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Anemia

Free Subscription Articles published in Br J Haematol Retrieve available abstracts of 257 articles: HTML format

Single Articles

July 2026
1. MANEEKESORN S, Choed-Amphai C, Chanthong S, Tantiworawit A, et al
   Oxidative stress and antioxidant capacity in hereditary elliptocytosis and hereditary pyropoikilocytosis.
   Br J Haematol. 2026;209:266-274.
   PubMed     Abstract available
   
   
   June 2026
2. WANG D, Zhou L, Hendrickson JE, Karafin MS, et al
   Impact of blood donor, component and recipient variables on antigen-specific alloantibodies.
   Br J Haematol. 2026;208:2212-2221.
   PubMed     Abstract available
   
   
   
3. ARCANJO GS, Silva AP, Diniz MV, Domingos IF, et al
   A genetic risk score based on BCL11A and HBS1L-MYB variants predicts clinical severity in Brazilian sickle cell anaemia patients.
   Br J Haematol. 2026;208:2203-2211.
   PubMed     Abstract available
   
   
   
4. THEOCHARAKI K, Delicou S, Ntzoura-Kani A, Simantiris N, et al
   Red blood cell membrane proteome as a reporter of disease severity, transfusion impact and genetic background in transfusion-dependent beta-thalassaemia.
   Br J Haematol. 2026;208:1980-1992.
   PubMed     Abstract available
   
   
   
5. TEMIYE E, Akinsete A, Joacquim A, Fakile U, et al
   Short-course blood transfusion therapy with hydroxyurea, a functional strategy in the management of stroke in children with sickle cell disease.
   Br J Haematol. 2026;208:2194-2202.
   PubMed     Abstract available
   
   
   
6. WU X, Yang Z, Zhang X, Lu S, et al
   Clinical features and maternal-fetal outcome of pregnancy with aplastic anaemia: A single-centre retrospective study.
   Br J Haematol. 2026;208:2222-2228.
   PubMed     Abstract available
   
   
   May 2026
7. YAMASHITA N, Kawakami T, Matsuzawa S, Miyairi S, et al
   Immunological features of acquired pure red cell aplasia: Specific human leucocyte antigen alleles, signal transducer and activator of transcription 3 mutations and a unique T-cell receptor beta motif.
   Br J Haematol. 2026;208:1797-1805.
   PubMed     Abstract available
   
   
   
8. SPATARO F, Desantis V, Solimando AG
   Decoding immune-driven erythroid failure in pure red cell aplasia.
   Br J Haematol. 2026;208:1887-1889.
   PubMed     Abstract available
   
   
   
9. DE WILDE JRA, Kuppens GZL, Boesveld ME, van Vuren AJ, et al
   In-depth analysis of osmotic gradient ektacytometry parameters across different genotypes in hereditary spherocytosis.
   Br J Haematol. 2026;208:1785-1796.
   PubMed     Abstract available
   
   
   
10. BOMBACI S, Quarello P, Del Borrello G, Barat V, et al
    Neonatal genetic screening of Glucose-6-phosphate dehydrogenase deficiency through next-generation sequencing.
    Br J Haematol. 2026;208:1777-1784.
    PubMed     Abstract available
    
    
    
11. RUIZ LOPEZ JN, Shao L, Jiang D, Bailey LS, et al
    A multicentre analysis of efficacy, safety and molecular response correlates of fostamatinib in warm autoimmune haemolytic anaemia and Evans syndrome.
    Br J Haematol. 2026;208:1878-1884.
    PubMed     Abstract available
    
    
    April 2026
12. ZHANG X, Shah BN, Han J, Nouraie M, et al
    Circulating erythropoietin concentration associates with thromboembolism in sickle cell disease.
    Br J Haematol. 2026 Apr 29. doi: 10.1111/bjh.70517.
    PubMed     Abstract available
    
    
    
13. SHIM YJ, Lee JH, Dayagi TW, Klaassen RJ, et al
    Expanding genetic landscape of inherited bone marrow failure syndromes: Insights from the Canadian Inherited Marrow Failure Registry (CIMFR) (2001-2023).
    Br J Haematol. 2026;208:1407-1418.
    PubMed     Abstract available
    
    
    
14. BRANDSEN RP, Klaassen I, de Caluwe R, Nur E, et al
    Circulating angiogenesis-related biomarkers in sickle cell retinopathy and maculopathy.
    Br J Haematol. 2026;208:1398-1406.
    PubMed     Abstract available
    
    
    
15. ALAM AU, Kaul P, Jain V, Wu C, et al
    Suboptimal screening and correction of maternal iron deficiency anaemia in the general population and in inherited bleeding disorders: A population-based cohort study.
    Br J Haematol. 2026;208:1389-1397.
    PubMed     Abstract available
    
    
    
16. RODRIGUEZ V, Sankar A, Stanek J, Rush C, et al
    Safety and efficacy of anti-coagulation for primary and secondary venous thromboembolism prophylaxis in hospitalized adolescents and young adults with sickle cell disease: An institutional experience.
    Br J Haematol. 2026;208:1380-1388.
    PubMed     Abstract available
    
    
    March 2026
17. ST-ONGE J, Hristova T, Charles C, Bereznyakova O, et al
    Stroke burden and functional impacts in adults with sickle cell disease.
    Br J Haematol. 2026;208:1063-1073.
    PubMed     Abstract available
    
    
    
18. MURAKHOVSKAYA I, Yazdanbakhsh K
    Warm autoimmune haemolytic anaemia: Clinical considerations.
    Br J Haematol. 2026;208:841-844.
    PubMed     Abstract available
    
    
    
19. MEENA SK, Kancharla A, Mohamed AI, James B, et al
    Excellent outcomes in children after haematopoietic stem cell transplantation for hepatitis-associated aplastic anaemia following liver transplantation.
    Br J Haematol. 2026;208:1009-1016.
    PubMed     Abstract available
    
    
    
20. KARKARE T, Cronin RM, Roche C, Young A, et al
    Infertility and family building perspectives among adults with sickle cell disease.
    Br J Haematol. 2026;208:1054-1062.
    PubMed     Abstract available
    
    
    
21. NAKAMURA F, Ishiyama K, Suzuki R, Maruyama H, et al
    Phase II study of the triple combination of rabbit ATG, ciclosporin and eltrombopag in patients with transfusion-dependent aplastic anaemia: West Japan Hematology Study Group (W-JHS) AA02 trial.
    Br J Haematol. 2026;208:1084-1092.
    PubMed     Abstract available
    
    
    
22. DECLEENE NF, Nguyen DT, Kirk SE, Helber HL, et al
    The diagnostic performance of the basic versus the detailed telomere Flow FISH test in young patients with aplastic anaemia.
    Br J Haematol. 2026;208:1093-1104.
    PubMed     Abstract available
    
    
    February 2026
23. VILLABONI S, Stuart-Smith S, De Kreuk A, Rees DC, et al
    Iron deficiency is associated with reduced levels of inflammation and haemolysis in patients with HbSS and HbSC and reduced clinical admissions in those with HbSC.
    Br J Haematol. 2026;208:683-690.
    PubMed     Abstract available
    
    
    
24. DONATY L, Giansily-Blaizot M, Bertchansky I, Cunat S, et al
    Iron overload in hereditary spherocytosis: Are genetic factors the cause?
    Br J Haematol. 2026;208:691-696.
    PubMed     Abstract available
    
    
    
25. RIZVI I, Solipuram D, Kaur N, Komel A, et al
    The enigma of sickle cell hepatopathy: Pathophysiology, clinical manifestations and therapy.
    Br J Haematol. 2026;208:421-436.
    PubMed     Abstract available
    
    
    January 2026
26. STINNETT PZ, Ogg RJ, Helton K, Wang W, et al
    Cerebral blood flow trajectories in paediatric sickle cell anaemia by age, region, and treatment associations.
    Br J Haematol. 2026;208:367-372.
    PubMed     Abstract available
    
    
    
27. MUSALLAM KM, Taher AT, Porter JB, Kattamis A, et al
    Achieving clinically meaningful changes in haemoglobin levels in patients with non-transfusion-dependent beta-thalassaemia treated with luspatercept: A post hoc analysis of the phase 2 BEYOND trial.
    Br J Haematol. 2026;208:348-352.
    PubMed     Abstract available
    
    
    
28. RECH JS, Santin A, Lionnet F, Mattioni S, et al
    Emergency department utilization patterns in adults living with sickle cell disease.
    Br J Haematol. 2026;208:285-294.
    PubMed     Abstract available
    
    
    
29. ISHIYAMA K, Yamazaki M, Maruyama H, Hosono N, et al
    Efficacy of ciclosporin monotherapy in non-severe aplastic anaemia not requiring transfusions: Results from a multicentre phase II study.
    Br J Haematol. 2026;208:295-303.
    PubMed     Abstract available
    
    
    December 2025
30. KALIBBALA D, Mboizi V, Nambatya G, Murungi S, et al
    Growth measurements in Ugandan children with sickle cell anaemia from a hydroxyurea (hydroxycarbamide) treatment trial relative to unaffected sibling controls.
    Br J Haematol. 2025;207:2539-2549.
    PubMed     Abstract available
    
    
    November 2025
31. BRONS N, Rigas AS, Kaspersen KA, Pedersen OB, et al
    A structural deletion in the 3'UTR of SLC11A2 is associated with altered iron status: Evidence from two large Danish cohorts.
    Br J Haematol. 2025;207:2123-2134.
    PubMed     Abstract available
    
    
    
32. CHE M, Wang C, Li Y, Li L, et al
    A single-centre, real-world study on the efficacy and recovery of inflammatory cytokine levels of C5 complement inhibitor therapy in patients with paroxysmal nocturnal haemoglobinuria.
    Br J Haematol. 2025;207:2109-2117.
    PubMed     Abstract available
    
    
    
33. GUINDO A, Cablay K, Kamate J, MacLean B, et al
    Systematic point-of-care newborn screening for sickle cell disease in rural Mali, West Africa.
    Br J Haematol. 2025;207:2118-2122.
    PubMed     Abstract available
    
    
    
34. WU L, Zhou M, Chen X, Mo W, et al
    Clinical outcomes of modified post-transplantation cyclophosphamide versus granulocyte colony-stimulating factor/anti-thymocyte globulin-based protocol in alternative donor transplantation for severe aplastic anaemia.
    Br J Haematol. 2025;207:2059-2071.
    PubMed     Abstract available
    
    
    
35. SEVANTHINI BR, Hegde S, Sridhar T, Trivedi D, et al
    Short-term risks and benefits of hydroxyurea (hydroxycarbamide)-induced transfusion independence in patients with beta-thalassaemia syndromes.
    Br J Haematol. 2025;207:2196-2199.
    PubMed     Abstract available
    
    
    
36. DWOMOH D, Abankwah DNY, Benneh-Akwasi Kuma AA, Quartey J, et al
    Effectiveness of hydroxyurea (hydroxycarbamide) in a national sickle cell disease programme in Ghana.
    Br J Haematol. 2025;207:2099-2108.
    PubMed     Abstract available
    
    
    October 2025
37. MUSALLAM KM, Vitrano A, Inzerillo A, Di Maggio R, et al
    Impact of lifetime anaemia and iron control on outcomes in beta-thalassaemia: Data from the longitudinal de-LIGHT study.
    Br J Haematol. 2025;207:1578-1588.
    PubMed     Abstract available
    
    
    
38. REVEL-VILK S, Ben-Ami T, Constantini N
    Is it time to offer routine screening for iron deficiency in healthy adolescent females?
    Br J Haematol. 2025;207:1242-1247.
    PubMed     Abstract available
    
    
    September 2025
39. CHANG M, Semakula D, Little JA, Kanter J, et al
    Grandchildren of GRNDaD: Shifts in disease-modifying therapy at the adolescent transition in sickle cell disease.
    Br J Haematol. 2025;207:1070-1075.
    PubMed     Abstract available
    
    
    
40. SHANGGUAN S, Cui X, Li J, Li N, et al
    Alu-mediated FANCD2 exonic deletion contributes to Fanconi anaemia.
    Br J Haematol. 2025;207:1076-1084.
    PubMed     Abstract available
    
    
    
41. CHAMBLISS C, Manci E, Fields E, Bueno J, et al
    Characterizing pregnancy outcomes in a humanized mouse model of sickle cell disease.
    Br J Haematol. 2025;207:813-823.
    PubMed     Abstract available
    
    
    
42. HAJJAJ OI, Callum J, Shehata N, Farrell A, et al
    Laboratory assessment of fetomaternal haemorrhage and Rh immune globulin management: Canadian practice and scoping review.
    Br J Haematol. 2025;207:723-736.
    PubMed     Abstract available
    
    
    
43. LEUNG WY, Lee TY, Hwang YY, Lee JT, et al
    Iron overload and morbidities in Chinese with non-transfusion-dependent thalassaemia.
    Br J Haematol. 2025;207:1058-1069.
    PubMed     Abstract available
    
    
    August 2025
44. ZHANG L, Liu Z, Zhao X, Hu B, et al
    Efficacy and safety of HRS-5965 monotherapy in complement inhibitor-naive patients with paroxysmal nocturnal haemoglobinuria.
    Br J Haematol. 2025;207:571-581.
    PubMed     Abstract available
    
    
    
45. TEAWTRAKUL N, Jetsrisuparb A, Pongudom S, Chansung K, et al
    Survival and thalassaemia-related complications in HbE/beta-thalassaemia and alpha-thalassaemia: A 10-year longitudinal study in Thailand.
    Br J Haematol. 2025;207:552-560.
    PubMed     Abstract available
    
    
    
46. LEE JW, Jang JH, Chiba S, Yoon SS, et al
    Romiplostim with ciclosporin A in patients with aplastic anaemia naive to immunosuppressive therapy: A phase 2/3 study.
    Br J Haematol. 2025;207:582-590.
    PubMed     Abstract available
    
    
    
47. AFZALI-HASHEMI L, Franse M, Baas KPA, Schrantee A, et al
    Assessment of neurocognitive functioning in sickle cell disease and thalassaemia and the association with silent cerebral infarcts, cerebral haemodynamics and oxygen metabolism.
    Br J Haematol. 2025;207:561-570.
    PubMed     Abstract available
    
    
    July 2025
48. LOH J, Kuo KHM, Georgescu I, Wang S, et al
    Risk factors for immediate postpartum sickle cell disease-specific maternal morbidity.
    Br J Haematol. 2025;207:225-234.
    PubMed     Abstract available
    
    
    
49. WILSON SR, Noubouossie D, Little JA, Karafin MS, et al
    Real-world assessment of acute red cell exchange for stroke in sickle cell disease.
    Br J Haematol. 2025;207:217-224.
    PubMed     Abstract available
    
    
    
50. DIAW M, Coly MS, Charlot K, Gallou-Guyot M, et al
    Physical activity, vaso-occlusive crises and pain in patients with sickle cell anaemia in Senegal.
    Br J Haematol. 2025;207:206-216.
    PubMed     Abstract available
    
    
    
51. SANTINI V, Consagra A
    How to use luspatercept and erythropoiesis-stimulating agents in low-risk myelodysplastic syndrome.
    Br J Haematol. 2025;207:15-26.
    PubMed     Abstract available
    
    
    June 2025
52. KUO KHM, Layton DM, Lal A, Vichinsky EP, et al
    Long-term efficacy and safety of mitapivat in non-transfusion-dependent alpha- or beta-thalassaemia: An open-label phase 2 study.
    Br J Haematol. 2025;206:1764-1773.
    PubMed     Abstract available
    
    
    
53. VISTICA SAMPINO E, Bonal DM, Chorzalska A, Morgan J, et al
    Alterations in the humoral immunophenotype in sickle cell disease.
    Br J Haematol. 2025;206:1774-1785.
    PubMed     Abstract available
    
    
    
54. RICCHI P
    The double edge of erythropoietic modulation in thalassaemia.
    Br J Haematol. 2025;206:1879-1880.
    PubMed     Abstract available
    
    
    
55. HARJU T, Raiskila S, Lohi O, Jarvela L, et al
    Increased incidence of autoimmune haemolytic anaemia with paroxysmal cold haemoglobinuria features in paediatric cases in a changing viral environment post-COVID-19 pandemic.
    Br J Haematol. 2025;206:1872-1876.
    PubMed     Abstract available
    
    
    
56. PALANI CD, Smith A, Cao X, Li B, et al
    Cholesterol-conjugated miR-29b induces fetal haemoglobin expression via gamma-globin promoter demethylation in the Townes mouse model for sickle cell anaemia.
    Br J Haematol. 2025;206:1786-1795.
    PubMed     Abstract available
    
    
    
57. ZAIDEL B, Garland S, Merkeley H
    Acute splenomegaly, haemolysis, and thrombocytopenia following luspatercept initiation in a patient with transfusion-dependent thalassaemia: A case report.
    Br J Haematol. 2025;206:1806-1810.
    PubMed     Abstract available
    
    
    
58. BRANDSEN RP, Diederen RMH, Klaassen I, Veldthuis M, et al
    The role of red blood cell characteristics and viscosity in sickle cell retinopathy and maculopathy.
    Br J Haematol. 2025;206:1796-1805.
    PubMed     Abstract available
    
    
    
59. MAEDA T, Matsuda A, Kanda J, Kawabata H, et al
    Comparison of severe aplastic anaemia and lower risk hypoplastic myelodysplastic neoplasms: Critical role of megakaryocyte count in distinguishing aplastic anaemia from myelodysplastic neoplasms.
    Br J Haematol. 2025;206:1689-1698.
    PubMed     Abstract available
    
    
    
60. JACOBS JW, Amorim L, Pirenne F, Tayou C, et al
    The wider perspective: Barriers and recommendations for transfusion support for patients with sickle cell disease in low- and middle-income countries.
    Br J Haematol. 2025;206:1585-1592.
    PubMed     Abstract available
    
    
    
61. BALCIUNIENE J, Yilmaz S, Chonat S, Grace RF, et al
    Real-world insights from a cohort of approximately 2000 individuals who were analysed using a freely available next-generation sequencing anaemia screening programme.
    Br J Haematol. 2025;206:1853-1856.
    PubMed     Abstract available
    
    
    May 2025
62. MACLEAN B, Fuller J, Lim J, Dugan C, et al
    Greater prevalence of anaemia and heavy menstrual bleeding reported in women of reproductive age in the United Kingdom compared to Australia.
    Br J Haematol. 2025;206:1479-1484.
    PubMed     Abstract available
    
    
    
63. DELICOU S, Manganas K, Diamantidis MD, Venou TM, et al
    Comparative analysis of mortality patterns and treatment strategies in thalassaemia and sickle cell disease patients: A 12-year study.
    Br J Haematol. 2025;206:1466-1478.
    PubMed     Abstract available
    
    
    
64. PRINCE EJ, Scott JL, Nwankwoala O, Ali-Houchens L, et al
    A young adult clinic to support integration into adult sickle cell disease care: If you build it, they will come.
    Br J Haematol. 2025;206:1458-1465.
    PubMed     Abstract available
    
    
    April 2025
65. HOVING V, Donker AE, Schols SEM, Swinkels DW, et al
    How I treat iron-refractory iron deficiency anaemia-An expert opinion-based treatment guidance for children and adults.
    Br J Haematol. 2025;206:1067-1076.
    PubMed     Abstract available
    
    
    
66. METAFUNI E, Brioschi FA, Patriarca A, Leoni C, et al
    Real-world evidence of pegcetacoplan in patients with paroxysmal nocturnal haemoglobinuria: A nationwide Italian study.
    Br J Haematol. 2025;206:1246-1249.
    PubMed     Abstract available
    
    
    
67. CORSIA A, Joseph L, Beeker N, Manceau S, et al
    Maternal and perinatal outcomes of sickle cell disease in pregnancy: A nationwide study in France.
    Br J Haematol. 2025;206:1218-1227.
    PubMed     Abstract available
    
    
    
68. ENACHE A, Carty SA, Babushok DV
    Origins of T-cell-mediated autoimmunity in acquired aplastic anaemia.
    Br J Haematol. 2025;206:1035-1053.
    PubMed     Abstract available
    
    
    
69. SINHA U, Setty S, Pilon C, Brown JJ, et al
    Systemic lupus erythematosus-associated autoantibodies in sickle cell disease: Spontaneous emergence in a patient and in transgenic sickle mice.
    Br J Haematol. 2025;206:1213-1217.
    PubMed     Abstract available
    
    
    March 2025
70. DE LIGT LA, Gaartman AE, Konte K, Thakoerdin S, et al
    Plasma inflammatory and angiogenic protein profiling of patients with sickle cell disease.
    Br J Haematol. 2025;206:954-964.
    PubMed     Abstract available
    
    
    
71. SCHECHTER AN
    Sickle cell anaemia therapy in 2025.
    Br J Haematol. 2025;206:842-845.
    PubMed     Abstract available
    
    
    
72. LONGORIA JN, Howell KE, Porter JS, Treadwell M, et al
    Depression, sleep and pain affect instrumental activities of daily living through cognitive functioning in adults with sickle cell disease: A report from the Sickle Cell Disease Implementation Consortium.
    Br J Haematol. 2025;206:944-953.
    PubMed     Abstract available
    
    
    
73. LI H, Sachdev V, Tian X, Nguyen ML, et al
    A machine learning-based workflow for predicting transplant outcomes in patients with sickle cell disease.
    Br J Haematol. 2025;206:919-923.
    PubMed     Abstract available
    
    
    February 2025
74. MAGGIO A, Napolitano M, Taher AT, Bou-Fakhredin R, et al
    Reframing thalassaemia syndrome as a benign haematopoietic stem cell disorder.
    Br J Haematol. 2025;206:464-477.
    PubMed     Abstract available
    
    
    
75. ZHANG J, Sun J, Huai W, Tang J, et al
    Elucidating loss-of-function mechanisms of monoallelic EPAS1 mutations underlying congenital hypoplastic anaemia in a paediatric anaemia cohort.
    Br J Haematol. 2025;206:585-595.
    PubMed     Abstract available
    
    
    
76. EL HOSS S, Bazoum H
    From old to new: Repurposed drugs in the battle towards curing sickle cell disease.
    Br J Haematol. 2025;206:795-797.
    PubMed     Abstract available
    
    
    
77. BHAT V, Potdar AA, Yu GK, Gibson G, et al
    Impact of hydroxycarbamide treatment on the whole-blood transcriptome in sickle cell disease.
    Br J Haematol. 2025;206:713-720.
    PubMed     Abstract available
    
    
    
78. GURNARI C, Visconte V
    Dissecting the genomic traits and clinical course of secondary myelodysplastic syndrome following aplastic anaemia: A milestone.
    Br J Haematol. 2025;206:790-791.
    PubMed     Abstract available
    
    
    
79. QI J, Wang T, Wang M, He P, et al
    Comparative study of the diversity of amino acids on human leucocyte antigen class II molecules in patients with acquired aplastic anaemia.
    Br J Haematol. 2025;206:735-748.
    PubMed     Abstract available
    
    
    
80. RAZ S, Koren A, Bogdanova AY, Gassmann M, et al
    Memantine treatment in sickle cell disease: A 1-year study of its effects on cognitive functions and neural processing.
    Br J Haematol. 2025;206:689-702.
    PubMed     Abstract available
    
    
    
81. SONGDEJ D, Teawtrakul N, Laoaroon N, Komvilaisak P, et al
    Impact of HbE mutation on the clinical severity of HbH disease: A multicentre study from Thailand.
    Br J Haematol. 2025;206:703-712.
    PubMed     Abstract available
    
    
    January 2025
82. GE S, Ali S, Haldane V, Bekdache C, et al
    An approach to Hemequity: Identifying the barriers and facilitators of iron deficiency reduction strategies in low- to middle-income countries.
    Br J Haematol. 2025 Jan 6. doi: 10.1111/bjh.19984.
    PubMed     Abstract available
    
    
    
83. KHAN AA, Laas CE, Brewin JN, Potter V, et al
    Development of a novel test of splenic function for use in a clinical diagnostic laboratory.
    Br J Haematol. 2025;206:320-330.
    PubMed     Abstract available
    
    
    
84. GEHRIE EA, Booth GS
    Contextualizing prophylactic red blood cell antigen matching in the lifelong care of sickle cell disease and thalassaemia patients.
    Br J Haematol. 2025;206:382-384.
    PubMed     Abstract available
    
    
    
85. GALADANCI NA, Kanter J
    Avascular necrosis in sickle cell disease needs more definitive treatment options.
    Br J Haematol. 2025;206:385-386.
    PubMed     Abstract available
    
    
    
86. PIECHNIK SK, Polzella P, Shah A, Vera-Aviles M, et al
    Myocardial iron intake following intravenous iron therapy with ferric carboxymaltose is sustained at 1 year despite recurrence of iron deficiency.
    Br J Haematol. 2025;206:349-352.
    PubMed     Abstract available
    
    
    
87. NOGUER M, Berthon P, Makowski C, Messonnier LA, et al
    Impaired physical ability in patients with transfusion-dependent beta-thalassaemia: Can regular physical activity be a countermeasure?
    Br J Haematol. 2025;206:86-93.
    PubMed     Abstract available
    
    
    
88. WOLF J, Blais-Normandin I, Bathla A, Keshavarz H, et al
    Red cell specifications for blood group matching in patients with haemoglobinopathies: An updated systematic review and clinical practice guideline from the International Collaboration for Transfusion Medicine Guidelines.
    Br J Haematol. 2025;206:94-108.
    PubMed     Abstract available
    
    
    
89. KOCHHAR M, McGann PT
    Sickle cell disease in India: Not just a mild condition.
    Br J Haematol. 2025;206:380-381.
    PubMed     Abstract available
    
    
    
90. SETH T, Udupi S, Jain S, Bhatwadekar S, et al
    Burden of vaso-occlusive crisis, its management and impact on quality of life of Indian sickle cell disease patients.
    Br J Haematol. 2025;206:296-309.
    PubMed     Abstract available
    
    
    
91. CASALE M, Toro G, Porcelli F, Quota A, et al
    Long-term outcomes of avascular necrosis in sickle cell disease using joint-specific patient-reported outcome measures: Results from a multicentre study.
    Br J Haematol. 2025;206:310-319.
    PubMed     Abstract available
    
    
    December 2024
92. LOTH G, Dumke CCK, Muratori RR, Pelegrina PD, et al
    Haematopoietic cell transplantation for 106 infants and preschoolers with acquired and inherited bone marrow failures.
    Br J Haematol. 2024;205:2387-2402.
    PubMed     Abstract available
    
    
    
93. SEGBEFIA CI, Smart LR, Stuber SE, Amissah-Arthur KN, et al
    Baseline characteristics of Ghanaian children and adults enrolled in PIVOT, a randomised clinical trial of hydroxyurea in HbSC disease in sub-Saharan Africa.
    Br J Haematol. 2024;205:2470-2480.
    PubMed     Abstract available
    
    
    November 2024
94. COSTA S, Minucci A, Kumawat A, De Bonis M, et al
    Pathogenic G6PD variants: Different clinical pictures arise from different missense mutations in the same codon.
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95. CINTHO OZAHATA M, Guo Y, Gomes I, Malta B, et al
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96. ELSHERIF L, Tang Y, Patillo KL, Wichlan D, et al
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97. GURNARI C, Lima ACM, Pagliuca S
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98. MARIN V, Huguenin Y, Bessi L, Weinmann L, et al
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99. ZAIMOKU Y, Sakai K, Tsuji N, Hosomichi K, et al
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    October 2024
100. GUPTA CL, Jaganathasamy N, Madkaikar M
     Microbiome in sickle cell disease: Pathophysiology and therapeutic insights.
     Br J Haematol. 2024;205:1279-1287.
     PubMed     Abstract available
     
     
     
101. GILTON M, Fernandes H, Martinez C, Leverger G, et al
     Association of paediatric autoimmune cytopenia and inflammatory bowel disease suggests a common genetic origin.
     Br J Haematol. 2024;205:1508-1515.
     PubMed     Abstract available
     
     
     
102. VALENTINI CG, Teofili L, Gehrie E
     Iron metabolism in sickle cell disease patients undergoing chronic red blood cell exchange: A delicate homeostasis in balance.
     Br J Haematol. 2024;205:1257-1259.
     PubMed     Abstract available
     
     
     
103. CONNES P, Nader E
     Could oxygen gradient ektacytometry help to detect sickle cell trait carriers at risk for kidney disorders or exercise-related complications?
     Br J Haematol. 2024;205:1260-1261.
     PubMed     Abstract available
     
     
     
104. RAMSAY Z, Ali A, Grant J, Asnani M, et al
     Exploring the role of viscosity-vaso-occlusion and haemolysis-endothelial dysfunction in pain sensitization among Jamaicans with sickle cell disease.
     Br J Haematol. 2024;205:1570-1580.
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105. M ROSS J, Forte S, Mercure-Corriveau N, Lemay AS, et al
     Automated red blood cell exchange with a post-procedure haematocrit targeted at 34% in the chronic management of sickle cell disease.
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106. ELLSWORTH P, Pawlinski IJ, Sielaty R, Ilich A, et al
     Hypertonicity and/or acidosis induce marked rheological changes under hypoxic conditions in sickle trait red blood cells.
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107. KATO S, Chagi K, Takagi Y, Hidaka M, et al
     Machine/deep learning-assisted hemoglobin level prediction using palpebral conjunctival images.
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108. LEE JM, Kim HS, Yoo J, Lee J, et al
     Genomic insights into inherited bone marrow failure syndromes in a Korean population.
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     September 2024
109. CATELLA J, Turpin E, Connes P, Nader E, et al
     Impaired microvascular function in patients with sickle cell anemia and leg ulcers improved with healing.
     Br J Haematol. 2024 Sep 24. doi: 10.1111/bjh.19785.
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110. STRAUSS JD, Brown DW, Zhou W, Dagnall C, et al
     Telomere length and clonal chromosomal alterations in peripheral blood of patients with severe aplastic anaemia.
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111. PRABAHRAN A, Durrani J, Coelho-Da Silva J, Shalhoub R, et al
     Safety and efficacy of immunosuppressive therapy for elderly patients with severe aplastic anaemia.
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112. ZHOU LY, Derebail VK, Desai PC, Elsherif L, et al
     Persistent albuminuria and chronic kidney disease in adults with sickle cell anaemia: Results from a multicenter natural history study.
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113. SADAF A, Dong M, Pfeiffer A, Korpik J, et al
     A pharmacokinetic-pharmacodynamic analysis of l-glutamine for the treatment of sickle cell disease: Implications for understanding the mechanism of action and evaluating response to therapy.
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114. NKOY AB, Mumaka FM, Ngonde A, Mafumba SK, et al
     Relevance of repeated analyses of albuminuria and glomerular filtration rate in African children with sickle cell anaemia.
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     PubMed     Abstract available
     
     
     
115. ZHOU X, Wagner V, Scheller L, Stanojkovska E, et al
     Changes in T-cell subsets, preexisting cytopenias and hyperferritinaemia correlate with cytopenias after BCMA targeted CAR T-cell therapy in relapsed/refractory multiple myeloma: Results from a prospective comprehensive biomarker study.
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     PubMed     Abstract available
     
     
     August 2024
116. GLENTHOJ A, Grace RF, Lander C, van Beers EJ, et al
     Comorbidities and complications in adult and paediatric patients with pyruvate kinase deficiency: Analysis from the Peak Registry.
     Br J Haematol. 2024;205:613-623.
     PubMed     Abstract available
     
     
     
117. KATZ BZ, Karny S
     Pursuing the elusive footsteps of malaria in peripheral blood smears utilizing artificial intelligence.
     Br J Haematol. 2024;205:414-415.
     PubMed     Abstract available
     
     
     
118. SHARMA A, Kumar A, Rawat K, Vij S, et al
     Novel TMPRSS6 variants and their impact on iron-refractory iron deficiency anaemia in pregnancy: A North Indian genotype phenotype study.
     Br J Haematol. 2024;205:686-698.
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119. RECH JS, Cohen A, Bartolucci P, Santin A, et al
     Shift in emergency department utilization by frequent attendees with sickle cell disease during the COVID-19 pandemic: A multicentre cohort study.
     Br J Haematol. 2024;205:463-472.
     PubMed     Abstract available
     
     
     
120. SEGBEFIA C, Luchtman-Jones L
     Seeing haemoglobin SC: Challenging the misperceptions.
     Br J Haematol. 2024;205:404-405.
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121. NELSON M, Noisette L, Pugh N, Gordeuk V, et al
     The clinical spectrum of HbSC sickle cell disease-not a benign condition.
     Br J Haematol. 2024;205:653-663.
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122. MOYSIS E, Brown BJ, Shokunbi W, Manescu P, et al
     Leveraging deep learning for detecting red blood cell morphological changes in blood films from children with severe malaria anaemia.
     Br J Haematol. 2024;205:699-710.
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123. SHANDLEY LM, Fasano RM, Spencer JB, Mertens AC, et al
     The impact of sickle cell disease and its treatment on ovarian reserve in reproductive-aged Black women.
     Br J Haematol. 2024;205:674-685.
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124. ROSSI M, Belinga S, Tolo A, Diop S, et al
     Determinants of the haemoglobin level in patients with sickle cell disease living in sub-Saharan Africa: Major impact of the country of residence and independent effects of leucocyte and platelet counts and haemolysis.
     Br J Haematol. 2024;205:664-673.
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125. PIOLATTO A, Gaglioti CM, Tesio N, Clemente MG, et al
     Deferasirox film-coated tablet-associated ulcerative colitis: An emerging pattern in thalassemia patients?
     Br J Haematol. 2024;205:719-721.
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126. HAN J, Zhang X, Shah BN, Saraf SL, et al
     Alkaline phosphatase as a marker for painful vaso-occlusive events and other acute complications in sickle cell disease.
     Br J Haematol. 2024;205:716-718.
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     July 2024
127. CATELLA J, Guillot N, Nader E, Skinner S, et al
     Controversies in the pathophysiology of leg ulcers in sickle cell disease.
     Br J Haematol. 2024;205:61-70.
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128. GOK V, Leblebisatan G, Gurlek Gokcebay D, Guler S, et al
     Pyruvate kinase deficiency in 29 Turkish patients with two novel intronic variants.
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129. CHEMINET G, Corbasson A, Charmettan M, Namaoui W, et al
     Assessment of fatigue in adult patients with sickle cell disease: Use of the functional assessment of chronic illness therapy-Fatigue (FACIT-fatigue) questionnaire.
     Br J Haematol. 2024;205:335-342.
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130. MAYRAND L, Elie J, Pinhas Y, Rignault-Bricard R, et al
     Sputum interleukin-6 level as a marker of severity during acute chest syndrome in children with sickle cell disease.
     Br J Haematol. 2024;205:329-334.
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131. PLAZA-FLORIDO A, Liem RI, Haddad F, Radom-Aizik S, et al
     Whole-blood transcriptome analysis reveals distinct gene expression signatures in paediatric patients with sickle cell anaemia before and after exercise.
     Br J Haematol. 2024;205:320-328.
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132. ZHANG L, Chang M, Liu C, Xu Y, et al
     A case of de novo -alpha(3.7) thalassaemia and the utility of CATSA for detecting de novo mutations in thalassaemia.
     Br J Haematol. 2024;205:360-363.
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133. PADENIYA P, Premawardhena A
     Obesity, liver steatosis and metabolic syndrome: The hidden enemies in transfusion-dependent thalassaemia.
     Br J Haematol. 2024;205:28-29.
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134. RUIZ MA, Zhang X, Mansilla MA, Zahr RS, et al
     Prevalence of kidney health genetic variants in adults with sickle cell nephropathy.
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135. KIM DH, Hong J, Shin DY, Kim I, et al
     Phase II trial of posaconazole prophylaxis during anti-thymocyte globulin treatment for aplastic anaemia and hypoplastic myelodysplastic syndrome.
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136. HANDS K, Daru J, Evans C, Kotze A, et al
     Identification and management of preoperative anaemia in adults: A British Society for Haematology Guideline update.
     Br J Haematol. 2024;205:88-99.
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     June 2024
137. GUARNERA L, Visconte V
     The metabolic fuel of paroxysmal nocturnal haemoglobinuria.
     Br J Haematol. 2024;204:2162-2164.
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138. SHAH FT, Nicolle S, Garg M, Pancham S, et al
     Guideline for the management of conception and pregnancy in thalassaemia syndromes: A British Society for Haematology Guideline.
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139. RICCHI P, Pistoia L, Positano V, Spasiano A, et al
     Liver steatosis in patients with transfusion-dependent thalassaemia.
     Br J Haematol. 2024;204:2458-2467.
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140. ZACCHEDDU E, Zappu A, Barella S, Clemente MG, et al
     Unplanned pregnancy in women with beta-thalassaemia treated with luspatercept.
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141. CHEN Y, Liu H, Wang C, Chen W, et al
     The histone demethylase JMJD1C regulates CPS1 expression and promotes the proliferation of paroxysmal nocturnal haemoglobinuria clones through cell metabolic reprogramming.
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142. DAVILA J, O'Brien SH, Mitchell WB, Manwani D, et al
     Evaluating thromboprophylaxis in the sickle cell disease population: Navigating the evidence gap.
     Br J Haematol. 2024;204:2184-2193.
     PubMed     Abstract available
     
     
     May 2024
143. PHONGPAO K, Pholngam N, Chokchaichamnankit D, Nuamsee K, et al
     Proteomic profiling of circulating beta-thalassaemia/haemoglobin E extra-cellular vesicles reveals that association with immunoglobulin induces membrane vesiculation.
     Br J Haematol. 2024;204:2025-2039.
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144. CASABIANCA M, Gauthier A, Nader E, Cannas G, et al
     Red blood cell senescence and vascular function in patients with hereditary spherocytosis with and without splenectomy.
     Br J Haematol. 2024;204:e41-e44.
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145. HAGRY J, Monnet X, Mekontso-Dessap A, Chantalat C, et al
     Comprehensive assessment, pain and ventilatory management during acute complications of adult sickle cell disease: A clinical practice survey in French intensive care units.
     Br J Haematol. 2024;204:e37-e40.
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146. MANARA R, Brotto D, Barillari MR, Costa G, et al
     Hearing loss in beta-thalassaemia: An Italian multicentre case-control study.
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147. LIPTON JM
     Understanding complex disease-related mechanisms: Rational therapies for Diamond-Blackfan anaemia.
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148. TOMBUL Z, Bahaj W, Ozturk M, Patel B, et al
     Ahemolytic PNH (white cell PNH): Clinical features and implications of a distinct phenotype of paroxysmal nocturnal haemoglobinuria.
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149. ROGER G, Denormandie P, Gobe T, Azzolina D, et al
     Left ventricular global longitudinal strain and acute myocardial injury in patients with sickle cell disease admitted to the intensive care unit for vaso-occlusive crisis.
     Br J Haematol. 2024;204:2007-2015.
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150. DUNCAN BB, Lotter JL, Superata J, Barranta ME, et al
     Treatment of refractory/relapsed Diamond-Blackfan anaemia with eltrombopag.
     Br J Haematol. 2024;204:2077-2085.
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151. BIANCHI C, Margot H, Fernandes H, Pasquet M, et al
     Autoimmune cytopenia and Kabuki syndrome in paediatrics: Insights in 11 patients.
     Br J Haematol. 2024;204:1899-1907.
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152. UKONMAANAHO EM, Dell'Anna S, Hakonen A, Wartiovaara-Kautto U, et al
     Biallelic hexokinase 1 (HK1) variants causative of non-spherocytic haemolytic anaemia: A case series with emphasis on the HK1 promoter variant and literature review.
     Br J Haematol. 2024;204:2040-2048.
     PubMed     Abstract available
     
     
     
153. GIORGETTI A, Nyilima S, Stoffel NU, Moretti D, et al
     Stable iron ((58)Fe) isotopic measurements in Kenyan toddlers during 3 months of iron supplementation demonstrate that half of the iron absorbed is lost.
     Br J Haematol. 2024;204:2057-2065.
     PubMed     Abstract available
     
     
     
154. MAEDA T, Matsuda A, Kanda J, Kawabata H, et al
     Clinical impact and characteristics of erythroid dysplasia in adult aplastic anaemia: Results from a multicentre registry.
     Br J Haematol. 2024;204:2086-2096.
     PubMed     Abstract available
     
     
     
155. NEYER PJ, Kabore B, Nakas CT, Diallo S, et al
     Increased erythroferrone levels in malarial anaemia.
     Br J Haematol. 2024;204:2066-2070.
     PubMed     Abstract available
     
     
     April 2024
156. ARCANJO GS, Souza MB, Domingos IF, Pereira-Martins DA, et al
     BMP6 and VDR gene polymorphisms are associated with osteonecrosis in a sickle cell anaemia cohort.
     Br J Haematol. 2024;204:1507-1514.
     PubMed     Abstract available
     
     
     
157. CHANG A, Wilson SR, Morris S, Wichlan D, et al
     Nocturnal hypoxaemia is common in adults with sickle cell anaemia.
     Br J Haematol. 2024;204:1495-1499.
     PubMed     Abstract available
     
     
     
158. JACOBS JW, Sharma D, Stephens LD, Figueroa Villalba CA, et al
     Thrombosis risk with haemoglobin C trait and haemoglobin C disease: A systematic review.
     Br J Haematol. 2024;204:1500-1506.
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159. KUNVARJEE B, Contreras Yametti GP, Blouin AG, Linder GE, et al
     Donor-specific antibody desensitization with daratumumab prior to haematopoietic cell transplant for sickle cell disease: A case report.
     Br J Haematol. 2024;204:1540-1544.
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     March 2024
160. EBEA-UGWUANYI PO, Vidyasagar S, Connor JR, Frazer DM, et al
     Oral iron therapy: Current concepts and future prospects for improving efficacy and outcomes.
     Br J Haematol. 2024;204:759-773.
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161. KULASEKARARAJ A, Cavenagh J, Dokal I, Foukaneli T, et al
     Guidelines for the diagnosis and management of adult aplastic anaemia: A British Society for Haematology Guideline.
     Br J Haematol. 2024;204:784-804.
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162. LEE GM, Batchvarova M, Delahunty M, Boateng L, et al
     Sickle red blood cells directly activate neutrophils.
     Br J Haematol. 2024;204:e28-e30.
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163. JONASSAINT CR, Parchuri E, O'Brien JA, Lalama CM, et al
     Mental health, pain and likelihood of opioid misuse among adults with sickle cell disease.
     Br J Haematol. 2024;204:1029-1038.
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164. HANSEN DL, Maquet J, Lafaurie M, Moller S, et al
     Primary autoimmune haemolytic anaemia is associated with increased risk of ischaemic stroke: A binational cohort study from Denmark and France.
     Br J Haematol. 2024;204:1072-1081.
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165. EARLY ML, Raja M, Luo A, Solow M, et al
     Blood pressure thresholds for the diagnosis of hypertensive disorders of pregnancy in sickle cell disease.
     Br J Haematol. 2024;204:1039-1046.
     PubMed     Abstract available
     
     
     
166. KISALI EP, Iversen PO, Makani J
     Low vitamin B(12) blood levels in sickle cell disease: Data from a large cohort study in Tanzania.
     Br J Haematol. 2024;204:1047-1053.
     PubMed     Abstract available
     
     
     
167. STEINBERG-SHEMER O, Yacobovich J, Noy-Lotan S, Dgany O, et al
     Biallelic hypomorphic variants in CAD cause uridine-responsive macrocytic anaemia with elevated haemoglobin-A2.
     Br J Haematol. 2024;204:1067-1071.
     PubMed     Abstract available
     
     
     
168. LIU H, Ding K, Zhang W, Xing L, et al
     A pilot study of orelabrutinib treatment in three cases of refractory/relapsed autoimmune haemolytic anaemia/Evans syndrome.
     Br J Haematol. 2024;204:1082-1085.
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169. MUNARETTO V, Corti P, Bertoni E, Tripodi SI, et al
     Acute chest syndrome in children with sickle cell disease: Data from a national AIEOP cohort identify priority areas of intervention in a hub-and-spoke system.
     Br J Haematol. 2024;204:1061-1066.
     PubMed     Abstract available
     
     
     February 2024
170. WARE RE, Quinn CT
     The bold promise of gene therapy for sickle cell disease.
     Br J Haematol. 2024;204:381-382.
     PubMed    
     
     
     
171. STEENSMA DP
     Revisiting the first reported case of aplastic anaemia.
     Br J Haematol. 2024;204:455-458.
     PubMed     Abstract available
     
     
     
172. KATAGIRI T, Iwasaki H, Fujieda A, Kasashima S, et al
     A case of hepatitis-associated aplastic anaemia following living-donor liver transplantation for fulminant hepatitis showing loss of heterozygosity in the 6p chromosome in the affected liver.
     Br J Haematol. 2024;204:623-627.
     PubMed     Abstract available
     
     
     
173. HUNT RC, Kimchi-Sarfaty C
     A synonymous variant is unmasked in thalassaemia.
     Br J Haematol. 2024;204:399-401.
     PubMed     Abstract available
     
     
     
174. KHWAJA J, Japzon N, Gabriel M, Raju K, et al
     Cold agglutinin disease and cryoglobulinaemia: A frequent coexistence with clinical impact.
     Br J Haematol. 2024;204:e21-e24.
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175. EARLY ML, Luo A, Solow M, Matusiak K, et al
     Natural history of blood pressure in sickle cell disease pregnancy.
     Br J Haematol. 2024;204:658-667.
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176. CHAKRAVORTY S, Drasar E, Kaya B, Kesse-Adu R, et al
     UK Haemoglobin Disorders Peer Review: A Quality Standards-based review programme for sickle cell disease and thalassaemia.
     Br J Haematol. 2024;204:668-676.
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177. SISLER I, McClish DK, Villella A, Valrie C, et al
     Impact of community health workers on quality of life in adolescents and young adults with sickle cell disease: The SHIP-HU study.
     Br J Haematol. 2024;204:649-657.
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178. GORIVALE M, Sawant P, Kargutkar N, Hariharan P, et al
     When a synonymous mutation breaks the silence in a thalassaemia patient.
     Br J Haematol. 2024;204:677-682.
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     January 2024
179. OYARBIDE U, Crane GM, Corey SJ
     The metabolic basis of inherited neutropenias.
     Br J Haematol. 2024;204:45-55.
     PubMed     Abstract available
     
     
     
180. PETERS C
     Haematopoietic stem cell transplantation in children with sickle cell disease: Still to do?
     Br J Haematol. 2024;204:22-23.
     PubMed     Abstract available
     
     
     
181. DANIEL Y, Henthorn J
     Lessons learnt in the screening and diagnosis of haemoglobinopathies.
     Br J Haematol. 2024;204:68-73.
     PubMed     Abstract available
     
     
     
182. SHOOK LM, Ware RE
     Screening for haemoglobin disorders: One size may not fit all.
     Br J Haematol. 2024;204:26-28.
     PubMed     Abstract available
     
     
     
183. CSEH A, Galimard JE, de la Fuente J, Isgro A, et al
     Busulfan-fludarabine- or treosulfan-fludarabine-based conditioning before allogeneic HSCT from matched sibling donors in paediatric patients with sickle cell disease: A study on behalf of the EBMT Paediatric Diseases and Inborn Errors Working Parties.
     Br J Haematol. 2024;204:e1-e5.
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184. GUINDO A, Cisse Z, Keita I, Desmonde S, et al
     Potential for a large-scale newborn screening strategy for sickle cell disease in Mali: A comparative diagnostic performance study of two rapid diagnostic tests (SickleScan(R) and HemotypeSC(R)) on cord blood.
     Br J Haematol. 2024;204:337-345.
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185. ALLALI S, Marquant F, Rignault-Bricard R, Taylor M, et al
     Oral famotidine reduces the plasma level of soluble P-selectin in children with sickle cell disease.
     Br J Haematol. 2024;204:346-351.
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     December 2023
186. PIZZO A, Porter JS, Carroll Y, Burcheri A, et al
     Provider prescription of hydroxyurea in youth and adults with sickle cell disease: A review of prescription barriers and facilitators.
     Br J Haematol. 2023;203:712-721.
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187. MISHKIN AD, Prince EJ, Leimbach EJ, Mapara MY, et al
     Psychiatric comorbidities in adults with sickle cell disease: A narrative review.
     Br J Haematol. 2023;203:747-759.
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     November 2023
188. GREEN NS, Rosano C, Bangirana P, Opoka R, et al
     Neurofilament light chain: A potential biomarker for cerebrovascular disease in children with sickle cell anaemia.
     Br J Haematol. 2023;203:460-467.
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189. BANDINI P, Borras N, Fernandez Mellid E, Martin-Fernandez L, et al
     First description of bone marrow failure syndrome in Spain caused by mutations in the ERCC6L2 gene.
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190. STEWART GW, Gibson JS, Rees DC
     The cation-leaky hereditary stomatocytosis syndromes: A tale of six proteins.
     Br J Haematol. 2023;203:509-522.
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191. NOVAK W, Berner J, Svaton M, Jimenez-Heredia R, et al
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192. SCULLY M, Rayment R, Clark A, Westwood JP, et al
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193. FERMO E, Zaninoni A, Vercellati C, Marcello AP, et al
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194. ISHIYAMA K, Yonemura Y, Kawaguchi T, Hosokawa K, et al
     A longitudinal analysis of paroxysmal nocturnal haemoglobinuria-type cells in patients with bone marrow failure: Results of a prospective multi-centre study in Japan.
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     October 2023
195. ALADJIDI N, Pincez T, Rieux-Laucat F, Nugent D, et al
     Paediatric-onset Evans syndrome: Breaking away from refractory immune thrombocytopenia.
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196. RANQUE B, Diaw M, Dembele AK, Lapoumeroulie C, et al
     Association of haemolysis markers, blood viscosity and microcirculation function with organ damage in sickle cell disease in sub-Saharan Africa (the BIOCADRE study).
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197. ALSULTAN A, Abujoub R, Alsudairy R, Memon S, et al
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198. HEBBEL RP, Milbauer L, Wei P
     A novel promoter of endothelial dysfunction in African Americans: Relevance to sickle cell anaemia.
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199. GIARDINO S, Pierri F, Faraci M
     How to optimize outcome of patients undergoing HLA-matched related haematopoietic stem cell transplantation in acquired and inherited bone marrow failure syndromes.
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     September 2023
200. ZHANG Y, Xie H, Liang G, Qin Y, et al
     A novel gain-of-function PIP4K2A mutation elevates the expression of beta-globin and aggravates the severity of alpha-thalassemia.
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201. NANNELLI C, Bosman A, Cunningham J, Dugue PA, et al
     Genetic variants causing G6PD deficiency: Clinical and biochemical data support new WHO classification.
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202. DE ALCANTARA PEDRO PP, Castro CHM, Pinheiro MM, Goncalves LM, et al
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203. HAN J, Saraf SL, Gordeuk VR
     Vaccination in sickle cell disease: Immunocompromised or immunocompetent?
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204. ESPERTI S, Nader E, Boisson C, Carin R, et al
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205. KNIGHT-MADDEN J, King L, Asnani M, Skyers N, et al
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206. NAKAHARA H, Cheedarla N, Verkerke HP, Cheedarla S, et al
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207. GUPTA A, Gooda R, Marouf R
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208. ZOLLER H, Wagner S, Schaefer B
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209. ASHER S, Shah R, Ings S, Horder J, et al
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210. DASARI S, Tse W, Wang J
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211. CHU Z, Cushway T, Wong M, Lim KX, et al
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212. MANGANAS K, Delicou S, Xydaki A, Kourakli A, et al
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213. JACOBS JW, Ding JJ, Tormey CA, Abels EA, et al
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     August 2023
214. ELSHERIF L, Kanthakumar P, Afolabi J, Stratton AF, et al
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215. GIBSON JS, Stewart GW
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216. NADER E, Conran N, Leonardo FC, Hatem A, et al
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217. HAMANI S, Lioure B, Nicolae A, Lipsker D, et al
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218. JOLY P, Nader E, Ketels F, Boisson C, et al
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219. ZHANG X, Han J, Shah BN, Saraf SL, et al
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220. MARTIN OY, Margulies S, Speller-Brown B, Majumdar S, et al
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     July 2023
221. RAI MP, Lee EJ, Bussel JB
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222. HAROUN E, Dutta D, Lim SH
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223. FERRONE FA
     More of the same? Voxelotor spawns a successor, but on what success does it build?
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224. DUFU K, Alt C, Strutt S, Partridge J, et al
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     June 2023
225. SHETH S, Taher AT, Coates TD, Kattamis A, et al
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226. WU J, Wang J, Tang N, Wang X, et al
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227. LIN Y, Del Giudice ME, Kron A, Meirovich H, et al
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228. PENG Y, Liang L, Zhang H, Liu H, et al
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229. BAIN BJ, Daniel Y, Henthorn J, de la Salle B, et al
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230. JACOBS JW, Stephens LD, Allen ES, Binns TC, et al
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231. GENDREAU S, Cecchini J, Perier F, Razazi K, et al
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232. TAKASAKI K, Friedman DF, Uter S, Vege S, et al
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233. LI J, Wang Y, Zhang Y, Zhang X, et al
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234. CHEMINET G, Brunetti A, Khimoud D, Ranque B, et al
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235. JARISCH A, Salzmann-Manrique E, Soerensen J, Sach G, et al
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     May 2023
236. GAVILLET M, Rufer N, Grandoni F, Rizzi M, et al
     Successful outcome of pregnancy post-allogeneic stem cell transplant despite severe RH1 alloimmunization: A case report.
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237. PICCIN A, Magzoub I, Hervig T
     The 'scintilla' starting vaso-occlusion in sickle cell disease.
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238. AN R, Man Y, Cheng K, Zhang T, et al
     Sickle red blood cell-derived extracellular vesicles activate endothelial cells and enhance sickle red cell adhesion mediated by von Willebrand factor.
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239. TOWERMAN AS, Guilliams KP, Guerriero R, Shinawi MS, et al
     Hyperammonemia and acute liver failure associated with deferasirox in two adolescents with sickle cell disease.
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240. LUNATI-ROZIE A, Janin A, Faubert E, Nony S, et al
     Use of minigene assays as a useful tool to confirm the pathogenic role of intronic variations of the ANK1 gene: Report of two cases of hereditary spherocytosis.
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241. TENNENBAUM J, Volle G, Pouchot J, Joseph L, et al
     Increased risk of venous thromboembolism in splenectomized patients with sickle cell disease.
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     April 2023
242. SICA M, Barone F, Nannelli C, Ricci P, et al
     The long-acting anti-C5 ravulizumab results in C3 binding to PNH red cells similar to its parental molecule eculizumab.
     Br J Haematol. 2023;201:e1-e4.
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243. KAPUR R
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244. ROSSI M, Pirenne F, Le Roux E, Smaine D, et al
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245. WANG YM, Loveless M, Miller E, Nelson AS, et al
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246. RABELO IB, Chiba AK, Moritz E, D'Amora P, et al
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247. JACOB M, Kawadler JM, Murdoch R, Ahmed M, et al
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248. KOREN A
     The continuing global challenges of treating patients with beta-thalassemia.
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249. JACOBS JW, Binns TC, Abels E, Tormey CA, et al
     Autoimmune haemolytic anaemia secondary to babesiosis: A review of reported cases and description of a novel association with cold antibody-mediated haemolytic anaemia.
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250. SUTRA DEL GALY A, Willems L, D'Aveni M, Pautas C, et al
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251. HOKLAND P, Daar S, Khair W, Sheth S, et al
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252. DONZE C, Benoit A, Thuret I, Faust C, et al
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253. EARLEY EJ, Kelly S, Fang F, Alencar CS, et al
     Genome-wide association study of early ischaemic stroke risk in Brazilian individuals with sickle cell disease implicates ADAMTS2 and CDK18 and uncovers novel loci.
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254. JACOBS JW, Booth GS, Guarente J, Schlafer D, et al
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     March 2023
255. TSITSIKAS DA, Rowe S, Bosch A, Hui C, et al
     Addition of plasma exchange to red cell exchange improves outcomes of fat embolism syndrome in sickle cell disease.
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256. MCKEAGUE S, Peake N, Lovelock D, Chow J, et al
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257. KOEHL B, Claude L, Reminy K, Tarer V, et al
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