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Articles published in Am J Hematol

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Single Articles


    October 2017
  1. GONZALES GF, Rubin de Celis V, Begazo J, Hinojosa MDR, et al
    Correcting the cut-off point of hemoglobin at high altitude favors misclassification of anemia, erythrocytosis and excessive erythrocytosis.
    Am J Hematol. 2017 Oct 6. doi: 10.1002/ajh.24932.
    PubMed     Text format    


  2. MARTINEZ C, Watson DJ, Shebl A, Wallenhorst C, et al
    Impact of screening and exclusion of high anti-A titer donors on the risk of hemolytic anemia with intravenous immunoglobulin treatment - a hospital-based cohort study in the US.
    Am J Hematol. 2017 Oct 6. doi: 10.1002/ajh.24931.
    PubMed     Text format    


  3. VAN TUIJN CFJ, Schimmel M, van Beers EJ, Nur E, et al
    Prospective evaluation of chronic organ damage in adult sickle cell patients: A seven-year follow-up study.
    Am J Hematol. 2017;92:E584-E590.
    PubMed     Text format     Abstract available


  4. SUN CW, Wu LC, Knopick PL, Bradley DS, et al
    Sickle cells produce functional immune modulators and cytotoxics.
    Am J Hematol. 2017;92:981-988.
    PubMed     Text format     Abstract available


  5. CAPPELLINI MD, Comin-Colet J, de Francisco A, Dignass A, et al
    Iron deficiency across chronic inflammatory conditions: International expert opinion on definition, diagnosis, and management.
    Am J Hematol. 2017;92:1068-1078.
    PubMed     Text format     Abstract available


    September 2017
  6. ESTEPP JH, Smeltzer MP, Kang G, Li C, et al
    A Clinically Meaningful Fetal Hemoglobin Threshold for Children with Sickle Cell Anemia During Hydroxyurea Therapy.
    Am J Hematol. 2017 Sep 14. doi: 10.1002/ajh.24906.
    PubMed     Text format     Abstract available


  7. ASARE EV, Olayemi E, Boafor T, Dei-Adomakoh Y, et al
    Implementation of multidisciplinary care reduces maternal mortality in women with sickle cell disease living in low-resource setting.
    Am J Hematol. 2017;92:872-878.
    PubMed     Text format     Abstract available


  8. BIALKOWSKI W, Kiss JE, Wright DJ, Cable R, et al
    Estimates of total body iron indicate 19 mg and 38 mg oral iron are equivalent for the mitigation of iron deficiency in individuals experiencing repeated phlebotomy.
    Am J Hematol. 2017;92:851-857.
    PubMed     Text format     Abstract available


    August 2017
  9. BODDU P, Garcia-Manero G, Ravandi F, Borthakur G, et al
    Clinical Outcomes in Adult Patients with Aplastic Anemia- a single institution experience.
    Am J Hematol. 2017 Aug 29. doi: 10.1002/ajh.24897.
    PubMed     Text format     Abstract available


    July 2017
  10. ALVAREZ O, Nottage K, Simpson LM, Wood J, et al
    Kidney Function of Transfused Children with Sickle Cell Anemia: Baseline Data from the TWiTCH Study with Comparison to Non-Transfused Cohorts.
    Am J Hematol. 2017 Jul 25. doi: 10.1002/ajh.24871.
    PubMed     Text format    


  11. HABARA AH, Shaikho EM, Steinberg MH
    Fetal Hemoglobin in Sickle Cell Anemia: The Arab-Indian Haplotype and New Therapeutic Agents.
    Am J Hematol. 2017 Jul 24. doi: 10.1002/ajh.24872.
    PubMed     Text format     Abstract available


  12. WITZIG TE, Zinzani PL, Habermann TM, Tuscano JM, et al
    Long-Term Analysis of Phase II Studies of Single-Agent Lenalidomide in Relapsed/Refractory Mantle Cell Lymphoma.
    Am J Hematol. 2017 Jul 11. doi: 10.1002/ajh.24854.
    PubMed     Text format     Abstract available


  13. YEE MEM, Lane PA, Archer DR, Joiner CH, et al
    Estimation of Glomerular Filtration Rate Using Serum Cystatin C and Creatinine in Adults with Sickle Cell Anemia.
    Am J Hematol. 2017 Jul 3. doi: 10.1002/ajh.24840.
    PubMed     Text format    


  14. GLASSBERG J, Minnitti C, Cromwell C, Cytryn L, et al
    Inhaled steroids reduce pain and sVCAM levels in individuals with sickle cell disease: A triple-blind, randomized trial.
    Am J Hematol. 2017;92:622-631.
    PubMed     Text format     Abstract available


    June 2017
  15. VASSEUR C, Domingues-Hamdi E, Pakdaman S, Barau C, et al
    Elevated soluble alpha-hemoglobin pool in Sickle Cell Anemia.
    Am J Hematol. 2017 Jun 24. doi: 10.1002/ajh.24835.
    PubMed     Text format    


  16. KASTHURI RS, Montifar M, Nelson J, Kim H, et al
    Prevalence and Predictors of Anemia in Hereditary Hemorrhagic Telangiectasia.
    Am J Hematol. 2017 Jun 22. doi: 10.1002/ajh.24832.
    PubMed     Text format    


  17. SHAIKHO EM, Farrell JJ, Alsultan A, Sebastiani P, et al
    Genetic Determinants of HbF in Saudi Arabian and African Benin Haplotype Sickle Cell Anemia.
    Am J Hematol. 2017 Jun 13. doi: 10.1002/ajh.24822.
    PubMed     Text format    


  18. QUINN CT, Saraf SL, Gordeuk VR, Fitzhugh CD, et al
    Losartan for the Nephropathy of Sickle Cell Anemia: A Phase-2, Multi-Center Trial.
    Am J Hematol. 2017 Jun 7. doi: 10.1002/ajh.24810.
    PubMed     Text format     Abstract available


  19. GOMPERTS E, Belcher JD, Otterbein LE, Coates TD, et al
    The role of carbon monoxide and heme oxygenase in the prevention of sickle cell disease vaso-occlusive crises.
    Am J Hematol. 2017;92:569-582.
    PubMed     Text format     Abstract available


    May 2017
  20. HANSEN BR, Bottner WA, Ravindran A, DeJesus R, et al
    A follow-up on Desiderosmia (olfactory craving), a novel symptom associated with iron deficiency anemia.
    Am J Hematol. 2017 May 31. doi: 10.1002/ajh.24806.
    PubMed     Text format    


  21. TAHER AT, Origa R, Perrotta S, Kourakli A, et al
    New film-coated tablet formulation of deferasirox is well tolerated in patients with thalassemia or lower-risk MDS: Results of the randomized, phase II ECLIPSE study.
    Am J Hematol. 2017;92:420-428.
    PubMed     Text format     Abstract available


    April 2017
  22. GALADANCI N, Abdullahi SU, Vance LD, Tabari AM, et al
    Feasibility Trial for Primary Stroke Prevention in Children with Sickle Cell Anemia in Nigeria (SPIN Trial).
    Am J Hematol. 2017 Apr 25. doi: 10.1002/ajh.24770.
    PubMed     Text format     Abstract available


  23. RAVINDRAN A, Sankaran J, Jacob EK, Kreuter JD, et al
    High prevalence of monoclonal gammopathy among patients with warm autoimmune hemolytic anemia.
    Am J Hematol. 2017 Apr 24. doi: 10.1002/ajh.24765.
    PubMed     Text format    


  24. COURONNE L, Tertian G, Boutron A, Picard V, et al
    A Somatic Mosaicism in the G6PD Gene Inducing a Late Onset Chronic non Spherocytic Hemolytic Anemia.
    Am J Hematol. 2017 Apr 10. doi: 10.1002/ajh.24760.
    PubMed     Text format    


  25. HANSEN JW, Sandholdt H, Siersma V, Orskov AD, et al
    "Anemia is present years before myelodysplastic syndrome diagnosis - results from the pre-diagnostic period".
    Am J Hematol. 2017 Apr 6. doi: 10.1002/ajh.24757.
    PubMed     Text format    


  26. GRALL M, Azoulay E, Galicier L, Provot F, et al
    Thrombotic thrombocytopenic purpura misdiagnosed as autoimmune cytopenia: Causes of diagnostic errors and consequence on outcome. Experience of the French thrombotic microangiopathies reference centre.
    Am J Hematol. 2017;92:381-387.
    PubMed     Text format     Abstract available


    March 2017
  27. NASSIN ML, Vergilio JA, Heeney MM, LaBelle JL, et al
    Neonatal Anemia: Revisiting the Enigmatic Pyknocyte.
    Am J Hematol. 2017 Mar 23. doi: 10.1002/ajh.24731.
    PubMed     Text format    


  28. LEWEN MO, Kavanagh PL, Sobota AE
    A comment on improving transcranial Doppler ultrasonography screening in children with sickle cell anemia.
    Am J Hematol. 2017 Mar 23. doi: 10.1002/ajh.24727.
    PubMed     Text format    


  29. MEKONTSO DESSAP A, Cecchini J, Chaar V, Marcos E, et al
    Telomere attrition in sickle cell anemia.
    Am J Hematol. 2017 Mar 15. doi: 10.1002/ajh.24721.
    PubMed     Text format    


  30. FARRUGGIA P, Puccio G, Ramenghi U, Colombatti R, et al
    Recombinant erythropoietin vs. blood transfusion care in infants with hereditary spherocytosis: A retrospective cohort study of A.I.E.O.P. patients (Associazione Italiana Emato-Oncologia Pediatrica).
    Am J Hematol. 2017 Mar 6. doi: 10.1002/ajh.24713.
    PubMed     Text format    


  31. PATNAIK MM, Tefferi A
    Refractory anemia with ring sideroblasts (RARS) and RARS with thrombocytosis (RARS-T): 2017 update on diagnosis, risk-stratification, and management.
    Am J Hematol. 2017;92:297-310.
    PubMed     Text format     Abstract available


    February 2017
  32. HANSEN BR, Bottner WA, Ravindran A, DeJesus R, et al
    Desiderosmia (olfactory craving): A novel symptom associated with iron deficiency anemia.
    Am J Hematol. 2017 Feb 27. doi: 10.1002/ajh.24706.
    PubMed     Text format    


  33. LEAF RK, O'Brien KL, Leaf DE, Drews RE, et al
    Autoimmune hemolytic anemia in a young man with acute hepatitis E infection.
    Am J Hematol. 2017 Feb 23. doi: 10.1002/ajh.24699.
    PubMed     Text format    


  34. WHIPPLE NS, Schwartz JR, Nottage KA
    DAT-positive Plasmodium ovale malaria presenting in a child with sickle cell anemia.
    Am J Hematol. 2017 Feb 17. doi: 10.1002/ajh.24691.
    PubMed     Text format    


  35. BENNANI NN, LaPlant BR, Ansell SM, Habermann TM, et al
    Efficacy of the oral mTORC1 inhibitor everolimus in relapsed or refractory indolent lymphoma.
    Am J Hematol. 2017 Feb 17. doi: 10.1002/ajh.24671.
    PubMed     Text format     Abstract available


  36. ALELUIA MM, Santiago RP, da Guarda CC, Fonseca TC, et al
    Genetic Modulation of Fetal Hemoglobin in Hydroxyurea-Treated Sickle Cell Anemia.
    Am J Hematol. 2017 Feb 13. doi: 10.1002/ajh.24680.
    PubMed     Text format    


  37. CHATURVEDI S, Labib Ghafuri D, Kassim A, Rodeghier M, et al
    Elevated tricuspid regurgitant jet velocity, reduced forced expiratory volume in 1 second, and mortality in adults with sickle cell disease.
    Am J Hematol. 2017;92:125-130.
    PubMed     Text format     Abstract available


  38. WRAY K, Allen A, Evans E, Fisher C, et al
    Hepcidin detects iron deficiency in Sri Lankan adolescents with a high burden of hemoglobinopathy: A diagnostic test accuracy study.
    Am J Hematol. 2017;92:196-203.
    PubMed     Text format     Abstract available


  39. VAN TUIJN CF, Sins JW, Fijnvandraat K, Biemond BJ, et al
    Daily pain in adults with sickle cell disease-a different perspective.
    Am J Hematol. 2017;92:179-186.
    PubMed     Text format     Abstract available


  40. DELVILLE M, Manceau S, Ait Abdallah N, Stolba J, et al
    Arterio-venous fistula for automated red blood cells exchange in patients with sickle cell disease: Complications and outcomes.
    Am J Hematol. 2017;92:136-140.
    PubMed     Text format     Abstract available


    January 2017
  41. DERMAN R, Roman E, Modiano MR, Okam MM, et al
    A randomized trial of iron isomaltoside versus iron sucrose in patients with iron deficiency anemia.
    Am J Hematol. 2017 Jan 4. doi: 10.1002/ajh.24633.
    PubMed     Text format     Abstract available


    December 2016
  42. JACOB SA, Novelli EM, Isenberg JS, Garrett ME, et al
    Thrombospondin-1 Gene Polymorphism is Associated with Estimated Pulmonary Artery Pressure in Patients with Sickle Cell Anemia.
    Am J Hematol. 2016 Dec 29. doi: 10.1002/ajh.24635.
    PubMed     Text format    


  43. RICCHI P, Costantini S, Spasiano A, Di Matola T, et al
    Myelolipoma among patients with thalassemia major and rare anemia with iron loading: A not so rare entity.
    Am J Hematol. 2016 Dec 22. doi: 10.1002/ajh.24622.
    PubMed     Text format    


  44. BAIN BJ
    Howell-Jolly bodies in acute hemolytic anemia.
    Am J Hematol. 2016 Dec 22. doi: 10.1002/ajh.24624.
    PubMed     Text format    


    October 2016
  45. GOODNOUGH LT, Comin-Colet J, Leal-Noval S, Ozawa S, et al
    Management of Anemia in Patients with Congestive Heart Failure.
    Am J Hematol. 2016 Oct 25. doi: 10.1002/ajh.24595.
    PubMed     Text format     Abstract available


  46. QUARMYNE MO, Dong W, Theodore R, Anand S, et al
    Hydroxyurea Effectiveness in Children and Adolescents with Sickle Cell Anemia: A Large Retrospective, Population-Based Cohort.
    Am J Hematol. 2016 Oct 19. doi: 10.1002/ajh.24587.
    PubMed     Text format     Abstract available


  47. MICHEL M, Terriou L, Roudot-Thoraval F, Hamidou M, et al
    A Randomized and Double-Blind Controlled Trial Evaluating the Safety and Efficacy of Rituximab for Warm Auto-Immune Hemolytic Anemia in Adults (the RAIHA study).
    Am J Hematol. 2016 Oct 3. doi: 10.1002/ajh.24570.
    PubMed     Text format     Abstract available


    September 2016
  48. QUINN CT, Smith EP, Arbabi S, Khera PK, et al
    Biochemical surrogate markers of hemolysis do not correlate with directly measured erythrocyte survival in sickle cell anemia.
    Am J Hematol. 2016 Sep 20. doi: 10.1002/ajh.24562.
    PubMed     Text format     Abstract available


  49. DONKER AE, Schaap CC, Novotny VM, Smeets R, et al
    Iron Refractory Iron Deficiency Anemia (IRIDA): A heterogeneous disease that is not always iron refractory.
    Am J Hematol. 2016 Sep 19. doi: 10.1002/ajh.24561.
    PubMed     Text format     Abstract available


  50. DEITERING S, Anslemo L, Burnett A, Jakeman B, et al
    Safety and effectiveness of extended versus shortened iron dextran infusion time for the treatment of iron deficiency anemia.
    Am J Hematol. 2016 Sep 15. doi: 10.1002/ajh.24555.
    PubMed     Text format    


  51. ATTA M, Brannigan ET, Bain BJ
    Cold autoimmune hemolytic anemia secondary to atypical pneumonia.
    Am J Hematol. 2016 Sep 6. doi: 10.1002/ajh.24550.
    PubMed     Text format    


    August 2016
  52. NARLA A, Davis NL, LaVasseur C, Wong C, et al
    Erythrocyte adenosine deaminase levels are elevated in Diamond Blackfan anemia but not in the 5q- syndrome.
    Am J Hematol. 2016 Aug 24. doi: 10.1002/ajh.24541.
    PubMed     Text format    


  53. CHATURVEDI S, Ghafuri DL, Glassberg J, Kassim AA, et al
    Rapidly progressive acute chest syndrome in individuals with sickle cell anemia.
    Am J Hematol. 2016 Aug 20. doi: 10.1002/ajh.24539.
    PubMed     Text format     Abstract available


  54. VATHIPADIEKAL V, Farrell JJ, Wang S, Edward HL, et al
    A Candidate Trans-acting Modulator of Fetal Hemoglobin Gene Expression in the Arab-Indian Haplotype of Sickle Cell Anemia: -ANTXR1 Variants and HbF.
    Am J Hematol. 2016 Aug 7. doi: 10.1002/ajh.24527.
    PubMed     Text format     Abstract available


    July 2016
  55. STEVENS H, Chua CC, Wallis M, Hew S, et al
    Fanconi anemia in 55 year-old identical twins first presenting as fatal post-chemotherapy pancytopenia.
    Am J Hematol. 2016 Jul 18. doi: 10.1002/ajh.24488.
    PubMed     Text format    


    June 2016
  56. CAOCCI G, La Nasa G, Bain BJ
    Erythroblast morphology in refractory anemia with ring sideroblasts.
    Am J Hematol. 2016 Jun 14. doi: 10.1002/ajh.24448.
    PubMed     Text format    


  57. VATHIPADIEKAL V, Alsultan A, Baltrusaitis K, Farrell JJ, et al
    Homozygosity for a haplotype in the HBG2-OR51B4 region is exclusive to Arab-Indian haplotype sickle cell anemia.
    Am J Hematol. 2016;91:E308-11.
    PubMed     Text format    


  58. RISITANO AM
    Paroxysmal nocturnal hemoglobinuria in the era of complement inhibition.
    Am J Hematol. 2016;91:359-60.
    PubMed     Text format    


  59. SHIREL T, Hubler CP, Shah R, Mager AB, et al
    Maternal opioid dose is associated with neonatal abstinence syndrome in children born to women with sickle cell disease.
    Am J Hematol. 2016;91:416-9.
    PubMed     Text format     Abstract available


  60. LOSCHI M, Porcher R, Barraco F, Terriou L, et al
    Impact of eculizumab treatment on paroxysmal nocturnal hemoglobinuria: a treatment versus no-treatment study.
    Am J Hematol. 2016;91:366-70.
    PubMed     Text format     Abstract available


    May 2016
  61. BALANDYA E, Reynolds T, Obaro S, Makani J, et al
    Alteration of Lymphocyte Phenotype and Function in Sickle Cell Anemia: Implications for Vaccine Responses.
    Am J Hematol. 2016 May 30. doi: 10.1002/ajh.24438.
    PubMed     Text format     Abstract available


  62. RISHI G, Secondes ES, Wallace DF, Subramaniam VN, et al
    Hematopoietic deletion of Transferrin Receptor 2 in mice leads to a block in erythroid differentiation during iron-deficient anemia.
    Am J Hematol. 2016 May 11. doi: 10.1002/ajh.24417.
    PubMed     Text format     Abstract available


  63. HEXNER EO, Luger SM, Reshef R, Jeschke GR, et al
    Infusion of CD3/CD28 costimulated umbilical cord blood T cells at the time of single umbilical cord blood transplantation may enhance engraftment.
    Am J Hematol. 2016;91:453-60.
    PubMed     Text format     Abstract available


  64. KAMMEYER R, Devnani R, Mehta R
    Cerebral fat embolism syndrome mimicking thrombotic thrombocytopenic purpura in a patient with hemoglobin SC disease.
    Am J Hematol. 2016;91:539-42.
    PubMed     Text format    


    April 2016
  65. URIO F, Lyimo M, Mtatiro SN, Cox SE, et al
    High Prevalence of Individuals with Low Concentration of Fetal Hemoglobin in F-cells in Sickle Cell Anemia in Tanzania.
    Am J Hematol. 2016 Apr 16. doi: 10.1002/ajh.24390.
    PubMed     Text format    


  66. MAURO FR, Coluzzi S, Paoloni F, Trastulli F, et al
    "Clinical characteristics and outcome of patients with autoimmune hemolytic anemia (AIHA) uniformly defined as primary by a diagnostic work-up".
    Am J Hematol. 2016 Apr 5. doi: 10.1002/ajh.24379.
    PubMed     Text format    


    March 2016
  67. SVAHN J, Bagnasco F, Cappelli E, Onofrillo D, et al
    Somatic, hematologic phenotype, long-term outcome and effect of hematopoietic stem cell transplantation. An analysis of 97 Fanconi Anemia patients from the Italian national database on behalf of the Marrow Failure Study Group of the AIEOP (Italian Ass
    Am J Hematol. 2016 Mar 25. doi: 10.1002/ajh.24373.
    PubMed     Text format     Abstract available


  68. O'CONNELL C, Horwood K, Nadamuni M
    Correction of refractory thrombocytopenia and anemia following withdrawal of extended release niacin.
    Am J Hematol. 2016 Mar 25. doi: 10.1002/ajh.24371.
    PubMed     Text format    


  69. WONG L, Smith S, Gilstrop M, Derman R, et al
    Safety and Efficacy of Rapid (1000 mg in one hour) Intravenous Iron Dextran for Treatment of Maternal Iron Deficient Anemia.
    Am J Hematol. 2016 Mar 11. doi: 10.1002/ajh.24361.
    PubMed     Text format     Abstract available


  70. SADREAMELI SC, Eakin MN, Robinson KT, Alade RO, et al
    Secondhand smoke is associated with more frequent hospitalizations in children with sickle cell disease.
    Am J Hematol. 2016;91:313-7.
    PubMed     Text format     Abstract available


  71. HILLMEN P, Muus P, Szer J, Hill A, et al
    Assessment of human antihuman antibodies to eculizumab after long-term treatment in patients with paroxysmal nocturnal hemoglobinuria.
    Am J Hematol. 2016;91:E16-7.
    PubMed     Text format    


  72. KNAPP E, Cohen H, Kutlar A, Ghalie R, et al
    Intrapatient variability in fetal hemoglobin measurements over time in sickle cell patients not on fetal hemoglobin inducing agents.
    Am J Hematol. 2016;91:E11-2.
    PubMed     Text format    


    February 2016
  73. PATNAIK MM, Lasho TL, Finke CM, Hanson CA, et al
    Predictors of survival in refractory anemia with ring sideroblasts and thrombocytosis (RARS-T) and the role of next-generation sequencing.
    Am J Hematol. 2016 Feb 13. doi: 10.1002/ajh.24332.
    PubMed     Text format     Abstract available


  74. PARTAIN DK, Botero JP, Shi M, Poterucha JJ, et al
    Spur Cell Anemia in the Setting of Progressive Liver Allograft Failure.
    Am J Hematol. 2016 Feb 13. doi: 10.1002/ajh.24331.
    PubMed     Text format    


  75. LUCHTMAN-JONES L, Pressel S, Hilliard L, Brown RC, et al
    Effects of hydroxyurea treatment for patients with hemoglobin SC disease.
    Am J Hematol. 2016;91:238-42.
    PubMed     Text format     Abstract available


  76. MCGANN PT, Schaefer BA, Paniagua M, Howard TA, et al
    Characteristics of a rapid, point-of-care lateral flow immunoassay for the diagnosis of sickle cell disease.
    Am J Hematol. 2016;91:205-10.
    PubMed     Text format     Abstract available


  77. ANEA CB, Lyon M, Lee IA, Gonzales JN, et al
    Pulmonary platelet thrombi and vascular pathology in acute chest syndrome in patients with sickle cell disease.
    Am J Hematol. 2016;91:173-8.
    PubMed     Text format     Abstract available


  78. LAYTON DM, Bain BJ
    Dehydrated hereditary stomatocytosis.
    Am J Hematol. 2016;91:266.
    PubMed     Text format    


    January 2016
  79. BOUCHNITA A, Eymard N, Moyo TK, Koury MJ, et al
    Bone marrow infiltration by multiple myeloma causes anemia by reversible disruption of erythropoiesis.
    Am J Hematol. 2016 Jan 9. doi: 10.1002/ajh.24291.
    PubMed     Text format     Abstract available


  80. CHATURVEDI S, DeBaun MR
    Evolution of sickle cell disease from a life-threatening disease of children to a chronic disease of adults: The last 40 years.
    Am J Hematol. 2016;91:5-14.
    PubMed     Text format     Abstract available


  81. RUND D
    Thalassemia 2016: Modern medicine battles an ancient disease.
    Am J Hematol. 2016;91:15-21.
    PubMed     Text format     Abstract available


  82. MINNITI CP, Kato GJ
    Critical Reviews: How we treat sickle cell patients with leg ulcers.
    Am J Hematol. 2016;91:22-30.
    PubMed     Text format     Abstract available


    November 2015
  83. BABUSHOK DV, Grignon AL, Li Y, Atienza J, et al
    Disrupted lymphocyte homeostasis in hepatitis-associated acquired aplastic anemia is associated with short telomeres.
    Am J Hematol. 2015 Nov 30. doi: 10.1002/ajh.24256.
    PubMed     Text format     Abstract available


  84. TEFFERI A, Cerquozzi S, Liaw J
    Bendamustine therapy associated resolution of anemia and splenomegaly in myelofibrosis.
    Am J Hematol. 2015 Nov 20. doi: 10.1002/ajh.24248.
    PubMed     Text format    


  85. VADHAN-RAJ S, Ford DC, Dahl NV, Bernard K, et al
    Safety and efficacy of ferumoxytol for the episodic treatment of iron deficiency anemia in patients with a history of unsatisfactory oral iron therapy: Results of a phase III, open-label, 6-month extension study.
    Am J Hematol. 2015 Nov 17. doi: 10.1002/ajh.24240.
    PubMed     Text format    


  86. FILLIATRE L, Broseus J, Pissard S, Mekki C, et al
    Amyl nitrite inhalation, a "volatile" anemia.
    Am J Hematol. 2015 Nov 3. doi: 10.1002/ajh.24229.
    PubMed     Text format    


  87. FOUQUET G, Guidez S, Petillon MO, Louni C, et al
    Lenalidomide is safe and active in Waldenstrom macroglobulinemia.
    Am J Hematol. 2015;90:1055-9.
    PubMed     Text format     Abstract available


  88. RICCHI P, Meloni A, Spasiano A, Neri MG, et al
    Extramedullary hematopoiesis is associated with lower cardiac iron loading in chronically transfused thalassemia patients.
    Am J Hematol. 2015;90:1008-12.
    PubMed     Text format     Abstract available


    October 2015
  89. GARDNER K, Thein SL
    Super-elevated LDH and thrombocytopenia are markers of a severe subtype of vaso-occlusive crisis in sickle cell disease.
    Am J Hematol. 2015;90:E206-7.
    PubMed     Text format    


  90. ANDOLFO I, Russo R, Manna F, Shmukler BE, et al
    Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis).
    Am J Hematol. 2015;90:921-6.
    PubMed     Text format     Abstract available


    September 2015
  91. HANKINS JS, McCarville MB, Rankine-Mullings A, Reid ME, et al
    Prevention of conversion to abnormal tcd with hydroxyurea in sickle cell anemia: A phase III international randomized clinical trial.
    Am J Hematol. 2015 Sep 28. doi: 10.1002/ajh.24198.
    PubMed     Text format     Abstract available


  92. AUERBACH M, Adamson JW
    How We Diagnose and Treat Iron Deficiency Anemia.
    Am J Hematol. 2015 Sep 26. doi: 10.1002/ajh.24201.
    PubMed     Text format     Abstract available


  93. CASTRO O, Kato GJ
    Iron restriction in sickle cell anemia: Time for controlled clinical studies.
    Am J Hematol. 2015 Sep 16. doi: 10.1002/ajh.24193.
    PubMed     Text format    


  94. FREEMAN AT, Ataga KI
    Pulmonary Endarterectomy as Treatment for Chronic Thromboembolic Pulmonary Hypertension in Sickle Cell Disease.
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  95. SALIBA AN, Taher AT
    Comment on "deferiprone versus deferoxamine in thalassemia intermedia: results from a 5-year long-term Italian multicenter randomized clinical trial".
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  96. LUND K, Chakravorty S, Toma S, Bain BJ, et al
    Compound heterozygosity for hemoglobins S and D.
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  97. O'REILLY MA, Millar SR, Buckley CM, Harrington JM, et al
    Smoking as an independent risk factor for macrocytosis in middle-aged adults: a population-based observational study.
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  98. CHANDRAN R, Moran A, Barash M, Hopper B, et al
    A case of acute chest syndrome complicated by diffuse cerebral infarcts in an adult with HbSbeta-thalassemia(.).
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  99. GRACE RF, Zanella A, Neufeld EJ, Morton DH, et al
    Erythrocyte pyruvate kinase deficiency: 2015 status report.
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  100. SINGER ST, Killilea D, Suh JH, Wang ZJ, et al
    Fertility in transfusion-dependent thalassemia men: effects of iron burden on the reproductive axis.
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  101. MELONI A, Restaino G, Missere M, De Marchi D, et al
    Pancreatic iron overload by T2* MRI in a large cohort of well treated thalassemia major patients: can it tell us heart iron distribution and function?
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  102. CHEN M, Loh SF, Yu SL, Nair S, et al
    Rapid and reliable preimplantation genetic diagnosis of common hemoglobin Bart's hydrops fetalis syndrome and hemoglobin H disease determinants using an enhanced single-tube decaplex polymerase chain reaction assay.
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  103. KOURELIS TV, Buckner JC, Gangat N, Patnaik MM, et al
    Temozolomide induced bone marrow Suppression--A single institution outcome analysis and review of the literature.
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    August 2015
  104. MCGANN PT, Tyburski EA, de Oliveira V, Santos B, et al
    An accurate and inexpensive color-based assay for detecting severe anemia in a limited-resource setting.
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  105. DEL MAR MANU-PEREIRA M, Gonzalez-Roca E, van Solinge WW, Llaudet-Planas E, et al
    Pyruvate kinase deficiency and severe congenital hemolytic anemia in a double heterozygous patient with paternal transmission of an early germ-line de novo mutation.
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  106. HERBAUX C, Duployez N, Badens C, Poret N, et al
    Incidence of ATRX mutations in myelodysplastic syndromes, the value of microcytosis.
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  107. DESAI PC, Deal AM, Pfaff ER, Qaqish B, et al
    Alloimmunization is associated with older age of transfused red blood cells in sickle cell disease.
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  108. FATTIZZO B, Zaninoni A, Nesa F, Sciumbata VM, et al
    Lessons from very severe, refractory, and fatal primary autoimmune hemolytic anemias.
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  109. GIRI N, Alter BP, Penrose K, Falk RT, et al
    Immune status of patients with inherited bone marrow failure syndromes.
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    July 2015
  110. ARCHER N, Galacteros F, Brugnara C
    2015 Clinical Trials Update in Sickle Cell Anemia.
    Am J Hematol. 2015 Jul 15. doi: 10.1002/ajh.24116.
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  111. STEENSMA DP, Dakhil SR, Novotny PJ, Sloan JA, et al
    A Randomized Comparison of Once Weekly Epoetin Alfa to Extended Schedule Epoetin or Darbepoetin in Chemotherapy-Associated Anemia.
    Am J Hematol. 2015 Jul 6. doi: 10.1002/ajh.24110.
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  112. ADEKILE A, Menzel S, Gupta R, Al-Sharida S, et al
    Response to hydroxyurea among Kuwaiti patients with sickle cell disease and elevated baseline HbF levels.
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  113. FOZZA C, Pardini S, Giannico DB, Targhetta C, et al
    Dramatic erythroid response to low-dose thalidomide in two patients with transfusion independent thalassemia and severe post-transfusional alloimmune hemolysis.
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  114. CALVARUSO G, Vitrano A, Di Maggio R, Lai E, et al
    Deferiprone versus deferoxamine in thalassemia intermedia: Results from a 5-year long-term Italian multicenter randomized clinical trial.
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  115. JASPERS A, Baron F, Maertens J, De Prijck B, et al
    Long-term safety follow-up of a randomized trial of darbepoetin alpha and intravenous iron following autologous hematopoietic cell transplantation.
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    June 2015
  116. JASPERS A, Baron F, Servais S, Lejeune M, et al
    Erythropoietin therapy after allogeneic hematopoietic cell transplantation has no impact on long-term survival.
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  117. WOOD JC, Pressel S, Rogers ZR, Odame I, et al
    Liver iron concentration measurements by MRI in chronically transfused children with sickle cell anemia: Baseline results from the TWiTCH trial.
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  118. PIETY NZ, Yang X, Lezzar D, George A, et al
    A rapid paper-based test for quantifying sickle hemoglobin in blood samples from patients with sickle cell disease.
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    May 2015
  119. NICHELE I, Ruggeri M, Rodeghiero F
    Effectiveness of lenalidomide in a patient with refractory anemia with ring sideroblasts and thrombocytosis with JAK2 (V617F) mutation.
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  120. RENELLA R
    Age-dependent pathophysiology of acute chest syndrome in children with sickle cell disease.
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  121. FIANCHI L, Pagano L, Piciocchi A, Candoni A, et al
    Characteristics and outcome of therapy-related myeloid neoplasms: Report from the Italian network on secondary leukemias.
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  122. FERRONE FA
    The delay time in sickle cell disease after 40 years: A paradigm assessed.
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  123. LANZKRON S, Carroll CP, Hill P, David M, et al
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  124. REESE JA, Bougie DW, Curtis BR, Terrell DR, et al
    Drug-induced thrombotic microangiopathy: Experience of the Oklahoma Registry and the BloodCenter of Wisconsin.
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  125. MANWANI D, Chen G, Carullo V, Serban S, et al
    Single-dose intravenous gammaglobulin can stabilize neutrophil Mac-1 activation in sickle cell pain crisis.
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    April 2015
  126. PICOT J, Ndour PA, Lefevre SD, El Nemer W, et al
    A biomimetic microfluidic chip to study the circulation and mechanical retention of red blood cells in the spleen.
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  127. SAVAGE WJ, Buchanan GR, Yawn BP, Afenyi-Annan AN, et al
    Evidence gaps in the management of sickle cell disease: A summary of needed research.
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  128. SCHIMMEL M, van Beers EJ, van Tuijn CF, Nur E, et al
    N-terminal pro-B-type natriuretic peptide, tricuspid jet flow velocity, and death in adults with sickle cell disease.
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  129. SCHMIDT PJ, Racie T, Westerman M, Fitzgerald K, et al
    Combination therapy with a Tmprss6 RNAi-therapeutic and the oral iron chelator deferiprone additively diminishes secondary iron overload in a mouse model of beta-thalassemia intermedia.
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