| Nano-sized zeolite-like metal-organic frameworks induced hematological effects on red blood cell. | Hao F, Yan XP | J Hazard Mater | 2022 |
| Homing in on haemoglobinopathies. | The Lancet Global Health | Lancet Glob Health | 2022 |
| Bloodstream Infections in Children With Sickle Cell Disease: 2010-2019. | Yee ME, Lai KW, Bakshi N, Grossman JK, Jaggi P, Mallis A, Wang YF, Jerris RC, Lane PA, Yildirim I | Pediatrics | 2022 |
| Mortality in β-thalassemia patients with confirmed pulmonary arterial hypertension on right heart catheterization. | Pinto VM, Musallam KM, Derchi GE, Graziadei G, Giuditta M, Origa R, Barella S, Casu G, Pasanisi A, Longo F, Casale M, Miceli R, Merella P, Tartaglione I, Piga A, Cappellini MD, Gianesin B, Forni GL | Blood | 2022 |
| Efficacy and Safety of Iron Chelation Therapy After Allogeneic Hematopoietic Stem Cell Transplantation in Pediatric Thalassemia Patients: A Retrospective Observational Study. | Kupesiz FT, Sivrice C, Akinel A, Kintrup GT, Guler E, Kupesiz A | J Pediatr Hematol Oncol | 2022 |
| Telehealth Use Before and During the COVID-19 Pandemic Among Children with Sickle Cell Anemia. | Reeves SL, Patel PN, Madden B, Ng S, Creary SE, Smith D, Ellimoottil C | Telemed J E Health | 2022 |
| Modern management of iron overload in thalassemia major patients guided by MRI techniques: real-world data from a long-term cohort study. | Bayraktaroglu S, Karadas N, Onen S, Karapinar DY, Aydinok Y | Ann Hematol | 2022 |
| Up-regulation of miR-130a is related to leg ulcers in sickle cell anaemia. | Batista THC, Santana RM, Sobreira MJ, Arcanjo GS, Domingos IF, Pereira-Martins DA, Falcão DA, Oliveira JMF, Batista JVGF, Weinhӓuser I, Hatzlhofer BL, Júnior WLB, Araujo AS, Dos Anjos AC, Costa FF, Saad MJA, Carvalho BM, Vasconcelos LRS, Lucena-Araujo AR, Bezerra MA | Br J Haematol | 2022 |
| Delayed Hemolytic Transfusion Reaction in Sickle Cell Disease: A Case Series. | Alwaheed AJ, Alqatari SG, AlSulaiman AS, AlSulaiman RS | Am J Case Rep | 2022 |
| Translating research to usual care of children with sickle cell disease in Northern Nigeria: lessons learned from the SPRING Trial Team. | Bello-Manga H, Haliru L, Tabari AM, Farouk B, Suleiman A, Bahago GY, Sani AM, Bauman AA, DeBaun MR, King AA | BMC Res Notes | 2022 |
| A rare case of adrenal extramedullary haematopoiesis in a Cypriot woman with β-thalassaemia. | Georgiou AC, Lisacek-Kiosoglous AB, Mariannis D, Christou S, Hadjianastassiou VG | Ann R Coll Surg Engl | 2022 |
| Liver Transplant in Hemoglobin SC Disease and Autoimmune Hepatitis: A Case Report. | Kim A, Assarzadegan N, Anders RA, Oshima K, Chaturvedi S, Weeks S, Kohli R, Lanzkron S, Gurakar A, Garonzik-Wang J, Chen PH | Exp Clin Transplant | 2022 |
| The pharmacokinetic and safety profile of single-dose deferiprone in subjects with sickle cell disease. | Soulières D, Mercier-Ross J, Fradette C, Rozova A, Tsang YC, Tricta F | Ann Hematol | 2022 |
| Lentiviral globin gene therapy with reduced-intensity conditioning in adults with β-thalassemia: a phase 1 trial. | Boulad F, Maggio A, Wang X, Moi P, Acuto S, Kogel F, Takpradit C, Prockop S, Mansilla-Soto J, Cabriolu A, Odak A, Qu J, Thummar K, Du F, Shen L, Raso S, Barone R, Di Maggio R, Pitrolo L, Giambona A, Mingoia M, Everett JK, Hokama P, Roche AM, Cantu VA, Adhikari H, Reddy S, Bouhassira E, Mohandas N, Bushman FD, Rivière I, Sadelain M | Nat Med | 2022 |
| Perforated Duodenal Ulcer Associated with Deferasirox in a Child with β-Thalassemia Major. | Zahra A, Ragab A, Al-Abboh H, Ismaiel A, Adekile AD | Hemoglobin | 2022 |
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| Busulfan-fludarabine- or treosulfan-fludarabine-based myeloablative conditioning for children with thalassemia major. | Lüftinger R, Zubarovskaya N, Galimard JE, Cseh A, Salzer E, Locatelli F, Algeri M, Yesilipek A, de la Fuente J, Isgrò A, Alseraihy A, Angelucci E, Smiers FJ, La La Nasa G, Zecca M, Fisgin T, Unal E, Kleinschmidt K, Peters C, Lankester A, Corbacioglu S, | Ann Hematol | 2022 |
| Quality of life and challenges experienced by the surviving adults with transfusion dependent thalassaemia in Malaysia: a cross sectional study. | Foong WC, Chean KY, Rahim FF, Goh AS, Yeoh SL, Yeoh AAC | Health Qual Life Outcomes | 2022 |
| Cost analysis of acute care resource utilization among individuals with sickle cell disease in a middle-income country. | Lobo C, Moura P, Fidlarczyk D, Duran J, Barbosa R, Oliveira T, do Nascimento EM, Bhakta N, Hankins JS | BMC Health Serv Res | 2022 |
| Biopsychosocial Factors Associated with Parenting Stress in Pediatric Sickle Cell Disease. | Johnson YL, Woodward K, Dampier C, Cohen L, Sil S | J Clin Psychol Med Settings | 2022 |
| Transition from Oxycodone to Buprenorphine/Naloxone in a Hospitalized Patient with Sickle Cell Disease: A Case Report. | Leyde S, Suen L, Pratt L, DeFries T | J Gen Intern Med | 2022 |
| l-glutamine, crizanlizumab, voxelotor, and cell-based therapy for adult sickle cell disease: Hype or hope? | Leibovitch JN, Tambe AV, Cimpeanu E, Poplawska M, Jafri F, Dutta D, Lim SH | Blood Rev | 2022 |
| Clonal hematopoiesis in sickle cell disease. | Liggett LA, Cato LD, Weinstock JS, Zhang Y, Nouraie SM, Gladwin MT, Garrett ME, Ashley-Koch A, Telen M, Custer B, Kelly S, Dinardo C, Sabino EC, Loureiro P, Carneiro-Proietti A, Maximo C, Reiner AP, Abecasis GR, Williams DA, Natarajan P, Bick AG, Sankaran VG | J Clin Invest | 2022 |
| Venous cerebral blood flow quantification and cognition in patients with sickle cell anemia. | Stotesbury H, Hales PW, Koelbel M, Hood AM, Kawadler JM, Saunders DE, Sahota S, Rees DC, Wilkey O, Layton M, Pelidis M, Inusa BP, Howard J, Chakravorty S, Clark CA, Kirkham FJ | J Cereb Blood Flow Metab | 2022 |
| Evolving Strategies in the Management of Sickle Cell Disease in the 21st Century and the Role of the Pediatrician. | Hardit V, Alvarez O, Ziga E, Alperstein W | Pediatr Ann | 2022 |
| Assessing and managing people with sickle cell disease presenting with vaso-occlusive crisis in the emergency department. | De D, Thakur I | Emerg Nurse | 2022 |
| Prevalence of Depression among Iranian Patients with Beta-Thalassemia Major: A Systematic Review and Meta-analysis. | Jaafari Z, Sadidi N, Abdolahinia Z, Shahesmaeili A | Iran J Med Sci | 2022 |
| A Novel Association of HbQ India Trait with Sickle Cell Anemia: a New Insight in Hemoglobinopathies. | Gupta RK, Verma KK, Singh G | SN Compr Clin Med | 2022 |
| Navigating Hemostasis of Bleeding Among Children With β-Thalassemia. | El-Beshlawy A, Rabah F, Hamed HM, Mahmoud AA, Al-Wakeel HA, Abdelhamid EM, El-Sonbaty MM, El Sissy M | J Pediatr Hematol Oncol | 2022 |
| Hydroxyurea and fetal hemoglobin effect on leg ulcers in patients with sickle cell disease. | Tolu SS, Crouch A, Choi J, Gao Q, Reyes-Gil M, Ogu UO, Vinces G, Minniti CP | Ann Hematol | 2022 |
| Extensive porto-splenic venous thrombosis postsplenectomy in a sickle cell disease: a rare complication. | Al Barhi T, Wali Y, Al Sibai S, Al Balushi Z | BMJ Case Rep | 2022 |
| Effect of Sickle Cell Trait on Total Hip Arthroplasty in a Matched Cohort. | Waters TL, Wilder JH, Ross BJ, Salas Z, Sherman WF | J Arthroplasty | 2022 |
| Gastrointestinal vaso-occlusive crisis in a woman with hemoglobin SC disease. | Clement JM, Li AY, Berg BW, Law JY, Baer MR | Am J Med | 2022 |
| Native cardiac magnetic resonance T1 mapping and cardiac mechanics as assessed by speckle tracking echocardiography in patients with beta-thalassaemia major. | See WS, So EK, Hwang GY, Chin L, Ip L, Lam WW, Ha SY, Cheung YF | Int J Cardiol Heart Vasc | 2022 |
| Spectrum of HBB gene mutations among 696 β-thalassemia patients and carriers in Southern Vietnam. | Xinh PT, Chuong HQ, Ha NTT, Tram HDB, Van Dong C, Thanh LVH, Hoa NTH, Nghia H, Binh NT, Dung PC, Vu HA | Mol Biol Rep | 2022 |
| Feasibility of early sirolimus cessation post non-myeloablative transplantation in adult patients with severe sickle cell disease. | Damlaj M, Alahmari B, Alaskar A, Alhejazi A, Alsadi H, Shehab-Eddine I, Alghamdi A, Almashaqbeh W, Alshobaki H, Mahasneh I, Alotaibi A, Alanazi T, Balili M, Quarshi M, Ahmed M, Alzahrani M | Bone Marrow Transplant | 2022 |
| Effects of corticosteroids in patients with sickle cell disease and acute complications: a systematic review and meta-analysis. | Lopinto J, Gendreau S, Berti E, Bartolucci P, Habibi A, Mekontso Dessap A | Haematologica | 2022 |
| Correction to: Modern management of iron overload in thalassemia major patients guided by MRI techniques: real‑world data from a long‑term cohort study. | Bayraktaroglu S, Karadas N, Onen S, Karapinar DY, Aydinok Y | Ann Hematol | 2022 |
| Etavopivat, a Pyruvate Kinase Activator in Red Blood Cells, for the Treatment of Sickle Cell Disease. | Schroeder P, Fulzele K, Forsyth S, Ribadeneira MD, Guichard S, Wilker E, Marshall CG, Drake A, Fessler R, Konstantinidis DG, Seu KG, Kalfa TA | J Pharmacol Exp Ther | 2022 |
| De novo mutation rates at the single-mutation resolution in a human gene-region associated with adaptation and genetic disease. | Melamed D, Nov Y, Malik A, Yakass MB, Bolotin E, Shemer R, Hiadzi EK, Skorecki KL, Livnat A | Genome Res | 2022 |
| Annual decline in lung function in adults with sickle cell disease is similar to that observed in adults with cystic fibrosis. | Hodges B, Ivy ZK, Cronin RM, Rodeghier M, DeBaun MR, Willen S | Blood Adv | 2022 |
| Correction to: Macular microvascular changes in children with transfusion-dependent beta-thalassemia. | AttaAllah HR, Mousa SO, Omar IAN | Graefes Arch Clin Exp Ophthalmol | 2022 |
| Newborn Screening and Clinical Profile of Children with Sickle Cell Disease in a Tribal Area of Gujarat. | Dave KK, Desai S, Italia Y, Mukherjee MB, Mehta P, Desai G | Indian Pediatr | 2022 |
| Effects of dual chelation therapy with deferasirox and deferoxamine in patients with beta thalassaemia major. | Zargari A, Wu S, Greenway A, Cheng K, Kaplan Z | Vox Sang | 2022 |
| Epigenomic analysis of KLF1 haploinsufficiency in primary human erythroblasts. | Heshusius S, Grech L, Gillemans N, Brouwer RWW, den Dekker XT, van IJcken WFJ, Nota B, Felice AE, van Dijk TB, von Lindern M, Borg J, van den Akker E, Philipsen S | Sci Rep | 2022 |
| COVID-19 and Sickle Cell Disease-Related Deaths Reported in the United States. | Payne AB, Schieve LA, Abe K, Hulihan M, Hooper WC, Hsu LL | Public Health Rep | 2022 |
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| Possible effects of sirolimus treatment on the long‑term efficacy of COVID‑19 vaccination in patients with β‑thalassemia: A theoretical perspective. | Zurlo M, Nicoli F, Borgatti M, Finotti A, Gambari R | Int J Mol Med | 2022 |
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| COVID -19 Precipitating Vaso-Occlusive Crisis in a Patient of Sickle Cell Anemia with Avascular Necrosis of Femur. | Khandual SP, Mallick R, Jhankar SK, Tudu K, Bariha PK, Mohapatra MK | J Assoc Physicians India | 2022 |
| Atrial Fibrillation in β-Thalassemia: Overview of Mechanism, Significance and Clinical Management. | Malagù M, Marchini F, Fiorio A, Sirugo P, Clò S, Mari E, Gamberini MR, Rapezzi C, Bertini M | Biology (Basel) | 2022 |
| Activation of STAT and SMAD Signaling Induces Hepcidin Re-Expression as a Therapeutic Target for β-Thalassemia Patients. | Saad HKM, Abd Rahman AA, Ab Ghani AS, Taib WRW, Ismail I, Johan MF, Al-Wajeeh AS, Al-Jamal HAN | Biomedicines | 2022 |
| Redox-Regulation of α-Globin in Vascular Physiology. | Kiger L, Keith J, Freiwan A, Fernandez AG, Tillman H, Isakson BE, Weiss MJ, Lechauve C | Antioxidants (Basel) | 2022 |
| Influence of Haptoglobin Polymorphism on Stroke in Sickle Cell Disease Patients. | Edwards O, Burris A, Lua J, Wilkie DJ, Ezenwa MO, Doré S | Genes (Basel) | 2022 |
| Importance of Sequencing , and Genes to Confirm the Diagnosis of High Oxygen Affinity Hemoglobin. | Filser M, Gardie B, Wemeau M, Aguilar-Martinez P, Giansily-Blaizot M, Girodon F | Genes (Basel) | 2022 |
| Clinical phenotypes of three children with sickle cell disease caused by HbS/Sicilian (δβ) -thalassemia deletion. | Aygun B, Bello A, Thompson AA, Davis L, Sun Y, Luo HY, Cui S, Chui DHK | Am J Hematol | 2022 |
| Glucose-6-phosphate dehydrogenase deficiency is more prevalent in Duffy-null red blood cell transfusion in sickle cell disease. | Yee ME, Francis RO, Luban NLC, Easley KA, Lough CM, Roback JD, Josephson CD, Fasano RM | Transfusion | 2022 |
| Acoustic radiation force impulse elastography for liver iron overload in β-thalassemia major: Is it going to cut it? | Alessandrino F, Cantisani V | J Clin Ultrasound | 2022 |
| Ultra-rare Hb Regina (:c.289C>G) with coinherited β-thalassaemia trait: solving the puzzle for extreme erythrocytosis. | Mallik N, Jamwal M, Sharma R, Singh N, Sharma P, Bansal D, Trehan A, Chhabra S, Das R | J Clin Pathol | 2022 |
| Successful use of veno-venous extracorporeal membrane oxygenation for acute chest syndrome in a child with sickle cell disease and SARS-CoV-2. | Koh W, Malik P, Whitehead J, Morales DLS, Hayes D | Pediatr Pulmonol | 2022 |
| Procedural adverse events in pediatric patients with sickle cell disease undergoing chronic automated red cell exchange. | Wade J, Yee MEM, Easley KA, Pahz S, Butler H, Zerra PE, Josephson CD, Fasano RM | Transfusion | 2022 |
| A Case Study in Process Improvement to Minimize Delays from Obtaining Blood for Red Cell Exchange for a Patient with Sickle Cell Disease and Multiple Red Blood Cell Alloantibodies. | Narayanan D, Hogan NB, Schaser KA, Ruegsegger P, Rose WN | Case Rep Hematol | 2022 |
| Transfusion Practice, Post-Transfusion Complications and Risk Factors in Sickle Cell Disease in Senegal, West Africa. | Seck M, Senghor AB, Loum M, Touré SA, Faye BF, Diallo AB, Keita M, Bousso SE, Guèye SM, Gadji M, Sall A, Touré AO, Diop S | Mediterr J Hematol Infect Dis | 2022 |
| The Effect of Alpha Thalassemia, HbF and HbC on Haematological Parameters of Sickle Cell Disease Patients in Ibadan, Nigeria. | Fasola FA, Babalola OA, Brown BJ, Odetunde A, Falusi AG, Olopade O | Mediterr J Hematol Infect Dis | 2022 |
| Benefit of Pulmonary Subspecialty Care for Children with Sickle Cell Disease and Asthma. | Saxena S, Afolabi-Brown O, Ballester L, Schmucker N, Smith-Whitley K, Allen J, Bhandari A | Pediatr Pulmonol | 2022 |
| Rare co-inherited alpha-thalassemia minor and beta-thalassemia minor with heterozygous H63D mutation mistaken as iron deficiency anemia: a case report. | Chaudhry AF, Malik Z, Shegos CJ | AME Case Rep | 2022 |
| Endothelial Activation Markers in Polytransfused Children with Beta Thalassemia: Study from a Tertiary Care Centre in India. | Pallewar TS, Sharma K, Sharma S, Chandra J, Nangia A | Indian J Hematol Blood Transfus | 2022 |
| Impact of HFE-2 and HAMP Gene Variations on Iron Overload in Pediatric Patients with Non-Transfusion Dependent Thalassemia: A Pilot Study. | Bharadwaj N, Peyam S, Bhatia P, Bhatia A, Das R, Singh M, Bansal D, Trehan A, Jain R | Indian J Hematol Blood Transfus | 2022 |
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| Revascularization Is Associated With a Reduced Stroke Risk in Patients With Sickle Cell-Associated Moyamoya Syndrome. | Newman S, McMahon JT, Boulter JH, Malcolm JG, Revuelta Barbero JM, Chern JJ, Barrow DL, Pradilla G | Neurosurgery | 2022 |
| Thrombospondin-1, Platelet Factor 4, and Galectin-1 are Associated with Engraftment in Patients with Sickle Cell Disease Who Underwent Haploidentical HSCT. | Shaikh A, Olkhanud PB, Gangaplara A, Kone A, Patel S, Gucek M, Fitzhugh CD | Transplant Cell Ther | 2022 |
| Therapeutic plasma exchange in the management of acute complications of sickle cell disease: A single centre experience. | Tsitsikas DA, Mihalca D, Hibbs S, Freeman T, Bello-Sanyaolu O, Orebayo F, Lewis N, Green L | Transfus Apher Sci | 2022 |
| The Importance of Functional and Feature-Tracking Cardiac MRI Parameters in Prediction of Adverse Cardiac Events and Cardiac Mortality in Thalassemia Patients. | Asadian S, Hosseini L, Rezaeian N | Acad Radiol | 2022 |
| Main Complications during Pregnancy and Recommendations for Adequate Antenatal Care in Sickle Cell Disease: A Literature Review. | Figueira CO, Surita FG, Fertrin K, Nobrega GM, Costa ML | Rev Bras Ginecol Obstet | 2022 |
| Omega 3 fatty acids - Potential modulators for oxidative stress and inflammation in the management of sickle cell disease. | Khan SA, Damanhouri GA, Ahmed TJ, Halawani SH, Ali A, Makki A, Khan SA | J Pediatr (Rio J) | 2022 |
| Hybrid bone SPECT/CT reveals spleen calcification in sickle cell mutation and beta-thalassemia. | Sakellariou K, Charalampidou S, Fotopoulos A, Sioka C | Nucl Med Rev Cent East Eur | 2022 |
| Challenges in the Diagnosis of Beta-thalassemia Syndrome: The Importance of Molecular Diagnosis. | Rameli N, Ramli M, Zulkafli Z, Hassan MN, Yusoff SM, Noor NHM, Hussin S, Kamarudin NKM, Yusoff YM, Bahar R | Oman Med J | 2022 |
| Sudden Death in Diabetic Ketoacidosis Complicated by Sickle Cell Trait. | Dau GE, Shah JJ, Walsh JC, Berran PJ | Am J Forensic Med Pathol | 2022 |
| Sideroblastic anaemia in a patient with sickle cell disease. | Vobugari N, Chaturvedi M, Schlam-Camhi IM, Smith HP | BMJ Case Rep | 2022 |
| GRNDaD: big data and sickle cell disease. | Lanzkron S, Manwani D, Desai P, Kanter J, Little J | Blood Adv | 2022 |
| Pharmacologic induction of PGC-1α stimulates fetal haemoglobin gene expression. | Sun Y, Habara A, Le CQ, Nguyen N, Chen R, Murphy GJ, Chui DHK, Steinberg MH, Cui S | Br J Haematol | 2022 |
| Neurocognitive risk in sickle cell disease: Utilizing neuropsychology services to manage cognitive symptoms and functional limitations. | Longoria JN, Heitzer AM, Hankins JS, Trpchevska A, Porter JS | Br J Haematol | 2022 |
| Description of Hb Évora (: c.106T>C) on an Unexpected Allele in a Swiss Family. | Truttmann R, Schmidt A, Hartmann B, Rusch S, Mendez A | Hemoglobin | 2022 |
| Reduced blood pressure in sickle cell disease is associated with decreased angiotensin converting enzyme (ACE) activity and is not modulated by ACE inhibition. | Brito PL, Dos Santos AF, Chweih H, Favero ME, Gotardo EMF, Silva JAF, Leonardo FC, Franco-Penteado CF, de Oliveira MG, Ferreira WA, Zaidan BC, Billis A, Baldanzi G, Mashima DA, Antunes E, Saad STO, Costa FF, Conran N | PLoS One | 2022 |
| From H1N1 to COVID-19: What we have seen in children with hemoglobinopathies. | Oliveira CM, Soares VJ, Rechenmacher C, Daudt LE, Michalowski MB | Clinics (Sao Paulo) | 2022 |
| Cerebral oxygen metabolic stress is increased in children with sickle cell anemia compared to anemic controls. | Fields ME, Mirro AE, Binkley MM, Guilliams KP, Lewis JB, Fellah S, Chen Y, Hulbert ML, An H, Ford AL, Lee JM | Am J Hematol | 2022 |
| Efficacy and Safety of Gene Therapy for β-Thalassemia. | Payen E | N Engl J Med | 2022 |
| Determinants of the point of sickling measured by oxygen gradient ektacytometry in sickle cell anaemia. | Joly P, Boisson C, Renoux C, Caillat N, Robert M, Gauthier-Vasserot A, Poutrel S, Cibiel A, Nader E, Connes P | Br J Haematol | 2022 |
| Opioid Use in Patients With Sickle Cell Disease During a Vaso-Occlusive Crisis: A Systematic Review. | Arzoun H, Srinivasan M, Sahib I, Fondeur J, Escudero Mendez L, Hamouda RK, Mohammed L | Cureus | 2022 |
| Sickle cell nephropathy: A review of novel biomarkers and their potential roles in early detection of renal involvement. | Safdar OY, Baghdadi RM, Alahmadi SA, Fakieh BE, Algaydi AM | World J Clin Pediatr | 2022 |
| Health State Utilities for Sickle Cell Disease: A Catalog Prepared From a Systematic Review. | Jiao B, Basu A, Ramsey S, Roth J, Bender MA, Quach D, Devine B | Value Health | 2022 |
| Experiences of African Americans Living With Sickle Cell Disease. | Wickersham KE, Dawson RM, Becker KP, Everhart KC, Miles HS, Schultz BE, Tucker CM, Wright PJ, Jenerette CM | J Transcult Nurs | 2022 |
| Size and density measurements of single sickle red blood cells using microfluidic magnetic levitation. | Goreke U, Bode A, Yaman S, Gurkan UA, Durmus NG | Lab Chip | 2022 |
| Sickle cell disease and COVID-19 in pregnant women. | Kolanska K, Vasileva R, Lionnet F, Santin A, Jaudi S, Dabi Y, Chabbert-Buffet N, Daraï E, Bornes M | J Gynecol Obstet Hum Reprod | 2022 |
| CRISPR/Cas9-based multiplex genome editing of BCL11A and HBG efficiently induces fetal hemoglobin expression. | Han Y, Tan X, Jin T, Zhao S, Hu L, Zhang W, Kurita R, Nakamura Y, Liu J, Li D, Zhang Z, Fang X, Huang S | Eur J Pharmacol | 2022 |
| Process and strategies for patient engagement and outreach in the Sickle Cell Disease (SCD) community to promote clinical trial participation. | Byrnes C, Botello-Harbaum M, Clemons T, Bailey L, Valdes KM, Coleman-Cowger VH | J Natl Med Assoc | 2022 |
| Nrf2 expands the intracellular pool of the chaperone AHSP in a cellular model of β-thalassemia. | Han G, Cao C, Yang X, Zhao GW, Hu XJ, Yu DL, Yang RF, Yang K, Zhang YY, Wang WT, Liu XZ, Xu P, Liu XH, Chen P, Xue Z, Liu DP, Lv X | Redox Biol | 2022 |
| Tocilizumab in the management of posttransfusion hyperhemolysis syndrome in sickle cell disease: The experience so far. | Meenan J, Hall R, Badle S, Chatterjee B, Win N, Tsitsikas DA | Transfusion | 2022 |
| Documented Viral Illness at the Time of Splenic Sequestration Does Not Affect the Odds of Recurrence in Children With Sickle Cell Disease. | Clement O, Fishbein J, Appiah-Kubi A, Aygun B | J Pediatr Hematol Oncol | 2022 |
| Haemoglobin Bristol-Alesha in a child with non-spherocytic severe haemolytic anaemia and marked anisochromic poikilocytosis with basophilic stippling and amorphous intracellular content. | Corrons JV, Bain BJ | Blood Cells Mol Dis | 2022 |
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| The ektacytometric elongation Index (EI) of erythrocytes, validation of a prognostic, rheological biomarker for patients with sickle cell disease. | Franck P, Buijs P, Meenhuis A, Dane M, Postma C, Spaans A, Gijsbertha N, Kuypers FA, Hudig C, Kerkhoffs JL | Eur J Haematol | 2022 |
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| Rare unstable and low oxygen affinity haemoglobin variant, Hb Hazebrouck, detected on Sysmex XN-9000. | Adam AS, Benyaich S, Colard M, Benghiat FS, Cotton F, Gulbis B | Clin Chem Lab Med | 2022 |
| Long-term outcomes of lentiviral gene therapy for the β-hemoglobinopathies: the HGB-205 trial. | Magrin E, Semeraro M, Hebert N, Joseph L, Magnani A, Chalumeau A, Gabrion A, Roudaut C, Marouene J, Lefrere F, Diana JS, Denis A, Neven B, Funck-Brentano I, Negre O, Renolleau S, Brousse V, Kiger L, Touzot F, Poirot C, Bourget P, El Nemer W, Blanche S, Tréluyer JM, Asmal M, Walls C, Beuzard Y, Schmidt M, Hacein-Bey-Abina S, Asnafi V, Guichard I, Poirée M, Monpoux F, Touraine P, Brouzes C, de Montalembert M, Payen E, Six E, Ribeil JA, Miccio A, Bartolucci P, Leboulch P, Cavazzana M | Nat Med | 2022 |
| Identification of novel HPFH-like mutations by CRISPR base editing that elevate the expression of fetal hemoglobin. | Ravi NS, Wienert B, Wyman SK, Bell HW, George A, Mahalingam G, Vu JT, Prasad K, Bandlamudi BP, Devaraju N, Rajendiran V, Syedbasha N, Pai AA, Nakamura Y, Kurita R, Narayanasamy M, Balasubramanian P, Thangavel S, Marepally S, Velayudhan SR, Srivastava A, DeWitt MA, Crossley M, Corn JE, Mohankumar KM | Elife | 2022 |
| Post-transplant CD34+ selected stem cell boost as an intervention for declining mixed chimerism following reduced intensity conditioning allogeneic stem cell transplant in children and young adults with sickle cell disease: A case series. | Ngwube A, Franay C, Shah N | Pediatr Hematol Oncol | 2022 |
| Prevalence of neuropathic pain in adolescents with sickle cell disease: A single-center experience. | Cregan M, Puri L, Kang G, Anghelescu D | Pediatr Blood Cancer | 2022 |
| A predictive algorithm for identifying children with sickle cell anemia among children admitted to hospital with severe anemia in Africa. | Olupot-Olupot P, Connon R, Kiguli S, Opoka RO, Alaroker F, Uyoga S, Nakuya M, Okiror W, Nteziyaremye J, Ssenyondo T, Nabawanuka E, Kayaga J, Williams Mukisa C, Amorut D, Muhindo R, Frost G, Walsh K, Macharia AW, Gibb DM, Walker AS, George EC, Maitland K, Williams TN | Am J Hematol | 2022 |
| Diagnostic value of fetal hemoglobin Bart's for evaluation of fetal α-thalassemia syndromes: application to prenatal characterization of fetal anemia caused by undiagnosed α-hemoglobinopathy. | Singha K, Yamsri S, Chaibunruang A, Srivorakun H, Sanchaisuriya K, Fucharoen G, Fucharoen S | Orphanet J Rare Dis | 2022 |
| Hb Mizuho (: c.206T>C): Pitfalls of Screening Tests in an Unstable Hemoglobin Variant Diagnosed after Targeted Next-Generation Sequencing. | Yadav DD, Jamwal M, Singh N, Sharma R, Das R, Trehan A, Bansal D, Chhabra S, Sharma P | Hemoglobin | 2022 |
| Voxelotor and albuminuria in adults with sickle cell anaemia. | Han J, Molokie RE, Hussain F, Njoku F, Gordeuk VR, Saraf SL | Br J Haematol | 2022 |
| COVID-19 Vaccine Perception and Hesitancy Among Patients With Sickle Cell Disease in the Western Region of Saudi Arabia. | Jan H, Waheeb A, AlAhwal H, Almohammadi A, Al-Marzouki A, Barefah A, Bahashawan S, Radhwi O | Cureus | 2022 |
| Awareness and Acceptance of Hematopoietic Stem Cell Transplantation for Sickle Cell Disease in Jazan Province, Saudi Arabia. | Hurissi E, Hakami A, Homadi J, Kariri F, Abu-Jabir E, Alamer R, Mobarki R, Jaly AA, Alamer E, Alhazmi AH | Cureus | 2022 |
| Neonatal Screening for Sickle Cell Disease in Congo. | Dokekias AE, Ocko Gokaba LT, Louokdom JS, Ocini LN, Galiba Atipo Tsiba FO, Ondzotto Ibatta CI, Kouandzi QN, Tamekue ST, Bango JC, Nziengui Mboumba JV, Kobawila SC | Anemia | 2022 |
| Pas-de-deux: African Plasmodium falciparum adaptations to sickle hemoglobin. | Matuschewski K, Maier AG | Trends Parasitol | 2022 |
| Genes modulating intestinal permeability and microbial community are dysregulated in sickle cell disease. | Poplawska M, Dutta D, Jayaram M, Chong NS, Salifu M, Lim SH | Ann Hematol | 2022 |
| Pain Burden in the CASiRe International Cohort of Sickle Cell Patients: United States and Ghana. | Zempsky WT, Yanaros M, Sayeem M, Boruchov D, Piccone CM, Manwani D, Strunk C, Tartaglione I, Colombatti R, Akatue S, Oteng B, Owda A, Bamfo R, Wilson S, Rivers A, Farooq F, Urbonya R, Boatemaa GD, Rao S, Inusa B, Antwi-Boasiako C, Segbefia C, Sey F, Andemariam B, Asare EV, Campbell AD | Pain Med | 2022 |
| A Systematic Review on the Management of Transfusion-Related Acute Lung Injury in Transfusion-Dependent Sickle Cell Disease. | Arzoun H, Srinivasan M, Adam M, Thomas SS, Lee B, Yarema A | Cureus | 2022 |
| Circulating Small Extracellular Vesicles May Contribute to Vaso-Occlusive Crises in Sickle Cell Disease. | Gemel J, Zhang J, Mao Y, Lapping-Carr G, Beyer EC | J Clin Med | 2022 |
| Plasma-Derived Hemopexin as a Candidate Therapeutic Agent for Acute Vaso-Occlusion in Sickle Cell Disease: Preclinical Evidence. | Gentinetta T, Belcher JD, Brügger-Verdon V, Adam J, Ruthsatz T, Bain J, Schu D, Ventrici L, Edler M, Lioe H, Patel K, Chen C, Nguyen J, Abdulla F, Zhang P, Wassmer A, Jain M, Mischnik M, Pelzing M, Martin K, Davis R, Didichenko S, Schaub A, Brinkman N, Herzog E, Zürcher A, Vercellotti GM, Kato GJ, Höbarth G | J Clin Med | 2022 |
| MicroRNAs miR-451a and Let-7i-5p Profiles in Circulating Exosomes Vary among Individuals with Different Sickle Hemoglobin Genotypes and Malaria. | Oxendine Harp K, Bashi A, Botchway F, Dei-Adomakoh Y, Iqbal SA, Wilson MD, Adjei AA, Stiles JK, Driss A | J Clin Med | 2022 |
| Shear-Stress-Gradient and Oxygen-Gradient Ektacytometry in Sickle Cell Patients at Steady State and during Vaso-Occlusive Crises. | Boisson C, Nader E, Renoux C, Gauthier A, Poutrel S, Bertrand Y, Stauffer E, Virot E, Hot A, Fort R, Cannas G, Joly P, Connes P | Cells | 2022 |
| Reactivation of γ-globin expression using a minicircle DNA system to treat β-thalassemia. | Ma SP, Gao XX, Zhou GQ, Zhang HK, Yang JM, Wang WJ, Song XM, Chen HY, Lu DR | Gene | 2022 |
| Evolutionary race: Malaria evolves to evade sickle cell protection. | Gómez-Díaz E, Ranford-Cartwright L | Cell Host Microbe | 2022 |
| Acute chest syndrome of sickle cell disease: genetics, risk factors, prognosis, and management. | Klings ES, Steinberg MH | Expert Rev Hematol | 2022 |
| Phenotypic variation in sickle cell disease: the role of beta globin haplotype, alpha thalassaemia and fetal haemoglobin in HbSS. | Serjeant GR | Expert Rev Hematol | 2022 |
| Pregnancy outcomes with hydroxyurea use in women with sickle cell disease. | Kroner BL, Hankins JS, Pugh N, Kutlar A, King AA, Shah NR, Kanter J, Glassberg J, Treadwell M, Gordeuk VR, | Am J Hematol | 2022 |
| Comment on: Oxygen gradient ektacytometry does not predict pain in children with sickle cell anaemia. | Sheehan VA, van Beers EJ, Connes P, van Wijk R, Rab MAE | Br J Haematol | 2022 |
| Long-read sequencing on the SMRT platform enables efficient haplotype linkage analysis in preimplantation genetic testing for β-thalassemia. | Wu H, Chen D, Zhao Q, Shen X, Liao Y, Li P, Chiu PCN, Zhou C | J Assist Reprod Genet | 2022 |
| Association and Risk Factors of Osteonecrosis of Femoral Head in Sickle Cell Disease: A Systematic Review. | Leandro MP, De Sá CKC, Filho DPS, De Souza LAA, Salles C, Tenório MCC, Paz CLDSL, Matos MAA | Indian J Orthop | 2022 |
| Multiplex Quantitative Real-Time Polymerase Chain Reaction and High-Resolution Melting Analysis for Identification of a Couple At-Risk of Having a Newborn with Severe Thalassemia. | Ruengdit C, Punyamung M, Khamphikham P, Pongpunyayuen P, Intasai N, Pornprasert S | Hemoglobin | 2022 |
| Fetal-like Hemoglobin in Sickle Cell Anemia. | Steinberg MH | N Engl J Med | 2022 |
| Scalable manufacturing platform for the production of methemoglobin as a non-oxygen carrying control material in studies of cell-free hemoglobin solutions. | Gu X, Hickey R, Rath A, Palmer AF | PLoS One | 2022 |
| The distinct longitudinal impact of pain catastrophizing on pain interference among youth living with sickle cell disease and chronic pain. | Schneider MB, Manikowski A, Cohen L, Dampier C, Sil S | J Behav Med | 2022 |
| Purinergic signaling is essential for full Psickle activation by hypoxia and by normoxic acid pH in mature human sickle red cells and in vitro-differentiated cultured human sickle reticulocytes. | Vandorpe DH, Rivera A, Ganter M, Dankwa S, Wohlgemuth JG, Dlott JS, Snyder LM, Brugnara C, Duraisingh M, Alper SL | Pflugers Arch | 2022 |
| An Evaluation for the Causes of Reduced Hb A and the Molecular Characterization of Variants in Hong Kong. | Chan NCN, Wong THY, Cheng KCK, Chan NPH, Ng MHL | Hemoglobin | 2022 |
| Direct antiglobulin test-negative autoimmune hemolytic anemia in a patient with β-thalassemia minor during pregnancy: A case report. | Zhou Y, Ding YL, Zhang LJ, Peng M, Huang J | World J Clin Cases | 2022 |
| Anaesthetic management of patients with sickle cell disease in obstetrics. | Stoddard K, Sohal M, Bedson R | BJA Educ | 2022 |
| Thalassemia-free and graft-versus-host-free survival: outcomes of hematopoietic stem cell transplantation for thalassemia major, Turkish experience. | Yesilipek MA, Uygun V, Kupesiz A, Karasu G, Ozturk G, Ertem M, Şaşmaz İ, Daloğlu H, Güler E, Hazar V, Fisgin T, Sezgin G, Kansoy S, Kuşkonmaz B, Akıncı B, Özbek N, İnce EÜ, Öztürkmen S, Küpesiz FT, Yalçın K, Anak S, Bozkurt C, Karakükçü M, Küpeli S, Albayrak D, Öniz H, Aksoylar S, Okur FV, Albayrak C, Yenigürbüz FD, Bozkaya İO, İleri T, Gürsel O, Karagün BŞ, Kintrup GT, Çelen S, Elli M, Aksoy BA, Yılmaz E, Tanyeli A, Akyol ŞT, Siviş ZÖ, Özek G, Uçkan D, Kartal İ, Atay D, Akyay A, Bilir ÖA, Çakmaklı HF, Kürekçi E, Malbora B, Akbayram S, Demir HA, Kılıç SÇ, Güneş AM, Zengin E, Özmen S, Antmen AB | Bone Marrow Transplant | 2022 |
| Factors associated with blood pressure variation in sickle cell disease patients: a systematic review and meta-analyses. | Nguweneza A, Oosterwyk C, Banda K, Nembaware V, Mazandu G, Kengne AP, Wonkam A | Expert Rev Hematol | 2022 |
| Immune Response of Adult Sickle Cell Disease Patients after COVID-19 Vaccination: The Experience of a Greek Center. | Varelas C, Gavriilaki E, Sakellari I, Klonizakis P, Koravou EE, Christodoulou I, Mavrikou I, Kourelis A, Chatzopoulou F, Chatzidimitriou D, Touloumenidou T, Papalexandri A, Anagnostopoulos A, Vlachaki E | J Clin Med | 2022 |
| Comparison of Ultra-Wide Field Photography to Ultra-Wide Field Angiography for the Staging of Sickle Cell Retinopathy. | Torres-Villaros H, Fajnkuchen F, Amari F, Janicot L, Giocanti-Aurégan A | J Clin Med | 2022 |
| Conditioning Regimens in Patients with β-Thalassemia Who Underwent Hematopoietic Stem Cell Transplantation: A Scoping Review. | Mulas O, Mola B, Caocci G, La Nasa G | J Clin Med | 2022 |
| Use of Deferasirox Film-Coated Tablets in Pediatric Patients with Transfusion Dependent Thalassemia: A Single Center Experience. | Adramerina A, Printza N, Hatzipantelis E, Symeonidis S, Tarazi L, Teli A, Economou M | Biology (Basel) | 2022 |
| Health-Related Quality of Life Assessments by Children and Adolescents with Sickle Cell Disease and Their Parents in Portugal. | Abadesso C, Pacheco S, Machado MC, Finley GA | Children (Basel) | 2022 |
| A Description of the Hemolytic Component in Sickle Leg Ulcer: The Role of Circulating miR-199a-5p, miR-144, and miR-126. | Santos EDC, Melo GIV, Santana PVB, Quadros IGS, Yahouédéhou SCMA, Guarda CCD, Santiago RP, Fiuza LM, Carvalho SP, Adorno EV, Kaneto CM, Fonseca TCC, Goncalves MS, Aleluia MM | Biomolecules | 2022 |
| Optimizing transfusion therapy for survivors of Haemoglobin Bart's hydrops fetalis syndrome: Defining the targets for haemoglobin-H fraction and | Amid A, Barrowman N, Odame I, Kirby-Allen M | Br J Haematol | 2022 |
| The hematopoietic saga of clonality in sickle cell disease. | Stonestrom AJ, Levine RL | J Clin Invest | 2022 |
| A microfluidic-informatics assay for quantitative physical occlusion measurement in sickle cell disease. | Zhang X, Chan T, Carbonella J, Gong X, Ahmed N, Liu C, Demandel I, Zhang J, Pashankar F, Mak M | Lab Chip | 2022 |
| GBT1118, a voxelotor analog, protects red blood cells from damage during severe hypoxia. | Tarasev M, Ferranti M, Herppich A, Hines P | Am J Transl Res | 2022 |
| Sickle cell disease as an accelerated aging syndrome. | Idris IM, Botchwey EA, Hyacinth HI | Exp Biol Med (Maywood) | 2022 |
| Expanded eligibility for emerging therapies in sickle cell disease in the UK - crizanlizumab and voxelotor. | Vora SM, Boyd S, Denny N, Jackson E, Roy NBA, Howard J, Lugthart S | Br J Haematol | 2022 |
| Coinheritance of HbO Arab/β0-thalassemia with Severe Manifestation in Newborn. | Kalai M, Moumni I, Ouragini H, Chaouechi D, Boudriga I, Menif S | Am J Perinatol | 2022 |
| Black Americans' willingness to participate in pediatric sickle cell clinical trials: A retrospective, systematic review. | Zanfardino S, Mazziotto V, Bodas P | Pediatr Blood Cancer | 2022 |
| Diagnosis of α-thalassemia Chiang Rai (--) deletion by melt curve analysis in Northern Thailand. | Ruengdit C, Khamphikham P, Punyamung M, Pongpunyayuen P, Pornprasert S | Scand J Clin Lab Invest | 2022 |
| An impact evaluation of two modes of care for sickle cell disease crises. | Skinner R, Breck A, Esposito D | J Comp Eff Res | 2022 |
| Extra-Medullary Hematopoiesis in Sickle Cell Disease Presenting as a Right Adrenal Mass. | Ajayi F, Nali MS, Ali R, Patel A, Shaaban H | Cureus | 2022 |
| The clinical and radiological effectiveness of autologous bone marrow derived osteoblasts (ABMDO) in the management of avascular necrosis of femoral head (ANFH) in sickle cell disease (SCD). | Sadat-Ali M, Al-Omran AS, AlTabash K, Acharya S, Hegazi TM, Al Muhaish MI | J Exp Orthop | 2022 |
| Two trade names of deferasirox (Osveral® and Exjade®) in reduction of iron overload parameters in major beta-thalassemia patients: A randomized open labeled clinical trial. | Rafati M, Karami H, Lashtoo-Aghaee B, Lashtoo-Aghaee B, Dabirian M, Avan R | Caspian J Intern Med | 2022 |
| A randomised double-blind placebo-controlled clinical trial of oral hydroxyurea for transfusion-dependent β-thalassaemia. | Yasara N, Wickramarathne N, Mettananda C, Silva I, Hameed N, Attanayaka K, Rodrigo R, Wickramasinghe N, Perera L, Manamperi A, Premawardhena A, Mettananda S | Sci Rep | 2022 |
| Effect of age, cerebral infarcts, vasculopathy and haemoglobin on cognitive function, in Tanzanian children with sickle cell anaemia. | Jacob M, Stotesbury H, Kija E, Saunders D, Mtei RJ, Tutuba H, Masanu U, Kilonzo M, Kazema R, Hood AM, Kirkham F, Dimitriou D, Makani J | Eur J Paediatr Neurol | 2022 |
| Reduction in Prevalence of Thrombotic Events in Sickle Cell Disease after Allogeneic Hematopoietic Transplantation. | Patel A, Wilkerson K, Chen H, Sharma D, Byrne M, Green J, Sengsayadeth S, Dholaria B, Savani B, Chinratanalab W, Jayani R, Gatwood K, Engelhardt BG, Kitko C, Connelly J, Kassim A | Transplant Cell Ther | 2022 |
| Third-generation sequencing: A novel tool detects complex variants in the α-thalassemia gene. | Long J, Sun L, Gong F, Zhang C, Mao A, Lu Y, Li J, Liu E | Gene | 2022 |
| Correlation of Asymmetric Dimethyl Arginine Level to Sickle Retinopathy in Children With Sickle Cell Disease. | Elhawary EE, Khedr SF, Nagy HM, El-Bradey MH, Elshanshory MR | J Pediatr Hematol Oncol | 2022 |
| Assessment of Liver Fibrosis by Transient Elastography in Children and Young Adults With Sickle Cell Disease With and Without Iron Overload. | Alvarez O, Cumming V, Fifi AC | J Pediatr Hematol Oncol | 2022 |
| Introduction of Hydroxyurea Therapy to a Cohort of Sickle Cell Patients in Northern Haiti. | Paul-Hanna M, Joseph W, Mondesir W, Faustino EVS, Canarie MF | J Pediatr Hematol Oncol | 2022 |
| Peripheral Blood Smear Detection of Asymptomatic Central Line Infection in a Patient With Sickle Cell Disease. | Carll TC, Mariani R, Schafernak K, Snowberger T, Jacobsen J, Gomez E, Su L | J Pediatr Hematol Oncol | 2022 |
| Enuresis and Hyperfiltration in Children With Sickle Cell Disease. | Zahr RS, Ding J, Kang G, Wang WC, Hankins JS, Ataga KI, Lebensburger JD, Porter JS | J Pediatr Hematol Oncol | 2022 |
| Whole blood versus red cell concentrates for children with severe anaemia: a secondary analysis of the Transfusion and Treatment of African Children (TRACT) trial. | George EC, Uyoga S, M'baya B, Kyeyune Byabazair D, Kiguli S, Olupot-Olupot P, Opoka RO, Chagaluka G, Alaroker F, Williams TN, Bates I, Mbanya D, Gibb DM, Walker AS, Maitland K, | Lancet Glob Health | 2022 |
| Globin vector regulatory elements are active in early hematopoietic progenitor cells. | Cabriolu A, Odak A, Zamparo L, Yuan H, Leslie C, Sadelain M | Mol Ther | 2022 |
| The unexpected impact of cabozantinib on red blood cells consumption in patients with transfusion-dependent thalassemia. | Costantini S, Meloni A, Spasiano A, Cinque P, Ricchi P | Ann Hematol | 2022 |
| Retinal and choroidal thickness in pediatric patients with sickle cell disease: a cross-sectional cohort study. | Prazeres J, Lucatto LF, Ferreira A, Moraes N, Braga JAP, Lima LH, Regatieri C, Maia M | Int J Retina Vitreous | 2022 |
| The Sickle Cell Disease Functional Assessment (SCD-FA) tool: a feasibility pilot study. | Oyedeji CI, Hall K, Luciano A, Morey MC, Strouse JJ | Pilot Feasibility Stud | 2022 |
| Healthcare resource utilization and direct costs of transfusion-dependent thalassemia patients in Dubai, United Arab Emirates: a retrospective cost-of-illness study. | Alshamsi S, Hamidi S, Narci HO | BMC Health Serv Res | 2022 |
| Accuracy of transcranial Doppler in detecting intracranial stenosis in patients with sickle cell anemia when compared to magnetic resonance angiography. | Krementz NA, Gardener HE, Torres L, Alkhalifah M, Campo-Bustillo I, Campo N, Koch S, Alvarez O, Rundek T, Romano JG | J Clin Ultrasound | 2022 |
| Nursing Education for the Acute Care Nurse on Pain Mechanisms of Sickle Cell Disease. | Evelyn AE, Kittelson S, Mandernach MW, Black V, Duckworth L, Wilkie DJ | J Contin Educ Nurs | 2022 |
| Autoimmune disease and sickle cell anaemia: 'Intersecting pathways and differential diagnosis'. | Piccin A, O'Connor-Byrne N, Daves M, Lynch K, Farshbaf AD, Martin-Loeches I | Br J Haematol | 2022 |
| Efficacy and Safety of Teriparatide in Beta-Thalassemia Major Associated Osteoporosis: A Real-Life Experience. | Gagliardi I, Celico M, Gamberini MR, Pontrelli M, Fortini M, Carnevale A, Napoli N, Zatelli MC, Ambrosio MR | Calcif Tissue Int | 2022 |
| Erythrocyte (red blood cell) dataset in thalassemia case. | Tyas DA, Ratnaningsih T, Harjoko A, Hartati S | Data Brief | 2022 |
| Advances in the diagnosis and treatment of sickle cell disease. | Brandow AM, Liem RI | J Hematol Oncol | 2022 |
| Growth Hormone/Insulin-Like Growth Factor 1 Axis Associated with Modifiers Factors in Children with Sickle Cell Anemia. | Costa-Júnior DAD, Santos APP, da Silva CM, Velloso-Rodrigues C | Endocr Metab Immune Disord Drug Targets | 2022 |
| Estimating the risk of child mortality attributable to sickle cell anaemia in sub-Saharan Africa: a retrospective, multicentre, case-control study. | Ranque B, Kitenge R, Ndiaye DD, Ba MD, Adjoumani L, Traore H, Coulibaly C, Guindo A, Boidy K, Mbuyi D, Ly ID, Offredo L, Diallo DA, Tolo A, Kafando E, Tshilolo L, Diagne I | Lancet Haematol | 2022 |
| Filling the data gaps on sickle cell anaemia in sub-Saharan Africa. | Williams TN | Lancet Haematol | 2022 |
| Assessment of serum endocan levels in patients with beta-thalassemia minor. | Khanmammadov N, Zorlu M, Ozer OF, Karatoprak C, Kıskaç M, Çakırca M | Rev Assoc Med Bras (1992) | 2022 |
| A Rare Hemoglobin Variant (β51Pro → His) Causing Misleading Measurements of Hemoglobin A. | Mackley MP, Morgenthau A, Elnenaei M, MacKenzie H | J Endocr Soc | 2022 |
| Hair-on-End Sign in a 9-Year-Old Girl Presenting with Acute Stroke in Sickle Cell Disease. | Ogwang E, Odongo CN, Namusisi J, Okello PA, Acan M | Int Med Case Rep J | 2022 |
| Tricuspid-valve regurgitant jet velocity as a risk factor for death in β-Thalassemia. | Derchi G, Musallam KM, Pinto VM, Graziadei G, Giuditta M, Barella S, Origa R, Casu G, Pasanisi A, Longo F, Casale M, Miceli R, Merella P, Gianesin B, Ameri P, Tartaglione I, Perrotta S, Piga A, Cappellini MD, Forni GL | Haematologica | 2022 |
| Prevalence and risk factors of hepatitis E virus infection among patients with β-thalassemia major in South of Iran. | Farshadpour F, Taherkhani R, Shaeri M | J Immunoassay Immunochem | 2022 |
| Relation between haptoglobin polymorphism and oxidative stress status, lipid profile, and cardiovascular risk in sickle cell anemia patients. | Kengne Fotsing CB, Pieme CA, Biapa Nya PC, Chedjou JP, Dabou S, Nguemeni C, Teto G, Mbacham WF, Gatsing D | Health Sci Rep | 2022 |
| Healthcare professionals' perceptions of implementing a decision support intervention for cascade screening for beta-thalassemia in Pakistan. | Ahmed S, Jafri H, Ahmed WN, Faran M, Rashid Y, Ehsan Y, Ahmed M | Eur J Hum Genet | 2022 |
| ETV6 Regulates Hemin-Induced Erythroid Differentiation of K562 Cells through Mediating the Raf/MEK/ERK Pathway. | Li Z, Sun MZ, Lv X, Guo C, Liu S | Biol Pharm Bull | 2022 |
| Outcomes of kidney donors with sickle cell trait: A preliminary analysis. | Hebert SA, Gandhi NV, Al-Amin S, Edwards AR, Murad DN, Nguyen DT, Graviss EA, Ibrahim HN | Clin Transplant | 2022 |
| Two co-inherited hemoglobin variants revealed by capillary electrophoresis during quantification of glycated hemoglobin. | Antonello G, Lo Monaco C, Napoli P, Solimando D, Curcio C, Barberio G, Maoggi S, Ivaldi G, Nigra M | Clin Chem Lab Med | 2022 |
| Immunogenicity of The BNT162b2 COVID-19 mRNA and ChAdOx1 nCoV-19 Vaccines in Patients with Hemoglobinopathies. | Radhwi OO, Jan H, Waheeb A, Alamri SS, Alahwal HM, Denetiu I, Almanzlawey A, Al-Marzouki AF, Almohammadi AT, Bahashwan SM, Barefah AS, Qari MH, Abuzenadah AM, Hashem AM | Vaccines (Basel) | 2022 |
| Fetal Hemoglobin in β Hemoglobinopathies: Is Enough Too Much? | Steinberg MH | Am J Hematol | 2022 |
| High Frequency of Post-Transfusion Microchimerism Among Multi-Transfused Beta-Thalassemic Patients. | Matsagos S, Verigou E, Kourakli A, Alexis S, Vrakas S, Argyropoulou C, Lazaris V, Spyropoulou P, Labropoulou V, Georgara N, Lykouresi M, Karakantza M, Alepi C, Symeonidis A | Front Med (Lausanne) | 2022 |
| Editorial: Red Blood Cell Vascular Adhesion and Deformability, Volume II. | Guizouarn H, Barshtein G | Front Physiol | 2022 |
| Magnetic Resonance Imaging Quantification of the Liver Iron Burden and Volume Changes Following Treatment With Thalidomide in Patients With Transfusion-Dependent -Thalassemia. | Che J, Luo T, Huang L, Lu Q, Yan D, Meng Y, Xie J, Chen W, Chen J, Long L | Front Pharmacol | 2022 |
| Comparison of the programmed freezer method and deep freezer method in the manufacturing of frozen red blood cell products. | Fuchizaki A, Yasui K, Tanaka M, Mitsuhashi H, Shimogaki K, Kimura T, Takihara Y, Hirayama F | Vox Sang | 2022 |
| Extramedullary haematopoiesis in patients with transfusion dependent β-thalassaemia (TDT): a systematic review. | A Subahi E, Ata F, Choudry H, Iqbal P, A AlHiyari M, T Soliman A, De Sanctis V, A Yassin M | Ann Med | 2022 |
| Risk and protective factors for severe COVID-19 infection in a cohort of patients with sickle cell disease. | Cai J, Chen-Goodspeed A, Idowu M | J Investig Med | 2022 |
| Lower Muscle and Blood Lactate Accumulation in Sickle Cell Trait Carriers in Response to Short High-Intensity Exercise. | Messonnier LA, Oyono-Enguéllé S, Vincent L, Dubouchaud H, Chatel B, Sanchez H, Malgoyre A, Martin C, Galactéros F, Bartolucci P, Thiriet P, Féasson L | Nutrients | 2022 |
| Endothelial superoxide dismutase 2 is decreased in sickle cell disease and regulates fibronectin processing. | Dosunmu-Ogunbi A, Yuan S, Shiwarski DJ, Tashman JW, Reynolds M, Feinberg A, Novelli EM, Shiva S, Straub AC | Function (Oxf) | 2022 |
| α-thalassemia in affected fetuses with hemoglobin E-β-thalassemia disease in a high-risk population in Thailand. | Yamsri S, Prommetta S, Srivorakun H, Taweenan W, Sanchaisuriya K, Chaibunruang A, Fucharoen G, Fucharoen S | Am J Transl Res | 2022 |
| Acute complications in children with sickle cell disease: Prevention and management. | Beck CE, Trottier ED, Kirby-Allen M, Pastore Y | Paediatr Child Health | 2022 |
| Reflex single-gene non-invasive prenatal testing is associated with markedly better detection of fetuses affected with single-gene recessive disorders at lower cost. | Riku S, Hedriana H, Carozza JA, Hoskovec J | J Med Econ | 2022 |
| Rheological Abnormalities in Human Erythrocytes Subjected to Oxidative Inflammation. | Maruyama T, Hieda M, Mawatari S, Fujino T | Front Physiol | 2022 |
| Letter to the Editor: Role of Ketamine in Vaso-Occlusive Crisis of Sickle Cell Disease. | Raghuraman MS | Saudi J Med Med Sci | 2022 |
| Adiponectin and Disease Severity in Sickle Cell Anemia Patients Attending a Tertiary Health Institution in Nnewi, Southeast Nigeria. | Okocha CE, Manafa PO, Igwe CN, Okite UP, Onah CE, Efobi C | Front Genet | 2022 |
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| Web Exclusive. Annals for Hospitalists Inpatient Notes - Clinical Pearls-Acute Pain Episodes in Sickle Cell Disease. | Strouse JJ, Brandow AM | Ann Intern Med | 2022 |
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| Disseminated spp. Endocarditis in a Beta-Thalassemia Patient after Asymptomatic COVID-19 Infection. | Cinteza E, Nicolescu A, Ciomartan T, Gavriliu LC, Voicu C, Carabas A, Popescu M, Margarint I | Diagnostics (Basel) | 2022 |
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| A Novel Hemoglobin Variant Hb Liaobu [α107(G14)Val→Leu, : c.322G>C] Detected by Matrix-Assisted Laser Desorption Ionization-Time-of-Flight Mass Spectrometry. | Tan XM, Liu YH, Shang X, Ye YH, Xu XM | Hemoglobin | 2022 |
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| Perspective on newborn screening (NBS): Evidence sharing on conditions to be included in NBS in Pakistan. | Majid H, Jafri L, Ahmed S, Humayun K, Kirmani S, Ali N, Moiz B, Khan AH, Afroze B | J Pak Med Assoc | 2022 |
| Association of early donor chimerism status with survival outcomes in post allogeneic haematopoietic stem cell transplant patients of nonmalignant diseases. | Sial N, Ahmed P, Wattoo FH, Ali N | J Pak Med Assoc | 2022 |
| Can We Perform the Maximal Treadmill Test on Individuals with Sickle Cell Disease? | Ahner MM, Motta SBD, Franzoni L | Arq Bras Cardiol | 2022 |
| Exercise Testing In Patients with Sickle Cell Disease: Safety, Feasibility and Potential Prognostic Implication. | Araújo CG, Resende MBS, Tupinambás JT, Dias RCTM, Barros FC, Vasconcelos MCM, Januário JN, Ribeiro ALP, Nunes MCP | Arq Bras Cardiol | 2022 |
| An Immersive Virtual Reality Curriculum for Pediatric Hematology Clinicians on Shared Decision-making for Hydroxyurea in Sickle Cell Anemia. | Real FJ, Hood AM, Davis D, Cruse B, Klein M, Johnson Y, McTate E, Brinkman WB, Hackworth R, Hackworth K, Quinn CT, Crosby LE | J Pediatr Hematol Oncol | 2022 |
| Transition Preparation and Satisfaction of Care Among Adolescents and Young Adults With Sickle Cell Disease at the Ghana Institute of Clinical Genetics. | Kwarteng-Siaw M, Benneh-Akwasi Kuma A, Green NS | J Pediatr Hematol Oncol | 2022 |
| Genotype-phenotype correlation in patients with deletional and nondeletional mutations of Hb H disease in Southwest of Iran. | Hamid M, Keikhaei B, Galehdari H, Saberi A, Sedaghat A, Shariati G, Mohammadi-Anaei M | Sci Rep | 2022 |
| An unusual left atrial Rosai-Dorfman involvement in sickle cell disease patient. | Hritani R, Ramsey Z, Lee R, Bates WB, Williams H, Garcia D, Kutlar A, Aljaroudi W | J Nucl Cardiol | 2022 |
| Bloodstream Infections in Children With Sickle Cell Disease: 2010-2019. | Yee ME, Lai KW, Bakshi N, et al. | Pediatr Infect Dis J | 2022 |
| Feature tracking microfluidic analysis reveals differential roles of viscosity and friction in sickle cell blood. | Szafraniec HM, Valdez JM, Iffrig E, Lam WA, Higgins JM, Pearce P, Wood DK | Lab Chip | 2022 |
| Screening for glucose dysregulation in β-thalassemia major (β-TM): An update of current evidences and personal experience. | De Sanctis V, Daar S, Soliman AT, Tzoulis P, Karimi M, Di Maio S, Kattamis C | Acta Biomed | 2022 |
| Long-term Survival after Hematopoietic Cell Transplant for Sickle Cell Disease Compared to the United States Population. | StMartin A, Hebert KM, Serret-Larmande A, Jouhet V, Hughes E, Stedman J, DeSain T, Pillion D, Lyons JC, Steinert P, Avillach P, Eapen M | Transplant Cell Ther | 2022 |
| GH/IGF-1 axis in a large cohort of ß-thalassemia major adult patients: a cross-sectional study. | Gagliardi I, Mungari R, Gamberini MR, Fortini M, Dassie F, Putti MC, Maffei P, Aliberti L, Bondanelli M, Zatelli MC, Ambrosio MR | J Endocrinol Invest | 2022 |
| Acute kidney injury in hospitalized children with sickle cell anemia. | Batte A, Menon S, Ssenkusu J, Kiguli S, Kalyesubula R, Lubega J, Mutebi EI, Opoka RO, John CC, Starr MC, Conroy AL | BMC Nephrol | 2022 |
| Fetal hemoglobin modulates neurocognitive performance in sickle cell anemia. | Heitzer AM, Longoria J, Rampersaud E, Rashkin SR, Estepp JH, Okhomina VI, Wang WC, Raches D, Potter B, Steinberg MH, King AA, Kang G, Hankins JS | Curr Res Transl Med | 2022 |
| Mitochondrial function in sickle cell disease. | Messonnier LA | Blood | 2022 |
| Hemogen /BRG1 cooperativity modulates promoter and enhancer activation during erythropoiesis. | Guo X, Dean A, Zhao Y, Kim J | Blood | 2022 |
| Gonadal Status and Sexual Function at Long-Term Follow-up after Allogeneic Stem Cell Transplantation in Adult Patients with Sickle Cell Disease. | Boga C, Asma S, Ozer C, Bulgan Kilicdag E, Kozanoglu I, Yeral M, Korur A, Gereklioglu C, Ozdogu H | Exp Clin Transplant | 2022 |
| Sickle Cell Intrahepatic Cholestasis: Extremely Rare but Fatal Complication of Sickle Cell Disease. | Khan A, Nashed B, Issa M, Khan MZ | Cureus | 2022 |
| Demand-only patient-controlled analgesia for treatment of acute vaso-occlusive pain in sickle cell disease. | Carullo V, Morrone K, Weiss M, Choi J, Gao Q, Pisharoty S, Moody K, Manwani D | Pediatr Blood Cancer | 2022 |
| Simultaneous newborn screening for sickle cell disease, biotinidase deficiency, and hereditary tyrosinemia type 1 with an optimized tandem mass spectrometry protocol. | Lobitz S, Frömmel C, Brose A, Blankenstein O, Turner C, Dalton RN, Daniel Y, Klein J | Ann Hematol | 2022 |
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| Abnormal Lower Extremity Hemodynamics at Doppler US in Children with Sickle Cell Anemia. | Komolafe OO, Adetiloye VA, Ayoola OO, Adefehinti O, Onwuka C | Radiology | 2022 |
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| β-thalassemia, and the advent of new Interventions beyond Transfusion and Iron chelation. | Chauhan W, Shoaib S, Fatma R, Zaka-Ur-Rab Z, Afzal M | Br J Clin Pharmacol | 2022 |
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| Case Report: Clinical and Hematological Characteristics of ε Thalassemia in an Italian Patient. | Fotzi I, Pegoraro F, Chiocca E, Casini T, Mogni M, Veltroni M, Favre C | Front Pediatr | 2022 |
| Plasma Interleukin-33 Cannot Predict Hip Osteonecrosis in Patients With Sickle Cell Disease: A Case-Control Study. | Agrawal AC, Mohapatra E, Nanda R, Bodhey NK, Sakale H, Garg AK | Cureus | 2022 |
| A Huge Subcapsular Splenic Cyst Like Hematoma in Sickle Cell Anemia. | Odeh AM, Boumarah KA, Alsumaien WA, Al-Abbad MT, Al-Ali AH, Alammar ZA, Alsuqair H, Albeladi AM, Alsuwaigh A, Omrani A, Almuhanna MM, Busbaih Z, Al-Shaban HR, Aldhameen AA | Cureus | 2022 |
| An Interesting and Rare Case of Hemoglobin D-Punjab Variant in Tamil Nadu. | Spandana R, Panneerselvam K, Mani S, Krishnamoorthy N | Cureus | 2022 |
| Transcranial Doppler sonography and the effect of haematopoietic stem cell transplantation in sickle cell disease. | Thurn S, Kleinschmidt K, Kovacic I, Wendl C, Linker RA, Corbacioglu S, Schlachetzki F | Neurol Res Pract | 2022 |
| Spinal cord compression: An unusual sequela of sickle cell disease. | Shekar M, Casini G, Donoho D, Mohila C, Kim TO, Fasipe T, Porea T | Pediatr Blood Cancer | 2022 |
| Regional anesthesia for sickle cell disease vaso-occlusive crisis: A single-center case series. | Karsenty C, Tubman VN, Liu CJ, Fasipe T, Wyatt KEK | Pediatr Blood Cancer | 2022 |
| Healthcare utilization and the quality of life of children and adolescents with sickle cell disease. | Moody KL | Pediatr Blood Cancer | 2022 |
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| Essential thrombocythemia complicating hemoglobin SC disease and presenting with priapism. | Nwogbo OV, Loghavi S | Blood | 2022 |
| β-Thalassemia Intermedia: Interaction of α-Globin Gene Triplication With β-thalassemia Heterozygous in Spain. | Ropero P, González Fernández FA, Nieto JM, Torres-Jiménez WM, Benavente C | Front Med (Lausanne) | 2022 |
| Bacteraemia and Septic Arthritis in a Sickle Cell Disease Patient. | Alqurashi M, Madani B, Mursi M, Eltayeb N | Eur J Case Rep Intern Med | 2022 |
| Favorable outcomes of patients with sickle cell disease hospitalized due to COVID-19: A report of three cases. | Tentolouris A, Stafylidis C, Siafarikas C, Dimopoulou MN, Makrodimitri S, Bousi S, Papalexis P, Damaskos C, Trakas N, Sklapani P, Spandidos DA, Epameinondas Georgakopoulou V | Exp Ther Med | 2022 |
| Outcome of Hydroxyurea Use in SCD and Evaluation of Patients' Perception and Experience in Nigeria. | Chianumba RI, Ofakunrin AOD, Morrice J, Olanrewaju O, Oniyangi O, Kuliya-Gwarzo A, Nnebe-Agumadu U, Isa HA, Nnodu OE | Front Genet | 2022 |
| Strategies to increase access to basic sickle cell disease care in low- and middle-income countries. | Dua M, Bello-Manga H, Carroll YM, Galadanci AA, Ibrahim UA, King AA, Olanrewaju A, Estepp JH | Expert Rev Hematol | 2022 |
| Molecular spectrum of thalassemia in tropical Hainan Island of southern China：high allele frequency with low health burden. | Lai Y, Tao F, Zou Y, Huang M, Lin K, Li Y, Huang W, Zhou W | J Genet Genomics | 2022 |
| Unstable hemoglobin Montreal II uncovered in an adult with unexplained hemolysis exacerbated by a presumed viral infection: a case report. | Medri C, Méndez A, Hammerer-Lercher A, Rovó A, Angelillo-Scherrer A | J Med Case Rep | 2022 |
| Successful haploidentical hematopoietic stem cell transplantation (HSCT) and durable engraftment by repeated donor lymphocyte infusions for a Chinese patient with transfusion-dependent hemoglobin (Hb) Hammersmith and massive splenomegaly. | Chan WYK, Chan NCN, So JCC, Lee PPW, Cheuk DKL, Ha SY, Chan GCF, Leung W | Pediatr Transplant | 2022 |
| Adjuvant low-dose ketamine for paediatric and young adult sickle cell vaso-occlusive episodes in the emergency department. | Cooper-Sood JB, Hagar W, Marsh A, Hoppe C, Agrawal AK | Br J Haematol | 2022 |
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| [Comparision of Allogeneic Hematopoietic Stem Cell Transplantation between Children with Thalassemia of Different Ages]. | Kang DL, Tan YH, Chen YM, Lu JY, Shi J, Yan XZ, Lu QY | Zhongguo Shi Yan Xue Ye Xue Za Zhi | 2022 |
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| Assessing Cerebrovascular Resistance in Patients With Sickle Cell Disease. | Sayin ES, Sobczyk O, Poublanc J, Mikulis DJ, Fisher JA, Kuo KHM, Duffin J | Front Physiol | 2022 |
| and Studies for the Investigation of γ-Globin Gene Induction by : A Pre-Clinical Study of HbF Inducers for β-Thalassemia. | Iftikhar F, Rahman S, Khan MBN, Khan K, Khan MN, Uddin R, Musharraf SG | Front Pharmacol | 2022 |
| Blood Component Requirements and Erythrocyte Transfusion and Mortality Related to Hemoglobin Deficit in Phase III Trial of Hemoglobin-Based Oxygen Carrier: HBOC-201. | Jahr JS, Williams JP | Am J Ther | 2022 |
| DNA testing for sickle cell anemia in Africa: Implementation choices for the Democratic Republic of Congo. | Ngole M, Race V, Mbayabo G, Lumbala P, Songo C, Lukusa PT, Devriendt K, Matthijs G, Lumaka A | J Clin Lab Anal | 2022 |
| How Would You Treat This Patient With Acute and Chronic Pain From Sickle Cell Disease? : Grand Rounds Discussion From Beth Israel Deaconess Medical Center. | Kanjee Z, Achebe MO, Smith WR, Burns RB | Ann Intern Med | 2022 |
| Hb New York, preliminary results concerning the hematologic characteristics and the effects on thalassemia. | Cheng Z, Zhu X, Zeng D, Feng Q, Tian B, Zheng H, Tan S, Zhu C | Mol Biol Rep | 2022 |
| Arginine Therapy and Cardiopulmonary Hemodynamics in Hospitalized Children with Sickle Cell Anemia: A Prospective Double-Blinded Randomized Placebo-Controlled Trial. | Onalo R, Cilliers A, Cooper P, Morris CR | Am J Respir Crit Care Med | 2022 |
| Validation of single-gene noninvasive prenatal testing for sickle cell disease. | Westin ER, Tsao DS, Atay O, Landry BP, Ye PP, Chandler-Brown D, Alford B, Hoskovec J, Subramaniam A, Pawlik KM, Kuper SG, Goldman FD, Townes TM, Sheehan VA | Am J Hematol | 2022 |
| A decade of molecular preimplantation genetic diagnosis of 350 blastomeres for beta-thalassemia combined with HLA typing, aneuploidy screening and sex selection in Iran. | Keshvar Y, Sabeghi S, Sharifi Z, Fatemi KS, Fouladi P, Younesi Khah S, Rahiminejad F, Joudaki A, Amini M, Bagherian H, Ghaffari Novin M, Movahedin M, Mojbafan M, Zeinali S | BMC Pregnancy Childbirth | 2022 |
| Attitudes and practices of unmarried adults towards sickle cell disease: emergent factors from a cross sectional study in Nigeria's capital. | Adigwe OP, Onavbavba G, Onoja SO | Hematology | 2022 |
| Breaking the Cycle: Care Coordination Interventions and Sickle Cell Readmissions. | No authors listed | Prof Case Manag | 2022 |
| Breaking the Cycle: Care Coordination Interventions and Sickle Cell Readmissions. | Edge NB | Prof Case Manag | 2022 |
| BEHAVIORAL CHARACTERISTICS OF CHILDREN WITH SICKLE CELL DISEASE. | Pereira FB, Pedroso GC, Resegue RM, Ribeiro MVV, Hokazono M, Braga JAP | Rev Paul Pediatr | 2021 |
| Correction of Hemoglobin E/Beta-Thalassemia Patient-Derived iPSCs Using CRISPR/Cas9. | Wattanapanitch M | Methods Mol Biol | 2021 |
| The spectrum of beta-thalassemia mutations in the 22 Arab countries: a systematic review. | Khan AM, Al-Sulaiti AM, Younes S, Yassin M, Zayed H | Expert Rev Hematol | 2021 |
| Recommendation to reality: Closing the transcranial Doppler screening gap for children with sickle cell anemia. | Singh A, Danda V, Van Swol L, Scott JP, Brandow AM, Panepinto JA | Pediatr Blood Cancer | 2021 |
| The Theoretical Basis of In Utero Hematopoietic Stem Cell Transplantation and Its Use in the Treatment of Blood Disorders. | Tai-MacArthur S, Lombardi G, Shangaris P | Stem Cells Dev | 2021 |
| Automatic identification of abnormal blood smear images using color and morphology variation of RBCS and central pallor. | Rahman S, Azam B, Khan SU, Awais M, Ali I, Ul Hussen Khan RJ | Comput Med Imaging Graph | 2021 |
| Modulation of red blood cell oxygen affinity with a novel allosteric modifier of hemoglobin is additive to the Bohr effect. | Evans BA, Ansari AK, Kamyszek RW, Salvagno M, Welsby J, Fuller M, Welsby I | Blood Cells Mol Dis | 2021 |
| MicroRNA expression patterns in HbE/β-thalassemia patients: The passwords to unlock fetal hemoglobin expression in β-hemoglobinopathies. | Das SS, Das S, Byram PK, Rahaman M, Dolai TK, Chatterjee A, Chakravorty N | Blood Cells Mol Dis | 2021 |
| Marrow Fat Content and Composition in β-Thalassemia: A Study using H-MRS. | Ismail UN, Azlan CA, Khairullah S, Azman RR, Omar NF, Md Shah MN, Yeong CH, Jackson N, Ng KH | J Magn Reson Imaging | 2021 |
| Use of Wise Device Technology to Measure Adherence to Hydroxyurea Therapy in Youth With Sickle Cell Disease. | Ingerski LM, Loew M, Porter JS, Su Y, Zhang H, Hankins JS, Wang WC | J Pediatr Hematol Oncol | 2021 |
| Thrombin generation in vivo and ex vivo in sickle cell disease patients. | Ladeira VS, de Oliveira Toledo SL, Ferreira LGR, Oliveira MM, Silva APF, de Oliveira WV, Duarte RCF, Renó CO, Dusse LMS, Dos Santos HL, Carvalho MDG, Pinheiro MB, Rios DRA | Thromb Res | 2021 |
| Induction of therapeutic levels of HbF in genome-edited primary β 39-thalassaemia haematopoietic stem and progenitor cells. | Mingoia M, Caria CA, Ye L, Asunis I, Marongiu MF, Manunza L, Sollaino MC, Wang J, Cabriolu A, Kurita R, Nakamura Y, Cucca F, Kan YW, Marini MG, Moi P | Br J Haematol | 2021 |
| Benserazide as a potential novel fetal hemoglobin inducer: an observational study in non-carriers of hemoglobin disorders. | Santos MEHP, Olops L, Vendrame F, Tavares AHJ, Leonardo DP, de Azevedo PC, Piovesana LG, Costa FF, Fertrin KY | Blood Cells Mol Dis | 2021 |
| Swaying sickle cell research forward in support of patient reported outcomes. | Lanzkron S, Smith-Whitley K | Am J Hematol | 2021 |
| Rare Disorders of Painful Erection: A Cohort Study of the Investigation and Management of Stuttering Priapism and Sleep-Related Painful Erection. | Johnson MJ, McNeillis V, Chiriaco G, Ralph DJ | J Sex Med | 2021 |
| If you Can't Assess It, How Can you Treat It? Improving Pain Management in Sickle Cell Disease. | Jonassaint CR | J Emerg Nurs | 2021 |
| Curcuminoids supplementation ameliorates iron overload, oxidative stress, hypercoagulability, and inflammation in non-transfusion-dependent β-thalassemia/Hb E patients. | Hatairaktham S, Masaratana P, Hantaweepant C, Srisawat C, Sirivatanauksorn V, Siritanaratkul N, Panichkul N, Kalpravidh RW | Ann Hematol | 2021 |
| Krüppel-like factor 1 (KLF1) gene single nucleotide polymorphisms in sickle cell disease and its association with disease-related morbidities. | Kumar R, Yadav R, Mishra S, Singh MPSS, Gwal A, Bharti PK, Rajasubramaniam S | Ann Hematol | 2021 |
| MRI-based R2* mapping in patients with suspected or known iron overload. | Aslan E, Luo JW, Lesage A, Paquin P, Cerny M, Chin AS, Olivié D, Gilbert G, Soulières D, Tang A | Abdom Radiol (NY) | 2021 |
| A painless, sudden loss of vision in sickle cell anaemia: central retinal artery occlusion. | Guillaume M, Lahary A, Zourdani L, Malandain E, Ozkul-Wermester O | Lancet | 2021 |
| Chronic graft-versus-host disease in children and adolescents with thalassemia after hematopoietic stem cell transplantation. | Lertkovit O, Anurathapan U, Hongeng S, Thokanit NS, Pakakasama S | Int J Hematol | 2021 |
| Mortality in sickle cell disease: A population-based study in an aboriginal community in the Gudalur Valley, Nilgiris, Tamil Nadu, India. | Sheshadri V, Shabeer P, Santhirapala V, Jayaram A, Krishnamurti L, Menon N | Pediatr Blood Cancer | 2021 |
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| "I'm in Pain; Why Don't You Believe Me?" Pain Management in Sickle Cell Disease. | Ellis G | Am J Bioeth | 2021 |
| Safety and benefits of automated red cell depletion-exchange compared to standard exchange in patients with sickle cell disease undergoing chronic transfusion. | Ziemba Y, Xu C, Fomani KM, Nandi V, Yuan T, Rehmani S, Sachais BS, Appiah-Kubi AO, Aygun B, Louie JE, Shi PA | Transfusion | 2021 |
| Hemoglobinopathy and pediatrics in the time of COVID-19. | Vilela TS, Braga JAP, Loggetto SR | Hematol Transfus Cell Ther | 2021 |
| Trial design of comparing patient-specific versus weight-based protocols to treat vaso-occlusive episodes in sickle cell disease (COMPARE-VOE). | Ibemere SO, Dubbs SB, Barnhart HX, Brown JL, Freiermuth CE, Kavanagh P, Paice JA, Strouse JJ, Wilkerson RG, Tanabe P, | Contemp Clin Trials | 2021 |
| Long noncoding RNA CCDC26 as a modulator of transcriptional switching between fetal and embryonic globins. | Hirano T, Tsuruda T, Tanaka Y, Harada H, Yamazaki T, Ishida A | Biochim Biophys Acta Mol Cell Res | 2021 |
| CRISPR/Cas9 gene editing for curing sickle cell disease. | Park SH, Bao G | Transfus Apher Sci | 2021 |
| Increased zinc and albumin but lowered copper in children with transfusion-dependent thalassemia. | Alhillawi ZH, Al-Hakeim HK, Moustafa SR, Maes M | J Trace Elem Med Biol | 2021 |
| CD14+ monocytes repress gamma globin expression at early stages of erythropoiesis. | Heshusius S, Heideveld E, von Lindern M, van den Akker E | Sci Rep | 2021 |
| Anxiety level and clinical course of patients with sickle cell disease during the COVID-19 outbreak. | Tezol O, Unal S | Arch Pediatr | 2021 |
| Association of sickle cell disease with anthropometric indices among under-five children: evidence from 2018 Nigeria Demographic and Health Survey. | Islam MR, Moinuddin M, Ahmed A, Rahman SM | BMC Med | 2021 |
| Undernutrition: a major but potentially preventable cause of poor outcomes in children living with sickle cell disease in Africa. | Williams TN | BMC Med | 2021 |
| Co-transcriptional splicing regulates 3' end cleavage during mammalian erythropoiesis. | Reimer KA, Mimoso CA, Adelman K, Neugebauer KM | Mol Cell | 2021 |
| Early genetic screening uncovered a high prevalence of thalassemia among 18 309 neonates in Guizhou, China. | Tan M, Bai Y, Zhang X, Sun J, Huang C, Tian R, Yang Y, Luo X, Su Q, Wu L, Zheng L, Xia J, Murong H, Zhu P, Yang F, Zhong X, Chen J, Chen Y | Clin Genet | 2021 |
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| Addressing unmet basic needs for children with sickle cell disease in the United States: clinic and staff perspectives. | Loo S, Brochier A, Wexler MG, Long K, Kavanagh PL, Garg A, Drainoni ML | BMC Health Serv Res | 2021 |
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| Ketamine for Sickle Cell Vaso-Occlusive Crises: A Systematic Review. | Alshahrani MS, Alghamdi MA | Saudi J Med Med Sci | 2021 |
| Nitric oxide and sickle cell disease-Is there a painful connection? | Hallmark L, Almeida LE, Kamimura S, Smith M, Quezado ZM | Exp Biol Med (Maywood) | 2021 |
| Transfusion and sickle cell anemia in Africa. | Diop S, Pirenne F | Transfus Clin Biol | 2021 |
| Cas9-AAV6 gene correction of beta-globin in autologous HSCs improves sickle cell disease erythropoiesis in mice. | Wilkinson AC, Dever DP, Baik R, Camarena J, Hsu I, Charlesworth CT, Morita C, Nakauchi H, Porteus MH | Nat Commun | 2021 |
| Coronavirus Disease 2019 (COVID-19) Infection in Children With Sickle Cell Disease: Case Series From Oman. | Al Sabahi A, Al Maskari N, Al Busaidi I, Albiroty KA, Alkhamisy A, Al Hinai K, Al Hinai M, Al Mashaikhi N, Alkendi J | J Pediatr Hematol Oncol | 2021 |
| Targeting the AnxA1/Fpr2/ALX pathway regulates neutrophil function, promoting thromboinflammation resolution in sickle cell disease. | Ansari J, Senchenkova EY, Vital SA, Al-Yafeai Z, Kaur G, Sparkenbaugh EM, Orr AW, Pawlinski R, Hebbel RP, Granger DN, Kubes P, Gavins FNE | Blood | 2021 |
| Dietary iron restriction improves markers of disease severity in murine sickle cell anemia. | Parrow NL, Violet PC, George NA, Ali F, Bhanvadia S, Wong R, Tisdale JF, Fitzhugh C, Levine M, Thein SL, Fleming RE | Blood | 2021 |
| Markers of ineffective erythropoiesis in non-transfusion dependent β-thalassaemia. | Khairullah S, Jackson N | Med J Malaysia | 2021 |
| Diverse manifestations of a sickle cell crisis. | Hashemzehi T, Bertok S, Figaszewska MJ, Batura D | BMJ Case Rep | 2021 |
| Epigenetic activities in erythroid cell gene regulation. | Wang Y, Yu L, Engel JD, Singh SA | Semin Hematol | 2021 |
| Epigenetic regulation of hemoglobin switching in non-human primates. | Molokie R, DeSimone J, Lavelle D | Semin Hematol | 2021 |
| Epigenetic modifier directed therapeutics to unleash healthy genes in unhealthy cells. | Jha BK, Saunthararajah Y | Semin Hematol | 2021 |
| Bayesian spatial modeling of transfusion-dependent β-thalassemia incidence rate in Fars Province, Southern Iran. | Haghpanah S, Asmarian N, Zekavat OR, Bordbar M, Karimi M, Zareifar S, Ramzi M, Safaei S | Spat Spatiotemporal Epidemiol | 2021 |
| Validity of the Malay EQ-5D-3L in the Malaysian Transfusion-Dependent Thalassemia Population. | Shafie AA, Chhabra IK, Hui Yi JW, Mohammed NS, Ibrahim HM | Value Health Reg Issues | 2021 |
| Skewed intracellular cytokine production of iNKT cells toward Th2-related responses in alloimmunized thalassemia patients. | Amirian N, Ranjbaran R, Shokrgozar N, Ataei S, Bazrafshan A, Sharifzadeh S | Cytokine | 2021 |
| It takes a village to raise a sickle cell warrior. | Power-Hays A | Pediatr Blood Cancer | 2021 |
| A phenotypic risk score for predicting mortality in sickle cell disease. | Sachdev V, Tian X, Gu Y, Nichols J, Sidenko S, Li W, Beri A, Layne WA, Allen D, Wu CO, Thein SL | Br J Haematol | 2021 |
| Extramedullary hematopoiesis in the facial sinus in a patient homozygous for Hemoglobin Lepore: the first case in literature. | Talarico V, Muraca L, Arcuri PP, Gigliotti F, Fortugno C, Miniero R, Raiola G, Galati MC | Eur Rev Med Pharmacol Sci | 2021 |
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| Screening of HbE by the New Screening Test: Alcohol HbE Test (AET). | Tatu T, Anusak K, Jawannatoom C | J Appl Lab Med | 2021 |
| Compensated hypogonadism in men with sickle cell disease. | Ribeiro APMR, Silva CS, Zambrano JCC, Miranda JOF, Molina CAF, Gomes CM, Miranda EP, de Bessa J | Clin Endocrinol (Oxf) | 2021 |
| Opioids and Sickle Cell Disease: From Opium to the Opioid Epidemic. | Ballas SK | J Clin Med | 2021 |
| CYP450 Mediates Reactive Oxygen Species Production in a Mouse Model of β-Thalassemia through an Increase in 20-HETE Activity. | Bou-Fakhredin R, Dia B, Ghadieh HE, Rivella S, Cappellini MD, Eid AA, Taher AT | Int J Mol Sci | 2021 |
| A systematic review of quality of life in sickle cell disease and thalassemia after stem cell transplant or gene therapy. | Badawy SM, Beg U, Liem RI, Chaudhury S, Thompson AA | Blood Adv | 2021 |
| PPARγ increases HUWE1 to attenuate NF-κB/p65 and sickle cell disease with pulmonary hypertension. | Jang AJ, Chang SS, Park C, Lee CM, Benza RL, Passineau MJ, Ma J, Archer DR, Sutliff RL, Hart CM, Kang BY | Blood Adv | 2021 |
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| Transfusion and Cellular Therapy in Pediatric Sickle Cell Disease. | Zheng Y, Chou ST | Clin Lab Med | 2021 |
| Successful four-factor preimplantation genetic testing: α- and β-thalassemia, human leukocyte antigen typing, and aneuploidy screening. | Chen D, Shen X, Xu Y, Ding C, Ye Q, Zhong Y, Xu Y, Zhou C | Syst Biol Reprod Med | 2021 |
| Genetic determinants of ferritin, haemoglobin levels and haemoglobin trajectories: results from Donor InSight. | Timmer T, Tanck M, Penkett C, Stirrups K, Gleadall N, de Kort W, van der Schoot E, van den Hurk K | Vox Sang | 2021 |
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| Risk Factors and Complications Among Pediatric Patients With Sickle Cell Anemia: A Single Tertiary Center Retrospective Study. | Alzahrani F, Fallatah AM, Al-Haddad FM, Khayyat ST, AlMehmadi WM, AlQahtani BG, Alamri RS | Cureus | 2021 |
| Tolerance and humoral immune response to the yellow fever vaccine in sickle cell disease children treated with hydroxyurea: a multicentre prospective study. | Koehl B, Aupiais C, Schinckel N, Mornand P, Odièvre MH, Niakate A, Brousse V, Ithier G, Missud F, Holvoet L, Benkerrou M, Sorge F, Faye A | J Travel Med | 2021 |
| The Rh blood group system and its role in alloimmunization rate among sickle cell disease and sickle thalassemia patients in Iran. | Jalali Far MA, Oodi A, Amirizadeh N, Mohammadipour M, Keikhaei Dehdezi B. | Mol Genet Genomic Med | 2021 |
| Core decompression with autologous bone marrow aspirate injection in humeral head osteonecrosis in adults with sickle cell disease. | Guerin G, Habibi A, Hernigou P, Zilber S | Int Orthop | 2021 |
| Noninvasive prenatal testing of α-thalassemia and β-thalassemia through population-based parental haplotyping. | Chen C, Li R, Sun J, Zhu Y, Jiang L, Li J, Fu F, Wan J, Guo F, An X, Wang Y, Fan L, Sun Y, Guo X, Zhao S, Wang W, Zeng F, Yang Y, Ni P, Ding Y, Xiang B, Peng Z, Liao C | Genome Med | 2021 |
| Assessment of Subclinical Renal Glomerular and Tubular Dysfunction in Children with Beta Thalassemia Major. | Mahmoud AA, Elian DM, Abd El Hady NM, Abdallah HM, Abdelsattar S, Khalil FO, Abd El Naby SA | Children (Basel) | 2021 |
| Hematopoietic-Stem-Cell-Targeted Gene-Addition and Gene-Editing Strategies for β-hemoglobinopathies. | Drysdale CM, Nassehi T, Gamer J, Yapundich M, Tisdale JF, Uchida N | Cell Stem Cell | 2021 |
| Non-transfusion-dependent thalassemia in Italy: less blues, no role of reds. | Tartaglione I, Manara R, di Concilio R, Quarta A, Ruffo GB, De Michele E, Ammendola F, Foderini MV, Raimo S, Santangelo G, Perrotta S | Ann Hematol | 2021 |
| Tranexamic acid use in a patient with sickle cell disease undergoing posterior scoliosis correction surgery: safely mitigating bleeding and vaso-occlusive crises. | Newall M, Hamdan TA, Lui DF, Ajayi B, Bishop T, Weil S | J Surg Case Rep | 2021 |
| Parameters affecting successful stem cell collections for genetic therapies in sickle cell disease. | Justus DG, Manis JP | Transfus Apher Sci | 2021 |
| On the possibility of a disabled life in capitalist ruins: Black workers with sickle cell disorder in England. | Dyson SM, Atkin KM, Berghs MJ, Greene AM | Soc Sci Med | 2021 |
| Neutrophil extracellular trap regulators in sickle cell disease: Modulation of gene expression of PADI4, neutrophil elastase, and myeloperoxidase during vaso-occlusive crisis. | Hounkpe BW, Chenou F, Domingos IF, Cardoso EC, Costa Sobreira MJV, Araujo AS, Lucena-Araújo AR, da Silva Neto PV, Malheiro A, Fraiji NA, Costa FF, Bezerra MAC, Santos MNN, De Paula EV | Res Pract Thromb Haemost | 2021 |
| ADAMTS13 and von Willebrand factor assessment in steady state and acute vaso-occlusive crisis of sickle cell disease. | Demagny J, Driss A, Stepanian A, Anguel N, Affo L, Roux D, Habibi A, Benghezal S, Capdenat S, Coppo P, Driss F, Veyradier A | Res Pract Thromb Haemost | 2021 |
| Simultaneous diagnosis of severe SARS-CoV-2 infection and sickle cell disease in two infants. | Parodi E, Voi V, Vania B, Lonardi P, Saracco P, Longobardo A, Grassitelli S, Peruzzi L, Scolfaro C, Piga A | Blood Transfus | 2021 |
| Detection and follow-up of a soluble alpha-haemoglobin pool in the red cells of stored blood units. | Domingues-Hamdi E, Vasseur C, Bodivit G, Jouard A, de Ménorval MA, Pirenne F, Chadebech P, Baudin-Creuza V | Blood Transfus | 2021 |
| Longitudinal Assessment of Retinal Thinning in Adults With and Without Sickle Cell Retinopathy Using Spectral-Domain Optical Coherence Tomography. | Lim JI, Niec M, Sun J, Cao D | JAMA Ophthalmol | 2021 |
| Sickle Cell Disease and the Eye-Everything Old Is New Again. | Scott AW | JAMA Ophthalmol | 2021 |
| Non-myeloablative human leukocyte antigen-matched related donor transplantation in sickle cell disease: outcomes from three independent centres. | Alzahrani M, Damlaj M, Jeffries N, Alahmari B, Singh A, Rondelli D, Tisdale JF, Saraf SL, Hsieh MM | Br J Haematol | 2021 |
| Thalassemia Patients from Baluchistan in Pakistan Are Infected with Multiple Hepatitis B or C Virus Strains. | Ahmed S, Ayub M, Naeem M, Nazir FH, Hussain A, Ghilzai D, Magnius LO, Sajjad A, Norder H | Am J Trop Med Hyg | 2021 |
| Hydroyxurea improves cerebral oxygen saturation in children with sickle cell anemia. | Karkoska K, Quinn CT, Niss O, Pfeiffer A, Dong M, Vinks AA, McGann PT | Am J Hematol | 2021 |
| Guideline on the peri-operative management of patients with sickle cell disease: Guideline from the Association of Anaesthetists. | Walker I, Trompeter S, Howard J, Williams A, Bell R, Bingham R, Bankes M, Vercueil A, Dalay S, Whitaker D, Elton C | Anaesthesia | 2021 |
| Are current interventions for preventing silent cerebral infarcts in people with sickle cell disease effective and safe? A Cochrane Review summary with commentary. | Gimigliano F | Dev Med Child Neurol | 2021 |
| Effects of red blood cell transfusion on global oxygenation in anemic critically ill patients. | Themelin N, Biston P, Massart J, Lelubre C, Piagnerelli M | Transfusion | 2021 |
| Quantification of pancreatic iron overload and fat infiltration and their correlation with glucose disturbance in pediatric thalassemia major patients. | Huang J, Shen J, Yang Q, Cheng Z, Chen X, Yu T, Zhong J, Su Y, Guo H, Liang B | Quant Imaging Med Surg | 2021 |
| Sofosbuvir/Ledipasvir for Treatment of Chronic Hepatitis C Infection in Adult Patients with β- Thalassemia Major: A Real-Life Study. | Elbedewy TA, Abd-Elsalam S, Mostafa SM, Abdellatif RS, Fouad A, Youssef M, Abo-Amer YE, Elsebaey MA | Endocr Metab Immune Disord Drug Targets | 2021 |
| Identification of Circulating Endocan-1 and Ether Phospholipids as Biomarkers for Complications in Thalassemia Patients. | Botta A, Forest A, Daneault C, Pantopoulos K, Tantiworawit A, Phrommintikul A, Chattipakorn S, Chattipakorn N, Des Rosiers C, Sweeney G | Metabolites | 2021 |
| Neuropathic Pain in Children with Sickle Cell Disease: The Hidden Side of the Vaso-Occlusive Crisis. | Sigalla J, Duparc Alegria N, Le Roux E, Toumazi A, Thiollier AF, Holvoet L, Benkerrou M, Dugue S, Koehl B | Children (Basel) | 2021 |
| Transcutaneous monitoring of hemoglobin derivatives during methemoglobinemia in rats using spectral diffuse reflectance. | Khatun F, Aizu Y, Nishidate I | J Biomed Opt | 2021 |
| Loss of alpha globin genes is associated with improved microvascular function in patients with sickle cell anemia. | Romana M, Reminy K, Moeckesch B, Charlot K, Hardy-Dessources MD, Doumdo L, Tressieres B, Etienne-Julan M, Lemonne N, Denton C, Coates T, Petras M, Antoine-Jonville S, Connes P | Am J Hematol | 2021 |
| Adaptable stewardship during a pandemic: a multifaceted approach to sustaining the blood supply for individuals with sickle cell disease. | Godby RC, Kornbrust A, Noubouossie D, Kanter J, Ogunsile FJ, Lima JLO, Singh N, Marques MB, Siniard RC | Int J Lab Hematol | 2021 |
| Variations in hemoglobin level and morbidity burden in non-transfusion-dependent β-thalassemia. | Musallam KM, Cappellini MD, Taher AT | Ann Hematol | 2021 |
| Orofacial manifestations of sickle cell disease: implications for dental clinicians. | Girgis S, Cheng L, Tsitsikas D, Sproat C | Br Dent J | 2021 |
| The use of luspatercept for thalassemia in adults. | Cappellini MD, Taher AT | Blood Adv | 2021 |
| Clinical predictors of poor outcomes in patients with sickle cell disease and COVID-19 infection. | Minniti CP, Zaidi AU, Nouraie M, Manwani D, Crouch GD, Crouch AS, Callaghan MU, Carpenter S, Jacobs C, Han J, Simon J, Glassberg J, Gordeuk VR, Klings ES | Blood Adv | 2021 |
| Longitudinal effect of disease-modifying therapy on tricuspid regurgitant velocity in children with sickle cell anemia. | Rai P, Joshi VM, Goldberg JF, Yates AM, Okhomina VI, Penkert R, Ataga KI, Kang G, Hankins JS | Blood Adv | 2021 |
| Cognitive performance as a predictor of healthcare transition in sickle cell disease. | Saulsberry-Abate AC, Partanen M, Porter JS, Podila PSB, Hodges JR, King AA, Wang WC, Schreiber JE, Zhao X, Kang G, Jacola LM, Hankins JS | Br J Haematol | 2021 |
| Absence of hydroxyurea-induced mutational effects supports higher utilisation for the treatment of sickle cell anaemia. | Ware RE, Dertinger SD | Br J Haematol | 2021 |
| Web-based expert system with quick response code for beta-thalassemia management. | Banjar HR, Zaher GF, Almutiry HS, Alshamarni ASA, Almouhana GI, Alahwal HM, Bahashwan S, Barefah AS, Alnajjar SA, Alharbi HM | Health Informatics J | 2021 |
| Differential diagnosis of thalassemia and iron deficiency anemia in pregnant women using new formulas from multidimensional analysis of red blood cells. | Xiao H, Wang Y, Ye Y, Yang C, Wu X, Wu X, Zhang X, Li T, Xiao J, Zhuang L, Qi H, Wang F | Ann Transl Med | 2021 |
| OCCURRENCE OF UNUSUAL HAEMOGLOBINOPATHIES IN BALOCHISTAN: HB SD AND HB SE - PRESENTATION WITH OSTEOMYELITIS. | Tauseef U, Anjum M, Ibrahim M, Baqai HS, Tauseef A, Tauseef M, Asghar MS, Zafar M, Rasheed U, Shaikh N | Rev Paul Pediatr | 2021 |
| Correlation of hepcidin and serum ferritin levels in thalassemia patients at Chiang Mai University Hospital. | Tantiworawit A, Khemakapasiddhi S, Rattanathammethee T, Hantrakool S, Chai-Adisaksopha C, Rattarittamrong E, Norasetthada L, Charoenkwan P, Srichairatanakool S, Fanhchaksai K | Biosci Rep | 2021 |
| Left ventricular deformation mechanics over time in patients with thalassemia major with and without iron overload. | Bonios MJ, Fountas E, Delaporta P, Kyrzopoulos S, Kattamis A, Adamopoulos SN, Tsiapras D | BMC Cardiovasc Disord | 2021 |
| Quality of life in Patients with β-thalassemia Major: Short-term and Long-term Effects after Haematopoietic Stem Cell Transplantation. | Zhai L, Liu Y, Huo R, Pan Z, Bin J, Li Z, Tang Q, Fan J | Curr Stem Cell Res Ther | 2021 |
| Sickle cell anemia/sickle cell disease and pregnancy outcomes among ethnic tribes in India: an integrative mini-review. | Ganesh B, Rajakumar T, Acharya SK, Kaur H | J Matern Fetal Neonatal Med | 2021 |
| Hyperhemolysis Syndrome in a Patient with Sickle Cell Disease: A Case Report. | Kalter JA, Gupta R, Greenberg MR, Miller AJ, Allen J | Clin Pract Cases Emerg Med | 2021 |
| Allogeneic stem cell transplantation with omidubicel in sickle cell disease. | Parikh S, Brochstein JA, Galamidi E, Schwarzbach A, Kurtzberg J | Blood Adv | 2021 |
| Rh alloimmunization in chronically transfused patients with thalassemia receiving RhD, C, E, and K matched transfusions. | Waldis SJ, Uter S, Kavitsky D, Flickinger C, Vege S, Friedman DF, Westhoff CM, Chou ST | Blood Adv | 2021 |
| Pediatric Neurodevelopmental Delays in Children 0 to 5 Years of Age With Sickle Cell Disease: A Systematic Literature Review. | Knight LMJ, King AA, Strouse JJ, Tanabe P | J Pediatr Hematol Oncol | 2021 |
| Psychometric Impact of Priapism on Lives of Adolescents and Adults With Sickle Cell Anemia: A Sequential Independent Mixed-Methods Design. | Idris IM, Bonnet K, Schlundt D, Abba A, Galadanci J, Burnett AL, DeBaun MR | J Pediatr Hematol Oncol | 2021 |
| Quality and Reliability of YouTube Videos on Sickle Cell Disease. | Om A, Mathew N, Nawaz A | J Pediatr Hematol Oncol | 2021 |
| Musculoskeletal imaging manifestations of beta-thalassemia. | Hajimoradi M, Haseli S, Abadi A, Chalian M | Skeletal Radiol | 2021 |
| Sickle cell disease-Under pressure. | Halabi CM, Hulbert ML | Pediatr Blood Cancer | 2021 |
| Genetics background of β-thalassemia (3.5 kb deletion) in Southern Thailand: Haplotype analysis using novel reverse dot blot hybridization. | Tepakhan W, Srewaradachpisal K, Kanjanaopas S, Jomoui W | Ann Hum Genet | 2021 |
| Usefulness of NGS for Diagnosis of Dominant Beta-Thalassemia and Unstable Hemoglobinopathies in Five Clinical Cases. | Rizzuto V, Koopmann TT, Blanco-Álvarez A, Tazón-Vega B, Idrizovic A, Díaz de Heredia C, Del Orbe R, Pampliega MV, Velasco P, Beneitez D, Santen GWE, Waisfisz Q, Elting M, Smiers FJW, de Pagter AJ, Kerkhoffs JH, Harteveld CL, Mañú-Pereira MDM | Front Physiol | 2021 |
| MRI detection of brain abnormality in sickle cell disease. | Stotesbury H, Kawadler JM, Saunders DE, Kirkham FJ | Expert Rev Hematol | 2021 |
| Efficient Clinical Counseling for Sickle Cell Disease. | Morrone KA, Manwani D, Cabana MD | J Natl Med Assoc | 2021 |
| Comparison of efficacy and safety of thalidomide vs hydroxyurea in patients with Hb E-β thalassemia - a pilot study from a tertiary care Centre of India. | Jain M, Chakrabarti P, Dolai TK, Ghosh P, Mandal PK, Baul SN, De R | Blood Cells Mol Dis | 2021 |
| Hepatic veno-occlusive disease/sinusoidal obstruction syndrome after hematopoietic stem cell transplantation for thalassemia major: incidence, management, and outcome. | Lai X, Liu L, Zhang Z, Shi L, Yang G, Wu M, Huang R, Liu R, Lai Y, Li Q | Bone Marrow Transplant | 2021 |
| Chronic osteo-articular changes in patients with sickle cell disease. | Ferreira TFA, Dos Santos APT, Leal AS, de Araújo Pereira G, Silva SS, Moraes-Souza H | Adv Rheumatol | 2021 |
| Evaluation of the Significance of Tear Ferning Patterns in beta-Thalassemia Patients. | Fagehi R, Abbadi IM, Abusharha A, Alanazi MA, Malhan H, El-Hiti GA, Masmali AM | Klin Monbl Augenheilkd | 2021 |
| Clinical and health-related quality of life outcomes of transfusion-dependent thalassaemia patients in Singapore. | Lam JCM, Lee SY, Koh PL, Fong SZ, Abdul-Kadir NI, Lim CY, Zhang X, Bhattacharyya R, Soh SY, Chan MY, Tan AM, Kuperan P, Ang AL | Blood Cells Mol Dis | 2021 |
| Sickle cell disease in India: a scoping review from a health systems perspective to identify an agenda for research and action. | Raman V, Seshadri T, Joice SV, N Srinivas P | BMJ Glob Health | 2021 |
| Evaluation of the High Resolution Melting Approach for Detection of β-Thalassemia Gene Mutations. | Tariq A, Khurshid S, Sajjad M | Hemoglobin | 2021 |
| Voxelotor for the treatment of sickle cell disease. | Vissa M, Vichinsky E | Expert Rev Hematol | 2021 |
| Emotion regulation, pain interference and affective symptoms in children and adolescents with sickle cell disease. | Miller M, Balsamo L, Pashankar F, Bailey CS | J Affect Disord | 2021 |
| Integrative holistic approaches for children, adolescents, and young adults with sickle cell disease: A single center experience. | Mahmood LA, Thaniel L, Martin B, Marguiles S, Reece-Stremtan S, Idiokitas R, Bettini E, Hardy SJ, Cohen I, Connolly M, Darbari DS | Complement Ther Med | 2021 |
| MicroRNAs in β-thalassemia. | Wang F, Ling L, Yu D | Am J Med Sci | 2021 |
| Clinical presentations and outcomes of COVID-19 infection in sickle cell disease patients: Case series from Komfo Anokye teaching hospital, Ghana. | Hardy YO, Amenuke DAY, Abukari Y, Oti-Acheampong A, Hutton-Mensah K, Amoah-Dankwah J, Amoabeng Kontoh S, Danso KA, Berchie PO, Otu-Ansah C | Clin Case Rep | 2021 |
| mutations and HbA2 level: Escaping the carrier screening programs. | Sharifi A, Mahdieh N | Clin Case Rep | 2021 |
| Implementation science research for the scale-up of evidence-based interventions for sickle cell disease in africa: a commentary. | Gyamfi J, Ojo T, Iwelunmor J, Ogedegbe G, Ryan N, Diawara A, Nnodu O, Wonkam A, Royal C, Peprah E | Global Health | 2021 |
| Characterisation of two unusual cases of haemoglobin Bart's hydrops foetalis caused by - and large novel α-globin gene cluster deletions. | Wang Y, Xiong Y, Liu C, Lu J, Wang J, Qin D, Liu L, Wu J, Zhao X, Fang L, Du L, Yin A | J Int Med Res | 2021 |
| Evidence-based interventions implemented in low-and middle-income countries for sickle cell disease management: A systematic review of randomized controlled trials. | Gyamfi J, Ojo T, Epou S, Diawara A, Dike L, Adenikinju D, Enechukwu S, Vieira D, Nnodu O, Ogedegbe G, Peprah E | PLoS One | 2021 |
| Patient Perspectives of Sickle Cell Management in the Emergency Department. | Crego N, Masese R, Bonnabeau E, Douglas C, Rains G, Shah N, Tanabe P | Crit Care Nurs Q | 2021 |
| Management of sickle cell disease: current practices and challenges in a northeastern region of the Democratic Republic of the Congo. | Kambale-Kombi P, Marini Djang'eing'a R, Alworong'a Opara JP, Minon JM, Boemer F, Bours V, Tonen-Wolyec S, Kayembe Tshilumba C, Batina-Agasa S | Hematology | 2021 |
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| Prevalence and distribution of major β-thalassemia mutations and HbE/β-thalassemia variant in Nepalese ethnic groups. | Lama R, Yusof W, Shrestha TR, Hanafi S, Bhattarai M, Hassan R, Zilfalil BA | Hematol Oncol Stem Cell Ther | 2021 |
| CRISPR/Cas9-mediated β-globin gene knockout in rabbits recapitulates human β-thalassemia. | Yang Y, Kang X, Hu S, Chen B, Xie Y, Song B, Zhang Q, Wu H, Ou Z, Xian Y, Fan Y, Li X, Lai L, Sun X | J Biol Chem | 2021 |
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| A Unique Monocyte Transcriptome Discriminates Sickle Cell Disease From Other Hereditary Hemolytic Anemias and Shows the Particular Importance of Lipid and Interferon Signaling. | van Vuren AJ, van Straaten S, Mokry M, van Wijk R, van Beers EJ | Hemasphere | 2021 |
| Pharmacokinetics and safety of ticagrelor in infants and toddlers with sickle cell disease aged <24 months. | Duniva Inusa BP, Inati A, Maes P, Githanga J, Ogutu B, Abboud MR, Miano M, Cela E, Nduba V, Niazi M, Åstrand M, Persson K, Berggren A, Carlson G | Pediatr Blood Cancer | 2021 |
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| Varied Age of First Presentation of Sickle Cell Disease: Case Presentations and Review. | Claeys A, Van Steijn S, Van Kesteren L, Damen E, Van Den Akker M | Case Rep Med | 2021 |
| Efficacy and Tolerance of Vascular Electrical Stimulation Therapy in the Management of Vaso-Occlusive Crises in Patients with Sickle Cell Disease: A Phase II Single-Centre Randomized Study in Ivory Coast. | Botti RP, Bokoum SS, L'Hermite E, Silue DA, Kouakou B, Bognini SA, Agoua SA, Mandeng Ma Linwa E, Ayemou R, Koffi KG | Adv Hematol | 2021 |
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| Transcranial Doppler Screening in a Current Cohort of Children With Sickle Cell Anemia: Results From the DISPLACE Study. | Kanter J, Phillips S, Schlenz AM, Mueller M, Dooley M, Sirline L, Nickel R, Brown RC, Hilliard L, Melvin CL, Adams RJ | J Pediatr Hematol Oncol | 2021 |
| Cognitive Functioning and Educational Support Plans in Youth With Sickle Cell Disease. | Connolly ME, Bills SE, Hardy SJ | J Pediatr Hematol Oncol | 2021 |
| First Observation of HbM-Saskatoon at the Origin of Neonatal Cyanosis in a Tunisian Baby. | Bouatrous E, Nouira S, Ben Khaled M, Ouederni M, Abbes S, Menif S, Ouragini H | J Pediatr Hematol Oncol | 2021 |
| Erythropoietin Concentration in Boys With p.His63Asp Polymorphism of the HFE Gene. | Kaczorowska-Hac B, Luszczyk M, Wasilewska E, Antosiewicz J, Kaczor JJ | J Pediatr Hematol Oncol | 2021 |
| Association of Anemia and Blood Pressure With Novel Markers of Diastolic Function in Pediatric Sickle Cell Disease. | Jhaveri S, Choueiter N, Manwani D, Ranabothu S, Morrone K, Hafeman M, Reidy K, Kaskel F, Mahgerefteh J | J Pediatr Hematol Oncol | 2021 |
| Hydroxyurea improves nitric oxide bioavailability in humanized sickle cell mice. | Taylor CM, Kasztan M, Sedaka R, Molina PA, Dunaway LS, Pollock JS, Pollock DM | Am J Physiol Regul Integr Comp Physiol | 2021 |
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| Hb S (: c.20A>T) Characteristics by High Performance Liquid Chromatography in Patients with Sickle Cell Disease Receiving the Novel Agent Voxelotor. | Tsitsikas DA, Kamal M, Braimoh A, Benson S, Abukar J | Hemoglobin | 2021 |
| In vivo HSPC gene therapy with base editors allows for efficient reactivation of fetal γ-globin in β-YAC mice. | Li C, Georgakopoulou A, Mishra A, Gil S, Hawkins RD, Yannaki E, Lieber A | Blood Adv | 2021 |
| Major Thalassemia, Screening or Treatment: An Economic Evaluation Study in Iran. | Esmaeilzadeh F, Ahmadi B, Vahedi S, Barzegari S, Rajabi A | Int J Health Policy Manag | 2021 |
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| P-selectin deficiency promotes liver senescence in sickle cell disease mice. | Vats R, Kaminski TW, Ju EM, Brozska T, Tutuncuoglu E, Tejero J, Novelli EM, Sundd P, Pradhan-Sundd T | Blood | 2021 |
| The potential hepatoprotective effect of metformin in hepatitis C virus-infected adolescent patients with beta thalassemia major: Randomised clinical trial. | Abdel Monem MS, Farid SF, Abbassi MM, Youssry I, Andraues NG, Hassany M, Selim YMM, El-Sayed MH | Int J Clin Pract | 2021 |
| Characteristics of sickle cell patients with frequent emergency department visits and hospitalizations. | Kidwell K, Albo C, Pope M, Bowman L, Xu H, Wells L, Barrett N, Patel N, Allison A, Kutlar A | PLoS One | 2021 |
| Adherence to hydroxyurea, health-related quality of life domains and attitudes towards a smartphone app among Irish adolescents and young adults with sickle cell disease. | Fogarty H, Gaul A, Syed S, Aleksejenko N, Geoghegan R, Conroy H, Crampton E, Ngwenya N, Tuohy E, McMahon C | Ir J Med Sci | 2021 |
| Long noncoding RNA HBBP1 enhances γ-globin expression through the ETS transcription factor ELK1. | Ma SP, Xi HR, Gao XX, Yang JM, Kurita R, Nakamura Y, Song XM, Chen HY, Lu DR | Biochem Biophys Res Commun | 2021 |
| Benserazide racemate and enantiomers induce fetal globin gene expression in vivo: Studies to guide clinical development for beta thalassemia and sickle cell disease. | Pace BS, Perrine S, Li B, Makala L, Xu H, Takezaki M, Wolf RF, Wang A, Xu X, Huang J, Alimardanov A, Tawa GJ, Sangerman J, Faller A, Zheng W, Toney L, Haugabook SJ | Blood Cells Mol Dis | 2021 |
| A pause in gene therapy: Reflecting on the unique challenges of sickle cell disease. | Leonard A, Tisdale JF | Mol Ther | 2021 |
| The Crisis of Sickle Cell Disease in Africa from Insights into Primary Prevention in Ghana and Nigeria: Notes from the Field. | Ezenwa MO, Dennis-Antwi JA, Dallas CM, Amarachukwu C, Ezema CI, Yao Y, Gallo AM, Wilkie DJ | J Immigr Minor Health | 2021 |
| The comfort ability program for adolescents with sickle cell pain: Evaluating feasibility and acceptability of an inpatient group-based clinical implementation. | Sil S, Lee JL, Klosky J, Vaz A, Mee L, Cochran S, Thompson B, Coakley R | Pediatr Blood Cancer | 2021 |
| Implementation of near-universal hydroxyurea uptake among children with sickle cell anemia: A single-center experience. | Karkoska K, Todd K, Niss O, Clapp K, Fenchel L, Kalfa TA, Malik P, Quinn CT, Ware RE, McGann PT | Pediatr Blood Cancer | 2021 |
| Sickle cell disease and ventricular myocardial strain: A systematic review. | Whipple NS, Joshi VM, Naik RJ, Mentnech T, McFarland MM, Nolan VG, Hankins JS | Pediatr Blood Cancer | 2021 |
| Red blood cell mannoses as phagocytic ligands mediating both sickle cell anaemia and malaria resistance. | Cao H, Antonopoulos A, Henderson S, Wassall H, Brewin J, Masson A, Shepherd J, Konieczny G, Patel B, Williams ML, Davie A, Forrester MA, Hall L, Minter B, Tampakis D, Moss M, Lennon C, Pickford W, Erwig L, Robertson B, Dell A, Brown GD, Wilson HM, Rees DC, Haslam SM, Alexandra Rowe J, Barker RN, Vickers MA | Nat Commun | 2021 |
| Impact of COVID-19 on vasooclusive crisis in patients with sickle cell anaemia. | Alkindi S, Elsadek RA, Al-Madhani A, Al-Musalhi M, AlKindi SY, Al-Khadouri G, Al Rawahi B, Al-Ruqeishi S, Al-Yazeedi J, Wali YA, Al Shamakhi S, Al Rawahi M, Pathare AV | Int J Infect Dis | 2021 |
| Novel retinal findings in β-thalassemia major: older age and higher ferritin level as the risk factors. | Kurnia KH, Elvioza , Sidik M, Sari TT, Prihartono J, Sitorus RS | Graefes Arch Clin Exp Ophthalmol | 2021 |
| Gene replacement of α-globin with β-globin restores hemoglobin balance in β-thalassemia-derived hematopoietic stem and progenitor cells. | Cromer MK, Camarena J, Martin RM, Lesch BJ, Vakulskas CA, Bode NM, Kurgan G, Collingwood MA, Rettig GR, Behlke MA, Lemgart VT, Zhang Y, Goyal A, Zhao F, Ponce E, Srifa W, Bak RO, Uchida N, Majeti R, Sheehan VA, Tisdale JF, Dever DP, Porteus MH | Nat Med | 2021 |
| The value of the red cell distribution width index versus other parameters in the differentiation between iron deficiency anemia and beta thalassemia trait among children in Mosul, Iraq. | Al-Numan AH, Al-Obeidi RA | Expert Rev Hematol | 2021 |
| Epigenetic inactivation of ERF reactivates γ-globin expression in β-thalassemia. | Bao X, Zhang X, Wang L, Wang Z, Huang J, Zhang Q, Ye Y, Liu Y, Chen D, Zuo Y, Liu Q, Xu P, Huang B, Fang J, Lao J, Feng X, Li Y, Kurita R, Nakamura Y, Yu W, Ju C, Huang C, Mohandas N, Li D, Zhao C, Xu X | Am J Hum Genet | 2021 |
| Descriptive analysis of sickle cell patients living in France: The PHEDRE cross-sectional study. | Gerardin M, Rousselet M, Couec ML, Masseau A, Guerlais M, Authier N, Deheul S, Roussin A, Micallef J, Djezzar S, , Feuillet F, Jolliet P, Victorri-Vigneau C | PLoS One | 2021 |
| Clinical Guideline Highlights for the Hospitalist: Management of Acute and Chronic Pain in Sickle Cell Disease. | Pham CD, Hua DT | J Hosp Med | 2021 |
| Molecular and Hematological Analysis of Alpha- and Beta-Thalassemia in a Cohort of Mexican Patients. | Rizo-de la Torre LDC, Rentería-López VM, Sánchez-López JY, Magaña-Torres MT, Ibarra-Cortés B, Perea-Díaz FJ | Genet Test Mol Biomarkers | 2021 |
| Characterization and identification of Prachinburi β -thalassemia: A novel-60 kb deletion in beta globin gene related to high levels of Hb F in heterozygous state. | Jomoui W, Tepakhan W | Int J Lab Hematol | 2021 |
| Relation of Serum Ferritin Level with Serum Hepcidin and Fucose Levels in Children with β-Thalassemia Major. | Al-Zuhairy SH, Darweesh MA, Othman MA | Hemoglobin | 2021 |
| Iatrogenic arteriovenous fistula in patient with sickle cell disease undergoing red blood cell exchange. | Guarente J, Palladino M, Babariya S, Hayes C, Blumhof B, Peedin AR, Karp JK | Transfusion | 2021 |
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| Gross and radiographic appearance of porotic hyperostosis and cribra orbitalia in thalassemia affected skulls. | Chaichun A, Yurasakpong L, Suwannakhan A, Iamsaard S, Arun S, Chaiyamoon A | Anat Cell Biol | 2021 |
| Nutritional perspectives on sickle cell disease in Africa: a systematic review. | Nartey EB, Spector J, Adu-Afarwuah S, Jones CL, Jackson A, Ohemeng A, Shah R, Koryo-Dabrah A, Kuma AB, Hyacinth HI, Steiner-Asiedu M | BMC Nutr | 2021 |
| Silent cerebral infarcts in sickle cell disease: Really silent? | Garnier-Crussard A, Cotton F, Desestret V, Krolak-Salmon P, Fort R | J Neuroradiol | 2021 |
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| Insight of fetal to adult hemoglobin switch: Genetic modulators and therapeutic targets. | Hariharan P, Nadkarni A | Blood Rev | 2021 |
| Effects of a positive thinking program on hope and sleep quality in Iranian patients with thalassemia: a randomized clinical trial. | Makaremnia S, Dehghan Manshadi M, Khademian Z | BMC Psychol | 2021 |
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| Mitochondrial reactive oxygen species scavenging attenuates thrombus formation in a murine model of sickle cell disease. | Annarapu G, Nolfi-Donegan D, Reynolds M, Wang Y, Shiva S | J Thromb Haemost | 2021 |
| Prophylactic antibiotics for preventing pneumococcal infection in children with sickle cell disease. | Rankine-Mullings AE, Owusu-Ofori S | Cochrane Database Syst Rev | 2021 |
| Assessment of cystatin C in pediatric sickle cell disease and β-thalassemia as a marker of subclinical cardiovascular dysfunction: a case-control study. | Hanna D, Beshir M, Khalifa N, Baz E, Elhewala A | Pediatr Hematol Oncol | 2021 |
| Vasculo-toxic and pro-inflammatory action of unbound haemoglobin, haem and iron in transfusion-dependent patients with haemolytic anaemias. | Vinchi F, Sparla R, Passos ST, Sharma R, Vance SZ, Zreid HS, Juaidi H, Manwani D, Yazdanbakhsh K, Nandi V, Silva AMN, Agarvas AR, Fibach E, Belcher JD, Vercellotti GM, Ghoti H, Muckenthaler MU | Br J Haematol | 2021 |
| Pain-Related Injustice Appraisals in Youth with Sickle Cell Disease: A Preliminary Investigation. | Miller MM, Rumble DD, Hirsh AT, Vervoort T, Crosby LE, Madan-Swain A, Lebensburger J, Hood AM, Trost Z | Pain Med | 2021 |
| Professionally responsible management of the ethical and social challenges of antenatal screening and diagnosis of β-thalassemia in a high-risk population. | Corda V, Murgia F, Dessolis F, Murru S, Chervenak FA, McCullough LB, Monni G | J Perinat Med | 2021 |
| Pseudothrombocytosis in a Case of Beta-thalassaemia Intermedia Masquerading as Myeloproliferative Neoplasm. | Purohit AHL, Bharti S, Kumar D, Bohra GK, Khichar S | Curr Med Imaging | 2021 |
| Calibration of T oximetry MRI for subjects with sickle cell disease. | Bush A, Vu C, Choi S, Borzage M, Miao X, Li W, Qin Q, Nederveen AJ, Coates TD, Wood JC | Magn Reson Med | 2021 |
| Cardiac pathophysiology in sickle cell disease. | Gbotosho OT, Taylor M, Malik P | J Thromb Thrombolysis | 2021 |
| The Impact of Environmental Factors on Monogenic Mendelian Diseases. | Tukker AM, Royal CD, Bowman AB, McAllister KA | Toxicol Sci | 2021 |
| Oxidative status in the β-thalassemia syndromes in Sri Lanka; a cross-sectional survey. | Allen A, Perera S, Mettananda S, Rodrigo R, Perera L, Darshana T, Moggach F, Jackson Crawford A, Heirene L, Fisher C, Olivieri N, Rees D, Premawardhena A, Allen S | Free Radic Biol Med | 2021 |
| Anti-sickling activities of two isolated compounds from the root of Combretum racemosum P. beauv. (Combretaceae). | Famojuro TI, Adeyemi AA, Ajayi TO, Fasola FA, Fukushi Y, Omotade OO, Moody JO | J Ethnopharmacol | 2021 |
| Hb Maruchi [α165 (E14) Ala>Pro; HBA1: c.196G>C]: A new thalassemia hemoglobinopathy related to the alpha1 globin gene. | Ropero P, M Nieto J, González Fernández FA, Villegas A, Benavente C | Clin Biochem | 2021 |
| Pituitary Volume and Iron Overload Evaluation by 3T MRI in Thalassemia. | Nayak AM, Choudhari A, Patkar DP, Merchant RH | Indian J Pediatr | 2021 |
| Pain Experiences of Adults With Sickle Cell Disease and Hematopoietic Stem Cell Transplantation: A Qualitative Study. | Abu Al Hamayel N, Waldfogel JM, Hannum SM, Brodsky RA, Bolaños-Meade J, Gamper CJ, Jones RJ, Dy SM | Pain Med | 2021 |
| Nephrotic syndrome on sickle cell disease: the impact of Hydroxyurea. | Cunha M, Simão C, Ferrão A, Palaré MJ | BMJ Case Rep | 2021 |
| Lysophosphatidic Acid-Activated Calcium Signaling Is Elevated in Red Cells from Sickle Cell Disease Patients. | Wang J, Hertz L, Ruppenthal S, El Nemer W, Connes P, Goede JS, Bogdanova A, Birnbaumer L, Kaestner L | Cells | 2021 |
| Automated Red Cell Exchange in the Management of Sickle Cell Disease. | Tsitsikas DA, Badle S, Hall R, Meenan J, Bello-Sanyaolu O, Orebayo F, Abukar J, Elmi M, Mulla A, Dave S, Lewis N, Sharma M, Chatterjee B, Amos RJ | J Clin Med | 2021 |
| and Its Virulence Factors HO and Pneumolysin Are Potent Mediators of the Acute Chest Syndrome in Sickle Cell Disease. | Gonzales J, Chakraborty T, Romero M, Mraheil MA, Kutlar A, Pace B, Lucas R | Toxins (Basel) | 2021 |
| Sickle Cell Disease: Role of Oxidative Stress and Antioxidant Therapy. | Vona R, Sposi NM, Mattia L, Gambardella L, Straface E, Pietraforte D | Antioxidants (Basel) | 2021 |
| Variability of Prognostic Results Based on Biological Parameters in Sickle Cell Disease Cohort Studies in Children: What Should Clinicians Know? | Sommet J, Roux EL, Koehl B, Haouari Z, Mohamed D, Baruchel A, Benkerrou M, Alberti C | Children (Basel) | 2021 |
| Mechanisms of Bone Impairment in Sickle Bone Disease. | Giordano P, Urbano F, Lassandro G, Faienza MF | Int J Environ Res Public Health | 2021 |
| Characterization and statistical modeling of glycosylation changes in sickle cell disease. | Ashwood HE, Ashwood C, Schmidt AP, Gundry RL, Hoffmeister KM, Anani WQ | Blood Adv | 2021 |
| Methylenetetrahydrofolate reductase polymorphisms as genetic markers to predict homocysteinemia and clinical severity in sickle cell disease. | Patel S, Nanda R, Hussain N, Mohapatra E, Patra PK | Biomark Med | 2021 |
| Persistence of CRISPR/Cas9 gene edited hematopoietic stem cells following transplantation: A systematic review and meta-analysis of preclinical studies. | Maganti HB, Bailey AJM, Kirkham AM, Shorr R, Pineault N, Allan DS | Stem Cells Transl Med | 2021 |
| Determinants of Care-Seeking Practices for Children with Sickle Cell Disease in Ekiti, Southwest Nigeria. | Olatunya OS, Babatola AO, Adeniyi AT, Lawal OA, Daramola AO, Agbesanwa TA, Olumuyiwa Ojo T, Ajayi PO, Ibijola AA, Komolafe AK, Adekile A | J Blood Med | 2021 |
| Distinct effects of V617F and exon12-mutated JAK2 expressions on erythropoiesis in a human induced pluripotent stem cell (iPSC)-based model. | Nilsri N, Jangprasert P, Pawinwongchai J, Israsena N, Rojnuckarin P | Sci Rep | 2021 |
| Hyperhemolysis Syndrome in a Patient With Sickle Cell Disease and Acute Chest Syndrome. | Shankar K, Shah D, Huffman DL, Peterson C, Bhagavatula R | Cureus | 2021 |
| Luspatercept: A Gigantic Step in the Treatment of Transfusion-Dependent β-Thalassemia Patients-a Quick Review. | Darvishi-Khezri H, Karami H | Adv Ther | 2021 |
| MetAP2 inhibition modifies hemoglobin S to delay polymerization and improves blood flow in sickle cell disease. | Demers M, Sturtevant S, Guertin KR, Gupta D, Desai K, Vieira BF, Li W, Hicks A, Ismail A, Gonçalves BP, Di Caprio G, Schonbrun E, Hansen S, Musayev FN, Safo MK, Wood DK, Higgins JM, Light DR | Blood Adv | 2021 |
| Sickle cell disease, interleukin-18, and arrhythmias. | Zhabyeyev P, Oudit GY | Blood | 2021 |
| Circulating mitochondrial DNA is a proinflammatory DAMP in sickle cell disease. | Tumburu L, Ghosh-Choudhary S, Seifuddin FT, Barbu EA, Yang S, Ahmad MM, Wilkins LHW, Tunc I, Sivakumar I, Nichols JS, Dagur PK, Yang S, Almeida LEF, Quezado ZMN, Combs CA, Lindberg E, Bleck CKE, Zhu J, Shet AS, Chung JH, Pirooznia M, Thein SL | Blood | 2021 |
| Is Busulfan Clearance Different in Patients With Sickle Cell Disease? Let's Clear Up That Case With Some Controls. | Remy A, Théorêt Y, Ansari M, Bittencourt H, Ducruet T, Nava T, Pastore Y, Rezgui MA, Krajinovic M, Kleiber N | J Pediatr Hematol Oncol | 2021 |
| A pilot study of the effect of rivaroxaban in sickle cell anemia. | Ataga KI, Elsherif L, Wichlan D, Wogu AF, Matsui N, Pawlinski R, Cai J, Key NS | Transfusion | 2021 |
| Therapeutic drug monitoring of intravenous busulfan in Thai children undergoing hematopoietic stem cell transplantation: A pilot study. | Jansing T, Sanpakit K, Tharnpanich T, Jiranantakan T, Niphandwongkorn V, Chindavijak B, Suansanae T | Pediatr Hematol Oncol | 2021 |
| Prevalence and association of malaria with ABO blood group and hemoglobin level in individuals visiting Mekaneeyesus Primary Hospital, Estie District, northwest Ethiopia: a cross-sectional study. | Tazebew B, Munshea A, Nibret E | Parasitol Res | 2021 |
| Perspectives on Building Sustainable Newborn Screening Programs for Sickle Cell Disease: Experience from Tanzania. | Bukini D, Nkya S, McCurdy S, Mbekenga C, Manji K, Parker M, Makani J | Int J Neonatal Screen | 2021 |
| A rare complex rearrangement in the β-globin gene cluster causing a novel homozygous γ( γδβ) -thalassemia. | Zhang X, Yang Y, Zhang H, Du Z, Liu H, Shen Y | Am J Hematol | 2021 |
| American Society of Hematology 2020 Podcast Collection: Sickle Cell Anaemia. | Russo G, Colombatti R | Adv Ther | 2021 |
| Whole-blood phenotyping to assess alloimmunization status in transfused sickle cell disease patients. | Tamagne M, Pakdaman S, Bartolucci P, Habibi A, Galactéros F, Pirenne F, Vingert B | Blood Adv | 2021 |
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| Intravenous Acetaminophen vs Intravenous Diclofenac Sodium in Management of Skeletal Vaso-occlusive Crisis Among Children with Homozygous Sickle Cell Disease: A Randomized Controlled Trial. | Panda PC, Mishra NR, Patra CS, Nayak BK, Panda SK | Indian Pediatr | 2021 |
| Improving access to healthcare for paediatric sickle cell disease patients: a qualitative study on healthcare professionals' views. | Houwing ME, Buddenbaum M, Verheul TCJ, de Pagter APJ, Philipsen JNJ, Hazelzet JA, Cnossen MH | BMC Health Serv Res | 2021 |
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| A Pragmatic Scoring Tool to Predict Hydroxyurea Response Among β-Thalassemia Major Patients in Pakistan. | Ansari SH, Hussain Z, Zohaib M, Parveen S, Kaleem B, Qamar H, Adil O, Khan MT, Shamsi TS | J Pediatr Hematol Oncol | 2021 |
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| Regarding chronic graft-versus-host disease in children and adolescents with thalassemia after hematopoietic stem cell transplantation. | Janowiak-Majeranowska A, Majeranowski A | Int J Hematol | 2021 |
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| Decreased activity and stability of pyruvate kinase in sickle cell disease: a novel target for mitapivat therapy. | Rab MAE, Bos J, van Oirschot BA, van Straaten S, Kosinski PA, Chubukov V, Kim H, Mangus H, Schutgens REG, Pasterkamp G, Dang L, Kung C, van Beers EJ, van Wijk R | Blood | 2021 |
| PIEZO1 and the mechanism of the long circulatory longevity of human red blood cells. | Rogers S, Lew VL | PLoS Comput Biol | 2021 |
| Allele-Specific Recombinase Polymerase Amplification to Detect Sickle Cell Disease in Low-Resource Settings. | Natoli ME, Chang MM, Kundrod KA, Coole JB, Airewele GE, Tubman VN, Richards-Kortum RR | Anal Chem | 2021 |
| Compound Heterozygote Hemoglobin Lepore-Baltimore Haplotype with β-Thalassemia. | Dixit S, Das H, Bal M, Khuntia HK, Ranjit M | Indian J Pediatr | 2021 |
| A Novel Frameshift Mutation, Deletion of HBB:c.199_202delAAAG [Codon 66/67 (-AAAG)] in β-Thalassemia Major Patients from the Western Region of Uttar Pradesh, India. | Chauhan W, Afzal M, Zaka-Ur-Rab Z, Noorani MS | Appl Clin Genet | 2021 |
| Severe Acute Chest Syndrome in a Sickle Cell Patient That Required Repeated Exchange Transfusion. | Saleh M, Asemota J | Cureus | 2021 |
| A novel deletion of the major regulatory element flanking the α-globin gene cluster as a cause of α -thalassemia. | Jiang F, Xu LL, Tang XW, Li DZ | Int J Lab Hematol | 2021 |
| The impact of vaso-occlusive crises and disease severity on quality of life and productivity among patients with sickle cell disease in the US. | Shafrin J, Thom HHZ, Keeney E, Gaunt DM, Zhao LM, Bhor M, Rizio AA, Bronté-Hall L, Shah N | Curr Med Res Opin | 2021 |
| Association between left ventricular strain and cardiac iron load in beta-thalassaemia major: a cardiac magnetic resonance study. | Alis D, Asmakutlu O, Topel C, Sahin AA, Karaarslan E | Acta Cardiol | 2021 |
| Pregnancy outcome in homozygous sickle cell disease: observations from the Jamaican Birth Cohort. | Lewis G, Thame M, Howitt C, Hambleton I, Serjeant GR | BJOG | 2021 |
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| Hydroxyurea Adherence Strategies for Persons with Sickle Cell Disease: A Systematic Review. | Vick L, Potts M, Jaskowiak M, Gibson RW | J Health Care Poor Underserved | 2021 |
| An extensive review to facilitate understanding of CRISPR technology as a gene editing possibility for enhanced therapeutic applications. | Rautela I, Uniyal P, Thapliyal P, Chauhan N, Bhushan Sinha V, Dev Sharma M | Gene | 2021 |
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| Mild α-Thalassemia Caused by a Mosaic α-Globin Gene Mutation. | Wang RY, Jiang F, Xu LL, Li DZ | Hemoglobin | 2021 |
| Dual-energy CT evidence of pulmonary microvascular occlusion in patients with sickle cell disease experiencing acute chest syndrome. | Dako F, Hossain R, Jeudy J, White C | Clin Imaging | 2021 |
| Gene Therapies for Transfusion-Dependent b-Thalassemia. | Soni S | Indian Pediatr | 2021 |
| Pubertal Development and its Determinants in Adolescents With Transfusion-Dependent Thalassemia. | Singh P, Samaddar S, Parakh N, Chandra J, Seth A | Indian Pediatr | 2021 |
| Vitamin C Deficiency and Oxidant Levels in Children With Transfusion-Dependent b-Thalassemia. | Bhat KV, Sharma RA, Sharma SM, Joshi P, Dias BF, Shah N, Setia M, Manglani MV | Indian Pediatr | 2021 |
| Correlation of dynamic membrane fluctuations in red blood cells with diabetes mellitus and cardiovascular risks. | Sohn M, Lee JE, Ahn M, Park Y, Lim S | Sci Rep | 2021 |
| Spontaneous osteonecrosis of the jaw in a β-Thalassemia intermedia patient. | Shi HA, Teo GN, Qiqi L, Tan BPD | J Stomatol Oral Maxillofac Surg | 2021 |
| Pulmonary thromboendarterectomy for pulmonary hypertension linked to thalassemia. | Izzat MB, Aljasem H, Izzat AW | Clin Case Rep | 2021 |
| COVID-19 pneumonia in a pediatric sickle cell patient requiring red blood cell exchange. | Walker SC, Murphy ML, Hendricks H, Dulek DE, Volanakis EJ, Borinstein SC | Clin Case Rep | 2021 |
| Hydroxyurea Use Among Children With Sickle Cell Disease at King Abdulaziz University Hospital in Jeddah City. | Alzahrani F, Albaz GF, AlSinan F, Alzuhayri J, Barnawi ZM, Melebari N, Al Twairgi TM | Cureus | 2021 |
| β-Hemoglobinopathies lead the way. | Saunthararajah Y | Blood | 2021 |
| Memory CD8 T cell compartment associated with delayed onset of infection and better parasite control in sickle-cell trait children. | Loiseau C, Traore B, Ongoiba A, Kayentao K, Doumbo S, Doumtabe D, de Sousa KP, Brady JL, Proietti C, Crompton PD, Doolan DL | Clin Transl Immunology | 2021 |
| Agonistic Anti-CD40 Antibody Triggers an Acute Liver Crisis With Systemic Inflammation in Humanized Sickle Cell Disease Mice. | Yalamanoglu A, Dubach IL, Schulthess N, Ingoglia G, Swindle DC, Humar R, Schaer DJ, Buehler PW, Irwin DC, Vallelian F | Front Immunol | 2021 |
| Opioids are not a major cause of death of patients with sickle cell disease. | Ballas SK | Ann Hematol | 2021 |
| Commentary: Extramedullary hematopoiesis in the facial sinus, is it the time to search actively for it in some patients with thalassemia intermedia? | Ricchi P | Eur Rev Med Pharmacol Sci | 2021 |
| Deficient mitophagy pathways in sickle cell disease. | Martino S, Arlet JB, Odièvre MH, Jullien V, Moras M, Hattab C, Lefebvre T, Gouya L, Ostuni MA, Lefevre SD, Le Van Kim C | Br J Haematol | 2021 |
| [Transfusions in pediatric care - common situations]. | Deschmann E, Andersson A, Frisk T, Magnusson M | Lakartidningen | 2021 |
| A Cross-Sectional Study of Detection of Beta Globin (HBB) Haplotypes Among Beta Thalassemia Patients. | Alsamiri A, Alzahrani F, Filimban N, Khojah A, Felimban R, Qadah T | Cureus | 2021 |
| Free Tissue Transfer in a Patient With Hemoglobin S-Beta-Thalassemia Disease and Mandibular Osteomyelitis. | Chang K, Bollig C, Sclaroff A, Pipkorn P | Otolaryngol Head Neck Surg | 2021 |
| Kneeling Was the First Step for Sickle Cell Disease. | Desai P, Little J, Kanter J, Bridges K, Andemariam B, Lanzkron S | Ann Intern Med | 2021 |
| A Budget Impact Analysis of Gene Therapy for Sickle Cell Disease: The Medicaid Perspective. | DeMartino P, Haag MB, Hersh AR, Caughey AB, Roth JA | JAMA Pediatr | 2021 |
| Gene Therapy for Sickle Cell Disease-A Debt to Be Paid. | Ozuah PO | JAMA Pediatr | 2021 |
| Safety and efficacy of deferasirox in patients with transfusion-dependent thalassemia: A 4-year single-center experience. | Zengin Ersoy G, Ayçiçek A, Odaman Al I, Bayram C, Arslantaş E, Özdemir GN, Uysalol EP, Şalcıoğlu Z, Akıcı F, Aydoğan G | Pediatr Hematol Oncol | 2021 |
| Association between carriers of the G allele of the + 45T> G variant of the ADIPOQ gene () and the cardiometabolic profile in sickle cell trait. | Bruno JB, Dal Ponte ES, Retamoso V, Maurer P, Berro LF, Manfredini V, da Costa Escobar Piccoli J | Heliyon | 2021 |
| Impact of oral -arginine supplementation on blood pressure dynamics in children with severe sickle cell vaso-occlusive crisis. | Onalo R, Cilliers A, Cooper P | Am J Cardiovasc Dis | 2021 |
| Evaluation of iron overload by cardiac and liver T2* in β-thalassemia: Correlation with serum ferritin, heart function and liver enzymes. | Khadivi Heris H, Nejati B, Rezazadeh K, Sate H, Dolatkhah R, Ghoreishi Z, Esfahani A | J Cardiovasc Thorac Res | 2021 |
| Pathophysiological Relevance of Renal Medullary Conditions on the Behaviour of Red Cells From Patients With Sickle Cell Anaemia. | Lu DC, Wadud R, Hannemann A, Rees DC, Brewin JN, Gibson JS | Front Physiol | 2021 |
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| The effect of endothelial Nitric Oxide Synthase G894T and T786C polymorphisms on Hypoxia-Inducible Factor-1 alpha expression in Sickle Cell Disease. | Armenis I, Kalotychou V, Tzanetea R, Konstantopoulos K, Rombos I | Nitric Oxide | 2021 |
| Experience with combination of hydroxyurea and low-dose thalidomide in transfusion-dependent beta thalassemia patients. | Bhurani D, Kapoor J, Yadav N, Khushoo V, Agrawal N, Ahmed R, Arora JS, Mehta P | Ann Hematol | 2021 |
| Distinct miRNA Signatures and Networks Discern Fetal from Adult Erythroid Differentiation and Primary from Immortalized Erythroid Cells. | Papasavva PL, Papaioannou NY, Patsali P, Kurita R, Nakamura Y, Sitarou M, Christou S, Kleanthous M, Lederer CW | Int J Mol Sci | 2021 |
| Proteome of Stored RBC Membrane and Vesicles from Heterozygous Beta Thalassemia Donors. | Tzounakas VL, Anastasiadi AT, Dzieciatkowska M, Karadimas DG, Stamoulis K, Papassideri IS, Hansen KC, D'Alessandro A, Kriebardis AG, Antonelou MH | Int J Mol Sci | 2021 |
| Telomere shortening correlates with disease severity in hemoglobin H disease patients. | Panjawatanan P, Charoenkwan P, Tantiworawit A, Strogatz D, Perry KE, Tuntiwechapikul W | Blood Cells Mol Dis | 2021 |
| Fluorescence spectroscopy as a novel technique for premarital screening of sickle cell disorders. | Devanesan S, AlSalhi MS, Masilamani V, Alqahtany F, Rajasekar A, Alenazi A, Farhat K | Photodiagnosis Photodyn Ther | 2021 |
| Response to: Acute Liver Failure in a Sickle Cell Patient. | Rizvi SA, Pandey A | J Pediatr Gastroenterol Nutr | 2021 |
| Acute Liver Failure in a Sickle Cell Patient. | Maji P, Malik R | J Pediatr Gastroenterol Nutr | 2021 |
| Voxelotor: alteration of sickle cell disease pathophysiology by a first-in-class polymerization inhibitor. | Glaros AK, Razvi R, Shah N, Zaidi AU | Ther Adv Hematol | 2021 |
| Improvement of SCD morbimortality in children: experience in a remote area of an African country. | Mbiya BM, Kalombo DK, Mukendi YN, Daubie V, Mpoyi JK, Biboyi PM, Disashi GT, Gulbis B | BMC Health Serv Res | 2021 |
| Sickle cell vaso-occlusion: The dialectic between red cells and white cells. | Conran N, Embury SH | Exp Biol Med (Maywood) | 2021 |
| Vasculopathy in Sickle Cell Disease: From Red Blood Cell Sickling to Vascular Dysfunction. | Nader E, Conran N, Romana M, Connes P | Compr Physiol | 2021 |
| Report of Two Novel Thalassemia Variants, : c.181delG and : c.121_126delAAGACC, in Chinese Individuals. | Chen X, Lin Z, Hu J, Chen S, Wen S, Wu A, Wu H, Huang J, Wang H, Sun J, Peng Z, Sun Y, Fu S | Hemoglobin | 2021 |
| Identification of Two Novel Thalassemia Variants, : c.263delA and : c.376dupC, in Chinese Individuals. | Liu L, Sun Y, Chen S, Yu C, Cao P, Sun J, Peng Z, Mao P | Hemoglobin | 2021 |
| One third of alloantibodies in patients with sickle cell disease transfused with African blood are missed by the standard red blood cell test panel. | Boateng LA, Schonewille H, Ligthart PC, Javadi A, Veldhuisen B, Osei-Akoto A, Dei-Adomakoh Y, Bates I, Van der Schoot CE | Haematologica | 2021 |
| Red cell transfusion and alloimmunization in sickle cell disease. | Linder GE, Chou ST | Haematologica | 2021 |
| A Comparative Evaluation of Capillary Electrophoresis, Cation-Exchange High-Performance Liquid Chromatography, and Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry for the Screening of Hemoglobin Variants. | Xu M, Wang Y, Xu A | Am J Clin Pathol | 2021 |
| Feasibility Study of the | Kakou Danho JB, Atiméré YN, Koné D, Yéo DD, Couitchéré L | Adv Hematol | 2021 |
| Investigations of Kidney Dysfunction-Related Gene Variants in Sickle Cell Disease Patients in Cameroon (Sub-Saharan Africa). | Ngo-Bitoungui VJ, Belinga S, Mnika K, Masekoameng T, Nembaware V, Essomba RG, Ngo-Sack F, Awandare G, Mazandu GK, Wonkam A | Front Genet | 2021 |
| How Do Red Blood Cells Die? | Thiagarajan P, Parker CJ, Prchal JT | Front Physiol | 2021 |
| Associations between TGF-1 Levels and Markers of Hemolysis, Inflammation, and Tissue Remodeling in Pediatric Sickle Cell Patients. | Santiago RP, Carvalho MOS, Figueiredo CVB, Fiuza LM, Oliveira RM, Yahouédéhou SCMA, Nascimento VML, Lyra IM, Araujo-Santos T, Luz NF, Aleluia MM, Guarda CC, Borges VM, Goncalves MS | Mediators Inflamm | 2021 |
| Complement in Sickle Cell Disease: Are We Ready for Prime Time? | Varelas C, Tampaki A, Sakellari I, Anagnostopoulos Α, Gavriilaki E, Vlachaki E | J Blood Med | 2021 |
| A systematic review of ketamine for the management of vaso-occlusive pain in sickle cell disease. | Harris EM, Vilk E, Heeney MM, Solodiuk J, Greco C, Archer NM | Pediatr Blood Cancer | 2021 |
| Hydroxyurea in children with sickle cell disease in a resource-poor setting: Monitoring and effects of therapy. A practical perspective. | Nnebe-Agumadu U, Adebayo I, Erigbuem I, James E, Kumode E, Nnodu O, Adekile A | Pediatr Blood Cancer | 2021 |
| Monitoring retinal pathology and cerebral injury in sickle cell disease using spectral-domain optical coherence tomography in pediatric patients. | Jin J, Kandula V, Miller RE | Pediatr Blood Cancer | 2021 |
| Epigenetic effects toward new insights as potential therapeutic target in B-thalassemia. | Eltaweel NH, ElKamah GY, Khairat R, Atia HAE, Amr KS | J Genet Eng Biotechnol | 2021 |
| Evidence for Prophylactic Transfusion during Pregnancy for Women with Sickle Cell Disease. | Whittington JR, Magann EF, Ounpraseuth ST, Chang JN, Whitcombe DD, Morrison JC | South Med J | 2021 |
| Cerebral Hemodynamics and Executive Function in Sickle Cell Anemia. | Prussien KV, Compas BE, Siciliano RE, Ciriegio AE, Lee CA, Kassim AA, DeBaun MR, Donahue MJ, Jordan LC | Stroke | 2021 |
| Will the changing therapeutic landscape meet the needs of patients with sickle cell disease? | Inusa BPD, Casale M, Campbell A, Archer N | Lancet Haematol | 2021 |
| RE: re: manuscript titled, | Felli E, Felli E, Muttillo EM, Memeo R, Giannelli V, Colasanti M, Pellicelli A, Diana M, Ettorre GM | HPB (Oxford) | 2021 |
| A Qualitative Analysis of State Medicaid Coverage Benefits for Allogeneic Hematopoietic Cell Transplantation (alloHCT) for Patients with Sickle Cell Disease (SCD). | Mupfudze TG, Preussler JM, Sees JA, SanCartier M, Arnold SD, Devine S | Transplant Cell Ther | 2021 |
| Gaps in Medicaid Coverage and Financial Toxicity: A Health Disparity in Hematopoietic Cell Transplantation for Sickle Cell Disease. | Krishnamurti L | Transplant Cell Ther | 2021 |
| P-Selectin Blockade in the Treatment of Painful Vaso-Occlusive Crises in Sickle Cell Disease: A Spotlight on Crizanlizumab. | Karki NR, Kutlar A | J Pain Res | 2021 |
| Fifteen-minute consultation: Recognition of sickle cell crises in the paediatric emergency department. | Patel S, Dadnam C, Hewitson R, Thakur I, Morgan J | Arch Dis Child Educ Pract Ed | 2021 |
| NLRP3 inflammasome and bruton tyrosine kinase inhibition interferes with upregulated platelet aggregation and in vitro thrombus formation in sickle cell mice. | Vogel S, Kamimura S, Arora T, Smith ML, Almeida LEF, Combs CA, Thein SL, Quezado ZMN | Biochem Biophys Res Commun | 2021 |
| Surrogate Markers of Subclinical Atherosclerosis and Its Associated Factors in Patients with β-Thalassemia Major. | Soltani D, Fakhrzadeh H, Sharifi F, Mahmoudi MJ, Mahmoudi E, Vasheghani-Farahani A | Hemoglobin | 2021 |
| The Changing Trends in Prenatal Diagnosis of Hemoglobinopathies in India: The Quest of a Single Center to Reduce the Burden of Disease over Three Decades. | Colah RB, Nadkarni AH, Gorakshakar AC, Sawant PM, Mehta PR, Gorivale MS, Hariharan P, Mohanty D, Ghosh K | Hemoglobin | 2021 |
| Dissemination of Evidence-Based Recommendations for Sickle Cell Disease to Primary Care and Emergency Department Providers in North Carolina: A Cost Benefit Analysis. | Tanabe P, Blewer AL, Bonnabeau E, Bosworth HB, Clayton DH, Crego N, Earls MF, Eason K, Forlines G, Rains G, Young M, Shah N | J Health Econ Outcomes Res | 2021 |
| Prevalence and clinical phenotype of the triplicated α-globin genes and its ethnic and geographical distribution in Guizhou of China. | Luo X, Zhang XM, Wu LS, Chen J, Chen Y | BMC Med Genomics | 2021 |
| Haematological abnormalities in children with sickle cell disease and non-severe malaria infection in western Kenya. | Kosiyo P, Otieno W, Gitaka J, Munde EO, Ouma C | BMC Infect Dis | 2021 |
| Central macular thickness in patients with sickle cell disease and no signs of retinopathy: a cross-sectional study of Jordanian patients. | Abu-Yaghi NE, AlNawaiseh AM, Khourshid IM, AlRawashdeh TJ, Rawashdeh MMA, Zghoul AM, Shafagoj AN, Alomairi YA, Muhsen SM, AlRyalat SS | J Int Med Res | 2021 |
| Incorrect Migration of Hemoglobin after Capillary Electrophoresis Software Update Complicates Diagnosis of an Infant with Hemoglobin S/Beta+ Thalassemia. | Manthei DM, Harro DM, Keren DF | J Appl Lab Med | 2021 |
| A Randomized Controlled Trial of Working Memory Training in Pediatric Sickle Cell Disease. | Hardy SJ, Bills SE, Meier ER, Schatz JC, Keridan KJ, Wise S, Hardy KK | J Pediatr Psychol | 2021 |
| Red Blood Cell Exchange in a Patient With Extramedullary Hematopoiesis and Cor Pulmonale Secondary to Beta Thalassemia. | Kopparthy P, Kelkar AH, Aggarwal K, De Filippis S, Fletcher B | Cureus | 2021 |
| Telomere length and telomere repeat-binding protein in children with sickle cell disease. | Suliman ME, Ansari MGA, Rayis MA, Hamza MA, Saeed AA, Mohammed AK, Al-Daghri NM | Pediatr Res | 2021 |
| Hb Murcia (β118(G19)His>Gln): A New Hemoglobin Variant Found in a Spanish Woman. | Fernández BG, Campuzano JBN, Rocamora DG, Nieto JM, Fernández FAG, Villegas A, Cuesta CB, Ropero P | Ann Lab Med | 2021 |
| Depression in adults with sickle cell disease: a systematic review of the methodological issues in assessing prevalence of depression. | Oudin Doglioni D, Chabasseur V, Barbot F, Galactéros F, Gay MC | BMC Psychol | 2021 |
| Single laser trapping for optical folding and rotation of red blood cells in sickle cell disease in response to hydroxyurea treatment. | Mohi SM, Saadon HL, Khalaf AA | Biochem Biophys Res Commun | 2021 |
| Compound heterozygotes of Hb Constant Spring and Hb Stanleyville II in HbE/β-thalassemia. | Chen L, Liang L, Liao S, Huang Y, Liang L, Li Y | Clin Chem Lab Med | 2021 |
| The pyruvate kinase activator mitapivat reduces hemolysis and improves anemia in a β-thalassemia mouse model. | Matte A, Federti E, Kung C, Kosinski PA, Narayanaswamy R, Russo R, Federico G, Carlomagno F, Desbats MA, Salviati L, Leboeuf C, Valenti MT, Turrini F, Janin A, Yu S, Beneduce E, Ronseaux S, Iatcenko I, Dang L, Ganz T, Jung CL, Iolascon A, Brugnara C, De Franceschi L | J Clin Invest | 2021 |
| Hb Bart's Hydrops Fetalis Syndrome and Hb H Disease Caused by Deletional Chiang Rai (- -) α-Thalassemia in Two Unrelated Thai Families. | Ruengdit C, Khamphikham P, Jinorose N, Pornprasert S | Hemoglobin | 2021 |
| Is sickle cell disease a risk factor for severe COVID-19 outcomes in hospitalized patients? A multicenter national retrospective cohort study. | Abdulrahman A, Wael M, AlAmmadi F, Almosawi Z, Alsherooqi R, Abduljalil M, Kumar N, AlQahtani M | EJHaem | 2021 |
| Sickle haemoglobin: How critical are laboratory quality measures for accurate identification? | Sana N, Shaikh MS | J Pak Med Assoc | 2021 |
| Cas9 protein delivery non-integrating lentiviral vectors for gene correction in sickle cell disease. | Uchida N, Drysdale CM, Nassehi T, Gamer J, Yapundich M, DiNicola J, Shibata Y, Hinds M, Gudmundsdottir B, Haro-Mora JJ, Demirci S, Tisdale JF | Mol Ther Methods Clin Dev | 2021 |
| Editorial: Frontiers in Hemoglobinopathies: New Insights and Methods. | Risoluti R, Colah R, Materazzi S | Front Mol Biosci | 2021 |
| Exercise-induced haemoglobin oxygen desaturation in patients with SCD. | Antwi-Boasiako C, Asare CP, Afriyie-Mensah JS, Hayfron-Benjamin C, Nuako I, Aryee R, Dankwah GB, Asare MM, Adutwum-Ofosu K | Am J Cardiovasc Dis | 2021 |
| Qualitative and quantitative magnetic resonance imaging evaluation of bone tissue vaso-occlusive events in patients with sickle cell disease. | Lins CF, Salmon CEG, de Souza LA, Moraes RS, Silva-Pinto AC, Matos MA, Nogueira-Barbosa MH | Bone | 2021 |
| Utilization of Discriminant Formulas in the Differentiation of Alpha Thalassemia, Beta Thalassemia, and Iron Deficiency in Premarital Setting. | Saboor M | Clin Lab | 2021 |
| Buprenorphine for Chronic Pain in a Pediatric Patient With Sickle-Cell Disease. | Irwin M, Gunther W, Keefer P, Saul D, Singh SA, Wright J, Smith MA | J Pain Symptom Manage | 2021 |
| Frequency of bacteremia in patients with sickle cell disease: a longitudinal study. | Al-Tawfiq JA, Rabaan AA, AlEdreesi MH | Ann Hematol | 2021 |
| Olinciguat, a stimulator of soluble guanylyl cyclase, attenuates inflammation, vaso-occlusion and nephropathy in mouse models of sickle cell disease. | Tchernychev B, Li H, Lee SK, Gao X, Ramanarasimhaiah R, Liu G, Hall KC, Bernier SG, Jones JE, Feil S, Feil R, Buys ES, Graul RM, Frenette PS, Masferrer JL | Br J Pharmacol | 2021 |
| Acute stroke in young adult secondary to moyamoya angiopathy unveiling HbE-β thalassemia. | Das S, Karmakar K, Mukherjee R, Panda S, Dubey S, Sarkar N, Ray BK | Ann Hematol | 2021 |
| Co-morbidities and mortality in patients with sickle cell disease in England: A 10-year cohort analysis using hospital episodes statistics (HES) data. | Piel FB, Jobanputra M, Gallagher M, Weber J, Laird SG, McGahan M | Blood Cells Mol Dis | 2021 |
| The flow of sickle blood in glass capillaries: Fundamentals and potential applications. | Brown CD, Aprelev AM, Aliprando M, Harkness EA, Ferrone FA | Biophys J | 2021 |
| Electronic Health Record-Embedded Individualized Pain Plans for Emergency Department Treatment of Vaso-occlusive Episodes in Adults With Sickle Cell Disease: Protocol for a Preimplementation and Postimplementation Study. | Luo L, King AA, Carroll Y, Baumann AA, Brambilla D, Carpenter CR, Colla J, Gibson RW, Gollan S, Hall G, Klesges L, Kutlar A, Lyon M, Melvin CL, Norell S, Mueller M, Potter MB, Richesson R, Richardson LD, Ryan G, Siewny L, Treadwell M, Zun L, Armstrong-Brown J, Cox L, Tanabe P | JMIR Res Protoc | 2021 |
| Effectiveness of placental volume measured by virtual organ computer-aided analysis in prediction of fetal hemoglobin Bart's disease in late first trimester. | Bootchaingam P, Charoenratana C, Tongsong T, Luewan S | J Clin Ultrasound | 2021 |
| Mapping PedsQL™ Generic Core Scales to EQ-5D-3L utility scores in transfusion-dependent thalassemia patients. | Shafie AA, Chhabra IK, Wong JHY, Mohammed NS | Eur J Health Econ | 2021 |
| Site-Specific Introduction of Negative Charges on the Protein Surface for Improving Global Functions of Recombinant Fetal Hemoglobin. | Kettisen K, Dicko C, Smeds E, Bülow L | Front Mol Biosci | 2021 |
| ZNF410 represses fetal globin by singular control of CHD4. | Vinjamur DS, Yao Q, Cole MA, McGuckin C, Ren C, Zeng J, Hossain M, Luk K, Wolfe SA, Pinello L, Bauer DE | Nat Genet | 2021 |
| Genetic therapies for the first molecular disease. | Doerfler PA, Sharma A, Porter JS, Zheng Y, Tisdale JF, Weiss MJ | J Clin Invest | 2021 |
| Stigma Associated With Sickle Cell Disease in Kumasi, Ghana. | Buser JM, Bakari A, Seidu AA, Paintsil V, Osei-Akoto A, Amoah R, Otoo B, Moyer CA | J Transcult Nurs | 2021 |
| Evaluation of Corneal Epithelial Thickness and Dry Eye Disease Tests in Thalassemic Adolescents. | Ebeid WM, Kenny MA, Badran TA | Clin Ophthalmol | 2021 |
| Patient-controlled analgesia in sickle-cell disease painful vaso-occlusive crises: should we add ketamine to morphine? | Zuccarini F, Aoragh A, Maggiore A, Kapessidou P | Minerva Anestesiol | 2021 |
| Peripartum considerations in sickle cell disease. | Ezihe-Ejiofor A, Jackson J | Curr Opin Anaesthesiol | 2021 |
| Presentation of two new mutations in the 3'untranslated region of the β-globin gene and evaluating the molecular spectrum of thalassemia mutations in the Mediterranean region of Turkey. | Arpaci A, Gul BU, Ozcan O, Ilhan G, El C, Dirican E, Elmacioglu S, Kaya H | Ann Hematol | 2021 |
| Hepatocellular carcinoma in patients with thalassemia in the post-DAA era: not a disappearing entity. | Ricchi P, Costantini S, Spasiano A, Cinque P, Esposito S, Filosa A | Ann Hematol | 2021 |
| The effect of scheduled routine blood transfusions on learning achievement of children with thalassemia: A study from Tangerang District Indonesia. | Sari RS, Rianti , Lutbis AA, Hasanah I | Enferm Clin | 2021 |
| The Potential of mHealth as a Game Changer for the Management of Sickle Cell Disease in India. | Kumar R, Das A | JMIR Mhealth Uhealth | 2021 |
| Social support networks of adults with sickle cell disease. | Desine S, Eskin L, Bonham VL, Koehly LM | J Genet Couns | 2021 |
| Characterizing bulk rigidity of rigid red blood cell populations in sickle-cell disease patients. | Gutierrez M, Shamoun M, Seu KG, Tanski T, Kalfa TA, Eniola-Adefeso O | Sci Rep | 2021 |
| Detection of Renal Insufficiency in a Cohort of Patients With Beta-thalassemia Major Using Cystatin-C. | Hamdy M, Shaheen I, El-Gammal ZM, Ramadan YM | J Pediatr Hematol Oncol | 2021 |
| Hb Hezhou [β64(E8)Gly→Ser; : c.193G>A]: A Novel Variant on the β-Globin Gene. | Zhao YL, Lin QF, He XW, Li YQ, Liang L | Hemoglobin | 2021 |
| The use of expanded carrier screening of gamete donors. | Payne MR, Skytte AB, Harper JC | Hum Reprod | 2021 |
| Sickle Cell Trait Modulates the Proteome and Phosphoproteome of -Infected Erythrocytes. | Chauvet M, Chhuon C, Lipecka J, Dechavanne S, Dechavanne C, Lohezic M, Ortalli M, Pineau D, Ribeil JA, Manceau S, Le Van Kim C, Luty AJF, Migot-Nabias F, Azouzi S, Guerrera IC, Merckx A | Front Cell Infect Microbiol | 2021 |
| Red cell alloantibodies in beta-thalassaemia major patients' blood referring to the regional blood transfusion center of Tehran, Iran. | Ebrahimisadr P, Bakhshandeh Z, Majidiani H | Bioimpacts | 2021 |
| Soluble MD-2 and Heme in Sickle Cell Disease Plasma Promote Pro-Inflammatory Signaling in Endothelial Cells. | Zhang P, Nguyen J, Abdulla F, Nelson AT, Beckman JD, Vercellotti GM, Belcher JD | Front Immunol | 2021 |
| Automated Oxygen Gradient Ektacytometry: A Novel Biomarker in Sickle Cell Anemia. | Sadaf A, Seu KG, Thaman E, Fessler R, Konstantinidis DG, Bonar HA, Korpik J, Ware RE, McGann PT, Quinn CT, Kalfa TA | Front Physiol | 2021 |
| Engraftment after autologous hematopoietic stem cell transplantation in patients mobilized with Plerixafor: A retrospective, multicenter study of a large series of patients. | Antelo ML, Altuna A, Gimeno JJ, Ferreiro JJ, Amunárriz C, Mateos JJ, Zalba S, Alkorta A, Rifón J, Arroyo JL, Uresandi A, Moreno JA, Nájera MJ, Pinzón S, García A, Vallejo JC, | Transfus Apher Sci | 2021 |
| Hematopoietic Cell Transplantation Outcomes among Medicaid and Privately Insured Patients with Sickle Cell Disease. | Mupfudze TG, Meyer C, Preussler JM, Mau LW, Bolon YT, Steinert P, Arnold SD, Saber W, Krishnamurti L | Transplant Cell Ther | 2021 |
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| Advances in neuroimaging to improve care in sickle cell disease. | Jordan LC, DeBaun MR, Donahue MJ | Lancet Neurol | 2021 |
| Sevuparin for the treatment of acute pain crisis in patients with sickle cell disease: a multicentre, randomised, double-blind, placebo-controlled, phase 2 trial. | Biemond BJ, Tombak A, Kilinc Y, Al-Khabori M, Abboud M, Nafea M, Inati A, Wali Y, Kristensen J, Kowalski J, Donnelly E, Ohd J, | Lancet Haematol | 2021 |
| Sevuparin trial for acute pain in sickle cell disease: the dog that did not bark. | Ellsworth P, Little JA | Lancet Haematol | 2021 |
| A pilot study of the acceptability, feasibility and safety of yoga for chronic pain in sickle cell disease. | Bakshi N, Cooley A, Ross D, Hawkins L, Sullivan M, Astles R, Sinha C, Katoch D, Peddineni M, Gee BE, Lane PA, Krishnamurti L | Complement Ther Med | 2021 |
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| PF-07059013: A non-covalent hemoglobin modulator favorably impacts disease state in a mouse model of sickle cell disease. | Knee KM, Jasuja R, Barakat A, Rao D, Wenzel Z, Jasti J, Novak J, Beaumont K, Piotrowski DW, Jeffrey P, Bulawa C, Murphy JE, Janz JM | Am J Hematol | 2021 |
| Implementing newborn screening for sickle cell disease in Korle Bu Teaching Hospital, Accra: Results and lessons learned. | Segbefia CI, Goka B, Welbeck J, Amegan-Aho K, Dwuma-Badu D, Rao S, Salifu N, Oppong SA, Odei E, Ohene-Frempong K, Odame I | Pediatr Blood Cancer | 2021 |
| Effect of transfusion therapy on intracranial stenosis in a child with sickle cell anaemia. | Brunelli N, Mohamed BP, Fuschi M, Qureshi A, Mazzucco S | Neurol Sci | 2021 |
| Emergency department utilization for sickle cell disease in St. Vincent and the Grenadines. | Williams SA, Henson S, Trimmingham S, Newman J, Kanter J | Pan Afr Med J | 2021 |
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| Acute Phase Responses Vary Between Children of HbAS and HbAA Genotypes During Infection. | Tetteh M, Addai-Mensah O, Siedu Z, Kyei-Baafour E, Lamptey H, Williams J, Kupeh E, Egbi G, Kwayie AB, Abbam G, Afrifah DA, Debrah AY, Ofori MF | J Inflamm Res | 2021 |
| Evaluation of the expression of red blood cell CD36, interleukin-6 and interleukin-8 in sickle cell anemia pediatric patients. | Abdul-Hussein HK, Al-Mammori HS, Hassan MK | Cytokine | 2021 |
| Hemoglobin Yamagata [132(H10)Lys→Asn; (: c.399A>T)]: a mosaic to be put together. | Iacomelli I, Barberio G, Pucci P, Monaco V, Maffei M, Mogni M, Curcio C, Maoggi S, Giulietti C, Harteveld CL, Ivaldi G | Clin Chem Lab Med | 2021 |
| Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. | Hu Y, Stilp AM, McHugh CP, Rao S, Jain D, Zheng X, Lane J, Méric de Bellefon S, Raffield LM, Chen MH, Yanek LR, Wheeler M, Yao Y, Ren C, Broome J, Moon JY, de Vries PS, Hobbs BD, Sun Q, Surendran P, Brody JA, Blackwell TW, Choquet H, Ryan K, Duggirala R, Heard-Costa N, Wang Z, Chami N, Preuss MH, Min N, Ekunwe L, Lange LA, Cushman M, Faraday N, Curran JE, Almasy L, Kundu K, Smith AV, Gabriel S, Rotter JI, Fornage M, Lloyd-Jones DM, Vasan RS, Smith NL, North KE, Boerwinkle E, Becker LC, Lewis JP, Abecasis GR, Hou L, O'Connell JR, Morrison AC, Beaty TH, Kaplan R, Correa A, Blangero J, Jorgenson E, Psaty BM, Kooperberg C, Walton RT, Kleinstiver BP, Tang H, Loos RJF, Soranzo N, Butterworth AS, Nickerson D, Rich SS, Mitchell BD, Johnson AD, Auer PL, Li Y, Mathias RA, Lettre G, Pankratz N, Laurie CC, Laurie CA, Bauer DE, Conomos MP, Reiner AP, | Am J Hum Genet | 2021 |
| Validation of a Questionnaire to Identify Respiratory Tract Infections in Children With Sickle Cell Disease. | De A, Anekwe CV, Kattan M, Yao Y, Jin Z, Brittenham GM, Lee MT | J Pediatr Hematol Oncol | 2021 |
| Spectrum of hemoglobin disorders in southern Odisha, India: a hospital based study. | Sahu P, Purohit P, Mantri S, Tudu R, Nayak J, Agrawalla SK, Behera SK, Patro MK, Karmee N, Tripathy D, Mishra B, Mishra DP | Porto Biomed J | 2021 |
| The Quality of Life of Thalassemic Patients: The Role of Endocrine Defect Compensation. | Mattia L, Samperi I, Monti S, Toscano V, Pugliese G, Poggi M | Endocr Metab Immune Disord Drug Targets | 2021 |
| Survival and causes of death in 2033 patients with non-transfusion-dependent β-thalassemia. | Musallam KM, Vitrano A, Meloni A, Pollina WA, Karimi M, El-Beshlawy A, Hajipour M, Di Marco V, Ansari SH, Filosa A, Ricchi P, Ceci A, Daar S, Vlachaki E, Singer ST, Naserullah ZA, Pepe A, Scondotto S, Dardanoni G, Bonifazi F, Sankaran VG, Vichinsky E, Taher AT, Maggio A | Haematologica | 2021 |
| Brain injury pathophysiology study by a multimodal approach in children with sickle cell anemia with no intra or extra cranial arteriopathy. | Brousse V, Pondarre C, Kossorotoff M, Arnaud C, Kamdem A, de Montalembert M, Boutonnat-Faucher B, Allali S, Bourdeau H, Charlot K, Bertil S, Da Costa L, Connes P, Grévent D, Verlhac S | Haematologica | 2021 |
| Sickle Cell Nephropathy: Screening Provides an Opportunity to Intervene. | Thomas CC, Sinha A | Indian J Pediatr | 2021 |
| Pulmonary complications of sickle cell disease: a narrative clinical review. | Pervaiz A, El-Baba F, Dhillon K, Daoud A, Soubani A | Adv Respir Med | 2021 |
| Hematopoietic stem cell transplantation for people with β-thalassaemia. | Sharma A, Jagannath VA, Puri L | Cochrane Database Syst Rev | 2021 |
| Poloxamer 188 for Sickle Cell Disease. | Zylke J | JAMA | 2021 |
| Effect of Poloxamer 188 vs Placebo on Painful Vaso-Occlusive Episodes in Children and Adults With Sickle Cell Disease: A Randomized Clinical Trial. | Casella JF, Barton BA, Kanter J, Black LV, Majumdar S, Inati A, Wali Y, Drachtman RA, Abboud MR, Kilinc Y, Fuh BR, Al-Khabori MK, Takemoto CM, Salman E, Sarnaik SA, Shah N, Morris CR, Keates-Baleeiro J, Raj A, Alvarez OA, Hsu LL, Thompson AA, Sisler IY, Pace BS, Noronha SA, Lasky JL, de Julian EC, Godder K, Thornburg CD, Kamberos NL, Nuss R, Marsh AM, Owen WC, Schaefer A, Tebbi CK, Chantrain CF, Cohen DE, Karakas Z, Piccone CM, George A, Fixler JM, Singleton TC, Moulton T, Quinn CT, de Castro Lobo CL, Almomen AM, Goyal-Khemka M, Maes P, Emanuele M, Gorney RT, Padgett CS, Parsley E, Kronsberg SS, Kato GJ, Gladwin MT | JAMA | 2021 |
| Rationally Designed Base Editors for Precise Editing of the Sickle Cell Disease Mutation. | Chu SH, Packer M, Rees H, Lam D, Yu Y, Marshall J, Cheng LI, Lam D, Olins J, Ran FA, Liquori A, Gantzer B, Decker J, Born D, Barrera L, Hartigan A, Gaudelli N, Ciaramella G, Slaymaker IM | CRISPR J | 2021 |
| Universal Gene Correction Approaches for β-hemoglobinopathies Using CRISPR-Cas9 and Adeno-Associated Virus Serotype 6 Donor Templates. | Lamsfus-Calle A, Daniel-Moreno A, Ureña-Bailén G, Rottenberger J, Raju J, Epting T, Marciano S, Heumos L, Baskaran P, S Antony J, Handgretinger R, Mezger M | CRISPR J | 2021 |
| Base Editors Flex Sights on Sickle-Cell Disease. | Cereseto A, Cradick TJ, Davies K | CRISPR J | 2021 |
| Optimisation of T2 and T2* sequences in MRI for better quantification of iron on transfused dependent sickle cell patients. | Ahmed A, Baldo A, Sulieman A, Mirghani H, Abolaban FA, Suliman II, Salih I | Sci Rep | 2021 |
| A Case of Hb Aalborg (: c.223G>C) with Chronic Obstructive Pulmonary Disease: A First Familial Presentation in Japan. | Takamura K, Komori T, Hashino Y, Suzuki T, Shiwaku A, Kikuchi H, Yamamoto M, Yamauchi H, Yamashiro Y | Hemoglobin | 2021 |
| Physiological and Aberrant γ-Globin Transcription During Development. | Barbarani G, Labedz A, Stucchi S, Abbiati A, Ronchi AE | Front Cell Dev Biol | 2021 |
| Bone Marrow Fat Distribution in Patients With β-Thalassemia: A Study Using Chemical Shift-Based Water-Fat MRI. | Ismail UN, Azlan CA, Khairullah S, Azman RR, Lee KJ, Yeong CH, Omar NF, Ramli N, Md Shah MN, Jackson N, Ng KH | Acad Radiol | 2021 |
| Development of a community outreach project: An interprofessional partnership for thalassemia families guided by nursing students. | Schmotzer G, Kohlbry P, Strehlow K, Rist E, Bales K, Foe M, Yasmashita R, Yu J | Nurse Educ Pract | 2021 |
| Priapism in Sickle Cell Disease: An Evaluation of the Knowledge of an at Risk Population in Jamaica. | Whyte N, Morrison-Blidgen B, Asnani M | Sex Med | 2021 |
| Predictive SNPs for β-thalassemia/HbE disease severity. | Munkongdee T, Tongsima S, Ngamphiw C, Wangkumhang P, Peerapittayamongkol C, Hashim HB, Fucharoen S, Svasti S | Sci Rep | 2021 |
| Comparing the Effectiveness of Education Versus Digital Cognitive Behavioral Therapy for Adults With Sickle Cell Disease: Protocol for the Cognitive Behavioral Therapy and Real-time Pain Management Intervention for Sickle Cell via Mobile Applications (CaRISMA) Study. | Badawy SM, Abebe KZ, Reichman CA, Checo G, Hamm ME, Stinson J, Lalloo C, Carroll P, Saraf SL, Gordeuk VR, Desai P, Shah N, Liles D, Trimnell C, Jonassaint CR | JMIR Res Protoc | 2021 |
| Low FEV is associated with fetal death in pregnant women with sickle cell disease. | Hayfron-Benjamin CF, Asare EV, Boafor T, Olayemi E, Dei-Adomakoh Y, Musah L, Mensah E, Beyuo T, Kassim AA, Rodeghier M, DeBaun MR, Oppong SA | Am J Hematol | 2021 |
| Delayed Severe Hemolytic Transfusion Reaction During Pregnancy in a Woman with β-Thalassemia Intermediate: Successful Outcome After Eculizumab Administration. | Cannas G, Dubreuil L, Fichez A, Gerfaud-Valentin M, Debard AL, Hot A | Am J Case Rep | 2021 |
| P-selectin and sickle cell disease: a balancing act. | Manwani D | Blood | 2021 |
| Screening for Cognitive Dysfunction Using the Rowland Universal Dementia Assessment Scale in Adults With Sickle Cell Disease. | Forté S, Blais F, Castonguay M, Fadiga N, Fortier-St-Pierre M, Couette M, Ward R, Béland S, Cohn M, Soulières D, Kuo KHM | JAMA Netw Open | 2021 |
| Intravenous Acetaminophen vs Intravenous Diclofenac in the Management of Painful Crisis in Sickle Cell Disease: Authors' Reply. | Mishra NR | Indian Pediatr | 2021 |
| Intravenous Acetaminophen vs Intravenous Diclofenac in the Management of Painful Crisis in Sickle Cell Disease. | Kumar R, Tripathy SK | Indian Pediatr | 2021 |
| Clinical Features and Outcome of Sickle Cell Disease in a Tertiary Center in Northern Lebanon: A Retrospective Cohort Study in a Local, Hospital-Associated Registry. | Inati A, Al Alam C, El Ojaimi C, Hamad T, Kanakamedala H, Pilipovic V, Sabah R | Hemoglobin | 2021 |
| Low incidence of COVID-19 severe complications in a large cohort of children with sickle cell disease: a protective role for basal interferon-1 activation? | Brousse V, Holvoet L, Pescarmona R, Viel S, Perret M, Visseaux B, Ferre VM, Ithier G, Le Van Kim C, Benkerrou M, Missud F, Koehl B | Haematologica | 2021 |
| [Rare thalassemia caused by novel nucleotide variants in the globin gene: four case reports and literature review]. | Da ZZ, Chen LH, Jiang HM, Wang GP | Zhonghua Xue Ye Xue Za Zhi | 2021 |
| Cardiovascular benefits of a home-based exercise program in patients with sickle cell disease. | de Araujo Junior JA, Antonelli Rossi DA, Carneiro Valadão TF, Milan-Mattos JC, Catai AM, Sato TO, Hueb JC, Zanati Bazan SG, Hokama POM, Hokama NK, Roscani MG | PLoS One | 2021 |
| Individual red blood cell nitric oxide production in sickle cell anemia: Nitric oxide production is increased and sickle shaped cells have unique morphologic change compared to discoid cells. | Suriany S, Xu I, Liu H, Ulker P, Fernandez GE, Sposto R, Borzage M, Wenby R, Meiselman HJ, Forman HJ, Coates TD, Detterich JA | Free Radic Biol Med | 2021 |
| Multifocal Osteonecrosis in a 3-Year-Old Child With Sickle Beta Plus Thalassemia. | Bhasin N, Price N, Desoky SM | J Pediatr Hematol Oncol | 2021 |
| Maintenance of a High Influenza Vaccination Rate and Improvement in Health Outcomes in a Pediatric Sickle Cell Disease Clinic. | Lo ZC, Sobota AE | J Pediatr Hematol Oncol | 2021 |
| The ethics of genetic screening for beta thalassemia in Vietnam. | Riquier MT | Dev World Bioeth | 2021 |
| Levels of angiotensin-converting enzyme 1 and 2 in serum and urine of children with Sickle Cell Disease. | Hsien HC, Casarini DE, Carvalhaes JTA, Ronchi FA, Oliveira LCG, Braga JAP | J Bras Nefrol | 2021 |
| Thalassemia and Priapism: A Literature Review of a Rare Association. | Sardar S, Ali EA, Yassin MA | Cureus | 2021 |
| Transcranial color-coded duplex sonography reliably identifies intracranial vasculopathy in adult patients with sickle cell disease. | Edjlali M, Gobin-Metteil MP, Mélé N, Maïer B, Habibi A, Kauv P, Hosseini H, Mas JL, Oppenheim C, Galactéros F, Bartolucci P, Calvet D | Am J Hematol | 2021 |
| A case of ischemic colitis in a patient with non transfusion dependent thalassemia (NTDT) infected by SARS-COV-2. | Ricchi P, Filosa A | Pediatr Hematol Oncol | 2021 |
| Luspatercept: A Review in Transfusion-Dependent Anaemia due to Myelodysplastic Syndromes or β-Thalassaemia. | Kang C, Syed YY | Drugs | 2021 |
| A double-blind, controlled, crossover trial of amlodipine on iron overload status in transfusion dependent β-thalassemia patients. | Karami H, Khalilzadeh Arjmandi H, Salehifar E, Darvishi-Khezri H, Dabirian M, Kosaryan M, Aliasgharian A, Akbarzadeh R, Naeimayi Aali R, Nasirzadeh A | Int J Clin Pract | 2021 |
| Selecting β-thalassemia Patients for Gene Therapy: A Decision-making Algorithm. | Baronciani D, Casale M, De Franceschi L, Graziadei G, Longo F, Origa R, Rigano P, Pinto V, Marchetti M, Gigante A, Forni GL | Hemasphere | 2021 |
| Molecular Spectrum of β-Thalassemia Mutations in Central to Eastern Thailand. | Panichchob P, Iamdeelert P, Wongsariya P, Wongsariya P, Wongwattanasanti P, Tepakhan W, Jomoui W | Hemoglobin | 2021 |
| Impact of a submaximal mono-articular exercise on the skeletal muscle function of patients with sickle cell disease. | Gouraud E, Connes P, Gauthier-Vasserot A, Faes C, Merazga S, Poutrel S, Renoux C, Boisson C, Joly P, Bertrand Y, Hot A, Cannas G, Hautier C | Eur J Appl Physiol | 2021 |
| Rapid and automated quantitation of dense red blood cells: A robust biomarker of hydroxyurea treatment response. | Sadaf A, Quinn CT, Korpik JB, Pfeiffer A, Reynaud M, Niss O, Malik P, Ware RE, Kalfa TA, McGann PT | Blood Cells Mol Dis | 2021 |
| Newborn screening for sickle cell disease in sub-Saharan Africa: Is the glass half-full yet? | Smart LR, Ware RE | Pediatr Blood Cancer | 2021 |
| "It Is Not Easy": Cultural Influences of Sickle Cell Disease Management in Rural, Eastern Sierra Leone | Ibemere SO, Shambley-Ebron DZ, Tanabe P, Jaja C | Qual Health Res | 2021 |
| Sickle Cell Disease in Jordan: The Experience of a Major Referral Center. | Oudat RI, Abualruz HS, Al-Shiek NKA, Al-Mashaqba EA, Al-Hiari RA, Alsoukhni HA, Hammad MAA | Med Arch | 2021 |
| Acyclovir induces fetal hemoglobin via downregulation of γ-globin repressors, BCL11A and SOX6 trans-acting factors. | Ali H, Khan F, Ghulam Musharraf S | Biochem Pharmacol | 2021 |
| Sickle Cell Disease and Pain: Is it all Vaso-occlusive Crises? | Ramsay Z, Bartlett R, Ali A, Grant J, Gordon-Strachan G, Asnani M | Clin J Pain | 2021 |
| Fat Embolism Syndrome in Sickle Cell β-Thalassemia Patient With Osteonecrosis: An Uncommon Presentation in a Young Adult. | Sangani V, Pokal M, Balla M, Merugu GP, Khokher W, Gayam V, Konala VM | J Investig Med High Impact Case Rep | 2021 |
| COVID-19 Mortality in a Pediatric Patient with Hemoglobin SC Disease and Alpha-Thalassemia Trait. | Motelow JE, Kahn S, Wilson PT | Case Rep Crit Care | 2021 |
| Opioid Use in Adults With Sickle Cell Disease Hospitalized During Vaso-Occlusive Crisis: A Systematic Review. | Osborne JC, Osakwe Z, Odlum M | J Hematol | 2021 |
| Novel therapies in β-thalassaemia. | Grech L, Borg K, Borg J | Br J Clin Pharmacol | 2021 |
| Decision making for hematopoietic stem cell transplantation in pediatric, adolescent, and young adult patients with a hemoglobinopathy-Shared or not? | Mekelenkamp H, Smiers F, Camp N, Stubenrouch F, Lankester A, de Vries M | Pediatr Blood Cancer | 2021 |
| Outcomes of allogeneic transplantation for hemoglobin Bart's hydrops fetalis syndrome in Hong Kong. | Chan WYK, Lee PPW, Lee V, Chan GCF, Leung W, Ha SY, Cheuk DKL | Pediatr Transplant | 2021 |
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| Gene Therapy in Global Health: Meeting the Needs of Chinese Patients with Beta-Thalassemia. | Flotte TR | Hum Gene Ther | 2021 |
| The hepcidin regulator erythroferrone is a new member of the erythropoiesis-iron-bone circuitry. | Castro-Mollo M, Gera S, Ruiz-Martinez M, Feola M, Gumerova A, Planoutene M, Clementelli C, Sangkhae V, Casu C, Kim SM, Ostland V, Han H, Nemeth E, Fleming R, Rivella S, Lizneva D, Yuen T, Zaidi M, Ginzburg Y | Elife | 2021 |
| Screening for new red blood cell alloantibodies after transfusion in patients with sickle cell disease. | Rankin A, Darbari D, Campbell A, Webb J, Mo YD, Jacquot C, Delaney M, Luban NLC, Nickel RS | Transfusion | 2021 |
| Multisystem Inflammatory Syndrome in a Pediatric Patient With Sickle Cell Disease and COVID-19: A Case Report. | Español MG, Gardner RV, Alicea-Marrero MM, Marrero-Rivera G, Bradford T, LeBlanc DM, Velez MC | J Pediatr Hematol Oncol | 2021 |
| Mortality and Causes of Death From Sickle Cell Disease in The Netherlands, 1985-2017. | Rettenbacher E, Zaal J, Heijboer H, van der Plas EM, Hof M, Biemond BJ, Fijnvandraat K, | J Pediatr Hematol Oncol | 2021 |
| Establishing Sickle Cell Disease Stroke Prevention Teams in Africa is Feasible: Program Evaluation Using the RE-AIM Framework. | Ghafuri DL, Abdullahi SU, Dambatta AH, Galadanci J, Tabari MA, Bello-Manga H, Idris N, Inuwa H, Tijjani A, Suleiman AA, Jibir BW, Gambo S, Gambo AI, Khalifa Y, Haliru L, Abdulrasheed S, Zakari MA, Greene BC, Trevathan E, Jordan LC, Aliyu MH, Baumann AA, DeBaun MR | J Pediatr Hematol Oncol | 2021 |
| Lactate dehydrogenase to carboxyhemoglobin ratio as a biomarker of heme release to heme processing is associated with higher tricuspid regurgitant jet velocity and early death in sickle cell disease. | van Vuren AJ, Minniti CP, Mendelsohn L, Baird JH, Kato GJ, van Beers EJ | Am J Hematol | 2021 |
| GATA zinc finger domain-containing protein 2A (GATAD2A) deficiency reactivates fetal haemoglobin in patients with β-thalassaemia through impaired formation of methyl-binding domain protein 2 (MBD2)-containing nucleosome remodelling and deacetylation (NuRD) complex. | Liang Y, Zhang X, Liu Y, Wang L, Ye Y, Tan X, Pu J, Zhang Q, Bao X, Wei X, Li D, Kurita R, Nakamura Y, Li D, Xu X | Br J Haematol | 2021 |
| Renal Medullary Carcinoma in an Adolescent With Unknown Sickle Cell Trait. | Noreña-Rengifo BD, Ochoa-Gaviria J, Vélez-Escobar A, Muñoz JP, Riveros-Ángel M | Cureus | 2021 |
| Fetal Cytokine Balance, Erythropoietin and Thalassemia but Not Placental Malaria Contribute to Fetal Anemia Risk in Tanzania. | Kabyemela ER, Fried M, Kurtis JD, Moses G, Gorres JP, Muehlenbachs A, Duffy PE | Front Immunol | 2021 |
| Transcranial Doppler Ultrasonography Imaging Studies in Children with Sickle Cell Anaemia in a Tertiary Hospital, Abuja, Nigeria. | Mohammed-Nafi'u R, Oniyangi O, Akano AO, Aikhionbare HA, Okon EJ | West Afr J Med | 2021 |
| Paternal Stress and Child Outcomes in Youth with Sickle Cell Disease. | Moody KL | J Pediatr Psychol | 2021 |
| Gene therapy as the new frontier for Sickle Cell Disease. | Garg H, Tatiossian KJ, Peppel K, Kato GJ, Herzog E | Curr Med Chem | 2021 |
| Inclusion of a shRNA targeting BCL11A into a β-globin expressing vector allows concurrent synthesis of curative adult and fetal hemoglobin. | Pires Lourenco S, Jarocha D, Ghiaccio V, Guerra A, Abdulmalik O, La P, Zezulin A, Smith-Whitley K, Kwiatkowski JL, Guzikowski V, Nakamura Y, Raabe T, Breda L, Rivella S | Haematologica | 2021 |
| Delta-globin gene expression improves sickle cell disease in a humanised mouse model. | Porcu S, Simbula M, Marongiu MF, Perra A, Poddie D, Perseu L, Kowalik MA, Littera R, Barella S, Caria CA, Demartis FR, Ristaldi MS | Br J Haematol | 2021 |
| Long-Term Effects of Iron Chelating Agents on Ocular Function in Patients with Thalassemia Major. | Nuzzi R, Geronazzo G, Tridico F, Nuzzi A, Caselgrandi P, Piga AG | Clin Ophthalmol | 2021 |
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| Towards manufactured red blood cells for the treatment of inherited anemia. | Pellegrin S, Severn CE, Toye AM | Haematologica | 2021 |
| Exome sequencing in high and low fetal haemoglobin Arab-Indian haplotype sickle cell disease. | Alnafie AN, Alateeq SA, Al-Muhanna FA, Alsulaiman AM, Alfarhan M, Buali W, Vatte CB, Cyrus C, Keating B, Al-Ali AK, Steinberg MH | Br J Haematol | 2021 |
| Corrigendum to: Tranexamic acid use in a patient with sickle cell disease undergoing posterior scoliosis correction surgery: safely mitigating bleeding and vaso-occlusive crises. | Newall M, Hamdan TA, Ajayi B, Weil S, Bishop T, Lui DF | J Surg Case Rep | 2021 |
| Large red cell-derived membrane particles are major contributors to hypercoagulability in sickle cell disease. | Smith RA, Mankelow TJ, Drizou D, Bullock T, Latham T, Trompeter S, Blair A, Anstee DJ | Sci Rep | 2021 |
| First Report of Nondeletional Hb H Disease Caused by an α2-Globin Gene Mutation: : c.184A>T. | Tian Q, Lei YL, Xu LL, Li DZ | Hemoglobin | 2021 |
| Deep sequencing applied to the analysis of viromes in patients with beta-thalassemia. | Valença IN, Santos RBD, Peronni KC, Sauvage V, Vandenbogaert M, Caro V, Silva Junior WAD, Covas DT, Silva-Pinto AC, Laperche S, Kashima S, Slavov SN | Rev Inst Med Trop Sao Paulo | 2021 |
| Hemoglobin F (HbF) inducers; History, Structure and Efficacies. | Hashemi Z, Ebrahimzadeh MA | Mini Rev Med Chem | 2021 |
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| Coagulation Abnormalities Due to COVID-19 in a Child with Thalassemia: Correspondence. | Mungmunpuntipantip R, Wiwanitkit V | Indian J Pediatr | 2021 |
| Development of an Online Reproductive Health Intervention for Individuals with Sickle Cell Disease or Trait. | Johnson-Mallard V, Oguntoye A, Eades N, Aldossary D, Kuenzli G, Ezenwa MO, Gallo AM, Wilkie DJ | Womens Health Rep (New Rochelle) | 2021 |
| Cost-effectiveness of a hypothetical cell or gene therapy cure for sickle cell disease. | Salcedo J, Bulovic J, Young CM | Sci Rep | 2021 |
| Detection of the : c.393T>G Mutation in Two Patients with Hypochromic Microcytic Anemia. | Zhao Q, Zhao SM, Zhang X, Chen SP, Sun J, Peng ZY, Sun Y, Fan C, Xing XD, Li R | Hemoglobin | 2021 |
| Differential Diagnosis of Low Hemoglobin. | Ianni CM, McDowall MP, Zuska IA | Dimens Crit Care Nurs | 2021 |
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| Letter to the Editor: Physicians' Opinions of COVID-19 Ambulatory Care Constraints: A Survey of Sickle Cell Clinicians. | Kenney MO, Becerra B, Beatty SA, Smith W | J Ambul Care Manage | 2021 |
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| Sickle-trait hemoglobin reduces adhesion to both CD36 and EPCR by Plasmodium falciparum-infected erythrocytes. | Petersen JEV, Saelens JW, Freedman E, Turner L, Lavstsen T, Fairhurst RM, Diakité M, Taylor SM | PLoS Pathog | 2021 |
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| SNAP: Supportive noninvasive ventilation for acute chest syndrome prevention in children with sickle cell disease. | Guenther CS, Pae VJ, Neri CM, Barry K, Duggan MA, Cohen RT | Pediatr Blood Cancer | 2021 |
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| MWC allosteric model explains unusual hemoglobin-oxygen binding curves from sickle cell drug binding. | Henry ER, Harper J, Glass KE, Metaferia B, Louis JM, Eaton WA | Biophys J | 2021 |
| Screening of blood donors for sickle cell trait using a DNA-based approach: Frequency in a multiethnic donor population. | Gowda L, Vege S, Kessler D, Shaz B, Westhoff CM | Transfusion | 2021 |
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| Proteomic discovery in sickle cell disease: Elevated neurogranin levels in children with sickle cell disease. | Lance EI, Faulcon LM, Fu Z, Yang J, Whyte-Stewart D, Strouse JJ, Barron-Casella E, Jones K, Van Eyk JE, Casella JF, Everett AD | Proteomics Clin Appl | 2021 |
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| The Influence of Health-Seeking Behaviors on the Health Literacy of Adolescents With Sickle Cell Disease. | Caldwell EP, Rosonet LE | J Pediatr Oncol Nurs | 2021 |
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| Assessment of Hemoglobin A2 stability at room temperature during 24 or 25 days as measured by high pressure liquid chromatography and capillary electrophoresis. | Hildrum JM, Fjeld B, Risahagen SM, Bernatek BJ, Klingenberg O | Int J Lab Hematol | 2021 |
| Impairment of Cerebrovascular Hemodynamics in Patients With Severe and Milder Forms of Sickle Cell Disease. | Afzali-Hashemi L, Baas KPA, Schrantee A, Coolen BF, van Osch MJP, Spann SM, Nur E, Wood JC, Biemond BJ, Nederveen AJ | Front Physiol | 2021 |
| Stable to improved cardiac and pulmonary function in children with high-risk sickle cell disease following haploidentical stem cell transplantation. | Friedman D, Dozor AJ, Milner J, D'Souza M, Talano JA, Moore TB, Shenoy S, Shi Q, Walters MC, Vichinsky E, Parsons SK, Braniecki S, Moorthy CR, Ayello J, Flower A, Morris E, Mahanti H, Fabricatore S, Klejmont L, van de Ven C, Baxter-Lowe LA, Cairo MS | Bone Marrow Transplant | 2021 |
| Disease severity impacts plerixafor-mobilized stem cell collection in patients with sickle cell disease. | Leonard A, Sharma A, Uchida N, Stroncek D, Panch SR, West K, Molloy E, Hughes TE, Hauffe S, Taylor T, Fitzhugh C, Hankins JS, Wilson M, Tsai SQ, Weiss MJ, Hsieh M, Tisdale JF | Blood Adv | 2021 |
| Transfusion management of severe anaemia in African children: a consensus algorithm. | Maitland K, Kiguli S, Olupot-Olupot P, Opoka RO, Chimalizeni Y, Alaroker F, Uyoga S, Kyeyune-Byabazaire D, M'baya B, Bates I, Williams TN, Munube D, Mbanya D, Molyneux EM, South A, Walker AS, Gibb DM, George EC, | Br J Haematol | 2021 |
| Iron Status in Newly Diagnosed -Thalassemia Major: High Rate of Iron Status due to Erythropoiesis Drive. | Susanah S, Rakhmilla LE, Ghozali M, Trisaputra JO, Moestopo O, Sribudiani Y, Idjradinata PS, Maskoen AM | Biomed Res Int | 2021 |
| Iron Overload in Transfusion-Dependent Indonesian Thalassemic Patients. | Fianza PI, Rahmawati A, Widihastha SH, Afifah S, Ghozali M, Indrajaya A, Pratama DMA, Prasetya D, Sihite TA, Syamsunarno MRAA, Setiabudi D, Fucharoen S, Panigoro R | Anemia | 2021 |
| Occlusal Disorders in Patients with Sickle Cell Disease: Critical Literature Review. | Lopes CMI, Lira SS, da Silva Oliveira JC, Alves E Luna AC, de Melo Valença PA, de Menezes VA | J Clin Pediatr Dent | 2021 |
| Mobile health use predicts self-efficacy and self-management in adolescents with sickle cell disease. | Hood AM, Nwankwo C, Walton A, McTate E, Joffe N, Quinn CT, Britto MT, Peugh J, Mara CA, Crosby LE | Transl Behav Med | 2021 |
| Living with thalassaemia in Papua New Guinea, the experience of children, adolescents and their families. | Nagiria VR, Vince JD, Duke T | J Paediatr Child Health | 2021 |
| Impact of the preparation method of red cell concentrates on transfusion indices in thalassemia patients: A randomized crossover clinical trial. | Gamberini MR, Fortini M, Stievano A, Calori E, Riontino MV, Ceccherelli G, Venturelli D, Chicchi R, Biguzzi R, Fagnoni F, Portararo GA, Lasagni D, Borotti E, Buonocore R, Govoni M, Reverberi R | Transfusion | 2021 |
| Preclinical evaluation for engraftment of CD34 cells gene-edited at the sickle cell disease locus in xenograft mouse and non-human primate models. | Uchida N, Li L, Nassehi T, Drysdale CM, Yapundich M, Gamer J, Haro-Mora JJ, Demirci S, Leonard A, Bonifacino AC, Krouse AE, Linde NS, Allen C, Peshwa MV, De Ravin SS, Donahue RE, Malech HL, Tisdale JF | Cell Rep Med | 2021 |
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| Anemia at Altitude: Thalassemia, Sickle Cell Disease, and Other Inherited Anemias. | DeLoughery TG | High Alt Med Biol | 2021 |
| Left ventricular systolic dyssynchrony index and endothelial dysfunction parameters as subclinical predictors of cardiovascular involvement in patients with beta-thalassemia major. | Solmaz H, Cabuk AK, Altin Z, Albudak Ozcan E, Ozdogan O | Echocardiography | 2021 |
| FT-4202, an oral PKR activator, has potent antisickling effects and improves RBC survival and Hb levels in SCA mice. | Shrestha A, Chi M, Wagner K, Malik A, Korpik J, Drake A, Fulzele K, Guichard S, Malik P | Blood Adv | 2021 |
| Natural history of alpha-thalassemia X-linked intellectual disability syndrome: A case report of a 45-year-old man. | Arvio M, Lähdetie J | Am J Med Genet A | 2021 |
| SLN124, a GalNac-siRNA targeting transmembrane serine protease 6, in combination with deferiprone therapy reduces ineffective erythropoiesis and hepatic iron-overload in a mouse model of β-thalassaemia. | Vadolas J, Ng GZ, Kysenius K, Crouch PJ, Dames S, Eisermann M, Nualkaew T, Vilcassim S, Schaeper U, Grigoriadis G | Br J Haematol | 2021 |
| Pleckstrin-2 is essential for erythropoiesis in β-thalassemic mice, reducing apoptosis and enhancing enucleation. | Feola M, Zamperone A, Moskop D, Chen H, Casu C, Lama D, Di Martino J, Djedaini M, Papa L, Martinez MR, Choesang T, Bravo-Cordero JJ, MacKay M, Zumbo P, Brinkman N, Abrams CS, Rivella S, Hattangadi S, Mason CE, Hoffman R, Ji P, Follenzi A, Ginzburg YZ | Commun Biol | 2021 |
| COVID-19 Presentation in Patients with Sickle Cell Disease: A Case Series. | Chen-Goodspeed A, Idowu M | Am J Case Rep | 2021 |
| Coordinated β-globin expression and α2-globin reduction in a multiplex lentiviral gene therapy vector for β-thalassemia. | Nualkaew T, Sii-Felice K, Giorgi M, McColl B, Gouzil J, Glaser A, Voon HPJ, Tee HY, Grigoriadis G, Svasti S, Fucharoen S, Hongeng S, Leboulch P, Payen E, Vadolas J | Mol Ther | 2021 |
| Hemodynamic response to sensory stimulation in mice: Comparison between functional ultrasound and optoacoustic imaging. | Robin J, Rau R, Lafci B, Schroeter A, Reiss M, Deán-Ben XL, Goksel O, Razansky D | Neuroimage | 2021 |
| Hemoglobin fractionation by Sebia Capillarys 2 Flex Piercing System as primary method for evaluation of hemoglobinopathies. | Poventud-Fuentes I, Garnett E, Vispo B, Elghetany MT, Devaraj S | Clin Chim Acta | 2021 |
| Molecular analysis of the erythroid phenotype of a patient with BCL11A haploinsufficiency. | Wessels MW, Cnossen MH, van Dijk TB, Gillemans N, Schmidt KLJ, van Lom K, Vinjamur DS, Coyne S, Kurita R, Nakamura Y, de Man SA, Pfundt R, Azmani Z, Brouwer RWW, Bauer DE, van den Hout MCGN, van IJcken WFJ, Philipsen S | Blood Adv | 2021 |
| Alternating and Concurrent True Hyperkalemia and Pseudohyperkalemia in Adult Sickle Cell Disease. | Onuigbo MA, Tan H, Sherman SE | Rambam Maimonides Med J | 2021 |
| Concurrent use of hydroxyurea and deferasirox in Californians with sickle cell disease. | Wong TE, Valle J, Paulukonis S | Health Sci Rep | 2021 |
| Cardiac Chamber Quantification by Echocardiography in Adults With Sickle Cell Disease: Need Attention to Eccentric Hypertrophy. | Koyuncu MB, Tombak A, Orscelik O, Koseci T, Turker A, Basir H, Akdeniz A, Tiftik EN | Cureus | 2021 |
| Investigating the Role of Ferritin in Determining Sexual Underdevelopment in Beta-Thalassemia Major Patients: A Cross-Sectional Analysis From Pakistan. | Shahid Z, Hassan S, Ghazanfar S, Kaneez M, Khan MS, Tariq HT, Jawad A, Shuaib A, Bhatti AA, Razzaq MT | Cureus | 2021 |
| Sickle Cell Disease and the Respiratory System: A Tangential Perspective to the Hematopulmonological Dilemma. | Sange I, Cherukuri PB, Parchuri V, Srinivas N, Ramanan SP, Sange AH, Modi S, Khot FA | Cureus | 2021 |
| Opioid-Induced Psychosis in a Patient With Sickle Cell Disease. | Tumenta T, Thanju A, Perera P, Kallikkadan J, Fouron P, Olupona T | Cureus | 2021 |
| A Retrospective Long-Term Study on Age at Menarche and Menstrual Characteristics in 85 Young Women with Transfusion-Dependent β-Thalassemia (TDT). | Di Maio S, Marzuillo P, Mariannis D, Christou S, Ellinides A, Christodoulides C, de Sanctis V | Mediterr J Hematol Infect Dis | 2021 |
| Acute soft head syndrome in a sickle cell disease patient. | Zadeh C, Rameh V, Atweh LA | J Radiol Case Rep | 2021 |
| Prevalence of occult hepatitis C virus infection in beta-thalassemia major patients in Ahvaz, Iran. | Nasimzadeh S, Azaran A, Jalilian S, Makvandi M, Seyedian SS, Keikhaei B, Mehr FJ | Arch Virol | 2021 |
| Matched related hematopoietic cell transplant for sickle cell disease with alemtuzumab: the Texas Children's Hospital experience. | John TD, Friend B, Yassine K, Sasa G, Bhar S, Salem B, Omer B, Craddock J, Doherty E, Martinez C, Heslop HE, Krance RA, Leung K | Bone Marrow Transplant | 2021 |
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| Platelet counts on peripheral blood and Mean Platelet Volume as markers of clinical severity in Sickle Cell Disease. | Silva CM, de Souza Medina S, de Melo Campos P, Costa FF, Saad STO, Benites BD | Blood Cells Mol Dis | 2021 |
| Hydroxyurea treatment and neurocognitive functioning in sickle cell disease from school age to young adulthood. | Heitzer AM, Longoria J, Okhomina V, Wang WC, Raches D, Potter B, Jacola LM, Porter J, Schreiber JE, King AA, Kang G, Hankins JS | Br J Haematol | 2021 |
| The effect of sickle cell anemia on the linear growth of Nigerian children. | Chikani UN, Bisi-Onyemaechi A, Ohuche I, Onu J, Ugege S, Ogugua C, Mbanefo N, Chime P, Emodi I | J Pediatr Endocrinol Metab | 2021 |
| Molecular and phenotype characterization of an elongated β-globin variant produced by HBB:C.313delA. | Lin W, Zhang Q, Shen Z, Qu X, Wang Q, Wei L, Qiu Y, Yang J, Xu X, Lao J | Int J Lab Hematol | 2021 |
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| Comparative Effectiveness of a Six-Week Treatment Course of Vitamin D and D in Children With Sickle Cell Anemia in Steady State With Hypovitaminosis D: A Randomized Clinical Trial. | Adekunle MO, Dada AO, Njokanma FO, Solarin AU, Animasahun BA, Lamina MO | J Hematol | 2021 |
| Frequencies of Beta Thalassemia Mutations Show Different Pattern in Bannu Region than Other Parts of Pashtun Population in Khyber Pakhtunkhwa Province Pakistan. | Rehman SU, Shakeel M, Azam M, Akhtar S, Ziaullah , Niazi R | Indian J Hematol Blood Transfus | 2021 |
| Unmanipulated Stem Cell Boost for Mixed Chimerism in Transfusion Dependent Thalassemia. | Garg A, Shivchhand A, Shah S, Shah K, Patel K, Panchal H, Patel A, Parikh S | Indian J Hematol Blood Transfus | 2021 |
| Role of Red Cell Indices in Screening for Beta Thalassemia Trait: an Assessment of the Individual Indices and Application of Machine Learning Algorithm. | Jahan A, Singh G, Gupta R, Sarin N, Singh S | Indian J Hematol Blood Transfus | 2021 |
| Prenatal Screening and Diagnosis of ß-Thalassemia in India: Is ARMS-PCR Enough? | Ghosh S, Chakrabarti S, Bhattacharyya M | Indian J Hematol Blood Transfus | 2021 |
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| Screening of Dry Blood Spots from Newborns by Two High Performance Liquid Chromatography (HPLC) Systems: A Comparison of Their Ability to Diagnose Both Sickle and Non-sickle Hemoglobinopathies. | Ramani Daruwalla M, Das Gupta A, Pawar R | Indian J Hematol Blood Transfus | 2021 |
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| High Systolic Blood Pressure, Anterior Segment Changes and Visual Impairment Independently Predict Sickle Cell Retinopathy. | Idris IM, Yusuf AA, Gwarzo DH, Kurawa MS, Shuaib A, Galadanci AA, Ibrahim H, Borodo AM, Jobbi YD, Danagundi MB, Borodo SB, Mohammed IY, Galadanci NA, Kuliya-Gwarzo A | Hemoglobin | 2021 |
| Evaluation of interference from hemoglobin C, D, E and S traits on measurements of hemoglobin A1c by fifteen methods. | Rohlfing C, Hanson S, Estey MP, Bordeleau P, Little RR | Clin Chim Acta | 2021 |
| Patient-reported neurocognitive symptoms influence instrumental activities of daily living in sickle cell disease. | Longoria JN, Pugh NL, Gordeuk V, Hsu LL, Treadwell M, King AA, Gibson R, Kayle M, Crego N, Glassberg J, Melvin CL, Hankins JS, Porter J | Am J Hematol | 2021 |
| Individuals with sickle cell disease and sickle cell trait demonstrate no increase in mortality or critical illness from COVID-19 - A fifteen hospital observational study in the Bronx, New York. | Hoogenboom WS, Fleysher R, Soby S, Mirhaji P, Mitchell WB, Morrone KA, Manwani D, Duong TQ | Haematologica | 2021 |
| Assessment of Renal function status in steady state Sickle Cell Anaemic children using urine human Neutrophil Gelatinase-associated Lipocalin and Albumin:Creatinine ratio. | Olawale OO, Adekanmbi AF, Sonuga AA, Sonuga OO, Akodu SO, Ogundeyi MM | Med Princ Pract | 2021 |
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| 'Look into Their Hearts' 7-Year-Old Boy with Sickle Cell Disease, Fever, Left Sixth and Seventh Cranial Nerve Palsy and Left Hemiplegia. | Jabateh SM, Mohsenibod H | J Trop Pediatr | 2021 |
| Interleukin 6 as a marker of severe bacterial infection in children with sickle cell disease and fever: a case-control study. | Rincón-López EM, Navarro Gómez ML, Hernández-Sampelayo Matos T, Aguilera-Alonso D, Dueñas Moreno E, Saavedra-Lozano J, Santiago García B, Santos Sebastián MDM, García Morín M, Beléndez Bieler C, Lorente Romero J, Cela de Julián E, | BMC Infect Dis | 2021 |
| Sickle Cell Disease and the Kidney: Pathophysiology and Novel Biomarkers. | Lemes RPG, Rocha Laurentino M, Castelo LR, Silva Junior G | Contrib Nephrol | 2021 |
| Analysis of δ-globin gene alleles in Tunisians: description of three new delta-thalassemia mutations. | Kasmi C, Amri Y, Hadj-Fredj S, Oueslati S, Dabboussi M, Mahjoub R, Hammami S, Aljane I, Mami FB, Jamoussi H, Messaoud T, Bibi A | Mol Biol Rep | 2021 |
| Activation of γ-globin gene expression by GATA1 and NF-Y in hereditary persistence of fetal hemoglobin. | Doerfler PA, Feng R, Li Y, Palmer LE, Porter SN, Bell HW, Crossley M, Pruett-Miller SM, Cheng Y, Weiss MJ | Nat Genet | 2021 |
| Evaluation of role of HPLC (Merits & Pitfalls), in the diagnosis of various hemoglobinopathies & thalassemic syndromes. | Baig MA, Swamy KB, Baksh AD, Bahashwan A, Moshrif Y, Al Sawat A, Al Mutairi N, Alharbi N | Indian J Pathol Microbiol | 2021 |
| Neurologic and Cognitive Outcomes in Sickle Cell Disease from Infancy through Adolescence. | Mayer SL, Fields ME, Hulbert ML | Neoreviews | 2021 |
| Neuroprotection: further evidence for the early and universal use of hydroxyurea in children with sickle cell disease. | Karkoska K | Br J Haematol | 2021 |
| The promise and role of point of care testing to reduce the global burden of sickle cell disease through early diagnosis and linkage to care. | Dexter D, McGann PT | Br J Haematol | 2021 |
| Impact of the human leucocyte antigen (HLA)-B leader peptide dimorphism and HLA-A expression on outcomes of stem cell transplantation for sickle cell disease. | Cappelli B, Scigliuolo GM, Boukouaci W, Rafii H, Volt F, Kenzey C, Maio KT, Chabannon C, Corbacioglu S, Rocha V, Ruggeri A, Gluckman E, Tamouza R | Br J Haematol | 2021 |
| A qualitative exploration of health-related quality of life and health behaviours in children with sickle cell disease and healthy siblings. | Constantinou C, Payne N, van den Akker O, Inusa B | Psychol Health | 2021 |
| Correction: Treatment of Acute Pain in Adults With Sickle Cell Disease in an Infusion Center Versus the Emergency Department. | Lanzkron S, Little J, Wang H, Field JJ, Shows JR, Haywood C Jr, Saheed M, Proudford M, Robertson D, Kincaid A, Burgess L, Green C, Seufert R, Brooks J, Piehet A, Griffin B, Arnold N, Frymark S, Wallace M, Al Hamayel NA, Huang CY, Segal JB, Varadhan R. | Ann Intern Med | 2021 |
| Clinical utility of Abbott Alinity hq extended red blood cell parameters in differentiating β-thalassemia trait and iron deficiency anemia. | Mukhtar Z, Valente S, Masi L, Lakos G, Papa F | Int J Lab Hematol | 2021 |
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| Increased Prevalence of Alloimmunization in Sickle Cell Disease? Should We Restore Blood Donation in French Guiana? | Conrath S, Vantilcke V, Parisot M, Maire F, Selles P, Elenga N | Front Med (Lausanne) | 2021 |
| Economic evaluation of betibeglogene autotemcel (Beti-cel) gene addition therapy in transfusion-dependent β-thalassemia. | Kansal AR, Reifsnider OS, Brand SB, Hawkins N, Coughlan A, Li S, Cragin L, Paramore C, Dietz AC, Caro JJ | J Mark Access Health Policy | 2021 |
| Rare Presentation of Right Adrenal Mass: Extramedullary Haematopoiesis in a Patient with Thalassaemia Intermedia. | Wong PS, Yong LS, Karim NAB, Gan EL, Toh SG, Adam NLB | J ASEAN Fed Endocr Soc | 2021 |
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| A Novel β-Thalassemia Mutation, : c.356_357delTT [Codon 118 (-TT)] in an Iraqi Kurd. | Atroshi SD, Al-Allawi N, Chui DHK, Najmabadi H, Khailany RA | Hemoglobin | 2021 |
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| Development of a High Resolution Melting Curve Analysis for the Detection of Hemoglobin δ-Chain Variants in Thailand and Identification of Hb A2-Walsgrave [codon 52 (GAT>CAT), Asp→His; HBD:c.157G>C] in a Pregnant Woman from Southern Thailand. | Prajantasen T, Prayalaw P, Panyasai S, Binlee S, Nongnuan S | Genet Test Mol Biomarkers | 2021 |
| Fostering equity in education and academic outcomes in children with sickle cell disease. | Miller M, Landsman R, Scott JP, Heffelfinger AK | Clin Neuropsychol | 2021 |
| SARS-CoV-2 infection in patients with β-thalassemia: The French experience. | Jean-Mignard E, De Luna G, Pascal L, Agouti I, Thuret I | Transfus Clin Biol | 2021 |
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| Drug utilization study and cost analysis of adult β-thalassemia major patient therapy at Dr. Soetomo General Hospital Surabaya. | Qatrunnada H, Suharjono , Bintoro SUY, Wahyuni S | J Basic Clin Physiol Pharmacol | 2021 |
| Perception to hydroxyurea therapy in patients with sickle cell disease: Report from 3 centers. | Korubo KI, Onodingene NM, Okoye HC, Omunakwe HE | Ann Afr Med | 2021 |
| Increased hemoglobin affinity for oxygen with GBT1118 improves hypoxia tolerance in sickle cell mice. | Dufu K, Williams AT, Muller CR, Walser CM, Lucas A, Eaker AM, Alt C, Cathers BE, Oksenberg D, Cabrales P | Am J Physiol Heart Circ Physiol | 2021 |
| COVID 19 pandemic and lockdown: A double whammy for patients with thalassemia. | Kakkar S, Anand V, Dewan P, Sobti P | Acta Biomed | 2021 |
| The Pancreatic changes affecting glucose homeostasis in transfusion dependent β- thalassemia (TDT): a short review. | De Sanctis V, Soliman A, Tzoulis P, Daar S, Fiscina B, Kattamis C | Acta Biomed | 2021 |
| Relationship Between Disease Severity and Resting Electrocardiograms of Adults With Sickle Cell Anemia in a Tertiary Institution in Southern Nigeria. | Dic-Ijiewere MO, Emorinken A, Obasohan AO, Okokhere PO, Dic-Ijiewere EO, Otumu OS | Cureus | 2021 |
| Follow-up of children with sickle cell anemia screened with transcranial Doppler and enrolled in a primary prevention program of ischemic stroke. | Sabarense AP, Silva CM, Muniz MBSR, Viana MB | Hematol Transfus Cell Ther | 2021 |
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| Unique Polymorphisms at , and Loci Associated with HbF in Kuwaiti Patients with Sickle Cell Disease. | Akbulut-Jeradi N, Fernandez MJ, Al Khaldi R, Sukumaran J, Adekile A | J Pers Med | 2021 |
| Successful Implementation of Newborn Screening for Hemoglobin Disorders in the Philippines. | Padilla CD, Therrell BL, Alcausin MMLB, de Castro RC, Gepte MBP, Reyes MEL, Jomento CM, Suarez RCN, Maceda EBG, Abarquez CG, Posecion JEWC, Andal AP, Elizaga ALG, Halili-Mendoza BC, Otayza MPVK, Hoppe CC | Int J Neonatal Screen | 2021 |
| Critical Role of Hemopexin Mediated Cytoprotection in the Pathophysiology of Sickle Cell Disease. | Ashouri R, Fangman M, Burris A, Ezenwa MO, Wilkie DJ, Doré S | Int J Mol Sci | 2021 |
| Cell and Gene Therapy for Anemia: Hematopoietic Stem Cells and Gene Editing. | Anurogo D, Yuli Prasetyo Budi N, Thi Ngo MH, Huang YH, Pawitan JA | Int J Mol Sci | 2021 |
| Treatment of sickle cell disease by increasing oxygen affinity of hemoglobin. | Henry ER, Metaferia B, Li Q, Harper J, Best RB, Glass KE, Cellmer T, Dunkelberger EB, Conrey A, Thein SL, Bunn HF, Eaton WA | Blood | 2021 |
| Comorbidities are risk factors for hospitalization and serious COVID-19 illness in children and adults with sickle cell disease. | Mucalo L, Brandow AM, Dasgupta M, Mason SF, Simpson PM, Singh A, Taylor BW, Woods KJ, Yusuf FI, Panepinto JA | Blood Adv | 2021 |
| Wild-type HIV infection after treatment with lentiviral gene therapy for β-thalassemia. | Hongeng S, Anurathapan U, Songdej D, Phuphuakrat A, Jongrak K, Parsons G, Deary B, Bonner M, Veres G, Asmal M | Blood Adv | 2021 |
| Prevalence and molecular spectrum of α- and β-globin gene mutations in Hainan, China. | Wang Z, Sun W, Chen H, Zhang Y, Wang F, Chen H, Zhou Y, Huang Y, Zhou X, Li Q, Ma Y | Int J Hematol | 2021 |
| Commonly used agent for acute pain management of sickle cell anemia in Saudi Emergency Department: A narrative review. | Hejazi RA, Mandourah NA, Alsulami AS, Bakhsh HT, Diri RM, Noor AO | Saudi Pharm J | 2021 |
| Distribution of β-Thalassemia and Other Hemoglobinopathies in Bangladeshi University Students and Ready-Made Garment Workers. | Islam MM, Hossain F, Sakib N, Zeba Z, Bhuiyan AKMI, Mamun MA, Kaggwa MM, Yoshimura K, Afrin S, Selim S, Hossain M | Risk Manag Healthc Policy | 2021 |
| Further evidence for the benefit of therapeutic plasma exchange for acute multi-organ failure syndrome refractory to red cell exchange in sickle cell disease. | Siddiqui RS, Ferman DA, Shi PA | J Clin Apher | 2021 |
| Severe Persistent Pain and Inflammatory Biomarkers in Sickle Cell Disease: An Exploratory Study. | Knisely MR, Tanabe PJ, Walker JKL, Yang Q, Shah NR | Biol Res Nurs | 2021 |
| A narrative review of in utero gene therapy: advances, challenges, and future considerations. | Yung NK, Maassel NL, Ullrich SJ, Ricciardi AS, Stitelman DH | Transl Pediatr | 2021 |
| Post-transfusion hyperhemolysis syndrome in a patient with beta thalassemia major. | Kasinathan G, Sathar J | Clin Case Rep | 2021 |
| An Autopsy Case of β-Thalassemia Major Illuminating the Pathological Spectrum of the Disease. | Sood R, Rastogi P, Bansal D, Das R, Sharma P, Gude G, Dhankar M | Hemoglobin | 2021 |
| Frequency of beta S globin gene haplotypes among sickle cell patients in Nigeria. | Adabale A, Makanjuola SBL, Akinbami A, Dosunmu A, Akanmu A, Javid FA, Ajonuma LC | J Int Med Res | 2021 |
| Prospective Newborn Screening for Sickle Cell Disease and Other Inherited Blood Disorders in Central Malawi. | Tegha G, Topazian HM, Kamthunzi P, Howard T, Tembo Z, Mvalo T, Chome N, Kumwenda W, Mkochi T, Hernandez A, Ataga KI, Hoffman IF, Ware RE | Int J Public Health | 2021 |
| Total Annual Economic Burden of Patients with Sickle Cell Disease in Steady State in Greece. | Tsolakidis V, Vlachaki E, Papaioannou M, Pantelidou D, Diamantidis M, Eleftheriou P, Kouvelas D, Pourzitaki C | Hemoglobin | 2021 |
| Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden (:c.178G>C) and Hb Quong Sze (:c.377T>C). | Du L, Bao X, He W, Qin D, Wang J, Xiong Y, Shi X, Ding H, Yao C, Wu J | J Int Med Res | 2021 |
| Allogeneic hematopoietic stem cell transplant for sickle cell disease: The why, who, and what. | Cimpeanu E, Poplawska M, Jimenez BC, Dutta D, Lim SH | Blood Rev | 2021 |
| Multiple inducers of endothelial NOS (eNOS) dysfunction in sickle cell disease. | Hebbel RP, Vercellotti GM | Am J Hematol | 2021 |
| Effects of hydroxyurea on brain function in children with sickle cell anemia. | Wang WC, Zou P, Hwang SN, Kang G, Ding J, Heitzer AM, Schreiber JE, Helton K, Hankins JS | Pediatr Blood Cancer | 2021 |
| Thrombocytopenia in a teen with sickle cell disease following COVID-19 vaccination. | Underdown MJ, Nuss R | Pediatr Blood Cancer | 2021 |
| A novel ATRX splice variant causing acquired HbH disease in myelodysplastic syndrome with excess blasts-1. | Mallik N, Singh N, Jamwal M, Chhabra S, Hira JK, Malhotra P, Das R, Sharma P | Cancer Genet | 2021 |
| Murine bone marrow mesenchymal stromal cells have reduced hematopoietic maintenance ability in sickle cell disease. | Tang A, Strat AN, Rahman M, Zhang H, Bao W, Liu Y, Shi D, An X, Manwani D, Shi P, Yazdanbakhsh K, Mendelson A | Blood | 2021 |
| The health literacy disparity in adolescents with sickle cell disease. | Perry Caldwell E, Killingsworth E | J Spec Pediatr Nurs | 2021 |
| Letter to the Editor in response to: Fetal hemoglobin levels in premature newborns. | Teofili L, Bianchi M, Valentini CG, Papacci P | J Pediatr Surg | 2021 |
| Disease burden and quality of life of in children with sickle cell disease in Italy: time to be considered a priority. | Colombatti R, Casale M, Russo G | Ital J Pediatr | 2021 |
| Oral ferroportin inhibitor vamifeport for improving iron homeostasis and erythropoiesis in β-thalassemia: current evidence and future clinical development. | Porter J, Taher A, Viprakasit V, Kattamis A, Coates TD, Garbowski M, Dürrenberger F, Manolova V, Richard F, Cappellini MD | Expert Rev Hematol | 2021 |
| De novo HBB frameshift mutation in a patient with dominant β-thalassemia major. | Zhou X, Chen T, Zhang Q, Qi M, Zhang L, Du J, Chi H, Shen B, Xu X, Lu Y | Int J Lab Hematol | 2021 |
| Evaluation of myocardial perfusion and function in patients with asymptomatic beta-thalassemia major using myocardial gated single-photon-emission computed tomography. | Omrani A, Rahimzadeh P, Aba A, Jafari E, Amini A, Assadi M | World J Nucl Med | 2021 |
| Content validation of a self-report daily diary in patients with sickle cell disease. | White MK, Saucier C, Bailey M, D'Alessio D, Foster A, St Pierre D, Raymond K | J Patient Rep Outcomes | 2021 |
| Eosinophilic Myocarditis in a Patient With Sickle Cell Disease. | Imran HM, Ather K, Gutman NH, Atalay MK, Poppas A | JACC Case Rep | 2021 |
| Efficacy and Safety of Thalidomide in Patients With Transfusion-Dependent Thalassemia. | Chandra J, Parakh N, Sidharth , Singh N, Sharma S, Goel M, Pemde H | Indian Pediatr | 2021 |
| Management of Thalassemia: Blood and Beyond. | Merchant R | Indian Pediatr | 2021 |
| Investigating the reasons for marriage among couples with thalassemia minor, in Iran. | Hasanshahi F, Khanjani N | J Community Genet | 2021 |
| Cerebral and skeletal muscle tissue oxygenation during exercise challenge in children and young adults with sickle cell anaemia. | Barriteau CM, Chiu A, Rodeghier M, Liem RI | Br J Haematol | 2021 |
| Subglottic concretion masquerading as foreign body in a child with β thalassemia major: an airway nightmare! | Parikh B, Sahu S, Gupta DK, Singh V | BMJ Case Rep | 2021 |
| Hb Calgary (: c.194G>T): A Highly Unstable Hemoglobin Variant with a β-Thalassemia Major Phenotype. | Martin G, Grimholt RM, Le D, Bechensteen AG, Klingenberg O, Fjeld B, Fourie T, Perrier R, Proven M, Henderson SJ, Roy NBA | Hemoglobin | 2021 |
| The Effect of : c.-121C>T Variant [-71 (C>T)] on the β-Globin Promoter: Case Series Study. | Rafat M, Allamehzadeh Z, Shekari M, Afsa M, Malekzadeh K | Hemoglobin | 2021 |
| Hb Lepore-Hong Kong: First Report of a Novel δ/β-Globin Gene Fusion in a Chinese Family. | Jiang F, Tang XW, Li J, Zhou JY, Zuo LD, Li DZ | Hemoglobin | 2021 |
| A Novel α-Globin Chain Variant, Hb Nanchang [: c.46G>A, Codon 15 (GT>GT) (Gly→Ser)], Detected by Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry. | Xu A, Chen W, Xie W, Zheng H, Zhou Y, Ji L | Hemoglobin | 2021 |
| Identifying elevated risk for future pain crises in sickle-cell disease using photoplethysmogram patterns measured during sleep: A machine learning approach. | Ji Y, Chalacheva P, Rosen CL, DeBaun MR, Coates TD, Khoo MCK | Front Digit Health | 2021 |
| Plasma Lipids and Lipoproteins in Sickle Cell Disease Patients in the Northern West Bank, Palestine. | Samarah F, Srour MA, Dumaidi K | Biomed Res Int | 2021 |
| Multimodal Imaging in Retinal Vascular Occlusions following Trauma - A Case of Sickle Cell Disease with Negative Sickling Test. | Sahu ES, Sachdeva M, Sen A, Karkhur S | J Ophthalmic Vis Res | 2021 |
| Relationship of oxidative stress and antioxidant response with vaso-occlusive crisis in sickle cell anaemia. | Engwa GA, Okolie A, Chidili JPC, Okore PA, Onu PC, Ugwu MO, Oko DE, Ferdinand PU | Afr Health Sci | 2021 |
| Exploring the potential utilities of 99mTc-labeled RBC-equilibrium radionuclide angiocardiography in transfusion-dependent β-thalassemia major patients. | Vadi SK, Sood A, Khadwal A, Parmar M, Bhatia A, Kashyap S, Bahl A, Mittal BR | Nucl Med Commun | 2021 |
| Altered cardiac reserve is a determinant of exercise intolerance in sickle cell anaemia patients. | Hammoudi N, Ceccaldi A, Haymann JP, Guedeney P, Nicolas-Jilwan F, Zeitouni M, Montalescot G, Lionnet F, Isnard R, Hatem SN | Eur J Clin Invest | 2021 |
| Low-dose aspirin for preventing intrauterine growth restriction and pre-eclampsia in sickle cell pregnancy (PIPSICKLE): a randomised controlled trial (study protocol). | Afolabi BB, Babah OA, Adeyemo TA, Odukoya OO, Ezeaka CV, Nwaiwu O, Oshodi YA, Ogunnaike BA | BMJ Open | 2021 |
| Transition Navigator Intervention improves transition readiness to adult care for youth with Sickle Cell Disease. | Manwani D, Doyle M, Davidson L, Mallea M, Silver EJ, Jackson J, Chhabra R, Morrone K, Minniti C, Rastogi D, Stein RE, Oyeku S, Bauman LJ | Acad Pediatr | 2021 |
| Excess heme upregulates heme oxygenase 1 and promotes cardiac ferroptosis in mice with sickle cell disease. | Menon AV, Liu J, Tsai HP, Zeng L, Yang S, Asnani A, Kim J | Blood | 2021 |
| A Rare and Successfully Managed Complication of Stem Cell Transplantation in an Adult Patient With Sickle Cell Disease: Bone Marrow Necrosis. | Ozdogu H, Boga C, Yeral M, Kozanoglu I, Gereklioglu C, Kocer NE | Exp Clin Transplant | 2021 |
| Analysis of clinical presentation, hematological factors, self-reported bed net usage, and malaria burden in sickle cell disease patients. | Harp KO, Botchway F, Dei-Adomakoh Y, Wilson MD, Mubasher M, Adjei AA, Thompson WE, Stiles JK, Driss A | EClinicalMedicine | 2021 |
| The Evolving Role of Next-Generation Sequencing in Screening and Diagnosis of Hemoglobinopathies. | Achour A, Koopmann TT, Baas F, Harteveld CL | Front Physiol | 2021 |
| Prevalence of β-S Globin Haplotypes in Jazan Region of Saudi Arabia. | Akhter MS, Mobarki AA, Hamali HA, Saboor M, Madkhali AM, Dobie G, Hobani YH, Eisa ZM | Clin Lab | 2021 |
| Transcriptional silencing of fetal hemoglobin expression by NonO. | Li X, Chen M, Liu B, Lu P, Lv X, Zhao X, Cui S, Xu P, Nakamura Y, Kurita R, Chen B, Huang DCS, Liu DP, Liu M, Zhao Q | Nucleic Acids Res | 2021 |
| Alpha haemoglobin-stabilising protein concentration in the red blood cells of patients with sickle cell anaemia with and without hydroxycarbamide treatment. | Vasseur C, Domingues-Hamdi E, Pakdaman S, Galactéros F, Baudin-Creuza V | Br J Haematol | 2021 |
| Sonographic Assessment of Some Abdominal Organs in Children with Sickle Cell Disease in Ilorin, Nigeria. | Muftaudeen B, Eze JC, Sidi M, Miftaudeen MN | J Med Ultrasound | 2021 |
| Identified barriers and facilitators to stroke risk screening in children with sickle cell anemia: results from the DISPLACE consortium. | Phillips SM, Schlenz AM, Mueller M, Melvin CL, Adams RJ, Kanter J | Implement Sci Commun | 2021 |
| Urinary Kringle Domain-Containing Protein HGFL: A Validated Biomarker of Early Sickle Cell Anemia-Associated Kidney Disease. | Nekhai S, Lin X, Soni S, Taye A, Smith N, Afangbedji N, Saraf SL, Gordeuk VR, Taylor JG, Jerebtsova M | Am J Nephrol | 2021 |
| Indirect Economic Burden of Sickle Cell Disease. | Holdford D, Vendetti N, Sop DM, Johnson S, Smith WR | Value Health | 2021 |
| Core Decompression and Bone Marrow Aspirate Concentrate in the Treatment of Femoral Head Avascular Necrosis in Pediatric Sickle Cell Disease: Can We Improve Natural History? | Griffith MS, Shaw KA, Hattaway JK, Schrader T | J Pediatr Orthop | 2021 |
| Alteration of grey matter volume is associated with pain and quality of life in children with sickle cell disease: Structural brain alteration and association with pain in sickle cell disease. | Wang Y, Hardy SJ, Ichesco E, Zhang P, Harris RE, Darbari DS | Transl Res | 2021 |
| Combination of lentiviral and genome editing technologies for the treatment of sickle cell disease. | Ramadier S, Chalumeau A, Felix T, Othman N, Aknoun S, Casini A, Maule G, Masson C, De Cian A, Frati G, Brusson M, Concordet JP, Cavazzana M, Cereseto A, El Nemer W, Amendola M, Wattellier B, Meneghini V, Miccio A | Mol Ther | 2021 |
| Contraceptive use and preferences among females with sickle cell disease. | Roe AH, Lang B, McAllister A, Gaitors MC, Smith-Whitley K, Schreiber CA, Sayani F | Contraception | 2021 |
| LUSPATERCEPT - A better strategy for thalassemia? | Patel MS, Raza IM, Hassan SZ | J Pak Med Assoc | 2021 |
| Influenza immunization coverage of children with sickle cell disease. | Peng HK, Dombkowski KJ, Freed GL, Creary SE, Smith D, Reeves SL | Vaccine | 2021 |
| Sickle cell trait: an unsound cause of death. | Lichtsinn HS, Weyand AC, McKinney ZJ, Wilson AM | Lancet | 2021 |
| Novel Substituted Piperidine-2,6-dione Derivatives for Treating Sickle Cell Disease and β-Thalassemia. | Sabnis RW | ACS Med Chem Lett | 2021 |
| Validation of Discharge Diagnosis of Sickle Cell Disease Vaso-Occlusive Episodes in the French Hospital Electronic Database. | Walter O, Maquet J, Derumeaux H, Moulis G, Lafaurie M | Clin Epidemiol | 2021 |
| Quality of Life and Related Factors in β-Thalassemia Patients. | Etemad K, Mohseni P, Aghighi M, Bahadorimonfared A, Hantooshzadeh R, Taherpour N, Piri N, Sotoodeh Ghorbani S, Malek F, Kheiry F, Khodami A, Valadbeigi T, Hajipour M | Hemoglobin | 2021 |
| Management of sickle cell disease in pregnancy. A British Society for Haematology Guideline. | Oteng-Ntim E, Pavord S, Howard R, Robinson S, Oakley L, Mackillop L, Pancham S, Howard J, | Br J Haematol | 2021 |
| Standardizing care of those at great risk: the importance of sickle cell in pregnancy practice guidelines. | Stratton P | Br J Haematol | 2021 |
| Analysis of Causes of Hospitalization Among Children with Sickle Cell Disease in a Group of Private Hospitals in Jeddah, Saudi Arabia. | Abd El-Ghany SM, Tabbakh AT, Nur KI, Abdelrahman RY, Etarji SM, Almuzaini BY | J Blood Med | 2021 |
| Evidence of new intragenic HBB haplotypes model for the prediction of beta-thalassemia in the Malaysian population. | Aziz NA, Taib WW, Kharolazaman NK, Ismail I, Al-Jamal HAN, Jamil NWWA, Esa E, Ibrahim H | Sci Rep | 2021 |
| Progression of central nervous system disease from pediatric to young adulthood in sickle cell anemia. | Champlin G, Hwang SN, Heitzer A, Ding J, Jacola L, Estepp JH, Wang W, Ataga KI, Owens CL, Newman J, King AA, Davis R, Kang G, Hankins JS | Exp Biol Med (Maywood) | 2021 |
| Drug Repurposing: Hydroxyurea Therapy Improves the Transfusion-Free Interval in HbE/Beta-Thalassemia-Major Patients with the I Polymorphism. | Ghosh D, Panja A, Saha D, Banerjee U, Datta AK, Basu A | Genet Test Mol Biomarkers | 2021 |
| The International Hemoglobinopathy Research Network (INHERENT): An international initiative to study the role of genetic modifiers in hemoglobinopathies. | Kountouris P, Stephanou C, Archer N, Bonifazi F, Giannuzzi V, Kuo KHM, Maggio A, Makani J, Mañú-Pereira MDM, Michailidou K, Nkya S, Nnodu OE, Trompeter S, Tshilolo L, Wonkam A, Zilfalil BA, Inusa BPD, Kleanthous M, | Am J Hematol | 2021 |
| Predictors associated with sickle cell nephropathy: a systematic review. | Maurício L, Ribeiro S, Santos L, Miranda DB | Rev Assoc Med Bras (1992) | 2021 |
| A unified model of human hemoglobin switching through single-cell genome editing. | Shen Y, Verboon JM, Zhang Y, Liu N, Kim YJ, Marglous S, Nandakumar SK, Voit RA, Fiorini C, Ejaz A, Basak A, Orkin SH, Xu J, Sankaran VG | Nat Commun | 2021 |
| Thalassemia and autoimmune diseases: Absence of evidence or evidence of absence? | El Hasbani G, Musallam KM, Uthman I, Cappellini MD, Taher AT | Blood Rev | 2021 |
| Luspatercept for β-thalassemia: beyond red blood cell transfusions. | Taher AT, Cappellini MD | Expert Opin Biol Ther | 2021 |
| Longitudinal study of glomerular hyperfiltration and normalization of estimated glomerular filtration in adults with sickle cell disease. | Derebail VK, Zhou Q, Ciccone EJ, Cai J, Ataga KI | Br J Haematol | 2021 |
| Developing an emergency department order set to treat acute pain in sickle cell disease. | Duroseau Y, Beenhouwer D, Broder MS, Brown B, Brown T, Gibbs SN, Jackson K, Liang S, Malloy M, Romney ML, Shani D, Simon J, Yermilov I | J Am Coll Emerg Physicians Open | 2021 |
| Incidence and predictors of bacterial infections in febrile children with sickle cell disease. | Alzahrani F, Alaidarous K, Alqarni S, Alharbi S | Int J Pediatr Adolesc Med | 2021 |
| Prevalence of HBV and HCV infection in beta-thalassemia major patients of Tabriz city, Iran. | Mirzaei G, Shamsasenjan K, Jafari B, Bagherizadeh Y, Sadafzadeh A, Bannazadeh-Baghi H, Sadeghi-Deylamdeh Z, Jafari-Sales A | New Microbes New Infect | 2021 |
| Importance of sickle cell trait counseling for adolescents and young adults. | Jacob SA, Meier ER | Pediatr Blood Cancer | 2021 |
| Abnormal regulation of microRNAs and related genes in pediatric β-thalassemia. | Wang H, Chen M, Xu S, Pan Y, Zhang Y, Huang H, Xu L | J Clin Lab Anal | 2021 |
| Compounded with hemoglobin Port Phillip and -α or -- deletions were identified in Chinese population. | Du L, Bao X, Qin D, Wang J, Yao C, Liang J, Chen J, Yin A | Mol Genet Genomic Med | 2021 |
| Preliminary Study of Coping, Perceived Control, and Depressive Symptoms in Youth with Sickle Cell Anemia. | Prussien KV, Siciliano RE, Ciriegio AE, Lee CA, DeBaun MR, Jordan LC, Compas BE | J Dev Behav Pediatr | 2021 |
| Co-Occurrence of Neurodevelopmental Disorders in Pediatric Sickle Cell Disease. | Lance EI, Cannon AD, Shapiro BK, Lee LC, Johnston MV, Casella JF | J Dev Behav Pediatr | 2021 |
| Hyperhaemolytic transfusion reaction in two β-thalassaemia major patients: The role of eculizumab. | Pantelidou D, Pilalas D, Daios S, Polychronopoulos G, Papadopoulou D, Perifanis V, Savopoulos C, Kaiafa G | J Clin Pharm Ther | 2021 |
| Refractory acquired thrombotic thrombocytopenic purpura in a patient with sickle cell trait successfully treated with caplacizumab. | Aggarwal V, Singer Z, Ledingham D, Othman I | Hematology | 2021 |
| IVS-II-16 (G>C) (: c.315+16G>C) or IVS-II-666 (C>T) (: c.316-185C>T) Mutations Trigger an Hb S (: c.20A>T)/β-Thalassemia Phenotype in an Hb S Trait Patient. | Uçucu S, Karabıyık T, Azik FM | Hemoglobin | 2021 |
| Developmental screening of three-year-old children with sickle cell disease compared to controls. | Wang W, Freeman M, Hamilton L, Carroll Y, Kang G, Moen J, Smeltzer MP, Schreiber J, Heitzer AM, Estepp J, Aygun B | Br J Haematol | 2021 |
| Comparisons of oxygen gradient ektacytometry parameters between sickle cell patients with or without α-thalassaemia. | Boisson C, Renoux C, Nader E, Gauthier A, Poutrel S, Rab M, Fort R, Bertrand Y, Stauffer E, Cannas G, Kebaili K, Virot E, Hot A, Sheehan V, van Beers E, van Wijk R, Joly P, Connes P | Br J Haematol | 2021 |
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| Fatal sickling-associated microvascular occlusive crisis in a young with sickle cell trait. | Mutreja D, K BP, Tvsvgk T | Autops Case Rep | 2021 |
| A Randomized Clinical Hypnosis Pilot Study: Improvements in Self-Reported Pain Impact in Adults with Sickle Cell Disease. | Wallen GR, Middleton KR, Kazmi NB, Yang L, Brooks AT | Evid Based Complement Alternat Med | 2021 |
| Quality of Life and Related Paraclinical Factors in Iranian Patients with Transfusion-Dependent Thalassemia. | Khodashenas M, Mardi P, Taherzadeh-Ghahfarokhi N, Tavakoli-Far B, Jamee M, Ghodrati N | J Environ Public Health | 2021 |
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| Mechanism and Applications of CRISPR/Cas-9-Mediated Genome Editing. | Asmamaw M, Zawdie B | Biologics | 2021 |
| The transfusion management of beta thalassemia in the United States. | Lal A, Wong T, Keel S, Pagano M, Chung J, Kamdar A, Rao L, Ikeda A, Puthenveetil G, Shah S, Yu J, Vichinsky E | Transfusion | 2021 |
| Effect of hydroxyurea therapy on intravascular hemolysis and endothelial dysfunction markers in sickle cell anemia patients. | Chenou F, Hounkpe BW, Domingos IF, Tonassé WV, Batista THC, Santana RM, Arcanjo GDS, Alagbe AE, Araújo ADS, Lucena-Araújo AR, Bezerra MAC, Costa FF, Sonati MF, De Paula EV, Dos Santos MNN | Ann Hematol | 2021 |
| Pregnancy outcomes in women affected by fetal alpha-thalassemia: a case control study. | Li J, Yan J, Huang Y, Wei J, Xie B, Zhu M, Jiang W | Sci Rep | 2021 |
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| Improving the Solubility and Oral Bioavailability of a Novel Aromatic Aldehyde Antisickling Agent (PP10) for the Treatment of Sickle Cell Disease. | Ahmed TA, El-Say KM, Abd-Allah FI, Omar AM, El-Araby ME, Muhammad YA, Pagare PP, Zhang Y, Mohmmad KA, Abdulmalik O, Safo MK | Pharmaceutics | 2021 |
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| Hospital Use and Mortality in Transition-Aged Patients With Sickle Cell Disease. | Fasipe T, Dongarwar D, Lopez E, Brown R, Abadom M, Mahoney DH, Salihu HM | Hosp Pediatr | 2021 |
| Hematological and molecular analysis of patients with G6PD deficiency revealed coexistent hereditary spherocytosis and alpha thalassemia. | Rizo-delaTorre LDC, Herrera-Tirado IM, Hernández-Peña R, Ibarra-Cortés B, Perea-Díaz FJ | Ann Hum Genet | 2021 |
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| The Alberta Newborn Screening Approach for Sickle Cell Disease: The Advantages of Molecular Testing. | Zhou JR, Ridsdale R, MacNeil L, Lilley M, Hoang S, Christian S, Blumenschein P, Wolan V, Bruce A, Singh G, Wright N, Parboosingh JS, Lamont RE, Sosova I | Int J Neonatal Screen | 2021 |
| Case report of active pulmonary TB in a sickle cell disease patient. | Okar L, Rezek M, Abdelhamid MT, Yassin MA | Ann Med Surg (Lond) | 2021 |
| Improved Characterization of Complex β-Globin Gene Cluster Structural Variants Using Long-Read Sequencing. | Rangan A, Hein MS, Jenkinson WG, Koganti T, Aleff RA, Hilker CA, Blommel JH, Porter TR, Swanson KC, Lundquist P, Nguyen PL, Shi M, He R, Viswanatha DS, Jen J, Klee EW, Kipp BR, Hoyer JD, Wieben ED, Oliveira JL | J Mol Diagn | 2021 |
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| The Post-Storage Performance of RBCs from Beta-Thalassemia Trait Donors Is Related to Their Storability Profile. | Anastasiadi AT, Paronis EC, Arvaniti VZ, Velentzas AD, Apostolidou AC, Balafas EG, Dzieciatkowska M, Kostomitsopoulos NG, Stamoulis K, Papassideri IS, D'Alessandro A, Kriebardis AG, Antonelou MH, Tzounakas VL | Int J Mol Sci | 2021 |
| Comparison of Two Alternative Procedures to Obtain Packed Red Blood Cells for β-Thalassemia Major Transfusion Therapy. | Schiroli D, Merolle L, Quartieri E, Chicchi R, Fasano T, De Luca T, Molinari G, Pulcini S, Pertinhez TA, Di Bartolomeo E, Biguzzi R, Baricchi R, Marraccini C | Biomolecules | 2021 |
| Cell erythroid maturation approach: a new paradigm in the road map towards a cure for β-thalassaemia syndromes. | Maggio A | Br J Haematol | 2021 |
| Revisiting fetal hemoglobin inducers in beta-hemoglobinopathies: a review of natural products, conventional and combinatorial therapies. | Mukherjee M, Rahaman M, Ray SK, Shukla PC, Dolai TK, Chakravorty N | Mol Biol Rep | 2021 |
| Total Hip Replacement in Sickle Cell Disease Patients with Avascular Necrosis of Head of Femur: A Retrospective Observational Study. | Al-Otaibi ML, Waliullah S, Kumar V | Indian J Orthop | 2021 |
| A call to start hydroxyurea by 6 months of age and before the advent of sickle cell disease complications. | Elenga N, Kayemba-Kay's S, Nacher M, Archer N | Pediatr Blood Cancer | 2021 |
| Evaluation of Stillbirth Among Pregnant People With Sickle Cell Trait. | Canelón SP, Butts S, Boland MR | JAMA Netw Open | 2021 |
| Rapid molecular diagnostics of large deletional β-thalassemia (3.5 kb and 45 kb) using colorimetric LAMP in various thalassemia genotypes. | Tepakhan W, Jomoui W | Heliyon | 2021 |
| Acute Chest Syndrome in Sickle Cell Disease: Clinical Presentation and Outcomes. The Experience of a Single Thalassemia and Sickle Cell Unit in a University Hospital. | Delicou S, Aggeli K, Magganas K, Patsourakos D, Xydaki A, Koskinas J | Hemoglobin | 2021 |
| Nationwide retrospective study of critically ill adults with sickle cell disease in France. | Agbakou M, Mekontso-Dessap A, Pere M, Voiriot G, Picard M, Bourenne J, Ehrmann S, Canet E, Boyer A, Nseir S, Tamion F, Thille AW, Argaud L, Pontis E, Quenot JP, Schneider F, Hot A, Capellier G, Aubron C, Razazi K, Masseau A, Brule N, Reignier J, Lascarrou JB | Sci Rep | 2021 |
| Clinical depression in children and adolescents with sickle cell anaemia: influencing factors in a resource-limited setting. | Ezenwosu O, Chukwu B, Ezenwosu I, Uwaezuoke N, Eke C, Udorah M, Idoko C, Ikefuna A, Emodi I | BMC Pediatr | 2021 |
| Deferiprone vs deferoxamine for transfusional iron overload in SCD and other anemias: a randomized, open-label, noninferiority study. | Kwiatkowski JL, Hamdy M, El Beshlawy A, Ebeid FSE, Badr M, AlShehri AAM, Kanter J, Inusa BDP, Adly A, Williams S, Kilinc Y, Lee D, Tricta F, Elalfy MS | Blood Adv | 2021 |
| Early oral switch to combined cefixime therapy for management of osteoarticular infections in pediatric sickle cell disease patients: A descriptive analysis. | Mohzari YA, Alshuraim R, Asdaq SMB, Aljobair F, Alrashed A, Alsowaida YS, Alamer A, Al Munjem MF, Al Musawa MI, Hatata M, Alzaaqi MA, Binrokan A, Alajlan SA, Abraham I, Alamer A | J Infect Public Health | 2021 |
| Preferences for Using a Mobile App in Sickle Cell Disease Self-management: Descriptive Qualitative Study. | Mayo-Gamble TL, Quasie-Woode D, Cunningham-Erves J, Rollins M, Schlundt D, Bonnet K, Murry VM | JMIR Form Res | 2021 |
| Sickle cell disease patients in two London trusts: Genotyping including RH variants. | Hui YMT, Gurung K, Layton DM, Ibidapo M, Grimsley S, Regan F | Transfus Med | 2021 |
| Longitudinal assessment of adhesion to vascular cell adhesion molecule-1 at steady state and during vaso-occlusive crises in sickle cell disease. | White J, Callaghan MU, Gao X, Liu K, Zaidi A, Tarasev M, Hines PC | Br J Haematol | 2021 |
| Non-Invasive Prenatal Test for β-Thalassemia and Sickle Cell Disease Using Probe Capture Enrichment and Next-Generation Sequencing of DNA in Maternal Plasma. | Erlich HA, López-Peña C, Carlberg KT, Shih S, Bali G, Yamaguchi KD, Salamon H, Das R, Lal A, Calloway CD | J Appl Lab Med | 2021 |
| Performance of an HRP-2 based (First Response®) and p-LDH-based (Optimal®) rapid diagnostic tests for diagnosis of malaria in paediatric sickle cell disease patients. | Adjei GO, Sulley AM, Goka BQ, Enweronu-Laryea C, Renner L, Alifrangis M, Kurtzhals JAL | Clin Infect Dis | 2021 |
| Myocardial longitudinal strain as the first herald of cardiac impairment in very early iron overload state: an echocardiography and biosusceptometry study on beta-thalassemia patients. | Barbero U, Fornari F, Gagliardi M, Fava A, Giorgi M, Alunni G, Gaglioti CM, Piga A, Ferrero GB, Longo F | Am J Cardiovasc Dis | 2021 |
| Risk of mortality from anemia and iron overload in non-transfusion-dependent β-thalassemia. | Musallam KM, Vitrano A, Meloni A, Addario Pollina S, Karimi M, El-Beshlawy A, Hajipour M, Di Marco V, Ansari SH, Filosa A, Ricchi P, Ceci A, Daar S, Vlachaki E, Singer ST, Naserullah ZA, Pepe A, Scondotto S, Dardanoni G, Bonifazi F, Sankaran VG, Vichinsky E, Taher AT, Maggio A, | Am J Hematol | 2021 |
| Oxygen gradient ektacytometry does not predict pain in children with sickle cell anaemia. | Nardo-Marino A, Petersen J, Brewin JN, Birgens H, Williams TN, Kurtzhals JAL, Rees DC, Glenthøj A | Br J Haematol | 2021 |
| Clinical Utility of the Addition of Molecular Genetic Testing to Newborn Screening for Sickle Cell Anemia. | Shook LM, Haygood D, Quinn CT | Front Med (Lausanne) | 2021 |
| Diminished ovarian reserve in young women with sickle cell anemia. | Pecker L, Hussain S, Mahesh J, Varadhan R, Christianson MS, Lanzkron S | Blood | 2021 |
| Novel histone deacetylase inhibitor CT-101 induces γ-globin gene expression in sickle erythroid progenitors with targeted epigenetic effects. | Junker LH, Li B, Zhu X, Koti S, Cerbone RE, Hendrick CL, Sangerman J, Perrine S, Pace BS | Blood Cells Mol Dis | 2021 |
| Hepcidin-to-Ferritin Ratio: A Potential Novel Index to Predict Iron Overload-Liver Fibrosis in ß-Thalassemia Major. | Zaman BA, Rasool SO, Merza MA, Abdulah DM | Transfus Clin Biol | 2021 |
| Predicting risk factors for thromboembolic complications in patients with sickle cell anaemia - lessons learned for prophylaxis. | Alkindi S, Al-Ghadani AR, Al-Zeheimi SR, Alkindi SY, Fawaz N, Ballas SK, Pathare AV | J Int Med Res | 2021 |
| Hepatobiliary Findings in Nigerian Children with Sickle Cell Anaemia. | Adeniyi OF, Akinsete AM, Odeghe EA, Okeke OF, Mokwenyei O, Kene-Udemezue B, Seyi-Olajide JO, Akinsulie A, Adeniran O, Adeniran O, Oyeleke G | West Afr J Med | 2021 |
| Trends in quality of care among children with sickle cell anemia. | Reeves SL, Freed GL, Madden B, Wu M, Miller L, Cogan L, Anders D, Creary SE, McCormick J, Dombkowski KJ | Pediatr Blood Cancer | 2021 |
| A novel SUPT5H variant associated with a beta-thalassaemia trait. | Charnay T, Cerino M, Gonnet K, Bonello-Palot N, Bréchard MP, Badens C | Br J Haematol | 2021 |
| Multiplex CRISPR/Cas9 genome editing in hematopoietic stem cells for fetal hemoglobin reinduction generates chromosomal translocations. | Samuelson C, Radtke S, Zhu H, Llewellyn M, Fields E, Cook S, Huang MW, Jerome KR, Kiem HP, Humbert O | Mol Ther Methods Clin Dev | 2021 |
| Safety, clinical and laboratory characteristics of donors with thalassemia minor in living donor kidney transplant: a case series. | Dinh NH, Beaupha SMC | BMC Nephrol | 2021 |
| Splenic infarction in sickle cell trait: A comprehensive systematic review of case studies. | Jefferson JM, Sims WM, Umeh N, Byeon YJJ, Abdallah KE, Bonham VL, Naik RP, Smith-Whitley K | EJHaem | 2021 |
| Optimizing sgRNA to Improve CRISPR/Cas9 Knockout Efficiency: Special Focus on Human and Animal Cell. | Shojaei Baghini S, Gardanova ZR, Zekiy AO, Shomali N, Tosan F, Jarahian M | Front Bioeng Biotechnol | 2021 |
| Coexistence of Relapsing Polychondritis and Sickle Cell Disease in a Child. | Tetteh BO, Yebuah FB, Amissah-Arthur MB, Dey D | Case Rep Rheumatol | 2021 |
| Cognitive Function in Adults with Beta-Thalassemia Major in Oman: A Pilot Study. | Daar S, Al Saadoon M, Wali Y, Al Mujaini R, Al Rahbi S, Chan MF, Al-Siyabi A, Alansary N, Mahadevan S, Al-Adawi S | Oman Med J | 2021 |
| Alterations of panoramic radiomorphometric indices in children and adolescents with beta-thalassemia major: A fractal analysis study. | Yagmur B, Tercanli-Alkis H, Tayfun-Kupesiz F, Karayilmaz H, Kupesiz OA | Med Oral Patol Oral Cir Bucal | 2021 |
| Tocilizumab for severe acute chest syndrome in a child with sickle cell disease and dramatically high interleukin-6 values in endotracheal and pleural fluids. | Allali S, Chhun S, de Montalembert M, Heilbronner C, Taylor M, Brice J, Elie J, Rignault-Bricard R, Maciel TT, Chareyre J, Hermine O | Am J Hematol | 2021 |
| Myocardial Performance Index Among Patients of Sickle Cell Disorder in Rural Teaching Hospital: A Case-Control Study. | Chaturvedi A, Kumar S, Acharya S, Gaidhane SA, Wanjari A, Talwar D | Cureus | 2021 |
| Two Sides of a Coin: Case Report of Unilateral Synangiosis and Contralateral Stroke Highlighting Consequences of Disease Progression and Efficacy of Revascularization in Sickle Cell Disease Associated Moyamoya Syndrome. | Slingerland AL, Karsten MB, Smith ER, Sobota AE, See AP | Acta Haematol | 2021 |
| Long noncoding RNAs transcribed downstream of the human β-globin locus regulate β-globin gene expression. | Higashi M, Ikehara T, Nakagawa T, Yoneda M, Hattori N, Ikeda M, Ito T | J Biochem | 2021 |
| Screening by Self-Report Underestimates Sickle Cell Trait in High-School Athletes. | Allen G, Smith MS, Bruner M, Agrawal K, Clugston JR, Prine BR | Cureus | 2021 |
| Fear of abortion and emotional divorce in women with minor thalassemia: a population-based study in Yazd, Iran. | Rahaei Z, Sahami MA, Bidaki R | BMC Womens Health | 2021 |
| Malaria protection due to sickle haemoglobin depends on parasite genotype. | Band G, Leffler EM, Jallow M, Sisay-Joof F, Ndila CM, Macharia AW, Hubbart C, Jeffreys AE, Rowlands K, Nguyen T, Gonçalves S, Ariani CV, Stalker J, Pearson RD, Amato R, Drury E, Sirugo G, d'Alessandro U, Bojang KA, Marsh K, Peshu N, Saelens JW, Diakité M, Taylor SM, Conway DJ, Williams TN, Rockett KA, Kwiatkowski DP | Nature | 2021 |
| An online alpha-thalassemia carrier discrimination model based on random forest and red blood cell parameters for low HbA cases. | Feng P, Li Y, Liao Z, Yao Z, Lin W, Xie S, Hu B, Huang C, Liu W, Xu H, Liu M, Gan W | Clin Chim Acta | 2021 |
| Oxidative stress and hepcidin expression in pediatric sickle cell anemia with iron overload. | Elbostany EA, Elghoroury EA, Thabet EH, Rashad AA, Rasheed EA, El-Saeed GSM, Abdelhalim DA, Abdelfattah SN, Salama II | Hematol Oncol Stem Cell Ther | 2021 |
| Perinatal outcomes in women with sickle cell disease: a matched cohort study from London, UK. | Oakley LL, Mitchell S, von Rege I, Hadebe R, Howard J, Robinson SE, Oteng-Ntim E | Br J Haematol | 2021 |
| Practice Patterns for the Acceptance of Medically Complex Living Kidney Donors with Hematuria, Sickle Cell Trait, Smoking, Illegal Drug Use, or Urological Issues: A Multinational Survey. | Arabi Z, Hamad A, Bukhari M, Altheaby A, Kaysi S | Avicenna J Med | 2021 |
| Curative therapy for hemoglobinopathies: an International Society for Cell & Gene Therapy Stem Cell Engineering Committee review comparing outcomes, accessibility and cost of ex vivo stem cell gene therapy versus allogeneic hematopoietic stem cell transplantation. | Leonard A, Bertaina A, Bonfim C, Cohen S, Prockop S, Purtill D, Russell A, Boelens JJ, Wynn R, Ruggeri A, Abraham A | Cytotherapy | 2021 |
| Early testicular maturation is sensitive to depletion of spermatogonial pool in sickle cell disease. | Benninghoven-Frey KM, Neuhaus N, Lahtinen AK, Krallmann C, Portela JMD, Jarisch A, Nordhoff V, Soave A, Ba Omar HAM, Sundin M, Langenskiöld C, Kliesch S, Stukenborg JB, Jahnukainen K | Haematologica | 2021 |
| Reasons for Hospitalization of Sickle Cell Disease Patients in the Eastern Province of Saudi Arabia: A Single-Center Study. | Zakaria OM, Buhalim RA, Al Jabr FA, AlSaeed MN, Al-Hajji IA, Al Saleh YA, Buhalim MA, Al Dehailan AM | Cureus | 2021 |
| Acute Myeloid Leukemia Case after Gene Therapy for Sickle Cell Disease. | Goyal S, Tisdale J, Schmidt M, Kanter J, Jaroscak J, Whitney D, Bitter H, Gregory PD, Parsons G, Foos M, Yeri A, Gioia M, Voytek SB, Miller A, Lynch J, Colvin RA, Bonner M | N Engl J Med | 2021 |
| Biologic and Clinical Efficacy of LentiGlobin for Sickle Cell Disease. | Kanter J, Walters MC, Krishnamurti L, Mapara MY, Kwiatkowski JL, Rifkin-Zenenberg S, Aygun B, Kasow KA, Pierciey FJ, Bonner M, Miller A, Zhang X, Lynch J, Kim D, Ribeil JA, Asmal M, Goyal S, Thompson AA, Tisdale JF | N Engl J Med | 2021 |
| Impact of hydroxyurea on lymphocyte subsets in children with sickle cell anemia. | Elsayh KI, Saad K, Hetta HF, Youssef MAM, Embaby MM, Mohamed IL, Abdel-Aziz SM, Zahran ZAM, Elhoufey A, Ghandour AMA, Zahran AM | Pediatr Res | 2021 |
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| Optimal strategies for carrier screening and prenatal diagnosis of α- and β-thalassemia. | Mensah C, Sheth S | Hematology Am Soc Hematol Educ Program | 2021 |
| Clinical trial considerations in sickle cell disease: patient-reported outcomes, data elements, and the stakeholder engagement framework. | Badawy SM | Hematology Am Soc Hematol Educ Program | 2021 |
| Optimizing management of sickle cell disease in patients undergoing surgery. | Oyedeji CI, Welsby IJ | Hematology Am Soc Hematol Educ Program | 2021 |
| Treatment dilemmas: strategies for priapism, chronic leg ulcer disease, and pulmonary hypertension in sickle cell disease. | Azbell RCG, Desai PC | Hematology Am Soc Hematol Educ Program | 2021 |
| How to avoid the problem of erythrocyte alloimmunization in sickle cell disease. | Pirenne F, Floch A, Habibi A | Hematology Am Soc Hematol Educ Program | 2021 |
| Evidence-Based Minireview: In young children with severe sickle cell disease, do the benefits of HLA-identical sibling donor HCT outweigh the risks? | Shah N, Krishnamurti L | Hematology Am Soc Hematol Educ Program | 2021 |
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| First Report of the 3'-Untranslated Region +1506 (A>C) [NM_000518.5: c.*32A>C] mutation on the β-Globin Gene in the Indian Population. | Sen A, Seenappa V, Chakrabarti P, Dolai TK | Hemoglobin | 2021 |
| Association of High-Intensity Exercise with Renal Medullary Carcinoma in Individuals with Sickle Cell Trait: Clinical Observations and Experimental Animal Studies. | Shapiro DD, Soeung M, Perelli L, Dondossola E, Surasi DS, Tripathi DN, Bertocchio JP, Carbone F, Starbuck MW, Van Alstine ML, Rao P, Katz MHG, Parker NH, Shah AY, Carugo A, Heffernan TP, Schadler KL, Logothetis C, Walker CL, Wood CG, Karam JA, Draetta GF, Tannir NM, Genovese G, Msaouel P | Cancers (Basel) | 2021 |
| Anemia Diagnostic System Based on Impedance Measurement of Red Blood Cells. | Cho H, Lee SR, Baek Y | Sensors (Basel) | 2021 |
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| A successful booster umbilical cord blood transplantation for a 10-year-old patient with beta-thalassemia major in India. | Ramanan V | Asian J Transfus Sci | 2021 |
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| Telehealth acceptability and opioid prescribing patterns of providers of painful chronic diseases during the COVID-19 pandemic: A survey of sickle cell providers. | Kenney MO, Becerra B, Beatty SA, Smith WR | J Opioid Manag | 2021 |
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| Angiotensin-converting enzyme (ACE) inhibitors for proteinuria and microalbuminuria in people with sickle cell disease. | Sasongko TH, Nagalla S | Cochrane Database Syst Rev | 2021 |
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| Early Myeloid Derived Suppressor Cells (eMDSCs) Are Associated With High Donor Myeloid Chimerism Following Haploidentical HSCT for Sickle Cell Disease. | Bhat DK, Olkhanud PB, Gangaplara A, Seifuddin F, Pirooznia M, Biancotto A, Fantoni G, Pittman C, Francis B, Dagur PK, Saxena A, McCoy JP, Pfeiffer RM, Fitzhugh CD | Front Immunol | 2021 |
| Using DNA testing for the precise, definite, and low-cost diagnosis of sickle cell disease and other Haemoglobinopathies: findings from Tanzania. | Christopher H, Burns A, Josephat E, Makani J, Schuh A, Nkya S | BMC Genomics | 2021 |
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| Placental transcriptome sequencing combined with bioinformatics predicts potential genes and circular RNAs associated with hemoglobin Bart's hydrops fetalis syndrome. | Deng L, Lu Y, Yang D, Yang F, Ruan H, Wei C, Lai K, Pang L | J Obstet Gynaecol Res | 2021 |
| Treatment of Erythroid Precursor Cells from β-Thalassemia Patients with Alkaloids: Induction of Fetal Hemoglobin Production. | Zuccato C, Cosenza LC, Zurlo M, Lampronti I, Borgatti M, Scapoli C, Gambari R, Finotti A | Int J Mol Sci | 2021 |
| The Practices of Anaesthesiologists in the Management of Patients with Sickle Cell Disease: Empirical Evidence from Cameroon. | Djomo Tamchom D, Kuitchet A, Ndikontar R, Nga Nomo S, Fouda H, Van Obbergh L | Healthcare (Basel) | 2021 |
| Cranial masses in sickle cell disease. | Gonçalves JRDS, Tribovane D, Pires M, Silva Lopes R, Inacio de Oliveira MR, Conceição C | J Pediatr | 2021 |
| A critical evaluation of crizanlizumab for the treatment of sickle cell disease. | Karki NR, Saunders K, Kutlar A | Expert Rev Hematol | 2021 |
| Retinopathy in Egyptian patients with sickle cell disease: A cross-sectional study. | Hassan T, Badr M, Hanna D, Arafa M, Elhewala A, Dabour S, Shehata S, Rahman DA | Medicine (Baltimore) | 2021 |
| Use of rivaroxaban in sickle cell disease and venous thromboembolism: A case report. | Rozi W, Ali EAH, Al-Mashdali AF, Abdelrazek M, Yassin MA | Medicine (Baltimore) | 2021 |
| Newborn Screening Practices for Beta-Thalassemia in the United States. | Bender MA, Hulihan M, Dorley MC, Aguinaga MDP, Ojodu J, Yusuf C | Int J Neonatal Screen | 2021 |
| Impact of a Residential Summer Camp Experience on Children With Sickle Cell Disease. | Yan AP, Sawhney M, Kirby-Allen M | Ochsner J | 2021 |
| Molecular and Haematological Characteristics of alpha-Thalassemia Deletions in Yogyakarta Special Region, Indonesia. | Husna N, Handayani NSN | Rep Biochem Mol Biol | 2021 |
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| NESTROFT-A Cost-Effective Mass Screening Tool for the Detection of β-Thalassemia Carrier Status in Anemic Pregnant Women: A Step Toward Reducing the National Disease Burden. | Gosavi M, Chavan R, Bellad MB | J Lab Physicians | 2021 |
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| COVID-19-associated rhabdomyolysis in a paediatric patient with sickle cell trait. | Kermond R, Cavazzoni E, Kilo T, Britton PN, Durkan A | J Paediatr Child Health | 2021 |
| Challenges of Managing Multiple Myeloma Patients with Sickle Cell Disease: A Case Report and Review of Literature. | Bou Zerdan M, Diacovo MJ, Chaulagain CP | Am J Case Rep | 2021 |
| Combined preoperative plasma exchange and red blood cell exchange transfusion in a renal transplant patient with protein S deficiency and hemoglobin SC disease. | Cook O, Cervi A, Laureano M, Gangji AS, Verhovsek M | Transfus Apher Sci | 2021 |
| High Dickkopf-1 levels are associated with chronic inflammation in children with sickle cell disease. | Giordano P, Vecchio GCD, Russo G, Palmieri VV, Piacente L, Fidone C, Urbano F, Faienza MF | Eur J Haematol | 2021 |
| What does the term 'sickle cell disease' mean? | Bain BJ, Littlewood T, Rees DC | Br J Haematol | 2021 |
| Publisher Correction: Sickle cell gene therapies approach watershed. | Sheridan C | Nat Biotechnol | 2021 |
| Stable Luminescent Poly(Allylaminehydrochloride)-Templated Copper Nanoclusters for Selectively Turn-Off Sensing of Deferasirox in β-Thalassemia Plasma. | Lin HJ, Wang CC, Kou HS, Cheng CW, Wu SM | Pharmaceuticals (Basel) | 2021 |
| Granulocyte Colony-Stimulating Factor is Safe and Well Tolerated following Allogeneic Transplantation in Patients with Sickle Cell Disease. | Shah NC, Bhoopatiraju S, Abraham A, Anderson E, Andreansky M, Bhatia M, Chaudhury S, Cuvelier GDE, Godder K, Grimley M, Hale G, Kamani N, Jacobsohn D, Ngwube A, Gilman AL, Skiles J, Yu LC, Shenoy S | Transplant Cell Ther | 2021 |
| SOD2 V16A Amplifies Vascular Dysfunction in Sickle Cell Patients by Curtailing Mitochondria Complex IV Activity. | Dosunmu-Ogunbi A, Yuan S, Reynolds M, Giordano L, Sanker S, Sullivan M, Stolz DB, Kaufman BA, Wood KC, Zhang Y, Shiva S, Nouraie SM, Straub AC | Blood | 2021 |
| Hb Dahua [β59(E3)Lys→Met; : c.179A>T] a Novel Variant on the β-Globin Gene. | Qin YY, Huang XJ, Ma YL, Qin JX, Liang L, Li YQ | Hemoglobin | 2021 |
| Dominant β-Thalassemia Phenotype Caused by Hb Dieppe (: c.383A>G): Another Case Report. | Chen HQ, Wu LS, Jiang F, Li DZ | Hemoglobin | 2021 |
| Stigma and quality of life in adults with sickle cell disease in Jamaica and the United States. | Bulgin D, Asnani M, Vorderstrasse A, Royal C, Pan W, Tanabe P | Psychol Health Med | 2021 |
| Case study of betibeglogene autotemcel gene therapy in an adult Greek patient with transfusion-dependent β-thalassaemia of a severe genotype. | Constantinou V, Papayanni PG, Mallouri D, Batsis I, Bouinta A, Papadopoulou D, Papadimitriou V, Kammenou M, Pantelidou D, Sotiropoulos D, Sakellari I, Anagnostopoulos A, Yannaki E | Br J Haematol | 2021 |
| Long-Term Effects of Allogeneic Hematopoietic Stem Cell Transplantation on Systemic Inflammation in Sickle Cell Disease Patients. | de Azevedo JTC, Costa TCM, Lima KC, Maciel TT, Palma PVB, Darrigo-Júnior LG, Setanni Grecco CE, Stracieri ABPL, Elias JB, Pieroni F, Guerino-Cunha RL, Pinto ACS, De Santis GC, Covas DT, Hermine O, Simões BP, Oliveira MC, Malmegrim KCR | Front Immunol | 2021 |
| Multisystem Inflammatory Syndrome in a Previously Vaccinated Adolescent Female With Sickle Cell Disease. | DeJong J, Sainato R, Forouhar M, Robinson D, Kunz A | Pediatr Infect Dis J | 2021 |
| Accelerated low-density neutrophil transition in sickle cell anaemia may contribute to disease pathophysiology. | Torres LS, Teles LIM, Shaul ME, Fridlender ZG, Santos I, Leonardo FC, de Melo Campos P, Benites BD, Olalla Saad ST, Costa FF, Conran N | Br J Haematol | 2021 |
| Clinical and genetic characteristics of hemoglobin H disease in Iran. | Abolghasemi H, Kamfar S, Azarkeivan A, Karimi M, Keikhaei B, Abolghasemi F, Radfar MH, Eshghi P, Alavi S | Pediatr Hematol Oncol | 2021 |
| Genetic research and clinical analysis of β-globin gene cluster deletions in the Chinese population of Fujian province: A 14-year single-center experience. | Chen M, Zhang M, Chen L, Lin N, Wang Y, Xu L, Huang H | J Clin Lab Anal | 2021 |
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| VCAM1, HMOX1 and NOS3 differential endothelial expression may impact sickle cell anemia vasculopathy. | Silva M, Coelho A, Vargas S, Faustino P | Blood Cells Mol Dis | 2021 |
| Acute venous thromboembolism after initiation of voxelotor for treatment of sickle cell disease. | Lemon N, Sterk E, Rech MA | Am J Emerg Med | 2021 |
| Health Status of Patients With β-Thalassemia in the West Bank: A Retrospective-Cohort Study. | Aldwaik R, Abu Mohor T, Idyabi I, Warasna S, Abdeen S, Karmi B, Abu Seir R | Front Med (Lausanne) | 2021 |
| Correlation between Serum Fatty Acid Binding Protein 4 (FABP4) Levels and Cardiac Function in Patients with Thalassemia Major. | Fianza PI, Rahmawati A, Afifah S, Praptama S, Ghozali M, Sihite TA, Setiabudi D, Syamsunarno MRAA, Fucharoen S, Panigoro R | Dis Markers | 2021 |
| Analyzing Effects of Sickle Cell Disease on Morphometric and Cranial Growth in Indian Population. | Menka K, Anand K, Jha MS, Goel A, Nasreen S, Palve DH | J Pharm Bioallied Sci | 2021 |
| Sickle Cell Disease and Psychosocial Well-Being: Comparison of Patients With Preclinical and Clinical Avascular Necrosis of the Femoral Head. | Tezol O, Karahan F, Unal S | Turk Arch Pediatr | 2021 |
| Priming With Red Blood Cells Allows Red Blood Cell Exchange for Sickle Cell Disease in Low-Weight Children. | Hequet O, Boisson C, Joly P, Revesz D, Kebaili K, Gauthier A, Renoux C, Creppy S, Nader E, Nicolas JF, Berard F, Cognasse F, Vocanson M, Bertrand Y, Connes P | Front Med (Lausanne) | 2021 |
| Life-Threatening Acute Chest Syndrome in a Patient With Sickle Cell Disease After Switching From Hydroxyurea Therapy to Partial Exchange Transfusions: A Case Report. | Kvam AK, Torp HA, Iversen PO | Cureus | 2021 |
| Lysine-specific histone demethylase 1 inhibition enhances robust fetal hemoglobin induction in human β-thalassemia/hemoglobin E erythroid cells. | Kaewsakulthong W, Pongpaksupasin P, Nualkaew T, Hongeng S, Fucharoen S, Jearawiriyapaisarn N, Sripichai O | Hematol Rep | 2021 |
| Aggravated Dental and Periodontal Status in Patients with Sickle Cell Disease and Its Association with Serum Ferritin. | Davidopoulou S, Pikilidou M, Yavropoulou MP, Kalogirou TE, Zebekakis P, Kalfas S | J Contemp Dent Pract | 2021 |
| Genotypic and Clinical Analysis of a Thalassemia Major Cohort: An Observational Study. | A T, Lambrou GI, Samartzi A, Vlachou E, Papassotiriou I, Geronikolou SA, Kanaka-Gantenbein C, Chrousos GP, Kattamis A | Adv Exp Med Biol | 2021 |
| Hidradenitis suppurativa is associated with iron deficiency anemia, anemia of chronic disease, and sickle cell anemia-A single-center retrospective cohort study. | Parameswaran A, Garshick MS, Revankar R, Lu CP, Chiu ES, Sicco KIL | Int J Womens Dermatol | 2021 |
| Hearing Loss in Beta-Thalassemia: Systematic Review. | Tartaglione I, Carfora R, Brotto D, Barillari MR, Costa G, Perrotta S, Manara R | J Clin Med | 2021 |
| Quality of Life and Burden of Disease in Italian Patients with Transfusion-Dependent Beta-Thalassemia. | Tedone F, Lamendola P, Lopatriello S, Cafiero D, Piovani D, Forni GL | J Clin Med | 2021 |
| The Impact of Sickle Cell Disease on Academic Performance among Affected Students. | Alhazmi A, Hakami K, Abusageah F, Jaawna E, Khawaji M, Alhazmi E, Zogel B, Qahl S, Qumayri G | Children (Basel) | 2021 |
| Retained Splenic Function in an Indian Population with Homozygous Sickle Cell Disease May Have Important Clinical Significance. | Serjeant B, Hambleton I, Serjeant G | Indian J Community Med | 2021 |
| A Novel Mutation in ATRX Causes Alpha-Thalassemia X-Linked Intellectual Disability Syndrome in a Han Chinese Family. | Wu S, Zheng Y, Xu C, Fu J, Xiong F, Yang F | Front Pediatr | 2021 |
| Barriers to Therapeutic Use of Hydroxyurea for Sickle Cell Disease in Nigeria: A Cross-Sectional Survey. | Okocha EC, Gyamfi J, Ryan N, Babalola O, Etuk EA, Chianumba R, Nwegbu M, Isa H, Madu AJ, Adegoke S, Nnebe-Agumandu U, Brown B, Peprah E, Nnodu OE | Front Genet | 2021 |
| Improved Non-Invasive Preimplantation Genetic Testing for Beta-Thalassemia Using Spent Embryo Culture Medium Containing Blastocoelic Fluid. | Ou Z, Deng Y, Liang Y, Chen Z, Sun L | Front Endocrinol (Lausanne) | 2021 |
| Do Genetic Polymorphisms Affect Fetal Hemoglobin (HbF) Levels in Patients With Sickle Cell Anemia Treated With Hydroxyurea? A Systematic Review and Pathway Analysis. | Sales RR, Nogueira BL, Tosatti JAG, Gomes KB, Luizon MR | Front Pharmacol | 2021 |
| Spontaneous epidural hematoma: A case report of rare crisis of sickle cell disease. | Takroni SY, Nasiri AM, Ahmed E, Alkharras RA | J Family Med Prim Care | 2021 |
| Inhibition of the Aquaporin-1 Cation Conductance by Selected Furan Compounds Reduces Red Blood Cell Sickling. | Chow PH, Cox CD, Pei JV, Anabaraonye N, Nourmohammadi S, Henderson SW, Martinac B, Abdulmalik O, Yool AJ | Front Pharmacol | 2021 |
| Free Flap Reconstruction and Its Management in Sickle Cell Trait: Lessons Learned from a Case. | Mehta R, Rao KN, Nagarkar NM, Aggarwal A | Indian J Surg Oncol | 2021 |
| Whole Blood Transcriptome Analysis in Children with Sickle Cell Anemia. | Gee BE, Pearson A, Buchanan-Perry I, Simon RP, Archer DR, Meller R | Front Genet | 2021 |
| Influence of High Hemoglobin-Oxygen Affinity on Humans During Hypoxia. | Webb KL, Dominelli PB, Baker SE, Klassen SA, Joyner MJ, Senefeld JW, Wiggins CC | Front Physiol | 2021 |
| Investigating the Efficacy and Safety of Thalidomide for Treating Patients With -Thalassemia: A Meta-Analysis. | Lu Y, Wei Z, Yang G, Lai Y, Liu R | Front Pharmacol | 2021 |
| Timed Average Mean Maximum Velocity (TAMMV) of Cerebral Blood Flow of Children and Adolescents with Sickle cell Disease: correlation with clinical and hematological profiles in country. | Chukwu B, Menezes L, Fukuda T, Filho J, Goncalves M | Malawi Med J | 2021 |
| Iron profile of pregnant sickle cell anemia patients in Odisha, India. | Sukla SK, Mohanty PK, Patel S, Das K, Hiregoudar M, Soren UK, Meher S | Hematol Transfus Cell Ther | 2021 |
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