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Articles published in
Br J Haematol
    September 2024
  1. 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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    August 2024
  2. 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.
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  3. KATZ BZ, Karny S
    Pursuing the elusive footsteps of malaria in peripheral blood smears utilizing artificial intelligence.
    Br J Haematol. 2024;205:414-415.
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  4. 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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  5. 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.
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  6. SEGBEFIA C, Luchtman-Jones L
    Seeing haemoglobin SC: Challenging the misperceptions.
    Br J Haematol. 2024;205:404-405.
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  7. 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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  8. 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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  9. 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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  10. 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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  11. 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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  12. 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
  13. 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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  14. 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.
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  15. 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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  16. 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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  17. 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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  18. 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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  19. 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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  20. 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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  21. 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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  22. 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
  23. GUARNERA L, Visconte V
    The metabolic fuel of paroxysmal nocturnal haemoglobinuria.
    Br J Haematol. 2024;204:2162-2164.
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  24. 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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  25. 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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  26. 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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  27. 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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  28. 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
  29. 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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  30. 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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  31. 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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  32. 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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  33. LIPTON JM
    Understanding complex disease-related mechanisms: Rational therapies for Diamond-Blackfan anaemia.
    Br J Haematol. 2024;204:1598-1599.
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  34. 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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  35. 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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  36. 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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  37. 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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  38. 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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  39. 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.
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  40. 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.
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  41. NEYER PJ, Kabore B, Nakas CT, Diallo S, et al
    Increased erythroferrone levels in malarial anaemia.
    Br J Haematol. 2024;204:2066-2070.
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    April 2024
  42. 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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  43. 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.
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  44. 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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  45. 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
  46. 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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  47. 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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  48. 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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  49. 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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  50. 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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  51. 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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  52. 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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  53. 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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  54. 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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  55. 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
  56. WARE RE, Quinn CT
    The bold promise of gene therapy for sickle cell disease.
    Br J Haematol. 2024;204:381-382.
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  57. STEENSMA DP
    Revisiting the first reported case of aplastic anaemia.
    Br J Haematol. 2024;204:455-458.
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  58. 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.
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  59. HUNT RC, Kimchi-Sarfaty C
    A synonymous variant is unmasked in thalassaemia.
    Br J Haematol. 2024;204:399-401.
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  60. 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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  61. 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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  62. 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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  63. 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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  64. 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
  65. OYARBIDE U, Crane GM, Corey SJ
    The metabolic basis of inherited neutropenias.
    Br J Haematol. 2024;204:45-55.
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  66. 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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  67. DANIEL Y, Henthorn J
    Lessons learnt in the screening and diagnosis of haemoglobinopathies.
    Br J Haematol. 2024;204:68-73.
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  68. SHOOK LM, Ware RE
    Screening for haemoglobin disorders: One size may not fit all.
    Br J Haematol. 2024;204:26-28.
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  69. 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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  70. 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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  71. 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
  72. 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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  73. 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
  74. 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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  75. 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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  76. 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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  77. 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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  78. 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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  79. 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
  80. 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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  81. 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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  82. 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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  83. 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
  84. 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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  85. 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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  86. 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.
    >> Share

  87. HAN J, Saraf SL, Gordeuk VR
    Vaccination in sickle cell disease: Immunocompromised or immunocompetent?
    Br J Haematol. 2023;202:916-918.
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  88. 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.
    >> Share

  89. 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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  90. 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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  91. GUPTA A, Gooda R, Marouf R
    Pseudo-Gaucher cells in a splenectomised Beta-Thalassemia patient.
    Br J Haematol. 2023;202:911.
    >> Share

  92. ZOLLER H, Wagner S, Schaefer B
    What is wrong in doing good?
    Br J Haematol. 2023;202:1089-1090.
    >> Share

  93. 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.
    >> Share

  94. 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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  95. 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.
    >> Share

  96. 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.
    >> Share

  97. 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
  98. 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.
    >> Share

  99. 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.
    >> Share

  100. 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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  101. 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.
    >> Share

  102. 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.
    >> Share

  103. 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.
    >> Share

  104. 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.
    >> Share

    July 2023
  105. RAI MP, Lee EJ, Bussel JB
    Maintenence rituximab following induction in autoimmune cytopenias.
    Br J Haematol. 2023;202:153-158.
    >> Share

  106. 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.
    >> Share

  107. FERRONE FA
    More of the same? Voxelotor spawns a successor, but on what success does it build?
    Br J Haematol. 2023;202:13-15.
    >> Share

  108. 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.
    >> Share

    June 2023
  109. 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.
    >> Share

  110. 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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  111. 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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  112. 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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  113. 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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  114. 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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  115. 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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  116. 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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  117. 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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  118. 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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  119. 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
  120. 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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  121. PICCIN A, Magzoub I, Hervig T
    The 'scintilla' starting vaso-occlusion in sickle cell disease.
    Br J Haematol. 2023;201:379-380.
    >> Share

  122. 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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  123. 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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  124. 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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  125. 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
  126. 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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  127. 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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  128. 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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  129. 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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  130. 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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  131. 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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  132. KOREN A
    The continuing global challenges of treating patients with beta-thalassemia.
    Br J Haematol. 2023;201:183-184.
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  133. 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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  134. 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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  135. 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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  136. 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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  137. 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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  138. 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
  139. IBEMERE SO, Oyedeji CI, Preiss L, Van Althuis LE, et al
    Characterising the prevalence of overweight and obese status among adults with sickle cell disease.
    Br J Haematol. 2023;200:633-642.
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  140. JOSEPH L, Corbasson A, Manceau S, Khimoud D, et al
    Safety of coronavirus disease 2019 vaccines in 213 adult patients with sickle cell disease.
    Br J Haematol. 2023;200:563-567.
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  141. 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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  142. 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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  143. 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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    February 2023
  144. POUTREL S, Boisson C, Nader E, Renoux C, et al
    Clinical severity and blood rheology in patients with sickle cell anaemia and co-existing autoimmune disease.
    Br J Haematol. 2023;200:e28-e31.
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  145. AGUWA CJ, Cannon AD, Casella JF, Shapiro BK, et al
    Current developmental screening practices in young children with sickle cell disease.
    Br J Haematol. 2023;200:377-380.
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  146. HEITZER AM, Schreiber JE, Yuan X, Wang F, et al
    Working memory and school readiness in preschool children with sickle cell disease compared to demographically matched controls.
    Br J Haematol. 2023;200:358-366.
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  147. HU J, Gong S, Chen K, Yang R, et al
    Haploidentical transplant for paediatric patients with severe thalassaemia using post-transplant cyclophosphamide and methotrexate: A prospectively registered multicentre trial from the Bone Marrow Failure Working Group of Hunan Province, China.
    Br J Haematol. 2023;200:329-337.
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  148. SIRIWORADETKUN S, Thiengtavor C, Thubthed R, Paiboonsukwong K, et al
    A comprehensive study of immune function and immunophenotyping of white blood cells from beta-thalassaemia/HbE patients on hydroxyurea supports the safety of the drug.
    Br J Haematol. 2023;200:367-376.
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  149. RICCHI P
    Liver fibrosis in young patients with transfusion-dependent thalassaemia (TDT), understanding the role of steatosis.
    Br J Haematol. 2023;200:399-400.
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  150. PADENIYA P, Ediriweera D, De Silva AP, Niriella M, et al
    The association between steatosis and liver damage in transfusion-dependent beta thalassaemia patients.
    Br J Haematol. 2023;200:517-523.
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    January 2023
  151. NGUYEN PC, Tiong IS, Westerman DA, Blombery P, et al
    A novel ATRX variant with splicing consequences in myelodysplastic syndrome with acquired alpha thalassaemia.
    Br J Haematol. 2023;200:e13-e16.
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  152. ZHU D, Liang G, Zhang Y, Wei X, et al
    Identification of haemolytic anaemia caused by glucose phosphate isomerase deficiency in a thalassaemia-endemic region: Correction of misdiagnosis and consideration of the cause of misdiagnosis.
    Br J Haematol. 2023;200:e8-e12.
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  153. MOISE KJ JR
    Immunomodulation for early-onset haemolytic disease of the fetus/newborn: Can we delay the need for intrauterine transfusions?
    Br J Haematol. 2023;200:11-12.
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  154. WILSON J
    Rasburicase-induced methaemoglobinaemia and catastrophic oxidative haemolysis in undiagnosed G6PD deficiency.
    Br J Haematol. 2023;200:7.
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  155. VAN DIJK MJ, van Oirschot BA, Stam-Slob MC, Waanders E, et al
    Heterozygosity for bisphosphoglycerate mutase deficiency expressing clinically as congenital erythrocytosis: A case series and literature review.
    Br J Haematol. 2023;200:249-255.
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    December 2022
  156. ZAMAN BA, Rasool SO, Abdo JM
    The effect of erythroferrone suppression by transfusion on the erythropoietin-erythroferrone-hepcidin axis in transfusion-dependent thalassaemia: A pre-post cohort study.
    Br J Haematol. 2022 Dec 19. doi: 10.1111/bjh.18619.
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  157. LI M, Liu L, Ding B, Song X, et al
    Refractory/relapse thrombocytopenia in a patient with Evans' syndrome successfully treated with zanubrutinib.
    Br J Haematol. 2022;199:e37-e42.
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  158. WINER JC, Yee ME, Ataga KI, Lebensburger JD, et al
    Patients with sickle cell disease who develop end-stage kidney disease continue to experience poor survival - A 19-year United States Renal Data System study.
    Br J Haematol. 2022;199:e43-e47.
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  159. DE LA IGLESIA INIGO S, Navarrete Bullon L, Stuckey R, Veiga Vaz A, et al
    Cauda equina syndrome secondary to extramedullary erythropoiesis in a transfusion-dependent thalassemia patient following treatment with luspatercept: A case report.
    Br J Haematol. 2022;199:e30-e33.
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  160. RAJPUT RV, Ma X, Boswell KL, Gaudinski M, et al
    Clinical outcomes and immune responses to SARS-CoV-2 vaccination in severe aplastic anaemia.
    Br J Haematol. 2022;199:679-687.
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  161. CONNELLY JA, Savani BN
    Irradiation-free, T-cell replete haploidentical transplant for Fanconi anaemia, weighing the benefits.
    Br J Haematol. 2022;199:639-641.
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  162. VIAL Y, Lainey E, Leblanc T, Baudouin V, et al
    De novo NUF2 variant in a novel inherited bone marrow failure syndrome including microcephaly and renal hypoplasia.
    Br J Haematol. 2022;199:739-743.
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    November 2022
  163. AMPOMAH MA, Drake JA, Anum A, Amponsah B, et al
    A case-control and seven-year longitudinal neurocognitive study of adults with sickle cell disease in Ghana.
    Br J Haematol. 2022;199:411-426.
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  164. XU L, Lu Y, Hu S, Li C, et al
    Unmanipulated haploidentical haematopoietic cell transplantation with radiation-free conditioning in Fanconi anaemia: A retrospective analysis from the Chinese Blood and Marrow Transplantation Registry Group.
    Br J Haematol. 2022;199:401-410.
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  165. HAN J, Zhang X, Molokie RE, Njoku FU, et al
    COVID-19 vaccination status and disease burden in patients with sickle cell disease.
    Br J Haematol. 2022;199:e21-e24.
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  166. OGUNSILE FJ, Stewart KJ, Kanter J, Lanzkron SM, et al
    An evaluation of cardiopulmonary endurance and muscular strength in adults living with sickle cell disease.
    Br J Haematol. 2022;199:597-602.
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  167. RODRIGUEZ CORTE J, Candal-Pedreira C, Ruano-Ravina A, Perez-Rios M, et al
    Home-based blood transfusion therapy: A systematic review.
    Br J Haematol. 2022;199:496-506.
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    October 2022
  168. TORTI L
    Life beyond alpha-thalassaemia: We are moving forward.
    Br J Haematol. 2022;199:11-13.
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  169. PAALVAST Y, Moazzen S, Sweegers M, Hogema B, et al
    A computational model for prediction of ferritin and haemoglobin levels in blood donors.
    Br J Haematol. 2022;199:143-152.
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  170. CONRAN N, de Alvarenga Maximo C, Oliveira T, Fertrin KY, et al
    Safe use of hydroxycarbamide in sickle cell disease patients hospitalized for painful vaso-occlusive episodes during the randomized, open-label HELPS study.
    Br J Haematol. 2022;199:153-157.
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  171. AKE-SITTIPAISARN S, Sirichotiyakul S, Srisupundit K, Luewan S, et al
    Outcomes of pregnancies complicated by haemoglobin H-constant spring and deletional haemoglobin H disease: A retrospective cohort study.
    Br J Haematol. 2022;199:122-129.
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  172. EYSSETTE-GUERREAU S, Khimoud D, Michaux K, Odievre MH, et al
    Severe cases of COVID-19 in children with sickle cell disease during the Omicron wave in France: a plea for vaccination.
    Br J Haematol. 2022;199:e8-e11.
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  173. ESPERTI S, Boisson C, Robert M, Nader E, et al
    Does G6PD deficiency cause further damage to red blood cells of patients with sickle cell anaemia?
    Br J Haematol. 2022;199:289-291.
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  174. QUARELLO P, Ramenghi U, Fagioli F
    Diamond-Blackfan anaemia with iron overload: A serious issue.
    Br J Haematol. 2022;199:171-172.
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  175. CHURCHILL D, Ali H, Moussa M, Donohue C, et al
    Maternal iron deficiency anaemia in pregnancy: Lessons from a national audit.
    Br J Haematol. 2022;199:277-284.
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  176. LECORNEC N, Castex MP, Reguerre Y, Moreau P, et al
    Agranulocytosis in patients with Diamond-Blackfan anaemia (DBA) treated with deferiprone for post-transfusion iron overload: A retrospective study of the French DBA cohort.
    Br J Haematol. 2022;199:285-288.
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    September 2022
  177. WULFTANGE WJ, Kucukal E, Man Y, An R, et al
    Antithrombin-III mitigates thrombin-mediated endothelial cell contraction and sickle red blood cell adhesion in microscale flow.
    Br J Haematol. 2022;198:893-902.
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  178. CORNELISSEN HM, Musekwa EM, Glashoff RH, Esser M, et al
    Peripheral-blood cytopenia, an early indicator of inborn errors of immunity.
    Br J Haematol. 2022;198:875-886.
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  179. ALIBERTI L, Gagliardi I, Gamberini MR, Ziggiotto A, et al
    Beta-thalassaemia major: Prevalence, risk factors and clinical consequences of hypercalciuria.
    Br J Haematol. 2022;198:903-911.
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  180. ARITA K, Murakami J, Iwaki N, Hosono N, et al
    An eltrombopag-induced remission of bone-marrow aplasia accompanied by marked leukoerythroblastosis and splenomegaly.
    Br J Haematol. 2022;198:e75-e77.
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  181. PATEL NG, Young D, Numan Y, Bhasin A, et al
    The utility of peripheral blood film and haemolysis markers in evaluation of haemolytic anaemia at a tertiary care hospital.
    Br J Haematol. 2022;198:927-929.
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  182. VERCELLATI C, Zaninoni A, Marcello AP, Fermo E, et al
    Changing trends of splenectomy in hereditary spherocytosis: The experience of a reference Centre in the last 40 years.
    Br J Haematol. 2022;198:912-915.
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  183. TANTRAVAHI SK, Huber BD, Vagher J, Maese L, et al
    Genome-wide uniparental disomy as a mechanism of immune escape in acquired aplastic anaemia.
    Br J Haematol. 2022;198:e78-e81.
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  184. SONGDEJ D, Kadegasem P, Tangbubpha N, Sasanakul W, et al
    Whole-exome sequencing uncovered genetic diagnosis of severe inherited haemolytic anaemia: Correlation with clinical phenotypes.
    Br J Haematol. 2022;198:1051-1064.
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    August 2022
  185. WILSON J
    Unlikely bedfellows - Sickle cells with malaria parasites.
    Br J Haematol. 2022 Aug 12. doi: 10.1111/bjh.18412.
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  186. MORICONI C, Dzieciatkowska M, Roy M, D'Alessandro A, et al
    Retention of functional mitochondria in mature red blood cells from patients with sickle cell disease.
    Br J Haematol. 2022;198:574-586.
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  187. ROY NBA, Da Costa L, Russo R, Bianchi P, et al
    The use of next-generation sequencing in the diagnosis of rare inherited anaemias: A Joint BSH/EHA Good Practice Paper.
    Br J Haematol. 2022;198:459-477.
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  188. NISHIMURA JI, Usuki K, Ramos J, Ichikawa S, et al
    Crovalimab for treatment of patients with paroxysmal nocturnal haemoglobinuria and complement C5 polymorphism: Subanalysis of the phase 1/2 COMPOSER study.
    Br J Haematol. 2022;198:e46-e50.
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  189. GAARTMAN AE, Strijdhorst A, van Es N, Tang MW, et al
    Limited value of the D-dimer based YEARS algorithm to rule out pulmonary embolism in sickle cell disease and sickle cell trait.
    Br J Haematol. 2022;198:e42-e45.
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  190. GREEN NS, Van Doren L, Licursi M, Billings DD, et al
    Anti-SARS-CoV-19 antibodies in children and adults with sickle cell disease: A single-site analysis in New York City.
    Br J Haematol. 2022;198:680-683.
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  191. SHARMA A, Leonard A, West K, Gossett JM, et al
    Optimizing haematopoietic stem and progenitor cell apheresis collection from plerixafor-mobilized patients with sickle cell disease.
    Br J Haematol. 2022;198:740-744.
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  192. URSULE-DUFAIT C, Bengoufa D, Theodorou I, Villesuzanne C, et al
    Heavy chain/light chain assay is a useful biomarker for diagnosis and management of patients with cold agglutinin disease.
    Br J Haematol. 2022;198:e67-e70.
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  193. OGBENNA AA, Akinsete AM, Kalejaiye OO, Matthew OK, et al
    Reduction in seroprevalence of viral transfusion-transmitted infections in southwest Nigeria in children with sickle cell disease using an enhanced screening strategy.
    Br J Haematol. 2022;198:745-752.
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  194. GELBENEGGER G, Jaeger U, Fillitz M, D'Sa S, et al
    Sustained sutimlimab response for 3 years in patients with cold agglutinin disease: A phase I, open-label, extension trial.
    Br J Haematol. 2022;198:e59-e62.
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    July 2022
  195. SCOTT C, Bartolovic K, Clark SA, Waithe D, et al
    Functional impairment of erythropoiesis in Congenital Dyserythropoietic Anaemia type I arises at the progenitor level.
    Br J Haematol. 2022;198:e10-e14.
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  196. COOPER-SOOD JB, Hagar W, Marsh A, Hoppe C, et al
    Adjuvant low-dose ketamine for paediatric and young adult sickle cell vaso-occlusive episodes in the emergency department.
    Br J Haematol. 2022;198:207-209.
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  197. BUESCHE G, Teoman H, Schneider RK, Ribezzo F, et al
    Evolution of severe (transfusion-dependent) anaemia in myelodysplastic syndromes with 5q deletion is characterized by a macrophage-associated failure of the eythropoietic niche.
    Br J Haematol. 2022;198:114-130.
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  198. CAUGHEY MC, Derebail VK, Carden MA, Novelli EM, et al
    Prevalence and outcomes of dehydration in adults with sickle cell trait: the Atherosclerosis Risk in Communities (ARIC) study.
    Br J Haematol. 2022;198:397-400.
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  199. GUO JJ, Cao L, Zhu HY, Miao Y, et al
    T-cell large granular lymphocytic leukaemia with atypical immunophenotypes: A single-centre retrospective analysis of 17 cases.
    Br J Haematol. 2022;198:e18-e22.
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  200. KONGKIATKAMON S
    Acute haemolysis following COVID-19 vaccination in a thalassaemic patient with G6PD deficiency.
    Br J Haematol. 2022;198:221.
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  201. EARLY ML, Linton E, Bosch A, Campbell T, et al
    The Montreal cognitive assessment as a cognitive screening tool in sickle cell disease: Associations with clinically significant cognitive domains.
    Br J Haematol. 2022;198:382-390.
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    June 2022
  202. DELAPORTA P, Terpos E, Solomou EE, Gumeni S, et al
    Immune response and adverse events after vaccination against SARS-CoV-2 in adult patients with transfusion-dependent thalassaemia.
    Br J Haematol. 2022;197:576-579.
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  203. PICCIN A, O'Connor-Byrne N, Daves M, Lynch K, et al
    Autoimmune disease and sickle cell anaemia: 'Intersecting pathways and differential diagnosis'.
    Br J Haematol. 2022;197:518-528.
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  204. HAN J, Molokie RE, Hussain F, Njoku F, et al
    Voxelotor and albuminuria in adults with sickle cell anaemia.
    Br J Haematol. 2022;197:e63-e64.
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  205. SHEEHAN VA, van Beers EJ, Connes P, van Wijk R, et al
    Comment on: Oxygen gradient ektacytometry does not predict pain in children with sickle cell anaemia.
    Br J Haematol. 2022;197:e61-e62.
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  206. JOLY P, Boisson C, Renoux C, Caillat N, et al
    Determinants of the point of sickling measured by oxygen gradient ektacytometry in sickle cell anaemia.
    Br J Haematol. 2022;197:e56-e58.
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  207. NARDO-MARINO A, Petersen J, Brewin JN, Birgens H, et al
    Oxygen gradient ektacytometry does not predict pain in children with sickle cell anaemia.
    Br J Haematol. 2022;197:609-617.
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  208. MARSHALL WH 5TH, Cleary EM, Della-Moretta S, Li R, et al
    Elevated tricuspid regurgitation velocity is associated with increased adverse haematologic events during pregnancy in women with sickle cell disease.
    Br J Haematol. 2022;197:795-801.
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    May 2022
  209. AMID A, Barrowman N, Odame I, Kirby-Allen M, et al
    Optimizing transfusion therapy for survivors of Haemoglobin Bart's hydrops fetalis syndrome: Defining the targets for haemoglobin-H fraction and "functional" haemoglobin level.
    Br J Haematol. 2022;197:373-376.
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  210. LONGORIA JN, Heitzer AM, Hankins JS, Trpchevska A, et al
    Neurocognitive risk in sickle cell disease: Utilizing neuropsychology services to manage cognitive symptoms and functional limitations.
    Br J Haematol. 2022;197:260-270.
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  211. BAIN BJ, Littlewood T, Rees DC
    What does the term 'sickle cell disease' mean?
    Br J Haematol. 2022;197:381-382.
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  212. ALTER BP, Giri N, McReynolds LJ, Altintas B, et al
    Fanconi anaemia: A syndrome with distinct subgroups.
    Br J Haematol. 2022;197:467-474.
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  213. VORA SM, Boyd S, Denny N, Jackson E, et al
    Expanded eligibility for emerging therapies in sickle cell disease in the UK - crizanlizumab and voxelotor.
    Br J Haematol. 2022;197:502-504.
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    April 2022
  214. TANIGUCHI T, Nakayama S, Tanaka H, Rai S, et al
    Novel prognostic predictor of haemoglobin-platelet index in diffuse large B-cell lymphoma, not otherwise specified: Anaemia and thrombocytopenia are associated with IL-6 production in lymphoma cells.
    Br J Haematol. 2022 Apr 22. doi: 10.1111/bjh.18208.
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  215. SUN Y, Habara A, Le CQ, Nguyen N, et al
    Pharmacologic induction of PGC-1alpha stimulates fetal haemoglobin gene expression.
    Br J Haematol. 2022;197:97-109.
    >> Share

  216. RIEU JB, Largeaud L, Da Costa L, Cougoul P, et al
    Unexplained iron overload with haemolytic anaemia should prompt looking for morphological changes in erythroid precursors.
    Br J Haematol. 2022;197:132.
    >> Share

  217. ROSS DM
    Iron chelation for myelofibrosis-related anaemia during treatment with a Janus kinase inhibitor.
    Br J Haematol. 2022;197:135-136.
    >> Share

  218. GARG M, Agarwal S, Altohami M
    A single dose of eculizumab terminated life-threatening haemolysis in idiopathic IgM-mediated warm autoimmune haemolytic anaemia: A case report.
    Br J Haematol. 2022;197:e28-e31.
    >> Share

  219. BATISTA THC, Santana RM, Sobreira MJ, Arcanjo GS, et al
    Up-regulation of miR-130a is related to leg ulcers in sickle cell anaemia.
    Br J Haematol. 2022;197:e16-e18.
    >> Share

  220. TORRES LS, Teles LIM, Shaul ME, Fridlender ZG, et al
    Accelerated low-density neutrophil transition in sickle cell anaemia may contribute to disease pathophysiology.
    Br J Haematol. 2022;197:232-235.
    >> Share

    March 2022
  221. MIODOWNIK H, Curtis SA, Olivia Ogu U, Bradford C, et al
    Frequent health care utilisation and avascular necrosis are associated with cannabis use in adults with sickle cell disease.
    Br J Haematol. 2022;196:e41-e44.
    >> Share

  222. CECCHI N, Giannotta JA, Barcellini W, Fattizzo B, et al
    A case of severe aplastic anaemia after SARS-CoV-2 vaccination.
    Br J Haematol. 2022;196:1334-1336.
    >> Share

  223. CONSTANTINOU V, Papayanni PG, Mallouri D, Batsis I, et al
    Case study of betibeglogene autotemcel gene therapy in an adult Greek patient with transfusion-dependent beta-thalassaemia of a severe genotype.
    Br J Haematol. 2022;196:1401-1404.
    >> Share

  224. CHARNAY T, Cerino M, Gonnet K, Bonello-Palot N, et al
    A novel SUPT5H variant associated with a beta-thalassaemia trait.
    Br J Haematol. 2022;196:e70-e71.
    >> Share

  225. TAMURA S, Hori Y, Hiroi T, Morimoto M, et al
    Pegcetacoplan for refractory paroxysmal nocturnal haemoglobinuria associated with the C5 genetic variant.
    Br J Haematol. 2022;196:e57-e60.
    >> Share

    February 2022
  226. RUND D
    Laboratory diagnosis of iron deficiency: look out for the 'PITTs'.
    Br J Haematol. 2022;196:464-465.
    >> Share

  227. XU LP, Yu Y, Cheng YF, Zhang YY, et al
    Development and validation of a mortality predicting scoring system for severe aplastic anaemia patients receiving haploidentical allogeneic transplantation.
    Br J Haematol. 2022;196:735-742.
    >> Share

  228. FLETCHER A, Forbes A, Svenson N, Wayne Thomas D, et al
    Guideline for the laboratory diagnosis of iron deficiency in adults (excluding pregnancy) and children.
    Br J Haematol. 2022;196:523-529.
    >> Share

  229. POPLAWSKA M, Dutta D, Jayaram M, Salifu M, et al
    Intestinal pathophysiological abnormalities in steady state and after vaso-occlusive crisis in murine sickle cell disease.
    Br J Haematol. 2022;196:777-780.
    >> Share

  230. GERRITSMA J, Bongaerts V, Eckhardt C, Heijboer H, et al
    Extended phenotyping does not preclude the occurrence of delayed haemolytic transfusion reactions in sickle cell disease.
    Br J Haematol. 2022;196:769-776.
    >> Share

  231. BARADE A, Aboobacker F, Korula A, Lakshmi K, et al
    Impact of donor telomere length on survival in patients undergoing matched sibling donor transplantation for aplastic anaemia.
    Br J Haematol. 2022;196:724-734.
    >> Share

  232. MAGGIO A
    Cell erythroid maturation approach: a new paradigm in the road map towards a cure for beta-thalassaemia syndromes.
    Br J Haematol. 2022;196:806-808.
    >> Share

  233. OAKLEY LL, Mitchell S, von Rege I, Hadebe R, et al
    Perinatal outcomes in women with sickle cell disease: a matched cohort study from London, UK.
    Br J Haematol. 2022;196:1069-1075.
    >> Share

  234. VLACHODIMITROPOULOU E, Garbowski M, Anne Solomon S, Abbasi N, et al
    Outcome predictors for maternal red blood cell alloimmunisation with anti-K and anti-D managed with intrauterine blood transfusion.
    Br J Haematol. 2022;196:1096-1104.
    >> Share

  235. JONASSAINT CR, Lukombo I, Feldman R, Driscoll J, et al
    Differences in the prevalence of mental health disorders among Black American adults with sickle cell disease compared to those with non-heritable medical conditions or no medical conditions.
    Br J Haematol. 2022;196:1059-1068.
    >> Share

  236. WHITE J, Callaghan MU, Gao X, Liu K, et al
    Longitudinal assessment of adhesion to vascular cell adhesion molecule-1 at steady state and during vaso-occlusive crises in sickle cell disease.
    Br J Haematol. 2022;196:1052-1058.
    >> Share

  237. TANEJA K, Verma C, Mahajan A
    Can ruxolitinib avert splenectomy in patients with thalassaemia: a short term case series.
    Br J Haematol. 2022;196:1111-1113.
    >> Share

  238. VENUGOPAL J, Wang J, Guo C, Eitzman DT, et al
    Interleukin-1 receptor antagonism leads to improved anaemia in a murine model of sickle cell disease and is associated with reduced ex vivo platelet-mediated erythrocyte sickling.
    Br J Haematol. 2022;196:1040-1051.
    >> Share

    January 2022
  239. NAVILLE AS, Lazaro E, Boutin J, Prot-Leurent C, et al
    Acquired glucose 6-phosphate dehydrogenase (G6PD) deficiency in a patient with Chronic Myelomonocytic Leukemia.
    Br J Haematol. 2022 Jan 6. doi: 10.1111/bjh.18037.
    >> Share

  240. BRODSKY RA, Lee JW, Nishimura JI, Szer J, et al
    Lactate dehydrogenase versus haemoglobin: which one is the better marker in paroxysmal nocturnal haemoglobinuria?
    Br J Haematol. 2022;196:264-265.
    >> Share

  241. RUND D
    A Paradigm shift in genotype-phenotype relationships in beta-thalassaemia.
    Br J Haematol. 2022;196:270-271.
    >> Share

  242. ROY NBA
    Iron overload in inherited anaemias: why one size can't fit all.
    Br J Haematol. 2022;196:266-267.
    >> Share

  243. SMITH WR, McClish DK, Lottenberg R, Sisler IY, et al
    A randomised controlled provider-blinded trial of community health workers in sickle cell anaemia: effects on haematologic variables and hydroxyurea adherence.
    Br J Haematol. 2022;196:193-203.
    >> Share

  244. CHAPIN J, Cohen AR, Neufeld EJ, Vichinsky E, et al
    An update on the US adult thalassaemia population: a report from the CDC thalassaemia treatment centres.
    Br J Haematol. 2022;196:380-389.
    >> Share

  245. MUSALLAM KM, Vitrano A, Meloni A, Addario Pollina S, et al
    Primary HBB gene mutation severity and long-term outcomes in a global cohort of beta-thalassaemia.
    Br J Haematol. 2022;196:414-423.
    >> Share

  246. SHAH FT, Porter JB, Sadasivam N, Kaya B, et al
    Guidelines for the monitoring and management of iron overload in patients with haemoglobinopathies and rare anaemias.
    Br J Haematol. 2022;196:336-350.
    >> Share

  247. CHEN N, Li Z, Huang Y, Xiao C, et al
    Iron parameters in pregnant women with beta-thalassaemia minor combined with iron deficiency anaemia compared to pregnant women with iron deficiency anaemia alone demonstrate the safety of iron supplementation in beta-thalassaemia minor during pregnan
    Br J Haematol. 2022;196:390-396.
    >> Share

  248. KIENZLE SL, Rodeghier M, Liem RI
    Heart rate variability associated with acute exercise challenge in children with sickle cell anaemia.
    Br J Haematol. 2022;196:397-401.
    >> Share

  249. ADEBAYO OC, Betukumesu DK, Nkoy AB, Adesoji OM, et al
    Clinical and genetic factors are associated with kidney complications in African children with sickle cell anaemia.
    Br J Haematol. 2022;196:204-214.
    >> Share

  250. GRIFFIN R, Panayiotou A, Allen P, Height S, et al
    What is the role of chest X-ray imaging in the acute management of children with sickle cell disease?
    Br J Haematol. 2022;196:402-413.
    >> Share

  251. COLMAN KS, Pavord S, Roy N
    A quality improvement project for the cost-effective management of maternal anaemia.
    Br J Haematol. 2022;196:445-448.
    >> Share

  252. VASSEUR C, Domingues-Hamdi E, Pakdaman S, Galacteros F, et al
    Alpha haemoglobin-stabilising protein concentration in the red blood cells of patients with sickle cell anaemia with and without hydroxycarbamide treatment.
    Br J Haematol. 2022;196:183-192.
    >> Share

  253. RISITANO AM, Peffault de Latour R
    How we('ll) treat paroxysmal nocturnal haemoglobinuria: diving into the future.
    Br J Haematol. 2022;196:288-303.
    >> Share

  254. DEXTER D, McGann PT
    Saving lives through early diagnosis: the promise and role of point of care testing for sickle cell disease.
    Br J Haematol. 2022;196:63-69.
    >> Share

  255. MANABE M, Hagiwara Y, Asada R, Tanizawa N, et al
    Acquired elliptocytosis in a patient with myelodysplastic syndrome harbouring a novel unbalanced whole-arm translocation, der(14;20)(q10;p10).
    Br J Haematol. 2022;196:7.
    >> Share

  256. BARRITEAU CM, Chiu A, Rodeghier M, Liem RI, et al
    Cerebral and skeletal muscle tissue oxygenation during exercise challenge in children and young adults with sickle cell anaemia.
    Br J Haematol. 2022;196:179-182.
    >> Share

  257. HUGHES AD, Kurre P
    The impact of clonal diversity and mosaicism on haematopoietic function in Fanconi anaemia.
    Br J Haematol. 2022;196:274-287.
    >> Share

  258. GABELLI M, Ademokun C, Cooper N, Amrolia PI, et al
    Pathogenesis, risk factors and therapeutic options for autoimmune haemolytic anaemia in the post-transplant setting.
    Br J Haematol. 2022;196:45-62.
    >> Share

    December 2021
  259. AOUN SA, Motabi I
    Cold agglutinin disease after COVID-19 vaccine.
    Br J Haematol. 2021;195:650.
    >> Share

  260. LIN J, Ye Y, Shang X, Zhang Y, et al
    TEA domain transcription factor 4 modulates repression of fetal haemoglobin by direct binding to the gamma-globin gene promoters.
    Br J Haematol. 2021;195:764-769.
    >> Share

  261. NAKAGAWA N, Ishiyama K, Tanabe M, Yoroidaka T, et al
    The effectiveness of immunosuppressive therapy in patients with aplastic anaemia secondary to chemoradiotherapy for cancers.
    Br J Haematol. 2021;195:770-780.
    >> Share

  262. BADAWY SM, Payne AB, Hulihan MM, Coates TD, et al
    Concordance with comprehensive iron assessment, hepatitis A vaccination, and hepatitis B vaccination recommendations among patients with sickle cell disease and thalassaemia receiving chronic transfusions: an analysis from the Centers for Disease Cont
    Br J Haematol. 2021;195:e160-e164.
    >> Share

  263. WILSON SR, Sears M, Williams E, Drapekin J, et al
    Gaps in the diagnosis and management of iron overload in sickle cell disease: a 'real-world' report from the GRNDaD registry.
    Br J Haematol. 2021;195:e157-e160.
    >> Share

    November 2021
  264. HALL R, Meenan J, Mihalca D, Katumba A, et al
    The real impact of COVID-19 on an East London Sickle cell population: results of a service-wide survey.
    Br J Haematol. 2021;195:532-535.
    >> Share

  265. LILES DK, Shah NR, Scullin B, Gordeuk VR, et al
    Long-term biological effects in sickle cell disease: insights from a post-crizanlizumab study.
    Br J Haematol. 2021;195:e150-e153.
    >> Share

  266. EL-AMIN N, Lauzon SD, Nietert PJ, Kanter J, et al
    Which adults with sickle cell disease need an evaluation for pulmonary embolism?
    Br J Haematol. 2021;195:447-455.
    >> Share

  267. WANG W, Freeman M, Hamilton L, Carroll Y, et al
    Developmental screening of three-year-old children with sickle cell disease compared to controls.
    Br J Haematol. 2021;195:621-628.
    >> Share

  268. BOISSON C, Renoux C, Nader E, Gauthier A, et al
    Comparisons of oxygen gradient ektacytometry parameters between sickle cell patients with or without alpha-thalassaemia.
    Br J Haematol. 2021;195:629-633.
    >> Share

  269. LAFAURIE M, Maquet J, Baricault B, Ekstrand C, et al
    Risk factors of hospitalisation for thrombosis in adults with primary immune thrombocytopenia, including disease-specific treatments: a French nationwide cohort study.
    Br J Haematol. 2021;195:456-465.
    >> Share

  270. RANKINE-MULLINGS A, Reid M, Soares D, Taylor-Bryan C, et al
    Hydroxycarbamide treatment reduces transcranial Doppler velocity in the absence of transfusion support in children with sickle cell anaemia, elevated transcranial Doppler velocity, and cerebral vasculopathy: the EXTEND trial.
    Br J Haematol. 2021;195:612-620.
    >> Share

  271. BALLAS SK, Kuypers FA, Gordeuk VR, Hankins JS, et al
    Time to rethink haemoglobin threshold guidelines in sickle cell disease.
    Br J Haematol. 2021;195:518-522.
    >> Share

    October 2021
  272. HE Z, Sun X, Wang S, Bai D, et al
    Ggct (gamma-glutamyl cyclotransferase) plays an important role in erythrocyte antioxidant defense and red blood cell survival.
    Br J Haematol. 2021;195:267-275.
    >> Share

  273. KARKOSKA K
    Neuroprotection: further evidence for the early and universal use of hydroxyurea in children with sickle cell disease.
    Br J Haematol. 2021;195:158-159.
    >> Share

  274. CAPPELLI B, Scigliuolo GM, Boukouaci W, Rafii H, et al
    Impact of the human leucocyte antigen (HLA)-B leader peptide dimorphism and HLA-A expression on outcomes of stem cell transplantation for sickle cell disease.
    Br J Haematol. 2021;195:e128-e131.
    >> Share

  275. HEITZER AM, Longoria J, Okhomina V, Wang WC, et al
    Hydroxyurea treatment and neurocognitive functioning in sickle cell disease from school age to young adulthood.
    Br J Haematol. 2021;195:256-266.
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  276. DEREBAIL VK, Zhou Q, Ciccone EJ, Cai J, et al
    Longitudinal study of glomerular hyperfiltration and normalization of estimated glomerular filtration in adults with sickle cell disease.
    Br J Haematol. 2021;195:123-132.
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    September 2021
  277. MASLAH N, Ravdan O, Drevon L, Verger E, et al
    Revisiting Diagnostic performances of serum erythropoietin level and JAK2 mutation for polycythemias: analysis of a cohort of 1090 patients with red cell mass measurement.
    Br J Haematol. 2021 Sep 25. doi: 10.1111/bjh.17848.
    >> Share

  278. BARCELLINI W, Fattizzo B, Giannotta JA, Quattrocchi L, et al
    COVID-19 in patients with paroxysmal nocturnal haemoglobinuria: an Italian multicentre survey.
    Br J Haematol. 2021;194:854-856.
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  279. MUNARETTO V, Voi V, Palazzi G, Notarangelo LD, et al
    Acute events in children with sickle cell disease in Italy during the COVID-19 pandemic: useful lessons learned.
    Br J Haematol. 2021;194:851-854.
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  280. HINES PC, Callaghan MU, Zaidi AU, Gao X, et al
    Flow adhesion of whole blood to P-selectin: a prognostic biomarker for vaso-occlusive crisis in sickle cell disease.
    Br J Haematol. 2021;194:1074-1082.
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  281. OTENG-NTIM E, Pavord S, Howard R, Robinson S, et al
    Management of sickle cell disease in pregnancy. A British Society for Haematology Guideline.
    Br J Haematol. 2021;194:980-995.
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  282. STRATTON P
    Standardizing care of those at great risk: the importance of sickle cell in pregnancy practice guidelines.
    Br J Haematol. 2021;194:950-953.
    >> Share

  283. GAARTMAN AE, Sayedi AK, Gerritsma JJ, de Back TR, et al
    Fluid overload due to intravenous fluid therapy for vaso-occlusive crisis in sickle cell disease: incidence and risk factors.
    Br J Haematol. 2021;194:899-907.
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  284. PECKER LH, Sharma D, Nero A, Paidas MJ, et al
    Knowledge gaps in reproductive and sexual health in girls and women with sickle cell disease.
    Br J Haematol. 2021;194:970-979.
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  285. RIEGER MJ, Stolz SM, Ludwig S, Benoit TM, et al
    Daratumumab in rituximab-refractory autoimmune haemolytic anaemia.
    Br J Haematol. 2021;194:931-934.
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  286. BOUDHABHAY I, Boutin E, Bartolucci P, Bornes MI, et al
    Impact of pre-eclampsia on renal outcome in sickle cell disease patients.
    Br J Haematol. 2021;194:1053-1062.
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  287. MALINOWSKI AK, Kuo KHM, Tomlinson GA, Palcu P, et al
    Distinct maternal and fetal pregnancy outcomes in women with sickle cell disease can be predicted using routine clinical and laboratory data.
    Br J Haematol. 2021;194:1063-1073.
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  288. SARAF SL
    The vasculopathic cord between pre-eclampsia and kidney function in sickle cell disease.
    Br J Haematol. 2021;194:947-949.
    >> Share

  289. KUMKHAEK C, Uchida N, Tisdale JF, Rodgers GP, et al
    Comparison of CD34(+) cells isolated from frozen cord blood and fresh adult peripheral blood of sickle cell disease patients in gene correction of the sickle mutation at late-stage erythroid differentiation.
    Br J Haematol. 2021;194:e80-e84.
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  290. GOTTGENS EL, Ligthart PC, Veldhuisen B, Veldthuis M, et al
    Rh-null phenotype and stomatocytosis.
    Br J Haematol. 2021;194:803.
    >> Share

  291. SCHEINBERG P
    Acquired severe aplastic anaemia: how medical therapy evolved in the 20th and 21st centuries.
    Br J Haematol. 2021;194:954-969.
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    August 2021
  292. NJOKU F, Zhang X, Shah BN, Machado RF, et al
    Biomarkers of clinical severity in treated and untreated sickle cell disease: a comparison by genotypes of a single center cohort and African Americans in the NHANES study.
    Br J Haematol. 2021;194:767-778.
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  293. ELSHERIF L, Scott LC, Wichlan D, Jones SK, et al
    Hydroxyurea therapy decreases coagulation and endothelial activation in sickle cell disease: a Longitudinal Study.
    Br J Haematol. 2021;194:e71-e73.
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  294. QUINN CT, Niss O, Dong M, Pfeiffer A, et al
    Early initiation of hydroxyurea (hydroxycarbamide) using individualised, pharmacokinetics-guided dosing can produce sustained and nearly pancellular expression of fetal haemoglobin in children with sickle cell anaemia.
    Br J Haematol. 2021;194:617-625.
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  295. TANGSRICHAROEN T, Natesirinilkul R, Phusua A, Fanhchaksai K, et al
    Severe neonatal haemolytic anaemia caused by compound heterozygous KLF1 mutations: report of four families and literature review.
    Br J Haematol. 2021;194:626-634.
    >> Share

    July 2021
  296. FATTIZZO B, Rizzo L, Giannotta JA, Mazzon F, et al
    Switching to an alternative recombinant erythropoietin agent in patients with myelodysplastic syndromes: a second honeymoon?
    Br J Haematol. 2021 Jul 26. doi: 10.1111/bjh.17722.
    >> Share

  297. KILLICK SB, Ingram W, Culligan D, Enright H, et al
    British Society for Haematology guidelines for the management of adult myelodysplastic syndromes.
    Br J Haematol. 2021;194:267-281.
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  298. MITTELMAN M, Oster HS
    Thrombocytopenia in myelodysplastic syndromes: time to lift the embargo on thrombomimetics?
    Br J Haematol. 2021;194:231-233.
    >> Share

  299. RASHKIN SR, Rampersaud E, Kang G, Ataga KI, et al
    Generalization of a genetic risk score for time to first albuminuria in children with sickle cell anaemia: SCCRIP cohort study results.
    Br J Haematol. 2021;194:469-473.
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  300. ESTEPP JH, Cong Z, Agodoa I, Kang G, et al
    What drives transcranial Doppler velocity improvement in paediatric sickle cell anaemia: analysis from the Sickle Cell Clinical Research and Intervention Program (SCCRIP) longitudinal cohort study.
    Br J Haematol. 2021;194:463-468.
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  301. ALNAFIE AN, Alateeq SA, Al-Muhanna FA, Alsulaiman AM, et al
    Exome sequencing in high and low fetal haemoglobin Arab-Indian haplotype sickle cell disease.
    Br J Haematol. 2021;194:e61-e64.
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  302. PERES L, Monedero Alonso D, Nudel M, Figeac M, et al
    Characterisation of Asp669Tyr Piezo1 cation channel activity in red blood cells: an unexpected phenotype.
    Br J Haematol. 2021;194:e51-e55.
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  303. VADOLAS J, Ng GZ, Kysenius K, Crouch PJ, et al
    SLN124, a GalNac-siRNA targeting transmembrane serine protease 6, in combination with deferiprone therapy reduces ineffective erythropoiesis and hepatic iron-overload in a mouse model of beta-thalassaemia.
    Br J Haematol. 2021;194:200-210.
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  304. TAHER AT, Viprakasit V, Cappellini MD, Kraus D, et al
    Haematological effects of oral administration of bitopertin, a glycine transport inhibitor, in patients with non-transfusion-dependent beta-thalassaemia.
    Br J Haematol. 2021;194:474-477.
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  305. WICKRAMASINGHE W, Dissanayake R, Raj R, Gooneratne L, et al
    The first report of allogeneic haematopoietic stem cell transplantations for bone marrow failure performed in Sri Lanka.
    Br J Haematol. 2021;194:e56-e58.
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  306. TAMAGNE M, Pakdaman S, Bartolucci P, Habibi A, et al
    Whole-blood CCR7 expression and chemoattraction in red blood cell alloimmunization.
    Br J Haematol. 2021;194:477-481.
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  307. RIEU JB, El Kassir A, Largeaud L, Dion J, et al
    Characteristic vacuolisation of granulocytic and erythroid precursors associated with VEXAS syndrome.
    Br J Haematol. 2021;194:8.
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  308. WARE RE, Dertinger SD
    Absence of hydroxyurea-induced mutational effects supports higher utilisation for the treatment of sickle cell anaemia.
    Br J Haematol. 2021;194:252-266.
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  309. PACE BS, Starlard-Davenport A, Kutlar A
    Sickle cell disease: progress towards combination drug therapy.
    Br J Haematol. 2021;194:240-251.
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    June 2021
  310. PATON C, Mathews L, Groarke EM, Rios O, et al
    COVID-19 infection in patients with severe aplastic anaemia.
    Br J Haematol. 2021;193:902-905.
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  311. HANDS K, Taylor C, Kotze A, Richards T, et al
    Preoperative patient blood management during the SARS-CoV-2 pandemic.
    Br J Haematol. 2021;193:1087-1092.
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  312. STEINBERG MH
    HbA2 induction: the merit of pancellularity in sickle cell disease.
    Br J Haematol. 2021;193:1032-1033.
    >> Share

  313. HILLS RK
    Diagnosing Diamond-Blackfan anaemia: 'Vorsprung durch Technik'.
    Br J Haematol. 2021;193:1030-1031.
    >> Share

  314. BLAISE D, Savani BN
    Alternative donor transplantation for severe aplastic anaemia in 2021: haplo donor, cord blood or both?
    Br J Haematol. 2021;193:863-864.
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  315. PORCU S, Simbula M, Marongiu MF, Perra A, et al
    Delta-globin gene expression improves sickle cell disease in a humanised mouse model.
    Br J Haematol. 2021;193:1228-1237.
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  316. VAN DOOIJEWEERT B, Broeks MH, van Beers EJ, Verhoeven-Duif NM, et al
    Dried blood spot metabolomics reveals a metabolic fingerprint with diagnostic potential for Diamond Blackfan Anaemia.
    Br J Haematol. 2021;193:1185-1193.
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  317. LIANG Y, Zhang X, Liu Y, Wang L, et al
    GATA zinc finger domain-containing protein 2A (GATAD2A) deficiency reactivates fetal haemoglobin in patients with beta-thalassaemia through impaired formation of methyl-binding domain protein 2 (MBD2)-containing nucleosome remodelling and deacetylatio
    Br J Haematol. 2021;193:1220-1227.
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  318. CHILDS RW, Tian X, Vo P, Purev E, et al
    Combined haploidentical and cord blood transplantation for refractory severe aplastic anaemia and hypoplastic myelodysplastic syndrome.
    Br J Haematol. 2021;193:951-960.
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  319. MAITLAND K, Kiguli S, Olupot-Olupot P, Opoka RO, et al
    Transfusion management of severe anaemia in African children: a consensus algorithm.
    Br J Haematol. 2021;193:1247-1259.
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  320. LAAS C, Lambert C, Senior McKenzie T, Sheldon E, et al
    Improving the laboratory diagnosis of pyruvate kinase deficiency.
    Br J Haematol. 2021;193:994-1000.
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  321. JANG T, Mo G, Stewart C, Egini O, et al
    Antibiotic use in adults during sickle cell vaso-occlusive crisis: Is it time for a controlled trial?
    Br J Haematol. 2021;193:1281-1283.
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  322. MARTINO S, Arlet JB, Odievre MH, Jullien V, et al
    Deficient mitophagy pathways in sickle cell disease.
    Br J Haematol. 2021;193:988-993.
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  323. XU Y, Alfaro-Magallanes VM, Babitt JL
    Physiological and pathophysiological mechanisms of hepcidin regulation: clinical implications for iron disorders.
    Br J Haematol. 2021;193:882-893.
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  324. JUNG M, Mehta PA, Jiang CS, Rosti RO, et al
    Comparison of the clinical phenotype and haematological course of siblings with Fanconi anaemia.
    Br J Haematol. 2021;193:971-975.
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    May 2021
  325. UYOGA S, George EC, Bates I, Olupot-Olupot P, et al
    Point-of-care haemoglobin testing in African hospitals: a neglected essential diagnostic test.
    Br J Haematol. 2021 May 15. doi: 10.1111/bjh.17431.
    >> Share

  326. BARCELLINI W, Colombatti R
    The impact of Parvovirus B19 on hereditary haemolytic anaemias.
    Br J Haematol. 2021;193:703-704.
    >> Share

  327. BOOTH GS, Savani BN, Langston AA
    Pure red blood cell aplasia: patient management pitfalls in major ABO-incompatible haematopoietic cell transplantation.
    Br J Haematol. 2021;193:701-702.
    >> Share

  328. ELBADRY MI, Khaled SAA, Ahmed NM, Abudeif A, et al
    Acute human parvovirus B19 infection triggers immune-mediated transient bone marrow failure syndrome, extreme direct hyperbilirubinaemia and acute hepatitis in patients with hereditary haemolytic anaemias: multicentre prospective pathophysiological st
    Br J Haematol. 2021;193:827-840.
    >> Share

  329. LONGVAL T, Galimard JE, Lepretre AC, Suarez F, et al
    Treatment for pure red cell aplasia after major ABO-incompatible allogeneic stem cell transplantation: a multicentre study.
    Br J Haematol. 2021;193:814-826.
    >> Share

  330. VINCHI F, Sparla R, Passos ST, Sharma R, et al
    Vasculo-toxic and pro-inflammatory action of unbound haemoglobin, haem and iron in transfusion-dependent patients with haemolytic anaemias.
    Br J Haematol. 2021;193:637-658.
    >> Share

  331. RUND D
    Intravenous iron: do we adequately understand the short- and long-term risks in clinical practice?
    Br J Haematol. 2021;193:466-480.
    >> Share

  332. SARAF SL, Zhang X, Shah BN, Raslan R, et al
    Engulfment and cell motility 1 (ELMO1) and apolipoprotein A1 (APOA1) as candidate genes for sickle cell nephropathy.
    Br J Haematol. 2021;193:628-632.
    >> Share

  333. DENTON CC, Detterich JA, Coates TD, Wood JC, et al
    Kidney iron deposition by R2* is associated with haemolysis and urinary iron.
    Br J Haematol. 2021;193:633-636.
    >> Share

    April 2021
  334. BERNARD F, Uppungunduri CRS, Meyer S, Cummins M, et al
    Excellent overall and chronic graft-versus-host-disease-free event-free survival in Fanconi anaemia patients undergoing matched related- and unrelated-donor bone marrow transplantation using alemtuzumab-Flu-Cy: the UK experience.
    Br J Haematol. 2021 Apr 14. doi: 10.1111/bjh.17418.
    >> Share

  335. CALABRETTA E, Moraleda JM, Iacobelli M, Jara R, et al
    COVID-19-induced endotheliitis: emerging evidence and possible therapeutic strategies.
    Br J Haematol. 2021;193:43-51.
    >> Share

  336. BENNETT R, Ruskova A
    Atezolizumab-induced pure red cell aplasia.
    Br J Haematol. 2021;193:10.
    >> Share

  337. LADU AI, Aiyenigba AO, Adekile A, Bates I, et al
    The spectrum of splenic complications in patients with sickle cell disease in Africa: a systematic review.
    Br J Haematol. 2021;193:26-42.
    >> Share

  338. SHAFIEE S, Gelebart P, Popa M, Hellesoy M, et al
    Preclinical characterisation and development of a novel myelodysplastic syndrome-derived cell line.
    Br J Haematol. 2021;193:415-419.
    >> Share

  339. CHENG Y, Shang X, Chen D, Pang D, et al
    MicroRNA-2355-5p regulates gamma-globin expression in human erythroid cells by inhibiting KLF6.
    Br J Haematol. 2021;193:401-405.
    >> Share

  340. QUINTINO DE OLIVEIRA B, Catto LFB, Santana BAA, Tellechea MF, et al
    Eltrombopag preferentially expands haematopoietic multipotent progenitors in human aplastic anaemia.
    Br J Haematol. 2021;193:410-414.
    >> Share

    March 2021
  341. SAULSBERRY-ABATE AC, Partanen M, Porter JS, Podila PSB, et al
    Cognitive performance as a predictor of healthcare transition in sickle cell disease.
    Br J Haematol. 2021;192:1082-1091.
    >> Share

  342. AL-SAMKARI H, Addonizio K, Glader B, Morton DH, et al
    The pyruvate kinase (PK) to hexokinase enzyme activity ratio and erythrocyte PK protein level in the diagnosis and phenotype of PK deficiency.
    Br J Haematol. 2021;192:1092-1096.
    >> Share

  343. EGOT M, Lasne D, Poirault-Chassac S, Mirault T, et al
    Role of oculocerebrorenal syndrome of Lowe (OCRL) protein in megakaryocyte maturation, platelet production and functions: a study in patients with Lowe syndrome.
    Br J Haematol. 2021;192:909-921.
    >> Share

  344. ATAGA KI, Staffa SJ, Brugnara C, Stocker JW, et al
    Haemoglobin response to senicapoc in patients with sickle cell disease: a re-analysis of the Phase III trial.
    Br J Haematol. 2021;192:e129-e132.
    >> Share

  345. OIKONOMOPOULOU C, Paisiou A, Komitopoulou A, Ioannidou ED, et al
    Increased incidence of autoimmune cytopenias after allogeneic haematopoietic stem cell transplantation using a matched unrelated donor in children with beta-thalassaemia.
    Br J Haematol. 2021;192:e127-e129.
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  346. SACHDEV V, Tian X, Gu Y, Nichols J, et al
    A phenotypic risk score for predicting mortality in sickle cell disease.
    Br J Haematol. 2021;192:932-941.
    >> Share

  347. RIBEIRO PR, Teixeira RDS, Souza AR, Pereira TCS, et al
    Blood plasma metabolomics of children and adolescents with sickle cell anaemia treated with hydroxycarbamide: a new tool for uncovering biochemical alterations.
    Br J Haematol. 2021;192:922-931.
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    February 2021
  348. CAIRO MS, Savani BN
    Haematopoietic progenitor cell transplantation in adults with symptomatic sickle cell disease: the time has arrived.
    Br J Haematol. 2021;192:678-680.
    >> Share

  349. OLSON TS
    Paediatric severe aplastic anaemia treatment: where to start?
    Br J Haematol. 2021;192:417-419.
    >> Share

  350. ALZAHRANI M, Damlaj M, Jeffries N, Alahmari B, et al
    Non-myeloablative human leukocyte antigen-matched related donor transplantation in sickle cell disease: outcomes from three independent centres.
    Br J Haematol. 2021;192:761-768.
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  351. YUAN S, Jordan LC, Davis LT, Cogswell PM, et al
    A cross-sectional, case-control study of intracranial arterial wall thickness and complete blood count measures in sickle cell disease.
    Br J Haematol. 2021;192:769-777.
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  352. GROARKE EM, Patel BA, Gutierrez-Rodrigues F, Rios O, et al
    Eltrombopag added to immunosuppression for children with treatment-naive severe aplastic anaemia.
    Br J Haematol. 2021;192:605-614.
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  353. HOTINSKI AK, Best OG, Thurgood LA, Lower KM, et al
    A biclonal case of chronic lymphocytic leukaemia with discordant mutational status of the immunoglobulin heavy chain variable region and bimodal CD49d expression.
    Br J Haematol. 2021;192:e77-e81.
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  354. DEMBELE AK, Lapoumeroulie C, Diaw M, Tessougue O, et al
    Cell-derived microparticles and sickle cell disease chronic vasculopathy in sub-Saharan Africa: A multinational study.
    Br J Haematol. 2021;192:634-642.
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  355. VITRANO A, Meloni A, Addario Pollina W, Karimi M, et al
    A complication risk score to evaluate clinical severity of thalassaemia syndromes.
    Br J Haematol. 2021;192:626-633.
    >> Share

  356. CASTLEMAN JS, Moise KJ Jr, Kilby MD
    Medical therapy to attenuate fetal anaemia in severe maternal red cell alloimmunisation.
    Br J Haematol. 2021;192:425-432.
    >> Share

    January 2021
  357. KULASEKARARAJ AG, Marsh JCW
    Romiplostim in aplastic anaemia - another tool in the armamentarium.
    Br J Haematol. 2021;192:15-16.
    >> Share

  358. MINGOIA M, Caria CA, Ye L, Asunis I, et al
    Induction of therapeutic levels of HbF in genome-edited primary beta(0) 39-thalassaemia haematopoietic stem and progenitor cells.
    Br J Haematol. 2021;192:395-404.
    >> Share


  359. Developing the evidence base for the management of autoimmune haemolytic anaemia (AIHA): the UK experience.
    Br J Haematol. 2021;192:e54-e57.
    >> Share

  360. SHARMA POUDYAL B, Gyawali B, Rondelli D
    The need for locally generated data in haematology: a real-world experience of aplastic anaemia in Nepal.
    Br J Haematol. 2021;192:e63-e65.
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  361. GREGOIRE-PELCHAT P, Pastore Y, Robitaille N, LeMay S, et al
    Comparison of two vitamin D supplementation strategies in children with sickle cell disease: a randomized controlled trial.
    Br J Haematol. 2021;192:385-394.
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  362. PATEL A, Gan K, Li AA, Weiss J, et al
    Machine-learning algorithms for predicting hospital re-admissions in sickle cell disease.
    Br J Haematol. 2021;192:158-170.
    >> Share

  363. JANG JH, Tomiyama Y, Miyazaki K, Nagafuji K, et al
    Efficacy and safety of romiplostim in refractory aplastic anaemia: a Phase II/III, multicentre, open-label study.
    Br J Haematol. 2021;192:190-199.
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  364. CHAN LKL, Mak VWM, Chan SCH, Yu ELM, et al
    Liver complications of haemoglobin H disease in adults.
    Br J Haematol. 2021;192:171-178.
    >> Share

  365. MTENGA J, Orf K, Zheng J, Chamba C, et al
    Haematopoietic stem cell transplantation in Tanzania.
    Br J Haematol. 2021;192:17-21.
    >> Share

  366. SPEICH C, Wegmuller R, Brittenham GM, Zeder C, et al
    Measurement of long-term iron absorption and loss during iron supplementation using a stable isotope of iron ((57) Fe).
    Br J Haematol. 2021;192:179-189.
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  367. MANARA R, Dalla Torre A, Lucchetta M, Ermani M, et al
    Visual cortex changes in children with sickle cell disease and normal visual acuity: a multimodal magnetic resonance imaging study.
    Br J Haematol. 2021;192:151-157.
    >> Share

    December 2020
  368. RUND D
    The evolution of clinical research in thalassaemia: where has all the funding gone?
    Br J Haematol. 2020;191:666-667.
    >> Share

  369. JOBANPUTRA M, Paramore C, Laird SG, McGahan M, et al
    Co-morbidities and mortality associated with transfusion-dependent beta-thalassaemia in patients in England: a 10-year retrospective cohort analysis.
    Br J Haematol. 2020;191:897-905.
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  370. URIO F, Nkya S, Rooks H, Mgaya JA, et al
    F cell numbers are associated with an X-linked genetic polymorphism and correlate with haematological parameters in patients with sickle cell disease.
    Br J Haematol. 2020;191:888-896.
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  371. FORTE S, Eng B, Verhovsek M, Soulieres D, et al
    Microcytosis in patients with haemoglobin C trait: is alpha-thalassaemia trait to blame?
    Br J Haematol. 2020;191:e129-e131.
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  372. TANG D, Liu S, Sun H, Qin X, et al
    All-trans-retinoic acid shifts Th1 towards Th2 cell differentiation by targeting NFAT1 signalling to ameliorate immune-mediated aplastic anaemia.
    Br J Haematol. 2020;191:906-919.
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  373. PECKER LH, Hussain S, Christianson MS, Lanzkron S, et al
    Hydroxycarbamide exposure and ovarian reserve in women with sickle cell disease in the Multicenter Study of Hydroxycarbamide.
    Br J Haematol. 2020;191:880-887.
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  374. VALI S, Mukhtar S, Nandi A, Wilson K, et al
    Cumulative outcome of pre-implantation genetic diagnosis for sickle cell disease: a 5-year review.
    Br J Haematol. 2020;191:875-879.
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    November 2020
  375. VERLHAC S, Gabor F, Paillard C, Chateil JF, et al
    Improved stenosis outcome in stroke-free sickle cell anemia children after transplantation compared to chronic transfusion.
    Br J Haematol. 2020 Nov 20. doi: 10.1111/bjh.17178.
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  376. WEI Z, Yang G, Huang Y, Peng P, et al
    A 15-years follow-up of deferasirox in beta-thalassaemia major patients with iron overload.
    Br J Haematol. 2020;191:e81-e83.
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  377. PEZINA-CANTU C, Gomez-De Leon A, Jaime-Perez JC, Colunga-Pedraza P, et al
    Pernicious anaemia can be treated effectively with a single high dose of cobalamin.
    Br J Haematol. 2020;191:e97-e100.
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  378. SIRIWORADETKUN S, Thubthed R, Thiengtavor C, Paiboonsukwong K, et al
    Elevated levels of circulating monocytic myeloid derived suppressor cells in splenectomised beta-thalassaemia/HbE patients.
    Br J Haematol. 2020;191:e72-e76.
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  379. HAN J, Holden CC, Ahluwalia AY, Molokie RE, et al
    Chronic opioid use can be reduced or discontinued after haematopoietic stem cell transplantation for sickle cell disease.
    Br J Haematol. 2020;191:e70-e72.
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  380. PEFFAULT DE LATOUR R, Brodsky RA, Ortiz S, Risitano AM, et al
    Pharmacokinetic and pharmacodynamic effects of ravulizumab and eculizumab on complement component 5 in adults with paroxysmal nocturnal haemoglobinuria: results of two phase 3 randomised, multicentre studies.
    Br J Haematol. 2020;191:476-485.
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  381. TOLE S, Dhir P, Pugi J, Drury LJ, et al
    Genotype-phenotype correlation in children with hereditary spherocytosis.
    Br J Haematol. 2020;191:486-496.
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    October 2020
  382. HERISHANU Y, Levi S, Kamdjou T, Bornstein Y, et al
    Obinutuzumab in the treatment of autoimmune haemolytic anaemia and immune thrombocytopenia in patients with chronic lymphocytic leukaemia/small lymphocytic lymphoma.
    Br J Haematol. 2020 Oct 23. doi: 10.1111/bjh.17105.
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  383. SHEHA D, El-Shayeb M, Eid Y, Amin M, et al
    Unfolding of sickle cell trait by coronavirus disease 2019 (COVID-19) infection.
    Br J Haematol. 2020;191:e38-e40.
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  384. PIKE A, Muus P, Munir T, Mitchell L, et al
    COVID-19 infection in patients on anti-complement therapy: The Leeds National Paroxysmal Nocturnal Haemoglobinuria service experience.
    Br J Haematol. 2020;191:e1-e4.
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  385. ROIZENBLATT S, Cabanas-Pedro AC, Figueiredo MS
    Rheumatoid arthritis and sickle cell disease: A potential association.
    Br J Haematol. 2020;191:e25-e28.
    >> Share

  386. BARGEHR C, Crazzolara R
    Cabot rings and other peripheral blood features of Imerslund-Grasbeck syndrome.
    Br J Haematol. 2020;191:11.
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  387. TEOFILI L, Papacci P, Orlando N, Bianchi M, et al
    Allogeneic cord blood transfusions prevent fetal haemoglobin depletion in preterm neonates. Results of the CB-TrIP study.
    Br J Haematol. 2020;191:263-268.
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  388. RICCHI P, Meloni A, Pistoia L, Spasiano A, et al
    Longitudinal follow-up of patients with thalassaemia intermedia who started transfusion therapy in adulthood: a cohort study.
    Br J Haematol. 2020;191:107-114.
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    September 2020
  389. NESR G, Koshy R, Foldes D, Kagdi H, et al
    Autoimmune haemolytic anaemia and a marked rise in the lymphocyte count associated with COVID-19 in a patient with treatment-naive chronic lymphocytic leukaemia: a case report.
    Br J Haematol. 2020;190:e326-e328.
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  390. OLATUNYA OS
    Poverty and severity of childhood sickle cell disease.
    Br J Haematol. 2020;190:819-821.
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  391. WOUTERS HJCM, Stam SP, van der Klauw MM, Bakker SJL, et al
    The association between haemoglobin concentrations and muscle mass determined from urinary creatinine excretion rate: a population-based cohort study.
    Br J Haematol. 2020;190:e349-e352.
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  392. GERARD D, Bourin S, Phulpin A, Picard V, et al
    Previously misdiagnosed red cell membrane disorder and familial consequences.
    Br J Haematol. 2020;190:810.
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  393. LIAPIS K, Vrachiolias G, Spanoudakis E, Kotsianidis I, et al
    Vacuolation of early erythroblasts with ring sideroblasts: a clue to the diagnosis of linezolid toxicity.
    Br J Haematol. 2020;190:809.
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  394. MCGINNIS E, Smith TW
    Clostridium perfringens sepsis with spherocytosis and green neutrophil inclusions.
    Br J Haematol. 2020;190:641.
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  395. DE SANTIS GC, Costa TCM, Santos FLS, da Silva-Pinto AC, et al
    Blood transfusion support for sickle cell patients during haematopoietic stem cell transplantation: a single-institution experience.
    Br J Haematol. 2020;190:e295-e297.
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  396. BELLO-MANGA H, Galadanci AA, Abdullahi S, Ali S, et al
    Low educational level of head of household, as a proxy for poverty, is associated with severe anaemia among children with sickle cell disease living in a low-resource setting: evidence from the SPRING trial.
    Br J Haematol. 2020;190:939-944.
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    August 2020
  397. APPIAH-KUBI A, Acharya S, Fein Levy C, Vlachos A, et al
    Varying presentations and favourable outcomes of COVID-19 infection in children and young adults with sickle cell disease: an additional case series with comparisons to published cases.
    Br J Haematol. 2020;190:e221-e224.
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  398. KULASEKARARAJ AG
    Regulatory cells in immune-mediated aplastic anaemia - not Tregs but Bregs.
    Br J Haematol. 2020;190:486-487.
    >> Share

  399. GIBSON JS
    A novel mechanism for pathogenesis of sickle cell disease with therapeutic implications: Band 3 tyrosine phosphorylation.
    Br J Haematol. 2020;190:488-489.
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  400. COLOMBATTI R, Andemariam B
    Microvasculopathy and biomarkers in sickle cell disease: the promise of non-invasive real-time in vivo tools.
    Br J Haematol. 2020;190:309-310.
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  401. MALINOWSKI AK
    Thrombotic microangiopathy in pregnancy: when you hear hoofbeats, consider the zebras?
    Br J Haematol. 2020;190:306-308.
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  402. MOURA PL, Dobbe JGG, Streekstra GJ, Rab MAE, et al
    Rapid diagnosis of hereditary haemolytic anaemias using automated rheoscopy and supervised machine learning.
    Br J Haematol. 2020;190:e250-e255.
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  403. ANDREWS C, Maze D, Murphy T, Sibai H, et al
    Combination treatment with CPX-351 and midostaurin in patients with secondary acute myeloid leukaemia that are FLT3 mutated: three cases and review of literature.
    Br J Haematol. 2020;190:467-470.
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  404. FILIPPIDOU M, Avgerinou G, Tsipou H, Tourkantoni N, et al
    Longitudinal evaluation of eltrombopag in paediatric acquired severe aplastic anaemia.
    Br J Haematol. 2020;190:e157-e159.
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  405. FUNG EB, Ahmad T, Killilea DW, Hussain R, et al
    Zinc supplementation improves markers of glucose homeostasis in thalassaemia.
    Br J Haematol. 2020;190:e162-e166.
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  406. LUEWAN S, Charoenkwan P, Sirichotiyakul S, Tongsong T, et al
    Fetal haemoglobin H-Constant Spring disease: a role for intrauterine management.
    Br J Haematol. 2020;190:e233-e236.
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  407. NOOMUNA P, Risinger M, Zhou S, Seu K, et al
    Inhibition of Band 3 tyrosine phosphorylation: a new mechanism for treatment of sickle cell disease.
    Br J Haematol. 2020;190:599-609.
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  408. TIMMERMANS SAMEG, Werion A, Spaanderman MEA, Reutelingsperger CP, et al
    The natural course of pregnancies in women with primary atypical haemolytic uraemic syndrome and asymptomatic relatives.
    Br J Haematol. 2020;190:442-449.
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  409. ZAIMOKU Y, Patel BA, Kajigaya S, Feng X, et al
    Deficit of circulating CD19(+) CD24(hi) CD38(hi) regulatory B cells in severe aplastic anaemia.
    Br J Haematol. 2020;190:610-617.
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  410. SAMARRON SL, Miller JW, Cheung AT, Chen PC, et al
    Homocysteine is associated with severity of microvasculopathy in sickle cell disease patients.
    Br J Haematol. 2020;190:450-457.
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  411. WILSON S, Ellsworth P, Key NS
    Pregnancy in sickle cell trait: what we do and don't know.
    Br J Haematol. 2020;190:328-335.
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    July 2020
  412. CHAKRAVORTY S, Rees D
    Commentary on sickle cell non-invasive prenatal testing article.
    Br J Haematol. 2020;190:20-21.
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  413. JEREBTSOVA M, Taye A, Smith N, Afangbedji N, et al
    Association between plasma and urinary orosomucoid and chronic kidney disease in adults with sickle cell disease.
    Br J Haematol. 2020;190:e45-e48.
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  414. PEDROSA AM, Lemes RPG
    Gene expression of HIF-1alpha and VEGF in response to hypoxia in sickle cell anaemia: Influence of hydroxycarbamide.
    Br J Haematol. 2020;190:e39-e42.
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  415. NARDO-MARINO A, Brousse V, Rees D
    Emerging therapies in sickle cell disease.
    Br J Haematol. 2020;190:149-172.
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  416. KATTAMIS A
    Diamond-Blackfan anaemia: understanding an old disease.
    Br J Haematol. 2020;190:14-15.
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  417. VAN CAMPEN J, Silcock L, Yau S, Daniel Y, et al
    A novel non-invasive prenatal sickle cell disease test for all at-risk pregnancies.
    Br J Haematol. 2020;190:119-124.
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  418. QUARELLO P, Garelli E, Carando A, Cillario R, et al
    A 20-year long term experience of the Italian Diamond-Blackfan Anaemia Registry: RPS and RPL genes, different faces of the same disease?
    Br J Haematol. 2020;190:93-104.
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    June 2020
  419. LUZZATTO L
    PNH phenotypes and their genesis.
    Br J Haematol. 2020;189:802-805.
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  420. HYACINTH HI, Idris IM
    Cognitive deficit in sickle cell disease: Is hydroxyurea part of the story?
    Br J Haematol. 2020;189:1014-1015.
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  421. GIRELLI D, Busti F
    ERFE regulation in sickle cell disease: complex but promising.
    Br J Haematol. 2020;189:1012-1013.
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  422. KHAMPHIKHAM P, Nualkaew T, Pongpaksupasin P, Kaewsakulthong W, et al
    High-level induction of fetal haemoglobin by pomalidomide in beta-thalassaemia/HbE erythroid progenitor cells.
    Br J Haematol. 2020;189:e240-e245.
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  423. BREWIN JN, Crowley MP, Kesse-Adu R, Stuart-Smith S, et al
    Catheter associated thromboses in patients with sickle cell anaemia and dual lumen Vortex apheresis ports are common and can be clinically asymptomatic.
    Br J Haematol. 2020;189:e198-e200.
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  424. PARTANEN M, Kang G, Wang WC, Krull K, et al
    Association between hydroxycarbamide exposure and neurocognitive function in adolescents with sickle cell disease.
    Br J Haematol. 2020;189:1192-1203.
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  425. RICHARDS SJ, Dickinson AJ, Cullen MJ, Griffin M, et al
    Presentation clinical, haematological and immunophenotypic features of 1081 patients with GPI-deficient (paroxysmal nocturnal haemoglobinuria) cells detected by flow cytometry.
    Br J Haematol. 2020;189:954-966.
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  426. PRATS-MARTIN C, Mezquita L, Garcia-Canale S, Jimenez-Jambrina M, et al
    Numerous abnormal mitoses in parvovirus B19-infected proerythroblasts.
    Br J Haematol. 2020;189:800.
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  427. MANGAONKAR AA, Thawer F, Son J, Ajebo G, et al
    Regulation of iron homeostasis through the erythroferrone-hepcidin axis in sickle cell disease.
    Br J Haematol. 2020;189:1204-1209.
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  428. AL-ALI HK, Griesshammer M, Foltz L, Palumbo GA, et al
    Primary analysis of JUMP, a phase 3b, expanded-access study evaluating the safety and efficacy of ruxolitinib in patients with myelofibrosis, including those with low platelet counts.
    Br J Haematol. 2020;189:888-903.
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  429. PATEL BJ, Barot SV, Kuzmanovic T, Kerr C, et al
    Distinctive and common features of moderate aplastic anaemia.
    Br J Haematol. 2020;189:967-975.
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    May 2020
  430. ANTELO G, Mangaonkar AA, Coltro G, Buradkar A, et al
    Response to erythropoiesis-stimulating agents in patients with WHO-defined myelodysplastic syndrome/myeloproliferative neoplasm with ring sideroblasts and thrombocytosis (MDS/MPN-RS-T).
    Br J Haematol. 2020;189:e104-e108.
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  431. SHAH BN, Hassan TO, Zhang X, McClain DA, et al
    Increased iron stores influence glucose metabolism in sickle cell anaemia.
    Br J Haematol. 2020;189:e184-e187.
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  432. SKINNER S, Ling Liu K, Lo M, Josset-Lamaugarny A, et al
    Alterations in vascular reactivity in a transgenic mouse model of sickle cell trait.
    Br J Haematol. 2020;189:e154-e157.
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  433. GOUVEIA C, Duarte M, Norte S, Alves P, et al
    Osteoarticular infections in paediatric sickle cell disease: in the era of multidrugresistant bacteria.
    Br J Haematol. 2020;189:e147-e150.
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  434. PHILIP KEJ, Sadaka AS, Polkey MI, Hopkinson NS, et al
    The prevalence and associated mortality of non-anaemic iron deficiency in older adults: a 14 years observational cohort study.
    Br J Haematol. 2020;189:566-572.
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  435. LEONARD A, Tisdale J, Abraham A
    Curative options for sickle cell disease: haploidentical stem cell transplantation or gene therapy?
    Br J Haematol. 2020;189:408-423.
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  436. MCCORMICK M, Richardson T, Warady BA, Novelli EM, et al
    Acute kidney injury in paediatric patients with sickle cell disease is associated with increased morbidity and resource utilization.
    Br J Haematol. 2020;189:559-565.
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    April 2020
  437. ALI JS, Andrasik F, Berlin KS, Porter J, et al
    Attention difficulties are associated with lower engagement in adult care amongst youth with sickle cell disease.
    Br J Haematol. 2020;189:e27-e30.
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  438. FAYAND A, Dzierzynski N, Georgin-Lavialle S, Bachmeyer C, et al
    The association of psychiatric comorbidities with emergency visits and hospitalisations in adult sickle-cell patients: a cohort study.
    Br J Haematol. 2020;189:e21-e23.
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  439. ROPER D, Layton M, Rees D, Lambert C, et al
    Laboratory diagnosis of G6PD deficiency. A British Society for Haematology Guideline.
    Br J Haematol. 2020;189:24-38.
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  440. THIENGTAVOR C, Siriworadetkun S, Paiboonsukwong K, Fucharoen S, et al
    Increased ferritin levels in non-transfusion-dependent beta degrees -thalassaemia/HbE are associated with reduced CXCR2 expression and neutrophil migration.
    Br J Haematol. 2020;189:187-198.
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  441. FUJISAWA M, Yasumoto A, Kato H, Sugawara Y, et al
    The role of anti-complement factor H antibodies in the development of atypical haemolytic uremic syndrome: a possible contribution to abnormality of platelet function.
    Br J Haematol. 2020;189:182-186.
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  442. NICKEL RS, Horan JT, Abraham A, Qayed M, et al
    Human leukocyte antigen (HLA) class I antibodies and transfusion support in paediatric HLA-matched haematopoietic cell transplant for sickle cell disease.
    Br J Haematol. 2020;189:162-170.
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  443. QUARTA A, Sgherza N, Pasanisi A, Solfrizzi MP, et al
    Switching from dispersible to film coated tablet formulation of deferasirox improves hemoglobin levels and transfusional interval in patients with transfusion-dependent-thalassemia.
    Br J Haematol. 2020;189:e60-e63.
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    March 2020
  444. AUERBACH M, Georgieff MK
    Guidelines for iron deficiency in pregnancy: hope abounds: Commentary to accompany: UK guidelines on the management of iron deficiency in pregnancy.
    Br J Haematol. 2020;188:814-816.
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  445. AGGARWAL A, Jamwal M, Sharma P, Sachdeva MUS, et al
    Deciphering molecular heterogeneity of Indian families with hereditary spherocytosis using targeted next-generation sequencing: First South Asian study.
    Br J Haematol. 2020;188:784-795.
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  446. HANSEN S, Wood DK, Higgins JM
    5-(Hydroxymethyl)furfural restores low-oxygen rheology of sickle trait blood in vitro.
    Br J Haematol. 2020;188:985-993.
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  447. CORNELISSE AC, Bergkamp FJM, Griffioen-Keijzer A
    Haemolytic anaemia: an unrecognised side effect of hydroxyurea?
    Br J Haematol. 2020;188:e80-e81.
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  448. STALLINGS AM, Majhail NS, Nowacki AS, Onimoe GI, et al
    Paediatric haematologists' attitudes regarding haematopoietic cell transplantation as treatment for sickle cell disease.
    Br J Haematol. 2020;188:976-984.
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  449. PAVORD S, Daru J, Prasannan N, Robinson S, et al
    UK guidelines on the management of iron deficiency in pregnancy.
    Br J Haematol. 2020;188:819-830.
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