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Anemia

Free Subscription Articles published in Ann Hematol Retrieve available abstracts of 70 articles: HTML format Text format

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January 2012
1. SILVA MR , Sendin SM, Velloso-Rodrigues C, Belisario AR, et al
   Unstable hemoglobin Rush [beta 101(G3) Glu>Gln, HBB:c.304G>C] in a Brazilian family with moderate hemolytic anemia.
   Ann Hematol. 2012.
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   December 2011
2. MILMAN N
   Postpartum anemia II: prevention and treatment.
   Ann Hematol. 2011.
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3. DA SILVA GB JR , Liborio AB, Daher Ede F
   New insights on pathophysiology, clinical manifestations, diagnosis, and treatment of sickle cell nephropathy.
   Ann Hematol. 2011;90:1371-9.
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4. YANG SH , Yeh YC, Chan YJ, Chou TY, et al
   A solitary pulmonary lymphomatoid granulomatosis-like lesion as the only manifestation of post-transplant lymphoproliferative disorder after hematopoietic stem-cell transplantation.
   Ann Hematol. 2011;90:1481-3.
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   November 2011
5. LOTFI R , Moeller P, Schmid M, Schrezenmeier H, et al
   Increased requirement for platelet transfusions concurrent with enhanced bleeding during romiplostim treatment in a patient with thrombocytopenia due to bone marrow failure.
   Ann Hematol. 2011;90:1357-9.
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6. CHAIBUNRUANG A , Fucharoen G, Jetsrisuparb A, Fucharoen S, et al
   Hemoglobin Lepore EF Bart's disease: a molecular, hematological, and diagnostic aspects.
   Ann Hematol. 2011;90:1337-40.
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   October 2011
7. AU WY , Ngai CW, Chan WM, Leung RY, et al
   Hemolysis and methemoglobinemia due to hepatitis E virus infection in patient with G6PD deficiency.
   Ann Hematol. 2011;90:1237-8.
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   September 2011
8. MOON JH , Lee SJ, Lee YJ, Kang BW, et al
   Pilot study on combination of azacitidine and low-dose cytarabine for patients with refractory anemia with excess blast.
   Ann Hematol. 2011.
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9. GHIO AJ
   Anemia and global iron fortification and supplementation.
   Ann Hematol. 2011.
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10. ZHENG M , Zheng K, Zhou J, Sun H, et al
    Tcf-1 gene silence suppresses downstream gene expression in CD4(+) T cells from bone marrow of aplastic anemia patients.
    Ann Hematol. 2011.
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11. SATER MS , Mahdi N, Al-Absi IK, Al-Subaie AM, et al
    Anti-annexin V IgG and IgM antibodies in sickle cell disease patients with vaso-occlusive crisis.
    Ann Hematol. 2011;90:1031-6.
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    August 2011
12. HOCHSMANN B , Rojewski M, Schrezenmeier H
    Paroxysmal nocturnal hemoglobinuria (PNH): higher sensitivity and validity in diagnosis and serial monitoring by flow cytometric analysis of reticulocytes.
    Ann Hematol. 2011;90:887-99.
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13. GREGORY GP , Opat S, Quach H, Shortt J, et al
    Failure of eculizumab to correct paroxysmal cold hemoglobinuria.
    Ann Hematol. 2011;90:989-90.
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14. DEEREN D
    A kidney transplant patient with pure red cell aplasia: first things first!
    Ann Hematol. 2011;90:991-2.
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15. SEO JY , Kim HJ, Kim SH
    Neutropenia in parvovirus B19-associated pure red cell aplasia.
    Ann Hematol. 2011;90:975-8.
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    July 2011
16. BOVEN LA , de Haar-Holleman A, Folman CC, Kraaijenhagen RJ, et al
    Diagnostic and therapeutic challenges of severe Rh e-specific IgA-mediated autoimmune hemolytic anemia.
    Ann Hematol. 2011.
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17. LITHANATUDOM P , Wannatung T, Leecharoenkiat A, Svasti S, et al
    Enhanced activation of autophagy in beta-thalassemia/Hb E erythroblasts during erythropoiesis.
    Ann Hematol. 2011;90:747-58.
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18. MUNKONGDEE T , Pichanun D, Butthep P, Klamchuen S, et al
    Quantitative analysis of Hb Bart's in cord blood by capillary electrophoresis system.
    Ann Hematol. 2011;90:741-6.
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19. MULLIER F , Lainey E, Fenneteau O, Da Costa L, et al
    Additional erythrocytic and reticulocytic parameters helpful for diagnosis of hereditary spherocytosis: results of a multicentre study.
    Ann Hematol. 2011;90:759-68.
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    June 2011
20. MILMAN N
    Postpartum anemia I: definition, prevalence, causes, and consequences.
    Ann Hematol. 2011.
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21. DONNINI I , Scappini B, Guidi S, Longo G, et al
    Acquired severe aplastic anemia after H1N1 influenza virus vaccination successfully treated with allogeneic bone marrow transplantation.
    Ann Hematol. 2011.
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22. CRISP RL , Solari L, Vota D, Garcia E, et al
    A prospective study to assess the predictive value for hereditary spherocytosis using five laboratory tests (cryohemolysis test, eosin-5'-maleimide flow cytometry, osmotic fragility test, autohemolysis test, and SDS-PAGE) on 50 hereditary spherocytosi
    Ann Hematol. 2011;90:625-34.
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    May 2011
23. CANNELLA L , Latagliata R, Breccia M, Carmosino I, et al
    Very short-term lenalidomide treatment associated with durable resolution of anemia in a patient with myelodysplastic syndrome with chromosome 5q deletion.
    Ann Hematol. 2011.
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24. GHOTI H , Fibach E, Dana M, Abu Shaban M, et al
    Oxidative stress contributes to hemolysis in patients with hereditary spherocytosis and can be ameliorated by fermented papaya preparation.
    Ann Hematol. 2011;90:509-13.
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    March 2011
25. DUHRSEN U , Kratz CP, Flotho C, Lauenstein T, et al
    Long-term outcome of hemizygous and heterozygous carriers of a germline GATA1 (G208R) mutation.
    Ann Hematol. 2011;90:301-6.
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26. FERRARIO A , Merli F, Luminari S, Stelitano C, et al
    Phase II fludarabine and cyclophosphamide for the treatment of indolent B cell non-follicular lymphomas: final results of the LL02 trial of the Gruppo Italiano per lo Studio dei Linfomi (GISL).
    Ann Hematol. 2011;90:323-30.
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27. CHOPRA A , Fisher C, Khunger JM, Pati H, et al
    Hemoglobin O(Indonesia) in India: a rare observation.
    Ann Hematol. 2011;90:353-4.
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28. YIN XL , Zhou TH, Peng L, Zhang XH, et al
    A case report of concomitant paroxysmal nocturnal hemoglobinuria and heterozygous beta-thalassemia.
    Ann Hematol. 2011;90:355-6.
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29. PATEL DK , Patel S, Mashon RS, Dash PM, et al
    Diverse phenotypic expression of sickle cell hemoglobin C disease in an Indian family.
    Ann Hematol. 2011;90:357-8.
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30. AKBARI MT , Hamid M, Izadyar M
    Identification of rare hemoglobin variant (Hb Fairfax) causing dominant beta-thalassemia phenotype in an Iranian family.
    Ann Hematol. 2011;90:349-51.
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    February 2011
31. TANPHAICHITR VS , Hirono A, Pung-Amritt P, Treesucon A, et al
    Chronic nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency: report of two families with novel mutations causing G6PD Bangkok and G6PD Bangkok Noi.
    Ann Hematol. 2011.
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32. FAN R , Wang W, Wang XQ, Lin GW, et al
    Incidence of adult acquired severe aplastic anemia was not increased in Shanghai, China.
    Ann Hematol. 2011.
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33. TRIPATHI A , Jerrell JM, Stallworth JR
    Cost-effectiveness of adenotonsillectomy in reducing obstructive sleep apnea, cerebrovascular ischemia, vaso-occlusive pain, and ACS episodes in pediatric sickle cell disease.
    Ann Hematol. 2011;90:145-50.
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34. GUPTA N , Mahapatra M, Rathi S, Kapoor R, et al
    Acute renal failure following antithymocyte globulin therapy for aplastic anaemia-report of two cases and review of literature.
    Ann Hematol. 2011;90:239-41.
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35. YU N , Kim HR, Cha YJ, Park EK, et al
    A novel frameshift mutation at codon 66 (HBB:c.del201A) in the beta-globin gene leads to beta-thalassemia.
    Ann Hematol. 2011;90:243-4.
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36. GUNDEL F , Eber S, Heep A
    A new ankyrin mutation (ANK1 EXON E9X) causing severe hereditary spherocytosis in the neonatal period.
    Ann Hematol. 2011;90:231-2.
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    January 2011
37. JAIME-PEREZ JC , Colunga-Pedraza PR, Gomez-Ramirez CD, Gutierrez-Aguirre CH, et al
    Danazol as first-line therapy for aplastic anemia.
    Ann Hematol. 2011.
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38. MILMAN N
    Anemia-still a major health problem in many parts of the world!
    Ann Hematol. 2011.
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39. LI Y , Li X, Ge M, Shi J, et al
    Long-term follow-up of clonal evolutions in 802 aplastic anemia patients: a single-center experience.
    Ann Hematol. 2011.
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40. DIOP S , Soudre F, Seck M, Gueye YB, et al
    Sickle-cell disease and malaria: evaluation of seasonal intermittent preventive treatment with sulfadoxine-pyrimethamine in Senegalese patients-a randomized placebo-controlled trial.
    Ann Hematol. 2011;90:23-7.
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41. VOSKARIDOU E , Plata E, Douskou M, Sioni A, et al
    Deferasirox effectively decreases iron burden in patients with double heterozygous HbS/beta-thalassemia.
    Ann Hematol. 2011;90:11-5.
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42. WEI XF , Shang X, He DQ, Huang JW, et al
    Molecular characterization of a novel 27.6-kb deletion causing alpha(+) thalassemia in a Chinese family.
    Ann Hematol. 2011;90:17-22.
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43. LI DZ , Liao C, Zhou JY, Xie XM, et al
    Mild hemoglobin H-constant spring disease with beta-thalassemia-a case report.
    Ann Hematol. 2011;90:123-4.
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    December 2010
44. BALDINI M , Forti S, Marcon A, Ulivieri FM, et al
    Endocrine and bone disease in appropriately treated adult patients with beta-thalassemia major.
    Ann Hematol. 2010;89:1207-13.
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45. HAYWOOD A , Dreau H, Timbs A, Schuh A, et al
    Screening for clinically significant non-deletional alpha thalassaemia mutations by pyrosequencing.
    Ann Hematol. 2010;89:1215-21.
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46. MARTINEZ-TRILLOS A , Gaya A, Maffioli M, Arellano-Rodrigo E, et al
    Efficacy and tolerability of hydroxyurea in the treatment of the hyperproliferative manifestations of myelofibrosis: results in 40 patients.
    Ann Hematol. 2010;89:1233-7.
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    November 2010
47. DIERICKX D , Verhoef G, Delannoy A
    Rituximab in patients with refractory autoimmune hemolytic anemia.
    Ann Hematol. 2010.
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48. DAVIS NF , McGuire BB, Lawlor L, O'Gorman P, et al
    Oral tranexamic acid as a novel treatment option for persistent haematuria in patients with sickle cell disease.
    Ann Hematol. 2010;89:1179-80.
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49. BERDOUKAS V , Carson S, Nord A, Dongelyan A, et al
    Combining two orally active iron chelators for thalassemia.
    Ann Hematol. 2010;89:1177-8.
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    October 2010
50. LEE YG , Kim I, Kim JH, Bae JY, et al
    Impact of cytokine gene polymorphisms on risk and treatment outcomes of aplastic anemia.
    Ann Hematol. 2010.
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51. YAGASAKI H , Kato M, Shimizu N, Shichino H, et al
    Autoimmune hemolytic anemia and autoimmune neutropenia in a child with erythroblastopenia of childhood (TEC) caused by human herpesvirus-6 (HHV-6).
    Ann Hematol. 2010.
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52. SVASTI S , Masaki S, Penglong T, Abe Y, et al
    Expression of microRNA-451 in normal and thalassemic erythropoiesis.
    Ann Hematol. 2010;89:953-8.
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    September 2010
53. OZSOYLU S , Aytekin MN
    Vitamin D deficiency and anemia.
    Ann Hematol. 2010.
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54. FODSTAD P , Dheyauldeen S, Rinde M, Bachmann-Harildstad G, et al
    Anti-VEGF with 3-week intervals is effective on anemia in a patient with severe hereditary hemorrhagic telangiectasia.
    Ann Hematol. 2010.
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55. ZHENG W , Liu Y, Chen D, Rong K, et al
    Complex interaction of Hb Q-Thailand and Hb E with alpha(0)-thalassemia and hereditary persistence of fetal hemoglobin in a Chinese family.
    Ann Hematol. 2010;89:883-8.
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56. SANSONE S , Rottensteiner J, Stocker J, Rosanelli C, et al
    Ciprofloxacin-induced acute haemolytic anaemia in a patient with glucose-6-phosphate dehydrogenase Mediterranean deficiency: a case report.
    Ann Hematol. 2010;89:935-7.
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    August 2010
57. RINALDI CR , Rinaldi P, Pane F, Camera A, et al
    Acquired Hb H disease associated with elevated Hb F level in patient affected by primary myelofibrosis.
    Ann Hematol. 2010;89:827-8.
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    July 2010
58. QI Z , Takamatsu H, Espinoza JL, Lu X, et al
    Autoantibodies specific to hnRNP K: a new diagnostic marker for immune pathophysiology in aplastic anemia.
    Ann Hematol. 2010.
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    June 2010
59. NIE L , Li L, Yang L, Zhang Y, et al
    HFE genotype and iron metabolism in Chinese patients with myelodysplastic syndromes and aplastic anemia.
    Ann Hematol. 2010.
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60. PENALVER FJ , Alvarez-Larran A, Diez-Martin JL, Gallur L, et al
    Rituximab is an effective and safe therapeutic alternative in adults with refractory and severe autoimmune hemolytic anemia.
    Ann Hematol. 2010.
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61. ROGHI A , Cappellini MD, Wood JC, Musallam KM, et al
    Absence of cardiac siderosis despite hepatic iron overload in Italian patients with thalassemia intermedia: an MRI T2* study.
    Ann Hematol. 2010;89:585-9.
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62. GIRISHA KM , Vahab SA, Dalal AB, Gopinath PM, et al
    Compound heterozygosity for HbD Punjab and polyadenylation signal mutation causes clinically asymptomatic mild hypochromia and microcytosis.
    Ann Hematol. 2010;89:625-6.
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    May 2010
63. MEHTA AR , Salaru G, Harrison JS
    Stomatocytosis heralding a case of acute Wilsonian crisis.
    Ann Hematol. 2010;89:527-9.
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    April 2010
64. VILAS-BOAS W , Cerqueira BA, Zanette AM, Reis MG, et al
    Arginase levels and their association with Th17-related cytokines, soluble adhesion molecules (sICAM-1 and sVCAM-1) and hemolysis markers among steady-state sickle cell anemia patients.
    Ann Hematol. 2010.
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65. ATTA EH , Dias DS, Marra VL, de Azevedo AM, et al
    Comparison between horse and rabbit antithymocyte globulin as first-line treatment for patients with severe aplastic anemia: a single-center retrospective study.
    Ann Hematol. 2010.
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66. SHARMA V , Kumar B, Saxena R
    Glutathione S-transferase gene deletions and their effect on iron status in HbE/beta thalassemia patients.
    Ann Hematol. 2010;89:411-4.
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67. PATHARE A , Taher A, Daar S
    Deferasirox (Exjade) significantly improves cardiac T2* in heavily iron-overloaded patients with beta-thalassemia major.
    Ann Hematol. 2010;89:405-9.
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68. GHOTI H , Rosenbaum H, Fibach E, Rachmilewitz EA, et al
    Decreased hemolysis following administration of antioxidant-fermented papaya preparation (FPP) to a patient with PNH.
    Ann Hematol. 2010;89:429-30.
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    March 2010
69. SUN WL , Kock L, Walder A, Erdel M, et al
    Successful treatment of MDS with lenalidomide, complicated by transient autoimmune hemolysis.
    Ann Hematol. 2010;89:327-9.
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    January 2010
70. CHAO YH , Peng CT, Harn HJ, Chan CK, et al
    Poor potential of proliferation and differentiation in bone marrow mesenchymal stem cells derived from children with severe aplastic anemia.
    Ann Hematol. 2010.
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