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Articles published in
Br J Haematol
    February 2026
  1. 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.
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  2. 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.
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  3. 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.
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    January 2026
  4. 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.
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  5. 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.
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  6. 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.
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  7. 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.
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    December 2025
  8. 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.
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    November 2025
  9. 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.
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  10. 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.
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  11. 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.
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  12. 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.
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  13. 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.
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  14. 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.
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    October 2025
  15. 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.
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  16. 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.
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    September 2025
  17. 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.
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  18. 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.
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  19. 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.
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  20. 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.
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  21. 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.
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    August 2025
  22. 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.
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  23. 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.
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  24. 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.
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  25. 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.
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    July 2025
  26. 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.
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  27. 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.
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  28. 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.
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  29. SANTINI V, Consagra A
    How to use luspatercept and erythropoiesis-stimulating agents in low-risk myelodysplastic syndrome.
    Br J Haematol. 2025;207:15-26.
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    June 2025
  30. 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.
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  31. 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.
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  32. RICCHI P
    The double edge of erythropoietic modulation in thalassaemia.
    Br J Haematol. 2025;206:1879-1880.
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  33. 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.
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  34. 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.
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  35. 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.
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  36. 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.
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  37. 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.
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  38. 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.
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  39. 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.
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    May 2025
  40. 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.
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  41. 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.
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  42. 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.
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    April 2025
  43. 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.
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  44. 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.
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  45. 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.
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  46. ENACHE A, Carty SA, Babushok DV
    Origins of T-cell-mediated autoimmunity in acquired aplastic anaemia.
    Br J Haematol. 2025;206:1035-1053.
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  47. 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.
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    March 2025
  48. 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.
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  49. SCHECHTER AN
    Sickle cell anaemia therapy in 2025.
    Br J Haematol. 2025;206:842-845.
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  50. 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.
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  51. 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.
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    February 2025
  52. 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.
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  53. 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.
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  54. 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.
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  55. 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.
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  56. 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.
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  57. 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.
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  58. 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.
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  59. 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.
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    January 2025
  60. 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.
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  61. 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.
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  62. 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.
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  63. GALADANCI NA, Kanter J
    Avascular necrosis in sickle cell disease needs more definitive treatment options.
    Br J Haematol. 2025;206:385-386.
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  64. 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.
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  65. 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.
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  66. 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.
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  67. KOCHHAR M, McGann PT
    Sickle cell disease in India: Not just a mild condition.
    Br J Haematol. 2025;206:380-381.
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  68. 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.
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  69. 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.
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    December 2024
  70. 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.
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  71. 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.
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    November 2024
  72. 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.
    Br J Haematol. 2024;205:1985-1994.
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  73. CINTHO OZAHATA M, Guo Y, Gomes I, Malta B, et al
    Genetic variants associated with white blood cell count amongst individuals with sickle cell disease.
    Br J Haematol. 2024;205:1974-1984.
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  74. ELSHERIF L, Tang Y, Patillo KL, Wichlan D, et al
    Association of biomarkers of endothelial function, coagulation activation and kidney injury with persistent albuminuria in sickle cell anaemia.
    Br J Haematol. 2024;205:1963-1973.
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  75. GURNARI C, Lima ACM, Pagliuca S
    HLA-lacking clones in aplastic anaemia: Adaptive or maladaptive?
    Br J Haematol. 2024;205:1681-1682.
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  76. MARIN V, Huguenin Y, Bessi L, Weinmann L, et al
    Beta-thalassaemia intermedia due to a complex alpha-globin rearrangement and a heterozygous beta thalassaemia mutation.
    Br J Haematol. 2024;205:1959-1962.
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  77. ZAIMOKU Y, Sakai K, Tsuji N, Hosomichi K, et al
    Haematopoietic regeneration by HLA-A*0206-deficient clones in severe aplastic anaemia without definitive immunosuppressive treatment.
    Br J Haematol. 2024;205:1995-1999.
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    October 2024
  78. GUPTA CL, Jaganathasamy N, Madkaikar M
    Microbiome in sickle cell disease: Pathophysiology and therapeutic insights.
    Br J Haematol. 2024;205:1279-1287.
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  79. 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.
    >> Share

  80. 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.
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  81. 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.
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  82. 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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  83. 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.
    Br J Haematol. 2024;205:1556-1564.
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  84. 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.
    Br J Haematol. 2024;205:1565-1569.
    >> Share

  85. KATO S, Chagi K, Takagi Y, Hidaka M, et al
    Machine/deep learning-assisted hemoglobin level prediction using palpebral conjunctival images.
    Br J Haematol. 2024;205:1590-1598.
    >> Share

  86. LEE JM, Kim HS, Yoo J, Lee J, et al
    Genomic insights into inherited bone marrow failure syndromes in a Korean population.
    Br J Haematol. 2024;205:1581-1589.
    >> Share

    September 2024
  87. 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.
    >> Share

  88. 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.
    Br J Haematol. 2024;205:1180-1187.
    >> Share

  89. 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.
    Br J Haematol. 2024;205:1170-1179.
    >> Share

  90. 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.
    Br J Haematol. 2024;205:1159-1169.
    >> Share

  91. 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.
    Br J Haematol. 2024;205:1147-1158.
    >> Share

  92. 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.
    Br J Haematol. 2024;205:1137-1146.
    >> Share

  93. 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.
    Br J Haematol. 2024;205:999-1010.
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    August 2024
  94. 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.
    >> Share

  95. KATZ BZ, Karny S
    Pursuing the elusive footsteps of malaria in peripheral blood smears utilizing artificial intelligence.
    Br J Haematol. 2024;205:414-415.
    >> Share

  96. 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.
    >> Share

  97. 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.
    >> Share

  98. SEGBEFIA C, Luchtman-Jones L
    Seeing haemoglobin SC: Challenging the misperceptions.
    Br J Haematol. 2024;205:404-405.
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  99. 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.
    >> Share

  100. 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.
    >> Share

  101. 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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  102. 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.
    >> Share

  103. 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.
    >> Share

  104. 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.
    >> Share

    July 2024
  105. 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.
    >> Share

  106. GOK V, Leblebisatan G, Gurlek Gokcebay D, Guler S, et al
    Pyruvate kinase deficiency in 29 Turkish patients with two novel intronic variants.
    Br J Haematol. 2024;205:236-242.
    >> Share

  107. 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.
    >> Share

  108. 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.
    >> Share

  109. 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.
    >> Share

  110. 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.
    >> Share

  111. PADENIYA P, Premawardhena A
    Obesity, liver steatosis and metabolic syndrome: The hidden enemies in transfusion-dependent thalassaemia.
    Br J Haematol. 2024;205:28-29.
    >> Share

  112. RUIZ MA, Zhang X, Mansilla MA, Zahr RS, et al
    Prevalence of kidney health genetic variants in adults with sickle cell nephropathy.
    Br J Haematol. 2024;205:316-319.
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  113. 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.
    Br J Haematol. 2024;205:356-359.
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  114. 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
  115. GUARNERA L, Visconte V
    The metabolic fuel of paroxysmal nocturnal haemoglobinuria.
    Br J Haematol. 2024;204:2162-2164.
    >> Share

  116. 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.
    Br J Haematol. 2024;204:2194-2209.
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  117. 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.
    >> Share

  118. ZACCHEDDU E, Zappu A, Barella S, Clemente MG, et al
    Unplanned pregnancy in women with beta-thalassaemia treated with luspatercept.
    Br J Haematol. 2024;204:2505-2507.
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  119. 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.
    Br J Haematol. 2024;204:2468-2479.
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  120. 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.
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    May 2024
  121. 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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  122. 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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  123. 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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  124. MANARA R, Brotto D, Barillari MR, Costa G, et al
    Hearing loss in beta-thalassaemia: An Italian multicentre case-control study.
    Br J Haematol. 2024;204:2016-2024.
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  125. LIPTON JM
    Understanding complex disease-related mechanisms: Rational therapies for Diamond-Blackfan anaemia.
    Br J Haematol. 2024;204:1598-1599.
    >> Share

  126. 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.
    Br J Haematol. 2024;204:2121-2124.
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  127. 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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  128. 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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  129. 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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  130. 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.
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  131. 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.
    >> Share

  132. 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.
    >> Share

  133. NEYER PJ, Kabore B, Nakas CT, Diallo S, et al
    Increased erythroferrone levels in malarial anaemia.
    Br J Haematol. 2024;204:2066-2070.
    >> Share

    April 2024
  134. 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.
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  135. 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.
    >> Share

  136. 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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  137. 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
  138. 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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  139. 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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  140. LEE GM, Batchvarova M, Delahunty M, Boateng L, et al
    Sickle red blood cells directly activate neutrophils.
    Br J Haematol. 2024;204:e28-e30.
    >> Share

  141. 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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  142. 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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  143. 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.
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  144. 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.
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  145. 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.
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  146. 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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  147. 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.
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    February 2024
  148. WARE RE, Quinn CT
    The bold promise of gene therapy for sickle cell disease.
    Br J Haematol. 2024;204:381-382.
    >> Share

  149. STEENSMA DP
    Revisiting the first reported case of aplastic anaemia.
    Br J Haematol. 2024;204:455-458.
    >> Share

  150. 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.
    >> Share

  151. HUNT RC, Kimchi-Sarfaty C
    A synonymous variant is unmasked in thalassaemia.
    Br J Haematol. 2024;204:399-401.
    >> Share

  152. 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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  153. 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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  154. 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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  155. 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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  156. 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
  157. OYARBIDE U, Crane GM, Corey SJ
    The metabolic basis of inherited neutropenias.
    Br J Haematol. 2024;204:45-55.
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  158. PETERS C
    Haematopoietic stem cell transplantation in children with sickle cell disease: Still to do?
    Br J Haematol. 2024;204:22-23.
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  159. DANIEL Y, Henthorn J
    Lessons learnt in the screening and diagnosis of haemoglobinopathies.
    Br J Haematol. 2024;204:68-73.
    >> Share

  160. SHOOK LM, Ware RE
    Screening for haemoglobin disorders: One size may not fit all.
    Br J Haematol. 2024;204:26-28.
    >> Share

  161. 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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  162. 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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  163. 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
  164. 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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  165. 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
  166. 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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  167. 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.
    Br J Haematol. 2023;203:e102-e107.
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  168. 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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  169. NOVAK W, Berner J, Svaton M, Jimenez-Heredia R, et al
    Evans syndrome caused by a deleterious mutation affecting the adaptor protein SASH3.
    Br J Haematol. 2023;203:678-683.
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  170. SCULLY M, Rayment R, Clark A, Westwood JP, et al
    A British Society for Haematology Guideline: Diagnosis and management of thrombotic thrombocytopenic purpura and thrombotic microangiopathies.
    Br J Haematol. 2023;203:546-563.
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  171. FERMO E, Zaninoni A, Vercellati C, Marcello AP, et al
    When alpha spectrin null alleles meet low expression alpha spectrin polymorphisms.
    Br J Haematol. 2023;203:684-687.
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    October 2023
  172. ALADJIDI N, Pincez T, Rieux-Laucat F, Nugent D, et al
    Paediatric-onset Evans syndrome: Breaking away from refractory immune thrombocytopenia.
    Br J Haematol. 2023;203:28-35.
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  173. 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).
    Br J Haematol. 2023;203:319-326.
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  174. ALSULTAN A, Abujoub R, Alsudairy R, Memon S, et al
    Human leucocyte antigen-matched related haematopoietic stem cell transplantation using low-dose cyclophosphamide, fludarabine and thymoglobulin in children with severe aplastic anaemia.
    Br J Haematol. 2023;203:255-263.
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  175. HEBBEL RP, Milbauer L, Wei P
    A novel promoter of endothelial dysfunction in African Americans: Relevance to sickle cell anaemia.
    Br J Haematol. 2023;203:e71-e73.
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    September 2023
  176. 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.
    Br J Haematol. 2023;202:1018-1023.
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  177. NANNELLI C, Bosman A, Cunningham J, Dugue PA, et al
    Genetic variants causing G6PD deficiency: Clinical and biochemical data support new WHO classification.
    Br J Haematol. 2023;202:1024-1032.
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  178. DE ALCANTARA PEDRO PP, Castro CHM, Pinheiro MM, Goncalves LM, et al
    Vertebral fractures and low lean mass in young men with sickle cell disease: Lack of association with bone mineral density and clinical characteristics.
    Br J Haematol. 2023;202:e46-e49.
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  179. HAN J, Saraf SL, Gordeuk VR
    Vaccination in sickle cell disease: Immunocompromised or immunocompetent?
    Br J Haematol. 2023;202:916-918.
    >> Share

  180. ESPERTI S, Nader E, Boisson C, Carin R, et al
    Mitochondria retention in mature RBCs from haemoglobin SC patients.
    Br J Haematol. 2023;202:e36-e38.
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  181. KNIGHT-MADDEN J, King L, Asnani M, Skyers N, et al
    Needs assessment in adults and parents of children living with sickle cell disease in Jamaica.
    Br J Haematol. 2023;202:e31-e35.
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  182. NAKAHARA H, Cheedarla N, Verkerke HP, Cheedarla S, et al
    Enhanced IgG immune response to COVID-19 vaccination in patients with sickle cell disease.
    Br J Haematol. 2023;202:937-941.
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  183. GUPTA A, Gooda R, Marouf R
    Pseudo-Gaucher cells in a splenectomised Beta-Thalassemia patient.
    Br J Haematol. 2023;202:911.
    >> Share

  184. ZOLLER H, Wagner S, Schaefer B
    What is wrong in doing good?
    Br J Haematol. 2023;202:1089-1090.
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  185. ASHER S, Shah R, Ings S, Horder J, et al
    Haematopoietic stem cell mobilisation followed by high-dose chemotherapy and autologous stem cell transplantation for patients with sickle cell disease and myeloma.
    Br J Haematol. 2023;202:1224-1227.
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  186. DASARI S, Tse W, Wang J
    Real-world evidence of incidence and outcomes of aplastic anaemia following administration of immune checkpoint inhibitors.
    Br J Haematol. 2023;202:1205-1208.
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  187. CHU Z, Cushway T, Wong M, Lim KX, et al
    Incidence and predictors of hypophosphataemia after ferric carboxymaltose use-A 3-year experience from a single institution in Singapore.
    Br J Haematol. 2023;202:1199-1204.
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  188. MANGANAS K, Delicou S, Xydaki A, Kourakli A, et al
    Predisposing factors for advanced liver fibrosis in patients with sickle cell disease.
    Br J Haematol. 2023;202:1192-1198.
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  189. JACOBS JW, Ding JJ, Tormey CA, Abels EA, et al
    Where do they go? The clinical conundrum of warm autoantibodies and their inability to cause haemolytic disease of the foetus and newborn.
    Br J Haematol. 2023;202:1213-1215.
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    August 2023
  190. ELSHERIF L, Kanthakumar P, Afolabi J, Stratton AF, et al
    Urinary angiotensinogen is associated with albuminuria in adults with sickle cell anaemia.
    Br J Haematol. 2023;202:669-673.
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  191. GIBSON JS, Stewart GW
    A critical role for altered red cell cation permeability in pathogenesis of sickle cell disease and other haemolytic anaemias.
    Br J Haematol. 2023;202:462-464.
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  192. NADER E, Conran N, Leonardo FC, Hatem A, et al
    Piezo1 activation augments sickling propensity and the adhesive properties of sickle red blood cells in a calcium-dependent manner.
    Br J Haematol. 2023;202:657-668.
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  193. HAMANI S, Lioure B, Nicolae A, Lipsker D, et al
    A Rare Cause of Refractory Anaemia hidden between Folds.
    Br J Haematol. 2023;202:712.
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  194. JOLY P, Nader E, Ketels F, Boisson C, et al
    Effects of pyruvate kinase activators on red blood cell properties in sickle cell disease.
    Br J Haematol. 2023;202:e27-e30.
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  195. ZHANG X, Han J, Shah BN, Saraf SL, et al
    Platelet count decline and high neutrophil count within the first day of admission for painful sickle cell vaso-occlusive episodes predict severe complications.
    Br J Haematol. 2023;202:e20-e23.
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  196. MARTIN OY, Margulies S, Speller-Brown B, Majumdar S, et al
    The evolution of the COVID-19 pandemic in paediatric patients with sickle cell disease: From Alpha to Omicron.
    Br J Haematol. 2023;202:479-484.
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    July 2023
  197. RAI MP, Lee EJ, Bussel JB
    Maintenence rituximab following induction in autoimmune cytopenias.
    Br J Haematol. 2023;202:153-158.
    >> Share

  198. HAROUN E, Dutta D, Lim SH
    Effects of GBT1118, a voxelotor analog, on intestinal pathophysiology in sickle cell disease.
    Br J Haematol. 2023;202:184-194.
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  199. FERRONE FA
    More of the same? Voxelotor spawns a successor, but on what success does it build?
    Br J Haematol. 2023;202:13-15.
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  200. DUFU K, Alt C, Strutt S, Partridge J, et al
    GBT021601 improves red blood cell health and the pathophysiology of sickle cell disease in a murine model.
    Br J Haematol. 2023;202:173-183.
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    June 2023
  201. SHETH S, Taher AT, Coates TD, Kattamis A, et al
    Management of luspatercept therapy in patients with transfusion-dependent beta-thalassaemia.
    Br J Haematol. 2023;201:824-831.
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  202. WU J, Wang J, Tang N, Wang X, et al
    An atypical patient with bone marrow failure syndrome-2 without microcephaly and learning disability in a Chinese family.
    Br J Haematol. 2023;201:e50-e53.
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  203. LIN Y, Del Giudice ME, Kron A, Meirovich H, et al
    A pilot feasibility trial of daily versus every other day oral iron supplementation in patients with iron deficiency anaemia.
    Br J Haematol. 2023;201:1000-1004.
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  204. PENG Y, Liang L, Zhang H, Liu H, et al
    Single-cell profiling of ineffective erythropoiesis in a mouse model of beta-thalassaemia intermedia.
    Br J Haematol. 2023;201:982-994.
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  205. BAIN BJ, Daniel Y, Henthorn J, de la Salle B, et al
    Significant haemoglobinopathies: A guideline for screening and diagnosis: A British Society for Haematology Guideline: A British Society for Haematology Guideline.
    Br J Haematol. 2023;201:1047-1065.
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  206. JACOBS JW, Stephens LD, Allen ES, Binns TC, et al
    Epidemiological and clinical features, therapeutic strategies and outcomes in patients with hyperhaemolysis: A systematic review.
    Br J Haematol. 2023;201:1025-1032.
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  207. GENDREAU S, Cecchini J, Perier F, Razazi K, et al
    Effect of high-flow oxygen therapy on regional oxygen saturation during vaso-occlusive pain crisis: An observational study.
    Br J Haematol. 2023;201:e58-e61.
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  208. TAKASAKI K, Friedman DF, Uter S, Vege S, et al
    Variant RHD alleles and Rh immunization in patients with sickle cell disease.
    Br J Haematol. 2023;201:1220-1228.
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  209. LI J, Wang Y, Zhang Y, Zhang X, et al
    Haematopoietic stem cell transplantation for hepatitis-associated aplastic anaemia and non-hepatitis-associated aplastic anaemia: A propensity score-matched analysis.
    Br J Haematol. 2023;201:1179-1191.
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  210. CHEMINET G, Brunetti A, Khimoud D, Ranque B, et al
    Acute chest syndrome in adult patients with sickle cell disease: The relationship with the time to onset after hospital admission.
    Br J Haematol. 2023;201:1229-1238.
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  211. JARISCH A, Salzmann-Manrique E, Soerensen J, Sach G, et al
    Donor-type red blood cell transfusion to deplete isoagglutinins prior to allogeneic stem cell transplantation from ABO major incompatible bone marrow donors.
    Br J Haematol. 2023;201:1159-1168.
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    May 2023
  212. 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.
    Br J Haematol. 2023;201:581-584.
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  213. PICCIN A, Magzoub I, Hervig T
    The 'scintilla' starting vaso-occlusion in sickle cell disease.
    Br J Haematol. 2023;201:379-380.
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  214. 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.
    Br J Haematol. 2023;201:552-563.
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  215. 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.
    Br J Haematol. 2023;201:e30-e33.
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  216. 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.
    Br J Haematol. 2023;201:e46-e49.
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  217. TENNENBAUM J, Volle G, Pouchot J, Joseph L, et al
    Increased risk of venous thromboembolism in splenectomized patients with sickle cell disease.
    Br J Haematol. 2023;201:793-796.
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    April 2023
  218. 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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  219. KAPUR R
    The potential of metabolomics as a predictive guide for clinical management in autoimmunity against red blood cells.
    Br J Haematol. 2023;201:13-14.
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  220. ROSSI M, Pirenne F, Le Roux E, Smaine D, et al
    Delayed haemolytic transfusion reaction in paediatric patients with sickle cell disease: A retrospective study in a French national reference centre.
    Br J Haematol. 2023;201:125-132.
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  221. WANG YM, Loveless M, Miller E, Nelson AS, et al
    Phenotypes of adults with Fanconi anaemia.
    Br J Haematol. 2023;201:133-139.
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  222. RABELO IB, Chiba AK, Moritz E, D'Amora P, et al
    Metabolomic profile in patients with primary warm autoimmune haemolytic anaemia.
    Br J Haematol. 2023;201:140-149.
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  223. JACOB M, Kawadler JM, Murdoch R, Ahmed M, et al
    Brain volume in Tanzanian children with sickle cell anaemia: A neuroimaging study.
    Br J Haematol. 2023;201:114-124.
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  224. KOREN A
    The continuing global challenges of treating patients with beta-thalassemia.
    Br J Haematol. 2023;201:183-184.
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  225. 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.
    Br J Haematol. 2023;201:364-369.
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  226. SUTRA DEL GALY A, Willems L, D'Aveni M, Pautas C, et al
    Haemolytic paroxysmal nocturnal haemoglobinuria in patients with myeloid neoplasms: A rare association with specific therapeutic implications.
    Br J Haematol. 2023;201:e16-e20.
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  227. HOKLAND P, Daar S, Khair W, Sheth S, et al
    Thalassaemia-A global view.
    Br J Haematol. 2023;201:199-214.
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  228. DONZE C, Benoit A, Thuret I, Faust C, et al
    beta-Thalassemia in childhood: Current state of health in a high-income country.
    Br J Haematol. 2023;201:334-342.
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  229. 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.
    Br J Haematol. 2023;201:343-352.
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  230. JACOBS JW, Booth GS, Guarente J, Schlafer D, et al
    Autoimmune haemolytic anaemia and immune thrombocytopenia following SARS-CoV-2 and non-SARS-CoV-2 vaccination: 32 Years of passive surveillance data.
    Br J Haematol. 2023;201:227-233.
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    March 2023
  231. 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.
    Br J Haematol. 2023;200:e50-e52.
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  232. MCKEAGUE S, Peake N, Lovelock D, Chow J, et al
    Acquired HbH disease diagnosed by HbA1c capillary electrophoresis.
    Br J Haematol. 2023;200:687.
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  233. KOEHL B, Claude L, Reminy K, Tarer V, et al
    Erythrocyte type 1 equilibrative nucleoside transporter expression in sickle cell disease and sickle cell trait.
    Br J Haematol. 2023;200:812-820.
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