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Ann Hematol
    May 2024
  1. BARDON-CANCHO EJ, Marco-Sanchez JM, Beneitez-Pastor D, Payan-Pernia S, et al
    Spanish registry of hemoglobinopathies and rare anemias (REHem-AR): demographics, complications, and management of patients with beta-thalassemia.
    Ann Hematol. 2024;103:1525-1539.
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  2. AL-KURAISHY HM, Mazhar Ashour MH, Saad HM, Batiha GE, et al
    COVID-19 and beta-thalassemia: in lieu of evidence and vague nexus.
    Ann Hematol. 2024;103:1423-1433.
    >> Share

    April 2024
  3. LOMMERSE IN, Hinnen C, van Vliet LM, Schubert B, et al
    Quality of life after immune suppressive therapy in aplastic anemia.
    Ann Hematol. 2024 Apr 5. doi: 10.1007/s00277-024-05731.
    >> Share

  4. DE CASTRO JNP, da Silva Costa SM, Camargo ACL, Ito MT, et al
    Comparative transcriptomic analysis of circulating endothelial cells in sickle cell stroke.
    Ann Hematol. 2024;103:1167-1179.
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  5. SHARMA A, Kumar A, Saha PK, Saha L, et al
    The role of TMPRSS6 gene polymorphism in iron resistance iron deficiency anaemia (IRIDA): a systematic review.
    Ann Hematol. 2024;103:1085-1102.
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  6. WANG J, Zhu H, Miao K
    Gilteritinib combined with venetoclax and azacitidine for relapsed acute myeloid leukemia cocurrent with pure red cell aplasia after allogeneic hematopoietic stem cell transplantation: a case report.
    Ann Hematol. 2024 Apr 1. doi: 10.1007/s00277-024-05714.
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    March 2024
  7. VALLEJO C, Rosell A, Xicoy B, Garcia C, et al
    A multicentre ambispective observational study into the incidence and clinical management of aplastic anaemia in Spain (IMAS study).
    Ann Hematol. 2024;103:705-713.
    >> Share

  8. LEONI S, Bou-Fakhredin R, Granata F, Cassinerio E, et al
    Acute liver injury after SARS-CoV-2 vaccination and luspatercept administration in a patient with beta-thalassemia.
    Ann Hematol. 2024;103:1025-1026.
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    February 2024
  9. SECK M, Manal B, Toure SA, Keita M, et al
    Challenges in the management of iron-deficiency anemia in Senegal, West Africa.
    Ann Hematol. 2024 Feb 3. doi: 10.1007/s00277-024-05626.
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  10. ZHA Q, Shi Y, Shi Z, Huang F, et al
    Loeys-Dietz syndrome with concomitant aplastic anemia.
    Ann Hematol. 2024 Feb 2. doi: 10.1007/s00277-024-05637.
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  11. SONGDEJ D, Surapolchai P, Komwilaisak P, Sripornsawan P, et al
    Molecular characteristics of hereditary red blood cell membrane disorders in Thailand: a multi-center registry.
    Ann Hematol. 2024;103:385-393.
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  12. GARCIA-MORIN M, Bardon-Cancho EJ, Belendez C, Dulin E, et al
    Madrid Newborn Sickle Cell Disease Cohort: clinical outcomes, stroke prevention and survival.
    Ann Hematol. 2024;103:373-383.
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  13. MURAKHOVSKAYA I, Crivera C, Leon A, Alemao E, et al
    Healthcare resource utilization of patients with warm autoimmune hemolytic anemia initiating first line therapy of oral corticosteroids with or without rituximab.
    Ann Hematol. 2024 Feb 1. doi: 10.1007/s00277-023-05613.
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    January 2024
  14. CHATTOPADHYAY S, Lionel S, Selvarajan S, Devasia AJ, et al
    Relapse and transformation to myelodysplastic syndrome and acute myeloid leukemia following immunosuppressive therapy for aplastic anemia is more common as compared to allogeneic stem cell transplantation with a negative impact on survival.
    Ann Hematol. 2024 Jan 20. doi: 10.1007/s00277-024-05621.
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  15. ZHANG Z, Wang X, Jiang J
    Screening results and mutation frequency analysis of G6PD deficiency in 1,291,274 newborns in Huizhou, China: a twenty-year experience.
    Ann Hematol. 2024;103:29-36.
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  16. ZULLO A, De Francesco V, Gatta L, Scaccianoce G, et al
    Small bowel lesions in patients with iron deficiency anaemia without overt bleeding: a multicentre study.
    Ann Hematol. 2024;103:1-4.
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  17. SCHREZENMEIER H, Kulasekararaj A, Mitchell L, de Latour RP, et al
    Predictors for improvement in patient-reported outcomes: post hoc analysis of a phase 3 randomized, open-label study of eculizumab and ravulizumab in complement inhibitor-naive patients with paroxysmal nocturnal hemoglobinuria.
    Ann Hematol. 2024;103:5-15.
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    December 2023
  18. DELGADINHO M, Veiga L, Ginete C, Santos B, et al
    Differential expression of adhesion molecules in sickle cell anemia and gut microbiome effect.
    Ann Hematol. 2023 Dec 28. doi: 10.1007/s00277-023-05589.
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  19. FU L, Zhang J, Wang R, Yang B, et al
    Clinical characteristics of hepatitis-associated aplastic anemia in children.
    Ann Hematol. 2023 Dec 12. doi: 10.1007/s00277-023-05566.
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  20. MCBRIDE HJ, Frazer-Abel A, Thiemann S, Lehto SG, et al
    Functional similarity of ABP 959 and eculizumab in simulated serum models of aHUS and NMOSD.
    Ann Hematol. 2023;102:3299-3309.
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    November 2023
  21. GONG Y, Zhang X, Chen X, Yang H, et al
    Warm autoimmune hemolytic anemia associated with SARS-CoV-2 infection responsive to eculizumab.
    Ann Hematol. 2023 Nov 27. doi: 10.1007/s00277-023-05549.
    >> Share

  22. STRASSER B, Heibl S, Hormann G, Haushofer A, et al
    Diamond-Blackfan anemia with very late and fatal onset aplasia in a 55-year-old patient with RPL11 mutation.
    Ann Hematol. 2023 Nov 23. doi: 10.1007/s00277-023-05553.
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  23. KITAMURA W, Kobayashi H, Iseki A, Wada H, et al
    Cold agglutinin-induced acrocyanosis without hemolytic anemia.
    Ann Hematol. 2023 Nov 9. doi: 10.1007/s00277-023-05538.
    >> Share

  24. POPE V, Hsia CC
    Safe utilization of ruxolitinib in simultaneous primary myelofibrosis and warm autoimmune hemolytic anemia.
    Ann Hematol. 2023 Nov 6. doi: 10.1007/s00277-023-05535.
    >> Share

  25. LOUZAO M, Vargas MT, Meseguer E, Pedrote Amador B, et al
    Successful use of thrombopoietin analogs in thrombocytopenia associated with MYH-9 mutation.
    Ann Hematol. 2023;102:3283-3284.
    >> Share

  26. SUN XH, Liu Q, Wu SN, Xu WH, et al
    Cytopenia: a report of haplo-cord transplantation in twin brothers caused by a novel germline GATA1 mutation and family survey.
    Ann Hematol. 2023;102:3177-3184.
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    October 2023
  27. SI T, Ma X, Zhu W, Zhou Y, et al
    Comment on: Association between anemia and depression: results from NHANES 2005-2018 and Mendelian randomization analyses.
    Ann Hematol. 2023 Oct 21. doi: 10.1007/s00277-023-05496.
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  28. KURITA N, Nishikii H, Maruyama Y, Suehara Y, et al
    Safety of romiplostim administered immediately after cord-blood transplantation: a phase 1 trial.
    Ann Hematol. 2023;102:2895-2902.
    >> Share

  29. DEENADAYALAN V, Litvin R, Vakil J, Kanemo P, et al
    Recent national trends in outcomes and economic disparities among adult sickle cell disease-related admissions.
    Ann Hematol. 2023;102:2659-2669.
    >> Share

  30. ROCCOTELLI D, Grande D, Cicco G, Palma A, et al
    Real-life experience with luspatercept in transfusion-dependent beta-thalassemia.
    Ann Hematol. 2023;102:2965-2967.
    >> Share

  31. CAN F, Yilmaz KN, Kosemehmetoglu OS, Akinci S, et al
    Comparison of different intravenous iron preparations in terms of total oxidant and total antioxidant status, single center data.
    Ann Hematol. 2023;102:2645-2650.
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    September 2023
  32. YOUSSEF MAM, Ghazaly MH, Abdelfattah MA
    Alternative treatment modality for severe aplastic anemia in a resource-limited setting: a single-institution prospective cohort study from Upper Egypt.
    Ann Hematol. 2023 Sep 13. doi: 10.1007/s00277-023-05440.
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  33. CHEN M, Ataga KI, Hankins JS, Zhang M, et al
    Age-related differences in risks and outcomes of 30-day readmission in adults with sickle cell disease.
    Ann Hematol. 2023;102:2329-2342.
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  34. SHOME DK, Das P, Akbar GA, Taha S, et al
    Molecular insights into hereditary elliptocytosis and pyropoikilocytosis: NGS uncovers multiple potential candidate genes.
    Ann Hematol. 2023;102:2343-2351.
    >> Share

  35. GREWAL US, Thotamgari SR, Gaddam SJ, Lakra R, et al
    Characteristics and outcomes associated with venous thrombotic complications among patients with paroxysmal nocturnal hemoglobinuria.
    Ann Hematol. 2023;102:2631-2632.
    >> Share

  36. HAYASHINO K, Fujiwara Y, Isokane Y, Tobita H, et al
    Paroxysmal nocturnal hemoglobinuria with ulcerative colitis.
    Ann Hematol. 2023;102:2625-2626.
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    August 2023
  37. SORIN B, Fadlallah J, Garzaro M, Vigneron J, et al
    Real-life use of mTOR inhibitor-based therapy in adults with autoimmune cytopenia highlights strong efficacy in relapsing/refractory multi-lineage autoimmune cytopenia.
    Ann Hematol. 2023;102:2059-2068.
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  38. VIPRAKASIT V, Hamdy MM, Hassab HMA, Sherief LM, et al
    Patient preference for deferasirox film-coated versus dispersible tablet formulation: a sequential-design phase 2 study in patients with thalassemia.
    Ann Hematol. 2023;102:2039-2049.
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  39. MUSALLAM KM, Ahmed W, Almarshoodi MO, Trad O, et al
    Establishment of the Abu Dhabi Emirate Thalassemia Longitudinal Cohort (AD-TLC): leveraging the power of observation.
    Ann Hematol. 2023;102:2277-2278.
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  40. SHIMAZU Y, Mizumoto C, Chonabayashi K, Hanyu Y, et al
    Successful treatment with cyclosporine of pure red cell aplasia induced by obinutuzumab bendamustine therapy.
    Ann Hematol. 2023;102:2291-2292.
    >> Share

    July 2023
  41. WANG Y, Guo D, Sui C, Qu Z, et al
    Association between anemia and depression: results from NHANES 2005-2018 and mendelian randomization analyses.
    Ann Hematol. 2023 Jul 22. doi: 10.1007/s00277-023-05374.
    >> Share

  42. HAMMAMI MB, Qasim A, Thakur R, Vegivinti CTR, et al
    Rasburicase-induced hemolytic anemia and methemoglobinemia: a systematic review of current reports.
    Ann Hematol. 2023 Jul 19. doi: 10.1007/s00277-023-05364.
    >> Share

  43. LIN F, Dong X, Zhang Y, Cheng Y, et al
    Time-dependent analysis of the impact on early cytomegalovirus reactivation of HLA mismatch and acute graft-versus-host disease after allogeneic hematopoietic cell transplantation from related donors in acquired aplastic anemia.
    Ann Hematol. 2023 Jul 13. doi: 10.1007/s00277-023-05332.
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  44. ZHAO J, Ma L, Zheng M, Su L, et al
    Meta-analysis of the results of haploidentical transplantation in the treatment of aplastic anemia.
    Ann Hematol. 2023 Jul 13. doi: 10.1007/s00277-023-05339.
    >> Share

  45. BODLA ZH, Hashmi M, Niaz F, Farooq U, et al
    Timing matters: An analysis of the relationship between red cell transfusion timing and hospitalization outcomes in sickle cell crisis patients using the National Inpatient Sample database.
    Ann Hematol. 2023;102:1669-1676.
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  46. DINGLI D, Maciejewski JP, Larratt L, Go RS, et al
    Relationship of paroxysmal nocturnal hemoglobinuria (PNH) granulocyte clone size to disease burden and risk of major vascular events in untreated patients: results from the International PNH Registry.
    Ann Hematol. 2023;102:1637-1644.
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  47. AU TY, Wisniewski OW, Benjamin S, Kubicki T, et al
    G6PD deficiency-does it alter the course of COVID-19 infections?
    Ann Hematol. 2023;102:1629-1636.
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    June 2023
  48. CANNAS G, Poutrel S, Heiblig M, Labussiere H, et al
    Sickle cell disease and acute leukemia: one case report and an extensive review.
    Ann Hematol. 2023 Jun 3:1-11. doi: 10.1007/s00277-023-05294.
    >> Share

    May 2023
  49. ARAUJO COSTA E, de Paula Ayres-Silva J
    Global profile of anemia during pregnancy versus country income overview: 19 years estimative (2000-2019).
    Ann Hematol. 2023 May 26. doi: 10.1007/s00277-023-05279.
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  50. WU LQ, Huang LF, Yang H, Ye BD, et al
    Comparison of haploidentical-allogeneic hematopoietic stem cell transplantation and intensive immunosuppressive therapy for patients with severe aplastic anemia with an absolute neutrophil count of zero: a retrospective study.
    Ann Hematol. 2023 May 17. doi: 10.1007/s00277-023-05256.
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  51. NIU H, Yan L, Yang L, Zhang M, et al
    High TOX expression on CD8(+) T cells in pure red cell aplasia.
    Ann Hematol. 2023;102:1247-1255.
    >> Share

  52. DONGERDIYE R, Bokde M, More TA, Saptarshi A, et al
    Targeted next-generation sequencing identifies eighteen novel mutations expanding the molecular and clinical spectrum of PKLR gene disorders in the Indian population.
    Ann Hematol. 2023;102:1029-1036.
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  53. BELISARIO AR, Simoes E Silva AC, Moura ICG, Carneiro-Proietti AB, et al
    Estimated glomerular filtration rate in Brazilian adults with sickle cell disease: results from the REDS-III multicenter cohort study.
    Ann Hematol. 2023;102:1019-1027.
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    April 2023
  54. ABDEL-SALAM A, Bassiouni ST, Goher AM, Shafie ES, et al
    Autoimmune Hemolytic Anemia in the Pediatric Age Group: The Egyptian Experience.
    Ann Hematol. 2023 Apr 24. doi: 10.1007/s00277-023-05230.
    >> Share

  55. TSILIKA M, Mitrou J, Antonakos N, Tseti IK, et al
    An active new formulation of iron carried by aspartyl casein for iron-deficiency anemia: results of the ACCESS trial.
    Ann Hematol. 2023 Apr 6. doi: 10.1007/s00277-023-05197.
    >> Share

  56. JONGKRAIJAKRA S, Doungngern T, Sripakdee W, Lekhakula A, et al
    A randomized controlled trial of thrice-weekly versus thrice-daily oral ferrous fumarate treatment in adult patients with iron-deficiency anemia.
    Ann Hematol. 2023 Apr 3:1-8. doi: 10.1007/s00277-023-05198.
    >> Share

  57. IGLESIAS-VAZQUEZ L, Gimeno M, Coronel P, Caspersen IH, et al
    Maternal factors associated with iron deficiency without anaemia in early pregnancy: ECLIPSES study.
    Ann Hematol. 2023;102:741-748.
    >> Share

  58. ZHANG Y, Pan J, Kang H, Peng S, et al
    Characteristics of inpatients with newly diagnosed multiple myeloma in hematology, nephrology, and orthopedic departments.
    Ann Hematol. 2023;102:801-809.
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    March 2023
  59. YANG K, Nie W, Huang Q, Liao G, et al
    Hematopoietic cell transplantation for congenital dyserythropoietic anemia IV caused by compound heterozygous KLF1 mutations.
    Ann Hematol. 2023 Mar 31. doi: 10.1007/s00277-023-05175.
    >> Share

  60. DING K, Liu Z, Ren Y, Liu H, et al
    Use of roxadustat (FG-4592) in ruxolitinib-treatment-related anemia of two myelofibrosis patients.
    Ann Hematol. 2023 Mar 13. doi: 10.1007/s00277-022-04997.
    >> Share

  61. AHMADI M, Beiranvand S, Poormansouri S, Matbouei M, et al
    Sense of coherence or self-efficacy as predictors of health-related quality of life in sickle cell disease patients.
    Ann Hematol. 2023;102:519-528.
    >> Share

    February 2023
  62. VERSTOVSEK S
    How I manage anemia related to myelofibrosis and its treatment regimens.
    Ann Hematol. 2023 Feb 14. doi: 10.1007/s00277-023-05126.
    >> Share

  63. WANG H, Liu H, Li L, Chen Y, et al
    Long noncoding RNA FAM157C contributes to clonal proliferation in paroxysmal nocturnal hemoglobinuria.
    Ann Hematol. 2023;102:299-309.
    >> Share

  64. FU X, Zhao X, Weng A, Zhang Q, et al
    Comparative efficacy and safety of restrictive versus liberal transfusion thresholds in anemic preterm infants: a meta-analysis of 12 randomized controlled trials.
    Ann Hematol. 2023;102:283-297.
    >> Share

  65. MELONI A, Pistoia L, Quota A, Messina G, et al
    Prognostic value of multiparametric cardiac magnetic resonance in sickle cell patients.
    Ann Hematol. 2023;102:261-270.
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    January 2023
  66. JIN Y, Li R, Lin S, Jia J, et al
    Correction to: A real‑world experience of eltrombopag plus rabbit antithymocyte immunoglobulin-based IST in Chinese patients with severe aplastic anemia.
    Ann Hematol. 2023 Jan 26. doi: 10.1007/s00277-023-05107.
    >> Share

  67. ZHANG L, Mao J, Lian Y, Liang Q, et al
    Mass cytometry analysis identifies T cell immune signature of aplastic anemia and predicts the response to cyclosporine.
    Ann Hematol. 2023 Jan 21:1-11. doi: 10.1007/s00277-023-05097.
    >> Share

  68. TANTAWY A, El-Sherif N, Makkeyah S, Eldeen NS, et al
    Sleep disordered breathing and its relation to stroke and pulmonary hypertension in children with sickle cell disease: a single-center cross-sectional study.
    Ann Hematol. 2023 Jan 16. doi: 10.1007/s00277-023-05099.
    >> Share

  69. SHEN Y, Liu Q, Li H, Liu W, et al
    Whole-exome sequencing identifies FANC heterozygous germline mutation as an adverse factor for immunosuppressive therapy in Chinese aplastic anemia patients aged 40 or younger: a single-center retrospective study.
    Ann Hematol. 2023 Jan 9. doi: 10.1007/s00277-023-05086.
    >> Share

  70. CURTIS S, Henny B, Joanna S, Betancourt J, et al
    Excess deaths among adults with sickle cell disease in 2020 compared to prior years.
    Ann Hematol. 2023;102:41-44.
    >> Share

    December 2022
  71. ZHANG JY, Li Y, Ma YS, Sun XJ, et al
    Clinical characteristics and prognostic factors in intracranial hemorrhage patients with hematological diseases.
    Ann Hematol. 2022;101:2617-2625.
    >> Share

    November 2022
  72. FUTAGI Y, Suga Y, Shimada T, Sai Y, et al
    Impact of antithymocyte globulin on blood cyclosporin A levels in aplastic anemia patients.
    Ann Hematol. 2022 Nov 26. doi: 10.1007/s00277-022-05063.
    >> Share

  73. MUSALLAM KM, Cappellini MD, Daar S, El-Beshlawy A, et al
    Magnitude of cumulative iron overload correlates with the severity of anemia in untreated non-transfusion-dependent beta-thalassemia.
    Ann Hematol. 2022 Nov 14. pii: 10.1007/s00277-022-05046.
    >> Share

  74. DELEHAYE F, Rouger J, Brossier D, Suttorp M, et al
    Prevalence of anemia at diagnosis of pediatric chronic myeloid leukemia and prognostic impact on the disease course.
    Ann Hematol. 2022 Nov 12. pii: 10.1007/s00277-022-05024.
    >> Share

  75. BANZIGER S, Weisshaar K, Arokoski R, Gerull S, et al
    Feasibility of electronic patient-reported outcome monitoring and self-management program in aplastic anemia and paroxysmal nocturnal hemoglobinuria-a pilot study (ePRO-AA-PNH).
    Ann Hematol. 2022 Nov 3. pii: 10.1007/s00277-022-05012.
    >> Share

  76. PIATTI G, Giuditta M, Consonni D, Cassinerio E, et al
    Cardiopulmonary testing in adult patients with beta-thalassemia major in comparison to healthy subjects.
    Ann Hematol. 2022;101:2445-2452.
    >> Share

  77. ZHANG R, Chen M, Yang C, Han B, et al
    Efficacy and steroid-sparing effect of tacrolimus in patients with autoimmune cytopenia.
    Ann Hematol. 2022;101:2421-2431.
    >> Share

  78. HAN B, Ji J, Zhang B, Bai H, et al
    The first successful expanded compassionate use of Iptacopan in a patient with paroxysmal nocturnal hemoglobinuria.
    Ann Hematol. 2022;101:2537-2539.
    >> Share

    October 2022
  79. FAN J, Lu R, Yu K, Zhang Y, et al
    Very severe aplastic anemia with papillary thyroid carcinoma: treatment with allo-HSCT-a case report and literature review.
    Ann Hematol. 2022 Oct 21. pii: 10.1007/s00277-022-05009.
    >> Share

  80. YANG W, Zhao X, He G, Chang H, et al
    Iron chelation of hetrombopag in aplastic anemia: a post hoc analysis of a phase II study.
    Ann Hematol. 2022 Oct 11. pii: 10.1007/s00277-022-04968.
    >> Share

  81. ROTH A, Barcellini W, Tvedt THA, Miyakawa Y, et al
    Sutimlimab improves quality of life in patients with cold agglutinin disease: results of patient-reported outcomes from the CARDINAL study.
    Ann Hematol. 2022;101:2169-2177.
    >> Share

  82. THEDSAWAD A, Wanachiwanawin W, Taka O, Hantaweepant C, et al
    Cut-off values for diagnosis of G6PD deficiency by flow cytometry in Thai population.
    Ann Hematol. 2022;101:2149-2157.
    >> Share

  83. LIU XD, Yang K, Xiao J, Huang H, et al
    Whole exome sequencing identifies a novel SPTB frameshift mutation causing hereditary spherocytosis in the Chinese population.
    Ann Hematol. 2022;101:2355-2357.
    >> Share

    September 2022
  84. HU J, Zhang L, Zhao X, Liu X, et al
    First-line immunosuppressive therapy with rATG and CsA for severe aplastic anemia: 15 years' experience.
    Ann Hematol. 2022 Sep 24. pii: 10.1007/s00277-022-04952.
    >> Share

  85. EL-AMIN N, Iness A, Cyrus JW, Sisler I, et al
    Anticoagulation strategies and recurrence of venous thromboembolic events in patients with sickle cell disease: a systematic review and meta-analysis.
    Ann Hematol. 2022;101:1931-1940.
    >> Share

  86. CELLA D, Sarda SP, Hsieh R, Fishman J, et al
    Changes in hemoglobin and clinical outcomes drive improvements in fatigue, quality of life, and physical function in patients with paroxysmal nocturnal hemoglobinuria: post hoc analyses from the phase III PEGASUS study.
    Ann Hematol. 2022;101:1905-1914.
    >> Share

  87. WONG RSM, Pullon HWH, Amine I, Bogdanovic A, et al
    Inhibition of C3 with pegcetacoplan results in normalization of hemolysis markers in paroxysmal nocturnal hemoglobinuria.
    Ann Hematol. 2022;101:1971-1986.
    >> Share

  88. PADRAO EMH, Bustos B, Mahesh A, Fonseca GHH, et al
    Phenotypes of sickle cell intensive care admissions: an unsupervised machine learning approach in a single-center retrospective cohort.
    Ann Hematol. 2022;101:1951-1957.
    >> Share

  89. MELONI A, Barbuto L, Pistoia L, Positano V, et al
    Frequency, pattern, and associations of renal iron accumulation in sickle/beta-thalassemia patients.
    Ann Hematol. 2022;101:1941-1950.
    >> Share

    August 2022
  90. JIN Y, Li R, Lin S, Jia J, et al
    A real-word experience of eltrombopag plus rabbit antithymocyte immunoglobulin-based IST in Chinese patients with severe aplastic anemia.
    Ann Hematol. 2022 Aug 27. pii: 10.1007/s00277-022-04966.
    >> Share

  91. BEYAR-KATZ O, Perry C, On YB, Amit O, et al
    Thrombopoietin receptor agonist for treating bone marrow aplasia following anti-CD19 CAR-T cells-single-center experience.
    Ann Hematol. 2022;101:1769-1776.
    >> Share

  92. ZHOU F, Zhang F, Zhang L, Wu Q, et al
    A multicentre trial of intensive immunosuppressive therapy combined with umbilical cord blood for the treatment of severe aplastic anaemia.
    Ann Hematol. 2022;101:1785-1794.
    >> Share

  93. PIRIYAKHUNTORN P, Tantiworawit A, Kasitanon N, Louthrenoo W, et al
    Prevalence and characteristics of inflammatory rheumatic diseases in patients with thalassemia.
    Ann Hematol. 2022;101:1667-1675.
    >> Share

  94. JAFRI F, Seong G, Jang T, Cimpeanu E, et al
    L-glutamine for sickle cell disease: more than reducing redox.
    Ann Hematol. 2022;101:1645-1654.
    >> Share

  95. LOBITZ S, Frommel C, Brose A, Blankenstein O, et al
    Simultaneous newborn screening for sickle cell disease, biotinidase deficiency, and hereditary tyrosinemia type 1 with an optimized tandem mass spectrometry protocol.
    Ann Hematol. 2022;101:1859-1860.
    >> Share

    July 2022
  96. AL-KURAISHY HM, Al-Gareeb AI, Kaushik A, Kujawska M, et al
    Hemolytic anemia in COVID-19.
    Ann Hematol. 2022 Jul 8. pii: 10.1007/s00277-022-04907.
    >> Share

  97. HAN B, Kim HJ, Yhim HY, Oh D, et al
    Sequential eradication of Helicobacter pylori as a treatment for immune thrombocytopenia in patients with moderate thrombocytopenia: a multicenter prospective randomized phase 3 study.
    Ann Hematol. 2022;101:1435-1445.
    >> Share

  98. JUNG EH, Park JH, Hwan Kim K, Kim JS, et al
    Characteristics of Sweet syndrome in patients with or without malignancy.
    Ann Hematol. 2022;101:1499-1508.
    >> Share

  99. ROPERO P, Gonzalez Fernandez FA, Nieto JM, Recasens V, et al
    Does size matter? Two new deletions in the HBB gene cause beta(0)-thalassemia.
    Ann Hematol. 2022;101:1465-1471.
    >> Share

  100. WU X, Cheng L, Liu X, Sun Y, et al
    Clinical characteristics and outcomes of 100 adult patients with pure red cell aplasia.
    Ann Hematol. 2022;101:1493-1498.
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  101. PATSOURAKOS D, Aggeli C, Gatzoulis KA, Delicou S, et al
    Left atrial deformation indices in beta-thalassemia major patients.
    Ann Hematol. 2022;101:1473-1483.
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  102. ADAM AS, Cotton F, Cantinieaux B, Benyaich S, et al
    Screening for hereditary spherocytosis in daily practice: what is the best algorithm using erythrocyte and reticulocyte parameters?
    Ann Hematol. 2022;101:1485-1491.
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  103. COSTANTINI S, Meloni A, Spasiano A, Cinque P, et al
    The unexpected impact of cabozantinib on red blood cells consumption in patients with transfusion-dependent thalassemia.
    Ann Hematol. 2022;101:1621-1623.
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    June 2022
  104. MA X, Zuo Y, Xu Z, Zhang Y, et al
    Comparable clinical outcomes of haploidentical hematopoietic stem cell transplantation in patients with hepatitis-associated aplastic anemia and non-hepatitis-associated aplastic anemia.
    Ann Hematol. 2022 Jun 23. pii: 10.1007/s00277-022-04885.
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  105. HWANG YY, Chan TSY, Chan FHY, Lau CWP, et al
    Eltrombopag as frontline treatment of aplastic anaemia in routine practice: implications on cost and efficacy.
    Ann Hematol. 2022;101:1163-1172.
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  106. ZHOU X, Jiang P, Gao L, Yang J, et al
    Immune reconstitution and survival of patients with parvovirus B19 related pure red cell aplasia after haplo-PBSCT.
    Ann Hematol. 2022;101:1333-1342.
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  107. ESCRIBANO SERRAT S, Del Campo Balguerias G, Martinez Nieto J, Medina Salazar F, et al
    Pincered red cells in hereditary spherocytosis.
    Ann Hematol. 2022;101:1393-1394.
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    May 2022
  108. PIRES DA SILVA BGP, Fonseca NP, Catto LFB, Pereira GC, et al
    The spectrum of paroxysmal nocturnal hemoglobinuria clinical presentation in a Brazilian single referral center.
    Ann Hematol. 2022;101:999-1007.
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  109. POPLAWSKA M, Dutta D, Jayaram M, Chong NS, et al
    Genes modulating intestinal permeability and microbial community are dysregulated in sickle cell disease.
    Ann Hematol. 2022;101:1009-1013.
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    April 2022
  110. KAYNAR LA, Gokcen S, Can F, Yegin ZA, et al
    Comparison of daily oral iron replacement therapy with every other day treatment in female reproductive age patients with iron-deficiency anemia.
    Ann Hematol. 2022 Apr 23. pii: 10.1007/s00277-022-04835.
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  111. WERNER R, Lohr B, Lodemann P, Chemnitz JM, et al
    Autoimmune basal ganglia encephalitis with hemolytic anemia.
    Ann Hematol. 2022 Apr 21. pii: 10.1007/s00277-022-04848.
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  112. PROCHASKA MT, Huisingh-Scheetz M, Meltzer D
    Sex differences in fatigue and symptoms of anemia in relation to hemoglobin level in hospitalized patients.
    Ann Hematol. 2022 Apr 11. pii: 10.1007/s00277-022-04830.
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  113. LI S, Guo P, Mi L, Chai X, et al
    A novel SPTB mutation causes hereditary spherocytosis via loss-of-function of beta-spectrin.
    Ann Hematol. 2022;101:731-738.
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    March 2022
  114. BAHATI YL, Delanghe J, Balaluka GB, Philippe J, et al
    Exploration of the relationship between anemia and iron and zinc deficiencies in children under 5 years of age living in the malaria endemic area of South Kivu/Democratic Republic of Congo.
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  115. TOLU SS, Crouch A, Choi J, Gao Q, et al
    Hydroxyurea and fetal hemoglobin effect on leg ulcers in patients with sickle cell disease.
    Ann Hematol. 2022;101:541-548.
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  116. LUFTINGER R, Zubarovskaya N, Galimard JE, Cseh A, et al
    Busulfan-fludarabine- or treosulfan-fludarabine-based myeloablative conditioning for children with thalassemia major.
    Ann Hematol. 2022;101:655-665.
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  117. BAYRAKTAROGLU S, Karadas N, Onen S, Karapinar DY, et al
    Modern management of iron overload in thalassemia major patients guided by MRI techniques: real-world data from a long-term cohort study.
    Ann Hematol. 2022;101:521-529.
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  118. SOULIERES D, Mercier-Ross J, Fradette C, Rozova A, et al
    The pharmacokinetic and safety profile of single-dose deferiprone in subjects with sickle cell disease.
    Ann Hematol. 2022;101:533-539.
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  119. LI S, Chen K, Huang C, Zhang N, et al
    First report of successful treatment for hemoglobin Bristol-Alesha by hemopoietic stem cell transplantation.
    Ann Hematol. 2022;101:617-619.
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  120. ROSETTI M, De la Salle B, Farneti G, Clementoni A, et al
    The added value of digital morphological analysis in the evaluation of peripheral blood films: the report of an UKNEQAS external quality assessment sample.
    Ann Hematol. 2022;101:729-730.
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  121. FARFAN-QUIROGA G, Hermosilla-Fernandez MDM, Feliu-Sanchez J, Najera-Irazu MJ, et al
    A new case of Bicetre hemoglobin in an adult male: clinical observations over a period of four years.
    Ann Hematol. 2022;101:701-702.
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    February 2022
  122. VIROT E, Thuret I, Jardel S, Herbrecht R, et al
    Pregnancy outcome in women with transfused beta-thalassemia in France.
    Ann Hematol. 2022;101:289-296.
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  123. MARTINS SR, Toledo SLO, da Silva AJ, Mendes FS, et al
    Endothelial dysfunction biomarkers in sickle cell disease: is there a role for ADMA and PAI-1?
    Ann Hematol. 2022;101:273-280.
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  124. DINGLI D, Matos JE, Lehrhaupt K, Krishnan S, et al
    The burden of illness in patients with paroxysmal nocturnal hemoglobinuria receiving treatment with the C5-inhibitors eculizumab or ravulizumab: results from a US patient survey.
    Ann Hematol. 2022;101:251-263.
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  125. HOSOKAWA K, Nakao S
    Assay sensitivity of flow cytometric PNH analysis: response to Brando and Gatti.
    Ann Hematol. 2022;101:461-464.
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  126. BRANDO B, Gatti A
    Re: Hosokawa K et al. Assay sensitivity of flow cytometric PNH analysis.
    Ann Hematol. 2022;101:459-460.
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  127. DAS S, Karmakar K, Mukherjee R, Panda S, et al
    Acute stroke in young adult secondary to moyamoya angiopathy unveiling HbE-beta thalassemia.
    Ann Hematol. 2022;101:449-451.
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    January 2022
  128. SUN YX, Feng Q, Wang SW, Li X, et al
    HLA-G-ILT2 interaction contributes to suppression of bone marrow B cell proliferation in acquired aplastic anemia.
    Ann Hematol. 2022 Jan 18. pii: 10.1007/s00277-022-04757.
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  129. GHANEM P, Marrone K, Shanbhag S, Brahmer JR, et al
    Current challenges of hematologic complications due to immune checkpoint blockade: a comprehensive review.
    Ann Hematol. 2022;101:1-10.
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  130. YILDIRIM N, Unal S, Yalcinkaya A, Karahan F, et al
    Evaluation of the relationship between intravascular hemolysis and clinical manifestations in sickle cell disease: decreased hemopexin during vaso-occlusive crises and increased inflammation in acute chest syndrome.
    Ann Hematol. 2022;101:35-41.
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  131. SOKOL J, Guman T, Chudej J, Hlebaskova M, et al
    Ixazomib, lenalidomide, and dexamethasone combination in "real-world" clinical practice in patients with relapsed/refractory multiple myeloma.
    Ann Hematol. 2022;101:81-89.
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  132. ABULHAMAIL A, AlShebli A, Merdad L, Wali S, et al
    Prevalence of and risk factors for obstructive sleep apnea in children with sickle cell: a multicentric cross sectional study.
    Ann Hematol. 2022;101:43-57.
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  133. TARTAGLIONE I, Manara R, di Concilio R, Quarta A, et al
    Non-transfusion-dependent thalassemia in Italy: less blues, no role of reds.
    Ann Hematol. 2022;101:241-242.
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  134. MUSALLAM KM, Cappellini MD, Daar S, Taher AT, et al
    Morbidity-free survival and hemoglobin level in non-transfusion-dependent beta-thalassemia: a 10-year cohort study.
    Ann Hematol. 2022;101:203-204.
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  135. ACQUAVIVA G, Nonne G, Murtas A, Longu F, et al
    Cytomegalovirus reactivation in patients under immunosuppressive treatment for autoimmune haemolytic anaemia.
    Ann Hematol. 2022;101:227-228.
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  136. DEBUREAUX PE, Ruggiu M, Mathis S, Mirouse A, et al
    Aggressive lymphoma, hemophagocytic lymphohistiocytosis, and G6PD crisis: a lytic cocktail.
    Ann Hematol. 2022;101:219-221.
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    December 2021
  137. EL-KHAZRAGY N, Matbouly S, Hanna DH, Mahran NA, et al
    Circulating miRNAs and tissue iron overload in transfusion-dependent beta-thalassemia major: novel predictors and follow-up guide.
    Ann Hematol. 2021;100:2909-2917.
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  138. KARIMI M, Zarei T, Bahmanimehr A, Aramesh A, et al
    Long-term safety and efficacy of hydroxyurea in patients with non-transfusion-dependent beta-thalassemia: a comprehensive single-center experience.
    Ann Hematol. 2021;100:2901-2907.
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    November 2021
  139. VIVES-CORRONS JL, Krishnevskaya E, Hernandez-Rodriguez I, Payan-Pernia S, et al
    Red cell ektacytometry in two patients with chronic hemolytic anemia and three new alpha-spectrin variants.
    Ann Hematol. 2021 Nov 29. pii: 10.1007/s00277-021-04723.
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  140. JIANG Z, Jiang X, Chen M
    Severe aplastic anemia in a patient with erythropoietic protoporphyria successfully treated by avatrombopag.
    Ann Hematol. 2021 Nov 26. pii: 10.1007/s00277-021-04726.
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  141. MATSUYAMA Y, Hosoi H, Horitani R, Kawamoto S, et al
    Management of warm autoimmune hemolytic anemia related to band 3-positive colon carcinoma.
    Ann Hematol. 2021 Nov 5. pii: 10.1007/s00277-021-04714.
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  142. DUCA L, Nava I, Tavazzi D, Marcon A, et al
    Epidemiological shift of glucose-6-phosphate dehydrogenase mutations in northern Italy in the last 15 years.
    Ann Hematol. 2021;100:2683-2688.
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  143. KULAGIN AD, Ptushkin VV, Lukina EA, Davydkin IL, et al
    Randomized multicenter noninferiority phase III clinical trial of the first biosimilar of eculizumab.
    Ann Hematol. 2021;100:2689-2698.
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  144. TEAWTRAKUL N, Chansai S, Yamsri S, Ungarreevittaya P, et al
    JAK2V617F mutation in patients with beta-thalassemia disease: prevalence and clinical characteristics.
    Ann Hematol. 2021;100:2863-2865.
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    October 2021
  145. EL FAKIH R, Alfraih F, Alhayli S, Ahmed SO, et al
    Frontline-matched sibling donor transplant of aplastic anemia patients using primed versus steady-state bone marrow grafts.
    Ann Hematol. 2021 Oct 31. pii: 10.1007/s00277-021-04708.
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  146. BIASSI TP, Guerra-Shinohara EM, Moretti PNS, de Freitas Dutra V, et al
    miRNA profile and disease severity in patients with sickle cell anemia.
    Ann Hematol. 2021 Oct 22. pii: 10.1007/s00277-021-04665.
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  147. PEREIRA-MARTINS DA, Coelho-Silva JL, Domingos IF, Weinhauser I, et al
    The ratio of ATP11C/PLSCR1 mRNA transcripts has clinical significance in sickle cell anemia.
    Ann Hematol. 2021 Oct 14. pii: 10.1007/s00277-021-04696.
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  148. SHOKRGOZAR N, Karimi M, Golmoghaddam H, Rezaei N, et al
    Expression of the immune checkpoint receptors CTLA-4, LAG-3, and TIM-3 in beta-thalassemia major patients: correlation with alloantibody production and regulatory T cells (Tregs) phenotype.
    Ann Hematol. 2021;100:2463-2469.
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  149. ABDULHAI F, Jaffa MA, Elias J, Zakka P, et al
    Digital thermography and vascular involvement in beta-thalassemia intermedia.
    Ann Hematol. 2021;100:2471-2477.
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    September 2021
  150. HIRAMOTO N, Yamazaki H, Nakamura Y, Uchida N, et al
    Total body irradiation-containing conditioning regimens without antithymocyte globulin in adults with aplastic anemia undergoing umbilical cord blood transplantation.
    Ann Hematol. 2021 Sep 21. pii: 10.1007/s00277-021-04664.
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  151. THONG EWS, Tan SS, Sethi SK, Chee YL, et al
    Falsely elevated serum vitamin B12 levels in a case of pernicious anemia.
    Ann Hematol. 2021 Sep 10. pii: 10.1007/s00277-021-04612.
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  152. WOUTERS HJCM, Conrads-Frank A, Koinig KA, Smith A, et al
    The anemia-independent impact of myelodysplastic syndromes on health-related quality of life.
    Ann Hematol. 2021 Sep 2. pii: 10.1007/s00277-021-04654.
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  153. JANG T, Mo G, Stewart C, Khoury L, et al
    Obesity and diabetes mellitus in patients with sickle cell disease.
    Ann Hematol. 2021;100:2203-2205.
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  154. BOGA C, Asma S, Leblebisatan G, Sen N, et al
    Comparison of the clinical course of COVID-19 infection in sickle cell disease patients with healthcare professionals.
    Ann Hematol. 2021;100:2195-2202.
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    August 2021
  155. CHENOU F, Hounkpe BW, Domingos IF, Tonasse WV, et al
    Effect of hydroxyurea therapy on intravascular hemolysis and endothelial dysfunction markers in sickle cell anemia patients.
    Ann Hematol. 2021 Aug 28. pii: 10.1007/s00277-021-04636.
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  156. YAMADA S, Kajikawa S, Nakagawa N, Kondo Y, et al
    Coombs' test positive autoimmune hemolytic anemia accompanied by myelodysplastic syndrome that became Coombs' test negative after azacitidine administration.
    Ann Hematol. 2021 Aug 27. pii: 10.1007/s00277-021-04652.
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  157. ATIPIMONPAT A, Siwaponanan P, Khuhapinant A, Svasti S, et al
    Extracellular vesicles from thalassemia patients carry iron-containing ferritin and hemichrome that promote cardiac cell proliferation.
    Ann Hematol. 2021;100:1929-1946.
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  158. TRANEKAER S, Hansen DL, Biemond BJ, Sorensen AL, et al
    Priapism in patients with hemolytic disorders: a nationwide retrospective cohort study.
    Ann Hematol. 2021;100:1947-1951.
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  159. SINGHA K, Fucharoen G, Fucharoen S
    delta-Hemoglobinopathies in Thailand: screening, molecular basis, genotype-phenotype interaction, and implication for prevention and control of thalassemia.
    Ann Hematol. 2021;100:1953-1963.
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  160. HOSOKAWA K, Ishiyama K, Ikemoto T, Sugimori C, et al
    The clinical significance of PNH-phenotype cells accounting for < 0.01% of total granulocytes detected by the Clinical and Laboratory Standards Institute methods in patients with bone marrow failure.
    Ann Hematol. 2021;100:1975-1982.
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  161. OKAMOTO H, Uoshima N, Kamitsuji Y, Kawata E, et al
    Paroxysmal nocturnal hemoglobinuria complicated with essential thrombocythemia harboring concomitant PIGA, CALR, and ASXL1 mutations.
    Ann Hematol. 2021;100:2113-2115.
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  162. ROBIER C, Hoefler G, Aubell K, Hubmann E, et al
    Acquired elliptocytosis as presenting sign of a myelodysplastic syndrome associated with deletion of chromosome 20 and mutations in TET2, DNMT3A, and U2AF1.
    Ann Hematol. 2021;100:2111-2112.
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  163. JAMWAL M, Mallik N, Aravindan AV, Jain A, et al
    Hemolytic erythrocytosis: an amalgamated phenotype from coinherited Chuvash polycythemia and G6PD Kerala-Kalyan with acquired transient stomatocytosis.
    Ann Hematol. 2021;100:2107-2109.
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    July 2021
  164. NORASETTHADA L, Wongkhantee S, Chaipokam J, Charoenprasert K, et al
    Adult aplastic anemia in Thailand: incidence and treatment outcome from a prospective nationwide population-based study.
    Ann Hematol. 2021 Jul 16. pii: 10.1007/s00277-021-04566.
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  165. YANG W, Zhao X, Peng G, Zhang L, et al
    Time and residual hematopoiesis are crucial for PNH clones escape in hepatitis-associated aplastic anemia.
    Ann Hematol. 2021 Jul 16. pii: 10.1007/s00277-021-04553.
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  166. CAO J, Pei R, Zhang P, Liu X, et al
    Successful haploidentical transplantation using plasma exchange and post-transplantation cyclophosphamide for severe aplastic anemia patients with anti-human leukocyte antigen donor-specific antibodies.
    Ann Hematol. 2021 Jul 6. pii: 10.1007/s00277-021-04497.
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  167. GOREN SAHIN D, Akay OM, Keklik M, Okan V, et al
    Clinical characteristics and therapeutic outcomes of paroxysmal nocturnal hemoglobinuria patients in Turkey: a multicenter experience.
    Ann Hematol. 2021;100:1667-1675.
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  168. ELZAEEM DI, Sharkawi EAE, Zaki EM, Ghobrial AG, et al
    Comparative study of IgG binding to megakaryocytes in immune and myelodysplastic thrombocytopenic patients.
    Ann Hematol. 2021;100:1701-1709.
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  169. NJUE L, Medri C, Keller P, Diepold M, et al
    The rare hemoglobin variant Hb Mizuho: report of a Swiss family and literature review.
    Ann Hematol. 2021;100:1677-1683.
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  170. RICCHI P, Costantini S, Spasiano A, Cinque P, et al
    Hepatocellular carcinoma in patients with thalassemia in the post-DAA era: not a disappearing entity.
    Ann Hematol. 2021;100:1907-1910.
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  171. MUSALLAM KM, Cappellini MD, Taher AT
    Variations in hemoglobin level and morbidity burden in non-transfusion-dependent beta-thalassemia.
    Ann Hematol. 2021;100:1903-1905.
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  172. TRAN QUANG V, Tarfi S, Loustau V, Moutereau S, et al
    A belated diagnosis of G6PD deficiency in an 81-year-old woman.
    Ann Hematol. 2021;100:1901-1902.
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    June 2021
  173. BATISTA JVGF, Pereira-Martins DA, Falcao DA, Domingos IF, et al
    Association of KLOTHO polymorphisms with clinical complications of sickle cell anemia.
    Ann Hematol. 2021 Jun 14. pii: 10.1007/s00277-021-04532.
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  174. KRECAK I, Cengic M, Skoric I, Nakic M, et al
    Concomitant autoimmune hemolytic anemia and pure red cell aplasia in a patient with chronic lymphocytic leukemia successfully treated with ibrutinib.
    Ann Hematol. 2021 Jun 10. pii: 10.1007/s00277-021-04570.
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  175. AL-TAWFIQ JA, Rabaan AA, AlEdreesi MH
    Frequency of bacteremia in patients with sickle cell disease: a longitudinal study.
    Ann Hematol. 2021;100:1411-1416.
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  176. ARPACI A, Gul BU, Ozcan O, Ilhan G, et al
    Presentation of two new mutations in the 3'untranslated region of the beta-globin gene and evaluating the molecular spectrum of thalassemia mutations in the Mediterranean region of Turkey.
    Ann Hematol. 2021;100:1429-1438.
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  177. BHURANI D, Kapoor J, Yadav N, Khushoo V, et al
    Experience with combination of hydroxyurea and low-dose thalidomide in transfusion-dependent beta thalassemia patients.
    Ann Hematol. 2021;100:1417-1427.
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  178. MAROUF R, Adekile AD, El-Muzaini H, Abdulla R, et al
    Neutrophil gelatinase-associated lipocalin as a biomarker of nephropathy in sickle cell disease.
    Ann Hematol. 2021;100:1401-1409.
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  179. TAMAI Y, Ito S, Hasegawa A
    Paroxysmal nocturnal haemoglobinuria associated with a novel phosphatidylinositol glycan class A (PIGA) mutation in a patient with Klinefelter syndrome.
    Ann Hematol. 2021;100:1625-1627.
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    May 2021
  180. HERBRETEAU L, Le Calloch R, Arnaud B, Cassou N, et al
    Eculizumab, a real-life successful treatment for refractory cold agglutinin-mediated auto-immune hemolytic anemia secondary to lymphoproliferative disorders.
    Ann Hematol. 2021 May 18. pii: 10.1007/s00277-021-04557.
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  181. QIN X, Zhu YP, Luo CJ, Zhou M, et al
    Optimizing conditioning regimen with low-dose irradiation or busulfan enables the outcome of transplantation from a 6-7/8 HLA-matched donor comparable to that from an 8/8 HLA-matched unrelated donor in severe aplastic anemia patients under 40 years.
    Ann Hematol. 2021 May 14. pii: 10.1007/s00277-021-04540.
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  182. BALLAS SK
    Opioids are not a major cause of death of patients with sickle cell disease.
    Ann Hematol. 2021;100:1133-1138.
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    April 2021
  183. MENDOZA E, Duque X, Moran S, Martinez-Andrade G, et al
    Hepcidin and other indicators of iron status, by alpha-1 acid glycoprotein levels, in a cohort of Mexican infants.
    Ann Hematol. 2021;100:879-890.
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  184. RAMSAY Z, Gabbadon CH, Asnani M
    Numb chin syndrome in sickle cell disease: a case series of Jamaican patients.
    Ann Hematol. 2021;100:913-919.
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  185. HATAIRAKTHAM S, Masaratana P, Hantaweepant C, Srisawat C, et al
    Curcuminoids supplementation ameliorates iron overload, oxidative stress, hypercoagulability, and inflammation in non-transfusion-dependent beta-thalassemia/Hb E patients.
    Ann Hematol. 2021;100:891-901.
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    March 2021
  186. YOUSSEF JG, Zahiruddin F, Youssef G, Padmanabhan S, et al
    G6PD deficiency and severity of COVID19 pneumonia and acute respiratory distress syndrome: tip of the iceberg?
    Ann Hematol. 2021;100:667-673.
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  187. SAEIDNIA M, Nowrouzi-Sohrabi P, Erfani M, Fazeli P, et al
    The effect of curcumin on serum copper, zinc, and zinc/copper ratio in patients with beta-thalassemia intermedia: a randomized double-blind clinical trial.
    Ann Hematol. 2021;100:627-633.
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  188. VERMA HK, Ratre YK, Bhaskar LVKS, Colombatti R, et al
    Erythrocyte microRNAs: a tiny magic bullet with great potential for sickle cell disease therapy.
    Ann Hematol. 2021;100:607-614.
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  189. HAGHPANAH S, Cohan N, Bordbar M, Bazrafshan A, et al
    Effects of three months of treatment with vitamin E and N-acetyl cysteine on the oxidative balance in patients with transfusion-dependent beta-thalassemia.
    Ann Hematol. 2021;100:635-644.
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  190. SCHULLER H, Klein F, Lubbert M, Prager EP, et al
    Hemolytic crisis in a patient treated with eculizumab for paroxysmal nocturnal hemoglobinuria possibly triggered by SARS-CoV-2 (COVID-19): a case report.
    Ann Hematol. 2021;100:841-842.
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  191. MISTRY RH, Kohut A, Ford P
    Correction of iron deficiency in hospitalized heart failure patients does not improve patient outcomes.
    Ann Hematol. 2021;100:661-666.
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    February 2021
  192. HSIEH TC, Sostin O
    Severe warm autoimmune hemolytic anemia in COVID-19 managed with least incompatible RBC product and glucocorticoids.
    Ann Hematol. 2021 Feb 18. pii: 10.1007/s00277-021-04457.
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  193. HATZLHOFER BLD, Pereira-Martins DA, de Farias Domingos I, Arcanjo GDS, et al
    Alpha thalassemia, but not beta(S)-globin haplotypes, influence sickle cell anemia clinical outcome in a large, single-center Brazilian cohort.
    Ann Hematol. 2021 Feb 13. pii: 10.1007/s00277-021-04450.
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  194. LADEIRA VS, Barbosa AR, Oliveira MM, Ferreira LGR, et al
    ADAMTS-13-VWF axis in sickle cell disease patients.
    Ann Hematol. 2021;100:375-382.
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  195. KUMAR R, Yadav R, Mishra S, Singh MPSS, et al
    Kruppel-like factor 1 (KLF1) gene single nucleotide polymorphisms in sickle cell disease and its association with disease-related morbidities.
    Ann Hematol. 2021;100:365-373.
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  196. BATISTA JVGF, Arcanjo GS, Batista THC, Sobreira MJ, et al
    Influence of UGT1A1 promoter polymorphism, alpha-thalassemia and beta(s) haplotype in bilirubin levels and cholelithiasis in a large sickle cell anemia cohort.
    Ann Hematol. 2021 Feb 1. pii: 10.1007/s00277-021-04422.
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    January 2021
  197. MARTYNOVA A, Chiu V, Mert M, Hermel D, et al
    Effectiveness and safety of tacrolimus with or without eltrombopag, as a part of immunosuppressive treatment of aplastic anemia in adults: a retrospective case series.
    Ann Hematol. 2021 Jan 9. pii: 10.1007/s00277-021-04401.
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  198. STACY S, Sheth S, Coleman B, Cerenzia W, et al
    An assessment of the continuing medical education needs of US physicians in the management of patients with beta thalassemia.
    Ann Hematol. 2021;100:27-35.
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    December 2020
  199. GIORDANO G, Napolitano M, Di Battista V, Lucchesi A, et al
    Oral high-dose sucrosomial iron vs intravenous iron in sideropenic anemia patients intolerant/refractory to iron sulfate: a multicentric randomized study.
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  200. WU Y, Yao Q, Zhong M, Wu J, et al
    Genetic research and clinical analysis of deletional Chinese (G)gamma(+)((A)gammadeltabeta)(0) -thalassemia and Southeast Asian HPFH in South China.
    Ann Hematol. 2020;99:2747-2753.
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  201. SINHA S, Jit BP, Patro ARK, Ray A, et al
    Influence of rs1042713 and rs1042714 polymorphisms of beta2-adrenergic receptor gene with erythrocyte cAMP in sickle cell disease patients from Odisha State, India.
    Ann Hematol. 2020;99:2737-2745.
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  202. PAZGAL I, Yahalom V, Shalev B, Raanani P, et al
    Alloimmunization and autoimmunization in adult transfusion-dependent thalassemia patients: a report from a comprehensive center in Israel.
    Ann Hematol. 2020;99:2731-2736.
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    November 2020
  203. MENDEZ M, Moreno-Carralero MI, Peri VL, Camacho-Galan R, et al
    Congenital dyserythropoietic anemia types Ib, II, and III: novel variants in the CDIN1 gene and functional study of a novel variant in the KIF23 gene.
    Ann Hematol. 2020 Nov 7. pii: 10.1007/s00277-020-04319.
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  204. RUAN J, Zuo W, Chen M, Yang C, et al
    Correction to: Eltrombopag is effective in patients with relapse/refractory aplastic anemia-report from a single center in China.
    Ann Hematol. 2020 Nov 2. pii: 10.1007/s00277-020-04301.
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  205. ABDULLAH N, Ismail N, Abd Jalal N, Mohd Radin F, et al
    Prevalence of anaemia and associated risk factors amongst The Malaysian Cohort participants.
    Ann Hematol. 2020;99:2521-2527.
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  206. DESAI RJ, Mahesri M, Globe D, Mutebi A, et al
    Clinical outcomes and healthcare utilization in patients with sickle cell disease: a nationwide cohort study of Medicaid beneficiaries.
    Ann Hematol. 2020;99:2497-2505.
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  207. BALLAS SK, Dampier C
    Risk factors associated with increased emergency department utilization in patients with sickle cell disease: a systematic literature review.
    Ann Hematol. 2020;99:2483-2495.
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  208. KIRITO K
    Expansion of paroxysmal nocturnal hemoglobinuria clones in MPLW515L mutation harboring primary myelofibrosis.
    Ann Hematol. 2020;99:2707-2709.
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  209. TRIPATHI P, Agarwal S, Gupta A, Mandal K, et al
    Biallelic rare 17 bp deletion mutation (HBB:c.380_396 del TGCAGGCTGCCTATCAG) in a transfusion depended form of thalassemia.
    Ann Hematol. 2020;99:2719-2722.
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    October 2020
  210. WAN K, Yin Y, Luo Z, Cheng J, et al
    Correction to: Remarkable response to roxadustat in a case of anti-erythropoietin antibody-mediated pure red cell aplasia.
    Ann Hematol. 2020 Oct 16. pii: 10.1007/s00277-020-04300.
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  211. ONISHI Y, Mori T, Yamazaki H, Takenaka K, et al
    Cyclosporine/methotrexate versus tacrolimus/methotrexate with or without anti-thymocyte globulin as GVHD prophylaxis in adult patients with aplastic anemia.
    Ann Hematol. 2020 Oct 9. pii: 10.1007/s00277-020-04290.
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  212. LAN Y, Chang L, Yi M, Cai Y, et al
    Long-term outcomes of 172 children with severe aplastic anemia treated with rabbit antithymocyte globulin and cyclosporine.
    Ann Hematol. 2020 Oct 8. pii: 10.1007/s00277-020-04296.
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  213. ONISHI Y, Yokoyama H, Katsuoka Y, Ito T, et al
    Low-dose lenalidomide and dexamethasone therapy after melphalan-prednisolone induction in elderly patients with newly diagnosed multiple myeloma.
    Ann Hematol. 2020;99:2351-2356.
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  214. FUREDER W, Sperr WR, Heibl S, Zebisch A, et al
    Prognostic factors and follow-up parameters in patients with paroxysmal nocturnal hemoglobinuria (PNH): experience of the Austrian PNH network.
    Ann Hematol. 2020;99:2303-2313.
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  215. BUTTARI B, Profumo E, Caprari P, Massimi S, et al
    Phenotypical and functional abnormalities of circulating neutrophils in patients with beta-thalassemia.
    Ann Hematol. 2020;99:2265-2277.
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  216. EL-GHAMRAWY M, Yassa ME, Tousson AMS, El-Hady MA, et al
    Association between BCL11A, HSB1L-MYB, and XmnI gammaG-158 (C/T) gene polymorphism and hemoglobin F level in Egyptian sickle cell disease patients.
    Ann Hematol. 2020;99:2279-2288.
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  217. CHUANG TY, Li JP, Weng TF, Wu KH, et al
    Combined chelation with high-dose deferiprone and deferoxamine to improve survival and restore cardiac function effectively in patients with transfusion-dependent thalassemia presenting severe cardiac complications.
    Ann Hematol. 2020;99:2289-2294.
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  218. FRIEDRICH C, Gay J, Alary AS, Arlet JB, et al
    Battle of the clones: paroxysmal nocturnal hemoglobinuria vs myelodysplastic syndrome.
    Ann Hematol. 2020;99:2459-2461.
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