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Anemia

Free Subscription Articles published in Br J Haematol Retrieve available abstracts of 140 articles: HTML format

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May 2009
1. HANKINS J , Aygun B
   Pharmacotherapy in sickle cell disease--state of the art and future prospects.
   Br J Haematol. 2009;145:296-308.
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2. ANUR P , Nemecek ER, Kurre P
   The evolving spectrum of 'non-classical' Diamond-Blackfan anaemia--a case of eADA positive pancytopenia in a young adult.
   Br J Haematol. 2009;145:428-30.
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   April 2009
3. SVAHN J , Fioredda F, Calvillo M, Molinari AC, et al
   Rituximab-based immunosuppression for autoimmune haemolytic anaemia in infants.
   Br J Haematol. 2009;145:96-100.
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4. TEACHEY DT , Greiner R, Seif A, Attiyeh E, et al
   Treatment with sirolimus results in complete responses in patients with autoimmune lymphoproliferative syndrome.
   Br J Haematol. 2009;145:101-6.
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5. PICCIN A , Smith OP, Murphy C, O'Marcaigh A, et al
   Splenectomy in sickle cell anaemia: a cause of further crises?
   Br J Haematol. 2009;145:144-6.
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   March 2009
6. PASHANKAR FD , Carbonella J, Bazzy-Asaad A, Friedman A, et al
   Longitudinal follow up of elevated pulmonary artery pressures in children with sickle cell disease.
   Br J Haematol. 2009;144:736-41.
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7. BRANDOW AM , Brousseau DC, Panepinto JA
   Postdischarge pain, functional limitations and impact on caregivers of children with sickle cell disease treated for painful events.
   Br J Haematol. 2009;144:782-8.
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8. LAWLER M , McCann SR, Marsh JC, Ljungman P, et al
   Serial chimerism analyses indicate that mixed haemopoietic chimerism influences the probability of graft rejection and disease recurrence following allogeneic stem cell transplantation (SCT) for severe aplastic anaemia (SAA): indication for routine asses
   Br J Haematol. 2009;144:933-45.
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9. WARDROP D , Steensma DP
   Is refractory anaemia with ring sideroblasts and thrombocytosis (RARS-T) a necessary or useful diagnostic category?
   Br J Haematol. 2009;144:809-17.
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10. BASU S , Kumar A
    Hair-on-end appearance in radiograph of skull and facial bones in a case of beta thalassaemia.
    Br J Haematol. 2009;144:807.
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    February 2009
11. TROMPETER S , Roberts I
    Haemoglobin F modulation in childhood sickle cell disease.
    Br J Haematol. 2009;144:308-16.
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12. SABINA RL , Wandersee NJ, Hillery CA
    Ca2+-CaM activation of AMP deaminase contributes to adenine nucleotide dysregulation and phosphatidylserine externalization in human sickle erythrocytes.
    Br J Haematol. 2009;144:434-45.
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13. TANG Y , Chen J, Young NS
    Expansion of haematopoietic stem cells from normal donors and bone marrow failure patients by recombinant hoxb4.
    Br J Haematol. 2009;144:603-12.
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14. HAAS PS , Roy NB, Gibbons RJ, Deville MA, et al
    The role of X-inactivation in the gender bias of patients with acquired alpha-thalassaemia and myelodysplastic syndrome (ATMDS).
    Br J Haematol. 2009;144:538-45.
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15. WENT R , Wright J, Webster R, Stamps R, et al
    Anti-Fy3 in sickle cell disease: a difficult transfusion problem.
    Br J Haematol. 2009;144:621-2.
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16. COUTINHO R , Bento C, Almeida H, Cunha E, et al
    Complex inheritance of chronic haemolytic anaemia.
    Br J Haematol. 2009;144:615-6.
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17. BAYLEY J , Pavlu J, Thompson M
    Striking bone marrow plasmacytosis in a patient with sickle cell anaemia.
    Br J Haematol. 2009;144:457.
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    January 2009
18. CRESCENZI B , La Starza R, Sambani C, Parcharidou A, et al
    Totipotent stem cells bearing del(20q) maintain multipotential differentiation in Shwachman Diamond syndrome.
    Br J Haematol. 2009;144:116-9.
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19. RAMIREZ JM , Schaad O, Durual S, Cossali D, et al
    Growth differentiation factor 15 production is necessary for normal erythroid differentiation and is increased in refractory anaemia with ring-sideroblasts.
    Br J Haematol. 2009;144:251-62.
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20. SCHEINBERG P , Wu CO, Nunez O, Young NS, et al
    Predicting response to immunosuppressive therapy and survival in severe aplastic anaemia.
    Br J Haematol. 2009;144:206-16.
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21. KUSUMAWIDJAJA D , Ghosh S, Ablett M
    Diffuse marrow abnormality on magnetic resonance imaging secondary to pernicious anaemia.
    Br J Haematol. 2009;144:145.
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    December 2008
22. KAO SY , Xu W, Brandwein JM, Lipton JH, et al
    Outcomes of older patients (> or = 60 years) with acquired aplastic anaemia treated with immunosuppressive therapy.
    Br J Haematol. 2008;143:738-43.
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23. MARIANI R , Pelucchi S, Pozzi M, Paolini V, et al
    Reduced expression of hepcidin in patients with myelodysplastic syndrome and myelofibrosis: the causes might be more heterogeneous than in thalassaemia.
    Br J Haematol. 2008;143:746-7.
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24. FITZGERALD JE , Simpson JA, Acheson AG
    The use of intravenous iron in patients with cancer related anaemia: don't overlook iron deficiency anaemia in colorectal cancer.
    Br J Haematol. 2008;143:754.
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    November 2008
25. FERRERO D , Darbesio A, Giai V, Genuardi M, et al
    Efficacy of a combination of human recombinant erythropoietin + 13-cis-retinoic acid and dihydroxylated vitamin D3 to improve moderate to severe anaemia in low/intermediate risk myelodysplastic syndromes.
    Br J Haematol. 2008.
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26. FURNESS CL , O'Driscoll S, Davenport M, Morrison G, et al
    Hydroxycarbamide and erythropoietin in the preoperative management of children with sickle cell anaemia undergoing moderate risk surgery.
    Br J Haematol. 2008.
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27. AU WY , Ha SY, Chow EY, Wan TS, et al
    A unique case of familial leukaemia: maternal puerperal leukaemia followed by infantile leukaemia with monosomy 7.
    Br J Haematol. 2008;143:445-6.
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28. NOLAN VG , Zhang Y, Lash T, Sebastiani P, et al
    Association between wind speed and the occurrence of sickle cell acute painful episodes: results of a case-crossover study.
    Br J Haematol. 2008;143:433-8.
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29. MARTIN FM , Prchal J, Nieva J, Saven A, et al
    Purification and characterization of sideroblasts from patients with acquired and hereditary sideroblastic anaemia.
    Br J Haematol. 2008;143:446-50.
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30. RUGGERI A , de Latour RP, Rocha V, Larghero J, et al
    Double cord blood transplantation in patients with high risk bone marrow failure syndromes.
    Br J Haematol. 2008;143:404-8.
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31. FANG CJ , Richards A, Liszewski MK, Kavanagh D, et al
    Advances in understanding of pathogenesis of aHUS and HELLP.
    Br J Haematol. 2008;143:336-48.
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32. BERNARDO ME , Zecca M, Piras E, Vacca A, et al
    Treosulfan-based conditioning regimen for allogeneic haematopoietic stem cell transplantation in patients with thalassaemia major.
    Br J Haematol. 2008;143:548-51.
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33. VASAVDA N , Badiger S, Rees D, Height S, et al
    The presence of alpha-thalassaemia trait blunts the response to hydroxycarbamide in patients with sickle cell disease.
    Br J Haematol. 2008;143:589-92.
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    October 2008
34. GREY-DAVIES E , Hows JM, Marsh JC
    Aplastic anaemia in association with coeliac disease: a series of three cases.
    Br J Haematol. 2008;143:258-60.
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    September 2008
35. AMENDOLA G , Di Concilio R, D'Urzo G, Danise P, et al
    Erythropoietin treatment can prevent blood transfusion in infantile pyknocytosis.
    Br J Haematol. 2008.
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36. FORZLEY BR , Sontrop JM, Macnab JJ, Chen S, et al
    Treating TTP/HUS with plasma exchange: a single centre's 25-year experience.
    Br J Haematol. 2008;143:100-6.
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37. PASSARELLO C , Giambona A, Prossomariti L, Ammirabile M, et al
    Hb Southern Italy: coexistence of two missence mutations (the Hb Sun Prairie alpha2 130 Ala --> Pro and Hb Caserta alpha2 26 Ala --> Thr) in a single HBA2 gene.
    Br J Haematol. 2008;143:138-42.
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38. LIONNET F , Bachmeyer C, Stankovic K, Tharaux PL, et al
    Efficacy of the endothelin receptor blocker bosentan for refractory sickle cell leg ulcers.
    Br J Haematol. 2008;142:991-2.
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39. MACK AK , McGowan Ii VR, Tremonti CK, Ackah D, et al
    Sodium nitrite promotes regional blood flow in patients with sickle cell disease: a phase I/II study.
    Br J Haematol. 2008;142:971-8.
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40. VLACHOS A , Ball S, Dahl N, Alter BP, et al
    Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference.
    Br J Haematol. 2008;142:859-76.
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41. LIU S , Bhattacharya S, Han A, Suragani RN, et al
    Haem-regulated eIF2alpha kinase is necessary for adaptive gene expression in erythroid precursors under the stress of iron deficiency.
    Br J Haematol. 2008;143:129-37.
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42. NTAIOS G , Chatzinikolaou A
    The spleen in beta thalassaemia minor: splenomegaly or just 'scanomegaly'?
    Br J Haematol. 2008;143:143.
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43. CAMASCHELLA C
    Recent advances in the understanding of inherited sideroblastic anaemia.
    Br J Haematol. 2008;143:27-38.
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44. ALMEIDA CB , Traina F, Lanaro C, Canalli AA, et al
    High expression of the cGMP-specific phosphodiesterase, PDE9A, in sickle cell disease (SCD) and the effects of its inhibition in erythroid cells and SCD neutrophils.
    Br J Haematol. 2008;142:836-44.
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    August 2008
45. WIN N , Roberts DJ
    Management of paroxysmal cold haemoglobinuria: not only avoiding cold but also keeping warm.
    Br J Haematol. 2008;142:668.
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46. KIDSON-GERBER G , Lindeman R
    Adherence to desferrioxamine and deferiprone and the impact of deferiprone co-prescription in thalassaemia major patients. Does the addition of deferiprone improve adherence?
    Br J Haematol. 2008;142:679-80.
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47. SAWADA K , Fujishima N, Hirokawa M
    Acquired pure red cell aplasia: updated review of treatment.
    Br J Haematol. 2008;142:505-14.
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    July 2008
48. UZIEL O , Reshef H, Ravid A, Fabian I, et al
    Oxidative stress causes telomere damage in Fanconi anaemia cells - a possible predisposition for malignant transformation.
    Br J Haematol. 2008;142:82-93.
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49. CUMMING V , King L, Fraser R, Serjeant G, et al
    Venous incompetence, poverty and lactate dehydrogenase in Jamaica are important predictors of leg ulceration in sickle cell anaemia.
    Br J Haematol. 2008;142:119-25.
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50. GU Y , Hu X, Liu C, Qv X, et al
    Interleukin (IL)-17 promotes macrophages to produce IL-8, IL-6 and tumour necrosis factor-alpha in aplastic anaemia.
    Br J Haematol. 2008;142:109-14.
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51. HANKINS JS , Fortner GL, McCarville MB, Smeltzer MP, et al
    The natural history of conditional transcranial Doppler flow velocities in children with sickle cell anaemia.
    Br J Haematol. 2008;142:94-9.
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52. ORIGA R , Satta S, Matta G, Galanello R, et al
    Glutathione S-transferase gene polymorphism and cardiac iron overload in thalassaemia major.
    Br J Haematol. 2008;142:143-5.
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53. KATODRITOU E , Zervas K, Terpos E, Brugnara C, et al
    Use of erythropoiesis stimulating agents and intravenous iron for cancer and treatment-related anaemia: the need for predictors and indicators of effectiveness has not abated.
    Br J Haematol. 2008;142:3-10.
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54. WESTERMAN M , Pizzey A, Hirschman J, Cerino M, et al
    Microvesicles in haemoglobinopathies offer insights into mechanisms of hypercoagulability, haemolysis and the effects of therapy.
    Br J Haematol. 2008;142:126-35.
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    June 2008
55. BRITTAIN JE , Knoll CM, Ataga KI, Orringer EP, et al
    Fibronectin bridges monocytes and reticulocytes via integrin alpha4beta1.
    Br J Haematol. 2008;141:872-81.
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56. LITTLEWOOD TJ , Alikhan R
    The use of intravenous iron in patients with cancer-related anaemia.
    Br J Haematol. 2008;141:751-6.
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57. WOOD JC , Claster S, Carson S, Menteer JD, et al
    Vitamin D deficiency, cardiac iron and cardiac function in thalassaemia major.
    Br J Haematol. 2008;141:891-4.
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58. MAMTANI M , Kulkarni H
    Influence of iron chelators on myocardial iron and cardiac function in transfusion-dependent thalassaemia: a systematic review and meta-analysis.
    Br J Haematol. 2008;141:882-90.
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    May 2008
59. KOSAKA N , Sugiura K, Yamamoto Y, Yoshioka Y, et al
    Identification of erythropoietin-induced microRNAs in haematopoietic cells during erythroid differentiation.
    Br J Haematol. 2008;.
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60. LIAPIS K , Bakiri M, Apostolidis J
    Erythroblastic synartesis in a patient with small lymphocytic lymphoma.
    Br J Haematol. 2008;.
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61. OLIVIERI NF , Muraca GM, O'Donnell A, Premawardhena A, et al
    Studies in haemoglobin E beta-thalassaemia.
    Br J Haematol. 2008;141:388-97.
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62. GANAPATHI KA , Shimamura A
    Ribosomal dysfunction and inherited marrow failure.
    Br J Haematol. 2008;141:376-87.
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63. THEIN SL
    Genetic modifiers of the beta-haemoglobinopathies.
    Br J Haematol. 2008;141:357-66.
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64. LISOWSKI L , Sadelain M
    Current status of globin gene therapy for the treatment of beta-thalassaemia.
    Br J Haematol. 2008;141:335-45.
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65. JELKMANN W
    Developments in the therapeutic use of erythropoiesis stimulating agents.
    Br J Haematol. 2008;141:287-97.
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66. PREMAWARDHENA A , Arambepola M, Katugaha N, Weatherall DJ, et al
    Is the beta thalassaemia trait of clinical importance?
    Br J Haematol. 2008;141:407-10.
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67. AN X , Mohandas N
    Disorders of red cell membrane.
    Br J Haematol. 2008;141:367-75.
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68. HAGAR W , Vichinsky E
    Advances in clinical research in sickle cell disease.
    Br J Haematol. 2008;141:346-56.
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69. PINTO FO , Roberts I
    Cord blood stem cell transplantation for haemoglobinopathies.
    Br J Haematol. 2008;141:309-24.
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70. CALZOLARI R , Pecoraro A, Borruso V, Troia A, et al
    Induction of gamma-globin gene transcription by hydroxycarbamide in primary erythroid cell cultures from Lepore patients.
    Br J Haematol. 2008;141:720-7.
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71. KARPAC CA , Li X, Terrell DR, Kremer Hovinga JA, et al
    Sporadic bloody diarrhoea-associated thrombotic thrombocytopenic purpura-haemolytic uraemic syndrome: an adult and paediatric comparison.
    Br J Haematol. 2008;141:696-707.
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72. CHEUNG YF , Chan GC, Ha SY
    Effect of deferasirox (ICL670) on arterial function in patients with beta-thalassaemia major.
    Br J Haematol. 2008;141:728-33.
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    April 2008
73. ARCASOY MO
    The non-haematopoietic biological effects of erythropoietin.
    Br J Haematol. 2008;141:14-31.
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74. BARTAKKE S , Abdelhaleem M, Carcao M
    Valproate-induced pure red cell aplasia and megakaryocyte dysplasia.
    Br J Haematol. 2008;141:133.
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75. SAUNTHARARAJAH Y , Molokie R, Saraf S, Sidhwani S, et al
    Clinical effectiveness of decitabine in severe sickle cell disease.
    Br J Haematol. 2008;141:126-9.
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76. EYLER CE , Jackson T, Elliott LE, De Castro LM, et al
    beta(2)-Adrenergic receptor and adenylate cyclase gene polymorphisms affect sickle red cell adhesion.
    Br J Haematol. 2008;141:105-8.
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77. ZOI K , Terpos E, Zoi C, Loukopoulos D, et al
    Increased CD177 (PRV1) expression in thalassaemia and the underlying erythropoietic activity.
    Br J Haematol. 2008;141:100-4.
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78. BASU S , Banerjee D, Chandra S, Chakrabarti A, et al
    Loss of phospholipid membrane asymmetry and sialylated glycoconjugates from erythrocyte surface in haemoglobin E beta-thalassaemia.
    Br J Haematol. 2008;141:92-9.
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79. KUMKHAEK C , Taylor JG 6th, Zhu J, Hoppe C, et al
    Fetal haemoglobin response to hydroxycarbamide treatment and sar1a promoter polymorphisms in sickle cell anaemia.
    Br J Haematol. 2008;141:254-9.
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80. GARVEY B
    Rituximab in the treatment of autoimmune haematological disorders.
    Br J Haematol. 2008;141:149-69.
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81. KULAGIN A , Lisukov I, Denisova V, Kruchkova I, et al
    Severe pancytopenia associated with a minor paroxysmal nocturnal haemoglobinuria clone and response to ciclosporin A in a heavily pretreated multiple myeloma patient.
    Br J Haematol. 2008;141:122-3.
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    March 2008
82. ZENT CS , Ding W, Schwager SM, Reinalda MS, et al
    The prognostic significance of cytopenia in chronic lymphocytic leukaemia/small lymphocytic lymphoma.
    Br J Haematol. 2008;.
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83. RAMOT Y , Koshkaryev A, Goldfarb A, Yedgar S, et al
    Phenylhydrazine as a partial model for beta-thalassaemia red blood cell hemodynamic properties.
    Br J Haematol. 2008;140:692-700.
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84. CHAUDHURY S , Auerbach AD, Kernan NA, Small TN, et al
    Fludarabine-based cytoreductive regimen and T-cell-depleted grafts from alternative donors for the treatment of high-risk patients with Fanconi anaemia.
    Br J Haematol. 2008;140:644-55.
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85. PALMER SR , Tefferi A, Hanson CA, Steensma DP, et al
    Platelet count is an IPSS-independent risk factor predicting survival in refractory anaemia with ringed sideroblasts.
    Br J Haematol. 2008;140:722-5.
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    February 2008
86. PEREZ-ALBUERNE ED , Eapen M, Klein J, Gross TJ, et al
    Outcome of unrelated donor stem cell transplantation for children with severe aplastic anemia.
    Br J Haematol. 2008;.
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87. KURAMITSU M , Hamaguchi I, Takuo M, Masumi A, et al
    Deficient RPS19 protein production induces cell cycle arrest in erythroid progenitor cells.
    Br J Haematol. 2008;140:348-59.
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88. KELAIDI C , Eclache V, Fenaux P
    The role of lenalidomide in the management of myelodysplasia with del 5q.
    Br J Haematol. 2008;140:267-78.
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89. QUINN CT , Sargent JW
    Daytime steady-state haemoglobin desaturation is a risk factor for overt stroke in children with sickle cell anaemia.
    Br J Haematol. 2008;140:336-9.
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90. GIRODON F , Garcon L, Bergoin E, Largier M, et al
    Usefulness of the eosin-5'-maleimide cytometric method as a first-line screening test for the diagnosis of hereditary spherocytosis: comparison with ektacytometry and protein electrophoresis.
    Br J Haematol. 2008;140:468-70.
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    January 2008
91. SARACCO P , Quarello P, Iori AP, Zecca M, et al
    Cyclosporin A response and dependence in children with acquired aplastic anaemia: a multicentre retrospective study with long-term observation follow-up.
    Br J Haematol. 2008;140:197-205.
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92. O'DRISCOLL S , Height SE, Dick MC, Rees DC, et al
    Serum lactate dehydrogenase activity as a biomarker in children with sickle cell disease.
    Br J Haematol. 2008;140:206-9.
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93. BOVERI E , Passamonti F, Rumi E, Pietra D, et al
    Bone marrow microvessel density in chronic myeloproliferative disorders: a study of 115 patients with clinicopathological and molecular correlations.
    Br J Haematol. 2008;140:162-8.
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94. HANKINS JS , Wynn LW, Brugnara C, Hillery CA, et al
    Phase I study of magnesium pidolate in combination with hydroxycarbamide for children with sickle cell anaemia.
    Br J Haematol. 2008;140:80-5.
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95. LITTERA R , Arras M, Ledda A, Caocci G, et al
    Long-term efficacy and tolerance of rituximab for post-transfusional alloimmune haemolytic anaemia in a thalassaemia patient.
    Br J Haematol. 2008;140:114-5.
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96. MORRIS ES , Darbyshire P, Fairlie F, Dalley CD, et al
    Two natural pregnancies following allogeneic transplantation for Fanconi anaemia.
    Br J Haematol. 2008;140:113.
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97. IMRAN A , Mawhinney R, Swirsky D, Hall C, et al
    Paravertebral extramedullary haemopoiesis occurring in a case of congenital dyserythropoietic anaemia type II.
    Br J Haematol. 2008;140:1.
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    December 2007
98. LANDGREN O , Gridley G, Check D, Caporaso NE, et al
    Acquired immune-related and inflammatory conditions and subsequent chronic lymphocytic leukaemia.
    Br J Haematol. 2007;139:791-8.
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    November 2007
99. WU CJ , Gladwin M, Tisdale J, Hsieh M, et al
    Mixed haematopoietic chimerism for sickle cell disease prevents intravascular haemolysis.
    Br J Haematol. 2007;139:504-7.
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100. STEENSMA DP , Porcher JC, Hanson CA, Lathrop CL, et al
     Prevalence of erythrocyte haemoglobin H inclusions in unselected patients with clonal myeloid disorders.
     Br J Haematol. 2007;139:439-42.
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101. GARRATTY G , Petz LD
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108. IYAMU EW , Ekekezie C, Woods GM
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115. BORGNA-PIGNATTI C
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116. GERTZ MA
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118. SOLOMOU EE , Wong S, Visconte V, Gibellini F, et al
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119. KIM JJ , Thrasher AJ, Jones AM, Davies EG, et al
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124. WANG C , Amato D
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128. HILL A , Richards SJ, Hillmen P
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130. ARCASOY MO , Gockerman JP
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134. DALLE JH , Champagne MA, Duval M
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135. NOOITGEDAGT JE , Harteveld CL, Starreveld JS, Versteegh FG, et al
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137. SARRAI M , Duroseau H, D'Augustine J, Moktan S, et al
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138. DAVIES JK , Guinan EC
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