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Articles published in Int J Hematol

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Single Articles


    November 2017
  1. FURUYAMA K, Kaneko K
    Iron metabolism in erythroid cells and patients with congenital sideroblastic anemia.
    Int J Hematol. 2017 Nov 14. doi: 10.1007/s12185-017-2368.
    PubMed     Text format     Abstract available


    October 2017
  2. IMATAKI O, Uchida S, Yokokura S, Uemura M, et al
    Anemia and hypogammaglobulinemia caused by Menetrier's disease.
    Int J Hematol. 2017 Oct 12. doi: 10.1007/s12185-017-2349.
    PubMed     Text format    


    September 2017
  3. CUI Q, Sha P, Chen H, Shen H, et al
    Modified immunosuppressive therapy with porcine antilymphocyte globulin plus delayed cyclosporine A in children with severe aplastic anemia.
    Int J Hematol. 2017 Sep 12. doi: 10.1007/s12185-017-2321.
    PubMed     Text format     Abstract available


    August 2017
  4. XU X, Li L, Xia W, Ding H, et al
    Successful management of a hydropic fetus with severe anemia and thrombocytopenia caused by anti-CD36 antibody.
    Int J Hematol. 2017 Aug 16. doi: 10.1007/s12185-017-2310.
    PubMed     Text format     Abstract available


  5. UPANAN S, McKie AT, Latunde-Dada GO, Roytrakul S, et al
    Hepcidin suppression in beta-thalassemia is associated with the down-regulation of atonal homolog 8.
    Int J Hematol. 2017;106:196-205.
    PubMed     Text format     Abstract available


    July 2017
  6. KUNIMOTO H, Nakajima H
    Epigenetic dysregulation of hematopoietic stem cells and preleukemic state.
    Int J Hematol. 2017;106:34-44.
    PubMed     Text format     Abstract available


  7. TOKI Y, Ikuta K, Kawahara Y, Niizeki N, et al
    Reticulocyte hemoglobin equivalent as a potential marker for diagnosis of iron deficiency.
    Int J Hematol. 2017;106:116-125.
    PubMed     Text format     Abstract available


    June 2017
  8. CHOI Y, Jo JC, Jeon HJ, Kim DW, et al
    Trend and treatment patterns of aplastic anemia in Korea, pure red cell aplasia and myelodysplastic syndrome in Korea: a nation-wide analysis.
    Int J Hematol. 2017 Jun 29. doi: 10.1007/s12185-017-2280.
    PubMed     Text format     Abstract available


  9. CHEUNG RS, Taniguchi T
    Recent insights into the molecular basis of Fanconi anemia: genes, modifiers, and drivers.
    Int J Hematol. 2017 Jun 19. doi: 10.1007/s12185-017-2283.
    PubMed     Text format     Abstract available


  10. LIU C, Zheng M, Zhang T, Fu R, et al
    TRAIL in CD8+ T cells from patients with severe aplastic anemia.
    Int J Hematol. 2017 Jun 19. doi: 10.1007/s12185-017-2279.
    PubMed     Text format     Abstract available


  11. ZHAO P, Gao Q, He Q, Tan J, et al
    Prevalence and clinical outcomes of hepatitis B virus infection in patients with aplastic anemia.
    Int J Hematol. 2017 Jun 13. doi: 10.1007/s12185-017-2276.
    PubMed     Text format     Abstract available


    May 2017
  12. URESHINO H, Kizuka H, Kusaba K, Sano H, et al
    5q- syndrome-like features as the first manifestation of myelodysplastic syndrome in a patient with an unbalanced whole-arm translocation der(5;19)(p10;q10).
    Int J Hematol. 2017;105:692-696.
    PubMed     Text format     Abstract available


    April 2017
  13. ABAZA Y, Yin CC, Bueso-Ramos CE, Wang SA, et al
    Primary autoimmune myelofibrosis: a case report and review of the literature.
    Int J Hematol. 2017;105:536-539.
    PubMed     Text format     Abstract available


    March 2017
  14. WU L, Mo W, Zhang Y, Zhou M, et al
    Vascular and perivascular niches, but not the osteoblastic niche, are numerically restored following allogeneic hematopoietic stem cell transplantation in patients with aplastic anemia.
    Int J Hematol. 2017 Mar 16. doi: 10.1007/s12185-017-2217.
    PubMed     Text format     Abstract available


  15. IKI S, Ohgi K, Suzuki K
    Eculizumab treatment improved renal hemosiderosis in a patient with paroxysmal nocturnal hemoglobinuria.
    Int J Hematol. 2017;105:231-232.
    PubMed     Text format    


  16. ZAHRAN AM, Saad K, Elsayh KI, Alblihed MA, et al
    Characterization of circulating CD4+ CD8+ double positive and CD4- CD8- double negative T-lymphocyte in children with beta-thalassemia major.
    Int J Hematol. 2017;105:265-271.
    PubMed     Text format     Abstract available


  17. KOMATSU N, Kirito K, Shimoda K, Ishikawa T, et al
    Assessing the safety and efficacy of ruxolitinib in a multicenter, open-label study in Japanese patients with myelofibrosis.
    Int J Hematol. 2017;105:309-317.
    PubMed     Text format     Abstract available


    February 2017
  18. WU L, Xu W, Xu L, Kong Q, et al
    Mitophagy is increased during erythroid differentiation in beta-thalassemia.
    Int J Hematol. 2017;105:162-173.
    PubMed     Text format     Abstract available


    January 2017
  19. HAYAKAWA J, Kanda J, Akahoshi Y, Harada N, et al
    Meta-analysis of treatment with rabbit and horse antithymocyte globulin for aplastic anemia.
    Int J Hematol. 2017 Jan 11. doi: 10.1007/s12185-017-2179.
    PubMed     Text format     Abstract available


  20. IKEBE T, Takata H, Sasaki H, Miyazaki Y, et al
    Hemophagocytic lymphohistiocytosis following influenza vaccination in a patient with aplastic anemia undergoing allogeneic bone marrow stem cell transplantation.
    Int J Hematol. 2017 Jan 4. doi: 10.1007/s12185-016-2177.
    PubMed     Text format    


    December 2016
  21. SEKIGUCHI N, Nishina S, Kawakami T, Sakai H, et al
    Oral cyclophosphamide was effective for Coombs-negative autoimmune hemolytic anemia in CD16+CD56- chronic lymphoproliferative disorder of NK-cells.
    Int J Hematol. 2016 Dec 27. doi: 10.1007/s12185-016-2170.
    PubMed     Text format     Abstract available


    November 2016
  22. ICHIMURA T, Yoshida K, Okuno Y, Yujiri T, et al
    Diagnostic challenge of Diamond-Blackfan anemia in mothers and children by whole-exome sequencing.
    Int J Hematol. 2016.
    PubMed     Text format     Abstract available


  23. NINOMIYA H, Obara N, Chiba S, Usuki K, et al
    Interim analysis of post-marketing surveillance of eculizumab for paroxysmal nocturnal hemoglobinuria in Japan.
    Int J Hematol. 2016;104:548-558.
    PubMed     Text format     Abstract available


    October 2016
  24. GUO Z, Gao HY, Zhang TY, Liu XD, et al
    Analysis of allogeneic hematopoietic stem cell transplantation with high-dose cyclophosphamide-induced immune tolerance for severe aplastic anemia.
    Int J Hematol. 2016.
    PubMed     Text format     Abstract available


    August 2016
  25. QI W, Yan L, Liu C, Fu R, et al
    Abnormal histone acetylation of CD8+ T cells in patients with severe aplastic anemia.
    Int J Hematol. 2016.
    PubMed     Text format     Abstract available


  26. NAKAO S
    Diagnostic problems in acquired bone marrow failure syndromes.
    Int J Hematol. 2016;104:151-2.
    PubMed     Text format    


  27. INOUE S, Kodjebacheva G, Scherrer T, Rice G, et al
    Adherence to hydroxyurea medication by children with sickle cell disease (SCD) using an electronic device: a feasibility study.
    Int J Hematol. 2016;104:200-7.
    PubMed     Text format     Abstract available


  28. FALCHI L, Grillo LM, Diuguid-Gerber JL, Eisenberger AB, et al
    Severe mechanical hemolysis in a patient with thalassemia minor who had undergone inappropriate splenectomy.
    Int J Hematol. 2016;104:147-8.
    PubMed     Text format    


  29. MIYATA T, Uchida Y, Yoshida Y, Kato H, et al
    No association between dysplasminogenemia with p.Ala620Thr mutation and atypical hemolytic uremic syndrome.
    Int J Hematol. 2016;104:223-7.
    PubMed     Text format     Abstract available


  30. MARSH JC, Mufti GJ
    Clinical significance of acquired somatic mutations in aplastic anaemia.
    Int J Hematol. 2016;104:159-67.
    PubMed     Text format     Abstract available


    July 2016
  31. LI Y, He H, Yang L, Li X, et al
    Therapeutic effect of Colla corii asini on improving anemia and hemoglobin compositions in pregnant women with thalassemia.
    Int J Hematol. 2016.
    PubMed     Text format     Abstract available


  32. CHUNCHARUNEE S, Wong R, Rojnuckarin P, Chang CS, et al
    Efficacy of rabbit antithymocyte globulin as first-line treatment of severe aplastic anemia: an Asian multicenter retrospective study.
    Int J Hematol. 2016.
    PubMed     Text format     Abstract available


  33. FU R, Yan S, Wang X, Wang G, et al
    A monocentric retrospective study comparing pulse cyclophosphamide therapy versus low dose rituximab in the treatment of refractory autoimmune hemolytic anemia in adults.
    Int J Hematol. 2016.
    PubMed     Text format     Abstract available


    June 2016
  34. TAKAHASHI N, Kameoka J, Takahashi N, Tamai Y, et al
    Causes of macrocytic anemia among 628 patients: mean corpuscular volumes of 114 and 130 fL as critical markers for categorization.
    Int J Hematol. 2016.
    PubMed     Text format     Abstract available


  35. HASHIMOTO K, Harada M, Kamijo Y
    Pure red cell aplasia induced by anti-erythropoietin antibodies, well-controlled with tacrolimus.
    Int J Hematol. 2016.
    PubMed     Text format     Abstract available


  36. SUZUKI T, Kobayashi H, Kawasaki Y, Okazuka K, et al
    Efficacy of combination therapy with anti-thymocyte globulin and cyclosporine A as a first-line treatment in adult patients with aplastic anemia: a comparison of rabbit and horse formulations.
    Int J Hematol. 2016.
    PubMed     Text format     Abstract available


  37. WAN Y, Chen X, An W, Ruan M, et al
    Clinical features, mutations and treatment of 104 patients of Diamond-Blackfan anemia in China: a single-center retrospective study.
    Int J Hematol. 2016.
    PubMed     Text format     Abstract available


  38. BACIGALUPO A, Giammarco S, Sica S
    Bone marrow transplantation versus immunosuppressive therapy in patients with acquired severe aplastic anemia.
    Int J Hematol. 2016.
    PubMed     Text format     Abstract available


  39. SIWAPONANAN P, Fucharoen S, Sirankapracha P, Winichagoon P, et al
    Elevated levels of miR-210 correlate with anemia in beta-thalassemia/HbE patients.
    Int J Hematol. 2016.
    PubMed     Text format     Abstract available


  40. YU F, Du Y, Han B
    A comparative analysis of clinical characteristics of patients with paroxysmal nocturnal hemoglobinuria between Asia and Europe/America.
    Int J Hematol. 2016;103:649-54.
    PubMed     Text format     Abstract available


  41. TANTIWORAWIT A, Charoenkwan P, Hantrakool S, Choeyprasert W, et al
    Iron overload in non-transfusion-dependent thalassemia: association with genotype and clinical risk factors.
    Int J Hematol. 2016;103:643-8.
    PubMed     Text format     Abstract available


  42. PIGATTO PD, Ronchi A, Guzzi G
    Iron overload, G6PD deficiency, and lead levels on blood smears.
    Int J Hematol. 2016;103:724.
    PubMed     Text format    


  43. MIYASAKA N, Miura O, Kawaguchi T, Arima N, et al
    Pregnancy outcomes of patients with paroxysmal nocturnal hemoglobinuria treated with eculizumab: a Japanese experience and updated review.
    Int J Hematol. 2016;103:703-12.
    PubMed     Text format     Abstract available


    May 2016
  44. DIAMANTIDIS MD, Neokleous N, Agapidou A, Vetsiou E, et al
    Iron chelation therapy of transfusion-dependent beta-thalassemia during pregnancy in the era of novel drugs: is deferasirox toxic?
    Int J Hematol. 2016;103:537-44.
    PubMed     Text format     Abstract available


    April 2016
  45. SUZUKI K, Muramatsu H, Okuno Y, Narita A, et al
    Immunosuppressive therapy for patients with Down syndrome and idiopathic aplastic anemia.
    Int J Hematol. 2016.
    PubMed     Text format     Abstract available


  46. NARITA A, Kojima S
    Biomarkers for predicting clinical response to immunosuppressive therapy in aplastic anemia.
    Int J Hematol. 2016.
    PubMed     Text format     Abstract available


  47. AIZAWA K, Kawasaki R, Tashiro Y, Hirata M, et al
    Epoetin beta pegol, but not recombinant erythropoietin, retains its hematopoietic effect in vivo in the presence of the sialic acid-metabolizing enzyme sialidase.
    Int J Hematol. 2016.
    PubMed     Text format     Abstract available


  48. HASEGAWA D
    The current perspective of low-grade myelodysplastic syndrome in children.
    Int J Hematol. 2016;103:360-4.
    PubMed     Text format     Abstract available


  49. MANABE A
    Guest Editorial: Inherited bone marrow failure and myelodysplasia in children: how much do we know about pediatric diseases?
    Int J Hematol. 2016;103:359.
    PubMed     Text format    


  50. DALLE JH, Peffault de Latour R
    Allogeneic hematopoietic stem cell transplantation for inherited bone marrow failure syndromes.
    Int J Hematol. 2016;103:373-9.
    PubMed     Text format     Abstract available


    March 2016
  51. IMASHUKU S, Muramatsu H, Sugihara T, Okuno Y, et al
    PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus.
    Int J Hematol. 2016.
    PubMed     Text format     Abstract available


  52. ZHU H, Xu W, Liu H, Wang H, et al
    Expression of activated molecules on CD5B lymphocytes in autoimmune hemolytic anemia.
    Int J Hematol. 2016.
    PubMed     Text format     Abstract available


  53. HATZIMICHAEL E, Briasoulis E
    Megaloblastic anemia presenting with skin hyperpigmentation.
    Int J Hematol. 2016.
    PubMed     Text format    


  54. FAN X, Kremer Hovinga JA, Shirotani-Ikejima H, Eura Y, et al
    Genetic variations in complement factors in patients with congenital thrombotic thrombocytopenic purpura with renal insufficiency.
    Int J Hematol. 2016;103:283-91.
    PubMed     Text format     Abstract available


    February 2016
  55. MORI T, Koh H, Onishi Y, Kako S, et al
    Impact of cyclophosphamide dose of conditioning on the outcome of allogeneic hematopoietic stem cell transplantation for aplastic anemia from human leukocyte antigen-identical sibling.
    Int J Hematol. 2016.
    PubMed     Text format     Abstract available


  56. KOOK H, Chung NG, Kang HJ, Im HJ, et al
    Acquired aplastic anemia in Korean children: treatment guidelines from the Bone Marrow Failure Committee of the Korean Society of Pediatric Hematology Oncology.
    Int J Hematol. 2016.
    PubMed     Text format     Abstract available


  57. KATSURADA T, Kawabata H, Kawabata D, Kawahara M, et al
    A Japanese family with X-linked sideroblastic anemia affecting females and manifesting as macrocytic anemia.
    Int J Hematol. 2016.
    PubMed     Text format     Abstract available


    January 2016
  58. ADDO L, Ikuta K, Tanaka H, Toki Y, et al
    The three isoforms of hepcidin in human serum and their processing determined by liquid chromatography-tandem mass spectrometry (LC-tandem MS).
    Int J Hematol. 2016;103:34-43.
    PubMed     Text format     Abstract available


    November 2015
  59. IKEDA F, Toki T, Kanezaki R, Terui K, et al
    ALDH2 polymorphism in patients with Diamond-Blackfan anemia in Japan.
    Int J Hematol. 2015.
    PubMed     Text format    


    October 2015
  60. WU L, Mo W, Zhang Y, Deng H, et al
    Impairment of hematopoietic stem cell niches in patients with aplastic anemia.
    Int J Hematol. 2015.
    PubMed     Text format     Abstract available


    August 2015
  61. XU ZZ, Zhao BB, Xiong H, Wei BW, et al
    Serum BAFF and APRIL levels in patients with autoimmune hemolytic anemia and their clinical significance.
    Int J Hematol. 2015.
    PubMed     Text format     Abstract available


    July 2015
  62. ONAY H, Aykut A, Karaca E, Durmaz A, et al
    Molecular spectrum of alpha-globin gene mutations in the Aegean region of Turkey: first observation of three alpha-globin gene mutations in the Turkish population.
    Int J Hematol. 2015;102:1-6.
    PubMed     Text format     Abstract available


    June 2015
  63. WANG M, Li X, Shi J, Shao Y, et al
    Outcome of a novel immunosuppressive strategy of cyclosporine, levamisole and danazol for severe aplastic anemia.
    Int J Hematol. 2015.
    PubMed     Text format     Abstract available


    April 2015
  64. YIGIT N, Covey S, Tam W
    Massive splenic hamartoma with bizarre stromal cells.
    Int J Hematol. 2015;101:315-6.
    PubMed     Text format    


  65. SAKURAGI M, Hayashi S, Maruyama M, Kabutomori O, et al
    Clinical significance of IPF% or RP% measurement in distinguishing primary immune thrombocytopenia from aplastic thrombocytopenic disorders.
    Int J Hematol. 2015;101:369-75.
    PubMed     Text format     Abstract available


    February 2015
  66. VANDER MEEREN S, Van Damme A, Jochmans K
    Prominent basophilic stippling and hemochromatosis in glucose-6-phosphate dehydrogenase deficiency.
    Int J Hematol. 2015;101:112-3.
    PubMed     Text format    


  67. UNAL S, Ozdemir O, Ozcimen AA, Oztas Y, et al
    Increase of serum fractalkine and fractalkine gene expression levels in sickle cell disease patients.
    Int J Hematol. 2015;101:114-8.
    PubMed     Text format     Abstract available


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