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COVID-19: Daily Top 10 Papers


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Articles published in Br J Haematol

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    June 2021
  1. 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.

  2. 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.

    April 2021
  3. 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.

    February 2021
  4. 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.

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

  6. 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.
    PubMed     Abstract available

  7. 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.
    PubMed     Abstract available

  8. 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.
    PubMed     Abstract available

  9. 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.

  10. 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.
    PubMed     Abstract available

  11. 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.
    PubMed     Abstract available

  12. 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.
    PubMed     Abstract available

    January 2021
    Romiplostim in aplastic anaemia - another tool in the armamentarium.
    Br J Haematol. 2021;192:15-16.

  14. 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.
    PubMed     Abstract available

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

  16. 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.

  17. 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.
    PubMed     Abstract available

  18. 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.
    PubMed     Abstract available

  19. 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.
    PubMed     Abstract available

  20. 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.
    PubMed     Abstract available

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

  22. 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.
    PubMed     Abstract available

  23. 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.
    PubMed     Abstract available

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

  25. 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.
    PubMed     Abstract available

  26. 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.
    PubMed     Abstract available

  27. 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.

  28. 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.
    PubMed     Abstract available

  29. 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.
    PubMed     Abstract available

  30. 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.
    PubMed     Abstract available

    November 2020
  31. 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.
    PubMed     Abstract available

  32. 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.

  33. 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.

  34. 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.

  35. 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.

  36. 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.
    PubMed     Abstract available

  37. 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.
    PubMed     Abstract available

    October 2020
  38. 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.

  39. 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.

  40. 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.

  41. ROIZENBLATT S, Cabanas-Pedro AC, Figueiredo MS
    Rheumatoid arthritis and sickle cell disease: A potential association.
    Br J Haematol. 2020;191:e25-e28.

  42. BARGEHR C, Crazzolara R
    Cabot rings and other peripheral blood features of Imerslund-Grasbeck syndrome.
    Br J Haematol. 2020;191:11.

  43. 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.
    PubMed     Abstract available

  44. 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.
    PubMed     Abstract available

    September 2020
  45. 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.

    Poverty and severity of childhood sickle cell disease.
    Br J Haematol. 2020;190:819-821.

  47. 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.

  48. 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.

  49. 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.

  50. MCGINNIS E, Smith TW
    Clostridium perfringens sepsis with spherocytosis and green neutrophil inclusions.
    Br J Haematol. 2020;190:641.

  51. 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.

  52. 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.
    PubMed     Abstract available

    August 2020
  53. KULASEKARARAJ AG, Lazana I, Large J, Posadas K, et al
    Terminal complement inhibition dampens the inflammation during COVID-19.
    Br J Haematol. 2020;190:e141-e143.

  54. KARIMI M, Haghpanah S, Azarkeivan A, Zahedi Z, et al
    Prevalence and mortality in beta-thalassaemias due to outbreak of novel coronavirus disease (COVID-19): the nationwide Iranian experience.
    Br J Haematol. 2020;190:e137-e140.

  55. 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.

    Regulatory cells in immune-mediated aplastic anaemia - not Tregs but Bregs.
    Br J Haematol. 2020;190:486-487.

    A novel mechanism for pathogenesis of sickle cell disease with therapeutic implications: Band 3 tyrosine phosphorylation.
    Br J Haematol. 2020;190:488-489.

  58. 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.

    Thrombotic microangiopathy in pregnancy: when you hear hoofbeats, consider the zebras?
    Br J Haematol. 2020;190:306-308.

  60. 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.

  61. 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.

  62. 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.

  63. 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.

  64. 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.

  65. 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.
    PubMed     Abstract available

  66. 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.
    PubMed     Abstract available

  67. 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.
    PubMed     Abstract available

  68. 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.
    PubMed     Abstract available

  69. 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.
    PubMed     Abstract available

    July 2020
  70. HEILBRONNER C, Berteloot L, Tremolieres P, Dupic L, et al
    Patients with sickle cell disease and suspected COVID-19 in a paediatric intensive care unit.
    Br J Haematol. 2020;190:e21-e24.

  71. SAHU KK, Siddiqui AD, Cerny J
    Managing sickle cell patients with COVID-19 infection: the need to pool our collective experience.
    Br J Haematol. 2020;190:e86-e89.

  72. LI M, Nguyen CB, Yeung Z, Sanchez K, et al
    Evans syndrome in a patient with COVID-19.
    Br J Haematol. 2020;190:e59-e61.

  73. MCCLOSKEY KA, Meenan J, Hall R, Tsitsikas DA, et al
    COVID-19 infection and sickle cell disease: a UK centre experience.
    Br J Haematol. 2020;190:e57-e58.

    Commentary on sickle cell non-invasive prenatal testing article.
    Br J Haematol. 2020;190:20-21.

  75. 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.

  76. 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.
    PubMed     Abstract available

  77. NARDO-MARINO A, Brousse V, Rees D
    Emerging therapies in sickle cell disease.
    Br J Haematol. 2020;190:149-172.
    PubMed     Abstract available

    Diamond-Blackfan anaemia: understanding an old disease.
    Br J Haematol. 2020;190:14-15.

  79. 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.
    PubMed     Abstract available

  80. 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.
    PubMed     Abstract available

    June 2020
  81. HUSSAIN FA, Njoku FU, Saraf SL, Molokie RE, et al
    COVID-19 infection in patients with sickle cell disease.
    Br J Haematol. 2020;189:851-852.

    PNH phenotypes and their genesis.
    Br J Haematol. 2020;189:802-805.

  83. HYACINTH HI, Idris IM
    Cognitive deficit in sickle cell disease: Is hydroxyurea part of the story?
    Br J Haematol. 2020;189:1014-1015.

  84. GIRELLI D, Busti F
    ERFE regulation in sickle cell disease: complex but promising.
    Br J Haematol. 2020;189:1012-1013.

  85. 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.

  86. 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.

  87. 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.
    PubMed     Abstract available

  88. 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.
    PubMed     Abstract available

  89. 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.

  90. 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.
    PubMed     Abstract available

  91. 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.
    PubMed     Abstract available

  92. 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.
    PubMed     Abstract available

    May 2020
  93. ZAGORSKI E, Pawar T, Rahimian S, Forman D, et al
    Cold Agglutinin Autoimmune Hemolytic Anemia Associated with Novel Coronavirus (COVID-19).
    Br J Haematol. 2020 May 27. doi: 10.1111/bjh.16892.
    PubMed     Abstract available

  94. ANGILERI F, Legare S, Marino Gammazza A, Conway de Macario E, et al
    Is molecular mimicry the culprit in the autoimmune hemolytic anemia affecting COVID-19 patients?
    Br J Haematol. 2020 May 26. doi: 10.1111/bjh.16883.
    PubMed     Abstract available

  95. LAZARIAN G, Quinquenel A, Bellal M, Siavellis J, et al
    Autoimmune hemolytic anemia associated with Covid-19 infection.
    Br J Haematol. 2020 May 6. doi: 10.1111/bjh.16794.
    PubMed     Abstract available

  96. LOPEZ C, Kim J, Pandey A, Huang T, et al
    Simultaneous Onset of COVID-19 and Autoimmune Hemolytic Anemia.
    Br J Haematol. 2020 May 5. doi: 10.1111/bjh.16786.
    PubMed     Abstract available

  97. ROY NBA, Telfer P, Eleftheriou P, de la Fuente J, et al
    Protecting vulnerable patients with inherited anaemias from unnecessary death during the COVID-19 pandemic.
    Br J Haematol. 2020;189:635-639.
    PubMed     Abstract available

  98. 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.

  99. 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.

  100. 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.

  101. 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.

  102. 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.
    PubMed     Abstract available

  103. 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.
    PubMed     Abstract available

  104. 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.
    PubMed     Abstract available

    April 2020
  105. 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.

  106. 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.

  107. 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.

  108. 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.
    PubMed     Abstract available

  109. 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.
    PubMed     Abstract available

  110. 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.
    PubMed     Abstract available

  111. 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.

    March 2020
  112. 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.

  113. 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.
    PubMed     Abstract available

  114. 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.
    PubMed     Abstract available

  115. CORNELISSE AC, Bergkamp FJM, Griffioen-Keijzer A
    Haemolytic anaemia: an unrecognised side effect of hydroxyurea?
    Br J Haematol. 2020;188:e80-e81.

  116. 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.
    PubMed     Abstract available

  117. 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.

    February 2020
  118. NZE C, Fortin B, Freedman R, Mandell E, et al
    Sudden death in sickle cell disease: current experience.
    Br J Haematol. 2020;188:e43-e45.

  119. SANCHEZ-PETITTO G, Drachenberg CB, Mannuel HD, Law JY, et al
    An unusual presentation of paroxysmal nocturnal haemoglobinuria.
    Br J Haematol. 2020;188:347.

  120. SHAH S, Sheth R, Shah K, Patel K, et al
    Safety and effectiveness of thalidomide and hydroxyurea combination in beta-thalassaemia intermedia and major: a retrospective pilot study.
    Br J Haematol. 2020;188:e18-e21.

  121. PEREIRA-MARTINS DA, Coelho-Silva JL, Domingos IF, Weinhauser I, et al
    Association between ANXA2*5681 polymorphism (rs7170178) and osteonecrosis in haemoglobin SS-genotyped patients.
    Br J Haematol. 2020;188:e8-e11.

  122. DUTTA D, Aujla A, Knoll BM, Lim SH, et al
    Intestinal pathophysiological and microbial changes in sickle cell disease: Potential targets for therapeutic intervention.
    Br J Haematol. 2020;188:488-493.
    PubMed     Abstract available

  123. SAITO-BENZ M, Flanagan P, Berry MJ
    Management of anaemia in pre-term infants.
    Br J Haematol. 2020;188:354-366.
    PubMed     Abstract available

    January 2020
  124. SCHOLS S, Nunn MA, Mackie I, Weston-Davies W, et al
    Successful treatment of a PNH patient non-responsive to eculizumab with the novel complement C5 inhibitor coversin (nomacopan).
    Br J Haematol. 2020;188:334-337.

  125. WANG Y, McReynolds LJ, Dagnall C, Katki HA, et al
    Pre-transplant short telomeres are associated with high mortality risk after unrelated donor haematopoietic cell transplant for severe aplastic anaemia.
    Br J Haematol. 2020;188:309-316.
    PubMed     Abstract available

    April 2019
  126. SCHOLZ GA, Leichtle AB, Scherer A, Arndt U, et al
    The links of hepcidin and erythropoietin in the interplay of inflammation and iron deficiency in a large observational study of rheumatoid arthritis.
    Br J Haematol. 2019 Apr 2. doi: 10.1111/bjh.15895.
    PubMed     Abstract available

  127. RUND D
    Bittersweet news for the adult sickle cell patient.
    Br J Haematol. 2019;185:9-10.

  128. ZHOU J, Han J, Nutescu EA, Galanter WL, et al
    Similar burden of type 2 diabetes among adult patients with sickle cell disease relative to African Americans in the U.S. population: a six-year population-based cohort analysis.
    Br J Haematol. 2019;185:116-127.
    PubMed     Abstract available

  129. NASHASHIBI J, Avraham GR, Schwartz N, Awni Y, et al
    Intravenous iron treatment reduces coagulability in patients with iron deficiency anaemia: a longitudinal study.
    Br J Haematol. 2019;185:93-101.
    PubMed     Abstract available

  130. BELISARIO AR, Vieira ELM, de Almeida JA, Mendes FG, et al
    Low urinary levels of angiotensin-converting enzyme 2 may contribute to albuminuria in children with sickle cell anaemia.
    Br J Haematol. 2019;185:190-193.

  131. MORISSENS M, Castro Rodriguez J, Azerad MA, Besse-Hammer T, et al
    Added value of speckle tracking in the evaluation of cardiac function in patients with sickle cell disease.
    Br J Haematol. 2019;185:151-153.

  132. BRUNSON A, Keegan THM, Mahajan A, Paulukonis S, et al
    Cancer specific survival in patients with sickle cell disease.
    Br J Haematol. 2019;185:128-132.
    PubMed     Abstract available

  133. DAY ME, Rodeghier M, Driggers J, Bean CJ, et al
    A significant proportion of children of African descent with HbSbeta(0) thalassaemia are inaccurately diagnosed based on phenotypic analyses alone.
    Br J Haematol. 2019;185:153-156.

    March 2019
  134. GRACE RF, Mark Layton D, Barcellini W
    How we manage patients with pyruvate kinase deficiency.
    Br J Haematol. 2019;184:721-734.
    PubMed     Abstract available

  135. WHITE J, Lindgren M, Liu K, Gao X, et al
    Sevuparin blocks sickle blood cell adhesion and sickle-leucocyte rolling on immobilized L-selectin in a dose dependent manner.
    Br J Haematol. 2019;184:873-876.

  136. PELLEGRIN S, Haydn-Smith KL, Hampton-O'Neil LA, Hawley BR, et al
    Transduction with BBF2H7/CREB3L2 upregulates SEC23A protein in erythroblasts and partially corrects the hypo-glycosylation phenotype associated with CDAII.
    Br J Haematol. 2019;184:876-881.

  137. ALTER BP, Giri N
    Serum alpha fetoprotein levels in Fanconi anaemia.
    Br J Haematol. 2019;184:1074-1076.

  138. BERGER G, van den Berg E, Smetsers S, Leegte BK, et al
    Fanconi anaemia presenting as acute myeloid leukaemia and myelodysplastic syndrome in adulthood: a family report on co-occurring FANCC and CHEK2 mutations.
    Br J Haematol. 2019;184:1071-1073.

  139. JIANG H, Zhang H, Wang Y, Qi W, et al
    Sirolimus for the treatment of multi-resistant pure red cell aplasia.
    Br J Haematol. 2019;184:1055-1058.

  140. SALEM B, Mitchell R, DeFor TE, Tryon R, et al
    Elevations in serum alpha fetoprotein levels in patients with Fanconi anaemia.
    Br J Haematol. 2019;184:1032-1035.

  141. KANTER J, Heath LE, Knorr J, Agbenyega ET, et al
    Novel findings from the multinational DOVE study on geographic and age-related differences in pain perception and analgesic usage in children with sickle cell anaemia.
    Br J Haematol. 2019;184:1058-1061.

    February 2019
  142. MCGOWAN KE, Malinowski AK, Schuh AC, Whittle W, et al
    Aplastic anaemia in pregnancy - a single centre, North American series.
    Br J Haematol. 2019;184:436-439.
    PubMed     Abstract available

  143. LUZZATTO L, Notaro R
    The "escape" model: a versatile mechanism for clonal expansion.
    Br J Haematol. 2019;184:465-466.

  144. RAVERA S, Degan P, Sabatini F, Columbaro M, et al
    Altered lipid metabolism could drive the bone marrow failure in fanconi anaemia.
    Br J Haematol. 2019;184:693-696.

  145. DARBARI DS, Liljencrantz J, Ikechi A, Martin S, et al
    Pain and opioid use after reversal of sickle cell disease following HLA-matched sibling haematopoietic stem cell transplant.
    Br J Haematol. 2019;184:690-693.

  146. MARKUS C, Saxon B, Metz M
    Ferritin as a functional biomarker of iron status in children and young adults.
    Br J Haematol. 2019;184:640-642.

  147. MALINOWSKI AK, Cheung P, Yang J, D'Souza R, et al
    Cord gas parameters in infants born to women with sickle cell disease: a retrospective matched cohort study.
    Br J Haematol. 2019;184:653-657.

  148. MAJUMDAR S, Tirona R, Mashegu H, Desai J, et al
    A phase 1 dose-finding study of intravenous L-citrulline in sickle cell disease: a potential novel therapy for sickle cell pain crisis.
    Br J Haematol. 2019;184:634-636.

    January 2019
  149. BARTELS M, Bierings M
    How I manage children with Diamond-Blackfan anaemia.
    Br J Haematol. 2019;184:123-133.
    PubMed     Abstract available

  150. ALEXANDRE-HEYMANN L, Dubert M, Diallo DA, Diop S, et al
    Prevalence and correlates of growth failure in young African patients with sickle cell disease.
    Br J Haematol. 2019;184:253-262.
    PubMed     Abstract available

  151. THROWER A, Ciccone EJ, Maitra P, Derebail VK, et al
    Effect of renin-angiotensin-aldosterone system blocking agents on progression of glomerulopathy in sickle cell disease.
    Br J Haematol. 2019;184:246-252.
    PubMed     Abstract available

  152. KANTER J, Abboud MR, Kaya B, Nduba V, et al
    Ticagrelor does not impact patient-reported pain in young adults with sickle cell disease: a multicentre, randomised phase IIb study.
    Br J Haematol. 2019;184:269-278.
    PubMed     Abstract available

  153. SHAH A, Wray K, James T, Shine B, et al
    Serum hepcidin potentially identifies iron deficiency in survivors of critical illness at the time of hospital discharge.
    Br J Haematol. 2019;184:279-281.

    December 2018
  154. NAKAYAMA S, Taniguchi T, Tanaka H, Espinoza JL, et al
    Interleukin-17-producing angioimmunoblastic T-cell lymphoma with Evans syndrome.
    Br J Haematol. 2018 Dec 28. doi: 10.1111/bjh.15733.

  155. PARK S, Greenberg P, Yucel A, Farmer C, et al
    Clinical effectiveness and safety of erythropoietin-stimulating agents for the treatment of low- and intermediate-1-risk myelodysplastic syndrome: a systematic literature review.
    Br J Haematol. 2018 Dec 13. doi: 10.1111/bjh.15707.
    PubMed     Abstract available

    November 2018
  156. YANAMANDRA U, Senee H, Yanamadra S, Das SK, et al
    Erythropoietin and ferritin response in native highlanders aged 4-19 years from the Leh-Ladakh region of India.
    Br J Haematol. 2018 Nov 26. doi: 10.1111/bjh.15553.
    PubMed     Abstract available

    June 2018
  157. HAN J, Zhang X, Saraf SL, Gowhari M, et al
    Risk factors for vitamin D deficiency in sickle cell disease.
    Br J Haematol. 2018;181:828-835.
    PubMed     Abstract available

  158. GUEDENEY P, Lionnet F, Ceccaldi A, Stankovic Stojanovic K, et al
    Cardiac manifestations in sickle cell disease varies with patient genotype.
    Br J Haematol. 2018;181:664-671.
    PubMed     Abstract available

  159. KARAFIN MS, Westlake M, Hauser RG, Tormey CA, et al
    Risk factors for red blood cell alloimmunization in the Recipient Epidemiology and Donor Evaluation Study (REDS-III) database.
    Br J Haematol. 2018;181:672-681.
    PubMed     Abstract available

    May 2018
  160. QURESHI A, Kaya B, Pancham S, Keenan R, et al
    Guidelines for the use of hydroxycarbamide in children and adults with sickle cell disease: A British Society for Haematology Guideline.
    Br J Haematol. 2018;181:460-475.

  161. SAULTIER P, Loosveld M, Benoist JF, Michel G, et al
    Pancytopenia and megaloblastic erythropoiesis reveal a novel GIF mutation.
    Br J Haematol. 2018;181:304.

    How I manage patients with cold agglutinin disease.
    Br J Haematol. 2018;181:320-330.
    PubMed     Abstract available

  163. JONASSAINT CR, Birenboim A, Jorgensen DR, Novelli EM, et al
    The association of smartphone-based activity space measures with cognitive functioning and pain sickle cell disease.
    Br J Haematol. 2018;181:395-397.

  164. DAGUR PK, McCoy JP, Nichols J, Mendelsohn L, et al
    Haem augments and iron chelation decreases toll-like receptor 4 mediated inflammation in monocytes from sickle cell patients.
    Br J Haematol. 2018;181:552-554.

    April 2018
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    Renal protection by atorvastatin in a murine model of sickle cell nephropathy.
    Br J Haematol. 2018;181:111-121.
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  166. RANKINE-MULLINGS AE, Morrison-Levy N, Soares D, Aldred K, et al
    Transcranial Doppler velocity among Jamaican children with sickle cell anaemia: determining the significance of haematological values and nutrition.
    Br J Haematol. 2018;181:242-251.
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  167. SOUSOS N, Sinakos E, Klonizakis P, Adamidou D, et al
    Deferasirox improves liver fibrosis in beta-thalassaemia major patients. A five-year longitudinal study from a single thalassaemia centre.
    Br J Haematol. 2018;181:140-142.

    March 2018
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    Platelets at the crossroads of thrombosis, inflammation and haemolysis.
    Br J Haematol. 2018;180:761-767.
    PubMed     Abstract available

  169. RICCHI P, Meloni A, Spasiano A, Costantini S, et al
    The impact of liver steatosis on the ability of serum ferritin levels to be predictive of liver iron concentration in non-transfusion-dependent thalassaemia patients.
    Br J Haematol. 2018;180:721-726.
    PubMed     Abstract available

  170. JIANG Z, Luo HY, Farrell JJ, Zhang Z, et al
    A variant Sp1 (R218Q) transcription factor might enhance HbF expression in beta(0) -thalassaemia homozygotes.
    Br J Haematol. 2018;180:755-757.

  171. PEPE A, Gamberini MR, Missere M, Pistoia L, et al
    Gender differences in the development of cardiac complications: a multicentre study in a large cohort of thalassaemia major patients to optimize the timing of cardiac follow-up.
    Br J Haematol. 2018;180:879-888.
    PubMed     Abstract available

  172. KERAGALA CB, Draxler DF, McQuilten ZK, Medcalf RL, et al
    Haemostasis and innate immunity - a complementary relationship: A review of the intricate relationship between coagulation and complement pathways.
    Br J Haematol. 2018;180:782-798.
    PubMed     Abstract available

    February 2018
  173. TJON JM, de Groot MR, Sypkens Smit SMA, de Wreede LC, et al
    Short-term efficacy and safety of antithymocyte globulin treatment in elderly patients with acquired aplastic anaemia.
    Br J Haematol. 2018;180:459-462.

  174. REES DC, Robinson S, Howard J
    How I manage red cell transfusions in patients with sickle cell disease.
    Br J Haematol. 2018;180:607-617.
    PubMed     Abstract available

  175. WILLEN SM, Rodeghier M, Strunk RC, Bacharier LB, et al
    Aeroallergen sensitization predicts acute chest syndrome in children with sickle cell anaemia.
    Br J Haematol. 2018;180:571-577.
    PubMed     Abstract available

  176. EKONG A, Berg L, Amos RJ, Tsitsikas DA, et al
    Regular automated red cell exchange transfusion in the management of stuttering priapism complicating sickle cell disease.
    Br J Haematol. 2018;180:585-588.

  177. VACLAVU L, Baldew ZAV, Gevers S, Mutsaerts HJMM, et al
    Intracranial 4D flow magnetic resonance imaging reveals altered haemodynamics in sickle cell disease.
    Br J Haematol. 2018;180:432-442.
    PubMed     Abstract available

    January 2018
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    Paediatric amendment to adult BSH Guidelines for aplastic anaemia.
    Br J Haematol. 2018;180:201-205.

  179. WONKAM A, Mnika K, Ngo Bitoungui VJ, Chetcha Chemegni B, et al
    Clinical and genetic factors are associated with pain and hospitalisation rates in sickle cell anaemia in Cameroon.
    Br J Haematol. 2018;180:134-146.
    PubMed     Abstract available

  180. PAIKARI A, Sheehan VA
    Fetal haemoglobin induction in sickle cell disease.
    Br J Haematol. 2018;180:189-200.
    PubMed     Abstract available

  181. CREASEY T, Biss T, Lambert J, Smith F, et al
    Pyridoxine-sensitive X-linked 'sideroblastic' anaemia in the absence of ring sideroblasts - molecular diagnosis.
    Br J Haematol. 2018;180:10.

  182. BIERINGS M, Bonfim C, Peffault De Latour R, Aljurf M, et al
    Transplant results in adults with Fanconi anaemia.
    Br J Haematol. 2018;180:100-109.
    PubMed     Abstract available

  183. CLARK B, Shooter C, Smith F, Brawand D, et al
    Beta thalassaemia intermedia due to co-inheritance of three unique alpha globin cluster duplications characterised by next generation sequencing analysis.
    Br J Haematol. 2018;180:160-164.

    December 2017
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    Association of aplastic anaemia and lymphoma: a report from the severe aplastic anaemia working party of the European Society of Blood and Bone Marrow Transplantation.
    Br J Haematol. 2017 Dec 19. doi: 10.1111/bjh.15074.

  185. NAIR M, Churchill D, Robinson S, Nelson-Piercy C, et al
    Association between maternal haemoglobin and stillbirth: a cohort study among a multi-ethnic population in England.
    Br J Haematol. 2017;179:829-837.
    PubMed     Abstract available

  186. HAYMANN JP, Hammoudi N, Stankovic Stojanovic K, Galacteros F, et al
    Renin-angiotensin system blockade promotes a cardio-renal protection in albuminuric homozygous sickle cell patients.
    Br J Haematol. 2017;179:820-828.
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    November 2017
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    Erythrophagocytosis by T-cell lymphoma cells in a patient with hereditary spherocytosis post-splenectomy.
    Br J Haematol. 2017 Nov 16. doi: 10.1111/bjh.15028.

  188. BREWIN J, Kaya B, Chakravorty S
    How I manage sickle cell patients with high transcranial doppler results.
    Br J Haematol. 2017;179:377-388.
    PubMed     Abstract available

  189. ZAPPIA KJ, Guo Y, Retherford D, Wandersee NJ, et al
    Characterization of a mouse model of sickle cell trait: parallels to human trait and a novel finding of cutaneous sensitization.
    Br J Haematol. 2017;179:657-666.
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  190. WINCHENNE A, Cecchini J, Deux JF, De Prost N, et al
    A clinical risk score for pulmonary artery thrombosis during acute chest syndrome in adult patients with sickle cell disease.
    Br J Haematol. 2017;179:627-634.
    PubMed     Abstract available

  191. SACHDEV V, Sidenko S, Wu MD, Minniti CP, et al
    Skeletal and myocardial microvascular blood flow in hydroxycarbamide-treated patients with sickle cell disease.
    Br J Haematol. 2017;179:648-656.
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  192. MICHELOZZI IM, Pievani A, Pagni F, Antolini L, et al
    Human aplastic anaemia-derived mesenchymal stromal cells form functional haematopoietic stem cell niche in vivo.
    Br J Haematol. 2017;179:669-673.

    October 2017
  193. CABANAS-PEDRO AC, Roizenblatt S, de Souza AAL, Tufik S, et al
    Periodic limb movement in sleep and sickle cell disease: a neglected association?
    Br J Haematol. 2017;179:154-157.
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  194. VASSEUR C, Domingues-Hamdi E, Ledudal K, Le Corvoisier P, et al
    Red blood cells free alpha-haemoglobin pool: a biomarker to monitor the beta-thalassemia intermedia variability. The ALPHAPOOL study.
    Br J Haematol. 2017;179:142-153.
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  195. AL BALUSHI HWM, Wali Y, Al Awadi M, Al-Subhi T, et al
    The super sickling haemoglobin HbS-Oman: a study of red cell sickling, K+ permeability and associations with disease severity in patients heterozygous for HbA and HbS-Oman (HbA/S-Oman genotype).
    Br J Haematol. 2017;179:256-265.
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  196. KORMANN R, Jannot AS, Narjoz C, Ribeil JA, et al
    Roles of APOL1 G1 and G2 variants in sickle cell disease patients: kidney is the main target.
    Br J Haematol. 2017;179:323-335.
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    September 2017
  197. DI MAGGIO R, Maggio A
    The new era of chelation treatments: effectiveness and safety of 10 different regimens for controlling iron overloading in thalassaemia major.
    Br J Haematol. 2017;178:676-688.
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  198. NARITA A, Muramatsu H, Okuno Y, Sekiya Y, et al
    Development of clinical paroxysmal nocturnal haemoglobinuria in children with aplastic anaemia.
    Br J Haematol. 2017;178:954-958.
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  199. PUNARO E, Feltrin KY, Reis F
    Magnetic resonance imaging in acaeruloplasminaemia - a rare differential diagnosis of microcytic anaemia with iron overload.
    Br J Haematol. 2017;178:837.

    August 2017
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    Telomere length and somatic mutations in correlation with response to immunosuppressive treatment in aplastic anaemia.
    Br J Haematol. 2017;178:603-615.
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  201. GEARD A, Pule GD, Chetcha Chemegni B, Ngo Bitoungui VJ, et al
    Clinical and genetic predictors of renal dysfunctions in sickle cell anaemia in Cameroon.
    Br J Haematol. 2017;178:629-639.
    PubMed     Abstract available

  202. MOCKESCH B, Connes P, Charlot K, Skinner S, et al
    Association between oxidative stress and vascular reactivity in children with sickle cell anaemia and sickle haemoglobin C disease.
    Br J Haematol. 2017;178:468-475.
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  203. BROWN FC, Collett M, Tremblay CS, Rank G, et al
    Loss of Dynamin 2 GTPase function results in microcytic anaemia.
    Br J Haematol. 2017;178:616-628.
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  204. LANCELOT M, White J, Sarnaik S, Hines P, et al
    Low molecular weight heparin inhibits sickle erythrocyte adhesion to VCAM-1 through VLA-4 blockade in a standardized microfluidic flow adhesion assay.
    Br J Haematol. 2017;178:479-481.

  205. ROSE C, Callebaut I, Pascal L, Oudin C, et al
    Lethal ALAS2 mutation in males X-linked sideroblastic anaemia.
    Br J Haematol. 2017;178:648-651.

  206. FISHER AE, Oduro AKY, Adzaku F, Telfer P, et al
    Presentations of sickle cell disease patients to hospital in Ghana: key findings from a preliminary study at Volta Regional Hospital.
    Br J Haematol. 2017;178:489-491.

    July 2017
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    How I manage patients with Fanconi anaemia.
    Br J Haematol. 2017;178:32-47.
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  208. BRUNSON A, Lei A, Rosenberg AS, White RH, et al
    Increased incidence of VTE in sickle cell disease patients: risk factors, recurrence and impact on mortality.
    Br J Haematol. 2017;178:319-326.
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  209. CHELI E, Roze J, Garrot T, Tagarist S, et al
    Usefulness of the EMA flow cytometric test in the diagnosis of hereditary spherocytosis post-transfusion.
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    June 2017
  210. DUCASSOU S, Leverger G, Fernandes H, Chambost H, et al
    Benefits of rituximab as a second-line treatment for autoimmune haemolytic anaemia in children: a prospective French cohort study.
    Br J Haematol. 2017;177:751-758.
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  211. COATES TD, Wood JC
    How we manage iron overload in sickle cell patients.
    Br J Haematol. 2017;177:703-716.
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  212. MAKUBI A, Roberts DJ
    Investigation and treatment for iron deficiency in heart failure: the unmet need in Lower and Middle Income Countries.
    Br J Haematol. 2017;177:896-904.
    PubMed     Abstract available

  213. TUBMAN VN, Makani J
    Turf wars: exploring splenomegaly in sickle cell disease in malaria-endemic regions.
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  214. JONKER FAM, Te Poel E, Bates I, Boele van Hensbroek M, et al
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  215. TLUWAY F, Makani J
    Sickle cell disease in Africa: an overview of the integrated approach to health, research, education and advocacy in Tanzania, 2004-2016.
    Br J Haematol. 2017;177:919-929.
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  216. MWANGI MN, Prentice AM, Verhoef H
    Safety and benefits of antenatal oral iron supplementation in low-income countries: a review.
    Br J Haematol. 2017;177:884-895.
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  217. MAKUBI A, Mmbando BP, Novelli EM, Lwakatare J, et al
    Rates and risk factors of hypertension in adolescents and adults with sickle cell anaemia in Tanzania: 10 years' experience.
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  218. MACKAREL J, Iatan M, Kumar L, Storey L, et al
    In support of upfront stem cell transplantation as first-line therapy for paediatric patients with idiopathic severe aplastic anaemia who lack a sibling donor.
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    May 2017
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    British Committee for Standards in Haematology guidelines for aplastic anemia: Single centre retrospective review finds no compelling evidence for the recommended higher platelet count threshold of 20 x 109 /L - RESPONSE to Yan et al.
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  220. ALLALI S, Peyrard T, Amiranoff D, Cohen JF, et al
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  221. CYBULSKA A, Meintker L, Ringwald J, Krause SW, et al
    Measurements of immature platelets with haematology analysers are of limited value to separate immune thrombocytopenia from bone marrow failure.
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    The genomics of inherited bone marrow failure: from mechanism to the clinic.
    Br J Haematol. 2017;177:526-542.
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