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Articles published in Br J Haematol

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Single Articles


    February 2018
  1. 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.
    PubMed     Text format    


  2. 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     Text format     Abstract available


  3. 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     Text format     Abstract available


  4. 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.
    PubMed     Text format    


  5. 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     Text format     Abstract available


    January 2018
  6. SAMARASINGHE S, Veys P, Vora A, Wynn R, et al
    Paediatric amendment to adult BSH Guidelines for aplastic anaemia.
    Br J Haematol. 2018;180:201-205.
    PubMed     Text format    


  7. 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     Text format     Abstract available


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


  9. 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.
    PubMed     Text format    


  10. 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     Text format     Abstract available


  11. 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.
    PubMed     Text format    


    December 2017
  12. 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     Text format     Abstract available


  13. 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.
    PubMed     Text format     Abstract available


    November 2017
  14. 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     Text format     Abstract available


  15. 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.
    PubMed     Text format     Abstract available


  16. 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     Text format     Abstract available


  17. 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.
    PubMed     Text format     Abstract available


  18. 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.
    PubMed     Text format    


    October 2017
  19. 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.
    PubMed     Text format     Abstract available


  20. 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.
    PubMed     Text format     Abstract available


  21. 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.
    PubMed     Text format     Abstract available


  22. 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.
    PubMed     Text format     Abstract available


    September 2017
  23. 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.
    PubMed     Text format     Abstract available


  24. 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.
    PubMed     Text format     Abstract available


  25. 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.
    PubMed     Text format    


    August 2017
  26. PARK HS, Park SN, Im K, Kim SM, et al
    Telomere length and somatic mutations in correlation with response to immunosuppressive treatment in aplastic anaemia.
    Br J Haematol. 2017;178:603-615.
    PubMed     Text format     Abstract available


  27. 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     Text format     Abstract available


  28. 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.
    PubMed     Text format     Abstract available


  29. 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.
    PubMed     Text format     Abstract available


  30. 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.
    PubMed     Text format    


  31. 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.
    PubMed     Text format    


  32. 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.
    PubMed     Text format    


    July 2017
  33. DUFOUR C
    How I manage patients with Fanconi anaemia.
    Br J Haematol. 2017;178:32-47.
    PubMed     Text format     Abstract available


  34. 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.
    PubMed     Text format     Abstract available


  35. 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.
    Br J Haematol. 2017;178:180.
    PubMed     Text format    


    June 2017
  36. 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.
    PubMed     Text format     Abstract available


  37. COATES TD, Wood JC
    How we manage iron overload in sickle cell patients.
    Br J Haematol. 2017;177:703-716.
    PubMed     Text format     Abstract available


  38. 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     Text format     Abstract available


  39. TUBMAN VN, Makani J
    Turf wars: exploring splenomegaly in sickle cell disease in malaria-endemic regions.
    Br J Haematol. 2017;177:938-946.
    PubMed     Text format     Abstract available


  40. JONKER FAM, Te Poel E, Bates I, Boele van Hensbroek M, et al
    Anaemia, iron deficiency and susceptibility to infection in children in sub-Saharan Africa, guideline dilemmas.
    Br J Haematol. 2017;177:878-883.
    PubMed     Text format     Abstract available


  41. 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.
    PubMed     Text format     Abstract available


  42. 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.
    PubMed     Text format     Abstract available


  43. 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.
    Br J Haematol. 2017;177:930-937.
    PubMed     Text format     Abstract available


  44. 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.
    Br J Haematol. 2017;177:806-808.
    PubMed     Text format    


    May 2017
  45. KILLICK SB, Bown N, Cavenagh J, Dokal I, et al
    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.
    Br J Haematol. 2017 May 23. doi: 10.1111/bjh.14766.
    PubMed     Text format    


  46. ALLALI S, Peyrard T, Amiranoff D, Cohen JF, et al
    Prevalence and risk factors for red blood cell alloimmunization in 175 children with sickle cell disease in a French university hospital reference centre.
    Br J Haematol. 2017;177:641-647.
    PubMed     Text format     Abstract available


  47. 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.
    Br J Haematol. 2017;177:612-619.
    PubMed     Text format     Abstract available


  48. HOPPE C, Jacob E, Styles L, Kuypers F, et al
    Simvastatin reduces vaso-occlusive pain in sickle cell anaemia: a pilot efficacy trial.
    Br J Haematol. 2017;177:620-629.
    PubMed     Text format     Abstract available


  49. WEGMAN-OSTROSKY T, Savage SA
    The genomics of inherited bone marrow failure: from mechanism to the clinic.
    Br J Haematol. 2017;177:526-542.
    PubMed     Text format     Abstract available


  50. STANLEY N, Olson TS, Babushok DV
    Recent advances in understanding clonal haematopoiesis in aplastic anaemia.
    Br J Haematol. 2017;177:509-525.
    PubMed     Text format     Abstract available


  51. MEUNIER B, Loosveld M, Grados A, Rico A, et al
    Bone marrow erythrophagocytosis and reticulocytopenia in autoimmune haemolytic anaemia.
    Br J Haematol. 2017;177:346.
    PubMed     Text format    


  52. CHARLOT K, Hierso R, Lemonne N, Romana M, et al
    Changes in autonomic nervous activity during vaso-occlusive crisis in patients with sickle cell anaemia.
    Br J Haematol. 2017;177:484-486.
    PubMed     Text format    


    April 2017
  53. SINAKOS E, Kountouras D, Koskinas J, Zachou K, et al
    Treatment of chronic hepatitis C with direct-acting antivirals in patients with beta-thalassaemia major and advanced liver disease.
    Br J Haematol. 2017 Apr 25. doi: 10.1111/bjh.14640.
    PubMed     Text format     Abstract available


  54. HOSOKAWA K, Kajigaya S, Keyvanfar K, Qiao W, et al
    Whole transcriptome sequencing identifies increased CXCR2 expression in PNH granulocytes.
    Br J Haematol. 2017;177:136-141.
    PubMed     Text format     Abstract available


  55. BHATIA P, Singh A, Hegde A, Jain R, et al
    Systematic evaluation of paediatric cohort with iron refractory iron deficiency anaemia (IRIDA) phenotype reveals multiple TMPRSS6 gene variations.
    Br J Haematol. 2017;177:311-318.
    PubMed     Text format     Abstract available


  56. KULASEKARARAJ AG
    Clonal dominance of PNH- another piece to the jigsaw.
    Br J Haematol. 2017;177:9-10.
    PubMed     Text format    


  57. PIPPARD MJ
    Microcytic anaemias in childhood and iron-refractory iron deficiency anaemia.
    Br J Haematol. 2017;177:167-168.
    PubMed     Text format    


  58. HILL QA, Stamps R, Massey E, Grainger JD, et al
    Guidelines on the management of drug-induced immune and secondary autoimmune, haemolytic anaemia.
    Br J Haematol. 2017;177:208-220.
    PubMed     Text format    


  59. KAWADLER JM, Clark CA, McKinstry RC, Kirkham FJ, et al
    Brain atrophy in paediatric sickle cell anaemia: findings from the silent infarct transfusion (SIT) trial.
    Br J Haematol. 2017;177:151-153.
    PubMed     Text format    


    March 2017
  60. PUREV E, Tian X, Aue G, Pantin J, et al
    Allogeneic transplantation using CD34+ selected peripheral blood progenitor cells combined with non-mobilized donor T cells for refractory severe aplastic anaemia.
    Br J Haematol. 2017;176:950-960.
    PubMed     Text format     Abstract available


  61. LU J, Lee JH, Huang SY, Qiu L, et al
    Continuous treatment with lenalidomide and low-dose dexamethasone in transplant-ineligible patients with newly diagnosed multiple myeloma in Asia: subanalysis of the FIRST trial.
    Br J Haematol. 2017;176:743-749.
    PubMed     Text format     Abstract available


  62. HIERSO R, Lemonne N, Villaescusa R, Lalanne-Mistrih ML, et al
    Exacerbation of oxidative stress during sickle vaso-occlusive crisis is associated with decreased anti-band 3 autoantibodies rate and increased red blood cell-derived microparticle level: a prospective study.
    Br J Haematol. 2017;176:805-813.
    PubMed     Text format     Abstract available


  63. TAHER AT
    Clinical utility of serum ferritin thresholds for guiding iron chelation therapy when magnetic resonance imaging is unavailable in patients with non-transfusion-dependent thalassaemias - response to Ang et al.
    Br J Haematol. 2017;176:989-990.
    PubMed     Text format    


  64. GILL H, Leung GM, Lopes D, Kwong YL, et al
    The thrombopoietin mimetics eltrombopag and romiplostim in the treatment of refractory aplastic anaemia.
    Br J Haematol. 2017;176:991-994.
    PubMed     Text format    


  65. WU MY, He Y, Yan JM, Li DZ, et al
    A novel selective deletion of the major alpha-globin regulatory element (MCS-R2) causing alpha-thalassaemia.
    Br J Haematol. 2017;176:984-986.
    PubMed     Text format    


    February 2017
  66. DRASAR E, Fitzpatrick E, Gardner K, Awogbade M, et al
    Interim assessment of liver damage in patients with sickle cell disease using new non-invasive techniques.
    Br J Haematol. 2017;176:643-650.
    PubMed     Text format     Abstract available


  67. PECKER LH, Schaefer BA, Luchtman-Jones L
    Knowledge insufficient: the management of haemoglobin SC disease.
    Br J Haematol. 2017;176:515-526.
    PubMed     Text format     Abstract available


  68. MANARA R, Talenti G, Rampazzo P, Ermani M, et al
    Longitudinal evaluation of cerebral white matter hyperintensities lesion volume in children with sickle cell disease.
    Br J Haematol. 2017;176:485-487.
    PubMed     Text format    


  69. HILL QA, Stamps R, Massey E, Grainger JD, et al
    The diagnosis and management of primary autoimmune haemolytic anaemia.
    Br J Haematol. 2017;176:395-411.
    PubMed     Text format    


  70. BABUSHOK DV, Stanley N, Xie HM, Huang H, et al
    Clonal Replacement Underlies Spontaneous Remission in Paroxysmal Nocturnal Haemoglobinuria.
    Br J Haematol. 2017;176:487-490.
    PubMed     Text format    


    January 2017
  71. VITRANO A, Calvaruso G, Lai E, Colletta G, et al
    The era of comparable life expectancy between thalassaemia major and intermedia: Is it time to revisit the major-intermedia dichotomy?
    Br J Haematol. 2017;176:124-130.
    PubMed     Text format     Abstract available


  72. PORTER JB, Cappellini MD, Kattamis A, Viprakasit V, et al
    Iron overload across the spectrum of non-transfusion-dependent thalassaemias: role of erythropoiesis, splenectomy and transfusions.
    Br J Haematol. 2017;176:288-299.
    PubMed     Text format     Abstract available


  73. KOSINSKI PD, Croal PL, Leung J, Williams S, et al
    The severity of anaemia depletes cerebrovascular dilatory reserve in children with sickle cell disease: a quantitative magnetic resonance imaging study.
    Br J Haematol. 2017;176:280-287.
    PubMed     Text format     Abstract available


  74. DOWLING MM, Quinn CT, Ramaciotti C, Kanter J, et al
    Increased prevalence of potential right-to-left shunting in children with sickle cell anaemia and stroke.
    Br J Haematol. 2017;176:300-308.
    PubMed     Text format     Abstract available


  75. GUIDOTTI F, Piatti G, Marcon A, Cassinerio E, et al
    Pulmonary dysfunction in thalassaemia major: is there any relationship with body iron stores?
    Br J Haematol. 2017;176:309-314.
    PubMed     Text format     Abstract available


  76. DOWLING MM, Kirkham FJ
    Stroke in sickle cell anaemia is more than stenosis and thrombosis: the role of anaemia and hyperemia in ischaemia.
    Br J Haematol. 2017;176:151-153.
    PubMed     Text format    


  77. DAVIS BA, Allard S, Qureshi A, Porter JB, et al
    Guidelines on red cell transfusion in sickle cell disease. Part I: principles and laboratory aspects.
    Br J Haematol. 2017;176:179-191.
    PubMed     Text format    


  78. DAVIS BA, Allard S, Qureshi A, Porter JB, et al
    Guidelines on red cell transfusion in sickle cell disease Part II: indications for transfusion.
    Br J Haematol. 2017;176:192-209.
    PubMed     Text format    


  79. LA GIOIA A, Bombara M, Fiorini F, Fiorini M, et al
    Pseudo-Chediak-Higashi granules and other unusual cytoplasmic inclusions in refractory anaemia with excess blasts-2.
    Br J Haematol. 2017;176:156.
    PubMed     Text format    


    June 2016
  80. COUQUE N, Girard D, Ducrocq R, Boizeau P, et al
    Improvement of medical care in a cohort of newborns with sickle-cell disease in North Paris: impact of national guidelines.
    Br J Haematol. 2016;173:927-37.
    PubMed     Text format     Abstract available


  81. THOMAS MR, Robinson S, Scully MA
    How we manage thrombotic microangiopathies in pregnancy.
    Br J Haematol. 2016;173:821-30.
    PubMed     Text format     Abstract available


  82. KORDE N, Zhang Y, Loeliger K, Poon A, et al
    Monoclonal gammopathy-associated pure red cell aplasia.
    Br J Haematol. 2016;173:876-83.
    PubMed     Text format     Abstract available


    May 2016
  83. ASNANI M, Serjeant G, Royal-Thomas T, Reid M, et al
    Predictors of renal function progression in adults with homozygous sickle cell disease.
    Br J Haematol. 2016;173:461-8.
    PubMed     Text format     Abstract available


  84. LEONARDO FC, Brugnerotto AF, Domingos IF, Fertrin KY, et al
    Reduced rate of sickle-related complications in Brazilian patients carrying HbF-promoting alleles at the BCL11A and HMIP-2 loci.
    Br J Haematol. 2016;173:456-60.
    PubMed     Text format     Abstract available


    April 2016
  85. SANDOR B, Marin M, Lapoumeroulie C, Rabai M, et al
    Effects of Poloxamer 188 on red blood cell membrane properties in sickle cell anaemia.
    Br J Haematol. 2016;173:145-9.
    PubMed     Text format     Abstract available


  86. RIDER TG, Grace RJ, Newman JA
    Autoimmune haemolytic anaemia occurring during ibrutinib therapy for chronic lymphocytic leukaemia.
    Br J Haematol. 2016;173:326-7.
    PubMed     Text format    


  87. DANILOV AV
    Autoimmune haemolytic anaemia occurring during ibrutinib therapy for chronic lymphocytic leukaemia--response to Rider et al.
    Br J Haematol. 2016;173:327-8.
    PubMed     Text format    


    March 2016
  88. QUARELLO P, Garelli E, Carando A, Mancini C, et al
    Ribosomal RNA analysis in the diagnosis of Diamond-Blackfan Anaemia.
    Br J Haematol. 2016;172:782-5.
    PubMed     Text format     Abstract available


  89. JIANG Z, Luo HY, Huang S, Farrell JJ, et al
    The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) beta(0) -thalassaemia homozygotes.
    Br J Haematol. 2016;172:958-65.
    PubMed     Text format     Abstract available


  90. SOMMET J, Alberti C, Couque N, Verlhac S, et al
    Clinical and haematological risk factors for cerebral macrovasculopathy in a sickle cell disease newborn cohort: a prospective study.
    Br J Haematol. 2016;172:966-77.
    PubMed     Text format     Abstract available


    February 2016
  91. MIANO M
    How I manage Evans Syndrome and AIHA cases in children.
    Br J Haematol. 2016;172:524-34.
    PubMed     Text format     Abstract available


  92. CAMASCHELLA C, Nai A
    Ineffective erythropoiesis and regulation of iron status in iron loading anaemias.
    Br J Haematol. 2016;172:512-23.
    PubMed     Text format     Abstract available


  93. RIVAS-DELGADO A, Matutes E, Rozman M
    Recurrent pure red cell aplasia in a hepatorenal transplant recipient with chronic parvovirus B19 infection.
    Br J Haematol. 2016;172:495.
    PubMed     Text format    


    January 2016
  94. KILLICK SB, Bown N, Cavenagh J, Dokal I, et al
    Guidelines for the diagnosis and management of adult aplastic anaemia.
    Br J Haematol. 2016;172:187-207.
    PubMed     Text format    


  95. VAN DER LAND V, Mutsaerts HJ, Engelen M, Heijboer H, et al
    Risk factor analysis of cerebral white matter hyperintensities in children with sickle cell disease.
    Br J Haematol. 2016;172:274-84.
    PubMed     Text format     Abstract available


  96. RUGGERI M, Rodeghiero F
    Thrombotic risk in patients with immune haemolytic anaemia.
    Br J Haematol. 2016;172:144-6.
    PubMed     Text format    


  97. WOOD JC, Cohen AR, Pressel SL, Aygun B, et al
    Organ iron accumulation in chronically transfused children with sickle cell anaemia: baseline results from the TWiTCH trial.
    Br J Haematol. 2016;172:122-30.
    PubMed     Text format     Abstract available


  98. INAGUMA Y, Akatsuka Y, Hosokawa K, Maruyama H, et al
    Induction of HLA-B*40:02-restricted T cells possessing cytotoxic and suppressive functions against haematopoietic progenitor cells from a patient with severe aplastic anaemia.
    Br J Haematol. 2016;172:131-4.
    PubMed     Text format    


    November 2015
  99. KOTZE A, Harris A, Baker C, Iqbal T, et al
    British Committee for Standards in Haematology Guidelines on the Identification and Management of Pre-Operative Anaemia.
    Br J Haematol. 2015;171:322-31.
    PubMed     Text format    


  100. SALIM O, Yucel OK, Karatas G, Alan S, et al
    Cutaneous thrombosis as the presenting finding of paroxysmal nocturnal haemoglobinuria.
    Br J Haematol. 2015;171:296.
    PubMed     Text format    


  101. LIU Q, Zhao X, Xu N, Huang P, et al
    Frontline therapy of severe aplastic anaemia with fludarabine, cyclophosphamide and ciclosporin.
    Br J Haematol. 2015;171:427-30.
    PubMed     Text format    


    October 2015
  102. CHIRICO V, Lacquaniti A, Piraino B, Cutrupi M, et al
    Thalassaemia major and infectious risk: High Mobility Group Box-1 represents a novel diagnostic and prognostic biomarker.
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  103. CANCIO MI, Helton KJ, Schreiber JE, Smeltzer MP, et al
    Silent cerebral infarcts in very young children with sickle cell anaemia are associated with a higher risk of stroke.
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    September 2015
  104. OLUWASANJO A, Alese O, Swierczynski S, Forman D, et al
    Rasburicase-induced methaemoglobinaemia and G6PD deficiency in an unusual suspect.
    Br J Haematol. 2015;170:595.
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  105. BROUSSE V, Kossorotoff M, de Montalembert M
    How I manage cerebral vasculopathy in children with sickle cell disease.
    Br J Haematol. 2015;170:615-25.
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  106. DIEP RT, Busani S, Simon J, Punzalan A, et al
    Cough and wheeze events are temporally associated with increased pain in individuals with sickle cell disease without asthma.
    Br J Haematol. 2015;170:732-4.
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  107. MANDA S, Dunbar N, Marx-Wood CR, Danilov AV, et al
    Ibrutinib is an effective treatment of autoimmune haemolytic anaemia in chronic lymphocytic leukaemia.
    Br J Haematol. 2015;170:734-6.
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  108. ATAGA KI, Stocker J
    The trials and hopes for drug development in sickle cell disease.
    Br J Haematol. 2015;170:768-80.
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  109. STEINBERG MH, Rodgers GP
    HbA2 : biology, clinical relevance and a possible target for ameliorating sickle cell disease.
    Br J Haematol. 2015;170:781-7.
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  110. SOBOTA A, Sabharwal V, Fonebi G, Steinberg M, et al
    How we prevent and manage infection in sickle cell disease.
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  111. MANTELLI M, Avanzini MA, Rosti V, Ingo DM, et al
    Comprehensive characterization of mesenchymal stromal cells from patients with Fanconi anaemia.
    Br J Haematol. 2015;170:826-36.
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  112. GARDNER K, Hoppe C, Mijovic A, Thein SL, et al
    How we treat delayed haemolytic transfusion reactions in patients with sickle cell disease.
    Br J Haematol. 2015;170:745-56.
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    August 2015
  113. CAUGHEY MC, Poole C, Ataga KI, Hinderliter AL, et al
    Estimated pulmonary artery systolic pressure and sickle cell disease: a meta-analysis and systematic review.
    Br J Haematol. 2015;170:416-24.
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  114. KUO KH, Ward R, Kaya B, Howard J, et al
    A comparison of chronic manual and automated red blood cell exchange transfusion in sickle cell disease patients.
    Br J Haematol. 2015;170:425-8.
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    July 2015
  115. WOLFROMM A, Rodriguez C, Michel M, Habibi A, et al
    Spectrum of adult Parvovirus B19 infection according to the underlying predisposing condition and proposals for clinical practice.
    Br J Haematol. 2015;170:192-9.
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  116. FORSTER L, McCooke J, Bellgard M, Joske D, et al
    Differential gene expression analysis in early and late erythroid progenitor cells in beta-thalassaemia.
    Br J Haematol. 2015;170:257-67.
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  117. NICKEL RS, Hendrickson JE, Yee MM, Bray RA, et al
    Red blood cell transfusions are associated with HLA class I but not H-Y alloantibodies in children with sickle cell disease.
    Br J Haematol. 2015;170:247-56.
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  118. WOOD JC
    Estimating tissue iron burden: current status and future prospects.
    Br J Haematol. 2015;170:15-28.
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  119. KEY NS, Connes P, Derebail VK
    Negative health implications of sickle cell trait in high income countries: from the football field to the laboratory.
    Br J Haematol. 2015;170:5-14.
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  120. SHOOTER C, Senior McKenzie T, Oakley M, Jacques T, et al
    First reported duplication of the entire beta globin gene cluster causing an unusual sickle cell trait phenotype.
    Br J Haematol. 2015;170:128-31.
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    June 2015
  121. MORRIS CR, Kim HY, Klings ES, Wood J, et al
    Dysregulated arginine metabolism and cardiopulmonary dysfunction in patients with thalassaemia.
    Br J Haematol. 2015;169:887-98.
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  122. MARTINEZ-GIRON R, Martinez-Torre S
    False positive cervical smear in a patient with pernicious anaemia.
    Br J Haematol. 2015;169:766.
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  123. HAMZIC E, Whiting K, Gordon Smith E, Pettengell R, et al
    Characterization of bone marrow mesenchymal stromal cells in aplastic anaemia.
    Br J Haematol. 2015;169:804-13.
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  124. STROCCHIO L, Zecca M, Comoli P, Mina T, et al
    Treosulfan-based conditioning regimen for allogeneic haematopoietic stem cell transplantation in children with sickle cell disease.
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  125. HIROKAWA M, Sawada K, Fujishima N, Teramura M, et al
    Long-term outcome of patients with acquired chronic pure red cell aplasia (PRCA) following immunosuppressive therapy: a final report of the nationwide cohort study in 2004/2006 by the Japan PRCA collaborative study group.
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  126. VIDLER JB, Gardner K, Amenyah K, Mijovic A, et al
    Delayed haemolytic transfusion reaction in adults with sickle cell disease: a 5-year experience.
    Br J Haematol. 2015;169:746-53.
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    May 2015
  127. HOWARD J, Hart N, Roberts-Harewood M, Cummins M, et al
    Guideline on the management of acute chest syndrome in sickle cell disease.
    Br J Haematol. 2015;169:492-505.
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  128. NICKEL RS, Osunkwo I, Garrett A, Robertson J, et al
    Immune parameter analysis of children with sickle cell disease on hydroxycarbamide or chronic transfusion therapy.
    Br J Haematol. 2015;169:574-83.
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  129. COLOMBATTI R, Ermani M, Rampazzo P, Manara R, et al
    Cognitive evoked potentials and neural networks are abnormal in children with sickle cell disease and not related to the degree of anaemia, pain and silent infarcts.
    Br J Haematol. 2015;169:597-600.
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    April 2015
  130. OTENG-NTIM E, Ayensah B, Knight M, Howard J, et al
    Pregnancy outcome in patients with sickle cell disease in the UK--a national cohort study comparing sickle cell anaemia (HbSS) with HbSC disease.
    Br J Haematol. 2015;169:129-37.
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  131. PENMAN BS, Gupta S, Weatherall DJ
    Epistasis and the sensitivity of phenotypic screens for beta thalassaemia.
    Br J Haematol. 2015;169:117-28.
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  132. WASSIE E, Finke C, Gangat N, Lasho TL, et al
    A compendium of cytogenetic abnormalities in myelofibrosis: molecular and phenotypic correlates in 826 patients.
    Br J Haematol. 2015;169:71-6.
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  133. DONKER AE, Brons PP, Swinkels DW
    Microcytic anaemia with low transferrin saturation, increased serum hepcidin and non-synonymous TMPRSS6 variants: not always iron-refractory iron deficiency anaemia.
    Br J Haematol. 2015;169:150-1.
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  134. HELLER M, Luckit J
    Bone marrow trephine track as incidental finding on CT scanning for anaemia and splenomegaly.
    Br J Haematol. 2015;169:155.
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  135. AYGUN B, Mortier NA, Kesler K, Lockhart A, et al
    Therapeutic phlebotomy is safe in children with sickle cell anaemia and can be effective treatment for transfusional iron overload.
    Br J Haematol. 2015;169:262-6.
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    March 2015
  136. WANG R, Yoshida K, Toki T, Sawada T, et al
    Loss of function mutations in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan anaemia.
    Br J Haematol. 2015;168:854-64.
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  137. WALLACE DF, Secondes ES, Rishi G, Ostini L, et al
    A critical role for murine transferrin receptor 2 in erythropoiesis during iron restriction.
    Br J Haematol. 2015;168:891-901.
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  138. PIGA A, Fracchia S, Lai ME, Cappellini MD, et al
    Deferasirox effect on renal haemodynamic parameters in patients with transfusion-dependent beta thalassaemia.
    Br J Haematol. 2015;168:882-90.
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    February 2015
  139. DUFOUR C, Pillon M, Socie G, Rovo A, et al
    Outcome of aplastic anaemia in children. A study by the severe aplastic anaemia and paediatric disease working parties of the European group blood and bone marrow transplant.
    Br J Haematol. 2015 Feb 14. doi: 10.1111/bjh.13297.
    PubMed     Text format     Abstract available


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