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Anemia

Free Subscription Articles published in Br J Haematol Retrieve available abstracts of 217 articles: HTML format

Single Articles

September 2025
1. CHANG M, Semakula D, Little JA, Kanter J, et al
   Grandchildren of GRNDaD: Shifts in disease-modifying therapy at the adolescent transition in sickle cell disease.
   Br J Haematol. 2025;207:1070-1075.
   PubMed     Abstract available
   
   
   
2. SHANGGUAN S, Cui X, Li J, Li N, et al
   Alu-mediated FANCD2 exonic deletion contributes to Fanconi anaemia.
   Br J Haematol. 2025;207:1076-1084.
   PubMed     Abstract available
   
   
   
3. CHAMBLISS C, Manci E, Fields E, Bueno J, et al
   Characterizing pregnancy outcomes in a humanized mouse model of sickle cell disease.
   Br J Haematol. 2025;207:813-823.
   PubMed     Abstract available
   
   
   
4. HAJJAJ OI, Callum J, Shehata N, Farrell A, et al
   Laboratory assessment of fetomaternal haemorrhage and Rh immune globulin management: Canadian practice and scoping review.
   Br J Haematol. 2025;207:723-736.
   PubMed     Abstract available
   
   
   
5. LEUNG WY, Lee TY, Hwang YY, Lee JT, et al
   Iron overload and morbidities in Chinese with non-transfusion-dependent thalassaemia.
   Br J Haematol. 2025;207:1058-1069.
   PubMed     Abstract available
   
   
   August 2025
6. ZHANG L, Liu Z, Zhao X, Hu B, et al
   Efficacy and safety of HRS-5965 monotherapy in complement inhibitor-naive patients with paroxysmal nocturnal haemoglobinuria.
   Br J Haematol. 2025;207:571-581.
   PubMed     Abstract available
   
   
   
7. TEAWTRAKUL N, Jetsrisuparb A, Pongudom S, Chansung K, et al
   Survival and thalassaemia-related complications in HbE/beta-thalassaemia and alpha-thalassaemia: A 10-year longitudinal study in Thailand.
   Br J Haematol. 2025;207:552-560.
   PubMed     Abstract available
   
   
   
8. LEE JW, Jang JH, Chiba S, Yoon SS, et al
   Romiplostim with ciclosporin A in patients with aplastic anaemia naive to immunosuppressive therapy: A phase 2/3 study.
   Br J Haematol. 2025;207:582-590.
   PubMed     Abstract available
   
   
   
9. AFZALI-HASHEMI L, Franse M, Baas KPA, Schrantee A, et al
   Assessment of neurocognitive functioning in sickle cell disease and thalassaemia and the association with silent cerebral infarcts, cerebral haemodynamics and oxygen metabolism.
   Br J Haematol. 2025;207:561-570.
   PubMed     Abstract available
   
   
   July 2025
10. LOH J, Kuo KHM, Georgescu I, Wang S, et al
    Risk factors for immediate postpartum sickle cell disease-specific maternal morbidity.
    Br J Haematol. 2025;207:225-234.
    PubMed     Abstract available
    
    
    
11. WILSON SR, Noubouossie D, Little JA, Karafin MS, et al
    Real-world assessment of acute red cell exchange for stroke in sickle cell disease.
    Br J Haematol. 2025;207:217-224.
    PubMed     Abstract available
    
    
    
12. DIAW M, Coly MS, Charlot K, Gallou-Guyot M, et al
    Physical activity, vaso-occlusive crises and pain in patients with sickle cell anaemia in Senegal.
    Br J Haematol. 2025;207:206-216.
    PubMed     Abstract available
    
    
    
13. SANTINI V, Consagra A
    How to use luspatercept and erythropoiesis-stimulating agents in low-risk myelodysplastic syndrome.
    Br J Haematol. 2025;207:15-26.
    PubMed     Abstract available
    
    
    June 2025
14. KUO KHM, Layton DM, Lal A, Vichinsky EP, et al
    Long-term efficacy and safety of mitapivat in non-transfusion-dependent alpha- or beta-thalassaemia: An open-label phase 2 study.
    Br J Haematol. 2025;206:1764-1773.
    PubMed     Abstract available
    
    
    
15. VISTICA SAMPINO E, Bonal DM, Chorzalska A, Morgan J, et al
    Alterations in the humoral immunophenotype in sickle cell disease.
    Br J Haematol. 2025;206:1774-1785.
    PubMed     Abstract available
    
    
    
16. RICCHI P
    The double edge of erythropoietic modulation in thalassaemia.
    Br J Haematol. 2025;206:1879-1880.
    PubMed     Abstract available
    
    
    
17. HARJU T, Raiskila S, Lohi O, Jarvela L, et al
    Increased incidence of autoimmune haemolytic anaemia with paroxysmal cold haemoglobinuria features in paediatric cases in a changing viral environment post-COVID-19 pandemic.
    Br J Haematol. 2025;206:1872-1876.
    PubMed     Abstract available
    
    
    
18. PALANI CD, Smith A, Cao X, Li B, et al
    Cholesterol-conjugated miR-29b induces fetal haemoglobin expression via gamma-globin promoter demethylation in the Townes mouse model for sickle cell anaemia.
    Br J Haematol. 2025;206:1786-1795.
    PubMed     Abstract available
    
    
    
19. ZAIDEL B, Garland S, Merkeley H
    Acute splenomegaly, haemolysis, and thrombocytopenia following luspatercept initiation in a patient with transfusion-dependent thalassaemia: A case report.
    Br J Haematol. 2025;206:1806-1810.
    PubMed     Abstract available
    
    
    
20. BRANDSEN RP, Diederen RMH, Klaassen I, Veldthuis M, et al
    The role of red blood cell characteristics and viscosity in sickle cell retinopathy and maculopathy.
    Br J Haematol. 2025;206:1796-1805.
    PubMed     Abstract available
    
    
    
21. MAEDA T, Matsuda A, Kanda J, Kawabata H, et al
    Comparison of severe aplastic anaemia and lower risk hypoplastic myelodysplastic neoplasms: Critical role of megakaryocyte count in distinguishing aplastic anaemia from myelodysplastic neoplasms.
    Br J Haematol. 2025;206:1689-1698.
    PubMed     Abstract available
    
    
    
22. JACOBS JW, Amorim L, Pirenne F, Tayou C, et al
    The wider perspective: Barriers and recommendations for transfusion support for patients with sickle cell disease in low- and middle-income countries.
    Br J Haematol. 2025;206:1585-1592.
    PubMed     Abstract available
    
    
    
23. BALCIUNIENE J, Yilmaz S, Chonat S, Grace RF, et al
    Real-world insights from a cohort of approximately 2000 individuals who were analysed using a freely available next-generation sequencing anaemia screening programme.
    Br J Haematol. 2025;206:1853-1856.
    PubMed     Abstract available
    
    
    May 2025
24. MACLEAN B, Fuller J, Lim J, Dugan C, et al
    Greater prevalence of anaemia and heavy menstrual bleeding reported in women of reproductive age in the United Kingdom compared to Australia.
    Br J Haematol. 2025;206:1479-1484.
    PubMed     Abstract available
    
    
    
25. DELICOU S, Manganas K, Diamantidis MD, Venou TM, et al
    Comparative analysis of mortality patterns and treatment strategies in thalassaemia and sickle cell disease patients: A 12-year study.
    Br J Haematol. 2025;206:1466-1478.
    PubMed     Abstract available
    
    
    
26. PRINCE EJ, Scott JL, Nwankwoala O, Ali-Houchens L, et al
    A young adult clinic to support integration into adult sickle cell disease care: If you build it, they will come.
    Br J Haematol. 2025;206:1458-1465.
    PubMed     Abstract available
    
    
    April 2025
27. HOVING V, Donker AE, Schols SEM, Swinkels DW, et al
    How I treat iron-refractory iron deficiency anaemia-An expert opinion-based treatment guidance for children and adults.
    Br J Haematol. 2025;206:1067-1076.
    PubMed     Abstract available
    
    
    
28. METAFUNI E, Brioschi FA, Patriarca A, Leoni C, et al
    Real-world evidence of pegcetacoplan in patients with paroxysmal nocturnal haemoglobinuria: A nationwide Italian study.
    Br J Haematol. 2025;206:1246-1249.
    PubMed     Abstract available
    
    
    
29. CORSIA A, Joseph L, Beeker N, Manceau S, et al
    Maternal and perinatal outcomes of sickle cell disease in pregnancy: A nationwide study in France.
    Br J Haematol. 2025;206:1218-1227.
    PubMed     Abstract available
    
    
    
30. ENACHE A, Carty SA, Babushok DV
    Origins of T-cell-mediated autoimmunity in acquired aplastic anaemia.
    Br J Haematol. 2025;206:1035-1053.
    PubMed     Abstract available
    
    
    
31. SINHA U, Setty S, Pilon C, Brown JJ, et al
    Systemic lupus erythematosus-associated autoantibodies in sickle cell disease: Spontaneous emergence in a patient and in transgenic sickle mice.
    Br J Haematol. 2025;206:1213-1217.
    PubMed     Abstract available
    
    
    March 2025
32. DE LIGT LA, Gaartman AE, Konte K, Thakoerdin S, et al
    Plasma inflammatory and angiogenic protein profiling of patients with sickle cell disease.
    Br J Haematol. 2025;206:954-964.
    PubMed     Abstract available
    
    
    
33. SCHECHTER AN
    Sickle cell anaemia therapy in 2025.
    Br J Haematol. 2025;206:842-845.
    PubMed     Abstract available
    
    
    
34. LONGORIA JN, Howell KE, Porter JS, Treadwell M, et al
    Depression, sleep and pain affect instrumental activities of daily living through cognitive functioning in adults with sickle cell disease: A report from the Sickle Cell Disease Implementation Consortium.
    Br J Haematol. 2025;206:944-953.
    PubMed     Abstract available
    
    
    
35. LI H, Sachdev V, Tian X, Nguyen ML, et al
    A machine learning-based workflow for predicting transplant outcomes in patients with sickle cell disease.
    Br J Haematol. 2025;206:919-923.
    PubMed     Abstract available
    
    
    February 2025
36. MAGGIO A, Napolitano M, Taher AT, Bou-Fakhredin R, et al
    Reframing thalassaemia syndrome as a benign haematopoietic stem cell disorder.
    Br J Haematol. 2025;206:464-477.
    PubMed     Abstract available
    
    
    
37. ZHANG J, Sun J, Huai W, Tang J, et al
    Elucidating loss-of-function mechanisms of monoallelic EPAS1 mutations underlying congenital hypoplastic anaemia in a paediatric anaemia cohort.
    Br J Haematol. 2025;206:585-595.
    PubMed     Abstract available
    
    
    
38. EL HOSS S, Bazoum H
    From old to new: Repurposed drugs in the battle towards curing sickle cell disease.
    Br J Haematol. 2025;206:795-797.
    PubMed     Abstract available
    
    
    
39. BHAT V, Potdar AA, Yu GK, Gibson G, et al
    Impact of hydroxycarbamide treatment on the whole-blood transcriptome in sickle cell disease.
    Br J Haematol. 2025;206:713-720.
    PubMed     Abstract available
    
    
    
40. GURNARI C, Visconte V
    Dissecting the genomic traits and clinical course of secondary myelodysplastic syndrome following aplastic anaemia: A milestone.
    Br J Haematol. 2025;206:790-791.
    PubMed     Abstract available
    
    
    
41. QI J, Wang T, Wang M, He P, et al
    Comparative study of the diversity of amino acids on human leucocyte antigen class II molecules in patients with acquired aplastic anaemia.
    Br J Haematol. 2025;206:735-748.
    PubMed     Abstract available
    
    
    
42. RAZ S, Koren A, Bogdanova AY, Gassmann M, et al
    Memantine treatment in sickle cell disease: A 1-year study of its effects on cognitive functions and neural processing.
    Br J Haematol. 2025;206:689-702.
    PubMed     Abstract available
    
    
    
43. SONGDEJ D, Teawtrakul N, Laoaroon N, Komvilaisak P, et al
    Impact of HbE mutation on the clinical severity of HbH disease: A multicentre study from Thailand.
    Br J Haematol. 2025;206:703-712.
    PubMed     Abstract available
    
    
    January 2025
44. GE S, Ali S, Haldane V, Bekdache C, et al
    An approach to Hemequity: Identifying the barriers and facilitators of iron deficiency reduction strategies in low- to middle-income countries.
    Br J Haematol. 2025 Jan 6. doi: 10.1111/bjh.19984.
    PubMed     Abstract available
    
    
    
45. KHAN AA, Laas CE, Brewin JN, Potter V, et al
    Development of a novel test of splenic function for use in a clinical diagnostic laboratory.
    Br J Haematol. 2025;206:320-330.
    PubMed     Abstract available
    
    
    
46. GEHRIE EA, Booth GS
    Contextualizing prophylactic red blood cell antigen matching in the lifelong care of sickle cell disease and thalassaemia patients.
    Br J Haematol. 2025;206:382-384.
    PubMed     Abstract available
    
    
    
47. GALADANCI NA, Kanter J
    Avascular necrosis in sickle cell disease needs more definitive treatment options.
    Br J Haematol. 2025;206:385-386.
    PubMed     Abstract available
    
    
    
48. PIECHNIK SK, Polzella P, Shah A, Vera-Aviles M, et al
    Myocardial iron intake following intravenous iron therapy with ferric carboxymaltose is sustained at 1 year despite recurrence of iron deficiency.
    Br J Haematol. 2025;206:349-352.
    PubMed     Abstract available
    
    
    
49. NOGUER M, Berthon P, Makowski C, Messonnier LA, et al
    Impaired physical ability in patients with transfusion-dependent beta-thalassaemia: Can regular physical activity be a countermeasure?
    Br J Haematol. 2025;206:86-93.
    PubMed     Abstract available
    
    
    
50. WOLF J, Blais-Normandin I, Bathla A, Keshavarz H, et al
    Red cell specifications for blood group matching in patients with haemoglobinopathies: An updated systematic review and clinical practice guideline from the International Collaboration for Transfusion Medicine Guidelines.
    Br J Haematol. 2025;206:94-108.
    PubMed     Abstract available
    
    
    
51. KOCHHAR M, McGann PT
    Sickle cell disease in India: Not just a mild condition.
    Br J Haematol. 2025;206:380-381.
    PubMed     Abstract available
    
    
    
52. SETH T, Udupi S, Jain S, Bhatwadekar S, et al
    Burden of vaso-occlusive crisis, its management and impact on quality of life of Indian sickle cell disease patients.
    Br J Haematol. 2025;206:296-309.
    PubMed     Abstract available
    
    
    
53. CASALE M, Toro G, Porcelli F, Quota A, et al
    Long-term outcomes of avascular necrosis in sickle cell disease using joint-specific patient-reported outcome measures: Results from a multicentre study.
    Br J Haematol. 2025;206:310-319.
    PubMed     Abstract available
    
    
    December 2024
54. LOTH G, Dumke CCK, Muratori RR, Pelegrina PD, et al
    Haematopoietic cell transplantation for 106 infants and preschoolers with acquired and inherited bone marrow failures.
    Br J Haematol. 2024;205:2387-2402.
    PubMed     Abstract available
    
    
    
55. SEGBEFIA CI, Smart LR, Stuber SE, Amissah-Arthur KN, et al
    Baseline characteristics of Ghanaian children and adults enrolled in PIVOT, a randomised clinical trial of hydroxyurea in HbSC disease in sub-Saharan Africa.
    Br J Haematol. 2024;205:2470-2480.
    PubMed     Abstract available
    
    
    November 2024
56. COSTA S, Minucci A, Kumawat A, De Bonis M, et al
    Pathogenic G6PD variants: Different clinical pictures arise from different missense mutations in the same codon.
    Br J Haematol. 2024;205:1985-1994.
    PubMed     Abstract available
    
    
    
57. CINTHO OZAHATA M, Guo Y, Gomes I, Malta B, et al
    Genetic variants associated with white blood cell count amongst individuals with sickle cell disease.
    Br J Haematol. 2024;205:1974-1984.
    PubMed     Abstract available
    
    
    
58. ELSHERIF L, Tang Y, Patillo KL, Wichlan D, et al
    Association of biomarkers of endothelial function, coagulation activation and kidney injury with persistent albuminuria in sickle cell anaemia.
    Br J Haematol. 2024;205:1963-1973.
    PubMed     Abstract available
    
    
    
59. GURNARI C, Lima ACM, Pagliuca S
    HLA-lacking clones in aplastic anaemia: Adaptive or maladaptive?
    Br J Haematol. 2024;205:1681-1682.
    PubMed     Abstract available
    
    
    
60. MARIN V, Huguenin Y, Bessi L, Weinmann L, et al
    Beta-thalassaemia intermedia due to a complex alpha-globin rearrangement and a heterozygous beta thalassaemia mutation.
    Br J Haematol. 2024;205:1959-1962.
    PubMed     Abstract available
    
    
    
61. ZAIMOKU Y, Sakai K, Tsuji N, Hosomichi K, et al
    Haematopoietic regeneration by HLA-A*0206-deficient clones in severe aplastic anaemia without definitive immunosuppressive treatment.
    Br J Haematol. 2024;205:1995-1999.
    PubMed     Abstract available
    
    
    October 2024
62. GUPTA CL, Jaganathasamy N, Madkaikar M
    Microbiome in sickle cell disease: Pathophysiology and therapeutic insights.
    Br J Haematol. 2024;205:1279-1287.
    PubMed     Abstract available
    
    
    
63. GILTON M, Fernandes H, Martinez C, Leverger G, et al
    Association of paediatric autoimmune cytopenia and inflammatory bowel disease suggests a common genetic origin.
    Br J Haematol. 2024;205:1508-1515.
    PubMed     Abstract available
    
    
    
64. VALENTINI CG, Teofili L, Gehrie E
    Iron metabolism in sickle cell disease patients undergoing chronic red blood cell exchange: A delicate homeostasis in balance.
    Br J Haematol. 2024;205:1257-1259.
    PubMed     Abstract available
    
    
    
65. CONNES P, Nader E
    Could oxygen gradient ektacytometry help to detect sickle cell trait carriers at risk for kidney disorders or exercise-related complications?
    Br J Haematol. 2024;205:1260-1261.
    PubMed     Abstract available
    
    
    
66. RAMSAY Z, Ali A, Grant J, Asnani M, et al
    Exploring the role of viscosity-vaso-occlusion and haemolysis-endothelial dysfunction in pain sensitization among Jamaicans with sickle cell disease.
    Br J Haematol. 2024;205:1570-1580.
    PubMed     Abstract available
    
    
    
67. M ROSS J, Forte S, Mercure-Corriveau N, Lemay AS, et al
    Automated red blood cell exchange with a post-procedure haematocrit targeted at 34% in the chronic management of sickle cell disease.
    Br J Haematol. 2024;205:1556-1564.
    PubMed     Abstract available
    
    
    
68. ELLSWORTH P, Pawlinski IJ, Sielaty R, Ilich A, et al
    Hypertonicity and/or acidosis induce marked rheological changes under hypoxic conditions in sickle trait red blood cells.
    Br J Haematol. 2024;205:1565-1569.
    PubMed     Abstract available
    
    
    
69. KATO S, Chagi K, Takagi Y, Hidaka M, et al
    Machine/deep learning-assisted hemoglobin level prediction using palpebral conjunctival images.
    Br J Haematol. 2024;205:1590-1598.
    PubMed     Abstract available
    
    
    
70. LEE JM, Kim HS, Yoo J, Lee J, et al
    Genomic insights into inherited bone marrow failure syndromes in a Korean population.
    Br J Haematol. 2024;205:1581-1589.
    PubMed     Abstract available
    
    
    September 2024
71. 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.
    PubMed     Abstract available
    
    
    
72. STRAUSS JD, Brown DW, Zhou W, Dagnall C, et al
    Telomere length and clonal chromosomal alterations in peripheral blood of patients with severe aplastic anaemia.
    Br J Haematol. 2024;205:1180-1187.
    PubMed     Abstract available
    
    
    
73. PRABAHRAN A, Durrani J, Coelho-Da Silva J, Shalhoub R, et al
    Safety and efficacy of immunosuppressive therapy for elderly patients with severe aplastic anaemia.
    Br J Haematol. 2024;205:1170-1179.
    PubMed     Abstract available
    
    
    
74. ZHOU LY, Derebail VK, Desai PC, Elsherif L, et al
    Persistent albuminuria and chronic kidney disease in adults with sickle cell anaemia: Results from a multicenter natural history study.
    Br J Haematol. 2024;205:1159-1169.
    PubMed     Abstract available
    
    
    
75. SADAF A, Dong M, Pfeiffer A, Korpik J, et al
    A pharmacokinetic-pharmacodynamic analysis of l-glutamine for the treatment of sickle cell disease: Implications for understanding the mechanism of action and evaluating response to therapy.
    Br J Haematol. 2024;205:1147-1158.
    PubMed     Abstract available
    
    
    
76. NKOY AB, Mumaka FM, Ngonde A, Mafumba SK, et al
    Relevance of repeated analyses of albuminuria and glomerular filtration rate in African children with sickle cell anaemia.
    Br J Haematol. 2024;205:1137-1146.
    PubMed     Abstract available
    
    
    
77. ZHOU X, Wagner V, Scheller L, Stanojkovska E, et al
    Changes in T-cell subsets, preexisting cytopenias and hyperferritinaemia correlate with cytopenias after BCMA targeted CAR T-cell therapy in relapsed/refractory multiple myeloma: Results from a prospective comprehensive biomarker study.
    Br J Haematol. 2024;205:999-1010.
    PubMed     Abstract available
    
    
    August 2024
78. GLENTHOJ A, Grace RF, Lander C, van Beers EJ, et al
    Comorbidities and complications in adult and paediatric patients with pyruvate kinase deficiency: Analysis from the Peak Registry.
    Br J Haematol. 2024;205:613-623.
    PubMed     Abstract available
    
    
    
79. KATZ BZ, Karny S
    Pursuing the elusive footsteps of malaria in peripheral blood smears utilizing artificial intelligence.
    Br J Haematol. 2024;205:414-415.
    PubMed     Abstract available
    
    
    
80. 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.
    PubMed     Abstract available
    
    
    
81. RECH JS, Cohen A, Bartolucci P, Santin A, et al
    Shift in emergency department utilization by frequent attendees with sickle cell disease during the COVID-19 pandemic: A multicentre cohort study.
    Br J Haematol. 2024;205:463-472.
    PubMed     Abstract available
    
    
    
82. SEGBEFIA C, Luchtman-Jones L
    Seeing haemoglobin SC: Challenging the misperceptions.
    Br J Haematol. 2024;205:404-405.
    PubMed     Abstract available
    
    
    
83. 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.
    PubMed     Abstract available
    
    
    
84. 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.
    PubMed     Abstract available
    
    
    
85. 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.
    PubMed     Abstract available
    
    
    
86. 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.
    PubMed     Abstract available
    
    
    
87. 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.
    PubMed    
    
    
    
88. 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.
    PubMed    
    
    
    July 2024
89. 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.
    PubMed     Abstract available
    
    
    
90. 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.
    PubMed     Abstract available
    
    
    
91. 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.
    PubMed     Abstract available
    
    
    
92. 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.
    PubMed     Abstract available
    
    
    
93. 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.
    PubMed     Abstract available
    
    
    
94. 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.
    PubMed    
    
    
    
95. PADENIYA P, Premawardhena A
    Obesity, liver steatosis and metabolic syndrome: The hidden enemies in transfusion-dependent thalassaemia.
    Br J Haematol. 2024;205:28-29.
    PubMed     Abstract available
    
    
    
96. RUIZ MA, Zhang X, Mansilla MA, Zahr RS, et al
    Prevalence of kidney health genetic variants in adults with sickle cell nephropathy.
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    PubMed     Abstract available
    
    
    
97. KIM DH, Hong J, Shin DY, Kim I, et al
    Phase II trial of posaconazole prophylaxis during anti-thymocyte globulin treatment for aplastic anaemia and hypoplastic myelodysplastic syndrome.
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    PubMed    
    
    
    
98. 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.
    PubMed     Abstract available
    
    
    June 2024
99. GUARNERA L, Visconte V
    The metabolic fuel of paroxysmal nocturnal haemoglobinuria.
    Br J Haematol. 2024;204:2162-2164.
    PubMed     Abstract available
    
    
    
100. SHAH FT, Nicolle S, Garg M, Pancham S, et al
     Guideline for the management of conception and pregnancy in thalassaemia syndromes: A British Society for Haematology Guideline.
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     PubMed     Abstract available
     
     
     
101. 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.
     PubMed     Abstract available
     
     
     
102. 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.
     PubMed    
     
     
     
103. 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.
     PubMed     Abstract available
     
     
     
104. DAVILA J, O'Brien SH, Mitchell WB, Manwani D, et al
     Evaluating thromboprophylaxis in the sickle cell disease population: Navigating the evidence gap.
     Br J Haematol. 2024;204:2184-2193.
     PubMed     Abstract available
     
     
     May 2024
105. 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.
     PubMed     Abstract available
     
     
     
106. 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.
     PubMed    
     
     
     
107. 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.
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     PubMed    
     
     
     
108. 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.
     PubMed     Abstract available
     
     
     
109. LIPTON JM
     Understanding complex disease-related mechanisms: Rational therapies for Diamond-Blackfan anaemia.
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     PubMed     Abstract available
     
     
     
110. 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.
     PubMed    
     
     
     
111. 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.
     PubMed     Abstract available
     
     
     
112. DUNCAN BB, Lotter JL, Superata J, Barranta ME, et al
     Treatment of refractory/relapsed Diamond-Blackfan anaemia with eltrombopag.
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     PubMed     Abstract available
     
     
     
113. 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.
     PubMed     Abstract available
     
     
     
114. 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.
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     PubMed     Abstract available
     
     
     
115. 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.
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     PubMed     Abstract available
     
     
     
116. 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.
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     PubMed     Abstract available
     
     
     
117. NEYER PJ, Kabore B, Nakas CT, Diallo S, et al
     Increased erythroferrone levels in malarial anaemia.
     Br J Haematol. 2024;204:2066-2070.
     PubMed     Abstract available
     
     
     April 2024
118. ARCANJO GS, Souza MB, Domingos IF, Pereira-Martins DA, et al
     BMP6 and VDR gene polymorphisms are associated with osteonecrosis in a sickle cell anaemia cohort.
     Br J Haematol. 2024;204:1507-1514.
     PubMed     Abstract available
     
     
     
119. CHANG A, Wilson SR, Morris S, Wichlan D, et al
     Nocturnal hypoxaemia is common in adults with sickle cell anaemia.
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120. JACOBS JW, Sharma D, Stephens LD, Figueroa Villalba CA, et al
     Thrombosis risk with haemoglobin C trait and haemoglobin C disease: A systematic review.
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121. 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.
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     PubMed    
     
     
     March 2024
122. 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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123. 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.
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124. LEE GM, Batchvarova M, Delahunty M, Boateng L, et al
     Sickle red blood cells directly activate neutrophils.
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125. 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.
     PubMed     Abstract available
     
     
     
126. 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.
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     PubMed     Abstract available
     
     
     
127. EARLY ML, Raja M, Luo A, Solow M, et al
     Blood pressure thresholds for the diagnosis of hypertensive disorders of pregnancy in sickle cell disease.
     Br J Haematol. 2024;204:1039-1046.
     PubMed     Abstract available
     
     
     
128. KISALI EP, Iversen PO, Makani J
     Low vitamin B(12) blood levels in sickle cell disease: Data from a large cohort study in Tanzania.
     Br J Haematol. 2024;204:1047-1053.
     PubMed     Abstract available
     
     
     
129. 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.
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     PubMed     Abstract available
     
     
     
130. 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.
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131. MUNARETTO V, Corti P, Bertoni E, Tripodi SI, et al
     Acute chest syndrome in children with sickle cell disease: Data from a national AIEOP cohort identify priority areas of intervention in a hub-and-spoke system.
     Br J Haematol. 2024;204:1061-1066.
     PubMed     Abstract available
     
     
     February 2024
132. WARE RE, Quinn CT
     The bold promise of gene therapy for sickle cell disease.
     Br J Haematol. 2024;204:381-382.
     PubMed    
     
     
     
133. STEENSMA DP
     Revisiting the first reported case of aplastic anaemia.
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134. KATAGIRI T, Iwasaki H, Fujieda A, Kasashima S, et al
     A case of hepatitis-associated aplastic anaemia following living-donor liver transplantation for fulminant hepatitis showing loss of heterozygosity in the 6p chromosome in the affected liver.
     Br J Haematol. 2024;204:623-627.
     PubMed     Abstract available
     
     
     
135. HUNT RC, Kimchi-Sarfaty C
     A synonymous variant is unmasked in thalassaemia.
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136. KHWAJA J, Japzon N, Gabriel M, Raju K, et al
     Cold agglutinin disease and cryoglobulinaemia: A frequent coexistence with clinical impact.
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137. EARLY ML, Luo A, Solow M, Matusiak K, et al
     Natural history of blood pressure in sickle cell disease pregnancy.
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138. 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.
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139. 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.
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140. GORIVALE M, Sawant P, Kargutkar N, Hariharan P, et al
     When a synonymous mutation breaks the silence in a thalassaemia patient.
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     January 2024
141. OYARBIDE U, Crane GM, Corey SJ
     The metabolic basis of inherited neutropenias.
     Br J Haematol. 2024;204:45-55.
     PubMed     Abstract available
     
     
     
142. PETERS C
     Haematopoietic stem cell transplantation in children with sickle cell disease: Still to do?
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     PubMed     Abstract available
     
     
     
143. DANIEL Y, Henthorn J
     Lessons learnt in the screening and diagnosis of haemoglobinopathies.
     Br J Haematol. 2024;204:68-73.
     PubMed     Abstract available
     
     
     
144. SHOOK LM, Ware RE
     Screening for haemoglobin disorders: One size may not fit all.
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145. 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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146. 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.
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147. 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
148. 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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149. 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
150. 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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151. 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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152. 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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153. 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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154. 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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155. 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
156. 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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157. 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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158. 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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159. 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
160. 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.
     PubMed     Abstract available
     
     
     
161. 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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162. 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.
     PubMed    
     
     
     
163. HAN J, Saraf SL, Gordeuk VR
     Vaccination in sickle cell disease: Immunocompromised or immunocompetent?
     Br J Haematol. 2023;202:916-918.
     PubMed     Abstract available
     
     
     
164. ESPERTI S, Nader E, Boisson C, Carin R, et al
     Mitochondria retention in mature RBCs from haemoglobin SC patients.
     Br J Haematol. 2023;202:e36-e38.
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165. 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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166. 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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167. GUPTA A, Gooda R, Marouf R
     Pseudo-Gaucher cells in a splenectomised Beta-Thalassemia patient.
     Br J Haematol. 2023;202:911.
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168. ZOLLER H, Wagner S, Schaefer B
     What is wrong in doing good?
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169. ASHER S, Shah R, Ings S, Horder J, et al
     Haematopoietic stem cell mobilisation followed by high-dose chemotherapy and autologous stem cell transplantation for patients with sickle cell disease and myeloma.
     Br J Haematol. 2023;202:1224-1227.
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170. 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.
     PubMed     Abstract available
     
     
     
171. 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.
     PubMed     Abstract available
     
     
     
172. MANGANAS K, Delicou S, Xydaki A, Kourakli A, et al
     Predisposing factors for advanced liver fibrosis in patients with sickle cell disease.
     Br J Haematol. 2023;202:1192-1198.
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173. 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
174. ELSHERIF L, Kanthakumar P, Afolabi J, Stratton AF, et al
     Urinary angiotensinogen is associated with albuminuria in adults with sickle cell anaemia.
     Br J Haematol. 2023;202:669-673.
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175. GIBSON JS, Stewart GW
     A critical role for altered red cell cation permeability in pathogenesis of sickle cell disease and other haemolytic anaemias.
     Br J Haematol. 2023;202:462-464.
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176. 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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177. HAMANI S, Lioure B, Nicolae A, Lipsker D, et al
     A Rare Cause of Refractory Anaemia hidden between Folds.
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178. JOLY P, Nader E, Ketels F, Boisson C, et al
     Effects of pyruvate kinase activators on red blood cell properties in sickle cell disease.
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179. 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.
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180. 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.
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     July 2023
181. RAI MP, Lee EJ, Bussel JB
     Maintenence rituximab following induction in autoimmune cytopenias.
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182. HAROUN E, Dutta D, Lim SH
     Effects of GBT1118, a voxelotor analog, on intestinal pathophysiology in sickle cell disease.
     Br J Haematol. 2023;202:184-194.
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183. FERRONE FA
     More of the same? Voxelotor spawns a successor, but on what success does it build?
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184. 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.
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     June 2023
185. SHETH S, Taher AT, Coates TD, Kattamis A, et al
     Management of luspatercept therapy in patients with transfusion-dependent beta-thalassaemia.
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186. WU J, Wang J, Tang N, Wang X, et al
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187. 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.
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188. PENG Y, Liang L, Zhang H, Liu H, et al
     Single-cell profiling of ineffective erythropoiesis in a mouse model of beta-thalassaemia intermedia.
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189. 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.
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190. JACOBS JW, Stephens LD, Allen ES, Binns TC, et al
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191. GENDREAU S, Cecchini J, Perier F, Razazi K, et al
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192. TAKASAKI K, Friedman DF, Uter S, Vege S, et al
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193. 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.
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194. CHEMINET G, Brunetti A, Khimoud D, Ranque B, et al
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