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Articles published in Ann Hematol

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Single Articles


    July 2018
  1. YAMAMOTO A, Meguri Y, Fukuda A, Kambara Y, et al
    A case of reversible cerebral vasoconstriction syndrome developing during treatment of adult aplastic anemia.
    Ann Hematol. 2018 Jul 10. pii: 10.1007/s00277-018-3430.
    PubMed     Text format    


  2. RINELLI M, Bellacchio E, Berardinelli F, Pascolini G, et al
    Structural modeling of a novel TERC variant in a patient with aplastic anemia and short telomeres.
    Ann Hematol. 2018 Jul 6. pii: 10.1007/s00277-018-3415.
    PubMed     Text format    


  3. CLE DV, Atta EH, Dias DSP, Lima CBL, et al
    Rabbit antithymocyte globulin dose does not affect response or survival as first-line therapy for acquired aplastic anemia: a multicenter retrospective study.
    Ann Hematol. 2018 Jul 5. pii: 10.1007/s00277-018-3416.
    PubMed     Text format     Abstract available


    June 2018
  4. MYINT ZW, Oo TH, Thein KZ, Tun AM, et al
    Copper deficiency anemia: review article.
    Ann Hematol. 2018 Jun 29. pii: 10.1007/s00277-018-3407.
    PubMed     Text format     Abstract available


  5. ARANDA N, Bedmar C, Arija V, Jardi C, et al
    Serum hepcidin levels, iron status, and HFE gene alterations during the first year of life in healthy Spanish infants.
    Ann Hematol. 2018;97:1071-1080.
    PubMed     Text format     Abstract available


    May 2018
  6. BOHME T, Medinger M, Suenderhauf C, Speer O, et al
    Severe anemia after trans-catheter arterial chemoembolization-an unusual presentation of hemoglobin Zurich.
    Ann Hematol. 2018 May 8. pii: 10.1007/s00277-018-3353.
    PubMed     Text format    


  7. CHATTERJEE T, Chakravarty A, Chakravarty S
    Hydroxyurea responses in clinically varied beta, HbE-beta thalassaemia and sickle cell anaemia patients of Eastern India.
    Ann Hematol. 2018;97:893-898.
    PubMed     Text format     Abstract available


  8. NEMTSAS P, Arnaoutoglou M, Perifanis V, Koutsouraki E, et al
    Polyneuropathy and myopathy in beta-thalassemia major patients.
    Ann Hematol. 2018;97:899-904.
    PubMed     Text format     Abstract available


  9. RAGHUNATHAN VM, Whitesell PL, Lim SH
    Sleep-disordered breathing in patients with sickle cell disease.
    Ann Hematol. 2018;97:755-762.
    PubMed     Text format     Abstract available


    April 2018
  10. MICHALAK SS, Rupa-Matysek J, Gil L
    Comorbidities, repeated hospitalizations, and age >/= 80 years as indicators of anemia development in the older population.
    Ann Hematol. 2018 Apr 9. pii: 10.1007/s00277-018-3321.
    PubMed     Text format     Abstract available


  11. MIRLOHI MS, Yaghooti H, Shirali S, Aminasnafi A, et al
    Increased levels of advanced glycation end products positively correlate with iron overload and oxidative stress markers in patients with beta-thalassemia major.
    Ann Hematol. 2018;97:679-684.
    PubMed     Text format     Abstract available


    March 2018
  12. RODGERS GM, Gilreath JA
    Eltrombopag as initial monotherapy for severe aplastic anemia-a case report.
    Ann Hematol. 2018 Mar 20. pii: 10.1007/s00277-018-3303.
    PubMed     Text format    


    February 2018
  13. GHAVAMZADEH A, Sotoudeh M, Hashemi Taheri AP, Alimoghaddam K, et al
    Liver fibrosis alleviation after co-transplantation of hematopoietic stem cells with mesenchymal stem cells in patients with thalassemia major.
    Ann Hematol. 2018;97:327-334.
    PubMed     Text format     Abstract available


    January 2018
  14. ZHAO L, Zhu H, Han B, Wang L, et al
    Influence of genetic polymorphisms of IL23R, STAT3, IL12B, and STAT4 on the risk of aplastic anemia and the effect of immunosuppressive therapy.
    Ann Hematol. 2018 Jan 12. pii: 10.1007/s00277-018-3227.
    PubMed     Text format     Abstract available


    December 2017
  15. VAN ZEVENTER IA, Schreurs JWGM, van den Berg E, Mulder AB, et al
    Efficacy of antithymocyte globulin as first-line treatment for aplastic anemia-a single-center experience.
    Ann Hematol. 2017 Dec 16. pii: 10.1007/s00277-017-3201.
    PubMed     Text format    


    November 2017
  16. SMART LR, Ambrose EE, Raphael KC, Hokororo A, et al
    Simultaneous point-of-care detection of anemia and sickle cell disease in Tanzania: the RAPID study.
    Ann Hematol. 2017 Nov 16. doi: 10.1007/s00277-017-3182.
    PubMed     Text format     Abstract available


  17. VISWESHWAR N, Jaglal M, Sokol L, Zuckerman K, et al
    Chemotherapy-related anemia.
    Ann Hematol. 2017 Nov 4. doi: 10.1007/s00277-017-3155.
    PubMed     Text format    


  18. FERRAO J, Silva M, Goncalves L, Gomes S, et al
    Widening the spectrum of deletions and molecular mechanisms underlying alpha-thalassemia.
    Ann Hematol. 2017;96:1921-1929.
    PubMed     Text format     Abstract available


  19. KLONIZAKIS P, Klaassen R, Sousos N, Liakos A, et al
    Evaluation of the Greek TranQol: a novel questionnaire for measuring quality of life in transfusion-dependent thalassemia patients.
    Ann Hematol. 2017;96:1937-1944.
    PubMed     Text format     Abstract available


  20. MAIRA D, Cassinerio E, Marcon A, Mancarella M, et al
    Progression of liver fibrosis can be controlled by adequate chelation in transfusion-dependent thalassemia (TDT).
    Ann Hematol. 2017;96:1931-1936.
    PubMed     Text format     Abstract available


    October 2017
  21. HOUSTON BL, Jayakar J, Wells RA, Lenis M, et al
    A predictive model of response to erythropoietin stimulating agents in myelodysplastic syndrome: from the Canadian MDS patient registry.
    Ann Hematol. 2017 Oct 3. doi: 10.1007/s00277-017-3137.
    PubMed     Text format     Abstract available


  22. VILLEGAS A, Nunez R, Gaya A, Cuevas-Ruiz MV, et al
    Presence of acute and chronic renal failure in patients with paroxysmal nocturnal hemoglobinuria: results of a retrospective analysis from the Spanish PNH Registry.
    Ann Hematol. 2017;96:1727-1733.
    PubMed     Text format     Abstract available


    September 2017
  23. YANG N, Chen J, Zhang H, Dai Z, et al
    Horse versus rabbit antithymocyte globulin in immunosuppressive therapy of treatment-naive aplastic anemia: a systematic review and meta-analysis.
    Ann Hematol. 2017 Sep 30. doi: 10.1007/s00277-017-3136.
    PubMed     Text format     Abstract available


  24. KEDAR P, Parmar V, Devendra R, Gupta V, et al
    Congenital dyserythropoietic anemia type II mimicking hereditary spherocytosis in Indian patient with SEC23B-Y462C mutations.
    Ann Hematol. 2017 Sep 7. doi: 10.1007/s00277-017-3116.
    PubMed     Text format    


  25. GRAZIADEI G, Casoni FM, Annoni F, Cortinovis I, et al
    Transcranial color Doppler in stroke-free adult patients with sickle cell disease.
    Ann Hematol. 2017;96:1547-1555.
    PubMed     Text format     Abstract available


  26. RICCHI P, Meloni A, Costantini S, Spasiano A, et al
    Soluble form of transferrin receptor-1 level is associated with the age at first diagnosis and the risk of therapeutic intervention and iron overloading in patients with non-transfusion-dependent thalassemia.
    Ann Hematol. 2017;96:1541-1546.
    PubMed     Text format     Abstract available


  27. RODEGHIERO F, Carli G
    Beyond immune thrombocytopenia: the evolving role of thrombopoietin receptor agonists.
    Ann Hematol. 2017;96:1421-1434.
    PubMed     Text format     Abstract available


    August 2017
  28. FUJIWARA T, Fukuhara N, Ichikawa S, Kobayashi M, et al
    A novel heterozygous ALAS2 mutation in a female with macrocytic sideroblastic anemia resembling myelodysplastic syndrome with ring sideroblasts: a case report and literature review.
    Ann Hematol. 2017 Aug 24. doi: 10.1007/s00277-017-3106.
    PubMed     Text format    


  29. ATTA EH, Lima CBL, Dias DSP, Cle DV, et al
    Predictors of early mortality after rabbit antithymocyte globulin as first-line treatment in severe aplastic anemia.
    Ann Hematol. 2017 Aug 16. doi: 10.1007/s00277-017-3086.
    PubMed     Text format     Abstract available


  30. LI Q, Luo C, Luo C, Wang J, et al
    Disease-specific hematopoietic stem cell transplantation in children with inherited bone marrow failure syndromes.
    Ann Hematol. 2017;96:1389-1397.
    PubMed     Text format     Abstract available


  31. WIEBKING V, Hutker S, Schmid I, Immler S, et al
    Reduced toxicity, myeloablative HLA-haploidentical hematopoietic stem cell transplantation with post-transplantation cyclophosphamide for sickle cell disease.
    Ann Hematol. 2017;96:1373-1377.
    PubMed     Text format     Abstract available


    July 2017
  32. KLAIHMON P, Vimonpatranon S, Noulsri E, Lertthammakiat S, et al
    Normalized levels of red blood cells expressing phosphatidylserine, their microparticles, and activated platelets in young patients with beta-thalassemia following bone marrow transplantation.
    Ann Hematol. 2017 Jul 26. doi: 10.1007/s00277-017-3070.
    PubMed     Text format     Abstract available


  33. ANTUNES FD, Propheta VGS, Vasconcelos HA, Cipolotti R, et al
    Neuropathic pain in patients with sickle cell disease: a cross-sectional study assessing teens and young adults.
    Ann Hematol. 2017;96:1121-1125.
    PubMed     Text format     Abstract available


    June 2017
  34. DE LACERDA MP, Guedes NR, Yamakawa PE, Pereira AD, et al
    Treatment of refractory autoimmune hemolytic anemia with venetoclax in relapsed chronic lymphocytic leukemia with (del17p).
    Ann Hematol. 2017 Jun 9. doi: 10.1007/s00277-017-3039.
    PubMed     Text format    


  35. TESSOULIN B, Thomare P, Delande E, Moynard J, et al
    Carboplatin instead of cisplatin in combination with dexamethasone, high-dose cytarabine with or without rituximab (DHAC+/-R) is an effective treatment with low toxicity in Hodgkin's and non-Hodgkin's lymphomas.
    Ann Hematol. 2017;96:943-950.
    PubMed     Text format     Abstract available


  36. SURAPOLCHAI P, Chuansumrit A, Sirachainan N, Kadegasem P, et al
    A molecular study on the role of alpha-hemoglobin-stabilizing protein in hemoglobin H disease.
    Ann Hematol. 2017;96:1005-1014.
    PubMed     Text format     Abstract available


  37. BALDINI M, Marcon A, Ulivieri FM, Seghezzi S, et al
    Bone quality in beta-thalassemia intermedia: relationships with bone quantity and endocrine and hematologic variables.
    Ann Hematol. 2017;96:995-1003.
    PubMed     Text format     Abstract available


  38. CASSINERIO E, Baldini IM, Alameddine RS, Marcon A, et al
    Pregnancy in patients with thalassemia major: a cohort study and conclusions for an adequate care management approach.
    Ann Hematol. 2017;96:1015-1021.
    PubMed     Text format     Abstract available


    May 2017
  39. CASTELLI R, Sciara S, Lambertenghi Deliliers G, Pantaleo G, et al
    Biosimilar epoetin alfa increases haemoglobin levels and brings cognitive and socio-relational benefits to elderly transfusion-dependent multiple myeloma patients: results from a pilot study.
    Ann Hematol. 2017;96:779-786.
    PubMed     Text format     Abstract available


  40. LAI YK, Lai NM, Lee SW
    Glucose-6-phosphate dehydrogenase deficiency and risk of diabetes: a systematic review and meta-analysis.
    Ann Hematol. 2017;96:839-845.
    PubMed     Text format     Abstract available


    April 2017
  41. YOUSSRY I, Soliman N, Ghamrawy M, Samy RM, et al
    Circulating microparticles and the risk of thromboembolic events in Egyptian beta thalassemia patients.
    Ann Hematol. 2017;96:597-603.
    PubMed     Text format     Abstract available


  42. ALASHKAR F, Vance C, Herich-Terhurne D, Preising N, et al
    Serologic response to meningococcal vaccination in patients with paroxysmal nocturnal hemoglobinuria (PNH) chronically treated with the terminal complement inhibitor eculizumab.
    Ann Hematol. 2017;96:589-596.
    PubMed     Text format     Abstract available


  43. CHEN M, Zhuang J, Zhou D, Xu Y, et al
    Outcome of anti-thymocyte immunoglobulin plus cyclosporine A for severe aplastic anaemia with chronic hepatitis B virus infection.
    Ann Hematol. 2017;96:581-587.
    PubMed     Text format     Abstract available


    March 2017
  44. GREGORY GP, Farrell A, Brown S
    Cold agglutinin disease complicated by acrocyanosis and necrosis.
    Ann Hematol. 2017;96:509-510.
    PubMed     Text format    


    February 2017
  45. PUIGVI L, Baumann T, Fernandez S, Castro P, et al
    Massive erythrophagocytosis by peripheral monocytes and neutrophils in parvovirus-B19 autoimmune hemolytic anemia.
    Ann Hematol. 2017 Feb 21. doi: 10.1007/s00277-017-2957.
    PubMed     Text format    


  46. KLAIHMON P, Phongpao K, Kheansaard W, Noulsri E, et al
    Microparticles from splenectomized beta-thalassemia/HbE patients play roles on procoagulant activities with thrombotic potential.
    Ann Hematol. 2017;96:189-198.
    PubMed     Text format     Abstract available


  47. WANG HC, Hsieh LL, Liu YC, Hsiao HH, et al
    The epidemiologic transition of thalassemia and associated hemoglobinopathies in southern Taiwan.
    Ann Hematol. 2017;96:183-188.
    PubMed     Text format     Abstract available


  48. BURKHARDT L, Lobitz S, Koustenis E, Rueckriegel SM, et al
    Cognitive and fine motor deficits in a pediatric sickle cell disease cohort of mixed ethnic origin.
    Ann Hematol. 2017;96:199-213.
    PubMed     Text format     Abstract available


    January 2017
  49. OUEDERNI M, Ben Khaled M, Mellouli F, Ben Fraj E, et al
    Myocardial and liver iron overload, assessed using T2* magnetic resonance imaging with an excel spreadsheet for post processing in Tunisian thalassemia major patients.
    Ann Hematol. 2017;96:133-139.
    PubMed     Text format     Abstract available


  50. BOGUSLAWSKA DM, Heger E, Machnicka B, Skulski M, et al
    A new frameshift mutation of the beta-spectrin gene associated with hereditary spherocytosis.
    Ann Hematol. 2017;96:163-165.
    PubMed     Text format    


  51. AL NAJJAR S, Adam S, Ahmed N, Qari M, et al
    Markers of endothelial dysfunction and leucocyte activation in Saudi and non-Saudi haplotypes of sickle cell disease.
    Ann Hematol. 2017;96:141-146.
    PubMed     Text format     Abstract available


    December 2016
  52. LIANG XH, Rong L, He G, He H, et al
    Polymorphisms of the TGF-beta1 gene and the risk of acquired aplastic anemia in a Chinese population.
    Ann Hematol. 2016.
    PubMed     Text format     Abstract available


  53. OH DH, Motorna O, Kong JB, Brown S, et al
    Linezolid-associated reticulocytopenia.
    Ann Hematol. 2016;95:2095-2097.
    PubMed     Text format    


    November 2016
  54. GROTH M, Singer S, Niedeggen C, Petermann-Meyer A, et al
    Development of a disease-specific quality of life questionnaire for patients with aplastic anemia and/or paroxysmal nocturnal hemoglobinuria (QLQ-AA/PNH)-report on phases I and II.
    Ann Hematol. 2016.
    PubMed     Text format     Abstract available


    October 2016
  55. ZHANG XH, Wang QM, Chen H, Chen YH, et al
    Clinical characteristics and risk factors of Intracranial hemorrhage in patients following allogeneic hematopoietic stem cell transplantation.
    Ann Hematol. 2016;95:1637-43.
    PubMed     Text format     Abstract available


  56. CRISP RL, Maltaneri RE, Vittori DC, Solari L, et al
    Red blood cell aquaporin-1 expression is decreased in hereditary spherocytosis.
    Ann Hematol. 2016;95:1595-601.
    PubMed     Text format     Abstract available


  57. PHONDEECHAREON T, Wattanapanitch M, U-Pratya Y, Damkham C, et al
    Generation of induced pluripotent stem cells as a potential source of hematopoietic stem cells for transplant in PNH patients.
    Ann Hematol. 2016;95:1617-25.
    PubMed     Text format     Abstract available


  58. URESHINO H, Miyahara M
    Unusual co-occurrence of Evans syndrome and pure red cell aplasia in elderly patient with prostate cancer.
    Ann Hematol. 2016;95:1743-4.
    PubMed     Text format    


  59. HUANG Y, Wang M, Yu C, Lei Y, et al
    Clinical presentation of the hemoglobin Youngstown variant in a Chinese family.
    Ann Hematol. 2016;95:1925-7.
    PubMed     Text format    


  60. BALAIAN E, Schuster C, Schonefeldt C, Germing U, et al
    Selective expansion of regulatory T cells during lenalidomide treatment of myelodysplastic syndrome with isolated deletion 5q.
    Ann Hematol. 2016;95:1805-10.
    PubMed     Text format     Abstract available


    September 2016
  61. VAGACE JM, Cardesa R, Corbacho A, Vazquez T, et al
    Etiopathological mechanisms and clinical characteristics of hyperhemolysis syndrome in Spanish patients with thalassemia.
    Ann Hematol. 2016;95:1419-27.
    PubMed     Text format     Abstract available


  62. LANZA F, Lazzari MC, Brambilla P, Di Martino G, et al
    An unusual association of paroxysmal nocturnal hemoglobinuria, myelodysplastic syndrome, and diffuse large B-cell non-Hodgkin lymphoma in a Caucasian man.
    Ann Hematol. 2016;95:1555-7.
    PubMed     Text format    


  63. HAGIWARA K, Kamesaki T, Kakimoto T, Fukushima K, et al
    Long-term follow-up of non-syphilitic paroxysmal cold hemoglobinuria in an adult.
    Ann Hematol. 2016;95:1547-9.
    PubMed     Text format    


    August 2016
  64. LOW MS, Vilcassim S, Fedele P, Grigoriadis G, et al
    Acute monocytic leukemia masked by hemolytic anemia and sclerotic lesions.
    Ann Hematol. 2016.
    PubMed     Text format    


  65. BAPTISTA LC, Costa ML, Ferreira R, Albuquerque DM, et al
    Abnormal expression of inflammatory genes in placentas of women with sickle cell anemia and sickle hemoglobin C disease.
    Ann Hematol. 2016.
    PubMed     Text format     Abstract available


  66. BELISARIO AR, Sales RR, Toledo NE, Muniz MB, et al
    Reticulocyte count is the most important predictor of acute cerebral ischemia and high-risk transcranial Doppler in a newborn cohort of 395 children with sickle cell anemia.
    Ann Hematol. 2016.
    PubMed     Text format     Abstract available


  67. ZAREI T, Haghpanah S, Parand S, Moravej H, et al
    Evaluation of bone mineral density in patients with hemoglobin H disease.
    Ann Hematol. 2016;95:1329-32.
    PubMed     Text format     Abstract available


  68. KARIMI M, Haghpanah S, Pishdad P, Rachmilewitz EA, et al
    Frequency of silent cerebral ischemia in patients with transfusion-dependent beta-thalassemia major compared to healthy individuals.
    Ann Hematol. 2016;95:1387.
    PubMed     Text format    


  69. ZAFARI M, Kosaryan M, Gill P, Alipour A, et al
    Non-invasive prenatal diagnosis of beta-thalassemia by detection of the cell-free fetal DNA in maternal circulation: a systematic review and meta-analysis.
    Ann Hematol. 2016;95:1341-50.
    PubMed     Text format     Abstract available


    July 2016
  70. VISWESHWAR N, Jaglal M, Booth C, Griffin P, et al
    AOHE: manuscript AOHE-D-16-00564 paroxysmal nocturnal hemoglobinuria with autoimmune hemolytic anemia following eculizumab therapy-with large granular lymphocytic leukemia.
    Ann Hematol. 2016.
    PubMed     Text format    


    June 2016
  71. PEREIRA J, Bento C, Manco L, Gonzalez A, et al
    Congenital dyserythropoietic anemia associated to a GATA1 mutation aggravated by pyruvate kinase deficiency.
    Ann Hematol. 2016.
    PubMed     Text format    


  72. RASO S, Napolitano M, Saccullo G, Siragusa S, et al
    Abdominal aortic thrombosis secondary to reactive thrombocytosis in a patient with iron deficiency anemia.
    Ann Hematol. 2016.
    PubMed     Text format    


  73. DEL ORBE BARRETO R, Arrizabalaga B, De la Hoz Rastrollo AB, Garcia-Orad A, et al
    Hereditary xerocytosis, a misleading anemia.
    Ann Hematol. 2016.
    PubMed     Text format    


  74. UPADHYE D, Jain D, Trivedi Y, Nadkarni A, et al
    Influence of single nucleotide polymorphisms in the BCL11A and HBS1L-MYB gene on the HbF levels and clinical severity of sickle cell anaemia patients.
    Ann Hematol. 2016;95:1201-3.
    PubMed     Text format    


    May 2016
  75. MUSA BM, Galadanci NA, Coker M, Bussell S, et al
    The global burden of pulmonary hypertension in sickle cell disease: a systematic review and meta-analysis.
    Ann Hematol. 2016.
    PubMed     Text format     Abstract available


  76. KARACAOGLU PK, Asma S, Korur A, Solmaz S, et al
    East Mediterranean region sickle cell disease mortality trial: retrospective multicenter cohort analysis of 735 patients.
    Ann Hematol. 2016;95:993-1000.
    PubMed     Text format     Abstract available


  77. CARLI G, Visco C, Falisi E, Perbellini O, et al
    Evans syndrome secondary to chronic lymphocytic leukaemia: presentation, treatment, and outcome.
    Ann Hematol. 2016;95:863-70.
    PubMed     Text format     Abstract available


  78. PIERINI A, Mancusi A, Terenzi A, Massei MS, et al
    New mechanism of lymphoma-induced bone marrow aplasia.
    Ann Hematol. 2016;95:1013-5.
    PubMed     Text format    


    April 2016
  79. O'NEILL C, Siddiqi I, Brynes RK, Vergara-Lluri M, et al
    Pegylated interferon for the treatment of early myelofibrosis: correlation of serial laboratory studies with response to therapy.
    Ann Hematol. 2016;95:733-8.
    PubMed     Text format     Abstract available


  80. POGGI M, Sorrentino F, Pugliese P, Smacchia MP, et al
    Longitudinal changes of endocrine and bone disease in adults with beta-thalassemia major receiving different iron chelators over 5 years.
    Ann Hematol. 2016;95:757-63.
    PubMed     Text format     Abstract available


  81. LARIBI K, Bolle D, Ghnaya H, Sandu A, et al
    Rituximab is an effective and safe treatment of relapse in elderly patients with resistant warm AIHA.
    Ann Hematol. 2016;95:765-9.
    PubMed     Text format     Abstract available


    March 2016
  82. DAO AT, Yamazaki H, Takamatsu H, Sugimori C, et al
    Cyclosporine restores hematopoietic function by compensating for decreased Tregs in patients with pure red cell aplasia and acquired aplastic anemia.
    Ann Hematol. 2016.
    PubMed     Text format     Abstract available


  83. TODO K, Ohmae T, Osamura T, Imamura T, et al
    Severe Helicobacter pylori gastritis-related thrombocytopenia and iron deficiency anemia in an adolescent female.
    Ann Hematol. 2016.
    PubMed     Text format    


  84. KELKITLI E, Ozturk N, Aslan NA, Kilic-Baygutalp N, et al
    Serum zinc levels in patients with iron deficiency anemia and its association with symptoms of iron deficiency anemia.
    Ann Hematol. 2016.
    PubMed     Text format     Abstract available


    February 2016
  85. HUANG Z, Shi J, Shao Y, Nie N, et al
    Clinical profile of megaloblastic anemia in China: a single center experience from MegA-1710 program over two decades.
    Ann Hematol. 2016.
    PubMed     Text format    


  86. PICH A, Godio L, Riera L, Cavaliere C, et al
    Myelodysplastic syndrome with del (5q) and JAK2(V617F) mutation transformed to acute myeloid leukaemia with complex karyotype.
    Ann Hematol. 2016;95:525-7.
    PubMed     Text format    


  87. SORNJAI W, Jaratsittisin J, Khungwanmaythawee K, Svasti S, et al
    Dysregulation of ferroportin gene expression in beta(0)-thalassemia/Hb E disease.
    Ann Hematol. 2016;95:387-96.
    PubMed     Text format     Abstract available


  88. KUNZ JB, Awad S, Happich M, Muckenthaler L, et al
    Significant prevalence of sickle cell disease in Southwest Germany: results from a birth cohort study indicate the necessity for newborn screening.
    Ann Hematol. 2016;95:397-402.
    PubMed     Text format     Abstract available


  89. KOWSARYAN M, Zafari M
    Which pamidronate protocol is the best for treating osteoporosis in beta-thalassemia major?
    Ann Hematol. 2016;95:383-6.
    PubMed     Text format     Abstract available


  90. DEVECI B, Kurtoglu A, Kurtoglu E, Salim O, et al
    Documentation of renal glomerular and tubular impairment and glomerular hyperfiltration in multitransfused patients with beta thalassemia.
    Ann Hematol. 2016;95:375-81.
    PubMed     Text format     Abstract available


    January 2016
  91. KIM JS, Jang JH, Yoon SS, Lee JH, et al
    Distinct subgroups of paroxysmal nocturnal hemoglobinuria (PNH) with cytopenia: results from South Korean National PNH Registry.
    Ann Hematol. 2016;95:125-33.
    PubMed     Text format     Abstract available


  92. KARIMI M, Toosi F, Haghpanah S, Pishdad P, et al
    The frequency of silent cerebral ischemia in patients with transfusion-dependent beta-thalassemia major.
    Ann Hematol. 2016;95:135-9.
    PubMed     Text format     Abstract available


  93. UZUNOVA L, Hook CE, Gattens M, Burke GA, et al
    Cold antibody autoimmune haemolytic anaemia in a child with diffuse large B cell lymphoma.
    Ann Hematol. 2016;95:151-2.
    PubMed     Text format    


  94. INOUE S, Khan I, Mushtaq R, Sanikommu SR, et al
    Pain management trend of vaso-occulsive crisis (VOC) at a community hospital emergency department (ED) for patients with sickle cell disease.
    Ann Hematol. 2016;95:221-5.
    PubMed     Text format     Abstract available


  95. VAN HAMEL PARSONS V, Gardner K, Patel R, Thein SL, et al
    Venous thromboembolism in adults with sickle cell disease: experience of a single centre in the UK.
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    December 2015
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    The long-term efficacy and tolerability of oral deferasirox for patients with transfusion-dependent beta-thalassemia in Taiwan.
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  97. ANDRES O, Eber S, Speer CP
    Early postnatal diagnosis of hereditary spherocytosis by combining light microscopy, acidified glycerol lysis test and eosin-5'-maleimide binding assay.
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  98. MEHTA PR, Upadhye DS, Sawant PM, Gorivale MS, et al
    Diverse phenotypes and transfusion requirements due to interaction of beta-thalassemias with triplicated alpha-globin genes.
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    November 2015
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    Incidence of testicular microlithiasis in patients with beta-thalassemia major.
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    October 2015
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    Left ventricular remodeling in patients with sickle cell disease: determinants factors and impact on outcome.
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    September 2015
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    Decitabine versus best supportive care in older patients with refractory anemia with excess blasts in transformation (RAEBt) - results of a subgroup analysis of the randomized phase III study 06011 of the EORTC Leukemia Cooperative Group and German MD
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  102. ST BERNARD R, Hsia CC
    Safe utilization of ibrutinib with or without steroids in chronic lymphocytic leukemia patients with autoimmune hemolytic anemia.
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  103. REHMAN S, Ahmed P, Saba N, Munir S, et al
    Association of GSTM1 and GSTT1 deletion polymorphisms with Pakistani aplastic anemia patients and controls and meta-analysis.
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  104. SAULTZ JN, Wu HM, Cataland S
    Headache prevalence following recovery from TTP and aHUS.
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  105. TABATA R, Tabata C, Yasumizu R, Kojima M, et al
    Severe sustained hypoplastic bone marrow after immunosuppressive therapy in malignant lymphoma cases with anti-centromere protein-B antibody.
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    August 2015
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    Angioimmunoblastic T-cell lymphomas presenting as autoimmune hemolytic anemias: clinical manifestations and circulating cytokine features.
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  107. NEMTSAS P, Arnaoutoglou M, Perifanis V, Koutsouraki E, et al
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    July 2015
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    Anemia among Muslim Bedouin and Jewish women of childbearing age in Southern Israel.
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  109. BIGLIARDI S, Morselli M, Potenza L, Riva G, et al
    Epidemiology and clinical outcome of lower respiratory tract infections by respiratory syncytial virus or parainfluenza virus type 3 in adults receiving treatment for either acute leukemia or severe aplastic anemia: a retrospective single center study
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  110. BOYER T, Grardel N, Copin MC, Roumier C, et al
    Paroxysmal nocturnal hemoglobinuria (PNH) and T cell large granular lymphocyte (LGL) leukemia-an unusual association: another cause of cytopenia in PNH.
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  111. MARTINEZ-LOPEZ J, Jimenez A, Sanchez-Calero J, Monteagudo D, et al
    Myeloproliferative neoplasm in a thalassaemic patient: response to treatment with a JAK inhibitor.
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  112. BAS M, Gumruk F, Gonc N, Cetin M, et al
    Biochemical markers of glucose metabolism may be used to estimate the degree and progression of iron overload in the liver and pancreas of patients with beta-thalassemia major.
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    June 2015
  113. CERVANTES F, Isola IM, Alvarez-Larran A, Hernandez-Boluda JC, et al
    Danazol therapy for the anemia of myelofibrosis: assessment of efficacy with current criteria of response and long-term results.
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    A 5-year follow-up in deferasirox treatment: improvement of cardiac and hepatic iron overload and amelioration in cardiac function in thalassemia major patients.
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    May 2015
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    Comparison and evaluation of three screening tests of hereditary spherocytosis in Chinese patients.
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  116. SO CC, Chan AY, Chan JC, Ma ES, et al
    Alpha thalassemia trait masquerading as hemoglobin H disease due to co-existing primary myelofibrosis.
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  117. KOUTSIS G, Karadima G, Panas M
    Symptomatic striopallidodentate calcinosis (Fahr's syndrome) in a thalassemic patient with hypoparathyroidism.
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