Humanit Med2014
Differences in quality of life between pediatric sickle cell patients who used hydroxyurea and those who did not.Nwenyi E, Leafman J, Mathieson K, Ezeobah N Int J Health Care Qual Assur2014
Co-inheritance of the rare β hemoglobin variants Hb Yaounde, Hb Görwihl and Hb City of Hope with other alterations in globin genes: impact in genetic counseling.Vinciguerra M, Passarello C, Leto F, Cassarà F, Cannata M, Maggio A, Giambona A Eur. J. Haematol.2014
Impact of long-term erythrocytapheresis on growth and peak height velocity of children with sickle cell disease.Bavle A, Raj A, Kong M, Bertolone S Pediatr Blood Cancer2014
Modeling the complex activity of sickle cell and thalassemia specialist nurses in England.Leary A, Anionwu EN Clin Nurse Spec2014
Beta-thalassaemia intermedia: evaluation of endocrine and bone complications.Baldini M, Marcon A, Cassin R, Ulivieri FM, Spinelli D, Cappellini MD, Graziadei G Biomed Res Int2014
A century after discovery of sickle cell disease: keeping hope alive!Mohanty D Indian J. Med. Res.2014
Induction of adult levels of β-globin in human erythroid cells that intrinsically express embryonic or fetal globin by transduction with KLF1 and BCL11A-XL.Trakarnsanga K, Wilson MC, Lau W, Singleton BK, Parsons SF, Sakuntanaga P, Kurita R, Nakamura Y, Anstee DJ, Frayne J Haematologica2014
Understanding sickle cell brain drain.Hulbert ML, Ford AL Blood2014
When Is the Optimal Time to Screen for Chlamydia in Adolescents and Young Adults With Sickle Cell Disease?Bluett-Mills G, Kanter J Clin Pediatr (Phila)2014
Sickle haemoglobin comes of age.Serjeant G Lancet Glob Health2014
An Unexpected Etiology of Priapism: Infection-Related Anti-Protein S Antibodies.Boissier E, Durant C, Vildy S, Glemain P, Lakhal K, Graveleau J, Masseau A, Fouassier M J Sex Med2014
Adverse events in cancer patients with sickle cell trait or disease: case reports.Swede H, Andemariam B, Gregorio DI, Jones BA, Braithwaite D, Rohan TE, Stevens RG Genet. Med.2014
Effects of the anti-receptor activator of nuclear factor kappa B ligand denusomab on beta thalassemia major-induced osteoporosis.Yassin MA, Soliman AT, De Sanctis V, Abdelrahman MO, Aziz Bedair EM, AbdelGawad M Indian J Endocrinol Metab2014
More blood for sickle cell anemia?Steinberg MH N. Engl. J. Med.2014
Controlled trial of transfusions for silent cerebral infarcts in sickle cell anemia.DeBaun MR, Gordon M, McKinstry RC, Noetzel MJ, White DA, Sarnaik SA, Meier ER, Howard TH, Majumdar S, Inusa BP, Telfer PT, Kirby-Allen M, McCavit TL, Kamdem A, Airewele G, Woods GM, Berman B, Panepinto JA, Fuh BR, Kwiatkowski JL, King AA, Fixler JM, Rhodes MM, Thompson AA, Heiny ME, Redding-Lallinger RC, Kirkham FJ, Dixon N, Gonzalez CE, Kalinyak KA, Quinn CT, Strouse JJ, Miller JP, Lehmann H, Kraut MA, Ball WS, Hirtz D, Casella JF N. Engl. J. Med.2014
The effect of prasugrel on ADP-stimulated markers of platelet activation in patients with sickle cell disease.Jakubowski JA, Zhou C, Winters KJ, Lachno DR, Howard J, Payne CD, Mant T, Jurcevic S, Frelinger AL Platelets2014
Sickle cell trait and incident ischemic stroke in the atherosclerosis risk in communities study.Caughey MC, Loehr LR, Key NS, Derebail VK, Gottesman RF, Kshirsagar AV, Grove ML, Heiss G Stroke2014
Structural Modification of Plasma Albumin in Sickle Cell Anemia.Ozgunes N, Oztas Y, Unal S, Yaman H Acta Haematol.2014
Deferasirox for iron chelation in multitransfused children with sickle cell disease; long-term experience in the East London clinical haemoglobinopathy network.Tsouana E, Kaya B, Gadong N, Hemmaway C, Newell H, Simmons A, Whitmarsh S, Telfer P Eur. J. Haematol.2014
Hemoglobin Q-Thailand and its combinations with other forms of thalassemia or hemoglobinopathies in northern Thailand.Panyasai S, Pornprasert S Clin. Lab.2014
A pilot study of manual chronic partial exchange transfusion in children with sickle disease.Aloni MN, Lê PQ, Heijmans C, Huybrechts S, Devalck C, Azzi N, Ngalula-Mujinga M, Ferster A Hematology2014
Abnormalities in renal tubular phosphate handling in children with sickle cell disease.Raj VM, Freundlich M, Hamideh D, Alvarez O, Seeherunvong W, Abitbol C, Katsoufis C, Chandar J, Ruiz P, Zilleruelo G Pediatr Blood Cancer2014
Hyperfiltration is associated with the development of microalbuminuria in patients with sickle cell anemia.Vazquez B, Shah B, Zhang X, Lash JP, Gordeuk VR, Saraf SL Am. J. Hematol.2014
Improved hydroxyurea effect with the use of text messaging in children with sickle cell anemia.Estepp JH, Winter B, Johnson M, Smeltzer MP, Howard SC, Hankins JS Pediatr Blood Cancer2014
Marriage and child bearing in patients with transfusion-dependent thalassemia major.Zafari M, Kosaryan M J. Obstet. Gynaecol. Res.2014
RBC alloimmunization and double alloantibodies in thalassemic patients.Azarkeivan A, Ahmadi MH, Zolfaghari S, Shaiegan M, Ferdowsi S, Rezaei N, Lotfi P Hematology2014
Platelet activation biomarkers in Berkeley sickle cell mice and the response to prasugrel.Ohno K, Tanaka H, Samata N, Jakubowski JA, Tomizawa A, Mizuno M, Sugidachi A Thromb. Res.2014
Impact of VEGFA -583C > T polymorphism on serum VEGF levels and the susceptibility to acute chest syndrome in pediatric patients with sickle cell disease.Redha NA, Mahdi N, Al-Habboubi HH, Almawi WY Pediatr Blood Cancer2014
How French paediatric emergency departments manage painful vaso-occlusive episodes in sickle cell disease patients.Galeotti C, Courtois E, Carbajal R Acta Paediatr.2014
Improvements in phenotype studies of hemoglobin disorders brought by advances in reversed-phase chromatography of globin chains.Riou J, Pissard S, Goossens M, Wajcman H Int J Lab Hematol2014
Quality of life among adults with beta-thalassemia major in western Saudi Arabia.Amoudi AS, Balkhoyor AH, Abulaban AA, Azab AM, Radi SA, Ayoub MD, Albayrouti BT Saudi Med J2014
Does cold hypersensitivity increase with age in sickle cell disease?Wang ZJ, Molokie RE, Wilkie DJ Pain2014
Increased circulating PEDF and low sICAM-1 are associated with sickle cell retinopathy.Cruz PR, Lira RP, Pereira Filho SA, Souza BB, Mitsuushi FN, Menaa F, Fertrin KY, Vasconcellos JP, Conran N, Costa FF, Melo MB Blood Cells Mol. Dis.2014
Mast Cell Activation Syndrome as a Significant Comorbidity in Sickle Cell Disease.Afrin LB Am. J. Med. Sci.2014
Quality of Life of Adolescents With Transfusion-dependent Thalassemia and Their Siblings: A Cross-Sectional Study.Ajij M, Pemde HK, Chandra J J. Pediatr. Hematol. Oncol.2014
Severe Hemolytic Transfusion Reaction Due to Anti-D in a D+ Patient With Sickle Cell Disease.Ipe TS, Wilkes JJ, Hartung HD, Westhoff CM, Chou ST, Friedman DF J. Pediatr. Hematol. Oncol.2014
Benefits of chronic blood transfusion in hemoglobin E/β thalassemia with pulmonary arterial hypertension.Chueamuangphan N, Patumanond J, Wongtheptien W, Nawarawong W, Sukonthasarn A, Chuncharunee S, Tawichasri C Int J Gen Med2014
Induction of fetal hemoglobin through enhanced translation efficiency of γ-globin mRNA.Hahn CK, Lowrey CH Blood2014
Effect of long-term transfusion therapy on the glycometabolic status and pancreatic Beta cell function in patients with Beta thalassemia major.Bhat KG, Periasamy PK J Family Med Prim Care2014
Vitamin D levels are low in adult patients with sickle cell disease in Jamaica and West Africa.Tayo BO, Akingbola TS, Salako BL, McKenzie CA, Reid M, Layden J, Osunkwo I, Plange-Rhule J, Luke A, Durazo-Arvizu R, Cooper RS BMC Hematol2014
Alloimmunization and autoimmunization in transfusion dependent thalassemia major patients: Study on 319 patients.Dhawan HK, Kumawat V, Marwaha N, Sharma RR, Sachdev S, Bansal D, Marwaha RK, Arora S Asian J Transfus Sci2014
Fever in children with sickle cell disease: are all fevers equal?Shihabuddin BS, Scarfi CA J Emerg Med2014
How Patients' Self-Disclosure about Sickle Cell Pain Episodes to Significant Others Relates to Living with Sickle Cell Disease.Derlega VJ, Janda LH, Miranda J, Chen IA, Goodman BM, Smith W Pain Med2014
Erythrocyte aggregation in homozygous sickle cell disease.Vayá A, Collado S, Alis R, Dasí MA Clin. Hemorheol. Microcirc.2014
A late onset sickle cell disease reveals a mosaic segmental uniparental isodisomy of chromosome 11p15.Vinatier I, Martin X, Costa JM, Bazin A, Giraudier S, Joly P Blood Cells Mol. Dis.2014
Beta thalassaemia intermedia due to silent alpha globin gene quadruplication in an infant.So CC, Chiang AK, Kan A, Lee V, Ng E Pathology2014
Hydroxyurea and growth in young children with sickle cell disease.Rana S, Houston PE, Wang WC, Iyer RV, Goldsmith J, Casella JF, Reed CK, Rogers ZR, Waclawiw MA, Thompson B, Pediatrics2014
HSP70 sequestration by free α-globin promotes ineffective erythropoiesis in β-thalassaemia.Arlet JB, Ribeil JA, Guillem F, Negre O, Hazoume A, Marcion G, Beuzard Y, Dussiot M, Moura IC, Demarest S, de Beauchêne IC, Belaid-Choucair Z, Sevin M, Maciel TT, Auclair C, Leboulch P, Chretien S, Tchertanov L, Baudin-Creuza V, Seigneuric R, Fontenay M, Garrido C, Hermine O, Courtois G Nature2014
Individualizing fetal hemoglobin augmenting therapy for β-type hemoglobinopathies patients.Gravia A, Chondrou V, Sgourou A, Papantoni I, Borg J, Katsila T, Papachatzopoulou A, Patrinos GP Pharmacogenomics2014
The Spectrum of β-Thalassemia Mutations in Hatay, Turkey: Reporting Three New Mutations.Aldemir O, Izmirli M, Kaya H Hemoglobin2014
A Local Equation for Differential Diagnosis of β-Thalassemia Trait and Iron Deficiency Anemia by Logistic Regression Analysis in Southeast Iran.Sargolzaie N, Miri-Moghaddam E Hemoglobin2014
[Genotypes of 1 571 cases of Hb H disease in Guangxi area].Fu C, Chen S, Zhang Q, He S, Wei Y, Chen Q, Tang Y, Zheng C Zhonghua Xue Ye Xue Za Zhi2014
[Molecular diagnosis for a novel deletion mutation of α thalassemia].Li Y, Chen Z, Zhao L, Wang L, Tian M, Huang H, Qin G, Chen S Zhonghua Xue Ye Xue Za Zhi2014
Pre-marital screening for beta thalassaemia in Pakistan: an insight.Shariq M, Moiz B, Zaidi N, Bin Azhar W, Iqbal W, Humaira A, Memon RN J Med Screen2014
Newborn screening for sickle cell disease: technical and legal aspects of a German pilot study with 38,220 participants.Frömmel C, Brose A, Klein J, Blankenstein O, Lobitz S Biomed Res Int2014
A mathematical model of sickle cell genome frequency in response to selective pressure from malaria.Liddell C, Owusu-Brackett N, Wallace D Bull. Math. Biol.2014
Time to define a new strategy for management of hepatocellular carcinoma in thalassaemia?Mancuso A, Perricone G Br. J. Haematol.2014
Hydroxycarbamide treatment in sickle cell disease: estimates of possible leukaemia risk and of hospitalization survival benefit.Castro O, Nouraie M, Oneal P Br. J. Haematol.2014
Patient reports of health outcome for adults living with sickle cell disease: development and testing of the ASCQ-Me item banks.Keller SD, Yang M, Treadwell MJ, Werner EM, Hassell KL Health Qual Life Outcomes2014
Red blood cell microparticles in hemoglobin E disorders.Chaichote W, Sae-Ung N, Fucharoen G, Fucharoen S Int J Lab Hematol2014
Proteinuria in patients with sickle cell disease.Alkhunaizi AM, Al-Khatti AA Saudi J Kidney Dis Transpl2014
Assessment of Ventricular Function in Adults with Sickle Cell Disease: Role of Two-Dimensional Speckle-Tracking Strain.Barbosa MM, Vasconcelos MC, Ferrari TC, Fernandes BM, Passaglia LG, Silva CM, Nunes MC J Am Soc Echocardiogr2014
Impaired pubertal development and testicular hormone function in males with sickle cell anemia.Martins PR, Kerbauy J, Moraes-Souza H, Pereira GD, Figueiredo MS, Verreschi IT Blood Cells Mol. Dis.2014
Adolescents with sickle cell disease in a rural community: are they ready to transition to adulthood?Mennito S, Hletko P, Ebeling M, Amann LA, Roberts J South. Med. J.2014
LIN28A Expression Reduces Sickling of Cultured Human Vasconcellos JF, Fasano RM, Lee YT, Kaushal M, Byrnes C, Meier ER, Anderson M, Rabel A, Braylan R, Stroncek DF, Miller JL PLoS ONE2014
Hematological parameters in combination with HbF levels are appropriate for screening of beta-thalassemia/HbE disease with HbF varying from 5 to 15%.Pornprasert S Clin. Lab.2014
Genetic counseling for thalassemia screening in resource limited setting: a case study.Joob B, Wiwanitkit V Clin. Lab.2014
High prevalence of thalassemia in migrant populations in Guangdong Province, China.Li B, Zhang XZ, Yin AH, Zhao QG, Wu L, Ma YZ, Luo MY, Yu SY BMC Public Health2014
α:Non-α and Gγ:Aγ globin chain ratios in thalassemia intermedia patients treated with hydroxyurea.Najjari A, Asouri M, Gouhari LH, Niaki HA, Nejad AS, Eslami SM, Abolghasemi H, Ataee R, Ebrahimi AA, Moshaei MR, Ahmadi AA Asian Pac J Trop Biomed2014
Impact of educational programme regarding chelation therapy on the quality of life for B-thalassemia major children.Samra OA, Auda W, Kamhawy H, Al-Tonbary Y Hematology2014
Incidence of sickle cell disease and other hemoglobin variants in 10,095 lebanese neonates.Khoriaty E, Halaby R, Berro M, Sweid A, Abbas HA, Inati A PLoS ONE2014
Immunologic effects of hydroxyurea in sickle cell anemia.Lederman HM, Connolly MA, Kalpatthi R, Ware RE, Wang WC, Luchtman-Jones L, Waclawiw M, Goldsmith JC, Swift A, Casella JF, Pediatrics2014
Growth Differentiation Factor 15 expression and regulation during erythroid differentiation in non-transfusion dependent thalassemia.Ronzoni L, Sonzogni L, Duca L, Graziadei G, Cappellini MD, Ferru E Blood Cells Mol. Dis.2014
The hypercoagulable status in common Mediterranean β-thalassaemia mutations trait.Labib HA, Etewa RL, Atia H Int J Lab Hematol2014
Moyamoya syndrome in sickle cell anaemia: a cause of recurrent stroke.Soares D, Bullock R, Ali S BMJ Case Rep2014
Acute liver function decompensation in a patient with sickle cell disease managed with exchange transfusion and endoscopic retrograde cholangiography.Papafragkakis H, Ona MA, Changela K, Sadanandan S, Jelin A, Anand S, Duddempudi S Therap Adv Gastroenterol2014
Hypertransfusion therapy in sickle cell disease in Nigeria.Adewoyin AS, Obieche JC Adv Hematol2014
Population based surveillance in sickle cell disease: Methods, findings and implications from the California registry and surveillance system in hemoglobinopathies project (RuSH).Paulukonis ST, Harris WT, Coates TD, Neumayr L, Treadwell M, Vichinsky E, Feuchtbaum LB Pediatr Blood Cancer2014
Association of alpha-thalassemia, TNF-alpha (-308G>A) and VCAM-1 (c.1238G>C) gene polymorphisms with cerebrovascular disease in a newborn cohort of 411 children with sickle cell anemia.Belisário AR, Nogueira FL, Rodrigues RS, Toledo NE, Cattabriga AL, Velloso-Rodrigues C, Duarte FO, Silva CM, Viana MB Blood Cells Mol. Dis.2014
Sickle Cell Disease Pain Management in Adolescents: A Literature Review.Wilson BH, Nelson J Pain Manag Nurs2014
Cerebral haemorrhagic risk in children with sickle-cell disease.Kossorotoff M, Brousse V, Grevent D, Naggara O, Brunelle F, Blauwblomme T, Gaussem P, Desguerre I, De Montalembert M Dev Med Child Neurol2014
Capacity building and stroke risk assessment in Nigerian children with sickle cell anaemia.Soyebi K, Adeyemo T, Ojewunmi O, James F, Adefalujo K, Akinyanju O Pediatr Blood Cancer2014
Known and new hemoglobin A2 variants in Thailand and implication for β-thalassemia screening.Panyasai S, Fucharoen G, Fucharoen S Clin. Chim. Acta2014
Noninvasive Buccal Swab Antigen Sample and Molecular Testing Provides Extended Antigen Typing for Patients with Hemoglobinopathies.Rampersad A, Hampton K, Duncan N, Roberson C, Slayten J, Davisson S, Aronowitz J, Shapiro A J. Pediatr.2014
ARKRAY ADAMS A1c HA-8180T Analyzer for Diagnosis of Thalassemia and Hemoglobinopathies Common in Southeast Asia.Kunwandee J, Srivorakun H, Fucharoen G, Sanchaisuriya K, Fucharoen S Lab Med2014
Blood and marrow transplantation for sickle cell disease: Is less more?Bolaños-Meade J, Brodsky RA Blood Rev.2014
Raman spectroscopy for a rapid diagnosis of sickle cell disease in human blood samples: a preliminary study.Filho AC, Silveira L, Yanai AL, Fernandes AB Lasers Med Sci2014
Iron overload causes osteoporosis in Thalassemia Major patients through interaction with TRPV1 channels.Rossi F, Perrotta S, Bellini G, Luongo L, Tortora C, Siniscalco D, Francese M, Torella M, Nobili B, Di Marzo V, Maione S Haematologica2014
Red Blood Cell Cluster Separation from Digital Images for use in Sickle Cell Disease.Gonzalez-Hidalgo M, Guerrero-Pena FA, Herold-Garcia S, Jaume-I-Capo A, Marrero-Fernandez PD IEEE J Biomed Health Inform2014
Hb Cibeles [α2 CD25(B6) (Gly → Asp)]: a novel alpha chain variant causing la Fuente-Gonzalo F, Nieto JM, Vinuesa L, Sevilla J, Díaz-Mediavilla J, Villegas A, González FA, Ropero P Int. J. Hematol.2014
Defining serum ferritin thresholds to predict clinically relevant liver iron concentrations for guiding deferasirox therapy when MRI is unavailable in patients with non-transfusion-dependent thalassaemia.Taher AT, Porter JB, Viprakasit V, Kattamis A, Chuncharunee S, Sutcharitchan P, Siritanaratkul N, Origa R, Karakas Z, Habr D, Zhu Z, Cappellini MD Br. J. Haematol.2014
Characterization of Transcription Factor Networks Involved in Umbilical Cord Blood CD34+ Stem Cells-Derived Erythropoiesis.Li B, Ding L, Yang C, Kang B, Liu L, Story MD, Pace BS PLoS ONE2014
First Reported Case of Proliferative Retinopathy in Hemoglobin SE Disease.Baciu P, Yang C, Fantin A, Darnley-Fisch D, Desai U Case Rep Ophthalmol Med2014
Mechanisms of plasma non-transferrin bound iron generation: insights from comparing transfused diamond blackfan anaemia with sickle cell and thalassaemia patients.Porter JB, Walter PB, Neumayr LD, Evans P, Bansal S, Garbowski M, Weyhmiller MG, Harmatz PR, Wood JC, Miller JL, Byrnes C, Weiss G, Seifert M, Grosse R, Grabowski D, Schmidt A, Fischer R, Nielsen P, Niemeyer C, Vichinsky E Br. J. Haematol.2014
Desferrithiocin: A Search for Clinically Effective Iron Chelators.Bergeron RJ, Wiegand J, McManis JS, Bharti N J. Med. Chem.2014
Perceived Discrimination, Patient Trust, and Adherence to Medical Recommendations Among Persons with Sickle Cell Disease.Haywood C, Lanzkron S, Bediako S, Strouse JJ, Haythornthwaite J, Carroll CP, Diener-West M, Onojobi G, Beach MC, J Gen Intern Med2014
Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel members.Yawn BP, Buchanan GR, Afenyi-Annan AN, Ballas SK, Hassell KL, James AH, Jordan L, Lanzkron SM, Lottenberg R, Savage WJ, Tanabe PJ, Ware RE, Murad MH, Goldsmith JC, Ortiz E, Fulwood R, Horton A, John-Sowah J JAMA2014
The challenge of creating an evidence-based guideline for sickle cell disease.DeBaun MR JAMA2014
Hematopoietic Stem Cell Transplantation for Sickle Cell Disease: State of the Science.Talano JA, Cairo MS Eur. J. Haematol.2014
Endocrinopathies, metabolic disorders and iron overload in major and intermedia thalassemia: serum ferritin as diagnostic and predictive marker associated with liver and cardiac T2* MRI assessment.Chirico V, Rigoli L, Lacquaniti A, Salpietro V, Piraino B, Amorini M, Salpietro C, Arrigo T Eur. J. Haematol.2014
Sickle cell disease and pulpal necrosis: a review of the literature for the primary care dentist.Basati MS Prim Dent J2014
Wheezing is Common in Children With Sickle Cell Disease When Compared With Controls.Galadanci NA, Liang WH, Galadanci AA, Aliyu MH, Jibir BW, Karaye IM, Inusa BP, Vermund SH, Strunk RC, DeBaun MR J. Pediatr. Hematol. Oncol.2014
Assessment of serum zinc levels of patients with thalassemia compared to their siblings.El Missiry M, Hamed Hussein M, Khalid S, Yaqub N, Khan S, Itrat F, Uderzo C, Faulkner L Anemia2014
Haplotype map of sickle cell anemia in Tunisia.Moumni I, Ben Mustapha M, Sassi S, Zorai A, Ben Mansour I, Douzi K, Chouachi D, Mellouli F, Bejaoui M, Abbes S Dis. Markers2014
Methaemoglobinemia - Faulty probe or faulty haemoglobin.Kishore K, Singh A, Sahu S, Patel GP Indian J Anaesth2014
Density-based separation in multiphase systems provides a simple method to identify sickle cell disease.Kumar AA, Patton MR, Hennek JW, Lee SY, D'Alesio-Spina G, Yang X, Kanter J, Shevkoplyas SS, Brugnara C, Whitesides GM Proc. Natl. Acad. Sci. U.S.A.2014
Endocrine function and bone disease during long-term chelation therapy with deferasirox in patients with β-thalassemia major.Casale M, Citarella S, Filosa A, De Michele E, Palmieri F, Ragozzino A, Amendola G, Pugliese U, Tartaglione I, Della Rocca F, Cinque P, Nobili B, Perrotta S Am. J. Hematol.2014
Microparticles as biomarkers of osteonecrosis of the hip in sickle cell disease.Marsh A, Schiffelers R, Kuypers F, Larkin S, Gildengorin G, van Solinge W, Hoppe C Br. J. Haematol.2014
Hemoglobin-based oxygen carriers: disclosed history and the way ahead: the relativity of safety.Weiskopf RB Anesth. Analg.2014
Multiplex amplification refractory mutation system (MARMS) for the detection of β-globin gene mutations among the transfusion-dependent β-thalassemia Malay patients in Kelantan, Northeast of Peninsular Malaysia.Hanafi S, Hassan R, Bahar R, Abdullah WZ, Johan MF, Rashid ND, Azman NF, Nasir A, Hassan S, Ahmad R, Othman A, Ibrahim MI, Sukeri S, Sulong S, Yusoff S, Mohamad NS, Hussein A, Hassan R, Yusoff N, Yahaya BH, Ismail E, Yussof NK, Salleh S, Zilfalil BA Am J Blood Res2014
Transfusion-independent β(0)-thalassemia after bone marrow transplantation failure: proposed involvement of high parental HbF and an epigenetic mechanism.Paciaroni K, Lucarelli G, Martelli F, Migliaccio AR, von Lindern M, Borg J, Gillemans N, van Dijk TB, Philipsen S Am J Blood Res2014
The transcription factor Miz-1 is required for embryonic and stress-induced erythropoiesis but dispensable for adult erythropoiesis.Kosan C, Rashkovan M, Ross J, Schaffer AM, Saba I, Lemsaddek W, Trudel M, Möröy T Am J Blood Res2014
Renal complications of beta-thalassemia major in children.Bakr A, Al-Tonbary Y, Osman G, El-Ashry R Am J Blood Res2014
Anxiety, depression and quality of life in patients with beta thalassemia major and their caregivers.Yengil E, Acipayam C, Kokacya MH, Kurhan F, Oktay G, Ozer C Int J Clin Exp Med2014
Association of genetic variations in the mitochondrial D-loop with β-thalassemia.Jamali L, Banoei MM, Khalili E, Dadgar S, Houshmand M Mitochondrial DNA2014
Thalassemia major and sickle cell disease in adolescents and young adults.Yacobovich J, Tamary H Acta Haematol.2014
Fetal outcomes in pregnant women with sickle cell disease.Al-Mendalawi MD, Al-Hunieni MN, Al-Khabori MK, Al-Farsi SH, Al-Riyami NM Saudi Med J2014
A cell-based high-throughput screen for novel chemical inducers of fetal hemoglobin for treatment of hemoglobinopathies.Peterson KR, Costa FC, Fedosyuk H, Neades RY, Chazelle AM, Zelenchuk L, Fonteles AH, Dalal P, Roy A, Chaguturu R, Li B, Pace BS PLoS ONE2014
Hemolysis-induced lethality involves inflammasome activation by heme.Dutra FF, Alves LS, Rodrigues D, Fernandez PL, de Oliveira RB, Golenbock DT, Zamboni DS, Bozza MT Proc. Natl. Acad. Sci. U.S.A.2014
Hydroxyurea Improves Oxygen Saturation in Children With Sickle Cell Disease.Pashankar FD, Manwani D, Lee MT, Green NS J. Pediatr. Hematol. Oncol.2014
β-Thalassemia Mutations in Western India: Outcome of Prenatal Diagnosis in a Hemoglobinopathies Project.Patel AP, Patel RB, Patel SA, Vaniawala SN, Patel DS, Shrivastava NS, Sharma NP, Zala JV, Parmar PH, Naik MR Hemoglobin2014
Adult sickle cell disease epidemiology and the potential role of a multidisciplinary comprehensive care center in a city with low prevalence.Binding A, Valentine K, Poon MC, Sayani FA Hemoglobin2014
Characterization of Hb Calvino (HBB: c.406G > A): A New Silent β-Globin Gene Variant Found in Coexistence with α-Thalassemia in a Family of African Origin.Marsella M, Salvagno G, Dolcini B, Ferlini A, Ravani A, Harteveld CL, Giordano PC, Borgna-Pignatti C Hemoglobin2014
N-Acetylcysteine Supplementation Reduces Oxidative Stress and DNA Damage in Children with β-Thalassemia.Ozdemir ZC, Koc A, Aycicek A, Kocyigit A Hemoglobin2014
Reduced plasma angiotensin II levels are reversed by hydroxyurea treatment in mice with sickle cell disease.Dos Santos AF, Almeida CB, Brugnerotto AF, Roversi FM, Pallis FR, Franco-Penteado CF, Lanaro C, Albuquerque DM, Leonardo FC, Costa FF, Conran N Life Sci.2014
Optimal method for early detection of cardiac disorders in thalassemia major patients: magnetic resonance imaging or echocardiography?Moussavi F, Ghasabeh MA, Roodpeyma S, Alavi S, Shakiba M, Gheiratmand R, Omidghaemi M Blood Res2014
Decreased plasma soluble erythropoietin receptor in high-altitude excessive erythrocytosis and Chronic Mountain Sickness.Villafuerte FC, Macarlupú JL, Anza-Ramírez C, Corrales-Melgar D, Vizcardo-Galindo G, Corante N, León-Velarde F J. Appl. Physiol.2014
Evaluation of the Sebia Minicap Flex Piercing capillary electrophoresis for hemoglobinopathy testing.Oyaert M, van Laer C, Claerhout H, Vermeersch P, Desmet K, Pauwels S, Kieffer D Int J Lab Hematol2014
The rate and cost of hospitalisation in children with sickle cell anaemia and its implications in a developing economy.Adegoke SA, Abioye-Kuteyi EA, Orji EO Afr Health Sci2014
Stroke prevalence amongst sickle cell disease patients in Nigeria: a multi-centre study.Jude MA, Aliyu GN, Nalado AM, Garba KU, Florence FO, Hassan A, Inyama M, Akinpelu O, Theresa N, Godswill IO, Sunday O, Ifeoma E, Anthony I, Batholomew C, Chide OE, Joseph O, Malachy I, Korubo K, Sabastine AU, Kingsley A, Nonyelu C, Ugwu A, Duru A, Anigbo C, Eze A, Chukwurah A, Ololo U, Omoti C, Agwu O, Iheanyi O Afr Health Sci2014
Physician Attitude, Awareness, and Knowledge Regarding Guidelines for Transcranial Doppler Screening in Sickle Cell Disease.Reeves SL, Fullerton HJ, Dombkowski KJ, Boulton ML, Braun TM, Lisabeth LD Clin Pediatr (Phila)2014
Homozygous hemoglobin S (HbSS) presenting with bilateral facial nerve palsy: a case report.Ogundunmade BG, Jasper US BMC Res Notes2014
Golden Tracheal Secretions and Bronchoalveolar Fluid During Acute Chest Syndrome in Sickle Cell Disease.Contou D, Mekontso Dessap A, Carteaux G, Brun-Buisson C, Maitre B, de Prost N Respir Care2014
Minor hemoglobins other than A2 in iron deficiency.Chandrashekar V Lab Med2014
High red blood cell nitric oxide synthase activation is not associated with improved vascular function and red blood cell deformability in sickle cell anaemia.Grau M, Mozar A, Charlot K, Lamarre Y, Weyel L, Suhr F, Collins B, Jumet S, Hardy-Dessources MD, Romana M, Lemonne N, Etienne-Julan M, Antoine-Jonville S, Bloch W, Connes P Br. J. Haematol.2014
Hematopoietic stem cell transplantation for people with ß-thalassaemia major.Jagannath VA, Fedorowicz Z, Al Hajeri A, Sharma A Cochrane Database Syst Rev2014
A Survey of the Pain Management of Acute Painful Crisis among Patients with Sickle Cell Disease at Two Centres in Jamaica.Augier R, Jenkins S, Bortolusso Ali S, Tennant I, Williams-Johnson J, Reid M West Indian Med J2014
Molecular analysis of abnormal hemoglobins in beta chain in Aegean region of Turkey and first reports of hemoglobin Andrew-Minneapolis and Hb Hinsdale from Turkey.Aykut A, Onay H, Durmaz A, Karaca E, Vergin C, Aydınok Y, Ozkınay F Hematology2014
MIR144 and MIR451 regulate human erythropoiesis via RAB14.Kim M, Tan YS, Cheng WC, Kingsbury TJ, Heimfeld S, Civin CI Br. J. Haematol.2014
Bio-content of Telferia occidentalis and their effect on methemoglobin formation in sickled erythrocytes.Atabo S, Bolanle JD, Aisha M, Alhaji UI Asian Pac J Trop Med2014
Effect of a novel oral active iron chelator: 1-(N-acetyl-6-aminohexyl)-3-hydroxy-2-methylpyridin-4-one (CM1) in iron-overloaded and non-overloaded mice.Chansiw N, Pangjit K, Phisalaphong C, Porter JB, Evans P, Fucharoen S, Srichairatanakool S Asian Pac J Trop Med2014
Prevalence of hepatitis C virus infection among thalassemia patients: a perspective from a multi-ethnic population of Pakistan.Din G, Malik S, Ali I, Ahmed S, Dasti JI Asian Pac J Trop Med2014
Endocrinopathies in adolescents with thalassaemia major receiving oral iron chelation therapy.Sharma R, Seth A, Chandra J, Gohain S, Kapoor S, Singh P, Pemde H Paediatr Int Child Health2014
Obstetrician-gynecologists' knowledge of sickle cell disease screening and management.Azonobi IC, Anderson BL, Byams VR, Grant AM, Schulkin J BMC Pregnancy Childbirth2014
Hemoglobin-albumin cluster incorporating a Pt nanoparticle: artificial O2 carrier with antioxidant activities.Hosaka H, Haruki R, Yamada K, Böttcher C, Komatsu T PLoS ONE2014
Clinical features and molecular analysis of Hb H disease in Taiwan.Chao YH, Wu KH, Wu HP, Liu SC, Peng CT, Lee MS Biomed Res Int2014
Shared decision making for hydroxyurea treatment initiation in children with sickle cell anemia.Crosby LE, Shook LM, Ware RE, Brinkman WB Pediatr Blood Cancer2014
Diagnosis of a rare double heterozygous Hb D Punjab/Hb Q India hemoglobinopathy using Sebia capillary zone electrophoresis.Parab S, Sakhare S, Sengupta C, Velumani A Indian J Pathol Microbiol2014
A systematic review and meta-analysis of deferiprone monotherapy and in combination with deferoxamine for reduction of iron overload in chronically transfused patients with β-thalassemia.Kuo KH, Mrkobrada M Hemoglobin2014
Altered erythropoiesis and iron metabolism in carriers of thalassemia.Guimarães JS, Cominal JG, Silva-Pinto AC, Olbina G, Ginzburg YZ, Nandi V, Westerman M, Rivella S, de Souza AM Eur. J. Haematol.2014
The Interaction Between Sickle Cell Disease and HIV Infection: A Systematic Review.Owusu ED, Visser BJ, Nagel IM, Mens PF, Grobusch MP Clin. Infect. Dis.2014
Ectodermal dysplasia associated with sickle cell disease.Volpato LE, Volpato MC, de Carvalhosa AA, Palma VC, Borges AH Case Rep Dent2014
Feasibility of a Newborn Screening and Follow-up Programme for Sickle Cell Disease among South Gujarat (India) Tribal Populations.Italia Y, Krishnamurti L, Mehta V, Raicha B, Italia K, Mehta P, Ghosh K, Colah R J Med Screen2014
[Gene distribution characteristics of deletional α-thalassemia in Guangxi region].Zhang Q, Fan X, He S, Fu C, Tang Y, Chen Q, Wei Y, Zheng C Zhonghua Xue Ye Xue Za Zhi2014
Subarachnoid haemorrhage and cerebral vasculopathy in a child with sickle cell anaemia.Inusa B, Casale M, Booth C, Lucas S BMJ Case Rep2014
Multiorgan failure after sickle cell vaso occlusive attack: integrated clinical and biological emergency.Cottin L, Rouvet C, Homedan C, Conté M, Mortaza S, Rousselet MC, Corby A, Le Guyader M, Zandecki M, Reynier P Ann. Biol. Clin. (Paris)2014
Fatal sepsis in a child with thalassemia major due to Serratia marcescens.Paksu MS, Karli A, Paksu S, Guney AK, Ozsevik SN, Belet N Pediatr Int2014
Compound heterozygous hemoglobin d-punjab/hemoglobin d-iran: a novel hemoglobinopathy.Gupta A, Saraf A, Dass J, Mehta M, Radhakrishnan N, Saxena R, Bhargava M Indian J Hematol Blood Transfus2014
Hypertriglyceridemia thalassemia syndrome: a report of 4 cases.Khera R, Singh M, Goel G, Gupta P, Singh T, Dubey AP Indian J Hematol Blood Transfus2014
Hb Knossos: HBB:c.82G>T Associated with HBB:c.315+1G>A Beta Zero Mutation Causes Thalassemia Intermedia.Nasouhipur H, Banihashemi A, Youssefi Kamangar R, Akhavan-Niaki H Indian J Hematol Blood Transfus2014
Down syndrome with transient myeloproliferative disorder and Beta-thalassemia major.Garg A, Singh A, Ramachandran M, Kapoor S Indian J Hematol Blood Transfus2014
Multiple vertebral necrosis in a sickle cell trait: a rare manifestations.Taksande BA, Kotpalliwar S, Sabarwal S, Patil M Indian J Hematol Blood Transfus2014
Fanconi anemia with incidental haemoglobin e trait: the first reported case in literature.Chakrabarti I, Saha A, Guha Mallick Sinha M, Krishna Goswami B, Das M Indian J Hematol Blood Transfus2014
Acute soft head syndrome in children with sickle cell anaemia in lagos, Nigeria.Akodu SO, Njokanma OF, Diaku-Akinwumi IN, Ubuane PO, Adediji UO Indian J Hematol Blood Transfus2014
Relevance of fibrinolytic protein (D-dimer) and fibrinopeptide A as markers of sickle cell anaemia vaso-occlusive crisis.Ekwere TA, Ebele U, Ekanem M, Ogunro PS Niger Postgrad Med J2014
Is undertransfusion a problem in modern clinical practice?Hibbs S, Miles D, Staves J, Murphy MF Transfusion2014
The evaluation of a new apheresis device for automated red blood cell exchange procedures in patients with sickle cell disease.Quirolo K, Bertolone S, Hassell K, Howard T, King KE, Rhodes DK, Bill J Transfusion2014
First Observation of Hemoglobin Jabalpur [Beta 3 (NA3) Leu>Pro] in the Turkish Population.Colak A, Toprak B, Yararbaş K, Akyol F, Ceylan C Turk J Haematol2014
Hemoglobin Lansing (Alpha) [HBA2 CD87 (HIS>GLU) (C>A)] in a Turkish Individual Resulting from Another Nucleotide Substitution.Akar N, Torun D, Oztürk A Turk J Haematol2014
Thalassemia Intermedia and Acute Lymphoblastic Leukemia: Is it a Coincidental Double Diagnosis?Tuğcu D, Karakaş Z, Gökçe M, Ağaoğlu L, Unüvar A, Sarıbeyoğlu E, Akçay A, Devecioğlu O Turk J Haematol2014
Survey of Hfe Gene C282Y Mutation in Turkish Beta-Thalassemia Patients and Healthy Population: A Preliminary Study.Unal S, Balta G, Gümrük F, Xu HG Turk J Haematol2014
Tumor Necrosis Factor-Superfamily 15 Gene Expression in Patients with Sickle Cell Disease.Ozçimen AA, Unal S, Canacankatan N, Antmen SE Turk J Haematol2014
MEK inhibitors, novel anti-adhesive molecules, reduce sickle red blood cell adhesion in vitro and in vivo, and vasoocclusion in vivo.Zennadi R PLoS ONE2014
C-reactive Protein and Disease Outcome in Nigerian Sickle Cell Disease Patients.Okocha C, Manafa P, Ozomba J, Ulasi T, Chukwuma G, Aneke J Ann Med Health Sci Res2014
Evaluation of creatine kinase activity and inorganic phosphate concentration in adult nigerian homozygous and heterozygous hemoglobin phenotypes.Nnadi E, Manafa P, Okocha E, Chukwuma G, Aneke J Ann Med Health Sci Res2014
Bilateral pulmonary embolism in an adolescent with sickle cell disease and a recent total hip arthroplasty: a case report and review of the literature.Burnham JM, Broussard M, Milbrandt T Iowa Orthop J2014
Musculoskeletal disorders in sickle cell anaemia--unusual associations.Umesh S, Ajit NE, Shobha V, Nazuralla S, Ross C, Choudhury R J Assoc Physicians India2014
Implication of globin gene expression, hemoglobin F and hemoglobin E levels on β-thalassemia/Hb E disease severity.Siriworadechkul S, Jindadamrongwech S, Chuncharunee S, Aupparakkitanon S Ann. Clin. Lab. Sci.2014
Prevalence of hemoglobin variants in a diabetic population at high risk of hemoglobinopathies and optimization of HbA1c monitoring by incorporating HPLC in the laboratory workup.Bouzid K, Ahmed HB, Kalai E, Blibeche S, Couque N, Khiari K, Bahlous A, Abdelmoula J Libyan J Med2014
The splenic syndrome in individuals with sickle cell trait.Goodman J, Hassell K, Irwin D, Witkowski EH, Nuss R High Alt. Med. Biol.2014
Whole exome sequencing identifies novel genes for fetal hemoglobin response to hydroxyurea in children with sickle cell anemia.Sheehan VA, Crosby JR, Sabo A, Mortier NA, Howard TA, Muzny DM, Dugan-Perez S, Aygun B, Nottage KA, Boerwinkle E, Gibbs RA, Ware RE, Flanagan JM PLoS ONE2014
The ethnic distribution of sickle cell disease in Sudan.Sabahelzain MM, Hamamy H Pan Afr Med J2014
Attitudes toward patients with sickle cell disease in a multicenter sample of emergency department providers.Freiermuth CE, Haywood C, Silva S, Cline DM, Kayle M, Sullivan D, Thornton V, Tanabe P Adv Emerg Nurs J2014
Sickle cell diseases and ileus.Helvaci MR, Aydogan A, Akkucuk S, Oruc C, Ugur M Int J Clin Exp Med2014
Guidelines for the primary prevention of stroke: a statement for healthcare professionals from the american heart association/american stroke association.Meschia JF, Bushnell C, Boden-Albala B, Braun LT, Bravata DM, Chaturvedi S, Creager MA, Eckel RH, Elkind MS, Fornage M, Goldstein LB, Greenberg SM, Horvath SE, Iadecola C, Jauch EC, Moore WS, Wilson JA, Stroke2014
Effects of hemoglobin variants on hemoglobin a1c values measured using a high-performance liquid chromatography method.Lorenzo-Medina M, De-La-Iglesia S, Ropero P, Nogueira-Salgueiro P, Santana-Benitez J J Diabetes Sci Technol2014
Generation of Human β-Thalassemia Induced Pluripotent Cell Lines by Reprogramming of Bone Marrow-Derived Mesenchymal Stromal Cells Using Modified mRNA.Varela I, Karagiannidou A, Oikonomakis V, Tzetis M, Tzanoudaki M, Siapati EK, Vassilopoulos G, Graphakos S, Kanavakis E, Goussetis E Cell Reprogram2014
An intriguing high performance liquid chromatogram of a double heterozygosity for Hb Q-India/Hb D-Punjab.Badyal RK, Chhabra S, Sharma P, Das R Hemoglobin2014
Immune response of thalassemia major patients in Indonesia with and without splenectomy.Sari TT, Gatot D, Akib AA, Bardosono S, Hadinegoro SR, Harahap AR, Idjradinata PS Acta Med Indones2014
Molecular characterization and phenotypical study of β-thalassemia in Tucumán, Argentina.Lazarte SS, Mónaco ME, Haro AC, Jiménez CL, Ledesma Achem ME, Issé BA Hemoglobin2014
Hb Youngstown [β101(G3)Glu → Ala; HBB: c.305A > C]: An unstable hemoglobin variant causing severe hemolytic anemia.Edward HL, Pisani LA, Rodriguez-Romero WE, Chaves-Villalobos J, Garcia-Quesada J, Harris NS, Luo HY, Steinberg MH, Forget BG, Chui DH Hemoglobin2014
Health-related quality of life in children with sickle cell anemia: Impact of blood transfusion therapy.Beverung LM, Strouse JJ, Hulbert ML, Neville K, Liem RI, Inusa B, Fuh B, King A, Meier ER, Casella J, DeBaun MR, Panepinto JA, Am. J. Hematol.2014
Sustained improvements in myocardial T2* over 2 years in severely iron-overloaded patients with beta thalassemia major treated with deferasirox or deferoxamine.Pennell DJ, Porter JB, Piga A, Lai YR, El-Beshlawy A, Elalfy M, Yesilipek A, Kilinç Y, Habr D, Musallam KM, Shen J, Aydinok Y, Am. J. Hematol.2014
Red blood cell nitric oxide synthase activation is increased in patients with sickle cell hemoglobin C disease.Mozar A, Grau M, Lamarre Y, Weyel L, Suhr F, Collins B, Hardy-Dessources MD, Romana M, Lemonne N, Etienne-Julan M, Bloch W, Connes P Am. J. Hematol.2014
Iron, Inflammation, and Early Death in Adults with Sickle Cell Disease.van Beers E, Yang Y, Raghavachari N, Tian X, Allen DT, Nichols JS, Mendelsohn L, Nekhai S, Gordeuk VR, Taylor JG, Kato GJ Circ. Res.2014
Oscillatory haematopoiesis in adults with sickle cell disease treated with hydroxycarbamide.Baird JH, Minniti CP, Lee JM, Tian X, Wu C, Jackson M, Alam S, Taylor JG, Kato GJ Br. J. Haematol.2014
Combined Chelation Therapy with Daily Oral Deferiprone and Twice-Weekly Subcutaneous Infusion of Desferrioxamine in Children with β-Thalassemia: 3-Year Experience.Songdej D, Sirachainan N, Wongwerawattanakoon P, Sasanakul W, Kadegasem P, Sungkarat W, Chuansumrit A Acta Haematol.2014
Hepatocellular carcinoma in thalassaemia - emerging issues and challenges for liver transplant.Mancuso A Aliment. Pharmacol. Ther.2014
Prophylactic antibiotics for preventing pneumococcal infection in children with sickle cell disease.Hirst C, Owusu-Ofori S Cochrane Database Syst Rev2014
Screening for sickle-cell trait at accession to the United States military.Webber BJ, Witkop CT Mil Med2014
Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania.Mtatiro SN, Singh T, Rooks H, Mgaya J, Mariki H, Soka D, Mmbando B, Msaki E, Kolder I, Thein SL, Menzel S, Cox SE, Makani J, Barrett JC PLoS ONE2014
Transfusions for silent cerebral infarcts in sickle cell anemia.van der Land V, Heijboer H, Fijnvandraat K N. Engl. J. Med.2014
Transfusions for silent cerebral infarcts in sickle cell anemia.DeBaun MR, Casella JF N. Engl. J. Med.2014
Molecular spectrum of α-globin gene defects in the Omani population.Hassan SM, Harteveld CL, Bakker E, Giordano PC Hemoglobin2014
An Alu element-mediated 28.5 kb α-thalassemia deletion found in a Chinese family.Yu J, Xie J, Luo L, Li Z Hemoglobin2014
Molecular characterization of a β-thalassemia intermedia patient presenting inferior vena cava thrombosis: interaction of the β-globin erythroid Krüppel-like factor binding site mutation with Hb E and α(+)-thalassemia.Prajantasen T, Teawtrakul N, Fucharoen G, Fucharoen S Hemoglobin2014
Early onset of fetal hydrops associated with the α-thalassemia - -(THAI) deletion.Yang Y, Li DZ Hemoglobin2014
Radix astragali induces in vitro and in vivo synthesis of fetal hemoglobin in non‑transfusion‑dependent β‑thalassemia: A preliminary study.Guo L, Qian X, Zhao D, Lu Z, Chen J, Wu Q, Xu M Mol Med Rep2014
Erythroexchange in sickle cell disease. A three-step procedure to remove more haemoglobin S.Govoni M Blood Transfus2014
Diminished anaerobic and aerobic exercise fitness in the hemoglobin e traits.Chidnok W, Jiraviriyakul A, Weerapun O, Wasuntarawat C J Sports Med Phys Fitness2014
Pathology image of the month: death in a young adult with sickle cell disease.France J, McGoey RR J La State Med Soc2014
Role of α-globin H helix in the building of tetrameric human hemoglobin: interaction with α-hemoglobin stabilizing protein (AHSP) and heme molecule.Domingues-Hamdi E, Vasseur C, Fournier JB, Marden MC, Wajcman H, Baudin-Creuza V PLoS ONE2014
Treatment for sickle cell disease in Africa: should we invest in haematopoietic stem cell transplantation?Pule G, Wonkam A Pan Afr Med J2014
[In Process Citation].Ondze-Kafata LI, Sanouiller A, Hedreville M, Hedreville S, Larifla L Pan Afr Med J2014
Autopsy findings and pattern of mortality in Nigerian sickle cell disease patients.Ogun GO, Ebili H, Kotila TR Pan Afr Med J2014
Health policy for sickle cell disease in Africa: experience from Tanzania on interventions to reduce under-five mortality.Makani J, Soka D, Rwezaula S, Krag M, Mghamba J, Ramaiya K, Cox SE, Grosse SD Trop. Med. Int. Health2014
Safety of stem cell mobilization in donors with sickle cell trait.Al-Khabori M, Al-Ghafri F, Al-Kindi S, Al-Riyami AZ, Al-Farsi K, Al-Huneini M, Dennison D, Al-Rawas A, Khan H, Daar S Bone Marrow Transplant.2014
Hepatobiliary Complications of Sickle Cell Disease among Children Admitted to Al Wahda Teaching Hospital, Aden, Yemen.Qhalib HA, Zain GH Sultan Qaboos Univ Med J2014
Non-invasive haemoglobin estimation in patients with thalassaemia major.Al Khabori MK, Al-Riyami AZ, Al-Farsi K, Al-Huneini M, Al-Hashim A, Al-Kemyani N, Al-Qarshoubi I, Khan H, Al-Amrani K, Daar S Sultan Qaboos Univ Med J2014
Efficacy of triphaladi avaleha on beejadushtijanya pandu (thalassemia).Patalia AY, Kori VK, Patel KS, Rajagopala S Ayu2014
Vasculopathy and Pulmonary Hypertension in Sickle Cell Disease.Potoka KP, Gladwin MT Am. J. Physiol. Lung Cell Mol. Physiol.2014
Genome editing for human gene therapy.Meissner TB, Mandal PK, Ferreira LM, Rossi DJ, Cowan CA Meth. Enzymol.2014
Oxidative Status and Plasma Lipid Profile in β-Thalassemia Patients.Boudrahem-Addour N, Izem-Meziane M, Bouguerra K, Nadjem N, Zidani N, Belhani M, Djerdjouri B Hemoglobin2014
Comparison of Bone Mineral Density Changes in Pediatric Thalassemic Patients With and Without Hematopoietic Stem Cell Transplant.Hamidieh AA, Mohajeri-Tehrani MR, Behfar M, Vaghari-Meher N, Alimoghaddam K, Mohseni F, Ghavamzadeh A, Larijani B, Hamidi Z Exp Clin Transplant2014
Defective nitric oxide metabolism in sickle cell disease.Kato GJ Pediatr Blood Cancer2014
Molecular Pathophysiology of Priapism: Emerging Targets.Anele UA, Morrison BF, Burnett AL Curr Drug Targets2014
The α-thalassemias.Piel FB, Weatherall DJ N. Engl. J. Med.2014
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Experiences of Pediatric Patients With Sickle Cell Disease in Rural Emergency Departments.Alston KJ, Valrie CR, Walcott C, Warner TD, Fuh B J. Pediatr. Hematol. Oncol.2014
The prevalence of zinc deficiency in patients with thalassemia in South East of iran, sistan and baluchistan province.Mashhadi MA, Sepehri Z, Heidari Z, Shirzaee E, Kiani Z Iran Red Crescent Med J2014
[Sickle cell disease: Pneumococcus escapes prevention and adapts to the disease. Consequences on vaccine design].Labie D, Elion J Med Sci (Paris)2014
[Thalassaemia diagnostics].Kusters E, Kerkhoffs JL, van Rossum AP Ned Tijdschr Geneeskd2014
No evidence of xenotropic murine leukemia virus-related virus infection in Brazilian multiply transfused patients with sickle cell disease and beta-thalassemia major.Slavov SN, Otaguiri KK, Macedo MD, Rocha-Júnior MC, Silva-Pinto AC, Kashima S, Covas DT New Microbiol.2014
A risk score for predicting pulmonary hypertension in patients with non-transfusion-dependent thalassemia in northeastern Thailand: The E-SAAN score.Teawtrakul N, Pussadhamma B, Ungprasert P, Prayalaw P, Fucharoen S, Jetsrisuparb A, Pongudom S, Sirijerachai C, Chansung K, Wanitpongpun C, Thongbuaban S, Thinkhamrop B, Chuncharunee S Hematology2014
Haemoglobin s interaction with Beta thalassaemia- a case report from assam, India.Pathak MS, Borah MS, Kalita D J Clin Diagn Res2014
Haematological characterisation and molecular basis of asian Indian inversion deletions delta Beta thalassemia: a case report.Khunger JM, Gupta M, Singh R, Kapoor R, Pandey HR J Clin Diagn Res2014
Extracellular vesicles in hematological disorders.Aharon A, Rebibo-Sabbah A, Tzoran I, Levin C Rambam Maimonides Med J2014
Transfusion-associated Anaplasma phagocytophilum infection in a pregnant patient with thalassemia trait: a case report.Shields K, Cumming M, Rios J, Wong MT, Zwicker JI, Stramer SL, Alonso CD Transfusion2014
Al-hijamah and oral honey for treating thalassemia, conditions of iron overload, and hyperferremia: toward improving the therapeutic outcomes.El Sayed SM, Baghdadi H, Abou-Taleb A, Mahmoud HS, Maria RA, Ahmed NS, Helmy Nabo MM J Blood Med2014
Oxidative stress is decreased in physically active sickle cell SAD mice.Charrin E, Aufradet E, Douillard A, Romdhani A, Souza GD, Bessaad A, Faes C, Chirico EN, Pialoux V, Martin C Br. J. Haematol.2014
A topical haemoglobin spray for oxygenating chronic venous leg ulcers: a pilot study.Norris R Br J Nurs2014
Implementation of transcranial Doppler ultrasonography screening and primary stroke prevention in urban and rural sickle cell disease populations.Hussain S, Nichols F, Bowman L, Xu H, Neunert C Pediatr Blood Cancer2014
Basal insulin requirement of youth with type 1 diabetes differs according to age.Urakami T, Kuwabara R, Habu M, Okuno M, Suzuki J, Takahashi S J Diabetes Investig2014
Lack of correlation between non-labile iron parameters, total carbonyl and malondialdehyde in major thalassemia.Al-Hakeim HK, Auda FM, Ali BM J Clin Biochem Nutr2014
Insulin-like Growth Factor-1 (IGF-1): Demographic, Clinical and Laboratory Data in 120 Consecutive Adult Patients with Thalassaemia Major.De Sanctis V, Soliman AT, Candini G, Yassin M, Raiola G, Galati MC, Elalaily R, Elsedfy H, Skordis N, Garofalo P, Anastasi S, Campisi S, Karimi M, Kattamis C, Canatan D, Kilinc Y, Sobti P, Fiscina B, El Kholy M Mediterr J Hematol Infect Dis2014
HbD Punjab/HbQ India Compound Heterozygosity: An Unusual Association.Colaco S, Surve R, Sawant P, Nadkarni A, Ghosh K, Colah R Mediterr J Hematol Infect Dis2014
Spectrum of Beta Globin Gene Mutations in Egyptian Children with β-Thalassemia.El-Shanshory M, Hagag A, Shebl S, Badria I, Abd Elhameed A, Abd El-Bar E, Al-Tonbary Y, Mansour A, Hassab H, Hamdy M, Alfy M, Sherief L, Sharaf E Mediterr J Hematol Infect Dis2014
Peripheral red blood cell split chimerism as a consequence of intramedullary selective apoptosis of recipient red blood cells in a case of sickle cell disease.Marziali M, Isgrò A, Sodani P, Gaziev J, Fraboni D, Paciaroni K, Gallucci C, Alfieri C, Roveda A, De Angelis G, Cardarelli L, Ribersani M, Andreani M, Lucarelli G Mediterr J Hematol Infect Dis2014
Non-thalassemic phenotype associated with the -83 (G > A) mutation of the β-globin gene promoter (HBB: c.-133G > A).Waye JS, Eng B, Hanna M, Hohenadel BA, Nakamura LN, Walker L Hemoglobin2014
Mutational spectrum of thalassemias and other hemoglobinopathies in West Bengal, Eastern India.Chatterjee T, Chakravarty A, Chakravarty S Hemoglobin2014
Prevalence of β-thalassemia trait and abnormal hemoglobins in Sanliurfa Province in southeast Turkey.Incebiyik A, Genc A, Hilali NG, Camuzcuoglu A, Camuzcuoglu H, Kilic A, Vural M Hemoglobin2014
Prenatal molecular diagnosis of β-thalassemia and sickle cell anemia in the Syrian population.Murad H, Moassas F, Jarjour R, Mukhalalaty Y, Al-Achkar W Hemoglobin2014
Erythropoietin levels in patients with sickle cell disease do not correlate with known inducers of erythropoietin.Pulte ED, McKenzie SE, Caro J, Ballas SK Hemoglobin2014
Medication Adherence Among Pediatric Patients With Sickle Cell Disease: A Systematic Review.Walsh KE, Cutrona SL, Kavanagh PL, Crosby LE, Malone C, Lobner K, Bundy DG Pediatrics2014
Deferasirox effect on renal haemodynamic parameters in patients with transfusion-dependent β thalassaemia.Piga A, Fracchia S, Lai ME, Cappellini MD, Hirschberg R, Habr D, Wegener A, Bouillaud E, Forni GL Br. J. Haematol.2014
Hemoglobin variant (hemoglobin Aalborg) mimicking interstitial pulmonary disease.Panou V, Jensen PD, Pedersen JF, Thomsen LP, Weinreich UM Pulm Med2014
Relationship between Serum Visfatin and Vascular Inflammation Markers Level in Beta Thalassemia Major Patients.Dehkordi EH, Nourbakhsh SM, Rostampour N, Boroujeni FA Int J Prev Med2014
[Sickle cell disease and diabetes: a rare combination in a black teenager in Lubumbashi, Democratic Republic of Congo].Ngombe LK, Mulangu AM, Kasole TL, Numbi OL Pan Afr Med J2014
Evaluation of high performance liquid chromatography (HPLC) pattern and prevalence of beta-thalassaemia trait among sickle cell disease patients in Lagos, Nigeria.Adeyemo T, Ojewunmi O, Oyetunji A Pan Afr Med J2014
Guidelines for screening, diagnosis and management of hemoglobinopathies.Ghosh K, Colah R, Manglani M, Choudhry VP, Verma I, Madan N, Saxena R, Jain D, Marwaha N, Das R, Mohanty D, Choudhary R, Agarwal S, Ghosh M, Ross C Indian J Hum Genet2014
Non-invasive prenatal diagnostic testing for β-thalassaemia using cell-free fetal DNA and next generation sequencing.Xiong L, Barrett AN, Hua R, Tan TZ, Ho SS, Chan JK, Zhong M, Choolani M Prenat. Diagn.2014
Primary stroke prevention in Nigerian children with sickle cell disease (SPIN): Challenges of conducting a feasibility trial.Galadanci NA, Abdullahi SU, Tabari MA, Abubakar S, Belonwu R, Salihu A, Neville K, Kirkham F, Inusa B, Shyr Y, Phillips S, Kassim AA, Jordan LC, Aliyu MH, Covert BV, DeBaun MR Pediatr Blood Cancer2014
Hyperbaric oxygen therapy in combination with systemic treatment of sickle cell disease presenting as central retinal artery occlusion: a case report.Canan H, Ulas B, Altan-Yaycioglu R J Med Case Rep2014
Sickle cell trait: not as benign as once thought.Khan U, Kleess L, Yeh J, Berko C, Kuehl S J Community Hosp Intern Med Perspect2014
β-Thalassaemia intermedia masquerading as β-thalassaemia major.Singh A, Varma S BMJ Case Rep2014
Renal function in adult Jamaicans with homozygous sickle cell disease.Asnani MR, Reid ME Hematology2014
A massive intestinal vaso-occlusive crisis or Knorr M, Bienemann K, Walde G, Kaufhold A, Schündeln MM Klin Padiatr2014
Hemoglobin expression in nonerythroid cells: novel or ubiquitous?Saha D, Patgaonkar M, Shroff A, Ayyar K, Bashir T, Reddy KV Int J Inflam2014
Emerging drugs for sickle cell anemia.Singh PC, Ballas SK Expert Opin Emerg Drugs2014
ADAMTS13 Levels in Young Patients With β-Thalassemia Major: Relation to Hepatitis C Virus Infection, Liver Cirrhosis, and Iron Overload.Hamed AA, Darwish YW, El-Sayed MH Clin. Appl. Thromb. Hemost.2014
Conjunctival microvascular haemodynamics in sickle cell retinopathy.Kord Valeshabad A, Wanek J, Zelkha R, Lim JI, Camardo N, Gaynes B, Shahidi M Acta Ophthalmol2014
Perfluorocarbon Emulsion Therapy Attenuates Pneumococcal Infection in Sickle Cell Mice.Helmi N, Andrew PW, Pandya HC J. Infect. Dis.2014
Attitudes among healthcare providers and patients diagnosed with sickle cell disease.O'Connor S, Hanes D, Lindsey A, Weiss M, Petty L, Overcash J Clin J Oncol Nurs2014
Prevalence of anemia, iron deficiency, thalassemia and glucose-6-phosphate dehydrogenase deficiency among hill-tribe school children in Omkoi District, Chiang Mai Province, Thailand.Yanola J, Kongpan C, Pornprasert S Southeast Asian J. Trop. Med. Public Health2014
Pulmonary hypertension in sickle cell disease.Hayes MM, Vedamurthy A, George G, Dweik R, Klings ES, Machado RF, Gladwin MT, Wilson KC, Thomson CC, Ann Am Thorac Soc2014
Duodenal perforation: an unusual complication of sickle cell anemia.Acıpayam C, Aldıç G, Akçora B, Çelikkaya ME, Aşkar H, Dorum BA Pan Afr Med J2014
Behavioral impact of sickle cell disease in young children with repeated hospitalization.Bakri MH, Ismail EA, Elsedfy GO, Amr MA, Ibrahim A Saudi J Anaesth2014
Suppression of erythropoiesis by dietary nitrate.Ashmore T, Fernandez BO, Evans CE, Huang Y, Branco-Price C, Griffin JL, Johnson RS, Feelisch M, Murray AJ FASEB J.2014
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X-linked thrombocytopenia with thalassaemia displays bone marrow reticulin fibrosis and enhanced angiogenesis: Comparisons with primary myelofibrosis.Aström M, Hahn-Strömberg V, Zetterberg E, Vedin I, Merup M, Palmblad J Am. J. Hematol.2014
Separation and determination of reduced vitamin C in polymerized hemoglobin-based oxygen carriers of the human placenta.Chen G, Mo L, Li S, Zhou W, Wang H, Liu J, Yang C Artif Cells Nanomed Biotechnol2014
Prominent role of platelets in the formation of circulating neutrophil-red cell heterocellular aggregates in sickle cell anemia.Dominical VM, Samsel L, Nichols JS, Costa FF, McCoy JP, Conran N, Kato GJ Haematologica2014
Flicking the switch: adult hemoglobin expression in erythroid cells derived from cord blood and human induced pluripotent stem cells.Cantú I, Philipsen S Haematologica2014
Glycoprotein B Genotyping of Human Cytomegalovirus Strains Isolated from Brazilian Patients with Sickle Cell Disease and Beta-Thalassemia Major.Slavov SN, Kashima S, Wagatsuma VM, Silva-Pinto AC, Martinez EZ, Favarin MD, Covas DT Viral Immunol.2014
Comparison of total haemoglobin mass measured with the optimized carbon monoxide rebreathing method across different Radiometer™ ABL-80 and OSM-3 hemoximeters.Turner G, Richardson AJ, Maxwell NS, Pringle JS Physiol Meas2014
Circuit Oxygenator Contributes to Extracorporeal Membrane Oxygenation-Induced Hemolysis.Williams DC, Turi JL, Hornik CP, Bonnadonna DK, Williford WL, Walczak RJ, Watt KM, Cheifetz IM ASAIO J.2014
Prevalence and distribution of iron overload in patients with transfusion-dependent anemias differs across geographic regions: results from the CORDELIA study.Aydinok Y, Porter JB, Piga A, Elalfy M, El-Beshlawy A, Kilinç Y, Viprakasit V, Yesilipek A, Habr D, Quebe-Fehling E, Pennell DJ Eur. J. Haematol.2014
Hepatitis E infection in a patient with transfusion-dependent β thalassemia.Sayani F, Goldberg D, Slaven L, Russell JE Am. J. Hematol.2014
[Analysis of thalassemia gene profiling of hemoglobin A2 as 2.5%-3.5%].Li Y, Chen Z, Qin G, Zhao L, Liang L, Guan L Zhonghua Xue Ye Xue Za Zhi2014
Heterogeneous red blood cell adhesion and deformability in sickle cell disease.Alapan Y, Little JA, Gurkan UA Sci Rep2014
Decreased heart rate variability is associated with increased transcranial Doppler velocities in children with sickle cell disease.Jones JB, Shatat IF, Egan BM, Paulo RC Ethn Dis2014
Perception of Pain Among Pediatric Patients With Sickle Cell Pain Crisis.Fosdal MB J Pediatr Oncol Nurs2014
Increase of serum fractalkine and fractalkine gene expression levels in sickle cell disease patients.Unal S, Ozdemir O, Ozcimen AA, Oztas Y Int. J. Hematol.2014
A genetic score for the prediction of beta-thalassemia severity.Danjou F, Francavilla M, Anni F, Satta S, Demartis FR, Perseu L, Manca M, Sollaino MC, Manunza L, Mereu E, Marceddu G, Pissard S, Joly P, Thuret I, Origa R, Borg J, Forni GL, Piga A, Lai ME, Badens C, Moi P, Galanello R Haematologica2014
Elevated Pulse Pressure is Associated with Hemolysis, Proteinuria and Chronic Kidney Disease in Sickle Cell Disease.Novelli EM, Hildesheim M, Rosano C, Vanderpool R, Simon M, Kato GJ, Gladwin MT PLoS ONE2014
Erythroid induction of K562 cells treated with mithramycin is associated with inhibition of raptor gene transcription and mammalian target of rapamycin complex 1 (mTORC1) functions.Finotti A, Bianchi N, Fabbri E, Borgatti M, Breveglieri G, Gasparello J, Gambari R Pharmacol. Res.2014
Correlation between Plasma Interleukin-3, the α/β Globin Ratio, and Globin mRNA Stability.Rouhi Dehnabeh S, Mahdian R, Ajdary S, Mostafavi E, Khatami S Anemia2014
Elevated erythropoietin and cytokines levels are related to impaired reticulocyte maturation in thalassemic patients.Butthep P, Wisedpanichkij R, Jindadamrongwech S, Fucharoen S Blood Cells Mol. Dis.2014
Heart Rate Recovery Is Impaired after Maximal Exercise Testing in Children with Sickle Cell Anemia.Alvarado AM, Ward KM, Muntz DS, Thompson AA, Rodeghier M, Fernhall B, Liem RI J. Pediatr.2014
Hb Souli, a 6 bp In-Frame Deletion on the HBA2 Gene (HBA2: c.[41-46delCCTGGG]) Leads to α-Thalassemia Intermedia, When in Trans to a Single α-Globin Gene Deletion.Kattamis A, Delaporta P, Fylaktou I, Vrettou C, Kyriakopoulou D, Stamoulakatou A, Papassotiriou I, Kanavakis E, Traeger-Synodinos J Hemoglobin2014
A New Hemoglobin Variant: Hb Meylan [β73(E17)Asp → Phe; HBB: c.220G>T; c.221A>T] with a Double Base Mutation at the Same Codon.Renoux C, Feray C, Joly P, Zanella-Cleon I, Garcia C, Lacan P, Couprie N, Francina A Hemoglobin2014
Reproductive issues in sickle cell disease.Smith-Whitley K Blood2014
Social stress increases expression of hemoglobin genes in mouse prefrontal cortex.Stankiewicz AM, Goscik J, Swiergiel AH, Majewska A, Wieczorek M, Juszczak GR, Lisowski P BMC Neurosci2014
Hydroxyurea Increases Plasma Concentrations of Microparticles and Reduces Coagulation Activation and Fibrinolysis in Patients with Sickle Cell Anemia.Brunetta DM, De Santis GC, Silva-Pinto AC, Oliveira de Oliveira LC, Covas DT Acta Haematol.2014
Activity of cytochrome P450 1A2 in relation to hepatic iron accumulation in transfusion-dependent β-thalassaemia major patients.Shteyer E, Nitzan I, Godfarb A, Hemed N, Revel-Vilk S Vox Sang.2014
A large cohort of β(+)-thalassemia in Thailand: Molecular, hematological and diagnostic considerations.Yamsri S, Singha K, Prajantasen T, Taweenan W, Fucharoen G, Sanchaisuriya K, Fucharoen S Blood Cells Mol. Dis.2014
Endothelial Function and Vascular Properties in Children with Sickle Cell Disease.Hadeed K, Hascoet S, Castex MP, Munzer C, Acar P, Dulac Y Echocardiography2014
Intensive management of high-utilizing adults with sickle cell disease lowers admissions.Koch KL, Karafin MS, Simpson P, Field JJ Am. J. Hematol.2014
Confirmation of a founder effect in a Northern European population of a new β-globin variant: HBB:c.23_26dup (codons 8/9 (+AGAA)).Marchi N, Pissard S, Cliquennois M, Vasseur C, Le Metayer N, Mereau C, Jouet JP, Georgel AF, Genin E, Rose C Eur. J. Hum. Genet.2014
An analysis of the NIH-supported sickle cell disease research portfolio.Gavini N, Hoots WK, Mensah GA, Hanspal M Blood Cells Mol. Dis.2014
Alpha thalassemia trait masquerading as hemoglobin H disease due to co-existing primary myelofibrosis.So CC, Chan AY, Chan JC, Ma ES Ann. Hematol.2014
Dengue virus infection of erythroid precursor cells is modulated by both thalassemia trait status and virus adaptation.Sornjai W, Khungwanmaythawee K, Svasti S, Fucharoen S, Wintachai P, Yoksan S, Ubol S, Wikan N, Smith DR Virology2014
Allogeneic Stem Cell Transplantation for Thalassemia Major.Mathews V, Srivastava A, Chandy M Hematol. Oncol. Clin. North Am.2014
Hematopoietic Stem Cell Transplantation for Patients with Sickle Cell Disease: Progress and Future Directions.Fitzhugh CD, Abraham AA, Tisdale JF, Hsieh MM Hematol. Oncol. Clin. North Am.2014
[Anti-erythrocyte and anti-HLA immunization in hemoglobinopathies].Ben Salah N, El Borgi W, Ben Lakhal F, Ben Mansour M, Gouider E, Gorgi Y, Bardi R, Zoueri B, Hafsia R Transfus Clin Biol2014
[Clinico-biological and Immunohaematological profile of patients with β-thalassemia in Tunisia: About 26 cases].Romdhane H, Amara H, Abdelkefi S, Souyeh N, Chakroun T, Jarrey I, Bouslama M, Belhedi S, Houissa B, Boughammoura L, Jemni Yacoub S Transfus Clin Biol2014
Klotho: its various functions and association with sickle cell disease Souza Pacheco AP, Goncalves M Rev Bras Hematol Hemoter2014
Characterization of mortality in children with sickle cell disease diagnosed through the Newborn Screening Program.Sabarense AP, Lima GO, Silva LM, Viana MB J Pediatr (Rio J)2014
Different patterns of myocardial iron distribution by whole-heart T2* magnetic resonance as risk markers for heart complications in thalassemia major.Meloni A, Restaino G, Borsellino Z, Caruso V, Spasiano A, Zuccarelli A, Valeri G, Toia P, Salvatori C, Positano V, Midiri M, Pepe A Int. J. Cardiol.2014
Effect of L-type calcium channel blocker (amlodipine) on myocardial iron deposition in patients with thalassaemia with moderate-to-severe myocardial iron deposition: protocol for a randomised, controlled trial.Shakoor A, Zahoor M, Sadaf A, Alvi N, Fadoo Z, Rizvi A, Quadri F, Tipoo FA, Khurshid M, Sajjad Z, Colan S, Hasan BS BMJ Open2014
Evaluation of a density-based rapid diagnostic test for sickle cell disease in a clinical setting in zambia.Kumar AA, Chunda-Liyoka C, Hennek JW, Mantina H, Lee SY, Patton MR, Sambo P, Sinyangwe S, Kankasa C, Chintu C, Brugnara C, Stossel TP, Whitesides GM PLoS ONE2014
Characterization of Hb Lepore Variants in the UK Population.Guo L, Kausar A, Old JM, Henderson SJ, Gallienne AE Hemoglobin2014
Association between somatic growth trajectory and cognitive functioning in young children with sickle cell disease.Puffer ES, Schatz JC, Roberts CW J Health Psychol2014
Polymorphism at BCL11A compared to HBS1L-MYB loci explains less of the variance in HbF in patients with sickle cell disease in Cameroon.Bitoungui VJ, Ngogang J, Wonkam A Blood Cells Mol. Dis.2014
Pulmonary hypertension in well-transfused thalassemia major patients.Meloni A, Detterich J, Pepe A, Harmatz P, Coates TD, Wood JC Blood Cells Mol. Dis.2014
Dietary supplementation with docosahexanoic acid (DHA) increases red blood cell membrane flexibility in mice with sickle cell disease.Wandersee NJ, Maciaszek JL, Giger KM, Hanson MS, Zheng S, Guo Y, Mickelson B, Hillery CA, Lykotrafitis G, Low PS, Hogg N Blood Cells Mol. Dis.2014
Hemoglobin C disease.Bain BJ Am. J. Hematol.2014
Identification of a novel variant of epsilon-gamma-delta-beta° thalassemia highlights limitations of next generation sequencing.Zebisch A, Schulz E, Grosso M, Lombardo B, Acierno G, Sill H, Iolascon A Am. J. Hematol.2014
Modulation of pain in pediatric sickle cell disease: Understanding the balance between endothelin mediated vasoconstriction and apelin mediated vasodilation.Smith TP, Schlenz AM, Schatz JC, Maitra R, Sweitzer SM Blood Cells Mol. Dis.2014
Beta-thalassemias: molecular, epidemiological, diagnostical and clinical aspects.Joly P, Pondarre C, Badens C Ann. Biol. Clin. (Paris)2014
Interventions for treating leg ulcers in people with sickle cell disease.Martí-Carvajal AJ, Knight-Madden JM, Martinez-Zapata MJ Cochrane Database Syst Rev2014
Keeping fetal hemoglobin in the loop.Grevet JD, Blobel GA Cell Cycle2014
Reversal of liver function without exchange transfusion in sickle cell intrahepatic cholestasis.Hosiriluck N, Rassameehiran S, Argueta E, Tijani L Proc (Bayl Univ Med Cent)2014
[Clinical consequences of alpha-thalassemia in the basque country, Spain. Impact of neonatal screening.]Aristizabal A, Merino S, Catediano E, Sasieta M, Aragües P, Navajas A An Pediatr (Barc)2014
Stroke and inherited thrombophilia in a Tunisian girl with sickle cell anemia.Nefissi RB, Ouali F, Massaoud T, Gritli N Clin. Chem. Lab. Med.2014
High resolution melting analytical platform for rapid prenatal and postnatal diagnosis of β-thalassemia common among Southeast Asian population.Prajantasen T, Fucharoen S, Fucharoen G Clin. Chim. Acta2014
From infancy to adolescence: fifteen years of continuous treatment with hydroxyurea in sickle cell anemia.Hankins JS, Aygun B, Nottage K, Thornburg C, Smeltzer MP, Ware RE, Wang WC Medicine (Baltimore)2014
Molecular analysis of beta-globin gene mutations among Thai beta-thalassemia children: results from a single center study.Boonyawat B, Monsereenusorn C, Traivaree C Appl Clin Genet2014
HMGB1 takes a "Toll" in sickle cell diseaseGupta K Blood2014
β-Globin Genes: Mutation Hot-Spots in the Global Thalassemia Belt.Kumar R, Sagar C, Sharma D, Kishor P Hemoglobin2014
Identification of Nondeletional α-Thalassemia in a Prenatal Screening Program by Reverse Dot-Blot in Southern China.Li J, Li R, Li D Hemoglobin2014
The use of rituximab to prevent severe delayed haemolytic transfusion reaction in immunized patients with sickle cell disease.Noizat-Pirenne F, Habibi A, Mekontso-Dessap A, Razazi K, Chadebech P, Mahevas M, Vingert B, Bierling P, Galactéros F, Bartolucci P, Michel M Vox Sang.2014
[Pseudotumor cerebri in children with sickle cell disease.]Butori P, Jean-Charles A, Elana G, Merle H J Fr Ophtalmol2014
Pregnancy outcome in patients with sickle cell disease in the UK - a national cohort study comparing sickle cell anaemia (HbSS) with HbSC disease.Oteng-Ntim E, Ayensah B, Knight M, Howard J Br. J. Haematol.2014
Epistasis and the sensitivity of phenotypic screens for beta thalassaemia.Penman BS, Gupta S, Weatherall DJ Br. J. Haematol.2014
First reported duplication of the entire beta globin gene cluster causing an unusual sickle cell trait phenotype.Shooter C, Senior McKenzie T, Oakley M, Jacques T, Clark B, Thein SL Br. J. Haematol.2014
Randomized trial of hypnosis as a pain and symptom management strategy in adults with sickle cell disease.Wallen GR, Middleton KR, Ames N, Brooks AT, Handel D Integr Med Insights2014
Left ventricular function by echocardiogram in children with sickle cell anaemia in Mumbai, Western India.Tidake A, Gangurde P, Taksande A, Mahajan A, Nathani P Cardiol Young2014
Hepcidin is suppressed by erythropoiesis in hemoglobin E β-thalassemia and β-thalassemia trait.Jones E, Pasricha SR, Allen A, Evans P, Fisher CA, Wray K, Premawardhena A, Bandara D, Perera A, Webster C, Sturges P, Olivieri NF, St Pierre T, Armitage AE, Porter JB, Weatherall DJ, Drakesmith H Blood2014
Changes in Coping, Pain and Activity following Cognitive-Behavioral Training: A Randomized Clinical Trial for Pediatric Sickle Cell Disease using Smartphones.Schatz J, Schlenz A, McClellan CB, Puffer ES, Hardy S, Pfeiffer M, Roberts CW Clin J Pain2014
Incidence of sickle cell trait - United States, 2010.Ojodu J, Hulihan MM, Pope SN, Grant AM MMWR Morb. Mortal. Wkly. Rep.2014
Effect of acetylsalicylic acid on thalassemia with pulmonary arterial hypertension.Chueamuangphan N, Wongtheptian W, Patumanond J, Sukonthasarn A, Chuncharunee S, Tawichasri C, Nawarawong W Int J Gen Med2014
Intravitreal Ranibizumab for Stage IV Proliferative Sickle Cell Retinopathy: A First Case Report.Mitropoulos PG, Chatziralli IP, Parikakis EA, Peponis VG, Amariotakis GA, Moschos MM Case Rep Ophthalmol Med2014
Decreased heart rate variability is associated with increased transcranial Doppler velocities in children with sickle cell disease.Jones JB, Shatat IF, Egan BM, Paulo RC Ethn Dis2014
[The pregnancy outcome in patients WITH β-thalassemia minor]. Akush Ginekol (Sofiia)2014
[Sickle cell disease: patients, racism and indifference].Deleuze J Rev Prat2014
[Hemoglobin disorders: an advantage against malaria, but the risk of severe disease].Bartolucci P Rev Prat2014
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[How to interpret an hemoglobin electrophoresis].Galacteros F Rev Prat2014
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[Chronic complications of sickle cell disease].Bartolucci P, Lionnet F Rev Prat2014
[Treatment with hydroxyurea has revolutionized the evolution of sickle cell disease ].Bartolucci P, de Montalembert M Rev Prat2014
[Risks associated with transfusions in sickle cell disease: delayed hemolytic transfusion reaction].Habibi A, Noizat-Pirenne F Rev Prat2014
[Indications for allogeneic hematopoietic stem cell transplantion in sickle cell disease].Benkerrou M Rev Prat2014
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[Thalassemia alpha].Pondarré C Rev Prat2014
α-thalassemia-associated hydrops fetalis: A rare cause of thyrotoxic cardiomyopathy.Tumian NR, Wong M, Wong CL J. Obstet. Gynaecol. Res.2014
Triterpenoid inducers of Nrf2 signaling as potential therapeutic agents in sickle cell disease: a review.Owusu-Ansah A, Choi SH, Petrosiute A, Letterio JJ, Huang AY Front Med2014
[Effects and clinical significance of virus load on red blood cell parameters in different stage of hepatitis B].Gao P, Xiao P, Yang YL, Chen QF, Mao XR, Zhao ZB, Shi L, Yang LZ, Zhou W Beijing Da Xue Xue Bao2014
The Association of Cytokine Levels With Cognitive Function in Children With Sickle Cell Disease and Normal MRI Studies of the Brain.Andreotti C, King AA, Macy E, Compas BE, DeBaun MR J. Child Neurol.2014
Effects of hemoglobin-based oxygen carriers on blood coagulation.Roghani K, Holtby RJ, Jahr JS J Funct Biomater2014
Sleep Disorders in Adult Sickle Cell Patients.Sharma S, Efird JT, Knupp C, Kadali R, Liles D, Shiue K, Boettger P, Quan SF J Clin Sleep Med2014
Hemoglobinopathy screening by osmotic fragility test based on flow cytometer or naked eye.Mohapatra R, Warang P, Ghosh K, Colah R Cytometry B Clin Cytom2014
Improved hematopoietic differentiation efficiency of gene-corrected beta-thalassemia induced pluripotent stem cells by CRISPR/Cas9 system.Song B, Fan Y, He W, Zhu D, Niu X, Wang D, Ou Z, Luo M, Sun XF Stem Cells Dev.2014
Quantification of Sickle Cells in the Peripheral Smear as a Marker of Disease Severity.Alvarez O, Montague NS, Marin M, O'Brien R, Rodriguez MM Fetal Pediatr Pathol2014
Modified desensitization protocols for a pediatric patient with anaphylactic reaction to deferoxamine.Surapolchai P, Poachanukoon O, Satayasai W, Silapamongkonkul P J Med Assoc Thai2014
Hickam's Dictum and the Rare Convergence of Antisynthetase Syndrome and Hemoglobin SC Disease.Wilkinson ST, Grunwald MR, Paik JJ, Ostrow LW, Gelber AC QJM2014
Meta-analysis on effectiveness of hydroxyurea to treat transfusion-dependent beta-thalassemia.Bayanzay K, Khan R Hematology2014
[Delayed haemolytic transfusion reaction: About 3 patients with sickle cell disease.]Bertrand E, Dumesnil C, Lahary A, Al Bagami M, Schneider P, Lévesque H, Vannier JP Rev Med Interne2014
Preliminary Results of Multiple Epiphyseal Drilling and Autologous Bone Marrow Implantation for Osteonecrosis of the Femoral Head Secondary to Sickle Cell Disease in Children.Novais EN, Sankar WN, Wells L, Carry PM, Kim YJ J Pediatr Orthop2014
Advances in sickle cell therapies in the hydroxyurea era.Field JJ, Nathan DG Mol. Med.2014
A novel inflammatory role for platelets in sickle cell disease.Davila J, Manwani D, Vasovic L, Avanzi M, Uehlinger J, Ireland K, Mitchell WB Platelets2014
The CCR5Δ32 polymorphism in Brazilian patients with sickle cell disease.Lopes MP, Santos MN, Faber EW, Bezerra MA, Hatzlhofer BL, Albuquerque DM, Zaccariotto TR, Ribeiro DM, Araújo Ada S, Costa FF, Sonati Mde F Dis. Markers2014
Environmental influences on daily emergency admissions in sickle-cell disease patients.Mekontso Dessap A, Contou D, Dandine-Roulland C, Hemery F, Habibi A, Charles-Nelson A, Galacteros F, Brun-Buisson C, Maitre B, Katsahian S Medicine (Baltimore)2014
Transcorneal oxygen therapy in two patients with traumatic hyphema and sickle cell trait.Padrón-Pérez N, Castany-Aregall M, Pueyo A, Carceller A Clin. Experiment. Ophthalmol.2014
The high oxygen affinity haemoglobin Nantes: a family case description.Artuso A, Balter R, Bonetti E, Zambon C, Ravani A, Dolcini B, Masieri MT, Salvagno GL, Zanotti R, Pizzolo G, Veneri D Blood Transfus2014
Mycobacterium avium Complex Infection in a Patient with Sickle Cell Disease and Severe Iron Overload.Shemisa K, Jafferjee N, Thomas D, Jacobs G, Meyerson HJ Case Rep Infect Dis2014
[RDBH-method and big DyeTM terminator technology in accurate diagnosis of β-thalassemia and the allelic polymorphism of β-globin cluster].Akbarova G Georgian Med News2014
Haptoglobin genotypes polymorphism as a risk factor for subclinical atherosclerosis in beta-thalassemia major children; a single center Egyptian study.Ragab SM, Safan MA, Badr EA, Ebeid OM Hematology2014
Significant Differences in Thymic Index of Thalassemia Major Patients.Oymak Y, Güzel B, Gümüş H, Dağlıoğlu E, Ayçiçek A, Koç A, Özyürük D Turk J Haematol2014
Serum Bcl-2 Levels in Patients with β-Thalassemia Minor: A Pilot Study.Yavaşoğlu İ, Sargın G, Kadıköylü G, Karul A, Bolaman Z Turk J Haematol2014
DNA damage: beta zero versus beta plus thalassemia.Sagar CS, Kumar R, Sharma DC, Kishor P Ann. Hum. Biol.2014
Evolution of α- and β-globin genes and their regulatory systems in light of the hypothesis of domain organization of the genome.Iarovaia OV, Ioudinkova ES, Petrova NV, Dolgushin KV, Kovina AV, Nefedochkina AV, Vassetzky YS, Razin SV Biochemistry Mosc.2014
Exertional sickling: questions and controversy.Blinder MA, Russel S Hematol Rep2014
Renal medullary carcinoma in a young white adult without sickle cell trait or disease.Mast Vilaseca R, Pons Escoda A Radiologia2014
Cilostazol and blood viscoelasticity in homozygous sickle cell disease.Lester DA, Richards AA, Younger-Coleman NO, Pepple DJ Br. J. Biomed. Sci.2014
Immunoglobulin levels and CD4 / CD8 counts in β- thalassemia major.Kadam PP, Manglani MV, Sharma SM, Sharma RA, Setia MS Indian Pediatr2014
Closure of chronic non healing ankle ulcer with low level laser therapy in a patient presenting with thalassemia intermedia: Case report.Dixit S, Agrawal PR, Sharma DK, Singh RP Indian J Plast Surg2014
Evaluation of caries-associated virulence of biofilms from Candida albicans isolated from saliva of pediatric patients with sickle-cell anemia.Brighenti FL, Medeiros AC, Matos BM, Ribeiro ZE, Koga-Ito CY J Appl Oral Sci2014
Profound sustained reticulocytopenia and anaemia in an adult patient with sickle cell disease.Win N, Lee E, Needs M, Homeida S, Stasi R Transfus Med2014
[Psychosocial impact of sickle cell disease in the parents of children living in Kinshasa, Democratic Republic of Congo: a qualitative study].Luboya E, Tshilonda JC, Ekila MB, Aloni MN Pan Afr Med J2014
Prevalence of metabolic syndrome in patients with minor beta thalassemia and its related factors: a cross-sectional study.Gozashti MH, Hasanzadeh A, Mashrouteh M J Diabetes Metab Disord2014
Prevalence of thalassaemia, iron-deficiency anaemia and glucose-6-phosphate dehydrogenase deficiency among Arab migrating nomad children, southern Islamic Republic of Iran.Pasalar M, Mehrabani D, Afrasiabi A, Mehravar Z, Reyhani I, Hamidi R, Karimi M East. Mediterr. Health J.2014
Wandering spleen with chronic torsion in a patient with thalassaemia.Ho CL Singapore Med J2014
Think about hemoglobinopathies.Shemer OS, Tamary H Isr. Med. Assoc. J.2014
In utero hematopoietic cell transplantation for hemoglobinopathies.Derderian SC, Jeanty C, Walters MC, Vichinsky E, MacKenzie TC Front Pharmacol2014
Pulmonary arterial hypertension in a patient with β-thalassemia intermedia and reversal with infusion epoprostenol then transition to oral calcium channel blocker therapy: review of literature.Ussavarungsi K, Burger CD Pulm Circ2014
Sickle erythrocytes and platelets augment lung leukotriene synthesis with downregulation of anti-inflammatory proteins: relevance in the pathology of the acute chest syndrome.Opene M, Kurantsin-Mills J, Husain S, Ibe BO Pulm Circ2014
Effect of zinc supplementation on viral response in patients with chronic hepatitis C and Beta thalassemia major, a pilot study.Abbasinazari M, Alavian SM, Behnava B, Asgharinia M, Salimi S, Keshvari M, Mehrnoush L, Karim P J Clin Diagn Res2014
Neonatal screening for sickle cell disease and other hemoglobinopathies in Rolla R, Castagno M, Zaffaroni M, Grigollo B, Colombo S, Piccotti S, Dellora C, Bona G, Bellomo G Clin. Lab.2014
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Comparison of deferiprone and deferrioxamine for the treatment of transfusional iron overload in children with beta thalassemia major.Waheed N, Ali S, Butt MA J Ayub Med Coll Abbottabad2014
Red blood cell alloimmunization in sickle cell disease: listen to your ancestors.Campbell-Lee SA, Kittles RA Transfus Med Hemother2014
The Cellie Coping Kit for Sickle Cell Disease: Initial acceptability and feasibility.Marsac ML, Klingbeil OG, Hildenbrand AK, Alderfer MA, Kassam-Adams N, Smith-Whitley K, Barakat LP Clin Pract Pediatr Psychol2014
Acute chest syndrome in severity of sickle cell diseases.Helvaci MR, Acipayam C, Aydogan A, Akkucuk S, Oruc C, Gokce C Int J Clin Exp Med2014
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Bloodless medicine: what to do when you can't transfuse.Resar LM, Frank SM Hematology Am Soc Hematol Educ Program2014
The science behind the hypoxic niche of hematopoietic stem and progenitors.Nombela-Arrieta C, Silberstein LE Hematology Am Soc Hematol Educ Program2014
Smoothing the crescent curve: sickle cell disease.Talano JA, Cairo MS Hematology Am Soc Hematol Educ Program2014
Red cell exchange: special focus on sickle cell disease.Kim HC Hematology Am Soc Hematol Educ Program2014
Breakthrough: new guidance for silent cerebral ischemia and infarction in sickle cell disease.Quinn CT Hematology Am Soc Hematol Educ Program2014
Does hydroxyurea prevent pulmonary complications of sickle cell disease?Buckner TW, Ataga KI Hematology Am Soc Hematol Educ Program2014
Pulmonary hypertension in sickle cell disease: diagnosis and management.Ataga KI, Klings ES Hematology Am Soc Hematol Educ Program2014
Reproductive issues in sickle cell disease.Smith-Whitley K Hematology Am Soc Hematol Educ Program2014
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Is supplementation efficacious in maintaining adequate plasma levels of vitamin a and e for thalassemic patients undergoing hematopoietic stem cell transplantation? A cross-sectional study.Hajimahmoodi M, Hadjibabaie M, Hamidieh AA, Ahmadvand A, Kazempanah S, Sadeghi N, Mansouri A, Ghavamzadeh A Iran J Pediatr2014
The Use of Analgesic Drugs in Patients with Sickle Cell Painful Crisis.Boyd I, Gossell-Williams M, Lee MG West Indian Med J2014
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Steroid treatment of protracted cholestatic hepatitis A in a child with β-thalassemia.Gökçe S, Çenesiz F, Özalp Akın E Turk J Gastroenterol2014
Recommendations for the management of sickle cell disease in South Africa.Alli NA, Patel M, Alli HD, Bassa F, Coetzee MJ, Davidson A, Essop MR, Lakha A, Louw VJ, Novitzky N, Philip V, Poole JE, Wainwright RD S. Afr. Med. J.2014
Mechanistic Studies of the Negative Epistatic Malaria-protective Interaction Between Sickle Cell Trait and α(+)thalassemia.Opi DH, Ochola LB, Tendwa M, Siddondo BR, Ocholla H, Fanjo H, Ghumra A, Ferguson DJ, Rowe JA, Williams TN EBioMedicine2014
Topical sodium nitrite for chronic leg ulcers in patients with sickle cell anaemia: a phase 1 dose-finding safety and tolerability trial.Minniti CP, Gorbach AM, Xu D, Hon YY, Delaney KM, Seidel M, Malik N, Peters-Lawrence M, Cantilena C, Nichols JS, Mendelsohn L, Conrey A, Grimes G, Kato GJ Lancet Haematol2014
Quantitative intravital two-photon excitation microscopy reveals absence of pulmonary vaso-occlusion in unchallenged Sickle Cell Disease mice.Bennewitz MF, Watkins SC, Sundd P Intravital2014
Frequency of red cell allo- and autoimmunization in patients with transfusion-dependent beta thalassemia and affecting factors.Koçyiğit C, Eliaçık K, Kanık A, Atabay B, Türker M Turk. J. Pediatr.2014
Extramedullary hematopoiesis in adrenal gland. An uncommon cause of adrenal incidentaloma in sickle cell disease.Azarpira N, Heidari Esfahani M, Paydar S Iran J Pediatr2014
Study of antisickling and vasorelaxant activities and acute toxicity assessment of crude extracts of leaves of Ficus sycomorus L. (Moraceae).Ramdé-Tiendrébéogo A, Tibiri A, Ouedraogo M, Ouédraogo S, Nacoulma OG, Guissou IP Pak. J. Biol. Sci.2014
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α(+)Thalassemia Antagonizes the Malaria-protective Effects of Sickle-Cell Trait.Amaratunga C, Fairhurst RM EBioMedicine2014
IMPAIRED ENDOTHELIAL FUNCTION IN PEDIATRIC HEMOGLOBIN E/β-THALASSEMIA PATIENTS WITH IRON OVERLOAD.Aphinives C, Kukongviriyapan U, Jetsrisuparb A, Kukongviriyapan V, Somparn N Southeast Asian J. Trop. Med. Public Health2014
Recurrent Nocardia Sepsis in a Patient With Sickle Cell Anemia Receiving Continuous Deferoxamine.Wessler JM, Adams DJ, Kunz AN, Babcock JG, Hartman KR J Pediatric Infect Dis Soc2014
Separation of hemoglobin variants by capillary electrophoresis.Cotton F, Gulbis BMethods Mol. Biol.2013
Transcranial Doppler ultrasonography in sickle cell disease: a study in omani patients.Gujjar AR, Zacharia M, Al-Kindi S, William R, Al Lamki Z, Wali Y, Bashir W, Jain R, Al-Asmi A, Pathare A J. Pediatr. Hematol. Oncol.2013
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Quantitative analysis of murine terminal erythroid differentiation in vivo: novel method to study normal and disordered erythropoiesis.Liu J, Zhang J, Ginzburg Y, Li H, Xue F, De Franceschi L, Chasis JA, Mohandas N, An X Blood2013
Lactate dehydrogenase and hemolysis in sickle cell disease.Ballas SK Blood2013
Proteomic analysis of ERK1/2-mediated human sickle red blood cell membrane protein phosphorylation.Soderblom EJ, Thompson JW, Schwartz EA, Chiou E, Dubois LG, Moseley MA, Zennadi R Clin Proteomics2013
The Molecular Basis of α-Thalassemia.Higgs DR Cold Spring Harb Perspect Med2013
Identification and molecular characterization of a novel 55 kb deletion recurrent in Southern Italy: the Italian (G) γ((A) γδβ)°-thalassemia.Lacerra G, Prezioso R, Musollino G, Piluso G, Mastrullo L, De Angioletti M Eur. J. Haematol.2013
Outcomes using lower vs higher hemoglobin thresholds for red blood cell transfusion.Carson JL, Carless PA, Hébert PC JAMA2013
Remote monitoring of pain and symptoms using wireless technology in children and adolescents with sickle cell disease.Jacob E, Duran J, Stinson J, Lewis MA, Zeltzer L J Am Acad Nurse Pract2013
Hemoglobin sickle cell disease in Brazil.Cabañas-Pedro AC, Braga JA, Camilo-Araújo RF, Silva AI, Vicari P, Figueiredo M Haematologica2013
Use of portable x-ray fluorescence (pxrf) in vivo as an alternative technique for the assessment of iron levels in patients with thalassemia and hemochromatosis.Estevam M, Appoloni CR Health Phys2013
Left Ventricular Dyssynchrony Is an Early Manifestation of Heart Involvement in Sickle Cell Anemia.Karakaş MF, Büyükkaya E, Kurt M, Celik M, Karakaş E, Büyükkaya S, Akçay AB, Sen N Echocardiography2013
Parental information, motivation, and adherence behaviors among children with sickle cell disease.Raphael JL, Butler AM, Rattler TL, Kowalkowski MA, Mueller BU, Giordano TP Pediatr Blood Cancer2013
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Relationships between systemic vascular resistance, blood rheology and nitric oxide in children with sickle cell anemia or sickle cell-hemoglobin C disease.Lamarre Y, Hardy-Dessources MD, Romana M, Lalanne-Mistrih ML, Waltz X, Petras M, Doumdo L, Blanchet-Deverly A, Martino J, Tressières B, Maillard F, Tarer V, Etienne-Julan M, Connes P Clin. Hemorheol. Microcirc.2013
A Case of Recurrent Psychosis during Sickle Cell Disease Crisis Treated Successfully with Ziprasidone.Spiegel DR, Messerschmidt C, Morewitz J, Akintola M Clin Schizophr Relat Psychoses2013
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Continuous Measurement of Hemoglobin: Methodological Approach and Lessons for the Future.Riou B Anesthesiology2013
Endocrinopathies in beta-thalassemia major. Prevalence, risk factors, and age at diagnosis in Northwest Saudi Arabia.Habeb AM, Al-Hawsawi ZM, Morsy MM, Al-Harbi AM, Osilan AS, Al-Magamsi MS, Zolaly MA Saudi Med J2013
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The Clinical and Laboratory Spectrum of Hb C [β6(A3)Glu→Lys, GAG>AAG] Disease.Cook CM, Smeltzer MP, Mortier NA, Kirk SE, Despotovic JM, Ware RE, Hankins JS Hemoglobin2013
A non-electrolyte haemolysis assay for diagnosis and prognosis of sickle cell disease.Milligan C, Rees DC, Ellory JC, Osei A, Browning JA, Hannemann A, Gibson JS J. Physiol. (Lond.)2013
Sickle hemoglobin disturbs normal coupling between erythrocyte O2 content, glycolysis and antioxidant capacity.Rogers SC, Ross JG, d'Avignon A, Gibbons LB, Gazit V, Hassan MN, McLaughlin D, Griffin S, Neumayr T, Debaun M, Debaun MR, Doctor A Blood2013
Developmental Function in Toddlers With Sickle Cell Anemia.Armstrong FD, Elkin TD, Brown RC, Glass P, Rana S, Casella JF, Kalpatthi RV, Pavlakis S, Mi Z, Wang WC, Pediatrics2013
Echocardiography in thalassemic patients on blood transfusions and chelation without heart failure.Rodrigues A, Guimarães-Filho FV, Braga JC, Rodrigues CS, Waib P, Fabron-Junior A, Tan DM, França AC, Okoshi MP, Okoshi K Arq. Bras. Cardiol.2013
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Hepatocellular carcinoma in hepatitis-negative patients with thalassemia intermedia: a closer look at the role of siderosis.Maakaron JE, Cappellini MD, Graziadei G, Ayache JB, Taher AT Ann Hepatol2013
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Thalassemia bone disease: the association between nephrolithiasis, bone mineral density and fractures.Wong P, Fuller PJ, Gillespie MT, Kartsogiannis V, Strauss BJ, Bowden D, Milat F Osteoporos Int2013
Identification of KAP-1-associated complexes negatively regulating the Ey and β-major globin genes in the β-globin locus.Yang D, Ma Z, Lin W, Yang J, Tian C, Wei H, Jiang Y, He F J Proteomics2013
Molecular and clinical evaluation of the acute human parvovirus B19 infection: comparison of two cases in children with sickle cell disease and discussion of the literature.Slavov SN, Kashima S, Silva-Pinto AC, Amarilla AA, Aquino VH, Covas DT Braz J Infect Dis2013
Evidence of Differential Selection for the -α(3.7) and -α(4.2) Single α-Globin Gene Deletions within the Same Population.Yap ZM, Sun KM, Teo CR, Tan AS, Chong SS Eur. J. Haematol.2013
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High prevalence of adrenal insufficiency in patients with sickle cell disease: results from a community hospital in the u.s.Makino J, Ndzengue A, Adekolujo S, Tipu A, Dogar UM, Mezher H, Sivasambu B, Trauber D, Guillaume E, Jaffe EA, Shiferaw-Deribe Z Exp. Clin. Endocrinol. Diabetes2013
Use of Serum Iron Status and Hemoglobin A2 Levels for Discrimination Between Iron Deficiency and Thalassemia Minor.Aslan D Pediatr Hematol Oncol2013
Sickle erythrocytes target cytotoxics to hypoxic tumor microvessels and potentiate a tumoricidal response.Terman DS, Viglianti BL, Zennadi R, Fels D, Boruta RJ, Yuan H, Dreher MR, Grant G, Rabbani ZN, Moon E, Lan L, Eble J, Cao Y, Sorg B, Ashcraft K, Palmer G, Telen MJ, Dewhirst MW PLoS ONE2013
Cardiac and hepatic iron and ejection fraction in thalassemia major: Multicentre prospective comparison of combined Deferiprone and Deferoxamine therapy against Deferiprone or Deferoxamine Monotherapy.Pepe A, Meloni A, Rossi G, Cuccia L, D Ascola GD, Santodirocco M, Cianciulli P, Caruso V, Romeo MA, Filosa A, Pitrolo L, Putti MC, Peluso A, Campisi S, Missere M, Midiri M, Gulino L, Positano V, Lombardi M, Ricchi P J Cardiovasc Magn Reson2013
Locus of control, depression and quality of life among persons with sickle cell disease in Jamaica.Gibson RC, Morgan KA, Abel WD, Sewell CA, Martin JS, Lowe GA, Haye WD, Edwards CL, O'Garo KN, Reid ME, Asnani MR Psychol Health Med2013
Craniofacial bone infarcts in sickle cell disease: clinical and radiological manifestations.Watanabe M, Saito N, Nadgir RN, Liao JH, Flower EN, Steinberg MH, Sakai O J Comput Assist Tomogr2013
The spectrum of β-thalassemia mutations in Gaza Strip, Palestine.Sirdah MM, Sievertsen J, Al-Yazji MS, Tarazi IS, Al-Haddad RM, Horstmann RD, Timmann C Blood Cells Mol. Dis.2013
Comparison of discriminative indices for iron deficiency anemia and β thalassemia trait in a Brazilian population.Matos JF, Dusse LM, Stubbert RV, Ferreira MR, Coura-Vital W, Fernandes AP, de Faria JR, Borges KB, Carvalho MD Hematology2013
Association between Sickle Cell Anemia and Pulp Necrosis.Costa CP, Thomaz EB, Souza Sde F J Endod2013
Systematic review of current and emerging strategies for reducing morbidity from malaria in sickle cell disease.Aneni EC, Hamer DH, Gill CJ Trop. Med. Int. Health2013
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Management of Hepatocellular Carcinoma in Homozygous β-Thalassemia Cirrhotic Patients.Gomatos IP, Alexakis N, Koskinas J, Smparounis SA, Katsaragakis S, Konstadoulakis MM, Zografos GC Am Surg2013
Induction of human fetal hemoglobin expression by denosine-2[prime],3[prime]-dialdehyde.He Y, Rank G, Zhang M, Ju J, Liu R, Xu Z, Brown F, Cerruti L, Ma C, Tan R, Jane SM, Zhao Q J Transl Med2013
Sickle Cell Disease in Pregnancy: Maternal Complications in a Medicaid-Enrolled Population.Boulet SL, Okoroh EM, Azonobi I, Grant A, Craig Hooper W Matern Child Health J2013
Clinical experience with fetal hemoglobin induction therapy in patients with β-thalassemia.Musallam KM, Taher AT, Cappellini MD, Sankaran VG Blood2013
Hypoxia Biomarkers, Oxidative Stress, and Circulating Microparticles in Pediatric Patients With Thalassemia in Upper Egypt.Elsayh KI, Zahran AM, El-Abaseri TB, Mohamed AO, El-Metwally TH Clin. Appl. Thromb. Hemost.2013
Hemoglobin variants and high-performance liquid chromatography.Nair S, Nadkarni AH, Ghosh K, Colah R Int J Lab Hematol2013
Genetic Heterogeneity of Beta Globin Mutations among Asian-Indians and Importance in Genetic Counselling and Diagnosis.Kumar R, Singh K, Panigrahi I, Agarwal S Mediterr J Hematol Infect Dis2013
Beta thalassemia major in a developing country: epidemiological, clinical and evolutionary aspects.Bejaoui M, Guirat N Mediterr J Hematol Infect Dis2013
Age at diagnosis of sickle cell anaemia in lagos, Nigeria.Akodu S, Diaku-Akinwumi I, Njokanma O Mediterr J Hematol Infect Dis2013
Characterization of Adult α- and β-Globin Elevated by Hydrogen Peroxide in Cervical Cancer Cells That Play A Cytoprotective Role Against Oxidative Insults.Li X, Wu Z, Wang Y, Mei Q, Fu X, Han W PLoS ONE2013
Erythrocyte NADPH oxidase activity modulated by Rac GTPases, PKC, and plasma cytokines contributes to oxidative stress in sickle cell disease.George A, Pushkaran S, Konstantinidis DG, Koochaki S, Malik P, Mohandas N, Zheng Y, Joiner CH, Kalfa TA Blood2013
Hair-on-end appearance in a case of thalassemia intermedia.Balikar R, Redkar NN, Patil MA, Pillai R BMJ Case Rep2013
Hemodynamic Predictors of Mortality in Adults with Sickle Cell Disease.Mehari A, Alam S, Tian X, Cuttica MJ, Barnett CF, Miles G, Xu D, Seamon C, Adams-Graves P, Castro OL, Minniti CP, Sachdev V, Taylor Vi JG, Kato GJ, Machado RF Am. J. Respir. Crit. Care Med.2013
Care Seeking for Pain in Young Adults with Sickle Cell Disease.Jenerette CM, Brewer CA, Ataga KI Pain Manag Nurs2013
Sickle Cell Disease with Double Stroke in a Moroccan Family.Hamzi K, Itto AB, Jouhadi Z, Slassi I, Nadifi S J. Mol. Neurosci.2013
Epidemiology of Bloodstream Infections in Children with Sickle Cell Disease.Ellison AM, Ota KV, McGowan KL, Smith-Whitley K Pediatr. Infect. Dis. J.2013
Triplex-forming Peptide Nucleic Acids Induce Heritable Elevations in Gamma-globin Expression in Hematopoietic Progenitor Cells.Chin JY, Reza F, Glazer PM Mol. Ther.2013
Successful Unrelated Cord Blood Transplantation For Homozygous α-Thalassemia.Gumuscu B, Thompson EI, Grovas AC, Zach TL, Warkentin PI, Coccia PF J. Pediatr. Hematol. Oncol.2013
Gene therapy for hemoglobinopathies: progress and challenge.Dong A, Rivella S, Breda L Transl Res2013
Serial echocardiographic left ventricular ejection fraction measurements: A tool for detecting thalassemia major patients at risk of cardiac death.Maggio A, Vitrano A, Calvaruso G, Barone R, Rigano P, Mancuso L, Cuccia L, Capra M, Pitrolo L, Prossomariti L, Filosa A, Caruso V, Gerardi C, Campisi S, Cianciulli P, Elefteriou A, Angastiniotis M, Hamza H, Telfer P, Walker JM, Phrommintikul A, Chattipakorn N Blood Cells Mol. Dis.2013
Age-related treatment patterns in sickle cell disease patients and the associated sickle cell complications and healthcare costs.Blinder MA, Vekeman F, Sasane M, Trahey A, Paley C, Duh MS Pediatr Blood Cancer2013
Thirty years experience in preventing haemoglobinopathies in Greece: achievements and potentials for optimization.Ladis V, Karagiorga-Lagana M, Tsatra I, Chouliaras G Eur. J. Haematol.2013
Incidence, Risk Factors, and Outcome of Portal Vein Thrombosis After Laparoscopic-Assisted Splenectomy in β-Thalassemia Patients: A Prospective Exploratory Study.Alexakis N, Dardamanis D, Albanopoulos K, Ptohis N, Skalistira M, Karagiorga M, Zografos G, Leandros E J Laparoendosc Adv Surg Tech A2013
Redox Reactions of Hemoglobin: Mechanisms of Toxicity and Control.Mollan T, Alayash AI Antioxid. Redox Signal.2013
In vivo comparison of myocardial T1 with T2 and T2* in thalassaemia major.Feng Y, He T, Carpenter JP, Jabbour A, Alam MH, Gatehouse PD, Greiser A, Messroghli D, Firmin DN, Pennell DJ J Magn Reson Imaging2013
1,25-Dihydroxyvitamin D(3) -induced intestinal calcium transport is impaired in β-globin knockout thalassemic mice.Charoenphandhu N, Kraidith K, Teerapornpuntakit J, Thongchote K, Khuituan P, Svasti S, Krishnamra N Cell Biochem. Funct.2013
Doppler Ultrasound Velocimetry of Middle Cerebral Arteries of Patients With Sickle Cell Disease at Aminu Kano Teaching Hospital: A Preliminary Report.Tabari AM, Ismail A Ultrasound Q2013
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Stem cell transplantation after reduced intensity conditioning for sickle cell disease.Matthes-Martin S, Lawitschka A, Fritsch G, Lion T, Grimm B, Breuer S, Boztug H, Karlhuber S, Holter W, Peters C, Minkov M Eur. J. Haematol.2013
Hb Plasencia [α125(H8)Leu→Arg (α2)] is a Frequent Cause of α(+)-Thalassemia in the Portuguese Population.Cunha E, Bento C, Oliveira A, Relvas L, Neves J, Gameiro M, Barros C, Araújo A, Macedo A, Rocha P, Costa R, Maia T, Ribeiro ML Hemoglobin2013
Comparative Assessment of Deferiprone and Deferasirox in Thalassemia Major Patients in the First Two Decades-Single Centre Experience.Zachariah M, Tony S, Bashir W, Al Rawas A, Wali Y, Pathare A Pediatr Hematol Oncol2013
Strokes and hemoglobinopathies in Burkina Faso.Napon C, Kaboré A, Ouédraogo M, Dravé A, Lompo L, Kaboré J Med Sante Trop2013
Changes of Bone Density in Pediatric Patients with β-thalassemia Major after Allogenic Hematopoietic Stem Cell Transplantation.Hamidieh AA, Hamidi Z, Nedaeifard L, Heshmat R, Alimoghaddam K, Larijani B, Ghavamzadeh A, Mohajeri-Tehrani MR Arch Iran Med2013
Microdeletion Of Exon 3 In The HBA2 Gene Associated With Mild α-Thalassemia Trait.Lambert A, Wong AY, Kominami Y, Smith VC, Reddy S, Wadsworth LD, Au NH, Macgillivray RT Hemoglobin2013
Influence of Lime Juice on the Severity of Sickle Cell Anemia.Adegoke SA, Shehu UA, Mohammed LO, Sanusi Y, Oyelami OA J Altern Complement Med2013
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The Transfusion Alternatives Preoperatively in Sickle Cell Disease (TAPS) study: a randomised, controlled, multicentre clinical trial.Howard J, Malfroy M, Llewelyn C, Choo L, Hodge R, Johnson T, Purohit S, Rees DC, Tillyer L, Walker I, Fijnvandraat K, Kirby-Allen M, Spackman E, Davies SC, Williamson LM Lancet2013
Preoperative transfusion in patients with sickle-cell disease.Goldsmith JC, Wang WC Lancet2013
Hb Treviso [α91(FG3)Leu→Phe (α2)]: A New Slightly Unstable Hemoglobin Variant with Moderately Decreased Oxygen Affinity.Barberio G, Leone D, Ivaldi G, Giordano PC Hemoglobin2013
Low cost biosensor-based molecular differential diagnosis of α-thalassemia (Southeast Asia deletion).Wangmaung N, Promptmas C, Chomean S, Sanchomphu C, Ittarat W Clin. Chem. Lab. Med.2013
Detection of Hb Constant Spring [α142, Term→Gln, TAA>CAA (α2)] in Heterozygotes Combined With β-Thalassemia.Li YQ, Li R, Li DZ Hemoglobin2013
Gγ-Xmn I Polymorphism: A Significant Determinant of β-Thalassemia Treatment Without Blood Transfusion.Ansari SH, Shamsi TS, Munzir S, Khan MT, Erum S, Perveen K, Farzana T, Ashraf M, Mehboob T, Moinuddin M J. Pediatr. Hematol. Oncol.2013
Hemoglobin Variants: Biochemical Properties and Clinical Correlates.Thom CS, Dickson CF, Gell DA, Weiss MJ Cold Spring Harb Perspect Med2013
Fetal Myocardial Performance (Tei) Index in Fetal Hemoglobin Bart's Disease.Luewan S, Tongprasert F, Srisupundit K, Tongsong T Ultraschall Med2013
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Trends in hospital admissions for sickle cell disease in England.Aljuburi G, Majeed A J Public Health (Oxf)2013
Trends in hospital admissions for sickle cell disease in England.Latinovic R, Streetly A J Public Health (Oxf)2013
Protection from sickle cell retinopathy is associated with elevated HbF levels and hydroxycarbamide use in children.Estepp JH, Smeltzer MP, Wang WC, Hoehn ME, Hankins JS, Aygun B Br. J. Haematol.2013
Hemoglobinopathy: molecular epidemiological characteristics and health effects on hakka people in the meizhou region, southern china.Lin M, Wen YF, Wu JR, Wang Q, Zheng L, Liu GR, Huang Y, Yang H, Lin F, Zhan XF, Lin CP, Yang HT, Weng QQ, Huang FT, Wang Y, Yao MQ, Chen HZ, Wu DH, Zeng JB, Zeng RX, Yang H, Li GC, Lu M, Zhu JJ, Xie LX, Wang JL, Yang LY PLoS ONE2013
Protection against Oxidative Stress in Beta Thalassemia/Hemoglobin E Erythrocytes by Inhibitors of Glutathione Efflux Transporters.Muanprasat C, Wongborisuth C, Pathomthongtaweechai N, Satitsri S, Hongeng S PLoS ONE2013
Effects of adenotonsillectomy on polysomnographic parameters in children with sickle cell disease.Finch P, Stocks RM, Smeltzer MP, Kimble A, Schoumacher R, Hankins JS Pediatr Blood Cancer2013
The impact of race and disease on sickle cell patient wait times in the emergency department.Haywood C, Tanabe P, Naik R, Beach MC, Lanzkron S Am J Emerg Med2013
Cost utility analysis of reduced intensity hematopoietic stem cell transplantation in adolescence and young adult with severe thalassemia compared to hypertransfusion and iron chelation program.Sruamsiri R, Chaiyakunapruk N, Pakakasama S, Sirireung S, Sripaiboonkij N, Bunworasate U, Hongeng S BMC Health Serv Res2013
Visual Diagnosis: A 31/2-year-old Boy With Sickle β-Thalassemia and a Groin Mass.Bagchi A, Elnawawi A, Sadanandan S Pediatr Rev2013
The prevention of thalassemia.Cao A, Kan YW Cold Spring Harb Perspect Med2013
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Hepatitis C in patients with β-thalassemia major. A single-centre experience.Triantos C, Kourakli A, Kalafateli M, Giannakopoulou D, Koukias N, Thomopoulos K, Lampropoulou P, Bartzavali C, Fragopanagou H, Kagadis GC, Christofidou M, Tsamandas A, Nikolopoulou V, Karakantza M, Labropoulou-Karatza C Ann. Hematol.2013
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Human T-cell lymphotropic virus type 1 Infection among U.S. Thalassemia Patients.Switzer W, Shankar A, Trimble S, Thompson AA, Giardina PJ, Cohen AR, Coates TD, Vichinsky E, Neufeld EJ, Boudreaux JM, Heneine PW AIDS Res. Hum. Retroviruses2013
Candidate sequence variants and fetal hemoglobin in children with sickle cell disease treated with hydroxyurea.Green NS, Ender KL, Pashankar F, Driscoll C, Giardina PJ, Mullen CA, Clark LN, Manwani D, Crotty J, Kisselev S, Neville KA, Hoppe C, Barral S PLoS ONE2013
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Fetal hemoglobin and hydroxycarbamide modulate both plasma concentration and cellular origin of circulating microparticles in sickle cell anemia children.Nébor D, Romana M, Santiago R, Vachiery N, Picot J, Broquere C, Chaar V, Doumdo L, Odièvre MH, Benkerrou M, Elion J Haematologica2013
Busulfan, Fludarabine and Alemtuzumab Conditioning and Unrelated Cord Blood Transplantation in Children with Sickle Cell Disease.Radhakrishnan K, Bhatia M, Geyer MB, Del Toro G, Jin Z, Baker C, Harrison L, Morris E, Baxter-Lowe LA, Cairo MS Biol. Blood Marrow Transplant.2013
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Novel Mutations Responsible for α-Thalassemia in Iranian Families.Bayat N, Farashi S, Hafezi-Nejad N, Faramarzi N, Ashki M, Vakili S, Imanian H, Khosravi M, And AA, Najmabadi H Hemoglobin2013
Thyroid function status and echocardiographic abnormalities in patients with Beta thalassemia major in bahrain.Garadah TS, Mahdi NA, Jaradat AM, Hasan ZA, Nagalla DS Clin Med Insights Cardiol2013
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Breast cancer in patients with sickle cell disease can be treated safely with weekly paclitaxel.Al Zaman AS Saudi Med J2013
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A simple, rapid, low-cost diagnostic test for sickle cell disease.Yang X, Kanter J, Piety NZ, Benton MS, Vignes SM, Shevkoplyas SS Lab Chip2013
High Throughput Molecular Confirmation of β-Thalassemia Mutations Using Novel TaqMan Probes.Kho SL, Chua KH, George E, Tan JA Sensors (Basel)2013
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Evaluation of the 5mg/g liver iron concentration threshold and its association with morbidity in patients with β-thalassemia intermedia.Musallam KM, Cappellini MD, Taher AT Blood Cells Mol. Dis.2013
Association in Cis of the Mutations +20 (C>T) in the 5' Untranslated Region and IVS-II-745 (C>G) on the β-Globin Gene.Ropero P, González FA, Cela E, Beléndez C, Cervera A, Martínez-Nieto J, Fuente-Gonzalo FD, Vinuesa L, Villegas A, Díaz-Mediavilla J Hemoglobin2013
Misdiagnosis of Hb D-Punjab/β-Thalassemia is a Potential Pitfall in Hemoglobinopathy Screening Programs: A Case Report.Belhoul KM, Bakir ML, Abdulrahman M Hemoglobin2013
Prevalence and Molecular Characterization of β-Thalassemia in the State of Bahia, Brazil: First Identification of Mutation HBB: c.135delC in Brazil.Fonseca SF, Moura Neto JP, Goncalves MS Hemoglobin2013
Risk Adopted Allogeneic Hematopoietic Stem Cell Transplantation Using a Reduced Intensity Regimen for Children with Thalassemia Major.Hussein AA, Al-Zaben A, Ghatasheh L, Natsheh A, Hammada T, Abdel-Rahman F, Abu-Jazar H, Sharma S, Najjar R, Frangoul H Pediatr Blood Cancer2013
Genetic mapping and exome sequencing identify two mutations associated with stroke protection in pediatric patients with sickle cell anemia.Flanagan JM, Sheehan V, Linder H, Howard TA, Wang YD, Hoppe CC, Aygun B, Adams RJ, Neale GA, Ware RE Blood2013
Wandering Pneumonia, Recurrent Hemoptysis, and Anemia in a Child With Sickle Cell Trait.Chauhan A, Urrego F, Warrier R Clin Pediatr (Phila)2013
Spectrum of α-thalassemia mutations including first observation of - -(FIL) deletion in Hatay Province, Turkey.Celik MM, Gunesacar R, Oktay G, Duran GG, Kaya H Blood Cells Mol. Dis.2013
Cerebral blood flow abnormalities in children with sickle cell disease: a systematic review.Behpour AM, Shah PS, Mikulis DJ, Kassner A Pediatr. Neurol.2013
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Sickle cell disease in pregnancy: trend and pregnancy outcomes at a tertiary hospital in Tanzania.Muganyizi PS, Kidanto H PLoS ONE2013
Retinal changes in children and adolescents with sickle cell disease attending a paediatric hospital in Cairo, Egypt: risk factors and relation to ophthalmic and cerebral blood flow.Tantawy AA, Andrawes NG, Adly AA, El Kady BA, Shalash AS Trans. R. Soc. Trop. Med. Hyg.2013
Exploring barriers and facilitators to clinical trial enrollment in the context of sickle cell anemia and hydroxyurea.Lebensburger JD, Sidonio RF, Debaun MR, Safford MM, Howard TH, Scarinci IC Pediatr Blood Cancer2013
Long Term Outcome and Evaluation of Organ Function in Pediatric Patients Undergoing Haploidentical and Matched Related Hematopoietic Cell Transplantation for Sickle Cell Disease.Dallas M, Triplett B, Shook D, Hartford C, Srinivasan A, Laver J, Ware R, Leung W Biol. Blood Marrow Transplant.2013
Wandering Spleen Associated With β-Thalassemia: A Case Report.Akhter MQ, Authoy F, Nabi J, Rahman MR, Hossain I, Hossain MM, Mamun AA, Chakrabarty P Mymensingh Med J2013
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A double-blind, randomized, multicenter phase 2 study of prasugrel versus placebo in adult patients with sickle cell disease.Wun T, Soulieres D, Frelinger AL, Krishnamurti L, Novelli EM, Kutlar A, Ataga KI, Knupp CL, McMahon LE, Strouse JJ, Zhou C, Heath LE, Nwachuku CE, Jakubowski JA, Riesmeyer JS, Winters KJ J Hematol Oncol2013
Natural history of hepatitis C in thalassemia major : a long-term prospective study.Eliana LM, Raffaella O, Fabrice D, Battista LG, Stefania V, Franco A, Claudia C, Patrizia F, Giovanna C, Renzo G Eur. J. Haematol.2013
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Mortality rates and age at death from sickle cell disease: u.s., 1979-2005.Lanzkron S, Carroll CP, Haywood C Public Health Rep2013
Acquired hemoglobin variants and exposure to glucose-6-phosphate dehydrogenase deficient red blood cell units during exchange transfusion for sickle cell disease in a patient requiring antigen-matched blood.Raciti PM, Francis RO, Spitalnik PF, Schwartz J, Jhang JS J Clin Apher2013
Assessment of communication modes in patients and families with sickle cell disease.Anderson C, Torres S, Gokuli S, Brandow AM, Panepinto JA Pediatr Blood Cancer2013
Mi2β-mediated silencing of the fetal γ-globin gene in adult erythroid cells.Amaya M, Desai M, Gnanapragasam MN, Wang SZ, Zhu SZ, Williams DC, Ginder GD Blood2013
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Haemoglobin variants among voluntary blood donors in Jos, Nigeria: the implications on blood transfusion.Damulak OD, Bolorunduro SA, Egesie JO, Yakubu K, Godit P, Smith OA Niger J Med2013
Value of magnetic resonance imaging T2* tests in detecting heart and liver iron overload in patients with β-thalassemia major.Wu XD, Jing YF, Pei FY, Chen JQ, Feng XQ, He YL, Zhang YM, Li CF Nan Fang Yi Ke Da Xue Xue Bao2013
PedsQL™ Sickle Cell Disease Module: Feasibility, Reliability, and Validity.Panepinto JA, Torres S, Bendo CB, McCavit TL, Dinu B, Sherman-Bien S, Bemrich-Stolz C, Varni JW Pediatr Blood Cancer2013
Antibiotics for treating acute chest syndrome in people with sickle cell disease.Martí-Carvajal AJ, Conterno LO, Knight-Madden JM Cochrane Database Syst Rev2013
Phytomedicines (medicines derived from plants) for sickle cell disease.Oniyangi O, Cohall DH Cochrane Database Syst Rev2013
Sistani Population: a Different Spectrum oF β-Thalassemia Mutations From other Ethnic Groups of Iran.Miri-Moghaddam E, Zadeh-Vakili A, Nikravesh A, Sanei Sistani S, Naroie-Nejad M Hemoglobin2013
Daytime pulse oximetry measurements may not predict nocturnal desaturations in adult sickle cell patients.Mehta H, Efird JT, Kadali RA, Boettger P, Liles D, Knupp C, Sharma S Ann. Hematol.2013
Sickle cell disease and venous thromboembolism: what the anticoagulation expert needs to know.Naik RP, Streiff MB, Lanzkron S J. Thromb. Thrombolysis2013
Sickle Cell Disease and Perioperative Considerations: Review and Retrospective Report.Stanley AC, Christian JM J. Oral Maxillofac. Surg.2013
Renal tubular dysfunction in children with sickle cell heamoglobinopathy.Badr M, El Koumi MA, Ali YF, Almonem NA, Hassan T, El-Morshedy S, El Rahman RA, Afify M Nephrology (Carlton)2013
Codon 62 (GTG>GCG, Val→Ala) (α1) (HBA1: c.188T>C) Causing Nondeletional α-Thalassemia in a Chinese Family.Liao C, Tang HS, Li R, Li DZ Hemoglobin2013
Identification of the First Mutation in a Bre Motif of the β-Globin Gene and its Inheritance with two Other α-Globin Gene Mutations in a Lebanese Family.Inati A, Abbas HA, Al-Danaf J, Souaid M, Kahale M, Koussa S, Nasr TA, Davis L, Luo HY, Chui DH Hemoglobin2013
Thalassemia and premarital screening: potential for implementation of a screening program among young people in pakistan.Mirza A, Ghani A, Pal A, Sami A, Hannan S, Ashraf Z, Iqbal S, Malik UZ, Hayat U, Fatmi Z Hemoglobin2013
Secular trends in the national and provincial births of new thalassemia cases in iran from 2001 to 2006.Hadipour Dehshal M, Ahmadvand A, Yousefi Darestani S, Manshadi M, Abolghasemi H Hemoglobin2013
Platelet Activation and Inhibition iN Sickle cell disease (PAINS) study.Frelinger AL, Jakubowski JA, Brooks JK, Carmichael SL, Berny-Lang MA, Barnard MR, Heeney MM, Michelson AD Platelets2013
Two decades of pre-marital screening for beta-thalassemia in central Iran.Zeinalian M, Nobari RF, Moafi A, Salehi M, Hashemzadeh-Chaleshtori M J Community Genet2013
Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype.Ngo D, Bae H, Steinberg MH, Sebastiani P, Solovieff N, Baldwin CT, Melista E, Safaya S, Farrer LA, Al-Suliman AM, Albuali WH, Al Bagshi MH, Naserullah Z, Akinsheye I, Gallagher P, Luo HY, Chui DH, Farrell JJ, Al-Ali AK, Alsultan A Blood Cells Mol. Dis.2013
Diminishing bias in sickle cell disease.Stewart R, Whiteman L Med Teach2013
Weight Status of Children With Sickle Cell Disease.Chawla A, Sprinz PG, Welch J, Heeney M, Usmani N, Pashankar F, Kavanagh P Pediatrics2013
Hemoglobin Shady Grove: A Novel Fetal Methemoglobin Variant.Marks A, Luo HY, Chui DH, Greenberg J Pediatr Blood Cancer2013
"You Just Have to Live With It": Coping With Sickle Cell Disease in Jamaica.Anderson M, Asnani M Qual Health Res2013
Predictors of Academic Achievement for School Age Children with Sickle Cell Disease.Smith KE, Patterson CA, Szabo MM, Tarazi RA, Barakat LP Adv Sch Ment Health Promot2013
Distinct sonographic features of acute appendicitis in sickle cell disease.Monib S, Donkol RH, Hassan A, Riaz AA Ann Saudi Med2013
Prevalence of iron overload complications among patients with b-thalassemia major treated at Dubai Thalassemia Centre.Belhoul KM, Bakir ML, Kadhim AM, Dewedar HE, Eldin MS, Alkhaja FA Ann Saudi Med2013
A review of acute chest syndrome in pediatric sickle cell disease.Abbas HA, Kahale M, Hosn MA, Inati A Pediatr Ann2013
Determining and Surveying the Role of Carnitine and Folic Acid to Decrease Fatigue in β-Thalassemia Minor Subjects.Tabei SM, Mazloom M, Shahriari M, Zareifar S, Azimi A, Hadaegh A, Karimi M Pediatr Hematol Oncol2013
Daily changes in pain, mood and physical function in children hospitalized for sickle cell disease pain.Zempsky WT, Palermo TM, Corsi JM, Lewandowski AS, Zhou C, Casella JF Pain Res Manag2013
Understanding the experiences of youth living with sickle cell disease: a photovoice pilot.Valenzuela JM, Vaughn LM, Crosby LE, Strong H, Kissling A, Mitchell MJ Fam Community Health2013
Multifocal osteoarticular infection caused by Salmonella non typhi in a child with sickle cell disease.Cabaret B, Couëc ML, Lorrot M, Launay E, Gras-Le Guen C Arch Pediatr2013
Sudden death in a case of sickle cell anemia: Post-mortem computed tomography and autopsy correlation from a radiologist's perspective.Abdul Rashid SN, Krauskopf A, Vonlanthen B, Thali MJ, Ruder TD Leg Med (Tokyo)2013
Hematological and hemorheological determinants of resting and exercise-induced hemoglobin oxygen desaturation in children with sickle cell disease.Waltz X, Romana M, Lalanne-Mistrih ML, Machado RF, Lamarre Y, Tarer V, Hardy-Dessources MD, Tressieres B, Divialle-Doumdo L, Petras M, Maillard F, Etienne-Julan M, Connes P Haematologica2013
Bone Mineral Density Patterns in Vitamin D Deficient African American Men With Sickle Cell Disease.Adams-Graves P, Daniels AB, Womack CR, Freire AX Am. J. Med. Sci.2013
Evaluation of h3 histone methylation and colony formation in erythroid progenitors treated with thalidomide and sodium butyrate.Fard AD, Kaviani S, Noruzinia M, Soleimani M, Abroun S, Chegeni R, Hajifathali A, Zonoubi Z, Ahmadvand M, Mohammadi MM, Saki N Lab Hematol2013
A pharmaco-economic evaluation of deferasirox for treating patients with iron overload caused by transfusion-dependent thalassemia in Taiwan.Ho WL, Chung KP, Yang SS, Lu MY, Jou ST, Chang HH, Yang YL, Lin DT, Lin KH J. Formos. Med. Assoc.2013
Novel Single Cell Functional Analysis of Red Blood Cells using Laser Tweezers Raman Spectroscopy: Application for Sickle Cell Disease.Liu R, Mao Z, Matthews DL, Li CS, Chan JW, Satake N Exp. Hematol.2013
The acute chest syndrome of sickle cell disease.Desai PC, Ataga KI Expert Opin Pharmacother2013
Updated role of nitric oxide in disorders of erythrocyte function.Kahn MJ, Maley JH, Lasker GF, Kadowitz PJ Cardiovasc Hematol Disord Drug Targets2013
Establishment of immortalized human erythroid progenitor cell lines able to produce enucleated red blood cells.Kurita R, Suda N, Sudo K, Miharada K, Hiroyama T, Miyoshi H, Tani K, Nakamura Y PLoS ONE2013
Thrombin Generation in Children with Sickle Cell Disease: Relationship with Age, Hemolysis, Transcranial Doppler Velocity and Hydroxyurea Treatment.Noubouossie DC, Lê PQ, Rozen L, Ziereisen F, Willems D, Demulder A, Ferster A Eur. J. Haematol.2013
Sickle cell disease--the American saga.Siddiqi AE, Jordan LB, Parker CS Ethn Dis2013
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Generation of Transgene-free Induced Pluripotent Stem Cells with Non-viral Methods.Wang T, Zhao HS, Zhang QL, Xu CL, Chang-Bai Liu A Chin. Med. Sci. J.2013
Pilot Study of Human Recombinant Hyaluronidase-Enhanced Subcutaneous Hydration and Opioid Administration for Sickle Cell Disease Acute Pain Episodes.Sandoval M, Coleman P, Govani R, Siddiqui S, Todd KH J Pain Palliat Care Pharmacother2013
Among emergency physicians, use of the term 'Sickler' is associated with negative attitudes towards people with sickle cell disease.Jeffrey G, Paula T, Lynne R, Michael D Am. J. Hematol.2013
Phenotypic and molecular changes of hemoglobinopathies in cancer.Abaza H, Gara Y, Ben Chaabene A, Douik H, Harzallah L, Boussen H, Guemira F Tunis Med2013
Problems in determining thalassemia carrier status in a program for prevention and control of severe thalassemia syndromes: a lesson from Thailand.Viprakasit V, Limwongse C, Sukpanichnant S, Ruangvutilert P, Kanjanakorn C, Glomglao W, Sirikong M, Utto W, Tanphaichitr VS Clin. Chem. Lab. Med.2013
Detection of fetal mutations causing hemoglobinopathies by non-invasive prenatal diagnosis from maternal plasma.D'Souza E, Sawant PM, Nadkarni AH, Gorakshakar A, Ghosh K, Colah RB J Postgrad Med2013
Reducing TMPRSS6 ameliorates hemochromatosis and β-thalassemia in mice.Guo S, Casu C, Gardenghi S, Booten S, Aghajan M, Peralta R, Watt A, Freier S, Monia BP, Rivella S J. Clin. Invest.2013
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Tertiary and quaternary effects in the allosteric regulation of animal hemoglobins.Ronda L, Bruno S, Bettati S Biochim. Biophys. Acta2013
Erythroid transcription factor EKLF/KLF1 mutation causing congenital dyserythropoietic anemia type IV in a patient of Taiwanese origin: Review of all reported cases and development of a clinical diagnostic paradigm.Jaffray JA, Mitchell WB, Gnanapragasam MN, Seshan SV, Guo X, Westhoff CM, Bieker JJ, Manwani D Blood Cells Mol. Dis.2013
Complex neonatal hemoglobin pattern due to co-inheritance of Hb Q-Thailand and Hb E.van Gammeren AJ, Jonkers M, Harteveld CL Int J Lab Hematol2013
Macrophages support pathological erythropoiesis in polycythemia vera and β-thalassemia.Ramos P, Casu C, Gardenghi S, Breda L, Crielaard BJ, Guy E, Marongiu MF, Gupta R, Levine RL, Abdel-Wahab O, Ebert BL, Van Rooijen N, Ghaffari S, Grady RW, Giardina PJ, Rivella S Nat. Med.2013
Prevalence of HBsAg and anti-HCV antibodies in homozygous sickle cell patients at Yaounde Central Hospital.Sack FN, Noah DN, Zouhaïratou H, Mbanya D Pan Afr Med J2013
Blood transfusion among thalassemia patients: A single Egyptian center experience.Ragab LA, Hamdy MM, Shaheen IA, Yassin RN Asian J Transfus Sci2013
Prevalence of common hemoglobin variants in an afro-descendent Ecuadorian population.Domínguez Y, Zurita C, Calvopiña D, Villacís J, Mora M BMC Res Notes2013
Genetic compound heterozygosity for Southeast Asian ovalocytosis and thalassemia in Thailand: prevalence and phenotypic analysis.Ngouprommin L, Sae-Ung N, Fucharoen S, Fucharoen G, Sanchaisuriya K, Jetsrisuparb A Clin. Genet.2013
Genomic variation in the MAP3K5 gene is associated with β-thalassemia disease severity and hydroxyurea treatment efficacy.Tafrali C, Paizi A, Borg J, Radmilovic M, Bartsakoulia M, Giannopoulou E, Giannakopoulou O, Stojiljkovic-Petrovic M, Zukic B, Poulas K, Stavrou EF, Lambropoulou P, Kourakli A, Felice AE, Papachatzopoulou A, Philipsen S, Pavlovic S, Georgitsi M, Patrinos GP Pharmacogenomics2013
Relationship between Malaria Incidence and IgG Levels to Plasmodium falciparum Merozoite Antigens in Malian Children: Impact of Hemoglobins S and C.Miura K, Diakite M, Diouf A, Doumbia S, Konate D, Keita AS, Moretz SE, Tullo G, Zhou H, Lopera-Mesa TM, Anderson JM, Fairhurst RM, Long CA PLoS ONE2013
Haptoglobin Preferentially Binds β but Not α Subunits Cross-Linked Hemoglobin Tetramers with Minimal Effects on Ligand and Redox Reactions.Jia Y, Wood F, Buehler PW, Alayash AI PLoS ONE2013
Biomarkers of hypochromia: the contemporary assessment of iron status and erythropoiesis.Urrechaga E, Borque L, Escanero JF Biomed Res Int2013
Deferasirox demonstrates a dose-dependent reduction in liver iron concentration and consistent efficacy across subgroups of non-transfusion-dependent thalassemia (NTDT) patients.Taher AT, Porter JB, Viprakasit V, Kattamis A, Chuncharunee S, Sutcharitchan P, Siritanaratkul N, Galanello R, Karakas Z, Lawniczek T, Habr D, Ros J, Zhang Y, Cappellini MD Am. J. Hematol.2013
Left ventricular hypertrabeculation / noncompaction in beta-thalassemia.Finsterer J, Stöllberger C Am. J. Hematol.2013
Effectiveness of the model for prenatal control of severe thalassemia.Tongsong T, Charoenkwan P, Sirivatanapa P, Wanapirak C, Piyamongkol W, Sirichotiyakul S, Srisupundit K, Tongprasert F, Luewan S, Ratanasiri T, Komwilaisak R, Saksiriwuttho P, Vuthiwong C, Punpuckdeekoon P, Panichkul P, Rueangchainikhom W, Choowong J, Orungrote N, Sarapak S, Kovavisarach E, Jaruyawongs P, Tansathit T, Phadungkiatwattana P, Rujiwetpongstorn J, Kor-Anantakul O, Suwanrath C, Hanprasertpong T, Pranpanus S Prenat. Diagn.2013
Asymmetric Dimethylarginine levels in Children with Sickle Cell Disease and its Correlation to Tricuspid Regurgitant Jet Velocity.El-Shanshory M, Badraia I, Donia A, Abd El-Hameed F, Mabrouk M Eur. J. Haematol.2013
Preimplantation genetic diagnosis, an alternative to conventional prenatal diagnosis of the hemoglobinopathies.Traeger-Synodinos J Int J Lab Hematol2013
New insights into sickle cell disease: a disease of hypoxia.Sun K, Xia Y Curr. Opin. Hematol.2013
Intra-Abdominal Umbilical Vein Varix Associated with Fetal Cardiac Failure: A Pitfall to the Prenatal Diagnosis of Alpha-Zero-Thalassemia.Rosenblatt J, Loberstajn A, Coulomb A, Stos B, Garel C, Abarah B, Bénifla JL, Jouannic JM Fetal. Diagn. Ther.2013
Angiotensin-converting enzyme (ACE) inhibitors for proteinuria and microalbuminuria in people with sickle cell disease.Sasongko TH, Nagalla S, Ballas SK Cochrane Database Syst Rev2013
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Intrafamilial Transmission of Hepatitis C Infection in Egyptian Multitransfused Thalassemia Patients.Said F, El Beshlawy A, Hamdy M, El Raziky M, Sherif M, Abdel Kader A, Ragab L J. Trop. Pediatr.2013
Fetal Haemoglobin and β-globin Gene Cluster Haplotypes among Sickle Cell Patients in Chhattisgarh.Bhagat S, Patra PK, Thakur AS J Clin Diagn Res2013
The influence of the BCL11A polymorphism on the phenotype of patients with beta thalassemia could be affected by the beta globin locus control region and/or the Xmn1-HBG2 genotypic background.Neishabury M, Zamani F, Keyhani E, Azarkeivan A, Abedini SS, Eslami MS, Kakroodi ST, Vesiehsari MJ, Najmabadi H Blood Cells Mol. Dis.2013
Next generation sequencing of SNPs for non-invasive prenatal diagnosis: challenges and feasibility as illustrated by an application to β-thalassaemia.Papasavva T, van Ijcken WF, Kockx CE, van den Hout MC, Kountouris P, Kythreotis L, Kalogirou E, Grosveld FG, Kleanthous M Eur. J. Hum. Genet.2013
A randomized phase I/II trial of HQK-1001, an oral fetal globin gene inducer, in β-thalassaemia intermedia and HbE/β-thalassaemia.Fucharoen S, Inati A, Siritanaratku N, Thein SL, Wargin WC, Koussa S, Taher A, Chaneim N, Boosalis M, Berenson R, Perrine SP Br. J. Haematol.2013
Treating iron overload in patients with non-transfusion-dependent thalassemia.Taher AT, Viprakasit V, Musallam KM, Cappellini MD Am. J. Hematol.2013
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Efficacy and safety of deferasirox at low and high iron burdens: results from the EPIC magnetic resonance imaging substudy.Porter JB, Elalfy MS, Taher AT, Aydinok Y, Chan LL, Lee SH, Sutcharitchan P, Habr D, Martin N, El-Beshlawy A Ann. Hematol.2013
Beta-S globin haplotypes in patients with sickle cell anemia: one approach to understand the diversity in Brazil.Okumura JV, Lobo CL, Bonini-Domingos CR Rev Bras Hematol Hemoter2013
Protective effect of flavonoids against reactive oxygen species production in sickle cell anemia patients treated with hydroxyurea.Henneberg R, Otuki MF, Furman AE, Hermann P, do Nascimento AJ, Leonart MS Rev Bras Hematol Hemoter2013
Molecular matching of red blood cells is superior to serological matching in sickle cell disease patients.da Costa DC, Pellegrino J, Guelsin GA, Ribeiro KA, Gilli SC, Castilho L Rev Bras Hematol Hemoter2013
Impact of iron overload on interleukin-10 levels, biochemical parameters and oxidative stress in patients with sickle cell anemia.Barbosa MC, Dos Santos TE, de Souza GF, de Assis LC, Freitas MV, Gonçalves RP Rev Bras Hematol Hemoter2013
Oxidative stress in sickle cell disease.Queiroz RF, Lima ES Rev Bras Hematol Hemoter2013
Comments on: molecular matching of red blood cells is superior to serological matching in sickle cell disease patients.Nance ST, Keller MA Rev Bras Hematol Hemoter2013
Does increased red blood cell deformability raise the risk for osteonecrosis in sickle cell anemia?Lemonne N, Lamarre Y, Romana M, Mukisi-Mukaza M, Hardy-Dessources MD, Tarer V, Mougenel D, Waltz X, Tressières B, Lalanne-Mistrih ML, Etienne-Julan M, Connes P Blood2013
Umbilical Cord Blood: An Evolving Stem Cell Source for Sickle Cell Disease Transplants.Shenoy S Stem Cells Transl Med2013
Application of Multiplex Ligation-Dependent Probe Amplification to Screen for β-Globin Cluster Deletions: Detection of Two Novel Deletions in a Multi Ethnic Population.Cui J, Azimi M, Baysdorfer C, Vichinsky EP, Hoppe CC Hemoglobin2013
Neuropathic pain in sickle cell disease triggered by Pain-Ease™.Rastogi S, Bird L, Karsli C Paediatr Anaesth2013
Hemoglobin A2 Lowered by Iron Deficiency and α -Thalassemia: Should Screening Recommendation for β -Thalassemia Change?Denic S, Agarwal MM, Al Dabbagh B, El Essa A, Takala M, Showqi S, Yassin J ISRN Hematol2013
The impact of migrations on the health services for rare diseases in europe: the example of haemoglobin disorders.Angastiniotis M, Vives Corrons JL, Soteriades ES, Eleftheriou A ScientificWorldJournal2013
Corepressor-dependent silencing of fetal hemoglobin expression by BCL11A.Xu J, Bauer DE, Kerenyi MA, Vo TD, Hou S, Hsu YJ, Yao H, Trowbridge JJ, Mandel G, Orkin SH Proc. Natl. Acad. Sci. U.S.A.2013
Evaluation of the SCKnowIQ Tool and Reproductive CHOICES Intervention Among Young Adults With Sickle Cell Disease or Sickle Cell Trait.Gallo AM, Wilkie DJ, Wang E, Labotka RJ, Molokie RE, Stahl C, Hershberger PE, Zhao Z, Suarez ML, Johnson B, Pullum C, Angulo R, Thompson A Clin Nurs Res2013
What's New in the Pathophysiology of Sickle Cell Disease?Adekile AD Med Princ Pract2013
Prevalence of Pneumococcal Bacteremia in Children with Sickle Cell Disease.Patel A, Zuzo A, Imran H, Siddiqui AH Pediatr Hematol Oncol2013
Changes in the quality of life of people with thalassemia major between 2001 and 2009.Gollo G, Savioli G, Balocco M, Venturino C, Boeri E, Costantini M, Forni GL Patient Prefer Adherence2013
Analysis of clinical phenotypes of compound heterozygotes of Hb J-Bangkok and β-thalassemia.Zhao Y, Shang X, Xiong F, Liu Y, Lou J, Xu X Zhonghua Yi Xue Yi Chuan Xue Za Zhi2013
Red blood cell alloimmunization: lessons from sickle cell disease.Treml A, King KE Transfusion2013
Low-dose ketamine as a potential adjuvant therapy for painful vaso-occlusive crises in sickle cell disease.Neri CM, Pestieau SR, Darbari DS Paediatr Anaesth2013
Effect of Antioxidant Therapy on Hepatic Fibrosis and Liver Iron Concentrations in β-Thalassemia Major Patients.Elalfy MS, Adly AA, Attia AA, Ibrahim FA, Mohammed AS, Sayed AM Hemoglobin2013
Coagulation profile of children with sickle cell anemia in steady state and crisis attending the university of Nigeria teaching hospital, Ituku-Ozalla, Enugu.Chinawa JM, Emodi IJ, Ikefuna AN, Ocheni S Niger J Clin Pract2013
Emergency Provider Analgesic Practices and Attitudes Toward Patients With Sickle Cell Disease.Glassberg JA, Tanabe P, Chow A, Harper K, Haywood C, Debaun MR, Richardson LD Ann Emerg Med2013
Clinical correlates of acute pulmonary events in children and adolescents with sickle cell disease.Paul R, Minniti CP, Nouraie M, Luchtman-Jones L, Campbell A, Rana S, Onyekwere O, Darbari DS, Ajayi O, Arteta M, Ensing G, Sable C, Dham N, Kato GJ, Gladwin MT, Castro OL, Gordeuk VR Eur. J. Haematol.2013
Genome-wide analysis shows that Ldb1 controls essential hematopoietic genes/pathways in mouse early development and reveals novel players in hematopoiesis.Mylona A, Andrieu-Soler C, Thongjuea S, Martella A, Soler E, Jorna R, Hou J, Kockx C, van Ijcken W, Lenhard B, Grosveld F Blood2013
Side effects of Deferasirox Iron Chelation in Patients with Beta Thalassemia Major or Intermedia.Al-Khabori M, Bhandari S, Al-Huneini M, Al-Farsi K, Panjwani V, Daar S Oman Med J2013
Transfusion and sickle cell disease.Boulat C Transfus Clin Biol2013
The Current Status of β-Thalassemia Major in Mainland China.Xu LH, Fang JP Hemoglobin2013
Interplay between coagulation and vascular inflammation in sickle cell disease.Sparkenbaugh E, Pawlinski R Br. J. Haematol.2013
A case of X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome with repeated apnea attacks due to laryngomalacia.Ebishima Y, Misaki T, Owa K, Okuno T, Wada T, Suehiro Y No To Hattatsu2013
Routine Paediatric Sickle Cell Disease (SCD) Outpatient Care in a Rural Kenyan Hospital: Utilization and Costs.Amendah DD, Mukamah G, Komba A, Ndila C, Williams TN PLoS ONE2013
Expression of Regulatory Platelet MicroRNAs in Patients with Sickle Cell Disease.Jain S, Kapetanaki MG, Raghavachari N, Woodhouse K, Yu G, Barge S, Coronnello C, Benos PV, Kato GJ, Kaminski N, Gladwin MT PLoS ONE2013
MicroRNA-486-3p Regulates γ-Globin Expression in Human Erythroid Cells by Directly Modulating BCL11A.Lulli V, Romania P, Morsilli O, Cianciulli P, Gabbianelli M, Testa U, Giuliani A, Marziali G PLoS ONE2013
Apolipoprotein E gene polymorphism and the risk of left ventricular dysfunction among Egyptian β-thalassemia major.El-Tagui MH, Hamdy MM, Shaheen IA, Agha H, Abd-Elfatah HA Gene2013
Association between the genetic polymorphisms of glutathione S-transferase (GSTM1 and GSTT1) and the clinical manifestations in sickle cell Oliveira Filho RA, Silva GJ, de Farias Domingos I, Hatzlhofer BL, da Silva Araújo A, de Lima Filho JL, Bezerra MA, Martins DB, de Araújo RF Blood Cells Mol. Dis.2013
The effect of hydroxcarbamide therapy on survival of children with sickle cell disease.Lopes de Castro Lobo C, Pinto JF, Nascimento EM, Moura PG, Cardoso GP, Hankins JS Br. J. Haematol.2013
Diagnostic testing for α-globin gene disorders in a heterogeneous North American population.Waye JS, Eng B Int J Lab Hematol2013
Prenatal and newborn screening for hemoglobinopathies.Hoppe CC Int J Lab Hematol2013
Maternal Complications and The Association with Baseline Variables in Pregnant Women with Sickle Cell Disease.Al-Farsi SH, Al-Riyami NM, Al-Khabori MK, Al-Hunaini MN Hemoglobin2013
Paradoxical protection from atherosclerosis and thrombosis in a mouse model of sickle cell disease.Wang H, Luo W, Wang J, Guo C, Wolffe SL, Wang J, Sun EB, Bradley KN, Campbell AD, Eitzman DT Br. J. Haematol.2013
Biologic complexity in sickle cell disease: implications for developing targeted therapeutics.Gee BE ScientificWorldJournal2013
A Case of Invasive Streptococcus pneumoniae in an Afebrile Adolescent With Sickle Cell Disease.Santoro JD, Case AE, El-Dahr J, Kanter J Clin Pediatr (Phila)2013
Plastrum testudinis induces γ-globin gene expression through epigenetic histone modifications within the γ-globin gene promoter via activation of the p38 MAPK signaling pathway.Qian X, Chen J, Zhao D, Guo L, Qian X Int. J. Mol. Med.2013
Predictors for Bacteremia in Febrile Sickle Cell Disease Children in the Post-7-Valent Pneumococcal Conjugate Vaccine Era.Chang TP, Kriengsoontorkij W, Chan LS, Wang VJ J. Pediatr. Hematol. Oncol.2013
Benefits of Delayed Fetal Hemoglobin (HbF) Switching in Sickle Cell Disease (SCD): A Case Report and Review of the Literature.Pack-Mabien AV, Imran H J. Pediatr. Hematol. Oncol.2013
Deferiprone-induced seizures in a patient with β-thalassemia major.Mallat NS, Beydoun A, Musallam KM, Koussa S, Taher AT Blood Cells Mol. Dis.2013
Silent β-Thalassemia Mutations at -101 (C>T) and -71 (C>T) and Their Coinheritance with the Sickle Cell Mutation in Bahrain.Al Moamen NJ, Mahdi F, Salman E, Thabet A, Abbas R, Al Arrayed S, Sanad H, Al Alawi A Hemoglobin2013
Sildenafil therapy in thalassemia patients with doppler-defined risk for pulmonary hypertension.Morris CR, Kim HY, Wood JC, Porter JB, Klings ES, Trachtenberg FL, Sweeters N, Olivieri NF, Kwiatkowski JL, Virzi L, Singer ST, Taher A, Neufeld EJ, Thompson AA, Sachdev V, Larkin S, Suh JH, Kuypers FA, Vichinsky EP Haematologica2013
Venous Thromboembolism in Adults with Sickle Cell Disease: A Serious and Under-recognized Complication.Naik RP, Streiff MB, Haywood C, Nelson JA, Lanzkron S Am. J. Med.2013
Evaluation and Comparison of Soluble Transferrin Receptor in Thalassemia Carriers and Iron Deficient Patients.Khatami S, Dehnabeh SR, Mostafavi E, Kamalzadeh N, Yaghmaei P, Saeedi P, Shariat F, Bagheriyan H, Zeinali S, Akbari MT Hemoglobin2013
Hydrodynamics of hemostasis in sickle-cell disease.Cohen SI, Mahadevan L Phys. Rev. Lett.2013
Assessment and management of iron overload in β-thalassaemia major patients during the 21st century: a real-life experience from the Italian Webthal project.Piga A, Longo F, Musallam KM, Cappellini MD, Forni GL, Quarta G, Chiavilli F, Commendatore F, Mulas S, Caruso V, Galanello R Br. J. Haematol.2013
Early complication in Sickle Cell Anemia children due to A(TA)_n TAA polymorphism at the promoter of UGT1A1 gene.Chaouch L, Talbi E, Moumni I, Ben Chaabene A, Kalai M, Chaouachi D, Mallouli F, Ghanem A, Abbes S Dis. Markers2013
Hemoglobin - source of reactive oxygen species .Zapora E, Jarocka I Postepy Hig Med Dosw (Online)2013
Cytochrome P450 2D6 Polymorphisms and Predicted Opioid Metabolism in African American Children With Sickle Cell Disease.Yee MM, Josephson C, Hill CE, Harrington R, Castillejo MI, Ramjit R, Osunkwo I J. Pediatr. Hematol. Oncol.2013
Hyperhemolysis in Sickle Cell Disease.Aragona E, Kelly MJ J. Pediatr. Hematol. Oncol.2013
Pain in Sickle Cell Disease #270.Minniti CP, Lu K, Groninger H J Palliat Med2013
Interaction of Hb Adana (HBA2: c.179G>A) with Deletional and Nondeletional α(+)-Thalassemia Mutations: Diverse Hematological and Clinical Features.Nainggolan IM, Harahap A, Ambarwati DD, Liliani RV, Megawati D, Swastika M, Setianingsih I Hemoglobin2013
Detection of β-globin Gene Mutations Among β-thalassaemia Carriers and Patients in Malaysia: Application of Multiplex Amplification Refractory Mutation System-Polymerase Chain Reaction.Hassan S, Ahmad R, Zakaria Z, Zulkafli Z, Abdullah WZ Malays J Med Sci2013
Prenatal diagnosis of haemoglobinopathies: our experience of 523 cases.Grosso M, Puzone S, Storino MR, Sessa R, Izzo P Clin. Chem. Lab. Med.2013
Barriers to Hematopoietic Cell Transplantation Clinical Trial Participation of African American and Black Youth With Sickle Cell Disease and Their Parents.Omondi NA, Ferguson SE, Majhail NS, Denzen EM, Buchanan GR, Haight AE, Labotka RJ, Rizzo JD, Murphy EA J. Pediatr. Hematol. Oncol.2013
Therapeutic potential of hematopoietic cells derived from pluripotent stem cells.Bouhassira EE Expert Opin Biol Ther2013
Alpha-(1,6)-fucosyltransferase (FUT8) inhibits hemoglobin production during differentiation of murine and K562 human erythroleukemia cells.Sasaki H, Toda T, Furukawa T, Mawatari Y, Takaesu R, Shimizu M, Wada R, Kato D, Utsugi T, Ohtsu M, Murakami Y J. Biol. Chem.2013
Effects of Antiretroviral Drugs for Prevention of HIV-Mother-to-Child Transmission on Hematological Parameters and Hemoglobin Synthesis in HIV-Uninfected Newborns With and Without Thalassemia Carrier.Wongnoi R, Oberdorfer P, Sirivatanapa P, Phanpong C, Pornprasert S Curr. HIV Res.2013
Assessment of hepatic and pancreatic iron overload in pediatric Beta-thalassemic major patients by t2* weighted gradient echo magnetic resonance imaging.Youssef DM, Fawzy Mohammad F, Ahmed Fathy A, Aly Abdelbasset M ISRN Hematol2013
Prevalence of High Blood Pressure, Heart Disease, Thalassemia, Sickle-Cell Anemia, and Iron-Deficiency Anemia among the UAE Adolescent Population.Barakat-Haddad C J Environ Public Health2013
Ineffective Erythropoiesis in β -Thalassemia.Ribeil JA, Arlet JB, Dussiot M, Cruz Moura I, Courtois G, Hermine O ScientificWorldJournal2013
Testosterone replacement therapy does not promote priapism in hypogonadal men with sickle cell disease: 12-month safety report.Morrison BF, Reid M, Madden W, Burnett AL Andrology2013
Genetic modifiers of sickle cell anemia in the BABY HUG cohort: Influence on laboratory and clinical phenotypes.Sheehan VA, Luo Z, Flanagan JM, Howard TA, Thompson BW, Wang WC, Kutlar A, Ware RE, Am. J. Hematol.2013
Usefulness of Pulsed Wave Tissue Doppler Imaging in Assessment of Left Ventricular Functions in Children with Beta-Thalassemia Major.Abdelmoktader AM, Azer HY Indian J Pediatr2013
Sirolimus and post transplant Cy synergistically maintain mixed chimerism in a mismatched murine model.Fitzhugh CD, Weitzel RP, Hsieh MM, Phang OA, Madison C, Luznik L, Powell JD, Tisdale JF Bone Marrow Transplant.2013
Erythrocyte deformability and aggregation in homozygous sickle cell disease.Vayá A, Collado S, Dasí MA, Pérez ML, Hernandez JL, Barragán E Clin. Hemorheol. Microcirc.2013
β-Thalassemia in Abu Dhabi: Consanguinity and Tribal Stratification are Major Factors Explaining the High Prevalence of the Disease.Denic S, Aden B, Nagelkerke N, Al Essa A Hemoglobin2013
A New β(0)-Thalassemia Mutation (codon 102, AAC>ATCAC) in Coexistence with a Heterozygous P4.2 Nippon Gene.Adhiyanto C, Yamashiro Y, Hattori Y, Nitta T, Hino M, Matar M, Takagi F, Kimoto M Hemoglobin2013
Thalassemia and Hemoglobinopathies in Thua Thien Hue Province, Central Vietnam.Nguyen HV, Sanchaisuriya K, Nguyen D, Phan HT, Siridamrongvattana S, Sanchaisuriya P, Fucharoen S, Fucharoen G, Schelp FP Hemoglobin2013
Elevated Serum Levels Of Cell Death Circulating Biomarkers, M30 And M65, In Patients With β-Thalassemia Major.Esmaeil N, Moayedi B, Gharagozloo M, Maracy MR Hemoglobin2013
Leg Ulcers in Sickle Cell Disease: Current Patterns and Practices.Delaney KM, Axelrod KC, Buscetta A, Hassell KL, Adams-Graves PE, Seamon C, Kato GJ, Minniti CP Hemoglobin2013
Longitudinal monitoring of cardiac siderosis using cardiovascular magnetic resonance (CMR) T2* in patients with thalassemia major on various chelation regimens: A 6 year study.Ambati SR, Randolph RE, Mennitt K, Kleinert DA, Weinsaft JW, Giardina PJ Am. J. Hematol.2013
Relationship between myocardial T2* values and cardiac volumetric and functional parameters in β-thalassemia patients evaluated by cardiac magnetic resonance in association with serum ferritin levels.Liguori C, Pitocco F, Di Giampietro I, de Vivo AE, Schena E, Cianciulli P, Zobel BB Eur J Radiol2013
Molecular and hematological studies in a large cohort of α(0)-thalassemia in northeast Thailand: Data from a single referral center.Chaibunruang A, Prommetta S, Yamsri S, Fucharoen G, Sae-Ung N, Sanchaisuriya K, Fucharoen S Blood Cells Mol. Dis.2013
Improved Clinical Outcomes of High Risk β Thalassemia Major Patients Undergoing a HLA Matched Related Allogeneic Stem Cell Transplant with a Treosulfan Based Conditioning Regimen and Peripheral Blood Stem Cell Grafts.Mathews V, George B, Viswabandya A, Abraham A, Ahmed R, Ganapule A, Sindhuvi E, Lakshmi KM, Srivastava A PLoS ONE2013
The Molecular Basis of β-Thalassemia.Thein SL Cold Spring Harb Perspect Med2013
Prenatal control of nondeletional α-thalassemia: first experience in mainland China.Li J, Li R, Zhou JY, Xie XM, Liao C, Li DZ Prenat. Diagn.2013
Sickle Cell Disease Related Mortality in the United States (1999-2009).Hamideh D, Alvarez O Pediatr Blood Cancer2013
The Emergency Department Sickle Cell Assessment of Needs and Strengths (ED-SCANS): Reliability and Validity.Tanabe P, Thornton VL, Martinovich Z, Todd KH, Wun T, Lyons JS Adv Emerg Nurs J2013
Adrenal insufficiency is prevalent in HbE / β thalassaemia paediatric patients irrespective of their clinical severity and transfusion requirement.Nakavachara P, Viprakasit V Clin. Endocrinol. (Oxf)2013
Extramedullary haematopoiesis presented as intrathoracic tumour in a patient with alpha-thalassaemia.Bobylev D, Zhang R, Haverich A, Krueger M J Cardiothorac Surg2013
Conservative management of Beta-thalassemia major cases in the sub-division level hospital of rural West Bengal, India.Bandyopadhyay U, Kundu D, Sinha A, Banerjee K, Bandyopadhyay R, Mandal T, Ray D J Nat Sci Biol Med2013
To respond or not to respond to hydroxyurea in thalassemia: a matter of stress adaptation?Ronchi A, Ottolenghi S Haematologica2013
Acute Care of Pediatric Patients With Sickle Cell Disease: A Simulation Performance Assessment.Burns TL, Debaun MR, Boulet JR, Murray GM, Murray DJ, Fehr JJ Pediatr Blood Cancer2013
The use of extracorporeal membrane oxygenation in pediatric patients with sickle cell disease.Kuo K, Cornell T, Shanley T, Odetola F, Annich G Perfusion2013
Thermal Pain and Sensory Processing in Children With Sickle Cell Disease.O'Leary JD, Crawford MW, Odame I, Shorten GD, McGrath PA Clin J Pain2013
Long-term treatment with deferiprone enhances left ventricular ejection function when compared to deferoxamine in patients with thalassemia major.Filosa A, Vitrano A, Rigano P, Calvaruso G, Barone R, Capra M, Cuccia L, Gagliardotto F, Pitrolo L, Prossomariti L, Casale M, Caruso V, Gerardi C, Campisi S, Cianciulli P, Rizzo M, D'Ascola G, Ciancio A, Maggio A Blood Cells Mol. Dis.2013
Transcranial Doppler Velocity and Brain MRI/MRA Changes in Children With Sickle Cell Anemia on Chronic Transfusions to Prevent Primary Stroke.Sheehan VA, Hansbury EN, Smeltzer MP, Fortner G, McCarville MB, Aygun B Pediatr Blood Cancer2013
Normalized Transcranial Doppler Velocities, Stroke Prevention and Improved Pulmonary Function after Stem Cell Transplantation in Children with Sickle Cell Anemia.Mynarek M, Bettoni da Cunha Riehm C, Brinkmann F, Weißenborn K, Tell-Lüersen M, Heuft HG, Maecker-Kolhoff B, Sykora KW Klin Padiatr2013
Immunomodulatory effects of silymarin in patients with β-thalassemia major.Gharagozloo M, Karimi M, Amirghofran Z Int. Immunopharmacol.2013
Prolongation of QTc Intervals and Risk of Death Among Patients with Sickle Cell Disease.Upadhya B, Ntim W, Brandon Stacey R, Henderson R, Leedy D, O'Brien FX, Knovich MA Eur. J. Haematol.2013
Interpreting elevated fetal hemoglobin in pathology and health at the basic laboratory level: new and known γ- gene mutations associated with hereditary persistence of fetal hemoglobin.Amato A, Cappabianca MP, Perri M, Zaghis I, Grisanti P, Ponzini D, Di Biagio P Int J Lab Hematol2013
Detection of Rare Beta Globin Gene Mutation [+22 5UTR(G>A)] in an Infant, Despite Prenatal Screening.Mahdavi MR, Karami H, Akbari MT, Jalali H, Roshan P Case Rep Hematol2013
Incidence of Serious Bacterial Infections in Febrile Children With Sickle Cell Disease.Bansil NH, Kim TY, Tieu L, Barcega B Clin Pediatr (Phila)2013
Morbidity among child travellers with sickle-cell disease visiting tropical areas: an observational study in a French tertiary care centre.Sommet J, Missud F, Holvoet L, Ithier G, Lorrot M, Benkerrou M, Faye A Arch. Dis. Child.2013
Tardive hip disease diagnosis in a young adult with sickle cell disease.Bokolombe A, Samato F, Lukinu T, Ekila M, Aloni M Afr Health Sci2013
Outcome of cholelithiasis in Sudanese children with Sickle Cell Anaemia (SCA) after 13 years follow-up.Attalla B, Karrar Z, Ibnouf G, Mohamed A, Abdelwahab O, Nasir EM, El Seed MA Afr Health Sci2013
Acute splenic sequestration in a pregnant woman with homozygous sickle-cell anemia.Maia CB, Nomura RM, Igai AM, Fonseca GH, Gualandro SM, Zugaib M Sao Paulo Med J2013
Transfusion suppresses erythropoiesis and increases hepcidin in adult patients with beta-thalassemia major: a longitudinal study.Pasricha SR, Frazer DM, Bowden DK, Anderson GJ Blood2013
Mild β(+)-Thalassemia Associated With Two Linked Sequence Variants: IVS-II-839 (T>C) and IVS-II-844 (C>A).Waye JS, Eng B, Hellens L, Hohenadel BA, Nakamura LM, Walker L Hemoglobin2013
Hb Grove City [β38(C4)Thr→Ser, ACC>AGC; HBB: c.116C>G]: A New Low Oxygen Affinity β Chain Variant.Taliercio RM, Ashton RW, Horwitz L, Swanson KC, Wendt PC, Hoyer JD, Oliveira JL Hemoglobin2013
Comparison of right and left side heart functions in patients with thalassemia major, patients with thalassemia intermedia, and control group.Noori N, Mohamadi M, Keshavarz K, Alavi SM, Mahjoubifard M, Mirmesdagh Y J Tehran Heart Cent2013
Cell-Free Hemoglobin and Its Scavenger Proteins: New Disease Models Leading the Way to Targeted Therapies.Schaer DJ, Buehler PW Cold Spring Harb Perspect Med2013
A randomized, placebo-control trial of arginine therapy for the treatment ofchildren with sickle cell disease hospitalized with vaso-occlusive pain episodes.Morris CR, Kuypers FA, Lavrisha L, Ansari M, Sweeters N, Stewart M, Gildengorin G, Neumayr L, Vichinsky EP Haematologica2013
Sepsis caused by Mycobacterium terrae complex in a patient with sickle cell disease.Esnakula AK, Mummidi SK, Oneal PA, Naab TJ BMJ Case Rep2013
Isolated cortical vein thrombosis in a patient with sickle cell disease: Treatment with decompressive craniotomy and anticoagulation and literature review.Hamamoto Filho PT, Gabarra RC, Braga GP, Ruiz E Resende LS, Bazan R, Zanini MA Neurol India2013
Natural antiband 3 antibodies in patients with sickle cell disease.Villaescusa R, Arce AA, Lalanne-Mistrih ML, Lamarre Y, Hierso R, Hernández C, Hardy-Dessources MD, C. R. Biol.2013
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Neuroradiologic Features in X-linked α-Thalassemia/Mental Retardation Syndrome.Wada T, Ban H, Matsufuji M, Okamoto N, Enomoto K, Kurosawa K, Aida N AJNR Am J Neuroradiol2013
Environmental tobacco smoke and airway obstruction in children with sickle cell anemia.Cohen RT, Strunk RC, Field JJ, Rosen CL, Kirkham FJ, Redline S, Stocks J, Rodeghier MJ, Debaun MR Chest2013
Decreased nitrite levels in erythrocytes of children with β-thalassemia/hemoglobin E.Suvachananonda T, Wankham A, Srihirun S, Tanratana P, Unchern S, Fucharoen S, Chuansumrit A, Sirachainan N, Sibmooh N Nitric Oxide2013
Association Between Baseline Fetal Hemoglobin Levels and Incidence of Severe Vaso-Occlusive Pain Episodes in Children With Sickle Cell Anemia.Bhatnagar P, Keefer JR, Casella JF, Barron-Casella EA, Bean CJ, Hooper CW, Payne AB, Arking DE, Debaun MR Pediatr Blood Cancer2013
Thrombospondin-1 and L-selectin are associated with silent cerebral infarct in children with sickle cell anaemia.Faulcon LM, Fu Z, Dulloor P, Barron-Casella E, Savage W, Jennings JM, Van Eyk JE, Debaun M, Casella JF, Everett A Br. J. Haematol.2013
Gigantic splenomegaly in a 27-year-old male of Southeast Asian descent with concurrent diagnosis of myeloproliferative neoplasm and hemoglobin H disease.Shi Y, Kulbacki E, Chui DH, Wang E Eur. J. Haematol.2013
Hb AHVAZ [α83(F4)Leu→Arg, CTG>CGG (α2); HBA2: c.251T>G],A NEW HEMOGLOBIN VARIANT OF THE α2-GLOBIN GENE.Hamid M, Shariati G, Saberi A, Galehdari H, Kaikhaei B, Mohammadi-Anaei M Hemoglobin2013
Transcranial Doppler in Sickle Cell Disease.Sarkar N, Sharma VK J. Pediatr. Hematol. Oncol.2013
Bacteremia Risk and Outpatient Management of Febrile Patients With Sickle Cell Disease.Baskin MN, Goh XL, Heeney MM, Harper MB Pediatrics2013
Differences in Pain Management Between Hematologists and Hospitalists Caring for Patients With Sickle Cell Disease Hospitalized for Vasoocclusive Crisis.Shah N, Rollins M, Landi D, Shah R, Bae J, De Castro LM Clin J Pain2013
A Stepwise α Thalassemia Screening Strategy in High Prevalence Areas.Alkindi SS, Zadjali SA, Daar SA, Sindhuvi E, Wali YA, Pathare AV, Venugopal S, Lapoumeroulie C, Srivastava A, Krishnamoorthy R Eur. J. Haematol.2013
Third party cord blood transplant boosts autologous hematopoiesis in a case of persistent bone marrow aplasia after double transplant failure for B-thalassemia major.Visani G, Picardi P, Guiducci B, Loscocco F, Giardini C, Lucesole M, Barulli S, Ricciardi T, Isidori A Mediterr J Hematol Infect Dis2013
Molecular characterization of β-thalassemia in four communities in South Gujarat-codon 30 (G → A) a predominant mutation in the Kachhiya Patel community.Bhukhanvala DS, Italia K, Sawant P, Colah R, Ghosh K, Gupte SC Ann. Hematol.2013
Birth of a healthy infant after preimplantation genetic diagnosis by sequential blastomere and trophectoderm biopsy for β-thalassemia and HLA genotyping.Milachich T, Timeva T, Ekmekci C, Beyazyurek C, Tac HA, Shterev A, Kahraman S Eur. J. Obstet. Gynecol. Reprod. Biol.2013
Left ventricular systolic function in sickle cell anemia: a meta-analysis.Poludasu S, Ramkissoon K, Salciccioli L, Kamran H, Lazar JM J. Card. Fail.2013
Variable Presentation of HB H Disease Due to Homozygosity for the Rare Polyadenylation Signal A T(Indian) (AATAAA>AATA- -) Mutation in Four Indian Families.Nair SB, Nadkarni AH, Ghosh K, Colah RB Hemoglobin2013
Investigation of Sickle-Cell Haemoglobin Polymerisation under Electrochemical Control.Iqbal Z, Li M, McKendry R, Horton M, Caruana DJ Chemphyschem2013
Quality of life in patients with sickle cell disease.Menezes AS, Len CA, Hilário MO, Terreri MT, Braga JA Rev Paul Pediatr2013
Current management of sickle cell disease in pregnancy.Andemariam B, Browning SL Clin. Lab. Med.2013
Validation of the Sickle Cell Disease Pain Burden Interview-Youth.Zempsky WT, O'Hara EA, Santanelli JP, Palermo TM, New T, Smith-Whitley K, Casella JF J Pain2013
α-Hemoglobin Stabilizing Protein (AHSP) Perturbs the Proximal Heme Pocket of Oxy-α-Hemoglobin and Weakens the Iron-Oxygen Bond.Dickson CF, Rich AM, D'Avigdor WM, Collins DA, Lowry JA, Mollan TL, Khandros E, Olson JS, Weiss MJ, Mackay JP, Lay PA, Gell DA J. Biol. Chem.2013
Hypoxia/reoxygenation stress increases markers of vaso-occlusive crisis in sickle SAD mice.Aufradet E, Desouza G, Bourgeaux V, Bessaad A, Campion Y, Canet-Soulas E, Pialoux V, Chirico EN, Chevrier AM, Godfrin Y, Martin C Clin. Hemorheol. Microcirc.2013
Age-related emergency department reliance (EDR) and health care resource utilization in patients with sickle cell disease (SCD).Blinder M, Vekeman F, Sasane M, Trahey A, Paley C, Magestro M, Duh MS Value Health2013
Key cost drivers in the cost of care for sickle cell disease patients: Results of a systematic literature search and a survey of payers and key opinion leaders.Jordan L, Duh MS, Vekeman F, Matter S, Bieri C, Sasane M Value Health2013
Expanding concepts of opioid-taking behavior in sickle cell disease: A multi-phase, mixed methods study.Alsalman AJ, Li Wong JK, Hassan NT, Smith WR Value Health2013
Biopsychosocial-spiritual determinants of opioid-taking behavior in sickle cell disease: A multi-phase, mixed methods study.Alsalman AJ, Li Wong JK, Hassan NT, Smith WR Value Health2013
Penicillin and amoxicillin prophylaxis in children with sickle cell disease (SCD): compliance and cost comparison.Zimmermann IR, Alexandre RF, Mosca M, Schneiders RE, do Nascimento JM, Gadelha CA Value Health2013
Outcome of patients with hemoglobinopathies given either cord blood or bone marrow transplantation from an HLA-identical sibling.Locatelli F, Kabbara N, Ruggeri A, Ghavamzadeh A, Roberts I, Li CK, Bernaudin F, Vermylen C, Dalle JH, Stein J, Wynn R, Cordonnier C, Pinto F, Angelucci E, Socié G, Gluckman E, Walters MC, Rocha V Blood2013
Cost-effectiveness of prospective red blood cell antigen matching to prevent alloimmunization among sickle cell patients.Kacker S, Ness PM, Savage WJ, Frick KD, Shirey RS, King KE, Tobian AA Transfusion2013
Oral Ketamine for Sickle Cell Crisis Pain Refractory to Opioids.Jennings CA, Bobb BT, Noreika DM, Coyne PJ J Pain Palliat Care Pharmacother2013
Hematological and Genetic Predictors of Daytime Hemoglobin Saturation in Tanzanian Children with and without Sickle Cell Anemia.Cox SE, Makani J, Newton CR, Prentice AM, Kirkham FJ ISRN Hematol2013
Outcome and challenges of kidney transplant in patients with sickle cell disease.Okafor UH, Aneke E J Transplant2013
PUFAs in sickle cell disease.Das UN Am. J. Clin. Nutr.2013
Distribution of thalassemias and associated hemoglobinopathies identified by prenatal diagnosis in Taiwan.Peng CT, Liu SC, Peng YC, Lin TH, Wang SJ, Le CY, Shih MC, Tien N, Lu JJ, Lin CY Blood Cells Mol. Dis.2013
Treatment of heart failure in adults with thalassemia major: response in patients randomised to deferoxamine with or without deferiprone.Porter JB, Wood J, Olivieri N, Vichinsky EP, Taher A, Neufeld E, Giardina P, Thompson A, Moore B, Evans P, Kim HY, Macklin EA, Trachtenberg F J Cardiovasc Magn Reson2013
Iron Overload and Glucose Metabolism in Subjects With β-Thalassaemia Major : An Overview.De Sanctis V, Soliman A, Yassin M Curr Diabetes Rev2013
Effect of zinc supplementation on serum antibody titers to heat shock protein 27 in patients with thalassemia major.Ghahramanlu E, Banihashem A, Mirhossini NZ, Hosseini G, Mostafavi-Toroghi H, Tavallaie S, Meshkat M, Ghayour-Mobarhan M, Ferns G Hematology2013
Rapid and inexpensive detection of common HBB gene mutations in Tunisian population by high-resolution melting analysis: Implication for molecular diagnosis.Ouragini H, Haddad F, Darragi I, Abbes S Hematology2013
Improvement of detection of paternally herited fetal mutant genes for β-globin in maternal plasma by PNA clamp.Huang K, Pan HF Zhonghua Xue Ye Xue Za Zhi2013
Coronary Microvascular function, Peripheral Endothelial Function and Carotid IMT in beta-thalassemia minor.Gullu H, Caliskan M, Caliskan Z, Unler GK, Ermisler E, Ciftci O, Guven A, Muderrisoglu H Thromb. Res.2013
Molecular Spectrum of β-Thalassemia in Fujian Province, Southeastern China.Huang H, Xu L, Lin N, He D, Li Y, Guo D, Wang L, Wang Y, Zhen L, Xu J, Lin Y Hemoglobin2013
Development of single-strand conformational polymorphism to screen for mutations in hotspot regions of beta-globin gene of beta-thalassemia patients of Sri Lanka.Dassanayake RS, Mahadevan K, Gunawardene YI Southeast Asian J. Trop. Med. Public Health2013
Serum ferritin levels in adults with sickle cell disease in Lagos, Nigeria.Akinbami AA, Dosunmu AO, Adediran AA, Oshinaike OO, Osunkalu VO, Ajibola SO, Arogundade OM J Blood Med2013
High prevalence of red blood cell alloimmunization in sickle cell disease despite transfusion from Rh-matched minority donors.Chou ST, Jackson T, Vege S, Smith-Whitley K, Friedman DF, Westhoff CM Blood2013
Iron regulation by hepcidin.Zhao N, Zhang AS, Enns CA J. Clin. Invest.2013
State of the art and new developments in molecular diagnostics for hemoglobinopathies in multiethnic societies.Harteveld CL Int J Lab Hematol2013
Death during an asthma exacerbation in an adult with sickle cell disease: An autopsy case study.Dhakal B, Giese K, Santo-Thomas L, Field JJ Am. J. Hematol.2013
Regulatory B cell compartment in transfused alloimmunized and non-alloimmunized patients with sickle cell disease.Bao W, Zhong H, Manwani D, Vasovic L, Uehlinger J, Lee MT, Sheth S, Shi P, Yazdanbankhsh K Am. J. Hematol.2013
Gene-centric association study of acute chest syndrome and painful crisis in sickle cell disease patients.Galarneau G, Coady S, Garrett ME, Jeffries N, Puggal M, Paltoo D, Soldano K, Guasch A, Ashley-Koch AE, Telen MJ, Kutlar A, Lettre G, Papanicolaou GJ Blood2013
Sickle Cell Trait: Is There an Increased VTE Risk in Pregnancy and the Postpartum?Pintova S, Cohen HW, Billett HH PLoS ONE2013
Asymptomatic bacteriuria in Nigerian children with sickle cell anemia.Adegoke SA, Adegun PT Indian J Nephrol2013
Genetic regulation of fetal haemoglobin in inherited bone marrow failure syndromes.Alter BP, Rosenberg PS, Day T, Menzel S, Giri N, Savage SA, Thein SL Br. J. Haematol.2013
The association between tricuspid regurgitation velocity and 5-year survival in a North West London population of patients with sickle cell disease in the United Kingdom.Zimbarra Cabrita I, Mohammed A, Layton M, Ghorashian S, Gilmore A, Cho G, Howard J, Anie KA, Desforges L, Bassett P, Grapsa J, Howard L, Mahalingam G, Dawson D, Pinto FJ, Nihoyannopoulos P, Davies SC, Gibbs JS Br. J. Haematol.2013
Parallel Assessment of Globin Lentiviral Transfer in Induced Pluripotent Stem Cells and Adult Hematopoietic Stem Cells Derived from the Same Transplanted β-Thalassemia Patient.Tubsuwan A, Abed S, Deichmann A, Kardel MD, Bartholomä C, Cheung A, Negre O, Kadri Z, Fucharoen S, von Kalle C, Payen E, Chrétien S, Schmidt M, Eaves CJ, Leboulch P, Maouche-Chrétien L Stem Cells2013
Decreased thrombin activity by a Congolese herbal medicine used in sickle cell anemia.Nsimba MM, Lami JN, Hayakawa Y, Yamamoto C, Kaji T J Ethnopharmacol2013
Novel One-Step Multiplex PCR-Based Method for HLA Typing and Preimplantational Genetic Diagnosis of β-Thalassemia.Fernández RM, Peciña A, Lozano-Arana MD, García-Lozano JC, Borrego S, Antiñolo G Biomed Res Int2013
Current Management of Sickle Cell Anemia.McGann PT, Nero AC, Ware RE Cold Spring Harb Perspect Med2013
The adolescent with sickle cell disease.Majumdar S Adolesc Med State Art Rev2013
Emodin can induce K562 cells to erythroid differentiation and improve the expression of globin genes.Ma YN, Chen MT, Wu ZK, Zhao HL, Yu HC, Yu J, Zhang JW Mol. Cell. Biochem.2013
Hb Southampton [B106(G8)Leu→PRO, CTG→CCG] in a Uruguayan woman.Pereira JA, López P, Costa FF, Sans M, Sonati Mde F Rev Bras Hematol Hemoter2013
Alpha chain hemoglobins with electrophoretic mobility similar to that of hemoglobin S in a newborn screening program.Silva MR, Sendin SM, Araujo IC, Pimentel FS, Viana MB Rev Bras Hematol Hemoter2013
Sexuality and sickle cell anemia.Côbo Vde A, Chapadeiro CA, Ribeiro JB, Moraes-Souza H, Martins PR Rev Bras Hematol Hemoter2013
α-chain hemoglobin variants with electrophoretic mobility similar to that of hemoglobin S in newborn screening programs.Sonati Mde F Rev Bras Hematol Hemoter2013
Sexuality and sickle cell disease.Figueiredo MS Rev Bras Hematol Hemoter2013
A unique cause of intestinal and splenic infarction in a sickle cell trait patient.Asfaw SH, Falk GA, Morris-Stiff G, Tuthill RJ, Moorman ML, Samotowka MA Case Rep Surg2013
Establishment and performance assessment of preparation technology of internal quality control products for blood transfusion compatibility testing.Yu Y, Ma C, Feng Q, Chen X, Guan X, Zhang X, Chen L, Lin Z, Pan J, Zhang T, Luo Q, Wang D Exp Ther Med2013
Automated red cell exchange: a simplified formula for how many red cell units to exchange and validity of haemoglobin S levels measured one to two hours later.Mandal S, Westra J, Apushkin M, Richa EM, Zibrat SJ, Toney L, Yeo KT, Baron JM, Baron BW Blood Transfus2013
The prevention of adverse reactions to transfusions in patients with haemoglobinopathies: a proposed algorithm.Bennardello F, Fidone C, Spadola V, Cabibbo S, Travali S, Garozzo G, Antolino A, Tavolino G, Falla C, Bonomo P Blood Transfus2013
Pulmonary Artery Pressure Correlates Directly with Spleen Volume in Non-Splenectomized Hemoglobin E/β-Thalassemia Patients.Atichartakarn V, Chuncharunee S, Yamwong S, Yingchoncharoen T, Jongjirasiri S, Archararit N, Udomsubpayakul U Acta Haematol.2013
A rare case of Moyamoya syndrome in a β-thalassemia major patient.Inati A, Tourjuman O, Bizri D, Dhayni R, Abbas HA, Tfaili H, Akouri G, Beydoun A Blood Cells Mol. Dis.2013
Plasma PTX3 levels in sickle cell disease patients, during vaso occlusion and acute chest syndrome (data from Saudi population).Elshazly SA, Heiba NM, Abdelmageed WM Hematology2013
Intellectual function evaluation of first generation immigrant children with sickle cell disease: the role of language and sociodemographic factors.Montanaro M, Colombatti R, Pugliese M, Migliozzi C, Zani F, Guerzoni ME, Manoli S, Manara R, Meneghetti G, Rampazzo P, Cavalleri F, Giordan M, Paolucci P, Basso G, Palazzi G, Sainati L Ital J Pediatr2013
Children with hemoglobin E/β-thalassemia have a high risk of being vitamin D deficient even if they get abundant sun exposure: A study from thailand.Nakavachara P, Viprakasit V Pediatr Blood Cancer2013
Intracranial blood flow velocities in patients with sickle cell disease and β-thalassemia intermedia.Abboud M, Maakaron J, Khoury R, Tamim H, Shehab M, Haddad F, Adams R, Taher A Am. J. Hematol.2013
Unusual cutaneous lesions indicating fat embolism syndrome in homozygous sickle cell disease.Bachmeyer C, Lionnet F, Stojanovic KS, Moguelet P, Aractingi S Am. J. Hematol.2013
Management of the thalassemias.Olivieri NF, Brittenham GM Cold Spring Harb Perspect Med2013
End stage renal disease in six patients with beta-thalassemia intermedia.Mallat NS, Musallam KM, Mallat SG, Ziyadeh FN, Koussa S, Taher AT Blood Cells Mol. Dis.2013
Analgesic efficacy of topical lidocaine for vaso-occlusive crisis in children with sickle cell disease.Rasolofo J, Poncelet M, Rousseau V, Marec-Berard P Arch Pediatr2013
Unusual low sickle cell hemoglobin level.Baklouti F, Delaunay J Haematologica2013
Non-transfusion-dependent thalassemias.Musallam KM, Rivella S, Vichinsky E, Rachmilewitz EA Haematologica2013
Gonadal function of beta-thalassemics following stem cell transplantation conditioned with myeloablative and reduced intensity regimens.Poomthavorn P, Chawalitdamrong P, Hongeng S, Mahachoklertwattana P, Pakakasama S, Khlairit P, Chailurkit LO J. Pediatr. Endocrinol. Metab.2013
Hematopoietic stem cell transplantation for people with sickle cell disease.Oringanje C, Nemecek E, Oniyangi O Cochrane Database Syst Rev2013
Splenectomy versus conservative management for acute sequestration crises in people with sickle cell disease.Owusu-Ofori S, Hirst C Cochrane Database Syst Rev2013
Transgenic sickle cell disease mice have high mortality and dysregulated immune responses after vaccination.Szczepanek SM, Secor ER, Bracken SJ, Guernsey L, Rafti E, Matson A, Thrall RS, Andemariam B Pediatr. Res.2013
Detection of a novel large deletion causing α-thalassemia in South China.Jia X, Huang R, Lei Z, Yao L, Wang L, Li Y, Meng D, Zhou Y, Liu J, Zhang X Exp. Mol. Pathol.2013
Polymorphism in the HMOX1 Gene is Associated with High Levels of Fetal Hemoglobin in Brazilian Patients with Sickle Cell Anemia.Gil GP, Ananina G, Oliveira MB, Costa FF, Silva MJ, Santos MN, Bezerra MA, Hatzlhofer BL, Araujo AS, Melo MB Hemoglobin2013
Protein antioxidants in thalassemia.Awadallah S Adv Clin Chem2013
Analysis of the beta-globin gene in DNA of suspected thalassemic great apes.Vuch J, Siori MS, Bigatti MP, Segat L, De Fabrizio G, Crovella S Genet. Mol. Res.2013
A heightened awareness: hemoglobin variants and HbA1c.Milojkovic R MLO Med Lab Obs2013
Information exploration system for sickle cell disease and repurposing of hydroxyfasudil.Essack M, Radovanovic A, Bajic VB PLoS ONE2013
The association of CD81 polymorphisms with alloimmunization in sickle cell disease.Tatari-Calderone Z, Tamouza R, Le Bouder GP, Dewan R, Luban NL, Lasserre J, Maury J, Lionnet F, Krishnamoorthy R, Girot R, Vukmanovic S Clin. Dev. Immunol.2013
Acquired alpha thalassemia associated with erythroleukemia.Anoop P, Roohi S Am. J. Hematol.2013
Low-molecular-weight heparins for managing vaso-occlusive crises in people with sickle cell disease.van Zuuren EJ, Fedorowicz Z Cochrane Database Syst Rev2013
Autoimmune haemolysis in unexpectedly mild sickle cell/hemoglobin C disease.Iskander D, O'Donovan E, Bain BJ Am. J. Hematol.2013
Prevalence of sickle cell disease, hemoglobin S, and hemoglobin C among haitian newborns.Rotz S, Arty G, Dall'amico R, De Zen L, Zanolli F, Bodas P Am. J. Hematol.2013
Pregnancy Outcomes in Women with Thalassemia in North America and the UK.Thompson AA, Kim HY, Singer ST, Vichinsky E, Eile J, Yamashita R, Giardina PA, Olivieri N, Parmar N, Trachtenberg F, Neufeld EJ, Kwiatkowski JL, Am. J. Hematol.2013
Dilemma in Differentiating between Acute Osteomyelitis and Bone Infarction in Children with Sickle Cell Disease: The Role of Ultrasound.Inusa BP, Oyewo A, Brokke F, Santhikumaran G, Jogeesvaran KH PLoS ONE2013
Is sickle cell anemia a neglected tropical disease?Ware RE PLoS Negl Trop Dis2013
Stroke in sickle cell anemia patients: A need for multidisciplinary approaches.Menaa F Atherosclerosis2013
Zinc supplements for treating thalassaemia and sickle cell disease.Swe KM, Abas AB, Bhardwaj A, Barua A, Nair NS Cochrane Database Syst Rev2013
Endothelial activation and inflammation biomarkers in children and adolescents with sickle cell disease.Hatzipantelis ES, Pana ZD, Gombakis N, Taparkou A, Tzimouli V, Kleta D, Zafeiriou DJ, Garipidou V, Kanakoudi F, Athanassiou M Int. J. Hematol.2013
KLF1 Gene Mutations in Chinese Adults with Increased Fetal Hemoglobin.Wang T, He Y, Zhou JY, Xie XM, Li J, Li R, Liao C, Li DZ Hemoglobin2013
Comparison between β-Thalassemia Minor and Normal Individuals using the Wechsler Adult Intelligence Scale.Zangiabadi N, Yarahmadi F, Darekordi A, Shabani M, Dadgar MM Hemoglobin2013
Molecular Epidemiological Survey of Hemoglobinopathies in the Wuxi Region of Jiangsu Province, Eastern China.Lin M, Han ZJ, Wang Q, Zheng L, Wang Y, Yang H, Huang Y, Lin F, Zhan XF, Lin CP, Wu JR, Luo ZY, Liu JB, Yan ZH, Zheng SY, Zheng JK, Lu M, Zhu JJ, Xie LX, Yang LY Hemoglobin2013
Utility Of The Multivariate Approach In Predicting β-Thalassemia Intermedia Or β-Thalassemia Major Types In Iranian Patients.Banan M, Bayat H, Namdar-Aligoodarzi P, Azarkeivan A, Kamali K, Daneshmand P, Zaker-Kandjani B, Najmabadi H Hemoglobin2013
Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia.Sahli CA, Bibi A, Ouali F, Fredj SH, Dakhlaoui B, Othmani R, Laouini N, Jouini L, Ouenniche F, Siala H, Touhami I, Becher M, Fattoum S, Toumi NE, Messaoud T Clin. Chem. Lab. Med.2013
Chest pain in sickle cell disease.Tonino SH, Nur E, Otten HM, Wykrzykowska JJ, Hoekstra JB, Biemond BJ Neth J Med2013
LIN28B-mediated expression of fetal hemoglobin and production of fetal-like erythrocytes from adult human erythroblasts ex vivo.Lee YT, de Vasconcellos JF, Yuan J, Byrnes C, Noh SJ, Meier ER, Kim KS, Rabel A, Kaushal M, Muljo SA, Miller JL Blood2013
Probing vasoocclusion phenomena in sickle cell anemia via mesoscopic simulations.Lei H, Karniadakis GE Proc. Natl. Acad. Sci. U.S.A.2013
HPLC-ESI-MS/MS analysis of hemoglobin peptides in tryptic digests of dried-blood spot extracts detects HbS, HbC, HbD, HbE, HbO-Arab, and HbG-Philadelphia mutations.Haynes CA, Guerra SL, Fontana JC, Dejesús VR Clin. Chim. Acta2013
Hemoglobin variants in Muslim community in South Gujarat, Western India.Bhukhanvala DS, Sorathiya S, Surve R, Nair S, Italia K, Colah R, Ghosh K, Gupte SC Int J Lab Hematol2013
Vascular endothelial growth factor in children with thalassemia major.Fahmey SS, Naguib HF, Abdelshafy SS, Alashry RE Mediterr J Hematol Infect Dis2013
Endothelial Nitric Oxide Synthase (eNOS) Gene Polymorphism is Associated with Age Onset of Menarche in Sickle Cell Disease Females of India.Nishank SS Mediterr J Hematol Infect Dis2013
Cardiac surgery in patients with sickle cell disease.Khandeparkar J, Porwal M, Mahajan V J Postgrad Med2013
Rapid prenatal diagnosis of common beta-thalassemia mutations in Southeast Asia using pyrosequencing.Ho SS, Huan PT, Leow GH, Ching LK, Chiu L, Law HY, Koay ES Prenat. Diagn.2013
A Sequence Variation: 713-8delC in the Transforming Growth Factor Beta 1 Gene Polymorphism in Thalassemia Major Patients.Singh K, Agarwal S, Shukla A, Gupta S J Clin Densitom2013
Male gender, increased blood viscosity, body mass index and triglyceride levels are independently associated with systemic relative hypertension in sickle cell anemia.Lamarre Y, Lalanne-Mistrih ML, Romana M, Lemonne N, Mougenel D, Waltz X, Tressières B, Etienne-Julan M, Tarer V, Hardy-Dessources MD, Connes P PLoS ONE2013
Stroke in patients with sickle cell disease.Webb J, Kwiatkowski JL Expert Rev Hematol2013
Combining gene therapy and fetal hemoglobin induction for treatment of β-thalassemia.Breda L, Rivella S, Zuccato C, Gambari R Expert Rev Hematol2013
Annotated Definition of BCL11A and HMIP-2 Haplotypes Through The Analysis of Sicilian β-Thalassemia Patients with High Levels of Fetal Hemoglobin.Buccheri MA, Spina S, Ruberto C, Lombardo T, Labie D, Ragusa A Hemoglobin2013
Growth and endocrine disorders in thalassemia: The international network on endocrine complications in thalassemia (I-CET) position statement and guidelines.De Sanctis V, Soliman AT, Elsedfy H, Skordis N, Kattamis C, Angastiniotis M, Karimi M, Yassin MA, El Awwa A, Stoeva I, Raiola G, Galati MC, Bedair EM, Fiscina B, El Kholy M Indian J Endocrinol Metab2013
Clinically meaningful measurement of pain in children with sickle cell disease.Myrvik MP, Brandow AM, Drendel AL, Yan K, Hoffmann RG, Panepinto JA Pediatr Blood Cancer2013
Novel dominant β-thalassemia: Hb Boston-Kuwait [Codon 139/140(+T)].Croteau SE, Luo HY, Lehmann LE, Chui DH, Neufeld EJ Pediatr Blood Cancer2013
Trends in blood transfusion among hospitalized children with sickle cell disease.Raphael JL, Oyeku SO, Kowalkowski MA, Mueller BU, Ellison AM Pediatr Blood Cancer2013
Mast cell activation contributes to sickle cell pathobiology and pain.Vincent L, Vang D, Nguyen J, Gupta M, Luk K, Ericson ME, Simone DA, Gupta K Blood2013
Deferasirox effectively reduces iron overload in non-transfusion-dependent thalassemia (NTDT) patients: 1-year extension results from the THALASSA study.Taher AT, Porter JB, Viprakasit V, Kattamis A, Chuncharunee S, Sutcharitchan P, Siritanaratkul N, Galanello R, Karakas Z, Lawniczek T, Habr D, Ros J, Zhu Z, Cappellini MD Ann. Hematol.2013
Identification of the Ca(2+) entry pathway involved in deoxygenation-induced phosphatidylserine exposure in red blood cells from patients with sickle cell disease.Cytlak UM, Hannemann A, Rees DC, Gibson JS Pflugers Arch.2013
Cardiovascular Function and Treatment in β-Thalassemia Major: A Consensus Statement From the American Heart Association.Pennell DJ, Udelson JE, Arai AE, Bozkurt B, Cohen AR, Galanello R, Hoffman TM, Kiernan MS, Lerakis S, Piga A, Porter JB, Walker JM, Wood J, Circulation2013
Sickle cell disease: time for a closer look at treatment options?Sheth S, Licursi M, Bhatia M Br. J. Haematol.2013
Prevalence of β thalassemia carrier state in Sindhi community of Wardha and evaluation of risk factors for β thalassemia trait.Rakholia R, Chaturvedi P Niger J Clin Pract2013
Prevalence and pattern of sickle cell disease in premarital couples in Southeastern Nigeria.Nnaji GA, Ezeagwuna DA, Nnaji I, Osakwe JO, Nwigwe AC, Onwurah OW Niger J Clin Pract2013
Effects of micro environmental factors on natural killer activity (NK) of Beta Thalassemia major patients.Atasever Arslan B, Erdem-Kuruca S, Karakas Z, Erman B, Ergen A Cell. Immunol.2013
Development of psychological and intellectual performance in transplanted sickle cell disease patients: A prospective study from pretransplant period to 5years after HSCT.Bockenmeyer J, Chamboredon E, Missud F, Benkerrou M, Holvoët L, Ithier G, Lescoeur B, Yakouben K, Ouachée-Chardin M, Rohrlich PS, Duval M, Baruchel A, Dalle JH Arch Pediatr2013
Genetic diversity of HCV among various high risk populations (IDAs, thalassemia, hemophilia, HD patients) in Iran.Rafiei A, Darzyani AM, Taheri S, Haghshenas M, Hosseinian A, Makhlough A Asian Pac J Trop Med2013
Hepcidin and β-thalassemia major.Nemeth E Blood2013
Genetic modulation of HbF in Brazilians with HbSC disease and sickle cell anemia.Barbosa CG, Aleluia AC, Pacheco AP, Paz SS, Zanette AM, Lyra IM, Steinberg MH, Milton JN, Goncalves MS Am. J. Hematol.2013
A dose-escalation phase IIa study of 2,2-dimethylbutyrate (HQK-1001), an oral fetal globin inducer, in sickle cell disease.Kutlar A, Reid M, Inati A, Taher A, Abboud MR, El-Beshlawy A, Buchanan GR, Smith H, Ataga K, Perrine S, Ghalie R Am. J. Hematol.2013
Liver stiffness increases acutely during sickle cell vaso-occlusive crisis.Koh C, Turner T, Zhao X, Minniti CP, Feld JJ, Simpson J, Demino M, Conrey AK, Jackson MJ, Seamon C, Kleiner DE, Kato GJ, Heller T Am. J. Hematol.2013
Cerebrovascular events in sickle cell-beta thalassemia treated with hydroxyurea: A single center prospective survey in adult Italians.Rigano P, Pecoraro A, Calvaruso G, Steinberg MH, Iannello S, Maggio A Am. J. Hematol.2013
Sickle-cell disease in Malawian children is associated with restrictive spirometry: a cross-sectional survey.Cook J, Jefferis O, Matchere P, Mbale E, Rylance J Int. J. Tuberc. Lung Dis.2013
UGT1A1 (TA)n genotyping in sickle-cell disease: High resolution melting (HRM) curve analysis or direct sequencing, what is the best way?Thomas V, Mazard B, Garcia C, Lacan P, Gagnieu MC, Joly P Clin. Chim. Acta2013
High-dose cyclophosphamide for severe aplastic anemia associated with β-thalassemia: a case report and literatures review.Zhao X, Li Y, Zhou K, Zhang L, Jing LP, Ye L, Peng GX, Li Y, Li JP, Fan HH, Song L, Zhang FK Zhonghua Xue Ye Xue Za Zhi2013
The Spectrum of β-Thalassemia Mutations In Baghdad, Central Iraq.Al-Allawi NA, Al-Mousawi BM, Badi AI, Jalal SD Hemoglobin2013
Hematological malignancies complicating β-thalassemia syndromes: a single center experience.Alavi S, Safari A, Sadeghi E, Amiri S Blood Res2013
Clinical factors and incidence of acute chest syndrome or pneumonia among children with sickle cell disease presenting with a Fever: a 17-year review.Chang TP, Kriengsoontorkij W, Chan LS, Wang VJ Pediatr Emerg Care2013
Hemostatic abnormalities in sickle cell disease.Lim MY, Ataga KI, Key NS Curr. Opin. Hematol.2013
A Pilot Study: The Effect of Healing Touch on Anxiety, Stress, Pain, Pain Medication Usage, and Physiological Measures in Hospitalized Sickle Cell Disease Adults Experiencing a Vaso-Occlusive Pain Episode.Thomas LS, Stephenson N, Swanson M, Jesse DE, Brown S J Holist Nurs2013
Longitudinal analysis of heart and liver iron in thalassemia major patients according to chelation treatment.Danjou F, Origa R, Anni F, Saba L, Cossa S, Podda G, Galanello R Blood Cells Mol. Dis.2013
Relationship between HLA-A, B alleles and red blood cell parameters of patients with --(SEA/αα) subtype of α(0)-thalassemia of Han ethnic population of Wuzhou city.Chen XQ, Li J, Cai YL, Li CJ, Ma YY, Huang DW, Li HF, Lu AY, Tang MZ Zhongguo Shi Yan Xue Ye Xue Za Zhi2013
Birth of children with severe β-thalassemia at a tertiary obstetric hospital: what are the reasons behind it?Yang Y, Li DZ Prenat. Diagn.2013
Circulating microparticles in children with sickle cell anemia: a heterogeneous procoagulant storm directed by hemolysis and fetal hemoglobin.Falanga A, Trinchero JA Haematologica2013
The Natural History of Sickle Cell Disease.Serjeant GR Cold Spring Harb Perspect Med2013
Type 1 diabetes mellitus in a patient with homozygous sickle cell anemia.Shoar Z, Rezvani G, De Luca F J. Pediatr. Endocrinol. Metab.2013
Efficacy and safety of interferon-based therapy in the treatment of adult thalassemic patients with chronic hepatitis C: a 12 years audit.Vafiadis I, Trilianos P, Vlachogiannakos J, Karagiorga M, Hatziliami A, Voskaridou E, Ladas SD Ann Hepatol2013
International survey of T2* cardiovascular magnetic resonance in beta thalassemia major.Carpenter JP, Roughton M, Pennell DJ Haematologica2013
South-Italy β-0-thalassaemia: a novel deletion not removing the γ-globin silencing element and with 3' breakpoint in a hsRTVL-H element, associated with β-0-thalassemia and high levels of Hb F.De Angioletti M, Sabato V, Musollino G, Prezioso R, Carestia C, Lacerra G Haematologica2013
Hematogenous Osteoarticular Infections of the Hand and the Wrist in Children With Sickle Cell Anemia: Preliminary Report.Tordjman D, Holvoet L, Benkerrou M, Ilharreborde B, Mazda K, Penneçot GF, Fitoussi F J Pediatr Orthop2013
Invasive Pneumococcal Disease among Children with and without Sickle Cell Disease in the United States, 1998-2009.Payne AB, Link-Gelles R, Azonobi I, Hooper WC, Beall BW, Jorgensen JH, Juni B, Moore M, Pediatr. Infect. Dis. J.2013
A Multiplex qPCR Gene Dosage Assay for Rapid Genotyping and Large-Scale Population Screening for Deletional α-Thalassemia.Zhou W, Wang G, Zhao X, Xiong F, Zhou S, Peng J, Cheng Y, Xu S, Xu X J Mol Diagn2013
Acute Splenic Syndrome in an African-American Male with Sickle Cell Trait on a Commercial Airplane Flight.Murano T, Fox AD, Anjaria D J Emerg Med2013
Erythrocyte-exchange in sickle-cell disease patients. A comparison between Caridian COBE Spectra and Optia cell separators.Perseghin P, Incontri A, Capra M Transfus. Apher. Sci.2013
Challenges in transfusion of patients with sickle cell disease.van Draat KF Transfus. Apher. Sci.2013
Haemoglobin S and β(Thal): Their Distribution in Maharashtra, India.Urade BP Int J Biomed Sci2013
Sildenafil Citrate-Restored eNOS and PDE5 Regulation in Sickle Cell Mouse Penis Prevents Priapism Via Control of Oxidative/Nitrosative Stress.Bivalacqua TJ, Musicki B, Hsu LL, Berkowitz DE, Champion HC, Burnett AL PLoS ONE2013
Development of gene therapy for blood disorders: an update.Nienhuis AW Blood2013
Noninvasive Prenatal Detection for Pathogenic CNVs: The Application in α-Thalassemia.Ge H, Huang X, Li X, Chen S, Zheng J, Jiang H, Zhang C, Pan X, Guo J, Chen F, Chen N, Fang Q, Jiang H, Wang W PLoS ONE2013
Neurodevelopmental Deficits Among Infants and Toddlers with Sickle Cell Disease.Glass P, Brennan T, Wang J, Luchtman-Jones L, Hsu L, Bass CM, Rana S, Martin B, Reed C, Cheng YI, Gordeuk V J Dev Behav Pediatr2013
Transcriptional Mechanisms Underlying Hemoglobin Synthesis.Katsumura KR, Devilbiss AW, Pope NJ, Johnson KD, Bresnick EH Cold Spring Harb Perspect Med2013
An investigation of the protective effect of alpha+-thalassaemia against severe Plasmodium falciparum amongst children in Kumasi, Ghana.Opoku-Okrah C, Gordge M, Kweku Nakua E, Abgenyega T, Parry M, Robertson C, Smith CL Int J Lab Hematol2013
Care of Children With Sickle Cell Disease in the Emergency Department: Parent and Provider Perspectives Inform Quality Improvement Efforts.Tanabe P, Dias N, Gorman L J Pediatr Oncol Nurs2013
Airways obstruction and pulmonary capillary blood volume in children with sickle cell disease.Wedderburn CJ, Rees D, Height S, Dick M, Rafferty GF, Lunt A, Greenough A Pediatr. Pulmonol.2013
Noninvasive prenatal diagnosis experience in the Çukurova Region of Southern Turkey: Detecting paternal mutations of sickle cell anemia and beta-thalassemia in cell-free fetal DNA using high-resolution melting analysis.Dundar Yenilmez E, Tuli A, Evrüke IC Prenat. Diagn.2013
Thyroid Doppler indices in patients with sickle cell disease.Karazincir S, Balci A, Yonden Z, Gali E, Daplan T, Beyoglu Y, Kaya H, Egilmez E Clin Imaging2013
Academic attainment findings in children with sickle cell disease.Epping AS, Myrvik MP, Newby RF, Panepinto JA, Brandow AM, Scott JP J Sch Health2013
The Role of the Inherited Disorders of Hemoglobin, the First Weatherall DJ Annu Rev Genomics Hum Genet2013
Combination therapy of deferasirox and deferoxamine shows significant improvements in markers of iron overload in a patient with β-thalassemia major and severe iron burden.Voskaridou E, Komninaka V, Karavas A, Terpos E, Akianidis V, Christoulas D Transfusion2013
Adipocytokines are related to haemolytic and inflammatory biomarkers in sickle cell beta thalassaemia.Makis A, Challa A, Hatzimichael E, Briasoulis E, Siamopoulou A, Chaliasos N Br. J. Haematol.2013
The Health of Adults Living with a Clinically Significant Haemoglobinopathy in NSW, Australia. The NSW Haemoglobinopathy Project.Crowther HJ, Lindeman R, Ho P, Allen E, Waite C, Matthews S, Jobburn K, Teo J, Day S, Seldon M, Rosenfeld D, Kerridge I Intern Med J2013
Cytomorphometric and cytomorphologic analysis of oral mucosa in children with sickle cell anemia.Paraizo JU, Rech IA, Azevedo-Alanis LR, Pianovski MA, De Lima AA, Machado MÂ J Cytol2013
Reversible Posterior Leukoencephalopathy Syndrome After Blood Transfusion in a Pediatric Patient With Sickle Cell Disease.Kolovou V, Zampakis P, Ginopoulou A, Varvarigou A, Kaleyias J Pediatr. Neurol.2013
Amlodipine Reduces Cardiac Iron Overload in Patients with Thalassemia Major: a Pilot Trial.Fernandes JL, Sampaio EF, Fertrin K, Coelho OR, Loggetto S, Piga A, Verissimo M, Saad ST Am. J. Med.2013
Longitudinal study of echocardiography-derived tricuspid regurgitant jet velocity in sickle cell disease.Desai PC, May RC, Jones SK, Strayhorn D, Caughey M, Hinderliter A, Ataga KI Br. J. Haematol.2013
Towards More Successful Gene Therapy Clinical Trials for β-Thalassemia.Drakopoulou E, Papanikolaou E, Georgomanoli M, Anagnou NP Curr. Mol. Med.2013
Detection of beta-thalassemia/hemoglobin E disease in samples which initially were diagnosed as homozygous hemoglobin E.Pornprasert S, Moriyama A, Kongthai K, Waneesorn J, Jaiping K, Treesuwan K, Hattori Y Clin. Lab.2013
Total antioxidant capacity and ischemia modified albumin in beta thalassemia.Awadallah S, Al Arrayed K, Bahareth E, Saeed Z Clin. Lab.2013
β-globin gene transfer to human bone marrow for sickle cell disease.Romero Z, Urbinati F, Geiger S, Cooper AR, Wherley J, Kaufman ML, Hollis RP, de Assin RR, Senadheera S, Sahagian A, Jin X, Gellis A, Wang X, Gjertson D, Deoliveira S, Kempert P, Shupien S, Abdel-Azim H, Walters MC, Meiselman HJ, Wenby RB, Gruber T, Marder V, Coates TD, Kohn DB J. Clin. Invest.2013
A Synthetic Model of Human Beta-Thalassemia Erythropoiesis Using CD34+ Cells from Healthy Adult Donors.Lee YT, Kim KS, Byrnes C, de Vasconcellos JF, Noh SJ, Rabel A, Meier ER, Miller JL PLoS ONE2013
Photo quiz: positive blood culture in a patient with sickle cell crisis.Suwantarat N, Jacobs MR J. Clin. Microbiol.2013
Pain and other non-neurological adverse events in children with sickle cell anemia and previous stroke who received hydroxyurea and phlebotomy or chronic transfusions and chelation: Results from the SWiTCH clinical trial.Alvarez O, Yovetich NA, Scott JP, Owen W, Miller ST, Schultz W, Lockhart A, Aygun B, Flanagan J, Bonner M, Mueller BU, Ware RE, Am. J. Hematol.2013
Impact of sickle cell disease and thalassemias in infants on birth outcomes.Whiteman V, Salinas A, Weldeselasse HE, August EM, Mbah AK, Aliyu MH, Salihu HM Eur. J. Obstet. Gynecol. Reprod. Biol.2013
A New High Affinity Variant Hb Aurillac (β141Leu→Val).Boursier G, Trouillier S, Blaizot MG, Igual H, Schved JF, Martinez PA Hemoglobin2013
Sickle cell anemia: reference values of cerebral blood flow determined by continuous arterial spin labeling MRI.Arkuszewski M, Krejza J, Chen R, Melhem ER Neuroradiol J2013
Progressive spinal cord compression due to epidural extramedullary hematopoiesis in thalassemia intermedia. A case report and literature review.Ghieda U, Elshimy M, El Beltagi AH Neuroradiol J2013
The proteomics and interactomics of human erythrocytes.Goodman SR, Daescu O, Kakhniashvili DG, Zivanic M Exp. Biol. Med. (Maywood)2013
The Role of a Low-Dose Ketamine-Midazolam Regimen in the Management of Severe Painful Crisis in Patients With Sickle Cell Disease.Tawfic QA, Faris AS, Kausalya R J Pain Symptom Manage2013
Incidence of hepatocellular carcinoma in patients with thalassemia who had hepatitis C.Ansari S, Azarkivan A, Halagi F Acta Med Iran2013
Analysis of β/α Globin Ratio by Using Relative qRT-PCR for Diagnosis of Beta-Thalassemia Carriers.Ranjbaran R, Okhovat MA, Mobarhanfard A, Aboualizadeh F, Abbasi M, Moezzi L, Golafshan HA, Behzad-Behbahani A, Bagheri M, Sharifzadeh S J. Clin. Lab. Anal.2013
Leg ulcers in patients with β-thalassaemia intermedia: a single centre's experience.Matta BN, Abbas O, Maakaron JE, Koussa S, Daderian RH, Taher AT J Eur Acad Dermatol Venereol2013
An Attempt to Induce Transient Immunosuppression Pre-erythrocytapheresis in a Girl With Sickle Cell Disease, a History of Severe Delayed Hemolytic Transfusion Reactions and Need for Hip Prosthesis.Cattoni A, Cazzaniga G, Perseghin P, Zatti G, Gaddi D, Cossio A, Biondi A, Corti P, Masera N Hematol Rep2013
Extent of silent cerebral infarcts in adult sickle-cell disease patients on magnetic resonance imaging: is there a correlation with the clinical severity of disease?Solomou E, Kraniotis P, Kourakli A, Petsas T Hematol Rep2013
Successful orthotopic liver transplantation in an adult patient with sickle cell disease and review of the literature.Blinder MA, Geng B, Lisker-Melman M, Crippin JS, Korenblat K, Chapman W, Shenoy S, Field JJ Hematol Rep2013
Fetal Red Blood Cell Hematology at Mid-Pregnancy Among Fetuses at Risk of Homozygous β-Thalassemia Disease.Srisupundit K, Wanapirak C, Sirichotiyakul S, Tongprasert F, Luewan S, Traisrisilp K, Tongsong T J. Pediatr. Hematol. Oncol.2013
Partial manual exchange reduces iron accumulation during chronic red cell transfusions for sickle cell disease.Savage WJ, Reddoch S, Wolfe J, Casella JF J. Pediatr. Hematol. Oncol.2013
Seroprevalence of parvovirus B19 antibodies and evidence of viremia among Nigerian patients with sickle cell anemia.Iwalokun BA, Iwalokun SO, Hodonu SO J Biomed Res2013
Pichia anomala (Candida pelliculosa) Fungemia in a Patient with Sickle Cell Disease.Chan AW, Cartwright EJ, Reddy SC, Kraft CS, Wang YF Mycopathologia2013
Determination of early cardiac deterioration in beta-thalassaemia major by echocardiography.Ozdogan O, Alp A, Turker M, Atabey B Acta Cardiol2013
Global burden of sickle cell anaemia is set to rise by a third by 2050.Biswas T BMJ2013
Psychosocial Burden of Sickle Cell Disease on Parents with an Affected Child in Cameroon.Wonkam A, Mba CZ, Mbanya D, Ngogang J, Ramesar R, Angwafo FF J Genet Couns2013
Ambulatory blood pressure monitoring for children with Beta-thalassemia major: a preliminary report.Tabatabaie M, Hooman N, Arjmandi-Rafsanjani K, Isa-Tafreshi R Iran J Kidney Dis2013
Deferasirox in Indian children with thalassemia major: 3 years experience.Dhamija M, Mahajan A, Kalra M, Virmani A Indian J Med Paediatr Oncol2013
β-thalassemia due to intronic LINE-1 insertion in the β-globin gene (HBB): molecular mechanisms underlying reduced transcript levels of the β-globinL1 allele.Lanikova L, Kucerova J, Indrak K, Divoka M, Issa JP, Papayannopoulou T, Prchal JT, Divoky V Hum. Mutat.2013
Sickle cell anaemia in a changing world.Fottrell E, Osrin D PLoS Med.2013
Transfusion in Sickle Cell Disease: Experience from a Gujarat Centre.Mehta V, Mistry A, Raicha B, Italia Y, Serjeant G Indian J Pediatr2013
In vivo activation of the human δ-globin gene: the therapeutic potential in β- thalassemic mice.Manchinu MF, Marongiu MF, Poddie D, Casu C, Latini V, Simbula M, Galanello R, Moi P, Cao A, Porcu S, Ristaldi MS Haematologica2013
Early Identification of Cardiovascular Involvement in Patients With β-Thalassemia Major.Cusmà Piccione M, Piraino B, Zito C, Khandheria BK, Di Bella G, De Gregorio C, Oreto L, Rigoli L, Ferraù V, Salpietro CD, Carerj S Am. J. Cardiol.2013
Respiratory muscle force and lung volume changes in a population of children with sickle cell disease.Ong BA, Caboot J, Jawad A, McDonough J, Jackson T, Arens R, Marcus CL, Smith-Whitley K, Mason TB, Ohene-Frempong K, Allen JL Br. J. Haematol.2013
Detection of glycemic abnormalities in adolescents with beta thalassemia using continuous glucose monitoring and oral glucose tolerance in adolescents and young adults with β-thalassemia major: Pilot study.Soliman AT, Yasin M, El-Awwa A, De Sanctis V Indian J Endocrinol Metab2013
The Prevalence of Factor V Leiden (G1691A) and Methylenetetrahydrofolate Reductase C677T Mutations in Sickle Cell Disease in Western India.Kangne HK, Jijina FF, Italia YM, Jain DL, Nadkarni AH, Ghosh KK, Colah RB Clin. Appl. Thromb. Hemost.2013
Cost-Utility Analysis of Deferiprone for the Treatment of β-Thalassaemia Patients with Chronic Iron Overload: A UK Perspective.Bentley A, Gillard S, Spino M, Connelly J, Tricta F Pharmacoeconomics2013
MP4CO, a pegylated hemoglobin saturated with carbon monoxide is a modulator of HO-1, inflammation and vaso-occlusion in transgenic sickle mice.Belcher JD, Young M, Chen C, Nguyen J, Burhop K, Tran P, Vercellotti GM Blood2013
β-thalassemia carriers in Afghanistan: a prevalence estimate.Delacour H, Brondeix A, Kedzierewicz R, Martin PV, Dulou R Ann. Biol. Clin. (Paris)2013
Genotype of thalassemia genes and the polymorphism of β- globin gene in Cantonese.Liu L, Jiang WY, Xu SY, Chen J, Chen LM, Tian QH, Wang JC Zhonghua Xue Ye Xue Za Zhi2013
The application of multiplex ligation-dependent probe amplification technology in diagnosis and prenatal diagnosis of α-thalassemia.Chen YJ, Yang XH, Zeng XQ, Qiao LL Zhonghua Xue Ye Xue Za Zhi2013
Hepcidin expression from monocyte of splenectomized and non-splenectomized patients with HbE-β-thalassemia.Pratummo K, Jetsrisuparb A, Fucharoen S, Tripatara A Hematology2013
A Non-Invasive Technique which Demonstrates the Iron in the Buccal Mucosa of Sickle Cell Anaemia and Thalassaemia Patients who Undergo Repeated Blood Transfusions.Chittamsetty H, Sekhar MS, Ahmed SA, Suri C, Palla S, Venkatesh SM, Tanveer S J Clin Diagn Res2013
Kidney dysfunction and beta S-haplotypes in patients with sickle cell disease.Rocha LB, da Silva Jn GB, Daher Ede F, Rocha HA, Elias DB, Gonçalves RP Rev Bras Hematol Hemoter2013
Sickle cell anemia: clinical diversity and beta S-globin haplotypes.Loggetto SR Rev Bras Hematol Hemoter2013
Quality of life among Iranian patients with beta-thalassemia major using the SF-36 questionnaire.Haghpanah S, Nasirabadi S, Ghaffarpasand F, Karami R, Mahmoodi M, Parand S, Karimi M Sao Paulo Med J2013
Comparison of pregnancy outcomes in women with sickle cell disease and trait.Zia S, Rafique M J Pak Med Assoc2013
Diagnostic applications of newborn screening for α-thalassaemias, haemoglobins E and H disorders using isoelectric focusing on dry blood spots.Jindatanmanusan P, Riolueang S, Glomglao W, Sukontharangsri Y, Chamnanvanakij S, Torcharus K, Viprakasit V Ann. Clin. Biochem.2013
Sickle cell disease and complex congenital cardiac surgery: a case report and review of the pathophysiology and perioperative management.Sanders D, Smith B, Sowell S, Nguyen D, Derby C, Eshun F, Nigro J Perfusion2013
Peripartum acute liver failure from a vaso-occlusive crisis in a patient with sickle cell trait.Khozaim K, Schellinger M, Cummings O, Robinson B J Perinatol2013
Complexity of the alpha-globin genotypes identified with thalassemia screening in Sardinia.Origa R, Paglietti ME, Sollaino MC, Desogus MF, Barella S, Loi D, Galanello R Blood Cells Mol. Dis.2013
Determining glomerular filtration rate in homozygous sickle cell disease: utility of serum creatinine based estimating equations.Asnani MR, Lynch O, Reid ME PLoS ONE2013
Perfluorocarbon emulsion improves oxygen transport of normal and sickle cell human blood in vitro.Filho IP, Pedro JR, Narayanan SV, Nguyen NM, Roseff SD, Spiess BD J Biomed Mater Res A2013
Pulmonary Artery Occlusion Pressure May Overdiagnose Pulmonary Artery Hypertension in Sickle Cell Disease.Sharma S, Efird J, Kadali R, Mehra S, Chohan H, Daggubati R, Liles D, Gouge C, Boettger P, Knupp C Clin Cardiol2013
Depression in subjects with beta-thalassemia minor.Keşkek SO, Kırım S, Turhan A, Turhan FG Ann. Hematol.2013
A 2-year-old girl with co-inherited cystic fibrosis and sickle cell-β+ thalassemia presenting with recurrent vaso-occlusive events during cystic fibrosis pulmonary exacerbations: a case report.Sobush KT, Thornburg CD, Voynow JA, Davis SD, Peterson-Carmichael SL J Med Case Rep2013
Clinical and molecular characterization of Hb Hofu in eastern India.Purohit P, Mashon RS, Patel S, Dehury S, Pattanayak C, Das K, Nair S, Italia K, Bag S, Colah R, Patel DK Int J Lab Hematol2013
Transfusion complications in thalassemia patients: a report from the Centers for Disease Control and Prevention.Vichinsky E, Neumayr L, Trimble S, Giardina PJ, Cohen AR, Coates T, Boudreaux J, Neufeld EJ, Kenney K, Grant A, Thompson AA, Transfusion2013
Subcortical and cerebellar volumetric deficits in paediatric sickle cell anaemia.Kawadler JM, Clayden JD, Kirkham FJ, Cox TC, Saunders DE, Clark CA Br. J. Haematol.2013
Relationship between antibiotic resistance and sickle cell anemia: preliminary evidence from a pediatric carriage study in Ghana.Donkor ES, Foster-Nyarko E, Enweronu-Laryea CC Infect Drug Resist2013
Lactate dehydrogenase and hemolysis in sickle cell disease.Kato GJ, Nouraie SM, Gladwin MT Blood2013
Hemoglobin disorders: a look to the future.Nathan DG Blood2013
Ideal donors, imperfect results in sickle cell disease.Thompson AA Blood2013
Seamless correction of the sickle cell disease mutation of the HBB gene in human induced pluripotent stem cells using TALENs.Sun N, Zhao H Biotechnol. Bioeng.2013
Unraveling restrictive chronic lung disease in sickle cell disease [Editorial].Jain S, Gladwin MT, Novelli EM Int. J. Tuberc. Lung Dis.2013
Therapeutic superiority and safety of combined hydroxyurea with recombinant human erythropoietin over hydroxyurea in young β-thalassemia intermedia patients.Elalfy MS, Adly AA, Ismail EA, Elhanawy Y, Elghamry IR Eur. J. Haematol.2013
Molecular epidemiological analysis of alpha- and beta-thalassemia in Fujian province.Xu L, Huang H, Wang Y, Zheng L, Wang L, Xu J, Huang X, Lin Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi2013
Laboratory diagnosis of homozygous alpha thalassaemia.Kyeremeh R, Acquaye JK, Asante PS, Dzudzor B West Afr J Med2013
Lung imaging during acute chest syndrome in sickle cell disease: computed tomography patterns and diagnostic accuracy of bedside chest radiograph.Mekontso Dessap A, Deux JF, Habibi A, Abidi N, Godeau B, Adnot S, Brun-Buisson C, Rahmouni A, Galacteros F, Maitre B Thorax2013
Is high pressure liquid chromatography an effective screening tool for characterization of molecular defects in hemoglobinopathies?Moorchung N, Phillip J, Sarkar RS, Prasad R, Dutta V Indian J Pathol Microbiol2013
Blood viscosity and the expression of inflammatory and adhesion markers in homozygous sickle cell disease subjects with chronic leg ulcers.Bowers AS, Reid HL, Greenidge A, Landis C, Reid M PLoS ONE2013
Search for antisickling agents from plants.Dash BP, Archana Y, Satapathy N, Naik SK Pharmacogn Rev2013
Would you terminate a pregnancy affected by sickle cell disease? Analysis of views of patients in Cameroon.Wonkam A, de Vries J, Royal CD, Ramesar R, Angwafo FF J Med Ethics2013
Pain over time and its effects on life in thalassemia.Oliveros O, Trachtenberg F, Haines D, Gerstenberger E, Martin M, Carson S, Green S, Calamaras D, Hess P, Yamashita R, Vichinsky E, Am. J. Hematol.2013
Right ventricular diastolic function in patients with thalassemia major.Demirkol S, Balta S, Cakar M Arq. Bras. Cardiol.2013
Sickle cell anemia and transfusion safety in Bamako, Mali. Seroprevalence of HIV, HBV and HCV infections and alloimmunization belonged to Rh and Kell systems in sickle cell anemia patients.Diarra AB, Guindo A, Kouriba B, Dorie A, Diabaté DT, Diawara SI, Fané B, Touré BA, Traoré A, Gulbis B, Diallo DA Transfus Clin Biol2013
Blood transfusion in Bangladesh with particular emphasis on the treatment of Thalassemia patients.Islam MB Transfus. Apher. Sci.2013
Sickle cell crisis and pregnancy.Parrish MR, Morrison JC Semin. Perinatol.2013
The Spectrum of β-Thalassemia Mutations in Kermanshah Province in West Iran and its Association with Hematological Parameters.Mehrabi M, Alibakhshi R, Fathollahi S, Farshchi MR Hemoglobin2013
Intraday Blood Rheological Changes Induced by Ramadan Fasting in Sickle Cell Trait Carriers.Diaw M, Connes P, Samb A, Sow AK, Sall ND, Sar FB, Ba A, Diop S, Niang MN, Tripette J Chronobiol. Int.2013
Medical management of beta-thalassaemia without blood transfusion: a myth or a reality?Shamsi T, Ansari S J Pak Med Assoc2013
Endothelin-1 receptor antagonists regulate cell surface-associated protein disulfide isomerase in sickle cell disease.Prado GN, Romero JR, Rivera A FASEB J.2013
Laboratory diagnosis of homozygous alpha thalassaemia.Kyeremeh R, Acquaye JK, Asante PS, Dzudzor B West Afr J Med2013
Nucleosomes and neutrophil activation in sickle cell disease painful crisis.Schimmel M, Nur E, Biemond BJ, van Mierlo GJ, Solati S, Brandjes DP, Otten HM, Schnog JJ, Zeerleder S Haematologica2013
Is sickle cell disease a possible risk factor for peripheral neuropathy after popliteal sciatic nerve block?Giabicani M, Compère V, Fourdrinier V, Dureuil B Br J Anaesth2013
Efficacy and safety of deferasirox compared with deferoxamine in sickle cell disease: 2-year results including pharmacokinetics and concomitant hydroxyurea.Vichinsky E, Torres M, Minniti CP, Barrette S, Habr D, Zhang Y, Files B, Am. J. Hematol.2013
Zinc supplementation improves bone density in patients with thalassemia: a double-blind, randomized, placebo-controlled trial.Fung EB, Kwiatkowski JL, Huang JN, Gildengorin G, King JC, Vichinsky EP Am. J. Clin. Nutr.2013
β- and α-Thalassemia Intermedia in Basra, Southern Iraq.Abdulwahid DA, Hassan MK Hemoglobin2013
Anemia in Patients with Coinherited Thalassemia and Glucose-6-Phosphate Dehydrogenase Deficiency.Pornprasert S, Phanthong S Hemoglobin2013
Assessment and prediction of pruritus in sickle cell disease patients: a preliminary study.Hanes D, Jefferson-Gordon J, Lindsey A, O'Connor S, Petty L, Weiss M, Nnadi M, Overcash J Clin Nurse Spec2013
Lefort 1 osteotomy in a beta-thalassemia major patient--a case report.Showkatbakhsh R, Behnia H, Jamilian A, Heydarpour M, Fetrati A Int J Orthod Milwaukee2013
Distal ulnar changes in children with thalassemia and deferiprone related arthropathy.Sharma R, Anand R, Chandra J, Seth A, Pemde H, Singh V Pediatr Blood Cancer2013
CRISPR/Cas9 systems targeting β-globin and CCR5 genes have substantial off-target activity.Cradick TJ, Fine EJ, Antico CJ, Bao G Nucleic Acids Res.2013
Hemoglobin variant analysis of whole blood and dried blood spots by MS.Edwards RL, Martin NJ, Cooper HJ Bioanalysis2013
Zinc finger protein 148 is dispensable for primitive and definitive hematopoiesis in mice.Nilton A, Sayin VI, Staffas A, Larsson E, Rolf J, Petit MM, Palmqvist L, Swolin B, Cardell S, Lindahl P PLoS ONE2013
Genome Wide Association Analysis of a Founder Population Identified TAF3 as a Gene for MCHC in Humans.Pistis G, Okonkwo SU, Traglia M, Sala C, Shin SY, Masciullo C, Buetti I, Massacane R, Mangino M, Thein SL, Spector TD, Ganesh S, Pirastu N, Gasparini P, Soranzo N, Camaschella C, Hart D, Green MR, Toniolo D PLoS ONE2013
Cyclosporine therapy during pregnancy in a patient with β-thalassemia major and autoimmune haemolytic anemia: a case report and review of the literature.Agapidou A, Vlachaki E, Theodoridis T, Economou M, Perifanis V Hippokratia2013
Massive haemolysis and methaemalbuminaemia in a patient with decompensated haemoglobin H disease.Joly P, Richard Colmant G, Varennes A, Francina A, Coppéré B, Delacour H Br. J. Haematol.2013
Role of Genetic Counselling in Prenatal Diagnosis of β-Thalassaemia in Pakistan.Bozdar M, Ahmed S, Jamy O, Tamoor Bin Hanif , Ali N, Khan Khattak SA J Coll Physicians Surg Pak2013
Burden of Anemia in Relation to Thalassemia and Iron Deficiency among Vietnamese Pregnant Women.Siridamrongvattana S, Van Hoa N, Sanchaisuriya K, Dung N, Hoa PT, Sanchaisuriya P, Fucharoen G, Fucharoen S, Schelp FP Acta Haematol.2013
Detection of unknown β-thalassemia cases from atypical HbA1c chromatograms.Desmons A, Guillard E, Jaisson S, Gillery P Clin. Chem. Lab. Med.2013
Hydroxyurea use and hospitalization trends in a comprehensive pediatric sickle cell program.Nottage KA, Hankins JS, Smeltzer M, Mzayek F, Wang WC, Aygun B, Gurney JG PLoS ONE2013
Deferasirox: appraisal of safety and efficacy in long-term therapy.Chaudhary P, Pullarkat V J Blood Med2013
Oral deferiprone for iron chelation in people with thalassaemia.Fisher SA, Brunskill SJ, Doree C, Chowdhury O, Gooding S, Roberts DJ Cochrane Database Syst Rev2013
Characteristics of Acute Care Utilization of a Delaware Adult Sickle Cell Disease Patient Population.Anderson N, Bellot J, Senu-Oke O, Ballas SK Popul Health Manag2013
Vasculopathy, inflammation and blood flow in leg ulcers of patients with sickle cell anemia.Minniti CP, Delaney KM, Gorbach AM, Xu D, Lee CC, Malik N, Koroulakis A, Antalek M, Maivelett J, Peters-Lawrence M, M Novelli E, Lanzkron SM, Axelrod KC, Kato GJ Am. J. Hematol.2013
Desferrioxamine mesylate for managing transfusional iron overload in people with transfusion-dependent thalassaemia.Fisher SA, Brunskill SJ, Doree C, Gooding S, Chowdhury O, Roberts DJ Cochrane Database Syst Rev2013
Bone marrow transplantation for thalassemia from alternative related donors: improved outcomes with a new approach.Gaziev J, Marziali M, Isgrò A, Sodani P, Paciaroni K, Gallucci C, Andreani M, Testi M, De Angelis G, Alfieri C, Cardarelli L, Ribersani M, Armiento D, Lucarelli G Blood2013
Using Photovoice to Explore the Unique Life Perspectives of Youth With Sickle Cell Disease: A Pilot Study.Stegenga K, Burks LM J Pediatr Oncol Nurs2013
The reproducibility of cardiac and liver T2* measurement in thalassemia major using two different software packages.Mavrogeni S, Bratis K, van Wijk K, Kyrou L, Kattamis A, Reiber JH Int J Cardiovasc Imaging2013
Long-term health-related quality of life evaluated more than twenty years after hematopoietic stem cell transplantation for thalassemia.La Nasa G, Caocci G, Efficace F, Dessì C, Vacca A, Piras E, Sanna M, Marcias M, Littera R, Carcassi C, Lucarelli G Blood2013
Detection of Hb H Disease Genotypes Common in Northern Thailand by Quantitative Real-Time Polymerase Chain Reaction and High Resolution Melting Analyses.Seeratanachot T, Sanguansermsri T, Shimbhu D Hemoglobin2013
Mapping Polymerization and Allostery of Hemoglobin S Using Point Mutations.Weinkam P, Sali A J Phys Chem B2013
Prevalence of Priapism and Its Awareness amongst Male Homozygous Sickle Cell Patients in Lagos, Nigeria.Adediran A, Wright K, Akinbami A, Dosunmu A, Oshinaike O, Osikomaiya B, Ajibola S, Ismail K, Uche E, Ojelabi O Adv Urol2013
Inhibition of Myeloperoxidase Decreases Vascular Oxidative Stress and Increases Vasodilatation in Sickle Cell Disease Mice.Zhang H, Xu H, Weihrauch D, Jones DW, Jing X, Shi Y, Gourlay D, Oldham KT, Hillery CA, Pritchard KA J. Lipid Res.2013
Audiologic and vestibular assessment in patients with β-thalassemia major receiving long-term transfusion therapy.Chao YH, Wu KH, Lin CY, Tsai MH, Peng CT, Wu HP, Lin CD Pediatr Blood Cancer2013
Chronic blood transfusion for primary and secondary stroke prevention in Nigerian children with sickle cell disease: A 5-year appraisal.Lagunju IA, Brown BJ, Sodeinde OO Pediatr Blood Cancer2013
Identification of One or Two α-Globin Gene Deletions by Isoelectric Focusing Electrophoresis.Agarwal AM, Nussenzveig RH, Hoke C, Lorey TS, Greene DN Am. J. Clin. Pathol.2013
L-arginine increases nitric oxide and attenuates pressor and heart rate responses to change in posture in sickle cell anemia subjects.Ogungbemi SI, Anigbogu CN, Kehinde MO, Jaja SI Niger J Physiol Sci2013
ABO (H) secretor status of sickle cell disease patients in Zaria, Kaduna State, Nigeria.Olorunshola KV, Audu L Niger J Physiol Sci2013
Sickle cell anaemia: Current therapies.Vermylen C Transfus. Apher. Sci.2013
Moyamoya syndrome associated with sickle cell trait in a child.Komur M, Unal S, Okuyaz C, Ozgur A Brain Dev.2013
Hematologic complications of pregnancy.Townsley DM Semin. Hematol.2013
Perinatal Outcome in Sickle Cell Anemia: A Prospective Study from India.Daigavane MM, Jena RK, Kar TJ Hemoglobin2013
Acute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemia.Bean CJ, Boulet SL, Yang G, Payne AB, Ghaji N, Pyle ME, Hooper WC, Bhatnagar P, Keefer J, Barron-Casella EA, Casella JF, Debaun MR Br. J. Haematol.2013
Gene Expression Analysis of the Brazilian Type of Hereditary Persistence of Fetal Hemoglobin: Identification of Genes that Could be Related to γ-Globin Activation.Roversi FM, da Cunha AF, Brugnerotto AF, Carazzolle MF, de Albuquerque DM, Lanaro C, Machado-Neto JA, Olalla Saad ST, da Costa FF Hemoglobin2013
Fatal dengue in patients with sickle cell disease or sickle cell anemia in curaçao: two case reports.Moesker FM, Muskiet FD, Koeijers JJ, Fraaij PL, Gerstenbluth I, van Gorp EC, Osterhaus AD PLoS Negl Trop Dis2013
Increased Reticulocytosis during Infancy Is Associated with Increased Hospitalizations in Sickle Cell Anemia Patients during the First Three Years of Life.Meier ER, Byrnes C, Lee YT, Wright EC, Schechter AN, Luban NL, Miller JL PLoS ONE2013
Low prevalence of cardiac siderosis in heavily iron loaded Egyptian thalassemia major patients.El Beshlawy A, El Tagui M, Hamdy M, El Ghamrawy M, Azim KA, Salem D, Said F, Samir A, Pierre TS, Pennell DJ Ann. Hematol.2013
Cystatin C, Beta2 Microglobulin, N-Acetyl-beta-D-glucosaminidase, Retinol-Binding Protein, and Endothelin 1 Levels in the Evaluation of Sickle Cell Disease Nephropathy.Unal S, Kotan C, Delibas A, Oztas Y Pediatr Hematol Oncol2013
Prevalence of Pulmonary Arterial Hypertension among Sickle Cell Disease Patients in AL Hassa.Al-Khoufi EA Glob J Health Sci2013
Transcranial Doppler Ultrasonography in Beta-thalassemia Major Patients Without and With Thrombocytosis.Shariat A, Nazeri M, Abolhasani Foroughi A, Karimi M Iran Red Crescent Med J2013
Causes and clinical significance of prolonged activated partial thromboplastin times in thalassaemia major.McFadyen J, Butler J, Malan E, Tran H Ann. Hematol.2013
Serum uric Acid: an early indicator of oxidative stress in Beta thalassemia population.Dasgupta S, Dasgupta A, Mukhopadhayay T, Bhattacharya S, Swaika B, Banarjee U, Chakrabarty P Mymensingh Med J2013
Identification of IVS-I (-1) (G > C) or Hb Monroe as a Report on the Beta-globin Gene with a Beta-thalassemia Minor Phenotype in South of Iran.Hamid M, Shariati G, Saberi A, Kaikhaei B, Galehdari H, Mohammadi-Anaei M Arch Iran Med2013
Clinical and molecular characteristics of hemoglobin New York in Guangxi populations.Li YQ, Huang HP, Yang WH, Chen ZZ, Zhao L, Huang HY, Qin GF Zhonghua Xue Ye Xue Za Zhi2013
Resveratrol accelerates erythroid maturation by activation of FOXO3 and ameliorates anemia in beta-thalassemic mice.Santos Franco S, De Falco L, Ghaffari S, Brugnara C, Sinclair DA, Mattè A, Iolascon A, Mohandas N, Bertoldi M, An X, Siciliano A, Rimmelé P, Cappellini MD, Michan S, Zoratti E, Janin A, De Franceschi L Haematologica2013
A pilot study of eptifibatide for treatment of acute pain episodes in sickle cell disease.Desai PC, Brittain JE, Jones SK, McDonald A, Wilson DR, Dominik R, Key NS, Parise LV, Ataga KI Thromb. Res.2013
Information-seeking coping behaviors during painful procedures in african-american children with sickle cell disease.Schlenz AM, Schatz J, McClellan CB, Sweitzer SM, Roberts CW Pain Manag Nurs2013
Evaluation of tissue doppler echocardiography and T2* magnetic resonance imaging in iron load of patients with thalassemia major.Saravi M, Tamadoni A, Jalalian R, Mahmoodi-Nesheli H, Hojati M, Ramezani S Caspian J Intern Med2013
Early detection of cardiac involvement in thalassemia: From bench to bedside perspective.Koonrungsesomboon N, Chattipakorn SC, Fucharoen S, Chattipakorn N World J Cardiol2013
Toward a stroke-free childhood in sickle cell disease: the 2013 sherman lecture.Adams RJ Stroke2013
Association between cardiac T2* magnetic resonance imaging values and endocrine function tests in patients with β-thalassemia major.Daar S, Musallam KM, Pathare A, Taher A Blood Cells Mol. Dis.2013
Hb Fulton-Georgia [α20(B1)His→Pro; HBA1: c.62A>C]: A New α-Globin Variant Coinherited with α-Thalassemia-2 (3.7 kb deletion) and Hb SC Disease.Zhuang L, Patel N, Bryant S, Kutlar A, Kutlar F, Young AN Hemoglobin2013
The Changing Epidemiology of β-Thalassemia in the Greek-Cypriot Population.Kyrri AR, Kalogerou E, Loizidou D, Ioannou C, Makariou C, Kythreotis L, Phylactides M, Kountouris P, Angastiniotis M, Modell B, Kleanthous M Hemoglobin2013
Low fetal hemoglobin rates in patients carrying Thai (δβ)0-deletion and Turkish (δβ)0-deletion/inversion strengthen the hypothesis that the 5'δ BCL11A binding site plays a major role in its fetal hemoglobin inhibitory regulation. Response to Ghedira ES, Pissard S Haematologica2013
The 12.6 kb-deletion in the β-globin gene cluster is the known Thai/Vietnamese (δβ)0-thalassemia commonly found in Southeast Asia.Chalaow N, Thein SL, Viprakasit V Haematologica2013
Sickle Cell Anemia: time for personalized prescription of hydroxyurea? Focus on Thornburg CD Am. J. Physiol., Cell Physiol.2013
Alpha thalassemia protects sickle cell anemia patients from macro-albuminuria through its effects on red blood cell rheological properties.Lamarre Y, Romana M, Lemonne N, Hardy-Dessources MD, Tarer V, Mougenel D, Waltz X, Tressières B, Lalanne-Mistrih ML, Etienne-Julan M, Connes P Clin. Hemorheol. Microcirc.2013
Prior exposure of endothelial cells to hydroxycarbamide alters the flow dynamics and adhesion of sickle red blood cells.Verger E, Schoëvaërt D, Carrivain P, Victor JM, Lapouméroulie C, Elion J Clin. Hemorheol. Microcirc.2013
Oxidative stress in sickle cell disease: An overview of erythrocyte redox metabolism and current antioxidant therapeutic strategies.Humberto Silva DG, Belini Junior E, de Almeida EA, Bonini-Domingos CR Free Radic. Biol. Med.2013
Hematopoietic stem cell mobilization for gene therapy: superior mobilization by the combination of Plerixafor plus GCSF in patients with thalassemia major.Yannaki E, Karponi G, Zervou F, Constantinou V, Bouinta A, Tachinopoulou V, Kotta K, Jonlin E, Papayannopoulou T, Anagnostopoulos A, Stamatoyannopoulos G Hum. Gene Ther.2013
Visual diagnosis: girl with sickle cell disease, abdominal pain, and elevated blood pressure ... A missed opportunity.Chuang E, Ng C, Ehrlich J Pediatr Rev2013
Comparison of automated red cell exchange transfusion and simple transfusion for the treatment of children with sickle cell disease acute chest syndrome.Saylors RL, Watkins B, Saccente S, Tang X Pediatr Blood Cancer2013
Hydroxyurea Is Associated With Lower Costs of Care of Young Children With Sickle Cell Anemia.Wang WC, Oyeku SO, Luo Z, Boulet SL, Miller ST, Casella JF, Fish B, Thompson BW, Grosse SD, Pediatrics2013
The Prevalence of the Beta Thalassemia Trait among the Pregnant Women who attended the ANC Clinic in a PHC, by using the NESTROF Test in Bangalore, Karnataka.Kulkarni P, Masthi NR, Niveditha S, Suvarna R J Clin Diagn Res2013
Study of Mutations in β-Thalassemia Trait among Blood Donors in Eastern Uttar Pradesh.Meena LP, Kumar K, Singh VK, Bharti A, Rahman SK, Tripathi K J Clin Diagn Res2013
Frequent red cell transfusions reduced vascular endothelial activation and thrombogenicity in children with sickle cell anemia and high stroke risk.Hyacinth HI, Adams RJ, Voeks JH, Hibbert JM, Gee BE Am. J. Hematol.2013
Reproductive Health Choices for Young Adults With Sickle Cell Disease or Trait: Randomized Controlled Trial Immediate Posttest Effects.Wilkie DJ, Gallo AM, Yao Y, Molokie RE, Stahl C, Hershberger PE, Zhao Z, Suarez ML, Labotka RJ, Johnson B, Angulo R, Angulo V, Carrasco J, Shuey D, Pelligra S, Wang E, Rogers DT, Thompson AA Nurs Res2013
Evidence review of hydroxyurea for the prevention of sickle cell complications in low-income countries.Mulaku M, Opiyo N, Karumbi J, Kitonyi G, Thoithi G, English M Arch. Dis. Child.2013
Isothermal Strand-Displacement Polymerase Reaction for Visual Detection of the Southeast Asian-Type Deletion of α-Thalassemia.Yu L, Wu W, Lie P, Liu Y, Zeng L J Mol Diagn2013
Clinical impact of Factor V Leiden, Prothrombin G20210A and MTHFR C677T mutations among sickle cell disease patients of Central India.Nishank SS, Singh M, Yadav R Eur. J. Haematol.2013
Sanfilippo syndrome, glucose-6-phosphate dehydrogenase deficiency and sickle cell/β(+) thalassemia in a child: The burden of consanguinity.Mohamed S Am. J. Med. Genet. A2013
2D DIGE based proteomics study of erythrocyte cytosol in sickle cell disease: altered proteostasis and oxidative stress.Basu A, Sutapa Saha , Karmakar S, Chakravarty S, Banerjee D, Dash BP, Chakrabartii A Proteomics2013
Hemoglobin levels and red blood cell indices in mid gestational fetuses with beta-thalassemia/HbE, beta-thalassemia trait or Hb E trait and normal fetuses.Srisupundit K, Wanapirak C, Sirichotiyakul S, Tongprasert F, Leuwan S, Traisrisilp K, Tongsong T Prenat. Diagn.2013
GLEE-ful for sickle cell pain?Kutlar A Blood2013
Haemoglobin SC disease presenting as hip pain and urinary retention.Tran J, Johnson RL, Jackson IS, Altschuler EL J Paediatr Child Health2013
Biochemical and immunological mechanisms by which sickle cell trait protects against malaria.Gong L, Parikh S, Rosenthal PJ, Greenhouse B Malar. J.2013
Distribution of alpha thalassaemia gene variants in diverse ethnic populations in malaysia: data from the institute for medical research.Ahmad R, Saleem M, Aloysious NS, Yelumalai P, Mohamed N, Hassan S Int J Mol Sci2013
Prevalence of intracranial stenosis and silent cerebral infarcts in children with sickle cell anemia and low risk of stroke.Arkuszewski M, Krejza J, Chen R, Ichord R, Kwiatkowski JL, Bilello M, Zimmerman R, Ohene-Frempong K, Melhem ER Int J Stroke2013
Beta-Thalassemia major and pregnancy.Gulino FA, Vitale SG, Fauzia M, Cianci S, Pafumi C, Palumbo MA Bratisl Lek Listy2013
Cardiomyocyte ultrastructural damage in β-thalassaemic mice.Sanyear C, Butthep P, Nithipongvanich R, Sirankapracha P, Winichagoon P, Fucharoen S, Svasti S Int J Exp Pathol2013
Early diagnosis of co-existent ß-thalassemia and alkaptonuria.Lodh M, Kerketta JA Indian J Hum Genet2013
Comparison of in-vitro and in-vivo response to fetal hemoglobin production and γ-mRNA expression by hydroxyurea in Hemoglobinopathies.Italia K, Jijina F, Merchant R, Swaminathan S, Nadkarni A, Gupta M, Ghosh K, Colah R Indian J Hum Genet2013
Unique pattern of mutations in β-thalassemia patients in Western Uttar Pradesh.Christopher AF, Kumari A, Chaudhary S, Hora S, Ali Z, Agrawal SC Indian J Hum Genet2013
Alpha thalassaemia due to non-deletional mutations on the -3.7 alpha globin fusion gene: laboratory diagnosis and clinical importance.Chow A, Ghassemifar R, Finlayson J Pathology2013
Treatment of chronic sickle cell leg ulcers with supplemental oxygen.Barnes SC J La State Med Soc2013
Circulating endothelial progenitor cells in adults with sickle cell disease.Rodrigo M, Mendelsohn L, Bereal-Williams C, Hunter L, Dalby CK, McGowan V, Hunter CJ, Machado RF, McCoy JP, Cannon RO, Kato GJ Pulm Circ2013
Counseling for prenatal diagnosis and termination of pregnancy due to thalassemia major: a survey of health care workers' practices in Malaysia.Ngim CF, Lai NM, Ibrahim H Prenat. Diagn.2013
Nocturnal enuresis in sickle cell disease and thalassemia major: associated factors in a clinical sample.Ekinci O, Celik T, Unal S, Oktay G, Toros F, Ozer C Int. J. Hematol.2013
Vaso-occlusion in sickle cell disease: pathophysiology and novel targeted therapies.Manwani D, Frenette PS Blood2013
Acute, Bilateral, Concurrent Central Retinal Artery Occlusion in Sickle Cell Disease After Use of Tadalafil (Cialis).Murthy RK, Perez L, Priluck JC, Grover S, Chalam KV JAMA Ophthalmol2013
Fetal Red Blood Cell Parameters in Thalassemia and Hemoglobinopathies.Karnpean R, Fucharoen G, Fucharoen S, Ratanasiri T Fetal. Diagn. Ther.2013
Two Unusual Cases of Haemoglobin Bart's Hydrops Fetalis due to Uniparental Disomy or Non-Paternity.Kou KO, Lee H, Lau B, Wong WS, Kan A, Tang M, Lau ET, Poon CF, Leung KY Fetal. Diagn. Ther.2013
Comparison of hematocrit/hemoglobin ratios in subjects with alpha-thalassemia, with subjects having chronic kidney disease and normal subjects.Insiripong S, Supattarobol T, Jetsrisuparb A Southeast Asian J. Trop. Med. Public Health2013
Sickle cell disease: taking a multidisciplinary approach.Apanah S, Rizzolo D JAAPA2013
Effect of sickle cell crises on glomerular filtration rate in children with sickle cell disease in Ilorin, Nigeria.Anigilaje EA, Adeniyi A, Adedoyin OT Indian J Nephrol2013
Plastic bronchitis in beta thalassemia minor.Yadav M, Tirpude S, Joshi JM Lung India2013
Prevalence of dentofacial abnormalities in children and adolescents with β-thalassaemia major.Elangovan A, Mungara J, Joseph E, Guptha V Indian J Dent Res2013
Reversal of paracentral occlusive retinopathy in a case of sickle cell disease using exchange transfusion.Gustave BW, Oliver SC, Mathias M, Velez-Montoya R, Quiroz-Mercado H, Olson JL, Mandava N, Bhandari R Ophthalmic Surg Lasers Imaging Retina2013
Regional consensus opinion for the management of Beta thalassemia major in the Arabian Gulf area.Qari MH, Wali Y, Albagshi MH, Alshahrani M, Alzahrani A, Alhijji IA, Almomen A, Aljefri A, Al Saeed HH, Abdullah S, Al Rustumani A, Mahour K, Mousa SA Orphanet J Rare Dis2013
Iron chelation therapy for non-transfusion-dependent thalassemia (NTDT): A status quo.Taher AT, Musallam KM, Viprakasit V, Porter JB, Cappellini MD Blood Cells Mol. Dis.2013
Pitfalls of using administrative data sets to describe clinical outcomes in sickle cell disease.Claster S, Termuhlen A, Schrager SM, Wolfson JA, Iverson E Pediatr Blood Cancer2013
PedsQL™ multidimensional fatigue scale in sickle cell disease: Feasibility, reliability, and validity.Panepinto JA, Torres S, Bendo CB, McCavit TL, Dinu B, Sherman-Bien S, Bemrich-Stolz C, Varni JW Pediatr Blood Cancer2013
Newborn screening program for hemoglobinopathies in Rio de Janeiro, Castro Lobo CL, Ballas SK, Domingos AC, Moura PG, do Nascimento EM, Cardoso GP, de Carvalho SM Pediatr Blood Cancer2013
Transcranial doppler and brain MRI in children with sickle cell disease and high hemoglobin F levels.Asbeutah A, Gupta R, Al-Saeid O, Ashebu S, Al-Sharida S, Mullah-Ali A, Mustafa NY, Adekile A Pediatr Blood Cancer2013
A prospective newborn screening and treatment program for sickle cell anemia in luanda, angola.McGann PT, Ferris MG, Ramamurthy U, Santos B, de Oliveira V, Bernardino L, Ware RE Am. J. Hematol.2013
The pathophysiological relationship and clinical significance of left atrial function and left ventricular diastolic dysfunction in β-thalassemia major.Kostopoulou AG, Tsiapras DP, Chaidaroglou AS, Degiannis DE, Farmakis D, Kremastinos DT Am. J. Hematol.2013
Newborn Screening for Sickle Cell Disease in India: The Need for Defining Optimal Clinical Care.Patel J, Serjeant GR Indian J Pediatr2013
Three most common nonsynonymous UGT1A6*2 polymorphisms (Thr181Ala, Arg184Serand Ser7Ala) and therapeutic response to deferiprone in β-thalassemia major patients.Dadheech S, Rao AV, Shaheen U, Hussien MD, Jain S, Jyothy A, Munshi A Gene2013
Managing misaligned paternity findings in research including sickle cell disease screening in Kenya: 'Consulting communities' to inform policy.Marsh V, Kombe F, Fitzpatrick R, Molyneux S, Parker M Soc Sci Med2013
Impact of heart magnetic resonance imaging on chelation choices, compliance with treatment and risk of heart disease in patients with thalassaemia major.Origa R, Danjou F, Cossa S, Matta G, Bina P, Dessì C, Defraia E, Foschini ML, Leoni G, Morittu M, Galanello R Br. J. Haematol.2013
A Retrospective Study to Assess the Utility of Frequent Laboratory Monitoring of Pediatric Patients With Sickle Cell Disease on Hydroxyurea.Nevin J, Myers L, Osunkwo I, Kanter J J. Pediatr. Hematol. Oncol.2013
Re: ambulatory blood pressure monitoring for children with Beta-thalassemia major: a preliminary report.Sadeghi Ghahrodi M, Einollahi B Iran J Kidney Dis2013
Detection of three common α-thalassemia in non-deletion types and six common thalassemia in deletion types by QF-PCR.Ju L, Xuehe Y, Kegan L, Wanrong P, Xunjin W, Kepeng F, Shanhuo Y, Lei S Clin. Biochem.2013
Images in clinical medicine. Extramedullary hematopoiesis in thalassemia.Hassanzadeh M N. Engl. J. Med.2013
Prenatal screening and counseling for genetic disorders.Maruotti GM, Sarno L, Simioli S, Castaldo G, Martinelli P J. Matern. Fetal. Neonatal. Med.2013
Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients.Jouini L, Sahli CA, Laaouini N, Ouali F, Youssef IB, Dakhlaoui B, Othmeni R, Ouennich F, Fredj SH, Siala H, Becher M, Toumi NE, Fattoum S, Hafsia R, Bibi A, Messaoud T Mol. Biol. Rep.2013
Fat-Soluble Antioxidant Vitamins, Iron Overload and Chronic Malnutrition in β-Thalassemia Major.Behera S, Dixit S, Bulliyya G, Kar SK Indian J Pediatr2013
Dynamics of α-Hb chain binding to its chaperone AHSP depends on heme coordination and redox state.Kiger L, Vasseur C, Domingues-Hamdi E, Truan G, Marden MC, Baudin-Creuza V Biochim. Biophys. Acta2013
Altered red cell and platelet adhesion in hemolytic diseases: Hereditary spherocytosis, paroxysmal nocturnal hemoglobinuria and sickle cell disease.Sakamoto TM, Canalli AA, Traina F, Franco-Penteado CF, Gambero S, Saad ST, Conran N, Costa FF Clin. Biochem.2013
UGT1A1 promoter polymorphism associated with serum bilirubin level in Saudi patients with sickle cell disease.Hamad Z, Aljedai A, Halwani R, Alsultan A Ann Saudi Med2013
Genome-wide meta-analysis of systolic blood pressure in children with sickle cell disease.Bhatnagar P, Barron-Casella E, Bean CJ, Milton JN, Baldwin CT, Steinberg MH, Debaun M, Casella JF, Arking DE PLoS ONE2013
Psychosocial Functioning In Adults With Beta-Thalassaemia Major: Evidence For Resilience.Zani B, Prati G J Health Psychol2013
Prevalence and genetic analysis of α-thalassemia and β-thalassemia in Chongqing area of China.Yao XY, Yu J, Chen SP, Xiao JW, Zheng QC, Liu HY, Zhang L, Xian Y, Zou L Gene2013
Evaluation of functional capacity for exercise in children and adolescents with sickle-cell disease through the six-minute walk test.Hostyn SV, Carvalho WB, Johnston C, Braga JA J Pediatr (Rio J)2013
Venous and Arterial Viscosity-associated Thrombosis in Hemoglobin SC Disease.Lionnet F Am. J. Med.2013
Thalassemic osteopathy: A new marker of bone deposition.Baldini M, Forti S, Orsatti A, Marcon A, Ulivieri FM, Airaghi L, Zanaboni L, Cappellini MD Blood Cells Mol. Dis.2013
Determination of glycated hemoglobin with special emphasis on biosensing methods.Pundir CS, Chawla S Anal. Biochem.2013
Endothelial nitric oxide synthase gene polymorphism is associated with sickle cell disease patients in India.Nishank SS, Singh MP, Yadav R, Gupta RB, Gadge VS, Gwal A J. Hum. Genet.2013
Haemoglobinopathies in nonendemic areas in recent years.Frezzotti A, Galeazzi M, Paladini C, Tocchini M Clin. Chem. Lab. Med.2013
Sickle cell pain management: are we missing the role of pronociception and neuropathic pain?Tawfic QA, Faris AS, Eipe N Paediatr Anaesth2013
Academic Performance and Intelligence Scores of Primary School-aged Children with Sickle Cell Anemia.Ezenwosu O, Emodi I, Ikefuna A, Chukwu B Pediatr Hematol Oncol2013
Effect of using bedside leukocyte filter on pulmonary functions in patients with thalassemia major.Hamed Ael S, Ragab IA, Kamel TB, Abd-El-Gawad AO Pediatr Hematol Oncol2013
The Effect of HFE Polymorphisms on Cardiac Iron Overload in Patients with Beta-Thalassemia Major.Turedi A, Oymak Y, Meşe T, Yaman Y, Bayraktaroglu S, Alpman A, Ozkinay F, Aydınok Y, Vergin C Pediatr Hematol Oncol2013
Extracellular hemin crisis triggers acute chest syndrome in sickle mice.Ghosh S, Adisa OA, Chappa P, Tan F, Jackson KA, Archer DR, Ofori-Acquah SF J. Clin. Invest.2013
Hydroxyurea is associated with lower prevalence of albuminuria in adults with sickle cell disease.Laurin LP, Nachman PH, Desai PC, Ataga KI, Derebail VK Nephrol. Dial. Transplant.2013
Deferasirox for the treatment of iron overload in non-transfusion-dependent thalassemia.Taher AT, Temraz S, Cappellini MD Expert Rev Hematol2013
Hematopoietic stem-cell transplantation for sickle cell disease: current evidence and opinions.Shenoy S Ther Adv Hematol2013
Prevalence and Risk Factors for Pulmonary Arterial Hypertension in a Large Group of β-Thalassemia Patients Using Right Heart Catheterization: A Webthal(R) Study.Derchi G, Galanello R, Bina P, Cappellini MD, Piga A, Lai ME, Quarta A, Casu G, Perrotta S, Pinto V, Musallam KM, Forni GL, Circulation2013
Clinical Presentation and Molecular Identification of Four Uncommon Alpha Globin Variants in Thailand. Initiation Codon Mutation of α2-Globin Gene (HBA2:c.1delA), Donor Splice Site Mutation of α1-Globin Gene (IVSI-1, HBA1:c.95 + 1G>A), Hemoglobin Queens Park/Chao Pra Ya (HBA1:c.98T>A) and Hemoglobin Westmead (HBA2:c.369C>G).Viprakasit V, Ekwattanakit S, Chalaow N, Riolueang S, Wijit S, Tanyut P, Chat-Uthai N, Tachavanich K Acta Haematol.2013
Association of Hemoglobin E-Saskatoon with Hemoglobin S: Report of the First Case Found in Brazil.Couto GK, Lorenzini PF, Pilger DA, Azevedo LA, Weber C, Macedo JL, Diedrich V, de Castro SM Acta Haematol.2013
Five Hemoglobin Variants in a Double Heterozygote for α- and β-Globin Chain Defects.Singha K, Fucharoen G, Fucharoen S Acta Haematol.2013
Spectrum of β-thalassemia mutations in Guizhou Province, PR China, including first observation of codon 121 (GAA>TAA) in Chinese population.Huang SW, Liu XM, Li GF, Su L, Wu X, Wang RL Clin. Biochem.2013
The regulatory role of the adrenergic agonists phenylephrine and isoproterenol on fetal hemoglobin expression and erythroid differentiation.Mei Y, Yin N, Jin X, He J, Yin Z Endocrinology2013
Association of care in a medical home and health care utilization among children with sickle cell disease.Raphael JL, Rattler TL, Kowalkowski MA, Brousseau DC, Mueller BU, Giordano TP J Natl Med Assoc2013
Integration of Administrative Data and Chart Review for Reporting Health Care Utilization Among Children With Sickle Cell Disease.Raphael JL, Tran XG, Mueller BU, Giardino AP Sage Open2013
Sustained nitric oxide (NO)-releasing compound reverses dysregulated NO signal transduction in priapism.Lagoda G, Sezen SF, Hurt KJ, Cabrini MR, Mohanty DK, Burnett AL FASEB J.2013
Alpha thalassemia gene mutations in neonates from Mazandaran, Iran, 2012.Jalali H, Mahdavi MR, Roshan P, Kosaryan M, Karami H, Mahdavi M Hematology2013
A killer revealed: 10-year experience with beta-thalassemia intermedia.Matta BN, Musallam KM, Maakaron JE, Koussa S, Taher AT Hematology2013
Hb Koln [β98(FG5) [GTG → ATG, Val → Met]: The first report from India.Warang P, Nair S, Nadkarni A, Kedar P, Bhave A, Ghosh K, Colah R Hematology2013
Compliance and satisfaction with deferasirox (Exjade(®)) compared with deferoxamine in patients with transfusion-dependent beta-thalassemia.Haghpanah S, Zarei T, Zahedi Z, Karimi M Hematology2013
Epistatic Interactions between Apolipoprotein E and Hemoglobin S Genes in Regulation of Malaria Parasitemia.Rougeron V, Woods CM, Tiedje KE, Bodeau-Livinec F, Migot-Nabias F, Deloron P, Luty AJ, Fowkes FJ, Day KP PLoS ONE2013
An ironic case of liver infections: Yersinia enterocolitis in the setting of thalassemia.Selsky N, Forouhar F, Wu GY World J. Gastroenterol.2013
Pain characteristics and age-related pain trajectories in infants and young children with sickle cell disease.Dampier C, Ely B, Brodecki D, Coleman C, Aertker L, Sendecki JA, Leiby B, Kesler K, Hyslop T, Stuart M Pediatr Blood Cancer2013
Diabetes mellitus in patients with thalassemia major.Li MJ, Peng SS, Lu MY, Chang HH, Yang YL, Jou ST, Lin DT, Lin KH Pediatr Blood Cancer2013
An erythroid enhancer of BCL11A subject to genetic variation determines fetal hemoglobin level.Bauer DE, Kamran SC, Lessard S, Xu J, Fujiwara Y, Lin C, Shao Z, Canver MC, Smith EC, Pinello L, Sabo PJ, Vierstra J, Voit RA, Yuan GC, Porteus MH, Stamatoyannopoulos JA, Lettre G, Orkin SH Science2013
Current sickle cell disease management practices in Nigeria.Galadanci N, Wudil BJ, Balogun TM, Ogunrinde GO, Akinsulie A, Hasan-Hanga F, Mohammed AS, Kehinde MO, Olaniyi JA, Diaku-Akinwumi IN, Brown BJ, Adeleke S, Nnodu OE, Emodi I, Ahmed S, Osegbue AO, Akinola N, Opara HI, Adegoke SA, Aneke J, Adekile AD Int Health2013
Lipoprotein Subfraction Profile and HDL-Associated Enzymes in Sickle Cell Disease Patients.Ozturk OH, Can Y, Yonden Z, Motor S, Oktay G, Kaya H, Aslan M Lipids2013
HO-1 and CO: fighters vs sickle cell disease?Araujo JA Blood2013
Extensive bone marrow necrosis and sickle cell disease.Pougnet L, Dagorne A, Sapin-Lory J, Boutefeu F, Nicolas X, Le Guen P, Drouillard I, Désidéri-Vaillant C Ann. Biol. Clin. (Paris)2013
Spectrum of renal manifestations in sickle cell disease.Cazenave M, Koehl B, Nochy D, Tharaux PL, Audard V Nephrol. Ther.2013
Quantification of HBG mRNA in primary erythroid cultures: prediction of the response to hydroxyurea in sickle cell and beta-thalassemia.Pecoraro A, Rigano P, Troia A, Calzolari R, Scazzone C, Maggio A, Steinberg MH, Marzo RD Eur. J. Haematol.2013
Phenotypic expression of Hb F in common high Hb F determinants in Thailand: roles of α-thalassemia, 5' δ-globin BCL11A binding region and 3' β-globin enhancer.Prakobkaew N, Fucharoen S, Fuchareon G, Siriratmanawong N Eur. J. Haematol.2013
Cardiac complications and diabetes in thalassaemia major: a large historical multicentre study.Pepe A, Meloni A, Rossi G, Caruso V, Cuccia L, Spasiano A, Gerardi C, Zuccarelli A, D'Ascola DG, Grimaldi S, Santodirocco M, Campisi S, Lai ME, Piraino B, Chiodi E, Ascioti C, Gulino L, Positano V, Lombardi M, Gamberini MR Br. J. Haematol.2013
Description of the Phenotypes of 63 Heterozygous, Homozygous and Compound Heterozygous Patients Carrying the Hb Groene Hart [α119(H2)Pro→Ser; HBA1: c.358C>T] Variant.Joly P, Lacan P, Garcia C, Francina A Hemoglobin2013
iACT - An interactive mHealth monitoring system to enhance psychotherapy for adolescents with sickle cell disease.Cheng C, Brown RC, Cohen LL, Venugopalan J, Stokes TH, Wang MD Conf Proc IEEE Eng Med Biol Soc2013
Renal medullary carcinoma in an adolescent with sickle cell anemia.Marsh A, Golden C, Hoppe C, Quirolo K, Vichinsky E Pediatr Blood Cancer2013
Surgical procedures and outcomes among children with sickle cell disease.Hyder O, Yaster M, Bateman BT, Firth PG Anesth. Analg.2013
Genetic and biochemical markers of hydroxyurea therapeutic response in sickle cell anemia.Silva DG, Belini Junior E, Carrocini GC, Torres LD, Ricci Júnior O, Lobo CL, Bonini-Domingos CR, de Almeida EA BMC Med. Genet.2013
Vitamin D Status in Thalassemia Major: an Update.Soliman A, De Sanctis V, Yassin M Mediterr J Hematol Infect Dis2013
Beta-globin Gene Mutations in Turkish Children with Beta-Thalassemia: Results from a Single Center Study.Fettah A, Bayram C, Yarali N, Isik P, Kara A, Culha V, Tunc B Mediterr J Hematol Infect Dis2013
Pain measurement as part of primary healthcare of adult patients with sickle cell disease.Signorelli AA, Ribeiro SB, Moraes-Souza H, de Oliveira LF, Ribeiro JB, da Silva SH, de Oliveira DF, Ribeiro MF Rev Bras Hematol Hemoter2013
Sociodemographic aspects and quality of life of patients with sickle cell anemia.Dos Santos JP, Gomes Neto M Rev Bras Hematol Hemoter2013
Dynamics of sickle cell disease as one of the determinants of quality of life.Ivo ML, Pinto AM Rev Bras Hematol Hemoter2013
Giant oral tumor in a child with malnutrition and sickle cell trait: Anesthetic challenges.Singh PM, Borle A, Trikha A J Anaesthesiol Clin Pharmacol2013
Structure of fully liganded Hb ζ2β2(s) trapped in a tense conformation.Safo MK, Ko TP, Abdulmalik O, He Z, Wang AH, Schreiter ER, Russell JE Acta Crystallogr. D Biol. Crystallogr.2013
Athens university thalassemia expertise unit: evolution, structure, perspectives and patients' expectations.Kattamis C, Sofocleous C, Ladis V, Kattamis A Georgian Med News2013
High prevalence of central hypothyroidism in adult patients with β-thalassemia major.De Sanctis V, Soliman A, Candini G, Campisi S, Anastasi S, Yassin M Georgian Med News2013
Growth hormone deficiency in adults with thalassemia: an overview and the I-cet recommendations.Soliman A, De Sanctis V, Elsedfy H, Yassin M, Skordis N, Karimi M, Sobti P, Raiola G, El Kholy M Georgian Med News2013
Distinctive Mutation Spectrum of the HBB Gene in an Urban Eastern Indian Population.Sahoo SS, Biswal S, Dixit M Hemoglobin2013
The Risk of Potential Thromboembolic, Renal and Cardiac Complications of Sickle Cell Trait.Bucknor MD, Goo JS, Coppolino ML Hemoglobin2013
Diagnostic utility of isoelectric focusing and high performance liquid chromatography in neonatal cord blood screening for thalassemia and non-sickling hemoglobinopathies.Uaprasert N, Settapiboon R, Amornsiriwat S, Sarnthammakul P, Thanapat T, Rojnuckarin P, Sutcharitchan P Clin. Chim. Acta2013
Docosahexaenoic and eicosapentaenoic acid supplementation does not exacerbate oxidative stress or intravascular haemolysis in homozygous sickle cell patients.Daak AA, Ghebremeskel K, Mariniello K, Attallah B, Clough P, Elbashir MI Prostaglandins Leukot. Essent. Fatty Acids2013
Management of sickle cell disease from childhood through adulthood.Kanter J, Kruse-Jarres R Blood Rev.2013
Induction of Multipotential Hematopoietic Progenitors from Human Pluripotent Stem Cells via Respecification of Lineage-Restricted Precursors.Doulatov S, Vo LT, Chou SS, Kim PG, Arora N, Li H, Hadland BK, Bernstein ID, Collins JJ, Zon LI, Daley GQ Cell Stem Cell2013
Painful Vaso-occlusive Crisis as a Prodromal Phase of Acute Chest Syndrome. Is Only One Chest X-ray Enough? A Case Report.Neocleous C, Spanou C, Adramerina A, Spyrou G, Tzanetis F Prague Med Rep2013
Prenatal Diagnosis of β-thalassemia in Twin Pregnancies in Iran.Kainimoghaddam Z, Valaei A, Bayat F, Taghavi Basmanj M, Navabmoghaddam F, Mortezazadeh M, Teimoori-Toolabi L, Ahmadi S, Sadegh S, Kordafshari A, Karimipoor M, Zeinali S Arch Iran Med2013
Pulmonary thromboembolism in a child with sickle cell hemoglobin d disease in the setting of acute chest syndrome.Villanueva H, Kuril S, Krajewski J, Sedrak A Case Rep Pediatr2013
Effect of congenital upregulation of hypoxia inducible factors on percentage of fetal hemoglobin in the blood.Salomon-Andonie J, Miasnikova G, Sergueeva A, Polyakova LA, Niu X, Nekhai S, Gordeuk VR Blood2013
Testosterone Induces Erythrocytosis via Increased Erythropoietin and Suppressed Hepcidin: Evidence for a New Erythropoietin/Hemoglobin Set Point.Bachman E, Travison TG, Basaria S, Davda MN, Guo W, Li M, Connor Westfall J, Bae H, Gordeuk V, Bhasin S J. Gerontol. A Biol. Sci. Med. Sci.2013
Newborn Blood Spot Screening for Sickle Cell Disease by Using Tandem Mass Spectrometry: Implementation of a Protocol to Identify Only the Disease States of Sickle Cell Disease.Moat SJ, Rees D, King L, Ifederu A, Harvey K, Hall K, Lloyd G, Morell C, Hillier S Clin. Chem.2013
Inhibitors of second messenger pathways and Ca(2+)-induced exposure of phosphatidylserine in red blood cells of patients with sickle cell disease.Gbotosho OT, Cytlak UM, Hannemann A, Rees DC, Tewari S, Gibson JS Pflugers Arch.2013
Nuclease-mediated gene editing by homologous recombination of the human globin locus.Voit RA, Hendel A, Pruett-Miller SM, Porteus MH Nucleic Acids Res.2013
Role of Chimerism Monitoring and Donor Lymphocyte Infusion in Eliminating the Risk of Graft Rejection Following HSCT in Thalassemia Patients-Review.Li ZF, Sun X Zhongguo Shi Yan Xue Ye Xue Za Zhi2013
Effect of Dexamethasone on G-CSF Mobilization of Peripheral Blood Stem Cells in Healthy Donors and Hematopoietic Reconstruction in the Recipients.Liu HS, Wang XN, Liu HB, Liu X, He PC, Chen LM, Xi JY, Wang MC, Li J, Zhang HT, Zhang M Zhongguo Shi Yan Xue Ye Xue Za Zhi2013
Genetic diagnosis of thalassemia mutations with free fetal DNA in pregnant plasma.Lin XR, You LX, Chen Y Zhongguo Shi Yan Xue Ye Xue Za Zhi2013
TALEN-mediated gene correction in integration-free β-thalassemia iPSCs.Ma N, Liao B, Zhang H, Wang L, Shan Y, Xue Y, Huang K, Chen S, Zhou X, Chen Y, Pei D, Pan G J. Biol. Chem.2013
Echocardiography in sickle cell anaemia patients under 20 years of age: a descriptive study in the Brazilian Western Amazon.Ribera MC, Ribera RB, Koifman RJ, Koifman S Cardiol Young2013
Impact of β-thalassemia trait carrier state on cardiovascular risk factors and metabolic profile in patients with newly diagnosed hypertension.Triantafyllou AI, Vyssoulis GP, Karpanou EA, Karkalousos PL, Triantafyllou EA, Aessopos A, Farmakis DT J Hum Hypertens2013
Dental infections increase the likelihood of hospital admissions among adult patients with sickle cell disease.Laurence B, Haywood C, Lanzkron S Community Dent Health2013
Molecular interactions of hemoglobin with resveratrol: potential protective antioxidant role and metabolic adaptations of the erythrocyte.Tellone E, De Rosa MC, Pirolli D, Russo A, Giardina B, Galtieri A, Ficarra S Biol. Chem.2013
An update on the recent literature on sickle cell bone disease.Osunkwo I Curr Opin Endocrinol Diabetes Obes2013
Efficacy of deferasirox for the treatment of iron overload in Chinese thalassaemia major patients: results from a prospective, open-label, multicentre clinical trial.Lai YR, Liu RR, Li CF, Huang SL, Li Q, Habr D, Martin N, Shen ZX Transfus Med2013
Optimizing adolescent transition to adult care for sickle cell disease.Cerns S, McCracken C, Rich C Medsurg Nurs2013
Hematological and hemorheological Determinants of the Six-Minute Walk Test Performance in Children with Sickle Cell Anemia.Waltz X, Romana M, Hardy-Dessources MD, Lamarre Y, Divialle-Doumdo L, Petras M, Tarer V, Hierso R, Baltyde KC, Tressières B, Lalanne-Mistrih ML, Maillard F, Hue O, Etienne-Julan M, Connes P PLoS ONE2013
The first five years of a preventive programme for haemoglobinopathies in Northeastern Iraq.Al-Allawi NA, Jalal SD, Ahmed NH, Faraj AH, Shalli A, Hamamy H J Med Screen2013
Universal newborn screening for haemoglobinopathies in Guadeloupe (French West Indies): A 27-year experience.Saint-Martin C, Romana M, Bibrac A, Brudey K, Tarer V, Divialle-Doumdo L, Petras M, Keclard-Christophe L, Lamothe S, Broquere C, Etienne-Julan M J Med Screen2013
Increased adhesive and inflammatory properties in blood outgrowth endothelial cells from sickle cell anemia patients.Sakamoto TM, Lanaro C, Ozelo MC, Garrido VT, Olalla-Saad ST, Conran N, Costa FF Microvasc. Res.2013
Cyclophosphamide-Associated Cardiotoxicity in a Child following Stem Cell Transplantation for β-Thalassemia Major: Case Report and Review of Literature.Meserve EE, Lehmann L, Perez-Atayde AR, Labelle JL Pediatr. Dev. Pathol.2013
Two Novel Mutations (HBG1: c.-250CT and HBG2: c.-250CT) Associated With Hereditary Persistence of Fetal Hemoglobin.Toma S, Tenorio M, Oakley M, Thein SL, Clark BE Hemoglobin2013
Optimizing the Dose of Hydroxyurea Therapy for Patients with β-Thalassemia Intermedia (Hb E-β-thalassemia): A Single Center Study from Eastern India.Bohara VV, Ray S, Chakrabarti P, Ray SS, Nath UK, Chaudhuri U Hemoglobin2013
Detection of Nine Mediterranean β-Thalassemia Mutations in Palestinians Using Three Restriction Enzyme Digest Panels: A Reliable Method for Developing Countries.Reading NS, Sirdah MM, Tarazi IS, Prchal JT Hemoglobin2013
Clinical and hematological effects of hydroxyurea therapy in sickle cell patients: a single-center experience in Brazil.Silva-Pinto AC, Angulo IL, Brunetta DM, Neves FI, Bassi SC, Santis GC, Covas DT Sao Paulo Med J2013
Non-invasive prenatal testing using massively parallel sequencing of maternal plasma DNA: from molecular karyotyping to fetal whole-genome sequencing.Lo YM Reprod. Biomed. Online2013
Oral manifestations and blood profile in patients with thalassemia trait.Wang YP, Yu-Fong Chang J, Wu YC, Cheng SJ, Chen HM, Sun A J. Formos. Med. Assoc.2013
Organizing national responses for rare blood disorders: the Italian experience with sickle cell disease in childhood.Colombatti R, Perrotta S, Samperi P, Casale M, Masera N, Palazzi G, Sainati L, Russo G, Orphanet J Rare Dis2013
Homozygous hemoglobin C disease.Dalia S, Zhang L Blood2013
Updates of the HbVar database of human hemoglobin variants and thalassemia mutations.Giardine B, Borg J, Viennas E, Pavlidis C, Moradkhani K, Joly P, Bartsakoulia M, Riemer C, Miller W, Tzimas G, Wajcman H, Hardison RC, Patrinos GP Nucleic Acids Res.2013
A GCH1 Haplotype Confers Sex Specific Susceptibility to Pain Crises and Altered Endothelial Function in Adults with Sickle Cell Anemia.Belfer I, Youngblood V, Darbari DS, Wang Z, Diaw L, Freeman L, Desai K, Dizon M, Allen D, Cunnington C, Channon K, Milton J, Hartley SW, Nolan V, Kato GJ, Steinberg MH, Goldman D, Taylor JG Am. J. Hematol.2013
Insurance Status as a Sociodemographic Risk Factor for Functional Outcomes and Health-related Quality of Life Among Youth With Sickle Cell Disease.Robinson MR, Daniel LC, O'Hara EA, Szabo MM, Barakat LP J. Pediatr. Hematol. Oncol.2013
Variable Genotype-Phenotype Correlations in Patients With a Rare Nondeletional α-thalassemia; Hb Pak Num Po (HBA1: c.396_397insT).Sanpakit K, Viprakasit V J. Pediatr. Hematol. Oncol.2013
Management of Refractory Pain in Hospitalized Adolescents With Sickle Cell Disease: Changing From Intravenous Opioids to Continuous Infusion Epidural Analgesia.New T, Venable C, Fraser L, Rosenberg E, Schmidt J, James-Herry A, Osunkwo I, Dampier C J. Pediatr. Hematol. Oncol.2013
The efficacy of vitamin k2 and calcitriol combination on thalassemic osteopathy.Ozdemir MA, Yilmaz K, Abdulrezzak U, Muhtaroglu S, Patiroglu T, Karakukcu M, Unal E J. Pediatr. Hematol. Oncol.2013
Morbidity pattern in hospitalized under five children with sickle cell disease.Jain D, Bagul AS, Shah M, Sarathi V Indian J. Med. Res.2013
Morbidity pattern of sickle cell disease in India: A single centre perspective.Tewari S, Rees D Indian J. Med. Res.2013
Asthma and hemoglobinopathy: When is supplemental oxygen required?Joseph L, Brickner-Braun I, Pinshow B, Goldberg S, Miskin H, Picard E Pediatr Int2013
Evaluation of clinical and laboratory correlates of sickle leg ulcers.Madu AJ, Ubesie A, Madu KA, Okwor B, Anigbo C Wound Repair Regen2013
A prospective study of tubular dysfunction in pediatric patients with Beta thalassemia major receiving deferasirox.Naderi M, Sadeghi-Bojd S, Valeshabad AK, Jahantigh A, Alizadeh S, Dorgalaleh A, Tabibian S, Bamedi T Pediatr Hematol Oncol2013
Association of iron overload and oxidative stress with insulin resistance in transfusion-dependent beta-thalassemia major and beta-thalassemia/HbE patients.Tangvarasittichai S, Pimanprom A, Choowet A, Tangvarasittichai O Clin. Lab.2013
A Generic, Flexible Protocol for Preimplantation Human Leukocyte Antigen Typing Alone or in Combination with a Monogenic Disease, for Rapid Case Work-up and Application.Kakourou G, Destouni A, Vrettou C, Traeger-Synodinos J, Kanavakis E Hemoglobin2013
Plasma zinc level in hepatitis C patients with or without Beta thalassemia major; is there any difference?Abbasinazari M, Behnava B, Panahi Y, Hajhossein Talasaz A, Salimi S, Keshvari M, Mehrnoush L, Karim P, Gholami Fesharaki M, Asgharinia M, Alavian SM Hepat Mon2013
Demonstration of iron in exfoliated buccal cells of β-thalassemia major patients.Bhat AA, Parwani RN, Wanjari SP J Cytol2013
Thalassaemic Osteopathy: a cross-sectional preliminary study from Sri Lanka.Dissanayake R, de Silva S, Lekamwasam S, Abeysekara G, Dissanayake VH J. Pediatr. Endocrinol. Metab.2013
Challenges for red blood cell biomarker discovery through proteomics.Barasa B, Slijper M Biochim. Biophys. Acta2013
Thalassemia and the hypercoagulable state.Sirachainan N Thromb. Res.2013
Consulting communities on feedback of genetic findings in international health research: sharing sickle cell disease and carrier information in coastal Kenya.Marsh V, Kombe F, Fitzpatrick R, Williams TN, Parker M, Molyneux S BMC Med Ethics2013
NF-κB Is Activated in CD4(+) iNKT Cells by Sickle Cell Disease and Mediates Rapid Induction of Adenosine A2A Receptors.Lin G, Field JJ, Yu JC, Ken R, Neuberg D, Nathan DG, Linden J PLoS ONE2013
Prospective evaluation for respiratory pathogens in children with sickle cell disease and acute respiratory illness.Srinivasan A, Wang WC, Gaur A, Smith T, Gu Z, Kang G, Leung W, Hayden RT Pediatr Blood Cancer2013
R2* as a surrogate measure of ferriscan iron quantification in thalassemia.Chan WC, Tejani Z, Budhani F, Massey C, Haider MA J Magn Reson Imaging2013
Parent education and biologic factors influence on cognition in sickle cell anemia.King AA, Strouse JJ, Rodeghier MJ, Compas BE, Casella JF, McKinstry RC, Noetzel MJ, Quinn CT, Ichord R, Dowling MM, Miller JP, Debaun MR Am. J. Hematol.2013
Building partnerships to target sickle cell anemia in africa.Tubman VN, Archer NM Am. J. Hematol.2013
Flow cytometry analyses reveal association between Lu/BCAM adhesion molecule and osteonecrosis in sickle cell disease.Picot J, Goudot C, Berkenou J, Galacteros F, Colin Y, Bartolucci P, Le Van Kim C Am. J. Hematol.2013
Comparison of maternal serum PlGF and sFlt-1 between pregnancies with and without fetal hemoglobin Bart's disease.Tongprasert F, Srisupundit K, Luewan S, Tongsong T Prenat. Diagn.2013
Applying molecular immunohaematology to regularly transfused thalassaemic patients in Thailand.Rujirojindakul P, Flegel WA Blood Transfus2013
Extramedullary haematopoiesis correlates with genotype and absence of cardiac iron overload in polytransfused adults with thalassaemia.Ricchi P, Ammirabile M, Spasiano A, Costantini S, Di Matola T, Pepe A, Cinque P, Pagano L, Casale M, Filosa A, Prossomariti L Blood Transfus2013
The contribution of red blood cells to thrombin generation in sickle cell disease: meizothrombin generation on sickled red blood cells.Whelihan MF, Mooberry MJ, Zachary V, Bradford RL, Ataga KI, Mann KG, Key NS J. Thromb. Haemost.2013
Assessment of left ventricular and atrial diastolic function using two-dimensional (2D) strain imaging in patients with β-thalassemia major.Karamanou AG, Hamodraka ES, Vrakas SC, Paraskevaidis I, Lekakis I, Kremastinos DT Eur. J. Haematol.2013
Red blood cell alloimmunization in sickle cell disease and in thalassaemia: current status, future perspectives and potential role of molecular typing.Matteocci A, Pierelli L Vox Sang.2013
Treating sickle cell anaemia with hydroxycarbamide.Pollack S Br. J. Haematol.2013
Human adipose tissue contains erythroid progenitors expressing fetal hemoglobin.Navarro A, Carbonell-Uberos F, Marín S, Miñana MD World J Stem Cells2013
Modulating hemoglobin nitrite reductase activity through allostery: A mathematical model.Rong Z, Alayash AI, Wilson MT, Cooper CE Nitric Oxide2013
Diffuse hepatic calcifications in a transfusion-dependent patient with Beta-thalassemia: a case report.Saki F, Bordbar MR, Imanieh MH, Karimi M Iran J Med Sci2013
Retinal Fiber Layer Thickness in Children with Thalessemia Major and Iron Deficiency Anemia.Aksoy A, Aslan L, Aslankurt M, Eser O, Garipardic M, Okumus S, Kaya G Semin Ophthalmol2013
Genetic variation in CD36, HBA, NOS3 and VCAM1 is associated to chronic haemolysis level in sickle cell anaemia: a longitudinal study.Coelho A, Dias A, Morais A, Nunes B, Ferreira E, Picanço I, Faustino P, Lavinha J Eur. J. Haematol.2013
An arresting sickle cell disease complication.Staley S, Hageman JR, Pinto N, Khan N Pediatr Ann2013
The prevalence of hypertension and abnormal kidney function in children with sickle cell disease --a cross sectional review.Bodas P, Huang A, O Riordan MA, Sedor JR, Dell KM BMC Nephrol2013
Bone marrow necrosis - initial presentation in sickle cell anemia.Shafiq M, Ali N Am J Case Rep2013
Early Complication in Sickle Cell Anemia Children due to A(TA)nTAA Polymorphism at the Promoter of UGT1A1 Gene.Chaouch L, Talbi E, Moumni I, Ben Chaabene A, Kalai M, Chaouachi D, Mallouli F, Ghanem A, Abbes S Dis. Markers2013
Association of hospital and provider types on sickle cell disease outcomes.Jan S, Slap G, Smith-Whitley K, Dai D, Keren R, Rubin DM Pediatrics2013
Neuropathic pain in patients with sickle cell disease.Brandow AM, Farley RA, Panepinto JA Pediatr Blood Cancer2013
Transcranial doppler ultrasonography in children with sickle cell anemia: Clinical and laboratory correlates for elevated blood flow velocities.Lagunju I, Sodeinde O, Brown B, Akinbami F, Adedokun B J Clin Ultrasound2013
Risky behaviours of Jamaican adolescents with sickle cell disease.Asnani MR, Bhatt K, Younger N, McFarlane S, Francis D, Gordon-Strachan G, Reid ME Hematology2013
Dexmedetomidine as sedative and analgesic in a patient of sickle cell disease for total hip replacement.Dhansura T, Kapadia S, Gandhi S Indian J Anaesth2013
Development of Phenotypic Screening Assays for γ-Globin Induction Using Primary Human Bone Marrow Day 7 Erythroid Progenitor Cells.Li H, Xie W, Gore ER, Montoute MN, Bee WT, Zappacosta F, Zeng X, Wu Z, Kallal L, Ames RS, Pope AJ, Benowitz A, Erickson-Miller CL J Biomol Screen2013
Carrier screening for inherited haemoglobin disorders among secondary school students and young adults in Latium, Italy.Amato A, Cappabianca MP, Lerone M, Colosimo A, Grisanti P, Ponzini D, Di Biagio P, Perri M, Gianni D, Rinaldi S, Piscitelli R J Community Genet2013
Oxidative Stress and β-Thalassemic Erythroid Cells behind the Molecular Defect.De Franceschi L, Bertoldi M, Matte A, Santos Franco S, Pantaleo A, Ferru E, Turrini F Oxid Med Cell Longev2013
Coagulation activation in children with sickle cell disease is associated with cerebral small vessel vasculopathy.Colombatti R, De Bon E, Bertomoro A, Casonato A, Pontara E, Omenetto E, Saggiorato G, Steffan A, Damian T, Cella G, Teso S, Manara R, Rampazzo P, Meneghetti G, Basso G, Sartori MT, Sainati L PLoS ONE2013
Coexistence of Two β-Globin Gene Deletions in a Chinese Girl with β-Thalassemia Minor.Huang G, Li P, Li YX, Ye LZ Hemoglobin2013
Masking of a β-Thalassemia Determinant by a Novel δ-Globin Gene Defect [Hb A2-Saurashtra or δ100(G2)Pro→Ser; HBD: c.301CT] in Cis.Colaco S, Trivedi A, Colah RB, Ghosh K, Nadkarni AH Hemoglobin2013
Hemoglobin Analyses in The Netherlands Reveal More Than 80 Different Variants Including Six Novel Ones.van Zwieten R, Veldthuis M, Delzenne B, Berghuis J, Groen J, Ait Ichou F, Clifford E, Harteveld CL, Stroobants AK Hemoglobin2013
The use and effectiveness of complementary and alternative medicine for pain in sickle cell anemia.Majumdar S, Thompson W, Ahmad N, Gordon C, Addison C Complement Ther Clin Pract2013
Bacteremia Caused by Microbacterium binotii in a Patient with Sickle Cell Anemia.Buss SN, Starlin R, Iwen PC J. Clin. Microbiol.2013
Biosafety Challenges for Use of Lentiviral Vectors in Gene Therapy.Rothe M, Modlich U, Schambach A Curr Gene Ther2013
The fc receptor polymorphisms and expression of neutrophil activation markers in patients with sickle cell disease from Western India.Kangne HK, Jijina FF, Italia YM, Jain DL, Nadkarni AH, Gupta M, Pradhan V, Mukesh RD, Ghosh KK, Colah RB Biomed Res Int2013
Transition From Pediatric to Adult Care in Sickle Cell Disease: Perspectives on the Family Role.Porter JS, Graff JC, Lopez AD, Hankins JS J Pediatr Nurs2013
Thrombospondin-1 inhibits ADAMTS13 activity in sickle cell disease.Novelli EM, Kato GJ, Hildesheim ME, Barge S, Meyer MP, Lozier J, Hassett AC, Ragni MV, Isenberg JS, Gladwin MT Haematologica2013
Linguistic markers of emotion in mothers of sickle cell carrier infants: What are they and what do they mean?Ahmad NY, Farrell MH Patient Educ Couns2013
Markers of endothelial dysfunction differ between subphenotypes in children with sickle cell disease.van der Land V, Peters M, Biemond BJ, Heijboer H, Harteveld CL, Fijnvandraat K Thromb. Res.2013
Validation and reliability of a disease-specific quality of life measure (the TranQol) in adults and children with thalassaemia major.Klaassen RJ, Barrowman N, Merelles-Pulcini M, Vichinsky EP, Sweeters N, Kirby-Allen M, Neufeld EJ, Kwiatkowski JL, Wu J, Vickars L, Blanchette VS, Forgie M, Yamashita R, Wong-Rieger D, Young NL Br. J. Haematol.2013
Hepatitis C and blood transfusion among children attending the Sickle Cell Clinic at Mulago Hospital, Uganda.Namasopo SO, Ndugwa C, Tumwine JK Afr Health Sci2013
Sickle cell retinopathy: diagnosis and treatment.Bonanomi MT, Lavezzo MM Arq Bras Oftalmol2013
Ketamine infusion for sickle cell pain crisis refractory to opioids: a case report and review of literature.Uprety D, Baber A, Foy M Ann. Hematol.2013
Newborn Screening for Hb H Disease by Determination of Hb Bart's Using the Sebia Capillary Electrophoresis System in Southern China.Liao C, Zhou JY, Xie XM, Tang HS, Li R, Li DZ Hemoglobin2013
A multiprofessional team for children living with sickle-cell anemia.Mensah S, Perrin A, Vandaele M Soins Pediatr Pueric2013
Effectiveness and acceptance of hydroxyurea in the treatment of severe forms of sickle cell disease: a prospective study of 65 cases.Mellouli F, Chouaibi S, Dhouib N, Ouederni M, Ben Khaled M, Abbes S, Bejaoui M Tunis Med2013
Blood transfusion for preventing primary and secondary stroke in people with sickle cell disease.Wang WC, Dwan K Cochrane Database Syst Rev2013
The diagnosis and molecular analysis of a novel 21.9kb deletion (Qinzhou type deletion) causing α(+) thalassemia.Long J, Yan S, Lao K, Pang W, Ye X, Sun L Blood Cells Mol. Dis.2013
Role of non-invasive assessment in prediction of preclinical cardiac affection in multi-transfused thalassaemia major patients.Othman KM, Elshazly SA, Heiba NM Hematology2013
Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign.Alsultan A, Alabdulaali MK, Griffin PJ, Alsuliman AM, Ghabbour HA, Sebastiani P, Albuali WH, Al-Ali AK, Chui DH, Steinberg MH Br. J. Haematol.2013
A phase 2 study of HQK-1001, an oral fetal haemoglobin inducer, in β-thalassaemia intermedia.Inati A, Kahale M, Perrine SP, Chui DH, Taher AT, Koussa S, Abi Nasr T, Abbas HA, Ghalie RG Br. J. Haematol.2013
Interaction of Normal and Sickle Hemoglobins for Sodium Dodecylsulphate and Hydrogen Peroxide at pH 5.0 and 7.2.Ezebuo FC, Eze SO, Lukong CB, Chilaka FC ISRN Hematol2013
Severe painful vaso-occlusive crises and mortality in a contemporary adult sickle cell anemia cohort study.Darbari DS, Wang Z, Kwak M, Hildesheim M, Nichols J, Allen D, Seamon C, Peters-Lawrence M, Conrey A, Hall MK, Kato GJ, Taylor Vi JG PLoS ONE2013
Decreased hematocrit-to-viscosity ratio and increased lactate dehydrogenase level in patients with sickle cell anemia and recurrent leg ulcers.Connes P, Lamarre Y, Hardy-Dessources MD, Lemonne N, Waltz X, Mougenel D, Mukisi-Mukaza M, Lalanne-Mistrih ML, Tarer V, Tressières B, Etienne-Julan M, Romana M PLoS ONE2013
Serum copeptin and cortisol do not accurately predict sickle cell anaemia vaso-occlusive crisis as C-reactive protein.Akinlade KS, Atere AD, Olaniyi JA, Rahamon SK, Adewale CO PLoS ONE2013
Glutathione redox system in β -thalassemia/Hb E patients.Kalpravidh RW, Tangjaidee T, Hatairaktham S, Charoensakdi R, Panichkul N, Siritanaratkul N, Fucharoen S ScientificWorldJournal2013
Renal medullary cancer in a patient with sickle cell trait.Alappan N, Marak CP, Chopra A, Joy PS, Dorokhova O, Guddati AK Case Rep Oncol Med2013
Fetal hemoglobin in sickle cell anemia: a glass half full?Steinberg MH, Chui DH, Dover GJ, Sebastiani P, Alsultan A Blood2013
Parental Problem-Solving Abilities and the Association of Sickle Cell Disease Complications with Health-Related Quality of Life for School-Age Children.Barakat LP, Daniel LC, Smith K, Renée Robinson M, Patterson CA J Clin Psychol Med Settings2013
Differential diagnostics of thalassemia minor by artificial neural networks model.Barnhart-Magen G, Gotlib V, Marilus R, Einav Y J. Clin. Lab. Anal.2013
α-Globin Gene Quadruplication and Heterozygous β-Thalassemia: A Not So Rare Cause of Thalassemia Intermedia.Origa R, Sollaino MC, Borgna-Pignatti C, Piga A, Feliu Torres A, Masile V, Galanello R Acta Haematol.2013
After the Introduction into the National Newborn Screening Program: Who Is Receiving Genetic Counseling for Hemoglobinopathies in The Netherlands.Kaufmann JO, Krapels IP, Van Brussel BT, Zekveld-Vroon RC, Oosterwijk JC, van Erp F, van Echtelt J, Zwijnenburg PJ, Petrij F, Bakker E, Giordano PC Public Health Genomics2013
Cardiopulmonary complications in sickle cell anemia.Rojas-Jiménez S, Lopera-Valle J, Yabur-Espítia M Arch Cardiol Mex2013
Airways obstruction and pulmonary capillary blood volume in children with sickle cell disease.Marzollo A, Colombatti R, Sainati L Pediatr. Pulmonol.2013
Mechanism-driven phase I translational study of trifluoperazine in adults with sickle cell disease.Molokie RE, Wilkie DJ, Wittert H, Suarez ML, Yao Y, Zhao Z, He Y, Wang ZJ Eur. J. Pharmacol.2013
A two-layered classifier based on the radial basis function for the screening of thalassaemia.Masala GL, Golosio B, Cutzu R, Pola R Comput. Biol. Med.2013
Dissecting the energies that stabilize sickle hemoglobin polymers.Wang Y, Ferrone FA Biophys. J.2013
Half of the Emirati Population Has Abnormal Red Cell Parameters: Challenges for Standards and Screening Guidelines.Al-Dabbagh B, Shawqi S, Yasin J, Al Essa A, Nagelkerke N, Denic S Hemoglobin2013
Evaluation of SWI in Children with Sickle Cell Disease.Winchell AM, Taylor BA, Song R, Loeffler RB, Grundlehner P, Hankins JS, Wang WC, Ogg RJ, Hillenbrand CM, Helton KJ AJNR Am J Neuroradiol2013
Association between rs267196 and rs267201 of BMP6 gene and osteonecrosis among Sickle Cell Aneamia patients.Chaouch L, Kalai M, Jbara MB, Chaabene AB, Darragi I, Chaouachi D, Mallouli F, Hafsia R, Ghanem A, Abbes S Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub2013
The Hb H Disease Genotypes in Southern China.Fang J, Chen L, Zeng R, Tian Q, Jiang W, Li H, Chen Z, Du C, Chen S Hemoglobin2013
Intravenous gammaglobulin as rescue therapy in a patient with sickle cell and septic shock.Romero-Legro I, Kadaria D, Murillo LC, Freire AX Tenn Med2013
β-Globin sleeping beauty transposon reduces red blood cell sickling in a patient-derived CD34(+)-based in vitro model.Sjeklocha LM, Wong PY, Belcher JD, Vercellotti GM, Steer CJ PLoS ONE2013
Genomic organization and differential signature of positive selection in the alpha and Beta globin gene clusters in two cetacean species.Nery MF, Arroyo JI, Opazo JC Genome Biol Evol2013
Sickle Cell Disease and HIV: A Case Highlighting Management Challenges for Children in a Resource-Limited Setting.Odera EB, Kwobah C, Stone G, Some F, Vreeman RC J Int Assoc Provid AIDS Care2013
Knowledge and attitude of secondary school students in Jos, Nigeria on sickle cell disease.Olakunle OS, Kenneth E, Olakekan AW, Adenike OB Pan Afr Med J2013
Glomerular filtration rate is altered in children with sickle cell disease: a comparison between Hb SS and Hb Paula RP, Nascimento AF, Sousa SM, Bastos PR, Barbosa AA Rev Bras Hematol Hemoter2013
Sickle Cell Disease: quality of life in patients with hemoglobin SS and SC disorders.Pereira SA, Brener S, Cardoso CS, Proietti AB Rev Bras Hematol Hemoter2013
Comments on renal abnormalities of sickle cell disease.Abbud-Filho M Rev Bras Hematol Hemoter2013
Clinical significance of circulating blood and endothelial cell microparticles in sickle-cell disease.Kasar M, Boğa C, Yeral M, Asma S, Kozanoglu I, Ozdogu H J. Thromb. Thrombolysis2013
Pneumococcal Vaccination Rates in Children With Sickle Cell Disease.Nero AC, Akuete K, Reeves SL, Dombkowski KJ J Public Health Manag Pract2013
Emerging science of hydroxyurea therapy for pediatric sickle cell disease.Green NS, Barral S Pediatr. Res.2013
Sildenafil Promotes eNOS Activation and Inhibits NADPH Oxidase in the Transgenic Sickle Cell Mouse Penis.Musicki B, Bivalacqua TJ, Champion HC, Burnett AL J Sex Med2013
Unexpected prevalence of hyperprolactinaemia associated with microprolactinoma and empty sella in a cohort of adult patients with non-transfusion-dependent thalassaemia: a prospective study.Ricchi P, Ammirabile M, Spasiano A, Costantini S, Vitale M, Di Matola T, Cinque P, Filosa A, Serino D Br. J. Haematol.2013
Trabeculectomy for Traumatic Hyphema in Sickle Cell Trait.Kaplowitz K, Nobe M, Abazari A, Honkanen R Semin Ophthalmol2013
Use of a clinical pathway to improve the acute management of vaso-occlusive crisis pain in pediatric sickle cell disease.Ender KL, Krajewski JA, Babineau J, Tresgallo M, Schechter W, Saroyan JM, Kharbanda A Pediatr Blood Cancer2013
New insights provided by a comparison of impaired deformability with erythrocyte oxidative stress for sickle cell disease.Barodka VM, Nagababu E, Mohanty JG, Nyhan D, Berkowitz DE, Rifkind JM, Strouse JJ Blood Cells Mol. Dis.2013
Determinants of academic performance in children with sickle cell anaemia.Ezenwosu OU, Emodi IJ, Ikefuna AN, Chukwu BF, Osuorah CD BMC Pediatr2013
Fetal hemoglobin and alpha thalassemia modulate the phenotypic expression of HbSD-Punjab.Patel DK, Purohit P, Dehury S, Das P, Dutta A, Meher S, Patel S, Bag S, Mashon RS, Das K Int J Lab Hematol2013
Thalassemias.Martin A, Thompson AA Pediatr. Clin. North Am.2013
Sickle cell disease in childhood: from newborn screening through transition to adult medical care.Quinn CT Pediatr. Clin. North Am.2013
Serum iron status of under-five children with sickle cell anaemia in lagos, Nigeria.Akodu SO, Diaku-Akinwumi IN, Kehinde OA, Njokanma OF Anemia2013
Stroke recurrence in Nigerian children with sickle cell disease treated with hydroxyurea.Lagunju IA, Brown BJ, Sodeinde OO Niger Postgrad Med J2013
Spectral detection of sickle cell anemia and thalassemia.Masilamani V, Al Salhi MS, Devanesan S, Algahtani FH, Abu-Salah KM, Ahamad I, Agastian P Photodiagnosis Photodyn Ther2013
Cost-effectiveness analysis of adding low dose ribavirin to peginterferon alfa-2a for treatment of chronic hepatitis C infected thalassemia major patients in iran.Mehrazmay A, Alavian SM, Moradi-Lakeh M, Mokhtari Payam M, Hashemi-Meshkini A, Behnava B, Miri SM, Karimi Elizee P, Tabatabaee SV, Keshvari M, Bagheri Lankarani K Hepat Mon2013
Sickle-cell disease: geographical distribution and population estimates.Piel FB Med Sci (Paris)2013
Newborn bloodspot results: predictive value of screen positive test for thalassaemia major.Streetly A, Latinovic R, Henthorn J, Daniel Y, Dormandy E, Darbyshire P, Mantio D, Fraser L, Farrar L, Will A, Tetlow L J Med Screen2013
Heme triggers TLR4 signaling leading to endothelial cell activation and vaso-occlusion in murine sickle cell disease.Belcher JD, Chen C, Nguyen J, Milbauer L, Abdulla F, Alayash AI, Smith A, Nath KA, Hebbel RP, Vercellotti GM Blood2013
Intravenous Magnesium Sulfate for Vaso-occlusive Episodes in Sickle Cell Disease.Goldman RD, Mounstephen W, Kirby-Allen M, Friedman JN Pediatrics2013
Severe Vitamin D Deficiency in a Patient With Sickle Cell Disease: A Case Study With Literature Review.Kaza PL, Moulton T J. Pediatr. Hematol. Oncol.2013
HbSD-Punjab: Clinical and Hematological Profile of a Rare Hemoglobinopathy.Oberoi S, Das R, Trehan A, Ahluwalia J, Bansal D, Malhotra P, Marwaha RK J. Pediatr. Hematol. Oncol.2013
Role of Red Cell Distribution Width in Screening for Hb E Trait in Population Screening for Hemoglobin Disorders.Nishad AA, de Silva IS, Perera HL, Pathmeswaran A, Kastutiratne KT, Premawardhena AP J. Pediatr. Hematol. Oncol.2013
Acute pulmonary complications of sickle cell disease.Knight-Madden J, Greenough A Paediatr Respir Rev2013
Malocclusion and treatment need in children and adolescents with sickle cell disease.Alves E Luna AC, Godoy F, de Menezes VA Angle Orthod2013
Hb Ullevaal [β78(EF2)Leu→Val; HBB: c.235C>G], a New Hemoglobin Variant Interfering with Hb A1c Measurement Using a Cation Exchange High Performance Liquid Chromatography Method.Grimholt RM, Sudmann AA, Piehler AP, Urdal P, Klingenberg O Hemoglobin2013
Molecular and Cellular Analysis of a Novel HBA2 Mutation (HBA2: c.94A>G) Shows Activation of a Cryptic Splice Site and Generation of a Premature Termination Codon.Qadah T, Finlayson J, Joly P, Ghassemifar R Hemoglobin2013
The Diminishing Trend of β-Thalassemia in Southern Iran From 1997 to 2011: The Impact of Preventive Strategies.Joulaei H, Shahbazi M, Nazemzadegan B, Rastgar M, Hadibarhaghtalab M, Heydari M, Ghaffarpasand F, Rahimi N Hemoglobin2013
Hematological characterization of compound heterozygous hemoglobin Hope/E patients with and without alpha-thalassemia-1 SEA type deletion.Pornprasert S Clin. Lab.2013
Sickle cell anemia: the impact of discovery, politics, and business.Xie LH, Doye AA, Conley E, Gwathmey JK J Health Care Poor Underserved2013
Somatic Growth and Lung Function in Sickle Cell Disease.Catanzaro T, Koumbourlis AC Paediatr Respir Rev2013
Lung Function in Sickle Cell Disease.Koumbourlis AC Paediatr Respir Rev2013
Prevalence and molecular analysis of β-thalassemia in children of Han ethnicity in Chongqing city.Yao XY, Zhang YM, Qin ZZ, Fan R, Zou L, Chen SP, Zhang L, Xie Q, Zhong XY, Xian Y, Yu J Zhonghua Er Ke Za Zhi2013
Lupus nephritis in a patient with sickle cell disease.Minocha V, Rana F Case Rep Hematol2013
Malnutrition in Sickle Cell Anemia: Implications for Infection, Growth, and Maturation.Hyacinth HI, Adekeye OA, Yilgwan CS J Soc Behav Health Sci2013
Abnormal Pulmonary Function and Associated Risk Factors in Children and Adolescents With Sickle Cell Anemia.Arteta M, Campbell A, Nouraie M, Rana S, Onyekwere OC, Ensing G, Sable C, Dham N, Darbari D, Luchtman-Jones L, Kato GJ, Gladwin MT, Castro OL, Minniti CP, Gordeuk VR J. Pediatr. Hematol. Oncol.2013
Predictors of Bacteremia Among Children With Sickle Cell Disease Presenting With Fever.Savlov D, Beck CE, Degroot J, Odame I, Friedman JN J. Pediatr. Hematol. Oncol.2013
An Intervention to Decrease Stigma in Young Adults With Sickle Cell Disease.Jenerette CM, Brewer CA, Edwards LJ, Mishel MH, Gil KM West J Nurs Res2013
Reproducibility of Detecting Silent Cerebral Infarcts in Pediatric Sickle Cell Anemia.Liem RI, Liu J, Gordon MO, Vendt BA, McKinstry RC, Kraut MA, Strouse JJ, Ball WS, Debaun MR J. Child Neurol.2013
Informing Children of Their Newborn Screening Carrier Result for Sickle Cell or Cystic Fibrosis: Qualitative Study of Parents' Intentions, Views and Support Needs.Ulph F, Cullinan T, Qureshi N, Kai J J Genet Couns2013
Adult Sickle Cell Quality of Life Measurement Information System (ASCQ-Me): Conceptual Model Based on Review of the Literature and Formative Research.Treadwell MJ, Hassell K, Levine R, Keller S Clin J Pain2013
Prophylactic versus selective blood transfusion for sickle cell disease in pregnancy.Okusanya BO, Oladapo OT Cochrane Database Syst Rev2013
An overview of hemoglobinopathies and the interpretation of newborn screening results.Chandrakasan S, Kamat D Pediatr Ann2013
Diagnosis and prevention of thalassemia.Ip HW, So CC Crit Rev Clin Lab Sci2013
Chelation therapy with oral solution of deferiprone in transfusional iron-overloaded children with hemoglobinopathies.Makis A, Chaliasos N, Alfantaki S, Karagouni P, Siamopoulou A Anemia2013
Pattern of chronic lung lesions in adults with sickle cell disease in Lagos, Nigeria.O Dosunmu A, A Akinola R, A Onakoya J, M Balogunt T, O Adeyeye O, A Akinbami A, M Arogundade O, T Brodie-Mends A Caspian J Intern Med2013
Mutation analysis for a Chinese family featuring X-linked alpha thalassemia/mental retardation syndrome.Lin S, Sun H, Song X, Chen L, Du M, Chen Z Zhonghua Yi Xue Yi Chuan Xue Za Zhi2013
Coping and Coping Assistance Among Children With Sickle Cell Disease and Their Parents.Hildenbrand AK, Barakat LP, Alderfer MA, Marsac ML J. Pediatr. Hematol. Oncol.2013
Cerebral Vascular Abnormalities in Pediatric Patients With Sickle Cell Disease After Hematopoietic Cell Transplant.Bodas P, Rotz S J. Pediatr. Hematol. Oncol.2013
Study of parents of β-thalassemia major children to determine cutoff values of hematological parameters for diagnosis of β-thalassemia trait and assessment of anemia in them.Bhukhanvala D, Seliya V, Shah A, Gupte S Indian J Med Sci2013
Asthma management in sickle cell disease.Gomez E, Morris CR Biomed Res Int2013
Dental and periodontal health status of Beta thalassemia major and sickle cell anemic patients: a comparative study.Singh J, Singh N, Kumar A, Kedia NB, Agarwal A J Int Oral Health2013
A Retrospective Review of Acupuncture Use for the Treatment of Pain in Sickle Cell Disease Patients: Descriptive Analysis From a Single Institution.Lu K, Cheng MJ, Ge X, Berger A, Xu D, Kato GJ, Minniti CP Clin J Pain2013
Acute Myocardial Ischemia in Association With Acute Respiratory Acidosis in Hemoglobin SC Disease: A Case Report.Gayanilo M, Nares M, Alvarez O, Swaminathan S J. Pediatr. Hematol. Oncol.2013
Red blood cell alloimmunization in sickle cell disease-prevalence and trends: a single-center cross-sectional study from United Kingdom.Mijovic A, Perera IG, Thein SL Transfusion2013
Massive hemothorax due to intrathoracic extramedullary hematopoiesis in a patient with beta thalassemia hemoglobin E disease.Tantraworasin A, Saeteng S J Med Assoc Thai2013
Sickle cell trait testing and athletic participation: a solution in search of a problem?Thompson AA Hematology Am Soc Hematol Educ Program2013
Consequences and management of iron overload in sickle cell disease.Porter J, Garbowski M Hematology Am Soc Hematol Educ Program2013
Transfusion therapy for sickle cell disease: a balancing act.Chou ST Hematology Am Soc Hematol Educ Program2013
Sickle cell disease pain management and the medical home.Raphael JL, Oyeku SO Hematology Am Soc Hematol Educ Program2013
Allogeneic transplantation strategies including haploidentical transplantation in sickle cell disease.Gluckman E Hematology Am Soc Hematol Educ Program2013
Vaso-occlusion in sickle cell disease: pathophysiology and novel targeted therapies.Manwani D, Frenette PS Hematology Am Soc Hematol Educ Program2013
Genetic association studies in β-hemoglobinopathies.Thein SL Hematology Am Soc Hematol Educ Program2013
A biopsychosocial-spiritual model of chronic pain in adults with sickle cell disease.Taylor LE, Stotts NA, Humphreys J, Treadwell MJ, Miaskowski C Pain Manag Nurs2013
The Spectrum of Ocular Alterations in Patients with β-Thalassemia Syndromes Suggests a Pathology Similar to Pseudoxanthoma Elasticum.Barteselli G, Dell'arti L, Finger RP, Charbel Issa P, Marcon A, Vezzola D, Mapelli C, Cassinerio E, Cappellini MD, Ratiglia R, Viola F Ophthalmology2013
Nondeletional α-Thalassemia (α2- IVS-1-116, A>G HBA2): An α2 Gene Point Mutation Detected in an African-American Female for the First Time.Dainer P, Patel N, Zhuang L, Carmichael H, Kutlar F Acta Haematol.2013
A Newly Modified Hemoglobin H Inclusion Test as a Secondary Screening for α-Thalassemia in Southeast Asian Populations.Fucharoen G, Yooyen K, Chaibunruang A, Fucharoen S Acta Haematol.2013
Fetal hemoglobin in sickle cell anemia.Nadkarni A, Dabke P, Colah RB, Ghosh K Blood Cells Mol. Dis.2013
Gender differences in severity of sickle cell diseases in non-smokers.Rami Helvaci M, Ayyildiz O, Gundogdu M Pak J Med Sci2013
A common signaling pathway is activated in erythroid cells expressing high levels of fetal hemoglobin: a potential role for cAMP-elevating agents in β-globin disorders.Ikuta T, Kuroyanagi Y, Odo N, Liu S J Blood Med2013
Combined Chelation Therapy with Deferoxamine and Deferiprone in β-Thalassemia Major: Compliance and Opinions of Young Thalassemic Patients.Hatzipantelis ES, Karasmanis K, Perifanis V, Vlachaki E, Tziomalos K, Economou M Hemoglobin2013
Severe α-Thalassemia Intermedia Due to a Compound Heterozygosity for the Highly Unstable Hb Adana (HBA2: c.179G>A) and a Novel Codon 24 (HBA2: c.75T>A) Mutation.Megawati D, Nainggolan IM, Swastika M, Susanah S, Mose JC, Harahap AR, Setianingsih I Hemoglobin2013
Hydroxyurea could be a good clinically relevant iron chelator.Italia K, Colah R, Ghosh K PLoS ONE2013
Airways obstruction and pulmonary capillary blood volume in children with sickle cell disease.Wedderburn CJ, Rees D, Height S, Dick M, Rafferty GF, Lunt A, Greenough A Pediatr. Pulmonol.2013
Ferritin trends do not predict changes in total body iron in patients with transfusional iron overload.Puliyel M, Sposto R, Berdoukas VA, Hofstra TC, Nord A, Carson S, Wood J, Coates TD Am. J. Hematol.2013
Transition from paediatric to adult care for patients with sickle cell Montalembert M, Guitton C, Br. J. Haematol.2013
Sickle cell disease and pregnancy outcomes: population-based study on 8.8 million births1).Alayed N, Kezouh A, Oddy L, Abenhaim HA J Perinat Med2013
Quality of life among children with beta-thalassemia major treated in Western Saudi Arabia.Ayoub MD, Radi SA, Azab AM, Abulaban AA, Balkhoyor AH, Bedair SW, Aljaouni SK, Kari JA Saudi Med J2013
Morphine is associated with acute chest syndrome in children hospitalized with sickle cell disease.Birken CS, Khambalia A, Dupuis A, Pastor A, Lee M, Padavattan K, Mekky M, Odame I, Parkin PC Hosp Pediatr2013
Hemoglobin Fontainebleau [a21(B2)Ala>Pro]: The second report from India.Mashon RS, Nair S, Sawant P, Colah RB, Ghosh K, Das S Indian J Hum Genet2013
Analysis of hemoglobin electrophoresis results and physicians investigative practices in Saudi Arabia.Mehdi SR, Al Dahmash BA Indian J Hum Genet2013
Usage of U7 small nuclear ribonucleic acid in gene therapy of hemoglobin D Punjab disorder: Rationale?Wiwanitkit V Indian J Hum Genet2013
Hemoglobin E disorder: Newborn screening program.Wiwanitkit V Indian J Hum Genet2013
Impact of Sickle Hemoglobinopathies on Pregnancy-Related Venous Thromboembolism.Porter B, Key NS, Jauk VC, Adam S, Biggio J, Tita A Am J Perinatol2013
Hyperhaemolysis syndrome responsive to splenectomy in a patient with δβ-thalassaemia: a discussion on underlying mechanisms.Vagace JM, Casado MS, Bajo R, Gervasini G Blood Transfus2013
Transcriptional regulators Myb and BCL11A interplay with DNA methyltransferase 1 in developmental silencing of embryonic and fetal β-like globin genes.Roosjen M, McColl B, Kao B, Gearing LJ, Blewitt ME, Vadolas J FASEB J.2013
Unrelated Donor Allogeneic Hematopoietic Stem Cell Transplantation for Patients with Hemoglobinopathies Using a Reduced-Intensity Conditioning Regimen and Third-Party Mesenchymal Stromal Cells.Kharbanda S, Smith AR, Hutchinson SK, McKenna DH, Ball JB, Lamb LS, Agarwal R, Weinberg KI, Wagner JE Biol. Blood Marrow Transplant.2013
Reply to Sun A J. Formos. Med. Assoc.2013
Molecular basis of transfusion dependent beta-thalassemia major patients in Sabah.Teh LK, George E, Lai MI, Tan JA, Wong L, Ismail P J. Hum. Genet.2013
The haematological phenotype and genotype analysis on 14 co-inheritance of hemoglobin Constant Spring and β-thalassemia.Li YQ, Yang T, Ling XZ, Liang L Zhonghua Xue Ye Xue Za Zhi2013
Oral manifestations and blood profile in thalassemia trait.Joob B, Wiwanitkit V J. Formos. Med. Assoc.2013
Iron Deficiency Anaemia among Pre-School Children with Sickle Cell Anaemia: Still a Rare Diagnosis?Akodu SO, Kehinde OA, Diaku-Akinwumi IN, Njokanma OF Mediterr J Hematol Infect Dis2013
Therapeutic value of combined therapy with deferasirox and silymarin on iron overload in children with Beta thalassemia.Hagag AA, Elfrargy MS, Gazar RA, El-Lateef AE Mediterr J Hematol Infect Dis2013
Sickle cell disease: management options and challenges in developing countries.Ansong D, Akoto AO, Ocloo D, Ohene-Frempong K Mediterr J Hematol Infect Dis2013
Addition of multimodal therapy to standard management of steady state sickle cell disease.Okpala I, Ezenwosu O, Ikefuna A, Duru A, Chukwu B, Madu A, Nwagha T, Ocheni S, Ibegbulam O, Emodi I, Anike U, Nonyelu C, Anigbo C, Agu K, Ajuba I, Chukwura A, Ugwu O, Ololo U ISRN Hematol2013
Frequency and origin of haplotypes associated with the beta-globin gene cluster in individuals with trait and sickle cell anemia in the Atlantic and Pacific coastal regions of Colombia.Fong C, Lizarralde-Iragorri MA, Rojas-Gallardo D, Barreto G Genet. Mol. Biol.2013
Arterial stiffness and pulse wave reflection in young adult heterozygous sickle cell carriers.Bayramoğlu T, Akkuş O, Nas K, Illyes M, Molnar F, Gürkan E, Bashırov MB, Demir S, Akkuş G, Acartürk E Turk J Haematol2013
β-Thalassemia Mutation At Codon 37 (Tgg>Tga) Detected In A Turkish Family.Güleç D, Bilgili S, Uzuncan N, Bozkaya G, Soyer N, Karaca B Turk J Haematol2013
Detection of Left Ventricular Regional Function in Asymptomatic Children with beta-Thalassemia Major by Longitudinal Strain and Strain Rate Imaging.Bay A, Başpınar O, Leblebisatan G, Yalçın AS, Irdem A Turk J Haematol2013
Low HbA2 Level in β-Thalassemia Trait.Ozsoylu S Turk J Haematol2013
National thalassemia prevention campaign: the talotır project.Canatan D, Aydınok Y, Kılınç Y, Karakaş Z, Saşmaz I, Apak H, Sarper N Turk J Haematol2013
A Case of Nonimmune Hydrops Fetalis Caused by Homozygous α-Thalassemia.Akar M, Dilli D, Dilmen U Turk J Haematol2013
Frequency and risk factors of endocrine complications in Turkish children and adolescents with sickle cell anemia.Ozen S, Unal S, Erçetin N, Taşdelen B Turk J Haematol2013
Diabetes monitoring in hemoglobinopathies.Shriraam M, Sridhar M Indian Pediatr2013
Longitudinal study on thyroid function in patients with thalassemia major: High incidence of central hypothyroidism by 18 years.Soliman AT, Al Yafei F, Al-Naimi L, Almarri N, Sabt A, Yassin M, De Sanctis V Indian J Endocrinol Metab2013
Cortisol response to low dose versus standard dose (back-to-back) adrenocorticotrophic stimulation tests in children and young adults with thalassemia major.Soliman AT, Yassin M, Majuid NM, Sabt A, Abdulrahman MO, De Sanctis V Indian J Endocrinol Metab2013
Does blood transfusion affect pituitary gonadal axis and sperm parameters in young males with sickle cell disease?Soliman AT, Yasin M, El-Awwa A, Abdelrahman MO, De Sanctis V Indian J Endocrinol Metab2013
Phenotypic heterogeneity of asian Indian inversion deletions gγ(aγδβ)0 breakpoint a and breakpoint B.Pandey S, Pandey S, Ranjan R, Mishra R, Sharma M, Saxena R Indian J Clin Biochem2013
Comparative efficacy and safety of deferoxamine, deferiprone and deferasirox on severe thalassemia: a meta-analysis of 16 randomized controlled trials.Xia S, Zhang W, Huang L, Jiang H PLoS ONE2013
Study of thyroid function in Egyptian children with β-thalassemia major and β-thalassemia intermedia.Abdel-Razek AR, Abdel-Salam A, El-Sonbaty MM, Youness ER J Egypt Public Health Assoc2013
What dentists should know about sickle cell disease.Devine BP Tex Dent J2013
Safety of pegfilgrastim (neulasta) in patients with sickle cell trait/anemia.Kasi PM, Patnaik MM, Peethambaram PP Case Rep Hematol2013
Beta-Thalassemia Major and Female Fertility: The Role of Iron and Iron-Induced Oxidative Stress.Roussou P, Tsagarakis NJ, Kountouras D, Livadas S, Diamanti-Kandarakis E Anemia2013
Diagnostic value of electrocardiography compared with echocardiography in measuring left ventricular mass index in major thalassemia patients over 10 years of age.Noori N, Mahjoubifard M, Alavi SM, Hosseini S, Sanati H, Mirmesdagh Y J Tehran Heart Cent2013
Brain Perfusion Impairment in Neurologically Asymptomatic Adult Patients with Sickle-Cell Disease Shown by Voxel-Based Analysis of SPECT Images.Deus-Silva L, Bonilha L, Damasceno BP, Costa AL, Yasuda CL, Costa FF, Santos AO, Etchebehere EC, Oquendo-Nogueira R, Fockink R, de Freitas CF, Camargo EE, Li LM, Cendes F, Saad ST Front Neurol2013
Frequencies of -308G/A (TNFA) and -509C/T (TGFB1) polymorphisms in sickle cell anemia patients from Brazil.Torres LS, Belini Júnior E, Silva DG, Lobo CL, Ruiz MA, Bonini-Domingos CR Genet. Mol. Res.2013
Wheezing Symptoms and Parental Asthma Are Associated with a Physician Diagnosis of Asthma in Children with Sickle Cell Anemia.Strunk RC, Cohen RT, Cooper BP, Rodeghier M, Kirkham FJ, Warner JO, Stocks J, Kirkby J, Roberts I, Rosen CL, Craven DI, Debaun MR, J. Pediatr.2013
Pulmonary hypertension in β thalassaemia.Anthi A, Orfanos SE, Armaganidis A Lancet Respir Med2013
Falciparum malaria infection in a case of sickle cell trait; unbalancing the balanced polymorphism.Amale A, Acharya S, Shukla S, Dubey S Indian J Hematol Blood Transfus2013
A Rare Case of Hemoglobin E Hemoglobinopathy with Gaucher's Disease.Chatterjee T, Dewan K, Ganguli P, Das S, Sharma A, Sahni AK, Nath P Indian J Hematol Blood Transfus2013
Carrier Screening for β Thalassemia in Pregnant Indian Women: Experience at a Single Center in Madhya Pradesh.Baxi A, Manila K, Kadhi P, Heena B Indian J Hematol Blood Transfus2013
Hematological Parameters and RBC TBARS Level of Q 10 Supplemented Tribal Sickle Cell Patients: A Hospital Based Study.Thakur AS, Littaru GP, Moesgaard S, Dan Sindberg C, Khan Y, Singh CM Indian J Clin Biochem2013
An update on thalassemia intermedia.Maakaron JE, Cappellini MD, Taher AT J Med Liban2013
Peg-interfon alpha-2a and low-dose ribavirin for treatment of hepatitis C virus infection in patients with sickle-cell anemia in Saudi Arabia.Agha A, Chakik R, Abdulhadi MM, Alsaudi D, Sammito G, Giannini EG Ann Saudi Med2013
Criteria for detection of alpha-thalassemia-1 Thai type deletion in routine laboratory.Pornprasert S, Punyamung M, Treesuwan K Clin. Lab.2013
Hypoxemia in Sickle Cell Disease: Significance And Management.Caboot JB, Allen JL Paediatr Respir Rev2013
Bone marrow transplantation for thalassemia: How much is a child's life worth?Kanwar VS South Asian J Cancer2013
Setting up low-risk bone marrow transplantation for children with thalassemia may facilitate pediatric cancer care.Faulkner LB South Asian J Cancer2013
Genotyping of beta thalassemia trait by high-resolution DNA melting analysis.Saetung R, Ongchai S, Charoenkwan P, Sanguansermsri T Southeast Asian J. Trop. Med. Public Health2013
Correlation between t2* cardiovascular magnetic resonance with left ventricular function and mass in adolescent and adult major thalassemia patients with iron overload.Djer MM, Anggriawan SL, Gatot D, Amalia P, Sastroasmoro S, Widjaja P Acta Med Indones2013
Brazilian Thalassemia Association protocol for iron chelation therapy in patients under regular transfusion.Veríssimo MP, Loggetto SR, Fabron Junior A, Baldanzi GR, Hamerschlak N, Fernandes JL, Araujo Ada S, Lobo CL, Fertrin KY, Berdoukas VA, Galanello R Rev Bras Hematol Hemoter2013
Oxidative stress and antioxidant status in beta-thalassemia heterozygotes.Ondei Lde S, Estevão Ida F, Rocha MI, Percário S, Souza DR, Pinhel MA, Bonini-Domingos CR Rev Bras Hematol Hemoter2013
Growth Parameters and Vitamin D status in Children with Thalassemia Major in Upper Egypt.Fahim FM, Saad K, Askar EA, Eldin EN, Thabet AF Int J Hematol Oncol Stem Cell Res2013
Evaluation of Novel Fetal Hemoglobin Inducer Drugs in Treatment of β-Hemoglobinopathy Disorders.Fard AD, Hosseini SA, Shahjahani M, Salari F, Jaseb K Int J Hematol Oncol Stem Cell Res2013
Evaluation of Signaling Pathways Involved in γ-Globin Gene Induction Using Fetal Hemoglobin Inducer Drugs.Rahim F, Allahmoradi H, Salari F, Shahjahani M, Fard AD, Hosseini SA, Mousakhani H Int J Hematol Oncol Stem Cell Res2013
Copper status in patients with thalassemia major in zahedan, iran.Mashhadi MA Int J Hematol Oncol Stem Cell Res2013
Prenatal Diagnosis of Different Polymorphisms of β-globin Gene in Ahvaz.Dehghanifard A, Shahjahani M, Galehdari H, Rahim F, Hamid F, Jaseb K, Asnafi AA, Jalalifar MA, Saki N Int J Hematol Oncol Stem Cell Res2013
Double heterozygous hemoglobin Q India/hemoglobin D Punjab hemoglobinopathy: Report of two rare cases.Mutreja D, Tyagi S, Tejwani N, Dass J Indian J Hum Genet2013
Piceatannol: a potential futuristic natural stilbene as fetal haemoglobin inducer.Kukreja A, Tandon S, Mishra A, Tiwari A J Clin Diagn Res2013
NESTROFT - A Valuable, Cost Effective Screening Test for Beta Thalassemia Trait in North Indian Punjabi Population.Piplani S, Manan R, Lalit M, Manjari M, Bhasin T, Bawa J J Clin Diagn Res2013
Osteoporosis in thalassemia major: an update and the I-CET 2013 recommendations for surveillance and treatment.De Sanctis V, Soliman AT, Elsedfy H, Yassin M, Canatan D, Kilinc Y, Sobti P, Skordis N, Karimi M, Raiola G, Galati MC, Bedair E, Fiscina B, El Kholy M Pediatr Endocrinol Rev2013
Correlation between serum leptin level and thyroid hormones in children with major beta-thalassemia .Shahramian I, Noori N, Ramezani A, Sharafi E, Akhlaghi E Iran J Ped Hematol Oncol2013
Quality of life in children with β-thalassemia major at center for special diseases.Kaheni S, Yaghobian M, Sharefzadah GH, Vahidi A, Ghorbani H, Abderahemi A Iran J Ped Hematol Oncol2013
A study of leptin serum concentrations in patients with major Beta-thalassemia.Shahramian I, Akhlaghi E, Ramezani A, Rezaee A, Noori N, Sharafi E Iran J Ped Hematol Oncol2013
Homozygous delta-beta Thalassemia in a Child: a Rare Cause of Elevated Fetal Hemoglobin.Verma S, Bhargava M, Mittal S, Gupta R Iran J Ped Hematol Oncol2013
Premarital Screening of Beta Thalassemia Minor in north-east of Iran.Hashemizadeh H, Noori R Iran J Ped Hematol Oncol2013
Evaluation of cardiac function in patients with thalassemia intermedia.Nouri N, Naderi M, Rajaie S, Dorgalaleh A, Tabibian Sh Iran J Ped Hematol Oncol2013
Knowledge, attitude and practice of premarital counseling for sickle cell disease among youth in Yaba, Nigeria.Oludarei GO, Ogili MC Afr J Reprod Health2013
Effect of health education on the knowledge and attitude to sickle cell disorder and screening practices among school of nursing students in Sokoto, Nigeria.Abiola AO, Ojika BO, Mannir B, Abba SK, Muhammad M, Ibrahim MT, Aschcroft BN, Akanmu SS Nig Q J Hosp Med2013
Beta thalassaemia in Nigeria: myth or fact?Kotila TR Afr J Med Med Sci2013
Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patients.Dabke PS, Colah RB, Ghosh KK, Nadkarni AH Hematology2013
Attenuation of serum ferritin and iron burden by intake of antioxidants in beta thalassemia major.Bhagat SS, Sarkar PD, Suryakar AN, Padalkar RK, Ghone RA, Patil SM, Hundekar PS Indian J. Physiol. Pharmacol.2013
Identification of patients with defects in the globin genes.Dell'edera D, Epifania AA, Milazzo GN, Leo M, Santacesaria C, Allegretti A, Mazzone E, Panetta P, Iammarino G, Lupo MG, Barbieri R, Lioi MB J Prenat Med2013
Serum procalcitonin as a predicting value in severity and prognosis of CAP in sickle cell-patients.Alsayed S, Marzouk S, Mousa E J Egypt Soc Parasitol2013
Sickle cell disease with osteogenesis imperfecta.Patil PL, Rao BV J Assoc Physicians India2013
Cardiac autonomic dysfunction in sickle cell anaemia and its correlation with QT parameters.Kolo PM, Sanya EO, Olanrewaju TO, Fawibe AE, Soladoye A Niger Med J2013
The Correlation between Troponin and Ferritin Serum Levels in the Patients with Major Beta-Thalassemia.Shahramian I, Razzaghian M, Ramazani AA, Ahmadi GA, Noori NM, Rezaee AR Int Cardiovasc Res J2013
Iron overload in Beta thalassaemia major and intermedia patients.Mishra AK, Tiwari A Maedica (Buchar)2013
Thalassaemia intermedia presenting with compressive myelopathy: a case report.Bhattacharyya B, Ghosh SK, Dhibar T, Chattopadhyay A, Ghosh SN, Bhadra AK, Ghorai PK J Indian Med Assoc2013
International thalassaemia day and present scenario of thalassaemia in West Bengal.Ghoshal AK, Bhattacharya M J Indian Med Assoc2013
Beta thalassaemia in Nigeria: myth or fact?Kotila TR Afr J Med Med Sci2013
Joint effusions and purpura in multiply-transfused adult beta-thalassemia- clinical pointers to diagnosis of scurvy.Prakash A, Pandey AK Kathmandu Univ Med J (KUMJ)2013
Sickle cell disease: new treatments and their rationale.Field JJ Clin Adv Hematol Oncol2013
Anemia and transfusion of red blood cells.Cortés Buelvas A Colomb. Med.2013
First successful lung transplantation for sickle cell disease with severe pulmonary arterial hypertension and pulmonary veno-occlusive disease.George MP, Novelli EM, Shigemura N, Simon MA, Feingold B, Krishnamurti L, Morrell MR, Gries CG, Haider S, Johnson BA, Crespo MM, Bhama JK, Bermudez C, Yousem SA, Toyoda Y, Champion HC, Pilewski JM, Gladwin MT Pulm Circ2013
Cellular, pharmacological, and biophysical evaluation of explanted lungs from a patient with sickle cell disease and severe pulmonary arterial hypertension.Rogers NM, Yao M, Sembrat J, George MP, Knupp H, Ross M, Sharifi-Sanjani M, Milosevic J, St Croix C, Rajkumar R, Frid MG, Hunter KS, Mazzaro L, Novelli EM, Stenmark KR, Gladwin MT, Ahmad F, Champion HC, Isenberg JS Pulm Circ2013
Dysregulation of ubiquitin-proteasome pathway and apolipoprotein A metabolism in sickle cell disease-related pulmonary arterial hypertension.Anjum F, Lazar J, Soh J, Albitar M, Gowda S, Hussain MM, Wadgaonkar R Pulm Circ2013
Diagnostic accuracy of spot and timed measurements of urinary albumin concentration to determine microalbuminuria in sickle cell disease.Asnani MR, Reid ME West Indian Med J2013
Frequency of beta-thalassemia trait in families of thalassemia major patients, Lahore.Majeed T, Akhter MA, Nayyar U, Riaz MS, Mannan J J Ayub Med Coll Abbottabad2013
KLF10 gene expression is associated with high fetal hemoglobin levels and with response to hydroxyurea treatment in β-hemoglobinopathy patients.Borg J, Phylactides M, Bartsakoulia M, Tafrali C, Lederer C, Felice AE, Papachatzopoulou A, Kourakli A, Stavrou EF, Christou S, Hou J, Karkabouna S, Lappa-Manakou C, Ozgur Z, van Ijcken W, von Lindern M, Grosveld FG, Georgitsi M, Kleanthous M, Philipsen S, Patrinos GPPharmacogenomics2012
The spine in β-thalassemia syndromes.Haidar R, Mhaidli H, Musallam KM, Taher ATSpine2012
Peroxiredoxin II is essential for preventing hemolytic anemia from oxidative stress through maintaining hemoglobin stability.Han YH, Kim SU, Kwon TH, Lee DS, Ha HL, Park DS, Woo EJ, Lee SH, Kim JM, Chae HB, Lee SY, Kim BY, Yoon do Y, Rhee SG, Fibach E, Yu DYBiochem. Biophys. Res. Commun.2012
Noninvasive Prenatal Diagnosis of Monogenic Diseases by Targeted Massively Parallel Sequencing of Maternal Plasma: Application to β-Thalassemia.Lam KW, Jiang P, Liao GJ, Chan KC, Leung TY, Chiu RW, Lo YMClin. Chem.2012
Association of xmn I polymorphism and hemoglobin e haplotypes on postnatal gamma globin gene expression in homozygous hemoglobin e.Ekwattanakit S, Monteerarat Y, Riolueang S, Tachavanich K, Viprakasit VAdv Hematol2012
Left ventricular rotational dynamics in Beta thalassemia major: a speckle-tracking echocardiographic study.Monte I, Buccheri S, Bottari V, Blundo A, Licciardi S, Romeo MAJ Am Soc Echocardiogr2012
Silent cerebral infarct in child patients with beta thalassaemia intermedia.Leblebisatan G, Bay A, Sirikci A, Kilincaslan H, Sonmezisik S, Leblebisatan S, Baspinar O, Dogan M, Yis UBlood Coagul. Fibrinolysis2012
High dose vitamin D therapy for chronic pain in children and adolescents with sickle cell disease: results of a randomized double blind pilot study.Osunkwo I, Ziegler TR, Alvarez J, McCracken C, Cherry K, Osunkwo CE, Ofori-Acquah SF, Ghosh S, Ogunbobode A, Rhodes J, Eckman JR, Dampier C, Tangpric