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Anemia

Free Subscription Articles published in Br J Haematol Retrieve available abstracts of 124 articles: HTML format Text format

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November 2011
1. ASHLEY-KOCH AE , Okocha EC, Garrett ME, Soldano K, et al
   MYH9 and APOL1 are both associated with sickle cell disease nephropathy.
   Br J Haematol. 2011;155:386-94.
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2. SHARPE CC , Thein SL
   Sickle cell nephropathy - a practical approach.
   Br J Haematol. 2011;155:287-97.
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   October 2011
3. QUINN CT , Stuart MJ, Kesler K, Ataga KI, et al
   Tapered oral dexamethasone for the acute chest syndrome of sickle cell disease.
   Br J Haematol. 2011;155:263-7.
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4. PELLAGATTI A , Cazzola M, Giagounidis A, Perry J, et al
   Marked down-regulation of nucleophosmin-1 is associated with advanced del(5q) myelodysplastic syndrome.
   Br J Haematol. 2011;155:272-4.
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5. STANKOVIC STOJANOVIC K , Thioliere B, Garandeau E, Lecomte I, et al
   Chronic myeloid leukaemia and sickle cell disease: could imatinib prevent vaso-occlusive crisis?
   Br J Haematol. 2011;155:271-2.
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   September 2011
6. GARBE E , Andersohn F, Bronder E, Klimpel A, et al
   Drug induced immune haemolytic anaemia in the Berlin Case-Control Surveillance Study.
   Br J Haematol. 2011;154:644-53.
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7. TUBSUWAN A , Munkongdee T, Jearawiriyapaisarn N, Boonchoy C, et al
   Molecular analysis of globin gene expression in different thalassaemia disorders: individual variation of beta(E) pre-mRNA splicing determine disease severity.
   Br J Haematol. 2011;154:635-43.
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8. LUCANIA G , Vitrano A, Filosa A, Maggio A, et al
   Chelation treatment in sickle-cell-anaemia: much ado about nothing?
   Br J Haematol. 2011;154:545-55.
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9. VOSKARIDOU E , Christoulas D, Terpos E
   Successful chelation therapy with the combination of deferasirox and deferiprone in a patient with thalassaemia major and persisting severe iron overload after single-agent chelation therapies.
   Br J Haematol. 2011;154:654-6.
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10. SMITH J , Rahilly M, Davidson K
    Extramedullary haematopoiesis secondary to hereditary spherocytosis.
    Br J Haematol. 2011;154:543.
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11. DRISS F , Moh-Klaren J, Pela AM, Tertian G, et al
    Regular automated erythrocytapheresis in sickle cell patients.
    Br J Haematol. 2011;154:656-9.
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    August 2011
12. CULLIS JO
    Diagnosis and management of anaemia of chronic disease: current status.
    Br J Haematol. 2011;154:289-300.
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13. VICHINSKY E , Bernaudin F, Forni GL, Gardner R, et al
    Long-term safety and efficacy of deferasirox (Exjade) for up to 5 years in transfusional iron-overloaded patients with sickle cell disease.
    Br J Haematol. 2011;154:387-97.
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14. BALAYSSAC-SIRANSY E , Connes P, Tuo N, Danho C, et al
    Mild haemorheological changes induced by a moderate endurance exercise in patients with sickle cell anaemia.
    Br J Haematol. 2011;154:398-407.
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15. GREEN L , De Lord C, Clark B, Cadet E, et al
    Transient aplastic crisis as presentation of a previously unknown G6PD deficiency with iron overload.
    Br J Haematol. 2011;154:288.
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16. MACHADO RF , Hildesheim M, Mendelsohn L, Remaley AT, et al
    NT-pro brain natriuretic peptide levels and the risk of death in the cooperative study of sickle cell disease.
    Br J Haematol. 2011;154:512-20.
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17. HANSON MS , Piknova B, Keszler A, Diers AR, et al
    Methaemalbumin formation in sickle cell disease: effect on oxidative protein modification and HO-1 induction.
    Br J Haematol. 2011;154:502-11.
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    July 2011
18. MCGANN PT , Howard TA, Flanagan JM, Lahti JM, et al
    Chromosome damage and repair in children with sickle cell anaemia and long-term hydroxycarbamide exposure.
    Br J Haematol. 2011;154:134-40.
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19. HODGSON K , Ferrer G, Pereira A, Moreno C, et al
    Autoimmune cytopenia in chronic lymphocytic leukaemia: diagnosis and treatment.
    Br J Haematol. 2011;154:14-22.
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20. SNOWDEN JA , Ahmedzai SH, Ashcroft J, D'Sa S, et al
    Guidelines for supportive care in multiple myeloma 2011.
    Br J Haematol. 2011;154:76-103.
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21. SILVY M , Di Cristofaro J, Beley S, Papa K, et al
    Identification of RHCE and KEL alleles in large cohorts of Afro-Caribbean and Comorian donors by multiplex SNaPshot and fragment assays: a transfusion support for sickle cell disease patients.
    Br J Haematol. 2011;154:260-70.
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22. MYERS KC , Bleesing JJ, Davies SM, Zhang X, et al
    Impaired immune function in children with Fanconi anaemia.
    Br J Haematol. 2011;154:234-40.
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23. GIULINO L , Guinan EC, Gillio AP, Drachtman RA, et al
    Sweet syndrome in patients with Fanconi anaemia: association with extracutaneous manifestations and progression of haematological disease.
    Br J Haematol. 2011;154:278-81.
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24. SINGER ST , Vichinsky EP, Sweeters N, Rachmilewitz E, et al
    Darbepoetin alfa for the treatment of anaemia in alpha- or beta- thalassaemia intermedia syndromes.
    Br J Haematol. 2011;154:281-4.
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    June 2011
25. HOPPE C , Kuypers F, Larkin S, Hagar W, et al
    A pilot study of the short-term use of simvastatin in sickle cell disease: effects on markers of vascular dysfunction.
    Br J Haematol. 2011;153:655-63.
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26. LUZZATTO L , Gianfaldoni G, Notaro R
    Management of paroxysmal nocturnal haemoglobinuria: a personal view.
    Br J Haematol. 2011;153:709-20.
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27. WOOD JC , Mo A, Gera A, Koh M, et al
    Quantitative computed tomography assessment of transfusional iron overload.
    Br J Haematol. 2011;153:780-5.
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28. LI J , Zhao Q, Xing W, Feng J, et al
    Interleukin-27 enhances the production of tumour necrosis factor-alpha and interferon-gamma by bone marrow T lymphocytes in aplastic anaemia.
    Br J Haematol. 2011;153:764-72.
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29. DARNIGE L , de Latour RP, Zemori L, Socie G, et al
    Antiphospholipid antibodies in patients with paroxysmal nocturnal haemoglobinuria receiving eculizumab.
    Br J Haematol. 2011;153:789-91.
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    May 2011
30. BERENTSEN S
    How I manage cold agglutinin disease.
    Br J Haematol. 2011;153:309-17.
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31. OSUNKWO I , Hodgman EI, Cherry K, Dampier C, et al
    Vitamin D deficiency and chronic pain in sickle cell disease.
    Br J Haematol. 2011;153:538-40.
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    April 2011
32. MOLLER HJ , Nielsen MJ, Bartram J, Dick MC, et al
    Soluble CD163 levels in children with sickle cell disease.
    Br J Haematol. 2011;153:105-10.
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33. QUINN CT , Johnson VL, Kim HY, Trachtenberg F, et al
    Renal dysfunction in patients with thalassaemia.
    Br J Haematol. 2011;153:111-7.
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34. THOMPSON AA , Cunningham MJ, Singer ST, Neufeld EJ, et al
    Red cell alloimmunization in a diverse population of transfused patients with thalassaemia.
    Br J Haematol. 2011;153:121-8.
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35. ATAGA KI , Reid M, Ballas SK, Yasin Z, et al
    Improvements in haemolysis and indicators of erythrocyte survival do not correlate with acute vaso-occlusive crises in patients with sickle cell disease: a phase III randomized, placebo-controlled, double-blind study of the Gardos channel blocker seni
    Br J Haematol. 2011;153:92-104.
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    March 2011
36. SARAF S , Farooqui M, Infusino G, Oza B, et al
    Standard clinical practice underestimates the role and significance of erythropoietin deficiency in sickle cell disease.
    Br J Haematol. 2011 Mar 21. doi: 10.1111/j.1365-2141.2010.08479.
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37. TAHER AT , Musallam KM, Cappellini MD, Weatherall DJ, et al
    Optimal management of beta thalassaemia intermedia.
    Br J Haematol. 2011;152:512-23.
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38. BEUTLER S , Beutler B
    Ernest Beutler: his life and contribution to medical science.
    Br J Haematol. 2011;152:543-50.
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39. KOZUMA Y , Sawahata Y, Takei Y, Chiba S, et al
    Procoagulant properties of microparticles released from red blood cells in paroxysmal nocturnal haemoglobinuria.
    Br J Haematol. 2011;152:631-9.
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40. TORIHARA H , Uechi T, Chakraborty A, Shinya M, et al
    Erythropoiesis failure due to RPS19 deficiency is independent of an activated Tp53 response in a zebrafish model of Diamond-Blackfan anaemia.
    Br J Haematol. 2011;152:648-54.
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41. WANG W , Brugnara C, Snyder C, Wynn L, et al
    The effects of hydroxycarbamide and magnesium on haemoglobin SC disease: results of the multi-centre CHAMPS trial.
    Br J Haematol. 2011;152:771-6.
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42. HAMMILL AM , Risinger MA, Joiner CH, Keddache M, et al
    Compound heterozygosity for two novel mutations in the erythrocyte protein 4.2 gene causing spherocytosis in a Caucasian patient.
    Br J Haematol. 2011;152:780-3.
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43. LEE P
    Response to the letter by Nicolas et al, BJH-2010-01422.
    Br J Haematol. 2011;152:785-6.
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44. DRASAR E , Igbineweka N, Vasavda N, Free M, et al
    Blood transfusion usage among adults with sickle cell disease - a single institution experience over ten years.
    Br J Haematol. 2011;152:766-70.
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    February 2011
45. PATRIZIA S , Arcangelo L, Carlo S
    Low dose intravenous bevacizumab for the treatment of anaemia in hereditary haemorrhagic telangiectasia.
    Br J Haematol. 2011;152:365.
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46. NICOLAS G , Deschemin JC, Ramsay AJ, Mayeux P, et al
    Is EPO therapy able to correct iron deficiency anaemia caused by matriptase-2 deficiency?
    Br J Haematol. 2011;152:498-500.
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    January 2011
47. RHODES M , Ashford L, Manes B, Calder C, et al
    Bone marrow transplantation in phosphoglycerate kinase (PGK) deficiency.
    Br J Haematol. 2011 Jan 11. doi: 10.1111/j.1365-2141.2010.08474.
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48. ATAGA KI , Brittain JE, Jones SK, May R, et al
    Association of soluble fms-like tyrosine kinase-1 with pulmonary hypertension and haemolysis in sickle cell disease.
    Br J Haematol. 2011 Jan 11. doi: 10.1111/j.1365-2141.2010.08410.
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49. ESKAZAN AE , Ar MC, Baslar Z
    Intracranial mass in a patient with thalassaemia major.
    Br J Haematol. 2011;152:126.
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50. NOETZLI LJ , Coates TD, Wood JC
    Pancreatic iron loading in chronically transfused sickle cell disease is lower than in thalassaemia major.
    Br J Haematol. 2011;152:229-33.
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51. RISITANO AM
    Immunosuppressive therapies in the management of immune-mediated marrow failures in adults: where we stand and where we are going.
    Br J Haematol. 2011;152:127-40.
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52. DANILOVA N , Sakamoto KM, Lin S
    Ribosomal protein L11 mutation in zebrafish leads to haematopoietic and metabolic defects.
    Br J Haematol. 2011;152:217-28.
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    December 2010
53. DALAL B , Al Riyami A, Yenson P
    Microangiopathic haemolytic anaemia and hyposplenism in angiosarcoma.
    Br J Haematol. 2010;151:413.
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54. SERJEANT GR
    One hundred years of sickle cell disease.
    Br J Haematol. 2010;151:425-9.
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55. RIGANO P , Pecoraro A, Calzolari R, Troia A, et al
    Desensitization to hydroxycarbamide following long-term treatment of thalassaemia intermedia as observed in vivo and in primary erythroid cultures from treated patients.
    Br J Haematol. 2010;151:509-15.
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56. MCMAHON L , Tamary H, Askin M, Adams-Graves P, et al
    A randomized phase II trial of Arginine Butyrate with standard local therapy in refractory sickle cell leg ulcers.
    Br J Haematol. 2010;151:516-24.
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57. LADIS V , Berdousi H, Gotsis E, Kattamis A, et al
    Deferasirox administration for the treatment of non-transfusional iron overload in patients with thalassaemia intermedia.
    Br J Haematol. 2010;151:504-8.
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    November 2010
58. ALI SB , Reid M, Fraser R, MooSang M, et al
    Seizures in the Jamaica cohort study of sickle cell disease.
    Br J Haematol. 2010;151:265-72.
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59. ALAHMAD A , Preuss KD, Schenk J, Fureder W, et al
    Desmoplakin and KIF20B as target antigens in patients with paroxysmal nocturnal haemoglobinuria.
    Br J Haematol. 2010;151:273-80.
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60. DELBINI P , Vaja V, Graziadei G, Duca L, et al
    Genetic variability of TMPRSS6 and its association with iron deficiency anaemia.
    Br J Haematol. 2010;151:281.
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61. CHOULIARAS GL , Kattamis A, Berdoukas V, Gotsis ED, et al
    Cardiac magnetic resonance in transfusion dependent thalassaemia: assessment of iron load and relationship to left ventricular ejection fraction.
    Br J Haematol. 2010;151:397-401.
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    October 2010
62. NUR E , Brandjes DP, Schnog JJ, Otten HM, et al
    Plasma levels of advanced glycation end products are associated with haemolysis-related organ complications in sickle cell patients.
    Br J Haematol. 2010;151:62-9.
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63. PENG H , Truksa J, Lee P
    EPO-mediated reduction in Hamp expression in vivo corrects iron deficiency anaemia in TMPRSS6 deficiency.
    Br J Haematol. 2010;151:106-9.
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    September 2010
64. SANCHEZ-CORRAL P , Melgosa M
    Advances in understanding the aetiology of atypical Haemolytic Uraemic Syndrome.
    Br J Haematol. 2010;150:529-42.
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65. GARDNER K , Bell C, Bartram JL, Allman M, et al
    Outcome of adults with sickle cell disease admitted to critical care - experience of a single institution in the UK.
    Br J Haematol. 2010;150:610-3.
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66. BARTRAM JL , Thein SL, Gardner K, Egberongbe Y, et al
    Outcome of children with sickle cell disease admitted to intensive care - a single institution experience.
    Br J Haematol. 2010;150:614-7.
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67. KAM GL , Wong WK, Koh M
    Iron deficiency anaemia: an unusual presentation of lymphangioma.
    Br J Haematol. 2010;150:645.
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68. PETRUZZELLI R , Gaudino S, Amendola G, Sessa R, et al
    Role of the cold shock domain protein A in the transcriptional regulation of HBG expression.
    Br J Haematol. 2010;150:689-99.
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69. NITTA H , Mihara K, Sakai A, Kimura A, et al
    Expansion of CD8+ /perforin+ effector memory T cells in the bone marrow of patients with thymoma-associated pure red cell aplasia.
    Br J Haematol. 2010;150:712-5.
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70. PARNES A , Nikiforow S, Berliner N, Vanasse GJ, et al
    Single nucleotide polymorphisms in the human TNF gene are associated with anaemia and neutropenia in a cohort of patients with de novo myelodysplastic syndrome.
    Br J Haematol. 2010;150:700-1.
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71. YAMAGUCHI H , Inokuchi K, Takeuchi J, Tamai H, et al
    Identification of TINF2 gene mutations in adult Japanese patients with acquired bone marrow failure syndromes.
    Br J Haematol. 2010;150:725-7.
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72. MARASCA R , Coluccio V, Santachiara R, Leonardi G, et al
    Pregnancy in PNH: another eculizumab baby.
    Br J Haematol. 2010;150:707-8.
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73. ANDO K , Tanaka Y, Hashimoto Y, Ohyashiki JH, et al
    PNH-phenotype cells in patients with idiopathic cytopenia of undetermined significance (ICUS) with megakaryocytic hypoplasia and thrombocytopenia.
    Br J Haematol. 2010;150:705-7.
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    August 2010
74. MARSH J , Socie G, Tichelli A, Schrezenmeier H, et al
    Should irradiated blood products be given routinely to all patients with aplastic anaemia undergoing immunosuppressive therapy with antithymocyte globulin (ATG)? A survey from the European Group for Blood and Marrow Transplantation Severe Aplastic Ana
    Br J Haematol. 2010;150:377-9.
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75. O'RIORDAN S , Hien TT, Miles K, Allen A, et al
    Large scale screening for haemoglobin disorders in southern Vietnam: implications for avoidance and management.
    Br J Haematol. 2010;150:359-64.
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76. DRAGONI F , Iori AP, Pignoloni P, Minotti C, et al
    Thrombophilic screening in patients with paroxysmal nocturnal haemoglobinuria: a pilot study.
    Br J Haematol. 2010;150:492-4.
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77. KOLNAGOU A , Kontoghiorghes GJ
    New golden era of chelation therapy in thalassaemia: the achievement and maintenance of normal range body iron stores.
    Br J Haematol. 2010;150:489-90.
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78. TAHER AT , Musallam KM, El-Beshlawy A, Karimi M, et al
    Age-related complications in treatment-naive patients with thalassaemia intermedia.
    Br J Haematol. 2010;150:486-9.
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79. TIMEUS F , Crescenzio N, Lorenzati A, Doria A, et al
    Paroxysmal nocturnal haemoglobinuria clones in children with acquired aplastic anaemia: a prospective single centre study.
    Br J Haematol. 2010;150:483-5.
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    July 2010
80. NOURAIE M , Reading NS, Campbell A, Minniti CP, et al
    Association of G6PD with lower haemoglobin concentration but not increased haemolysis in patients with sickle cell anaemia.
    Br J Haematol. 2010;150:218-25.
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81. ALTER BP , Giri N, Savage SA, Peters JA, et al
    Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study.
    Br J Haematol. 2010;150:179-88.
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82. ZHI G , Chen X, Newcomb W, Brown J, et al
    Purification of FANCD2 sub-complexes.
    Br J Haematol. 2010;150:88-92.
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83. RESTIVO PANTALONE G , Renda D, Valenza F, D'Amato F, et al
    Hepatocellular carcinoma in patients with thalassaemia syndromes: clinical characteristics and outcome in a long term single centre experience.
    Br J Haematol. 2010;150:245-7.
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84. ALIYU ZY , Suleiman A, Attah E, Mamman AI, et al
    NT-proBNP as a marker of cardiopulmonary status in sickle cell anaemia in Africa.
    Br J Haematol. 2010;150:102-7.
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85. SINAKOS E , Perifanis V, Vlachaki E, Tsatra I, et al
    Is liver stiffness really unrelated to liver iron concentration?
    Br J Haematol. 2010;150:247-8.
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    June 2010
86. COLOMBATTI R , Maschietto N, Varotto E, Grison A, et al
    Pulmonary hypertension in sickle cell disease children under 10 years of age.
    Br J Haematol. 2010.
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87. WEATHERALL DJ
    The importance of micromapping the gene frequencies for the common inherited disorders of haemoglobin.
    Br J Haematol. 2010;149:635-7.
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88. LOCASCIULLI A , Bacigalupo A, Bruno B, Montante B, et al
    Hepatitis-associated aplastic anaemia: epidemiology and treatment results obtained in Europe. A report of The EBMT aplastic anaemia working party.
    Br J Haematol. 2010;149:890-5.
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89. NIKPOUR M , Pellagatti A, Liu A, Karimi M, et al
    Gene expression profiling of erythroblasts from refractory anaemia with ring sideroblasts (RARS) and effects of G-CSF.
    Br J Haematol. 2010;149:844-54.
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90. KALFF A , Dowsing C, Grigg A
    The impact of a regular erythrocytapheresis programme on the acute and chronic complications of sickle cell disease in adults.
    Br J Haematol. 2010;149:768-74.
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91. ROCHA S , Costa E, Rocha-Pereira P, Ferreira F, et al
    Erythrocyte membrane protein destabilization versus clinical outcome in 160 Portuguese Hereditary Spherocytosis patients.
    Br J Haematol. 2010;149:785-94.
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92. COLAH R , Gorakshakar A, Phanasgaonkar S, D'Souza E, et al
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106. CHILVERS G , Szydlo R, Regan F
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