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Articles published in Am J Hematol

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    August 2021
  1. PEREZ-LAMAS L, Moreno-Jimenez G, Tenorio-Nunez MC, Velazquez-Kennedy K, et al
    Hemolytic crisis due to Covid-19 vaccination in a woman with cold agglutinin disease.
    Am J Hematol. 2021;96:E288-E291.
    PubMed    


  2. BOU-FAKHREDIN R, Daadaa H, Koussa S, Abou Nasr T, et al
    SARS-CoV-2 infection in patients with beta-thalassemia: Experience from Lebanon.
    Am J Hematol. 2021;96:E285-E288.
    PubMed    


    July 2021
  3. HANSEN DL, Berentsen S, Fattizzo B, Hansen PL, et al
    Seasonal variation in the incidence of cold agglutinin disease in Norway, Denmark, and Italy.
    Am J Hematol. 2021;96:E262-E265.
    PubMed    


  4. WAHEED A, Kuter DJ
    Iron overload after complement inhibitor treatment of Paroxysmal Nocturnal Hemoglobinuria.
    Am J Hematol. 2021;96:E235-E237.
    PubMed    


  5. MONTALBAN-BRAVO G, Kanagal-Shamanna R, Darbaniyan F, Siddiqui MT, et al
    Clinical, genomic, and transcriptomic differences between myelodysplastic syndrome/myeloproliferative neoplasm with ring sideroblasts and thrombocytosis (MDS/MPN-RS-T) and myelodysplastic syndrome with ring sideroblasts (MDS-RS).
    Am J Hematol. 2021;96:E246-E249.
    PubMed    


  6. KULASEKARARAJ AG, Brodsky RA, Hill A
    Monitoring of patients with paroxysmal nocturnal hemoglobinuria on a complement inhibitor.
    Am J Hematol. 2021;96:E232-E235.
    PubMed    


    June 2021
  7. GURUNG K, Bain BJ
    A normal mean cell volume does not exclude a diagnosis of megaloblastic anemia.
    Am J Hematol. 2021 Jun 24. doi: 10.1002/ajh.26283.
    PubMed    


  8. KIRK SE, Scheurer ME, Bernhardt MB, Mahoney DH, et al
    Phosphorus levels in children treated with intravenous ferric carboxymaltose.
    Am J Hematol. 2021;96:E215-E218.
    PubMed    


  9. PANAGIOTA V, Meggendorfer M, Kubasch AS, Gabdoulline R, et al
    Impact of PPM1D mutations in patients with myelodysplastic syndrome and deletion of chromosome 5q.
    Am J Hematol. 2021;96:E207-E210.
    PubMed    


  10. ZHANG X, Yang Y, Zhang H, Du Z, et al
    A rare complex rearrangement in the beta-globin gene cluster causing a novel homozygous (G) gamma((A) gammadeltabeta)(0) -thalassemia.
    Am J Hematol. 2021;96:E189-E193.
    PubMed    


    May 2021
  11. RAMIREZ MJ, Pujol R, Trujillo-Quintero JP, Minguillon J, et al
    Natural gene therapy by reverse mosaicism leads to improved hematology in Fanconi anemia patients.
    Am J Hematol. 2021 May 13. doi: 10.1002/ajh.26234.
    PubMed     Abstract available


  12. KIM SJ, Song J, Reading NS, Lautersztain J, et al
    Novel mechanism of hereditary pyropoikilocytosis phenotype due to co-inheritance of beta globin and alpha spectrin mutations.
    Am J Hematol. 2021;96:E150-E154.
    PubMed    


  13. KALANTAR-ZADEH K, Ganz T, Trumbo H, Seid MH, et al
    Parenteral iron therapy and phosphorus homeostasis: A review.
    Am J Hematol. 2021;96:606-616.
    PubMed     Abstract available


  14. BAIN BJ
    Alpha chain inclusions in peripheral blood erythroblasts and erythrocytes.
    Am J Hematol. 2021;96:630-631.
    PubMed    


    April 2021
  15. MAQUET J, Lafaurie M, Walter O, Sailler L, et al
    Epidemiology of autoimmune hemolytic anemia: a nationwide population-based study in France.
    Am J Hematol. 2021 Apr 30. doi: 10.1002/ajh.26213.
    PubMed    


  16. BARCELLINI W, Zaninoni A, Giannotta JA, Merati G, et al
    Circulating extracellular vesicles and cytokines in congenital and acquired hemolytic anemias.
    Am J Hematol. 2021;96:E129-E132.
    PubMed    


  17. MINNITI CP, Knight-Madden J, Tonda M, Gray S, et al
    The impact of voxelotor treatment on leg ulcers in patients with sickle cell disease.
    Am J Hematol. 2021;96:E126-E128.
    PubMed    


  18. AL-ALI AK, Alsulaiman A, Alfarhan M, Safaya S, et al
    Sickle cell disease in the Eastern Province of Saudi Arabia: Clinical and laboratory features.
    Am J Hematol. 2021;96:E117-E121.
    PubMed    


  19. MCGRATH M, Quint EH, Weyand AC
    Depression in adolescents and young adults with heavy menstrual bleeding in a referral clinic setting.
    Am J Hematol. 2021;96:E105-E108.
    PubMed    


  20. ARCHULETA J, van der Graaf M, Kaptein FHJ, Althaus L, et al
    Sudden death due to massive bone marrow sequestration crisis in a patient with sickle cell disease.
    Am J Hematol. 2021;96:E100-E102.
    PubMed    


  21. OSUNKWO I, Andemariam B, Minniti CP, Inusa BPD, et al
    Impact of sickle cell disease on patients' daily lives, symptoms reported, and disease management strategies: Results from the international Sickle Cell World Assessment Survey (SWAY).
    Am J Hematol. 2021;96:404-417.
    PubMed     Abstract available


  22. LANZKRON S, Smith-Whitley K
    Swaying sickle cell research forward in support of patient reported outcomes.
    Am J Hematol. 2021;96:402-403.
    PubMed    


    March 2021
  23. PATNAIK MM, Tefferi A
    Myelodysplastic syndromes with ring sideroblasts (MDS-RS) and MDS/myeloproliferative neoplasm with RS and thrombocytosis (MDS/MPN-RS-T) - "2021 update on diagnosis, risk-stratification, and management".
    Am J Hematol. 2021;96:379-394.
    PubMed     Abstract available


  24. DENTON CC, Shah P, Suriany S, Liu H, et al
    Loss of alpha-globin genes in human subjects is associated with improved nitric oxide-mediated vascular perfusion.
    Am J Hematol. 2021;96:277-281.
    PubMed     Abstract available


  25. MUSALLAM KM, Rivella S, Taher AT
    Management of non-transfusion-dependent beta-thalassemia (NTDT): The next 5 years.
    Am J Hematol. 2021;96:E57-E59.
    PubMed    


    February 2021
  26. ZUBICARAY J, Pagliara D, Sevilla J, Eikema DJ, et al
    Haplo-identical or mismatched unrelated donor hematopoietic cell transplantation for Fanconi anemia: results from the Severe Aplastic Anemia Working Party of the EBMT.
    Am J Hematol. 2021 Feb 19. doi: 10.1002/ajh.26135.
    PubMed     Abstract available


  27. ROMANA M, Reminy K, Moeckesch B, Charlot K, et al
    Loss of alpha globin genes is associated with improved microvascular function in patients with sickle cell anemia.
    Am J Hematol. 2021 Feb 13. doi: 10.1002/ajh.26126.
    PubMed    


  28. AUERBACH M, Henry D, DeLoughery TG
    Intravenous ferric derisomaltose for the treatment of iron deficiency anemia.
    Am J Hematol. 2021 Feb 13. doi: 10.1002/ajh.26124.
    PubMed     Abstract available


  29. KARKOSKA K, Quinn CT, Niss O, Pfeiffer A, et al
    Hydroyxurea improves cerebral oxygen saturation in children with sickle cell anemia.
    Am J Hematol. 2021 Feb 3. doi: 10.1002/ajh.26120.
    PubMed     Abstract available


  30. LEBENSBURGER JD, Aban I, Hilliard LM, Feig DI, et al
    Hyperuricemia and Abnormal Nocturnal Dipping Impact Glomerular Filtration Rate in Patients with Sickle Cell Anemia.
    Am J Hematol. 2021 Feb 1. doi: 10.1002/ajh.26115.
    PubMed    


  31. MUSALLAM KM, Cappellini MD, Viprakasit V, Kattamis A, et al
    Revisiting the non-transfusion-dependent (NTDT) vs. transfusion-dependent (TDT) thalassemia classification 10 years later.
    Am J Hematol. 2021;96:E54-E56.
    PubMed    


  32. SCHMIDT PJ, Fitzgerald K, Butler JS, Fleming MD, et al
    Global loss of Tfr2 with concomitant induced iron deficiency greatly ameliorates the phenotype of a murine thalassemia intermedia model.
    Am J Hematol. 2021;96:251-257.
    PubMed     Abstract available


    January 2021
  33. LUNATI A, Petit A, Lapillonne H, Gameiro C, et al
    VPS4A mutation in syndromic congenital hemolytic anemia without obvious signs of dyserythropoiesis.
    Am J Hematol. 2021 Jan 18. doi: 10.1002/ajh.26099.
    PubMed    


  34. GLADWIN MT, Kato GJ, Gordeuk VR
    Identifying adolescent and young adult patients with sickle cell disease at highest risk of death.
    Am J Hematol. 2021;96:9-11.
    PubMed    


  35. RAB MAE, Kanne CK, Bos J, van Oirschot BA, et al
    Oxygen gradient ektacytometry-derived biomarkers are associated with vaso-occlusive crises and correlate with treatment response in sickle cell disease.
    Am J Hematol. 2021;96:E29-E32.
    PubMed    


  36. ROSANWO TO, Kean LS, Archer NM
    End the pain: Start with antiracism.
    Am J Hematol. 2021;96:4-6.
    PubMed    


  37. OGU UO, Thomas M, Chan F, Vattappally L, et al
    L-glutamine use in adults with sickle cell disease: Clinical trials where success meets reality.
    Am J Hematol. 2021;96:E38-E40.
    PubMed    


  38. CHALACHEVA P, Ji Y, Rosen CL, DeBaun MR, et al
    Nocturnal peripheral vasoconstriction predicts the frequency of severe acute pain episodes in children with sickle cell disease.
    Am J Hematol. 2021;96:60-68.
    PubMed     Abstract available


  39. COSTA E, Tibalinda P, Sterzi E, Leufkens HMG, et al
    Making hydroxyurea affordable for sickle cell disease in Tanzania is essential (HASTE): How to meet major health needs at a reasonable cost.
    Am J Hematol. 2021;96:E2-E5.
    PubMed    


  40. SHAH P, Suriany S, Kato R, Bush AM, et al
    Tricuspid regurgitant jet velocity and myocardial tissue Doppler parameters predict mortality in a cohort of patients with sickle cell disease spanning from pediatric to adult age groups - revisiting this controversial concept after 16 years of additi
    Am J Hematol. 2021;96:31-39.
    PubMed     Abstract available


    December 2020
  41. KARKOSKA K, Quinn CT, Clapp K, McGann PT, et al
    Severe infusion-related reaction to crizanlizumab in an adolescent with sickle cell disease.
    Am J Hematol. 2020;95:E338-E339.
    PubMed    


  42. COHEN J, Khudanyan A, Lu J, Wing J, et al
    A multicenter study evaluating the effectiveness and safety of single-dose low molecular weight iron dextran vs single-dose ferumoxytol for the treatment of iron deficiency.
    Am J Hematol. 2020;95:1572-1577.
    PubMed     Abstract available


    November 2020
  43. DAVIS BH
    Assay for "fetal hemoglobin levels" in erythrocytes: Impact of new In Vitro Diagnostics regulation and expanded applications in sickle cell disease management.
    Am J Hematol. 2020;95:1230-1232.
    PubMed    


  44. ANGELUCCI E
    Can any new thalassemia therapy achieve a better than 97.4% cure rate?
    Am J Hematol. 2020;95:1233-1234.
    PubMed    


  45. HE Y, Jiang H, Li C, Zhu Y, et al
    Long-term results of the NF-08-TM protocol in stem cell transplant for patients with thalassemia major: A multi-center large-sample study.
    Am J Hematol. 2020;95:E297-E299.
    PubMed    


  46. RUSSO R, Marra R, Andolfo I, Manna F, et al
    Uridine treatment normalizes the congenital dyserythropoietic anemia type II-like hematological phenotype in a patient with homozygous mutation in the CAD gene.
    Am J Hematol. 2020;95:1423-1426.
    PubMed    


  47. MERLET AN, Feasson L, Bartolucci P, Hourde C, et al
    Muscle structural, energetic and functional benefits of endurance exercise training in sickle cell disease.
    Am J Hematol. 2020;95:1257-1268.
    PubMed     Abstract available


  48. HEBERT N, Rakotoson MG, Bodivit G, Audureau E, et al
    Individual red blood cell fetal hemoglobin quantification allows to determine protective thresholds in sickle cell disease.
    Am J Hematol. 2020;95:1235-1245.
    PubMed     Abstract available


  49. KUCUKAL E, Man Y, Hill A, Liu S, et al
    Whole blood viscosity and red blood cell adhesion: Potential biomarkers for targeted and curative therapies in sickle cell disease.
    Am J Hematol. 2020;95:1246-1256.
    PubMed     Abstract available


  50. DE CASTRO C, Grossi F, Weitz IC, Maciejewski J, et al
    C3 inhibition with pegcetacoplan in subjects with paroxysmal nocturnal hemoglobinuria treated with eculizumab.
    Am J Hematol. 2020;95:1334-1343.
    PubMed     Abstract available


    October 2020
  51. POLLYEA DA, Pratz K, Letai A, Jonas BA, et al
    Venetoclax with azacitidine or decitabine in patients with newly diagnosed acute myeloid leukemia: long term follow-up from a Phase 1b study.
    Am J Hematol. 2020 Oct 29. doi: 10.1002/ajh.26039.
    PubMed     Abstract available


  52. ONALO R, Cooper P, Cilliers A, Vorster BC, et al
    Randomized Control Trial of Oral Arginine Therapy for Children with Sickle Cell Anemia Hospitalized for Pain in Nigeria.
    Am J Hematol. 2020 Oct 19. doi: 10.1002/ajh.26028.
    PubMed     Abstract available


  53. WOLF M, Auerbach M, Kalra PA, Glaspy J, et al
    Safety of ferric derisomaltose and iron sucrose in patients with iron deficiency anemia: The FERWON-IDA/NEPHRO trials.
    Am J Hematol. 2020 Oct 7. doi: 10.1002/ajh.26015.
    PubMed    


    September 2020
  54. DEBEER T, Jordan LC, Lee CA, Patel NJ, et al
    Evidence of transfusion-induced reductions in cerebral capillary shunting in sickle cell disease.
    Am J Hematol. 2020;95:E228-E230.
    PubMed    


  55. SONI S
    Gene therapies for transfusion dependent beta-thalassemia: Current status and critical criteria for success.
    Am J Hematol. 2020;95:1099-1112.
    PubMed     Abstract available


  56. GALADANCI NA, Abdullahi SU, Ali Abubakar S, Wudil Jibir B, et al
    Moderate fixed-dose hydroxyurea for primary prevention of strokes in Nigerian children with sickle cell disease: Final results of the SPIN trial.
    Am J Hematol. 2020;95:E247-E250.
    PubMed    


  57. GEORGE A, Dinu B, Estrada N, Minard CG, et al
    Novel dose escalation to predict treatment with hydroxyurea (NDEPTH): A randomized controlled trial of a dose-prediction equation to determine maximum tolerated dose of hydroxyurea in pediatric sickle cell disease.
    Am J Hematol. 2020;95:E242-E244.
    PubMed    


  58. KNISELY MR, Pugh N, Kroner B, Masese R, et al
    Patient-reported outcomes in sickle cell disease and association with clinical and psychosocial factors: Report from the sickle cell disease implementation consortium.
    Am J Hematol. 2020;95:1066-1074.
    PubMed     Abstract available


  59. TISDALE JF, Pierciey FJ Jr, Bonner M, Thompson AA, et al
    Safety and feasibility of hematopoietic progenitor stem cell collection by mobilization with plerixafor followed by apheresis vs bone marrow harvest in patients with sickle cell disease in the multi-center HGB-206 trial.
    Am J Hematol. 2020;95:E239-E242.
    PubMed    


  60. SCARAMELLINI N, Consonni D, Cassinerio E, Arighi C, et al
    A holistic approach to iron chelation therapy in transfusion-dependent thalassemia patients with serum ferritin below 500 mug/L.
    Am J Hematol. 2020;95:E230-E232.
    PubMed    


  61. SIDANA S, Murray DL, Dasari S, Go RS, et al
    Glycosylation of immunoglobulin light chains is highly prevalent in cold agglutinin disease.
    Am J Hematol. 2020;95:E222-E225.
    PubMed    


  62. TSEU B, Siow W, Pushkaran B, Cheesebrough B, et al
    Beta thalassemia major and Noonan syndrome - Two genetic disorders manifest in the blood film.
    Am J Hematol. 2020;95:1113-1114.
    PubMed    


    August 2020
  63. WILDING C, Pelling D, Lund K, Bain BJ, et al
    Erythrophagocytosis by monocytes - an unusual observation in autoimmune hemolytic anemia.
    Am J Hematol. 2020 Aug 18. doi: 10.1002/ajh.25966.
    PubMed    


  64. JORDAN LC, Rodeghier M, Donahue MJ, DeBaun MR, et al
    Reduction in TCD velocity after regular blood transfusion therapy is associated with a change in hemoglobin S fraction in sickle cell anemia.
    Am J Hematol. 2020 Aug 10. doi: 10.1002/ajh.25954.
    PubMed    


  65. NAYMAGON L, Berwick S, Kessler A, Lancman G, et al
    The emergence of methemoglobinemia amidst the COVID-19 pandemic.
    Am J Hematol. 2020;95:E196-E197.
    PubMed    


  66. TAHER AT, Bou-Fakhredin R, Kreidieh F, Motta I, et al
    Care of patients with hemoglobin disorders during the COVID-19 pandemic: An overview of recommendations.
    Am J Hematol. 2020;95:E208-E210.
    PubMed    


  67. KUIPERS MT, van Zwieten R, Heijmans J, Rutten CE, et al
    Glucose-6-phosphate dehydrogenase deficiency-associated hemolysis and methemoglobinemia in a COVID-19 patient treated with chloroquine.
    Am J Hematol. 2020;95:E194-E196.
    PubMed    


  68. ODIEVRE MH, de Marcellus C, Ducou Le Pointe H, Allali S, et al
    Dramatic improvement after tocilizumab of severe COVID-19 in a child with sickle cell disease and acute chest syndrome.
    Am J Hematol. 2020;95:E192-E194.
    PubMed    


  69. MOTTA I, Migone De Amicis M, Pinto VM, Balocco M, et al
    SARS-CoV-2 infection in beta thalassemia: Preliminary data from the Italian experience.
    Am J Hematol. 2020;95:E198-E199.
    PubMed    


  70. MITRA A, Dwyre DM, Schivo M, Thompson GR 3rd, et al
    Leukoerythroblastic reaction in a patient with COVID-19 infection.
    Am J Hematol. 2020;95:999-1000.
    PubMed    


  71. MACRAE FL, Peacock-Young B, Bowman P, Baker SR, et al
    Patients with paroxysmal nocturnal hemoglobinuria demonstrate a prothrombotic clotting phenotype which is improved by complement inhibition with eculizumab.
    Am J Hematol. 2020;95:944-952.
    PubMed     Abstract available


  72. HARPER K, McIlwaine L, Leach M, Bain BJ, et al
    Giant proerythroblasts in pure red cell aplasia due to parvovirus B19 infection in a patient with rheumatoid arthritis.
    Am J Hematol. 2020;95:990-991.
    PubMed    


    July 2020
  73. DOMINGUES-HAMDI E, Vasseur C, Pakdaman S, Moutereau S, et al
    Hydroxycarbamide decreases the free alpha-hemoglobin pool in red blood cells of adult patients with sickle cell anemia.
    Am J Hematol. 2020 Jul 28. doi: 10.1002/ajh.25947.
    PubMed    


  74. GORDEUK VR, Shah BN, Zhang X, Thuma PE, et al
    CYB5R3(c) (.350C>G) and G6PD A Alleles Modify Severity of Anemia in Malaria and Sickle Cell Disease.
    Am J Hematol. 2020 Jul 22. doi: 10.1002/ajh.25941.
    PubMed     Abstract available


  75. SONG AB, Kuter DJ, Al-Samkari H
    Characterization of the Rate, Predictors, and Thrombotic Complications of Thrombocytosis in Iron Deficiency Anemia.
    Am J Hematol. 2020 Jul 3. doi: 10.1002/ajh.25925.
    PubMed     Abstract available


  76. DE LUNA G, Habibi A, Deux JF, Colard M, et al
    Rapid and severe Covid-19 pneumonia with severe acute chest syndrome in a sickle cell patient successfully treated with tocilizumab.
    Am J Hematol. 2020;95:876-878.
    PubMed    


  77. FAN BE, Ong KH, Chan SSW, Young BE, et al
    Blood and blood product use during COVID-19 infection.
    Am J Hematol. 2020;95:E158-E160.
    PubMed    


  78. BEERKENS F, John M, Puliafito B, Corbett V, et al
    COVID-19 pneumonia as a cause of acute chest syndrome in an adult sickle cell patient.
    Am J Hematol. 2020;95:E154-E156.
    PubMed    


  79. NOURAIE M, Darbari DS, Rana S, Minniti CP, et al
    Tricuspid regurgitation velocity and other biomarkers of mortality in children, adolescents and young adults with sickle cell disease in the United States: The PUSH study.
    Am J Hematol. 2020;95:766-774.
    PubMed     Abstract available


  80. VAN TUIJN CFJ, Gaartman AE, Nur E, Rijneveld AW, et al
    Incentive spirometry to prevent acute chest syndrome in adults with sickle cell disease; a randomized controlled trial.
    Am J Hematol. 2020;95:E160-E163.
    PubMed    


    June 2020
  81. ACHEBE MM, Glaspy J, Kalra PA, Auerbach M, et al
    A six month extension trial evaluating safety and efficacy of ferric derisomaltose in patients with iron deficiency anemia: The FERWON-EXT trial.
    Am J Hematol. 2020 Jun 29. doi: 10.1002/ajh.25920.
    PubMed    


  82. NUR E, Gaartman AE, van Tuijn CFJ, Tang MW, et al
    Vaso-occlusive crisis and acute chest syndrome in sickle cell disease due to 2019 novel coronavirus disease (COVID-19).
    Am J Hematol. 2020;95:725-726.
    PubMed    


  83. LIM SH, Dutta D
    Clinicopathologic consequences following discontinuation of rifaximin in patients with sickle cell disease.
    Am J Hematol. 2020;95:E151-E153.
    PubMed    


  84. HAUGHTON A, Stylian S, Bain BJ
    Stress erythropoiesis in hereditary spherocytosis.
    Am J Hematol. 2020;95:710-711.
    PubMed    


    May 2020
  85. LOFARO T, Bain BJ
    Schistocytosis is not always microangiopathic hemolytic anemia.
    Am J Hematol. 2020 May 10. doi: 10.1002/ajh.25861.
    PubMed    


  86. BIANCHI P, Fermo E, Lezon-Geyda K, van Beers EJ, et al
    Genotype-phenotype correlation and molecular heterogeneity in pyruvate kinase deficiency.
    Am J Hematol. 2020;95:472-482.
    PubMed     Abstract available


  87. SCHMIDT PJ, Hollowell ML, Fitzgerald K, Butler JS, et al
    Mild iron deficiency does not ameliorate the phenotype of a murine erythropoietic protoporphyria model.
    Am J Hematol. 2020;95:492-496.
    PubMed     Abstract available


  88. ROUMENINA LT, Chadebech P, Bodivit G, Vieira-Martins P, et al
    Complement activation in sickle cell disease: Dependence on cell density, hemolysis and modulation by hydroxyurea therapy.
    Am J Hematol. 2020;95:456-464.
    PubMed     Abstract available


  89. HADJIDEMETRIOU M
    Now I Am The Voice: "a journey of self-discovery through the eyes of a Thalassemic".
    Am J Hematol. 2020;95:E105-E107.
    PubMed    


    April 2020
  90. PROCHASKA MT, Zhang H, Alavi C, Meltzer DO, et al
    Fatigability: A new perspective on and patient-centered outcome measure for patients with anemia.
    Am J Hematol. 2020 Apr 15. doi: 10.1002/ajh.25803.
    PubMed    


  91. GIARDINO S, Peffault de Latour R, Aljurf M, Eikema DJ, et al
    Outcome of Patients with Fanconi Anemia developing myelodysplasia and acute leukemia who received Allogeneic Hematopoietic Stem Cell Transplantation: A retrospective analysis on Behalf of EBMT group.
    Am J Hematol. 2020 Apr 8. doi: 10.1002/ajh.25810.
    PubMed     Abstract available


  92. HWANG SR, O'Dowd T, Markovic SN, Wolanskyj-Spinner AP, et al
    Recurrent Checkpoint Inhibitor-Induced Warm Agglutinin Autoimmune Hemolytic Anemia in a Patient with Metastatic Melanoma.
    Am J Hematol. 2020 Apr 3. doi: 10.1002/ajh.25812.
    PubMed    


  93. AL-BUBSEREE B, Leach M, Jones R, Bain BJ, et al
    The hematological effects of copper deficiency.
    Am J Hematol. 2020;95:446.
    PubMed    


  94. ESPINOZA J, Shah P, Veluswamy S, Zeltzer L, et al
    Aura and mental stress are associated with reports of pain in sickle cell disease-a pilot study using a mobile application.
    Am J Hematol. 2020;95:E101-E103.
    PubMed    


  95. DUTTA D, Li K, Methe B, Lim SH, et al
    Rifaximin on intestinally-related pathologic changes in sickle cell disease.
    Am J Hematol. 2020;95:E83-E86.
    PubMed    


  96. VACLAVU L, Petr J, Petersen ET, Mutsaerts HJMM, et al
    Cerebral oxygen metabolism in adults with sickle cell disease.
    Am J Hematol. 2020;95:401-412.
    PubMed     Abstract available


  97. GONDELAUD F, Connes P, Nader E, Renoux C, et al
    Sialic acids rather than glycosaminoglycans affect normal and sickle red blood cell rheology by binding to four major sites on fibrinogen.
    Am J Hematol. 2020;95:E77-E80.
    PubMed    


    March 2020
  98. MANARA R, Canna A, Caiazza M, Ponticorvo S, et al
    White matter volume changes in adult beta-thalassemia: negligible and unrelated to anemia and cognitive performances.
    Am J Hematol. 2020 Mar 20. doi: 10.1002/ajh.25790.
    PubMed    


  99. CHOI S, Leahy RM, Wood JC
    Lower White Matter Volume in Beta-Thalassemia Associated with Anemia and Cognitive Performance.
    Am J Hematol. 2020 Mar 17. doi: 10.1002/ajh.25787.
    PubMed    


  100. IKWUANUSI I, Jordan LC, Lee CA, Patel NJ, et al
    Cerebral hemodynamics and metabolism are similar in sickle cell disease patients with hemoglobin SS and Sbeta(0) thalassemia phenotypes.
    Am J Hematol. 2020;95:E66-E68.
    PubMed    


  101. FOY BH, Li A, McClung JP, Ranganath R, et al
    Data-driven physiologic thresholds for iron deficiency associated with hematologic decline.
    Am J Hematol. 2020;95:302-309.
    PubMed     Abstract available


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    S100B has pleiotropic effects on vaso-occlusive manifestations in sickle cell disease.
    Am J Hematol. 2020;95:E62-E65.
    PubMed    


    February 2020
  103. SARNA K, Brittenham GM, Beall CM
    Current WHO hemoglobin thresholds for altitude and misdiagnosis of anemia among Tibetan highlanders.
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    PubMed    


  104. BELISARIO AR, de Almeida JA, Mendes FG, da Silva DMM, et al
    Prevalence and risk factors for albuminuria and glomerular hyperfiltration in a large cohort of children with sickle cell anemia.
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  105. TOLU S, Reyes-Gil M, Ogu UO, Thomas M, et al
    Inherited High Fetal Hemoglobin in Sickle Cell Anemia: Outcomes with Aging High HbF and Sickle Cell.
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  106. SCHECKEL CJ, Yanardag Acik D, Ravindran A, Marshall A, et al
    Hapticophagia: Tactile chew cravings in iron deficiency anemia.
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    PubMed    


  107. EATON WA
    Hemoglobin S polymerization and sickle cell disease: A retrospective on the occasion of the 70th anniversary of Pauling's Science paper.
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  108. ANDOLFO I, Rosato BE, Manna F, De Rosa G, et al
    Gain-of-function mutations in PIEZO1 directly impair hepatic iron metabolism via the inhibition of the BMP/SMADs pathway.
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  109. GENDREAU S, Scholer M, Cecchini J, Habibi A, et al
    Cerebral fat embolism in sickle cell disease.
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    January 2020
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    Hematologic Findings in a Large Sample of Patients with Anorexia Nervosa and Bulimia Nervosa.
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  111. STEINBERG MH
    Treating Sickle Cell Anemia: A New Era Dawns.
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  112. WILLEN SM, McNeil JB, Rodeghier M, Kerchberger VE, et al
    Haptoglobin genotype predicts severe acute vaso-occlusive pain episodes in children with sickle cell anemia.
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  113. QASRAWI A, Arora R, Ramlal R, Munker R, et al
    Allogenic hematopoietic stem cell transplantation for prolonged bone marrow aplasia after chimeric antigen receptor (CAR) T-cell therapy for relapsed diffuse large B-cell lymphoma.
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  114. RICHARD F, van Lier JJ, Roubert B, Haboubi T, et al
    Oral ferroportin inhibitor VIT-2763: First-in-human, phase 1 study in healthy volunteers.
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  115. RAB MAE, Kanne CK, Bos J, Boisson C, et al
    Methodological aspects of the oxygenscan in sickle cell disease: A need for standardization.
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  116. SCHYRR F, Dolci M, Nydegger M, Canellini G, et al
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  117. BAIN BJ
    Delta beta thalassemia.
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    December 2019
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    Characterizing the effect of exposure to microgravity on anemia, more space is worse.
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  119. KAKO S, Kanda Y, Onizuka M, Aotsuka N, et al
    Allogeneic hematopoietic stem cell transplantation for aplastic anemia with pre-transplant conditioning using fludarabine, reduced-dose cyclophosphamide, and low-dose thymoglobulin: a KSGCT prospective study.
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  120. NEUBERG D
    Dissecting the web of ischemic stroke, sickle cell trait, and chronic kidney disease.
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    November 2019
  121. ATAGA KI, Wichlan D, Elsherif L, Derebail VK, et al
    A pilot study of the effect of atorvastatin on endothelial function and albuminuria in sickle cell disease.
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  122. ANDOLFO I, Rosato BE, Marra R, De Rosa G, et al
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  123. HALKES C, de Wreede LC, Knol C, Simand C, et al
    Allogeneic stem cell transplantation for acquired pure red cell aplasia.
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    September 2019
  124. KARKI NR, Auerbach M
    Single total dose infusion of ferumoxytol (1020 mg in 30 minutes) is an improved method of administration of intravenous iron.
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    August 2019
  125. GALADANCI AA, Galadanci NA, Jibir BW, Abdullahi SU, et al
    Approximately 40,000 children with sickle cell anemia require screening with TCD and treating with hydroxyurea for stroke prevention in three states in northern Nigeria.
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  126. PATEL R, Kang S, Valeshabad AK, Shah BN, et al
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  127. BATHINI S, Holtzman NG, Koka R, Singh Z, et al
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  128. TAHER AT, Cappellini MD, Musallam KM
    Development of a thalassemia-related thrombosis risk scoring system.
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    July 2019
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  130. SOYOUNG CHOI BA, O'Neil SH, Joshi AA, Li J, et al
    Anemia Predicts Lower White Matter Volume and Cognitive Performance in Sickle and Non-Sickle Cell Anemia Syndrome.
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    June 2019
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  132. FATTIZZO B, Cavallaro F, Milesi G, Barcellini W, et al
    Iron mobilization in a real life cohort of aplastic anemia patients treated with eltrombopag.
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  134. DUTTA D, Methe BA, Morris A, Lim SH, et al
    Effects of rifaximin on circulating aged neutrophils in sickle cell disease.
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  135. NANKANJA R, Kadhumbula S, Tagoola A, Geisberg M, et al
    HemoTypeSC Demonstrates >99% Field Accuracy in a Sickle Cell Disease Screening Initiative in Children of Southeastern Uganda.
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  136. DUTTA D, Methe B, Morris A, Lim SH, et al
    Elevated urinary 3-indoxyl sulfate in sickle cell disease.
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  137. ITZEP NP, Jadhav SP, Kanne CK, Sheehan VA, et al
    Spontaneous healing of avascular necrosis of the femoral head in sickle cell disease.
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    May 2019
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  139. BRUNSON A, Keegan T, Mahajan A, White R, et al
    High Incidence of Venous Thromboembolism Recurrence in Patients with Sickle Cell Disease.
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  140. RAJAGOPAL R, Bennett R, Liang J, Royle G, et al
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  141. RAB MAE, van Oirschot BA, Bos J, Merkx TH, et al
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  142. VINER M, Zhou J, Allison D, Han J, et al
    The morbidity and mortality of end stage renal disease in sickle cell disease.
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  143. WALKER AL, Gaydos LM, Farzan R, De Castro L, et al
    Social media discussions provide new insight about perceptions of hydroxyurea in the sickle cell community.
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  144. WEISS M, Parisi Jun M, Sheth S
    Clinical and economic burden of regularly transfused adult patients with beta-thalassemia in the United States: A retrospective cohort study using payer claims.
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  145. HOFFMAN JF
    Erythrocyte ATP, a possible therapeutic approach for sickle cell disease.
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  146. BAO EL, Lareau CA, Brugnara C, Fulcher IR, et al
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    April 2019
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  148. KIM TO, Grimes AB, Kirk S, Arulselvan A, et al
    Association of a positive direct antiglobulin test with chronic immune thrombocytopenia and use of second line therapies in children: A multi-institutional review.
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  149. TAHER AT, Origa R, Perrotta S, Kouraklis A, et al
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  150. OYEDEJI C, Strouse JJ, Crawford RD, Garrett ME, et al
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  151. LEBENSBURGER JD, Aban I, Pernell B, Kasztan M, et al
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  152. ALLY M, Magesa P, Luzzatto L
    High frequency of acquired aplastic anemia in Tanzania.
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  153. REES C, Lund K, Bain BJ
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    March 2019
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  155. JORDAN LC, Juttukonda MR, Kassim AA, DeBaun MR, et al
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  156. VERCELLOTTI GM, Dalmasso AP, Schaid TR Jr, Nguyen J, et al
    Critical role of C5a in sickle cell disease.
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  157. CASALE M, Filosa A, Ragozzino A, Amendola G, et al
    Long-term improvement in cardiac magnetic resonance in beta-thalassemia major patients treated with deferasirox extends to patients with abnormal baseline cardiac function.
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  158. RODGERS GM, Kurtti AL, Gilreath JA
    Are eltrombopag plasma and skin hyperpigmentation related? The eyes have it.
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    February 2019
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    Clinical and Laboratory Features of Autoimmune Hemolytic Anemia Associated with Immune Checkpoint Inhibitors.
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  160. STEWART JT, Willen SM, Cohen R, Rodeghier M, et al
    BMI percentile is an independent predictor of increase in lung function in children with sickle cell anemia.
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  161. MARSHALL AL, Mann S, Wolanskyj-Spinner A
    Digital storytelling for hematology education: Interactive thalassemia module for graduate millennial learners.
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  163. OPPONG SA, Asare EV, Olayemi E, Boafor T, et al
    Multidisciplinary care results in similar maternal and perinatal mortality rates for women with and without SCD in a low-resource setting.
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  164. GURUPRASAD P, Mannino RG, Caruso C, Zhang H, et al
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  165. EISENGA MF, Wouters HJCM, Kieneker LM, van der Klauw MM, et al
    Active smoking and macrocytosis in the general population: Two population-based cohort studies.
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  166. TAHER A, Viprakasit V, Cappellini MD, Sutcharitchan P, et al
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  167. SHARARA AI, Rustom LBO, Marrache M, Rimmani HH, et al
    Sofosbuvir/velpatasvir for chronic hepatitis C infection in patients with transfusion-dependent thalassemia.
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    January 2019
  169. JIE Z, Jie M, Run-Hui W, Xue Z, et al
    Unusual presentations of sitosterolemia limited to hematological abnormalities: A report of 4 cases presenting with stomatocytic anemia and thrombocytopenia with macrothrombocytes.
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  171. OZCAN A, Saracoglu S, Verboon J, Karakukcu M, et al
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    Bone Marrow Transplantation for Adolescents and Young Adults with Sickle Cell Disease: Results of a Prospective Multicenter Pilot Study.
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  173. PATNAIK MM, Tefferi A
    Refractory Anemia with Ring Sideroblasts (RARS) and RARS with Thrombocytosis (RARS-T) - "2019 Update on Diagnosis, Risk-stratification, and Management".
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  174. BACIGALUPO A, Oneto R, Schrezenmeier H, Hochsmann B, et al
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  176. HAN J, Saraf SL, Molokie RE, Gordeuk VR, et al
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  177. HAN J, Saraf SL, Gowhari M, Jain S, et al
    High inpatient dose of opioid at discharge compared to home dose predicts readmission risk in sickle cell disease.
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    December 2018
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    November 2018
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    October 2018
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    September 2018
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    August 2018
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  202. MUNDY LM, Wohlfeil S
    A comment on the comparative safety of intravenous ferumoxytol versus ferric carboxymaltose in iron deficiency anemia.
    Am J Hematol. 2018 Jul 7. doi: 10.1002/ajh.25204.
    PubMed    


    June 2018
  203. PALMBLAD J, Sander B, Bain B, Klimkowska M, et al
    Congenital dyserythropoietic anemia type 1: a case with novel compound heterozygous mutations in the C15orf41 gene.
    Am J Hematol. 2018 Jun 8. doi: 10.1002/ajh.25157.
    PubMed    


  204. GANSNER JM, Furutani E, Campagna DR, Fleming MD, et al
    Pancreatic lipomatosis in Diamond-Blackfan anemia: The importance of genetic testing in bone marrow failure disorders.
    Am J Hematol. 2018 Jun 8. doi: 10.1002/ajh.25155.
    PubMed    


    May 2018
  205. TAYO BO, Akingbola TS, Saraf SL, Shah BN, et al
    Fixed Low-Dose Hydroxyurea for the Treatment of Adults with Sickle Cell Anemia in Nigeria.
    Am J Hematol. 2018 May 14. doi: 10.1002/ajh.25143.
    PubMed    


    April 2018
  206. ROY S, Rai P, Eiymo Mwa Mpollo MS, Chang KH, et al
    Angiotensin Receptor Signaling in Sickle Cell Anemia has a Reno-Protective effect on Urine Concentrating Ability but results in Sickle Glomerulopathy.
    Am J Hematol. 2018 Apr 20. doi: 10.1002/ajh.25118.
    PubMed    


  207. PENNA D, Nicolosi M, Vallapureddy RR, Szuber N, et al
    The impact of sex on disease phenotype and prognostic thresholds of anemia in myelodysplastic syndromes.
    Am J Hematol. 2018 Apr 16. doi: 10.1002/ajh.25114.
    PubMed    


    March 2018
  208. PERGOLA PE, Fishbane S, LeWinter RD, Neylan JF, et al
    Hemoglobin response to ferric citrate in patients with nondialysis-dependent chronic kidney disease and iron deficiency anemia.
    Am J Hematol. 2018 Mar 25. doi: 10.1002/ajh.25088.
    PubMed    


  209. DERMAN R, Roman E, Smith-Nguyen GN, Achebe MM, et al
    Iron isomaltoside is superior to iron sucrose in increasing hemoglobin in gynecological patients with iron deficiency anemia.
    Am J Hematol. 2018 Mar 23. doi: 10.1002/ajh.25094.
    PubMed    


  210. JORDAN LC, Williams DOR, Rodeghier MJ, Covert B, et al
    Children with sickle cell anemia with normal TCD and without silent infarcts have a low incidence of new strokes.
    Am J Hematol. 2018 Mar 9. doi: 10.1002/ajh.25085.
    PubMed     Abstract available


  211. BACIGALUPO A, Oneto R, Schrezenmeier H, Hochsmann B, et al
    First line treatment of aplastic anemia with thymoglobuline in europe and asia: Outcome of 955 patients treated 2001-2012.
    Am J Hematol. 2018 Mar 2. doi: 10.1002/ajh.25081.
    PubMed     Abstract available


  212. SCHMIDT PJ, Liu K, Visner G, Fitzgerald K, et al
    RNAi-mediated reduction of hepatic Tmprss6 diminishes anemia and secondary iron overload in a splenectomized mouse model of beta-thalassemia intermedia.
    Am J Hematol. 2018 Mar 2. doi: 10.1002/ajh.25079.
    PubMed     Abstract available


  213. GALADANCI NA, Umar Abdullahi S, Vance LD, Musa Tabari A, et al
    Feasibility trial for primary stroke prevention in children with sickle cell anemia in Nigeria (SPIN trial).
    Am J Hematol. 2018;93:E83.
    PubMed    


    February 2018
  214. ADKINSON NF, Strauss WE, Macdougall IC, Bernard KE, et al
    Comparative safety of intravenous ferumoxytol vs ferric carboxymaltose in iron deficiency anemia: A randomized trial.
    Am J Hematol. 2018 Feb 8. doi: 10.1002/ajh.25060.
    PubMed     Abstract available


  215. ASSI R, Kantarjian HM, Garcia-Manero G, Cortes JE, et al
    A phase II trial of ruxolitinib in combination with azacytidine in myelodysplastic syndrome/myeloproliferative neoplasms.
    Am J Hematol. 2018;93:277-285.
    PubMed     Abstract available


  216. JEREBTSOVA M, Saraf SL, Lin X, Lee G, et al
    Identification of ceruloplasmin as a biomarker of chronic kidney disease in urine of sickle cell disease patients by proteomic analysis.
    Am J Hematol. 2018;93:E45-E47.
    PubMed    


  217. ELALFY MS, Adly A, Awad H, Tarif Salam M, et al
    Safety and efficacy of early start of iron chelation therapy with deferiprone in young children newly diagnosed with transfusion-dependent thalassemia: A randomized controlled trial.
    Am J Hematol. 2018;93:262-268.
    PubMed     Abstract available


  218. KHAN AB, Kesse-Adu R, Breen C, Murphy PB, et al
    A descriptive study of the characteristics of older adults with sickle cell disease.
    Am J Hematol. 2018;93:E38-E40.
    PubMed    


  219. TANABE P, Silva S, Bosworth HB, Crawford R, et al
    A randomized controlled trial comparing two vaso-occlusive episode (VOE) protocols in sickle cell disease (SCD).
    Am J Hematol. 2018;93:159-168.
    PubMed     Abstract available


    January 2018
  220. PEFFAULT DE LATOUR R, Tabrizi R, Marcais A, Leblanc T, et al
    Nationwide Survey on the Use of Horse Antithymocyte Globulins (ATGAM) in Patients with Acquired Aplastic Anemia: A Report on Behalf of the French Reference Center for Aplastic Anemia.
    Am J Hematol. 2018 Jan 27. doi: 10.1002/ajh.25050.
    PubMed     Abstract available


  221. HERGOTT CB, Pozdnyakova O
    Evans syndrome secondary to undiagnosed chronic lymphocytic leukemia in a patient with unexplained bleeding.
    Am J Hematol. 2018 Jan 17. doi: 10.1002/ajh.25039.
    PubMed    


  222. JEREBTSOVA M, Saraf SL, Soni S, Afangbedji N, et al
    Urinary Orosomucoid is Associated with Progressive Chronic Kidney Disease Stage in Patients with Sickle Cell Anemia.
    Am J Hematol. 2018 Jan 12. doi: 10.1002/ajh.25036.
    PubMed    


  223. VANHINSBERGH L, Uthaya S, Bain BJ
    Methylene blue-induced Heinz body hemolytic anemia in a premature neonate.
    Am J Hematol. 2018 Jan 5. doi: 10.1002/ajh.25028.
    PubMed    


  224. ANDOLFO I, Russo R, Gambale A, Iolascon A, et al
    Hereditary stomatocytosis: An underdiagnosed condition.
    Am J Hematol. 2018;93:107-121.
    PubMed     Abstract available


  225. BARRETT A, Catherwood M, Thornton P, Murphy P, et al
    Transformation of MDS/MPN-RS-T to AML: Trisomy 13, resistant thrombocytosis and transient disease control with oral busulfan therapy.
    Am J Hematol. 2018;93:E16-E17.
    PubMed    


  226. NOLAN VG, Anderson SM, Smeltzer MP, Porter JS, et al
    Pediatric to adult care co-location transitional model for youth with sickle cell disease.
    Am J Hematol. 2018;93:E30-E32.
    PubMed    


  227. NICOLOSI M, Mudireddy M, Vallapureddy R, Gangat N, et al
    Lenalidomide therapy in patients with myelodysplastic syndrome/myeloproliferative neoplasm with ring sideroblasts and thrombocytosis (MDS/MPN-RS-T).
    Am J Hematol. 2018;93:E27-E30.
    PubMed    


  228. HAN J, Saraf SL, Kavoliunaite L, Jain S, et al
    Program expansion of a day hospital dedicated to manage sickle cell pain.
    Am J Hematol. 2018;93:E20-E21.
    PubMed    


  229. KAUFMAN HW, Niles JK, Gallagher DR, Rivera A, et al
    Revised prevalence estimate of possible Hereditary Xerocytosis as derived from a large U.S. Laboratory database.
    Am J Hematol. 2018;93:E9-E12.
    PubMed    


  230. GINWALLA M, AlMasoud A, Tofovic D, Alin T, et al
    Cardiovascular evaluation and management of iron overload cardiomyopathy in sickle cell disease.
    Am J Hematol. 2018;93:E7-E9.
    PubMed    


    December 2017
  231. FATTIZZO B, Zaninoni A, Gianelli U Prof, Zanella A Prof, et al
    Prognostic impact of bone marrow fibrosis and dyserythropoiesis in autoimmune hemolytic anemia.
    Am J Hematol. 2017 Dec 23. doi: 10.1002/ajh.25020.
    PubMed    


  232. WILLEN SM, Rodeghier M, Rosen CL, DeBaun MR, et al
    Sleep disordered breathing does not predict acute severe pain episodes in children with sickle cell anemia.
    Am J Hematol. 2017 Dec 20. doi: 10.1002/ajh.25013.
    PubMed     Abstract available


  233. WILLEN SM, Cohen R, Rodeghier M, Kirkham F, et al
    Age is the only predictor of small decrease in lung function in children with sickle cell anemia.
    Am J Hematol. 2017 Dec 11. doi: 10.1002/ajh.25003.
    PubMed     Abstract available


  234. DAVIES JOJ, Hart AC, De La Fuente J, Bain BJ, et al
    Macrophage activation syndrome and post-transplant microangiopathy following haploidentical bone marrow transplantation for sickle cell anemia.
    Am J Hematol. 2017 Dec 2. doi: 10.1002/ajh.24995.
    PubMed    


  235. DE FALCO L, Tortora R, Imperatore N, Bruno M, et al
    The role of tmprss6 and hfe variants in iron deficiency anemia in celiac disease.
    Am J Hematol. 2017 Dec 1. doi: 10.1002/ajh.24991.
    PubMed     Abstract available


  236. PINTO VM, Gianesin B, Balocco M, Bacigalupo L, et al
    Noninvasive monitoring of liver fibrosis in sickle cell disease: Longitudinal observation of a cohort of adult patients.
    Am J Hematol. 2017;92:E666-E668.
    PubMed    


  237. TAHER AT, Saliba AN, Kuo KH, Giardina PJ, et al
    Safety and pharmacokinetics of the oral iron chelator SP-420 in beta-thalassemia.
    Am J Hematol. 2017;92:1356-1361.
    PubMed     Abstract available


  238. NARBEY D, Habibi A, Chadebech P, Mekontso-Dessap A, et al
    Incidence and predictive score for delayed hemolytic transfusion reaction in adult patients with sickle cell disease.
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  239. SALIBA AN, Moukhadder HM, Harb A, Beydoun H, et al
    Causes of hospital admission in beta-thalassemia (CHAT) in Lebanon from 1995 to 2015: A pilot retrospective study from a tertiary care center.
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    PubMed    


  240. CAOCCI G, Orofino MG, Vacca A, Piroddi A, et al
    Long-term survival of beta thalassemia major patients treated with hematopoietic stem cell transplantation compared with survival with conventional treatment.
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    PubMed     Abstract available


  241. WORSHAM CM, Martin ST, Nouraie SM, Cohen RT, et al
    Clinical and laboratory findings associated with sleep disordered breathing in sickle cell disease.
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    PubMed    


  242. SCHARMAN CD, Burger D, Shatzel JJ, Kim E, et al
    Treatment of individuals who cannot receive blood products for religious or other reasons.
    Am J Hematol. 2017;92:1370-1381.
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    November 2017
  243. CASALE M, Borriello A, Scianguetta S, Roberti D, et al
    Hereditary hypochromic microcytic anemia associated with loss-of-function DMT1 gene mutations and absence of liver iron overload.
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  244. MACHARIA AW, Mochamah G, Uyoga S, Ndila CM, et al
    The clinical epidemiology of sickle cell anemia in Africa.
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  245. ALTMAN JK, Foran JM, Pratz KW, Trone D, et al
    Phase 1 Study of Quizartinib in Combination With Induction and Consolidation Chemotherapy in Patients With Newly Diagnosed Acute Myeloid Leukemia.
    Am J Hematol. 2017 Nov 15. doi: 10.1002/ajh.24974.
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  246. KHALEEL M, Puliyel M, Shah P, Sunwoo J, et al
    Individuals with sickle cell disease have a significantly greater vasoconstriction response to thermal pain than controls and have significant vasoconstriction in response to anticipation of pain.
    Am J Hematol. 2017;92:1137-1145.
    PubMed     Abstract available


  247. SOLOVEY A, Somani A, Belcher JD, Milbauer L, et al
    A monocyte-TNF-endothelial activation axis in sickle transgenic mice: Therapeutic benefit from TNF blockade.
    Am J Hematol. 2017;92:1119-1130.
    PubMed     Abstract available


  248. NADER E, Connes P, Lamarre Y, Renoux C, et al
    Plasmapheresis may improve clinical condition in sickle cell disease through its effects on red blood cell rheology.
    Am J Hematol. 2017;92:E629-E630.
    PubMed    


  249. SCHIMMEL M, Luken BM, Nur E, van Tuijn CFJ, et al
    Inflammatory and endothelial markers during vaso-occlusive crisis and acute chest syndrome in sickle cell disease.
    Am J Hematol. 2017;92:E634-E636.
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  250. ORIGA R, Tatti F, Zappu A, Leoni GB, et al
    Earlier initiation of transfusional and iron chelation therapies in recently born children with transfusion-dependent thalassemia.
    Am J Hematol. 2017;92:E627-E628.
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    October 2017
  251. 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.
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  252. 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.
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  253. 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     Abstract available


  254. 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.
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  255. 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.
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  256. WAHIDIYAT PA, Sekarsari D, Adnani NB, Putriasih SA, et al
    Association of pancreatic MRI R2* with blood glucose and cardiac MRI R2* among thalassemia major patients in Indonesia.
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    PubMed    


  257. AL-RIYAMI AZ, Iolascon A, Al-Zadjali S, Andolfo I, et al
    Targeted next generation sequencing identifies a novel beta-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis.
    Am J Hematol. 2017;92:E607-E609.
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    September 2017
  258. 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.
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  259. 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     Abstract available


  260. 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.
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  261. BARSHTEIN G, Goldschmidt N, Pries AR, Zelig O, et al
    Deformability of transfused red blood cells is a potent effector of transfusion-induced hemoglobin increment: A study with beta-thalassemia major patients.
    Am J Hematol. 2017;92:E559-E560.
    PubMed    


  262. SOOD R, Jiramongkolchai K, Streiff M, Gonzalez C, et al
    Look into my eyes: An unusual first presentation of sickle cell disease.
    Am J Hematol. 2017;92:968-971.
    PubMed    


  263. SIOW W, Matthey F, Bain BJ
    The significance of irregularly contracted cells and hemighosts in sickle cell disease.
    Am J Hematol. 2017;92:966-967.
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    August 2017
  264. BODDU P, Garcia-Manero G, Ravandi F, Borthakur G, et al
    Clinical Outcomes in Adult Patients with Aplastic Anemia- a single institution experience.
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    July 2017
  265. 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.
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  266. 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.
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  267. 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.
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  268. 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.
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  269. 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.
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    June 2017
  270. VASSEUR C, Domingues-Hamdi E, Pakdaman S, Barau C, et al
    Elevated soluble alpha-hemoglobin pool in Sickle Cell Anemia.
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  271. KASTHURI RS, Montifar M, Nelson J, Kim H, et al
    Prevalence and Predictors of Anemia in Hereditary Hemorrhagic Telangiectasia.
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  272. SHAIKHO EM, Farrell JJ, Alsultan A, Sebastiani P, et al
    Genetic Determinants of HbF in Saudi Arabian and African Benin Haplotype Sickle Cell Anemia.
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  273. QUINN CT, Saraf SL, Gordeuk VR, Fitzhugh CD, et al
    Losartan for the Nephropathy of Sickle Cell Anemia: A Phase-2, Multi-Center Trial.
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  274. 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.
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  275. HADJIDEMETRIOU M
    Thalassemia: Yesterday, Today, Tomorrow.
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  276. BALDINI M, Mancarella M, Cassinerio E, Marcon A, et al
    Adrenal insufficiency: An emerging challenge in thalassemia?
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  277. BRENNAN Y, Curnow J, Favaloro EJ
    2B or not 2B? A prothrombotic tendency masquerading as a bleeding disorder.
    Am J Hematol. 2017;92:584-590.
    PubMed    


  278. ANDERSON N, Eckman JR, Ballas SK
    Beyond the transition of adolescents and young adults with sickle cell disease to adult care: Role of geography.
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  279. RIVERA A, Vandorpe DH, Shmukler BE, Gallagher DR, et al
    Erythrocytes from hereditary xerocytosis patients heterozygous for KCNN4 V282M exhibit increased spontaneous Gardos channel-like activity inhibited by senicapoc.
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    PubMed    


  280. ROUMI JE, Moukhadder HM, Graziadei G, Pennisi M, et al
    Pregnancy in beta-thalassemia intermedia at two tertiary care centers in Lebanon and Italy: A follow-up report on fetal and maternal outcomes.
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  281. LAMBERT MP, Witmer CM, Kwiatkowski JL
    Therapy induced iron deficiency in children treated with eltrombopag for immune thrombocytopenia.
    Am J Hematol. 2017;92:E88-E91.
    PubMed    


  282. MINNITI CP, Vichinsky E
    Lifespan care in SCD: Whom to transition, the patients or the health care system?
    Am J Hematol. 2017;92:487-489.
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    May 2017
  283. 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.
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  284. 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.
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  285. HALAWI R, Cappellini MD, Taher A
    A higher prevalence of hematologic malignancies in patients with thalassemia: Background and culprits.
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  286. READING NS, Ruiz-Bonilla JA, Christensen RD, Caceres-Perkins W, et al
    A patient with both methemoglobinemia and G6PD deficiency: A therapeutic conundrum.
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  287. HALAWI R, Beydoun H, Cappellini MD, Ferla V, et al
    Hematologic malignancies in thalassemia: Adding new cases to the repertoire.
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  288. FURLAN L, Graziadei G, Colombo G, Forzenigo LV, et al
    K. pneumoniae liver abscess following deferoxamine subcutaneous self-injection.
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  289. ANGELUCCI E, Pilo F, Coates TD
    Transplantation in thalassemia: Revisiting the Pesaro risk factors 25 years later.
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    April 2017
  290. 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.
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  291. RAVINDRAN A, Sankaran J, Jacob EK, Kreuter JD, et al
    High prevalence of monoclonal gammopathy among patients with warm autoimmune hemolytic anemia.
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  292. 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.
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  293. 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.
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  294. 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.
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  295. LI LY, Liu ZY, Liu H, Liu CY, et al
    Deep sequencing of whole genome exon in paroxysmal nocturnal hemoglobinuria.
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  296. STEHOUWER N, Edge P, Katie Park B, Piccone C, et al
    Acute pain in adolescents and young adults with sickle cell disease: Delayed and increased opioid dosing following transition to adult care.
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  297. MANU PEREIRA MD, Ropero P, Loureiro C, Vives Corrons JL, et al
    Low affinity hemoglobinopathy (Hb Vigo) due to a new mutation of beta globin gene (c200 A>T; Lys>Ile). A cause of rare anemia misdiagnosis.
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    March 2017
  298. NASSIN ML, Vergilio JA, Heeney MM, LaBelle JL, et al
    Neonatal Anemia: Revisiting the Enigmatic Pyknocyte.
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    PubMed    


  299. LEWEN MO, Kavanagh PL, Sobota AE
    A comment on improving transcranial Doppler ultrasonography screening in children with sickle cell anemia.
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  300. 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    


  301. 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    


  302. 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     Abstract available


  303. SALIBA AN, Musallam KM, Cappellini MD, Graziadei G, et al
    Serum ferritin values between 300 and 800 ng/mL in nontransfusion-dependent thalassemia: A probability curve to guide clinical decision making when MRI is unavailable.
    Am J Hematol. 2017;92:E35-E37.
    PubMed    


  304. SCHOTTEN N, Laarakkers CM, Roelofs RW, Origa R, et al
    EPO and hepcidin plasma concentrations in blood donors and beta-thalassemia intermedia are not related to commercially tested plasma ERFE concentrations.
    Am J Hematol. 2017;92:E29-E31.
    PubMed    


  305. BARCELLINI W, Fattizzo B, Zaninoni A, Valli V, et al
    Clinical evolution of autoimmune cytopenias to idiopathic cytopenias/dysplasias of uncertain significance (ICUS/IDUS) and bone marrow failure syndromes.
    Am J Hematol. 2017;92:E26-E29.
    PubMed    


  306. GRAFFEO L, Vitrano A, Giambona A, Scondotto S, et al
    The heterozygote state for beta-thalassemia detrimentally affects health outcomes.
    Am J Hematol. 2017;92:E23-E25.
    PubMed    


  307. SOKOL KA, Veluswamy RR, Zimmerman BS, Tummalapalli SL, et al
    Atypical hemolytic uremic syndrome associated with Capnocytophaga canimorsus.
    Am J Hematol. 2017;92:322.
    PubMed    


    February 2017
  308. 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    


  309. 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    


  310. 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    


  311. 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     Abstract available


  312. 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    


  313. 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     Abstract available


  314. 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     Abstract available


  315. 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     Abstract available


  316. 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     Abstract available


    January 2017
  317. 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     Abstract available


  318. DAI Y, Sangerman J, Nouraie M, Faller AD, et al
    Effects of hydroxyurea on F-cells in sickle cell disease and potential impact of a second fetal globin inducer.
    Am J Hematol. 2017;92:E10-E11.
    PubMed    


    December 2016
  319. 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    


  320. 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    


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


    October 2016
  322. 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     Abstract available


  323. 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     Abstract available


  324. 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     Abstract available


    September 2016
  325. 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     Abstract available


  326. 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     Abstract available


  327. 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    


    May 2016
  328. KROPSHOFER G, Sopper S, Steurer M, Schwinger W, et al
    Successful management of mixed chimerism after bone marrow transplant in beta-thalassemia major.
    Am J Hematol. 2016 May 30. doi: 10.1002/ajh.24436.
    PubMed    


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