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Articles published in Am J Hematol

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    April 2021
  1. 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    


  2. 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    


  3. 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    


  4. 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    


  5. 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    


  6. 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    


  7. 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


  8. 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
  9. 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


  10. 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


  11. 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
  12. 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


  13. 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    


  14. 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


  15. 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


  16. 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    


  17. 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    


  18. 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
  19. 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    


  20. 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    


  21. 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    


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


  23. 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    


  24. 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


  25. 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    


  26. 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
  27. 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    


  28. 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
  29. 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    


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


  31. 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    


  32. 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    


  33. 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


  34. 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


  35. 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


  36. 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
  37. 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


  38. 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


  39. 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
  40. 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    


  41. 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


  42. 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    


  43. 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    


  44. 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


  45. 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    


  46. 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    


  47. 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    


  48. 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
  49. 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    


  50. 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    


  51. 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    


  52. 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    


  53. 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    


  54. 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    


  55. 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    


  56. 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    


  57. 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


  58. 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
  59. 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    


  60. 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


  61. 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


  62. 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    


  63. 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    


  64. 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    


  65. 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


  66. 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
  67. 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    


  68. 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    


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


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


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


  72. 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


  73. 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


  74. 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


  75. 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
  76. 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    


  77. 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


  78. 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    


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


  80. 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    


  81. 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    


  82. 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


  83. 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
  84. 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    


  85. 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    


  86. 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    


  87. 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


  88. ZHANG X, Shah BN, Zhang W, Saraf SL, et al
    S100B has pleiotropic effects on vaso-occlusive manifestations in sickle cell disease.
    Am J Hematol. 2020;95:E62-E65.
    PubMed    


    February 2020
  89. SARNA K, Brittenham GM, Beall CM
    Current WHO hemoglobin thresholds for altitude and misdiagnosis of anemia among Tibetan highlanders.
    Am J Hematol. 2020 Feb 25. doi: 10.1002/ajh.25765.
    PubMed    


  90. 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.
    Am J Hematol. 2020 Feb 21. doi: 10.1002/ajh.25763.
    PubMed    


  91. 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.
    Am J Hematol. 2020 Feb 18. doi: 10.1002/ajh.25759.
    PubMed    


  92. SCHECKEL CJ, Yanardag Acik D, Ravindran A, Marshall A, et al
    Hapticophagia: Tactile chew cravings in iron deficiency anemia.
    Am J Hematol. 2020 Feb 5. doi: 10.1002/ajh.25749.
    PubMed    


  93. EATON WA
    Hemoglobin S polymerization and sickle cell disease: A retrospective on the occasion of the 70th anniversary of Pauling's Science paper.
    Am J Hematol. 2020;95:205-211.
    PubMed     Abstract available


  94. 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.
    Am J Hematol. 2020;95:188-197.
    PubMed     Abstract available


  95. GENDREAU S, Scholer M, Cecchini J, Habibi A, et al
    Cerebral fat embolism in sickle cell disease.
    Am J Hematol. 2020;95:E41-E45.
    PubMed    


    January 2020
  96. WALSH K, Blalock DV, Mehler PS
    Hematologic Findings in a Large Sample of Patients with Anorexia Nervosa and Bulimia Nervosa.
    Am J Hematol. 2020 Jan 15. doi: 10.1002/ajh.25732.
    PubMed    


  97. STEINBERG MH
    Treating Sickle Cell Anemia: A New Era Dawns.
    Am J Hematol. 2020 Jan 10. doi: 10.1002/ajh.25724.
    PubMed    


  98. 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.
    Am J Hematol. 2020 Jan 9. doi: 10.1002/ajh.25728.
    PubMed    


  99. 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.
    Am J Hematol. 2020 Jan 9. doi: 10.1002/ajh.25725.
    PubMed    


  100. 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.
    Am J Hematol. 2020;95:68-77.
    PubMed     Abstract available


  101. RAB MAE, Kanne CK, Bos J, Boisson C, et al
    Methodological aspects of the oxygenscan in sickle cell disease: A need for standardization.
    Am J Hematol. 2020;95:E5-E8.
    PubMed    


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    Delta beta thalassemia.
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    PubMed    


    December 2019
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    Characterizing the effect of exposure to microgravity on anemia, more space is worse.
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  105. 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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  106. NEUBERG D
    Dissecting the web of ischemic stroke, sickle cell trait, and chronic kidney disease.
    Am J Hematol. 2019;94:1302.
    PubMed    


    November 2019
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    A pilot study of the effect of atorvastatin on endothelial function and albuminuria in sickle cell disease.
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    PubMed    


  108. ANDOLFO I, Rosato BE, Marra R, De Rosa G, et al
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  109. 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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    PubMed    


    September 2019
  110. 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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    PubMed    


    August 2019
  111. 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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  112. PATEL R, Kang S, Valeshabad AK, Shah BN, et al
    Kidney Ultrasound Findings According to Kidney Function in Sickle Cell Anemia.
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  113. BATHINI S, Holtzman NG, Koka R, Singh Z, et al
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  114. 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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  116. 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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    A prospective, multicenter, randomized comparison of iron isomaltoside 1000 versus iron sucrose in patients with iron deficiency anemia (the FERWON-IDA trial).
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  118. 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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  120. 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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  121. 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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    Elevated urinary 3-indoxyl sulfate in sickle cell disease.
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  123. 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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    Robust Clinical and Laboratory Response to Hydroxyurea Using Pharmacokinetically Guided Dosing for Young Children with Sickle Cell Anemia.
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  125. 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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  126. RAJAGOPAL R, Bennett R, Liang J, Royle G, et al
    High dose carfilzomib proteasome inhibition induces anemia by oxidative hemolysis: A case series of 8 patients from a single centre.
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  127. RAB MAE, van Oirschot BA, Bos J, Merkx TH, et al
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  128. 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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  129. 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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  130. 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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  131. HOFFMAN JF
    Erythrocyte ATP, a possible therapeutic approach for sickle cell disease.
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  132. BAO EL, Lareau CA, Brugnara C, Fulcher IR, et al
    Heritability of fetal hemoglobin, white cell count, and other clinical traits from a sickle cell disease family cohort.
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    April 2019
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  134. 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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  135. TAHER AT, Origa R, Perrotta S, Kouraklis A, et al
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  136. OYEDEJI C, Strouse JJ, Crawford RD, Garrett ME, et al
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  137. LEBENSBURGER JD, Aban I, Pernell B, Kasztan M, et al
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  138. ALLY M, Magesa P, Luzzatto L
    High frequency of acquired aplastic anemia in Tanzania.
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  139. REES C, Lund K, Bain BJ
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    March 2019
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    Normal Saline Bolus Use in Pediatric Emergency Departments is Associated with Worse Pain Control in Children with Sickle Cell Anemia and Vaso-occlusive Pain.
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  141. JORDAN LC, Juttukonda MR, Kassim AA, DeBaun MR, et al
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  142. VERCELLOTTI GM, Dalmasso AP, Schaid TR Jr, Nguyen J, et al
    Critical role of C5a in sickle cell disease.
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  143. 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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  144. RODGERS GM, Kurtti AL, Gilreath JA
    Are eltrombopag plasma and skin hyperpigmentation related? The eyes have it.
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    PubMed    


    February 2019
  145. LEAF RK, Ferreri C, Rangachari D, Mier J, et al
    Clinical and Laboratory Features of Autoimmune Hemolytic Anemia Associated with Immune Checkpoint Inhibitors.
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  146. 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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    PubMed    


  147. MARSHALL AL, Mann S, Wolanskyj-Spinner A
    Digital storytelling for hematology education: Interactive thalassemia module for graduate millennial learners.
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  148. DESAI PC, Kendel N, Huang Y, Heinlein M, et al
    Hypoxia in sickle cell disease due to right to left shunting.
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    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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  150. GURUPRASAD P, Mannino RG, Caruso C, Zhang H, et al
    Integrated automated particle tracking microfluidic enables high-throughput cell deformability cytometry for red cell disorders.
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  151. 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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  152. TAHER A, Viprakasit V, Cappellini MD, Sutcharitchan P, et al
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  153. 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
  155. 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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  157. OZCAN A, Saracoglu S, Verboon J, Karakukcu M, et al
    A mummy emerges from the grave: Scurvy confounding the clinical presentation of a child with Fanconi Anemia.
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  158. KRISHNAMURTI L, Neuberg DS, Sullivan KM, Kamani NR, et al
    Bone Marrow Transplantation for Adolescents and Young Adults with Sickle Cell Disease: Results of a Prospective Multicenter Pilot Study.
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  159. 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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    PubMed     Abstract available


  160. 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.
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  161. BIANCHI P, Fermo E, Glader B, Kanno H, et al
    Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency.
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    PubMed     Abstract available


  162. HAN J, Saraf SL, Molokie RE, Gordeuk VR, et al
    Use of metformin in patients with sickle cell disease.
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    PubMed    


  163. 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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  164. CHAPMAN MS, Kiritkumar K, Lund K, Bain BJ, et al
    An unusual hemoglobinopathy: compound heterozygosity for hemoglobins C and E.
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    December 2018
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  168. ARIGLIANI M, Dogara LG, Zubair R, Castriotta L, et al
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    November 2018
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    Iron, erythropoietin, and inflammation regulate hepcidin in Bmp2-deficient mice, but serum iron fails to induce hepcidin in Bmp6-deficient mice.
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    Preoperative Treatment of Anemia and Outcomes in Surgical Jehovah's Witness Patients.
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    October 2018
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    Effectiveness of Eculizumab in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH) With or Without Aplastic Anemia in the International PNH Registry.
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  173. AUSTIN A, Lund K, Bain BJ
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  174. SAMARASINGHE S, Clesham K, Iacobelli S, Sbianchi G, et al
    IMPACT OF T-CELL DEPLETION STRATEGIES ON OUTCOMES FOLLOWING HEMATOPOIETIC STEM CELL TRANSPLANTATION FOR IDIOPATHIC APLASTIC ANEMIA: A STUDY ON BEHALF OF THE EUROPEAN BLOOD AND MARROW TRANSPLANT (EBMT) SAA WORKING PARTY.
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  175. PRYCE A, Lund K, Shah M, Bain BJ, et al
    Pertussis - an uncommon cause of microangiopathic hemolytic anemia in an infant.
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    September 2018
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    Progressive Loss of Brain Volume in Children with Sickle Cell Anemia and Silent Cerebral Infarct: A Report from the Silent Cerebral Infarct Transfusion (SIT) Trial.
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  178. DI M, Bian J, Butera JN
    A new onset of thrombocytopenia and microangiopathic hemolytic anemia in the healthcare setting: A challenge for diagnosis.
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    FYN KYNASE IS A NOVEL MODULATOR OF ERYTHROPOIETIN SIGNALING AND STRESS ERYTHROPOIESIS.
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    August 2018
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  181. LEE SE, Park SS, Jeon YW, Yoon JH, et al
    Optimal conditioning regimen for haplo-identical stem cell transplantation in adult patients with acquired severe aplastic anemia: Prospective de-escalation study of TBI and ATG dose.
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  182. VAN STRAATEN S, Biemond BJ, Kerkhoffs JL, Gitz-Francois J, et al
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    July 2018
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    Management of anemia in patients who decline blood transfusion.
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    Predictors of refractoriness to therapy and healthcare resource utilization in 378 patients with primary autoimmune hemolytic anemia from 8 Italian Reference Centers.
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  188. MUNDY LM, Wohlfeil S
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    June 2018
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    Congenital dyserythropoietic anemia type 1: a case with novel compound heterozygous mutations in the C15orf41 gene.
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    May 2018
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    April 2018
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    March 2018
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  196. JORDAN LC, Williams DOR, Rodeghier MJ, Covert B, et al
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  197. BACIGALUPO A, Oneto R, Schrezenmeier H, Hochsmann B, et al
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    February 2018
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    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


  201. 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


  202. 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    


  203. 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


  204. 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    


  205. 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
  206. 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


  207. 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    


  208. 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    


  209. 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    


  210. 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


  211. 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    


  212. 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    


  213. 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    


  214. 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    


  215. 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    


  216. 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
  217. 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    


  218. 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


  219. 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


  220. 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    


  221. 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


  222. 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    


  223. 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


  224. 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.
    Am J Hematol. 2017;92:1340-1348.
    PubMed     Abstract available


  225. 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.
    Am J Hematol. 2017;92:E652-E653.
    PubMed    


  226. 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.
    Am J Hematol. 2017;92:1303-1310.
    PubMed     Abstract available


  227. WORSHAM CM, Martin ST, Nouraie SM, Cohen RT, et al
    Clinical and laboratory findings associated with sleep disordered breathing in sickle cell disease.
    Am J Hematol. 2017;92:E649-E651.
    PubMed    


  228. 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.
    PubMed     Abstract available


    November 2017
  229. 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.
    Am J Hematol. 2017 Nov 27. doi: 10.1002/ajh.24988.
    PubMed    


  230. MACHARIA AW, Mochamah G, Uyoga S, Ndila CM, et al
    The clinical epidemiology of sickle cell anemia in Africa.
    Am J Hematol. 2017 Nov 23. doi: 10.1002/ajh.24986.
    PubMed     Abstract available


  231. 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.
    PubMed     Abstract available


  232. 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


  233. 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


  234. 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    


  235. 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.
    PubMed    


  236. 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.
    PubMed    


    October 2017
  237. 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    


  238. 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    


  239. 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


  240. 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     Abstract available


  241. 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     Abstract available


  242. 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.
    Am J Hematol. 2017;92:E620-E621.
    PubMed    


  243. 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.
    PubMed    


    September 2017
  244. 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     Abstract available


  245. 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


  246. 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     Abstract available


  247. 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    


  248. 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    


  249. 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.
    PubMed    


    August 2017
  250. 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     Abstract available


    July 2017
  251. 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    


  252. 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     Abstract available


  253. 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     Abstract available


  254. 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    


  255. 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     Abstract available


    June 2017
  256. 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    


  257. 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    


  258. 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    


  259. 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     Abstract available


  260. 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     Abstract available


  261. HADJIDEMETRIOU M
    Thalassemia: Yesterday, Today, Tomorrow.
    Am J Hematol. 2017;92:490-492.
    PubMed    


  262. BALDINI M, Mancarella M, Cassinerio E, Marcon A, et al
    Adrenal insufficiency: An emerging challenge in thalassemia?
    Am J Hematol. 2017;92:E119-E121.
    PubMed    


  263. 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    


  264. ANDERSON N, Eckman JR, Ballas SK
    Beyond the transition of adolescents and young adults with sickle cell disease to adult care: Role of geography.
    Am J Hematol. 2017;92:E110-E112.
    PubMed    


  265. 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.
    Am J Hematol. 2017;92:E108-E110.
    PubMed    


  266. 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.
    Am J Hematol. 2017;92:E96-E99.
    PubMed    


  267. 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    


  268. 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.
    PubMed    


    May 2017
  269. 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    


  270. 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     Abstract available


  271. HALAWI R, Cappellini MD, Taher A
    A higher prevalence of hematologic malignancies in patients with thalassemia: Background and culprits.
    Am J Hematol. 2017;92:414-416.
    PubMed    


  272. READING NS, Ruiz-Bonilla JA, Christensen RD, Caceres-Perkins W, et al
    A patient with both methemoglobinemia and G6PD deficiency: A therapeutic conundrum.
    Am J Hematol. 2017;92:474-477.
    PubMed    


  273. HALAWI R, Beydoun H, Cappellini MD, Ferla V, et al
    Hematologic malignancies in thalassemia: Adding new cases to the repertoire.
    Am J Hematol. 2017;92:E68-E70.
    PubMed    


  274. FURLAN L, Graziadei G, Colombo G, Forzenigo LV, et al
    K. pneumoniae liver abscess following deferoxamine subcutaneous self-injection.
    Am J Hematol. 2017;92:480-481.
    PubMed    


  275. ANGELUCCI E, Pilo F, Coates TD
    Transplantation in thalassemia: Revisiting the Pesaro risk factors 25 years later.
    Am J Hematol. 2017;92:411-413.
    PubMed    


    April 2017
  276. 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     Abstract available


  277. 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    


  278. 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    


  279. 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    


  280. 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     Abstract available


  281. LI LY, Liu ZY, Liu H, Liu CY, et al
    Deep sequencing of whole genome exon in paroxysmal nocturnal hemoglobinuria.
    Am J Hematol. 2017;92:E51-E53.
    PubMed    


  282. 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.
    Am J Hematol. 2017;92:E40-E42.
    PubMed    


  283. 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.
    Am J Hematol. 2017;92:E38-E40.
    PubMed    


    March 2017
  284. 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    


  285. 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    


  286. 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    


  287. 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    


  288. 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


  289. 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    


  290. 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    


  291. 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    


  292. 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    


  293. 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
  294. 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    


  295. 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    


  296. 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    


  297. 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


  298. 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    


  299. 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.
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    Hepcidin detects iron deficiency in Sri Lankan adolescents with a high burden of hemoglobinopathy: A diagnostic test accuracy study.
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    Daily pain in adults with sickle cell disease-a different perspective.
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    Arterio-venous fistula for automated red blood cells exchange in patients with sickle cell disease: Complications and outcomes.
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    January 2017
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    A randomized trial of iron isomaltoside versus iron sucrose in patients with iron deficiency anemia.
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    Effects of hydroxyurea on F-cells in sickle cell disease and potential impact of a second fetal globin inducer.
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    PubMed    


    December 2016
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    Thrombospondin-1 Gene Polymorphism is Associated with Estimated Pulmonary Artery Pressure in Patients with Sickle Cell Anemia.
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  306. 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.
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  307. BAIN BJ
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    PubMed    


    October 2016
  308. GOODNOUGH LT, Comin-Colet J, Leal-Noval S, Ozawa S, et al
    Management of Anemia in Patients with Congestive Heart Failure.
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    Hydroxyurea Effectiveness in Children and Adolescents with Sickle Cell Anemia: A Large Retrospective, Population-Based Cohort.
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    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).
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    September 2016
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    Biochemical surrogate markers of hemolysis do not correlate with directly measured erythrocyte survival in sickle cell anemia.
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    Iron Refractory Iron Deficiency Anemia (IRIDA): A heterogeneous disease that is not always iron refractory.
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    Safety and effectiveness of extended versus shortened iron dextran infusion time for the treatment of iron deficiency anemia.
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    May 2016
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    Successful management of mixed chimerism after bone marrow transplant in beta-thalassemia major.
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    PubMed    


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