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  Anemia

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Articles published in Ann Hematol

Retrieve available abstracts of 143 articles:
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Single Articles


    April 2025
  1. TAYLOR KJ, Singer S, Langemeijer S, Kelly RJ, et al
    What are the most important quality of life domains for patients with aplastic anemia and paroxysmal nocturnal hemoglobinuria?
    Ann Hematol. 2025 Apr 29. doi: 10.1007/s00277-025-06377.
    PubMed    


  2. LIU X, Chai X, Yu Q, Wang W, et al
    Clinical features and outcomes in large granular lymphocyte leukemia - associated pure red cell aplasia with STAT3 mutation.
    Ann Hematol. 2025 Apr 23. doi: 10.1007/s00277-025-06371.
    PubMed     Abstract available


  3. CHEN T, Song J, Xing L, Chen J, et al
    From severe aplastic anemia with TERT variant to Wilson disease - associations or not.
    Ann Hematol. 2025 Apr 21. doi: 10.1007/s00277-025-06370.
    PubMed     Abstract available


  4. LI J, Shi Y, Zhang B, Yang W, et al
    The efficacy of immunosuppressive therapy with or without thrombopoietin receptor agonist in elderly patients with severe aplastic anemia.
    Ann Hematol. 2025 Apr 7. doi: 10.1007/s00277-025-06335.
    PubMed     Abstract available


  5. RAMESH M, Fakhari-Tehrani Y, Deenadayalan V, Padhi P, et al
    Impact of protein-energy malnutrition on outcomes of patients with sickle cell disease: an analysis of the National inpatient sample.
    Ann Hematol. 2025;104:2171-2177.
    PubMed     Abstract available


  6. MANNING JE, Ciantar E, Griffin M, Kelly RJ, et al
    Paroxysmal nocturnal haemoglobinuria in pregnancy-a systematic review with meta analysis.
    Ann Hematol. 2025;104:2517-2525.
    PubMed     Abstract available


  7. AL-AWADHI A, Alwehaidah MS, Al-Sabaan K, Al-Ajmi N, et al
    Assessment of ferritin and hepcidin levels in splenectomised and non-splenectomised beta-thalassemia major patients and exploring a potential correlation with von Willebrand factor and ADAMTS-13.
    Ann Hematol. 2025;104:2229-2238.
    PubMed     Abstract available


  8. YUSUP M, He G, Qin Y, Tuerxun N, et al
    Efficacy and influencing factors of immunosuppressive therapy for pure red cell aplasia: meta-analysis and systematic review.
    Ann Hematol. 2025;104:2189-2206.
    PubMed     Abstract available


  9. RODRIGUEZ NG, Franciss G, Perez E, Maryam Z, et al
    Understanding the role of asthma in acute chest syndrome: a comparative analysis of patients with and without asthma.
    Ann Hematol. 2025;104:2179-2187.
    PubMed     Abstract available


  10. JIANG F, Wu J, Yang M, Chen X, et al
    An unusual transfusion-dependent hemoglobin H disease caused by a novel complex inverted duplication involving the alpha-globin regulatory elements and alpha-thalassemia--SEA deletion.
    Ann Hematol. 2025;104:2529-2535.
    PubMed     Abstract available


    March 2025
  11. STEMPEL JM, Wang R, Lee AI, Zeidan AM, et al
    Initial management of patients with acquired aplastic anemia in the United States: results from a large national claims database.
    Ann Hematol. 2025 Mar 19. doi: 10.1007/s00277-025-06307.
    PubMed     Abstract available


  12. ROMANELLO KS, da Silva JPMO, Torres FF, Teixeira KKL, et al
    Unraveling the multifaceted roles of peroxiredoxins in sickle cell anemia: implications in redox and inflammation adaptations.
    Ann Hematol. 2025 Mar 14. doi: 10.1007/s00277-025-06294.
    PubMed     Abstract available


  13. LIU T, Fillbrunn M, Zhang S, Chen J, et al
    Treatment patterns and healthcare resource utilization in ruxolitinib-treated patients with myelofibrosis with and without anemia: a real-world analysis.
    Ann Hematol. 2025 Mar 12. doi: 10.1007/s00277-025-06279.
    PubMed     Abstract available


  14. REKAYA S, Ben Fraj I, Hamdi R, Ben Taieb A, et al
    Sideroblastic anemia in children: challenges in diagnosis and management in three cases.
    Ann Hematol. 2025 Mar 5. doi: 10.1007/s00277-025-06266.
    PubMed     Abstract available


  15. KAWAKAMI T, Kawakami F, Matsuzawa S, Yamane T, et al
    Mutational heterogeneities in STAT3 and clonal hematopoiesis-related genes in acquired pure red cell aplasia.
    Ann Hematol. 2025;104:1471-1479.
    PubMed     Abstract available


  16. KEESARI PR, Vegivinti CTR, Rajamanuri M, Mustafa A, et al
    Racial disparities in cardiovascular manifestations among patients with sickle cell trait: analysis of national inpatient sample data (2016-2020).
    Ann Hematol. 2025;104:1501-1506.
    PubMed     Abstract available


  17. LAI D, Chen D, Chen X, Zhou R, et al
    Effect of major ABO blood group mismatched HSCT on blood transfusion and clinical outcomes in AA patients.
    Ann Hematol. 2025;104:1931-1947.
    PubMed     Abstract available


  18. KARGAR M, Kaydani GA, Keikhaei B, Saki N, et al
    Association between HLA-DRB1*04, HLA-DQB1*03, and HLA-DQB1*06 with alloimmunization in transfusion-dependent patients with thalassemia: the first case-control study in Iran.
    Ann Hematol. 2025;104:1493-1499.
    PubMed     Abstract available


  19. BODE AL, Borja-Montes OF, Quazi MA, Mumtaz A, et al
    Sickle cell disease and opioid overdose outcomes in the United States: a nationwide analysis.
    Ann Hematol. 2025;104:1551-1561.
    PubMed     Abstract available


  20. LI Y, Feng Y, Wei Y, Huang J, et al
    The impact of various types of alpha-thalassemia on perinatal complications and pregnancy outcomes in pregnant women.
    Ann Hematol. 2025;104:1541-1550.
    PubMed     Abstract available


  21. HUANG L, Zhang Q, Ye Y, Long Y, et al
    Rapid detection of genetic modifiers of beta-thalassemia based on MALDI-TOF MS.
    Ann Hematol. 2025;104:1481-1492.
    PubMed     Abstract available


  22. SCHNEDL WJ, Leixner G, Voill-Glaninger A, Michaelis S, et al
    Combined heterozygosity for hemoglobin Pakse, alpha-thalassemia and for hemoglobin E, beta- thalassemia ? first appearance in Europe.
    Ann Hematol. 2025;104:2059-2064.
    PubMed     Abstract available


  23. ALHARBI M, Bawek S, Lund I, Glenn ST, et al
    Rare case of pure red cell aplasia secondary to smoldering multiple myeloma successfully treated with daratumumab - case report and review of the literature.
    Ann Hematol. 2025;104:2027-2034.
    PubMed     Abstract available


  24. TAN Z, Zhang X, Feng J, Zhao Y, et al
    Hematopoietic stem cell transplantation and immunosuppressive therapy: implications of clonal haematopoiesis.
    Ann Hematol. 2025;104:1877-1886.
    PubMed     Abstract available


    February 2025
  25. CHEN L, Wei X, Zheng C, Liu X, et al
    Novel AK-1 gene variants combined with thalassemia causing rare hereditary non-spherocytic hemolytic anemia in a Chinese family.
    Ann Hematol. 2025 Feb 28. doi: 10.1007/s00277-025-06289.
    PubMed     Abstract available


  26. YAN Q, Zhang Y, Wei L, Liu X, et al
    Assessment of anemia recovery using peripheral blood smears by deep semi-supervised learning.
    Ann Hematol. 2025 Feb 21. doi: 10.1007/s00277-025-06254.
    PubMed     Abstract available


  27. LIU A, Jacobs-McFarlane C, Sebastiani P, Glassberg J, et al
    Plasma free hemoglobin is associated with LDH, AST, total bilirubin, reticulocyte count, and the hemolysis score in patients with sickle cell anemia.
    Ann Hematol. 2025 Feb 19. doi: 10.1007/s00277-025-06253.
    PubMed     Abstract available


  28. CHEN X, Yu Q, Qin C, Zhang Y, et al
    Combining immunosuppressive therapy with low dosage eltrombopag in Chinese patients with severe aplastic anemia: mild aggravation of hepatic injury.
    Ann Hematol. 2025 Feb 5. doi: 10.1007/s00277-025-06210.
    PubMed     Abstract available


  29. AMMAR M, Kmiha S, Maalej M, Felhi R, et al
    Identification of a novel truncated pathogenic variant in PUS1 gene in two siblings of consanguineous Tunisian family: intrafamilial phenotypic variability related to mtDNA copy number.
    Ann Hematol. 2025;104:943-952.
    PubMed     Abstract available


  30. WU T, Ren Z, Liu X, Xing Z, et al
    Systematic identification and validation of ceRNA-driven regulatory mechanisms in pediatric beta-Thalassemia major.
    Ann Hematol. 2025;104:963-972.
    PubMed     Abstract available


  31. ARLET JB, Bernaudin F, Deme-Ly I, Coulibaly B, et al
    Use of hydroxyurea in French-speaking Sub-Saharan Africa.
    Ann Hematol. 2025;104:937-941.
    PubMed     Abstract available


  32. LIU Y, Liu M, He X, Yang L, et al
    Molecular landscape of CD8(+) T cells in pure red cell aplasia.
    Ann Hematol. 2025;104:953-961.
    PubMed     Abstract available


  33. MAHADEVIA H, Ponvilawan B, Madan U, Sharma P, et al
    A review on disease modifying pharmacologic therapies for sickle cell disease.
    Ann Hematol. 2025;104:881-893.
    PubMed     Abstract available


  34. XING L, Liang W, Li Y, Xiao J, et al
    Concurrent inhibited erythropoiesis in a case of VEXAS syndrome.
    Ann Hematol. 2025;104:1255-1258.
    PubMed     Abstract available


  35. RIEDL J, Pfeilstocker M, Farr A, Hausler G, et al
    Management of paroxysmal nocturnal hemoglobinuria with low-level hemolysis in pregnancy- a report of two cases.
    Ann Hematol. 2025;104:1249-1253.
    PubMed     Abstract available


  36. GOLDSCHMIDT V, Apodaca EI, Galvez KM, Wannesson B, et al
    Clinical characteristics and management of paroxysmal nocturnal haemoglobinuria in Latin America: a narrative review.
    Ann Hematol. 2025;104:867-879.
    PubMed     Abstract available


    January 2025
  37. YANG K, Li Q, Zhuang X, Ma H, et al
    A retrospective analysis of autoimmune hemolytic anemia after allogeneic hematopoietic stem cell transplantation for transfusion-dependent beta-thalassemia: focus on T and B lymphocyte reconstitution.
    Ann Hematol. 2025 Jan 3. doi: 10.1007/s00277-024-06157.
    PubMed     Abstract available


  38. KULASEKARARAJ A, Brodsky R, Schrezenmeier H, Griffin M, et al
    Ravulizumab demonstrates long-term efficacy, safety and favorable patient survival in patients with paroxysmal nocturnal hemoglobinuria.
    Ann Hematol. 2025;104:81-94.
    PubMed     Abstract available


  39. ZHUANG J, Huang N, Zheng Y, Zhang N, et al
    First clinical and pedigree study of rare HBB: c.316-90 A > G variant in beta-globin gene in Chinese population using third-generation sequencing.
    Ann Hematol. 2025;104:75-80.
    PubMed     Abstract available


    December 2024
  40. JANG T, Burnside RD, Chaffin J, Seifert R, et al
    Severe aplastic anemia with acquired X chromosome clonality as a sole abnormality.
    Ann Hematol. 2024 Dec 31. doi: 10.1007/s00277-024-06166.
    PubMed     Abstract available


  41. GAO M, Huang X, Gao S, Wang S, et al
    Similar outcomes between HLA-haploid and matched sibling donor hematopoietic stem cell transplantation: a multicenter, retrospective study and severe aplastic anemia transplant-specific prognostic scoring system.
    Ann Hematol. 2024 Dec 12. doi: 10.1007/s00277-024-06051.
    PubMed     Abstract available


  42. PINES M, Kleinert D, Thomas C, Mensah C, et al
    Real-world experience with iron chelation therapy in transfusion-dependent thalassemia: impact of the oral chelators' era.
    Ann Hematol. 2024;103:5229-5234.
    PubMed     Abstract available


  43. DAWUDI Y, Azoyan L, Bonjour M, Steichen O, et al
    COVID-19 outcomes among patients with sickle cell disease or sickle cell trait compared to the general population: a systematic review and meta-analyses.
    Ann Hematol. 2024;103:5071-5083.
    PubMed     Abstract available


  44. DINGLI D, Rizio AA, Broderick L, LaGasse K, et al
    Health-related quality of life and symptom-specific functional impairment among patients treated with parenterally administered complement inhibitors for paroxysmal nocturnal hemoglobinuria.
    Ann Hematol. 2024;103:5213-5227.
    PubMed     Abstract available


  45. FAN L, Cao L, Luo Y, Gao F, et al
    Roxadustat combined with immunosuppressants for treatment of pure red cell aplasia with kidney injury.
    Ann Hematol. 2024;103:5925-5927.
    PubMed     Abstract available


  46. MOTTA I, Delbini P, Scaramellini N, Ghiandai V, et al
    Enzyme replacement therapy improves erythropoiesis and iron dysregulation in Gaucher disease.
    Ann Hematol. 2024;103:5113-5121.
    PubMed     Abstract available


  47. GUO X, Lin S, Zhang X, Li M, et al
    Integrated metabolomic and microbiome analysis identifies Cupriavidus metallidurans as a potential therapeutic target for beta-thalassemia.
    Ann Hematol. 2024;103:5169-5179.
    PubMed     Abstract available


    November 2024
  48. LOH JB, Ross JM, Musallam KM, Kuo KHM, et al
    Trans-acting genetic modifiers of clinical severity in heterozygous beta-Thalassemia trait.
    Ann Hematol. 2024;103:4437-4447.
    PubMed     Abstract available


  49. DE SANTIS M, Tonutti A, Motta F, Todisco G, et al
    Approaches for the diagnosis and treatment of VEXAS syndrome: the importance of clinical suspicion and the use of methotrexate.
    Ann Hematol. 2024;103:4789-4791.
    PubMed     Abstract available


    October 2024
  50. CAHUAPAZA-GUTIERREZ NL
    Aplastic Anemia in the light of the COVID-19 pandemic: infection, vaccination, and pathophysiologic mechanisms.
    Ann Hematol. 2024 Oct 23. doi: 10.1007/s00277-024-06052.
    PubMed     Abstract available


  51. DONGERDIYE R, Kedar PS, Saptarshi A, Sampagar A, et al
    Non-syndromic congenital sideroblastic anaemia; phenotype, and genotype of 15 Indian patients.
    Ann Hematol. 2024;103:3987-3998.
    PubMed     Abstract available


  52. ZHANG M, Liu M, Yang L, Liu Y, et al
    Increased ferroptosis of erythrocytes is associated with myelodysplastic syndromes.
    Ann Hematol. 2024;103:4009-4020.
    PubMed     Abstract available


    September 2024
  53. CHEN WT, Wang SW, Huang Y, Tang RM, et al
    The effect of hetrombopag combined with conventional treatment on immune function and quality of life in patients with severe aplastic anemia.
    Ann Hematol. 2024 Sep 5. doi: 10.1007/s00277-024-05964.
    PubMed     Abstract available


  54. EBEID FSE, Aly NH, Shaheen NM, Abdellatif SMA, et al
    Safety and efficacy of L-Glutamine in reducing the frequency of acute complications among patients with sickle cell disease: A randomized controlled study.
    Ann Hematol. 2024;103:3493-3506.
    PubMed     Abstract available


  55. EZZAT EM, Bakr S, Golam RM, Abdelgyed BA, et al
    Adipocyte fatty acid-binding protein (FABP4) as a potential biomarker for predicting metabolically driven low-grade and organ damage in thalassemia syndromes.
    Ann Hematol. 2024;103:3473-3482.
    PubMed     Abstract available


  56. JAJODIA E, Menghani H, Arora N, Jitani A, et al
    De-novo ATR-16 syndrome associated with inherited hemoglobin Evanston causing HbH phenotype: a rare occurrence.
    Ann Hematol. 2024;103:3805-3810.
    PubMed     Abstract available


  57. PATSOURAKOS D, Aggeli C, Dimitroglou Y, Delicou S, et al
    Speckle tracking echocardiography and beta-thalassemia major. A systematic review.
    Ann Hematol. 2024;103:3335-3356.
    PubMed     Abstract available


    August 2024
  58. SHEN S, Hu Q, Yang C, Jiang Z, et al
    Adding hetrombopag to cyclosporine a improved response of patients with newly diagnosed transfusion-dependent non-severe aplastic anemia.
    Ann Hematol. 2024 Aug 23. doi: 10.1007/s00277-024-05941.
    PubMed    


  59. LI X, Shangguan X, Wang H, Wang Q, et al
    Comparison of efficacy of eltrombopag combined with immunosuppression in the treatment of severe aplastic anemia and very severe aplastic anemia: real-world data and evidence.
    Ann Hematol. 2024 Aug 1. doi: 10.1007/s00277-024-05910.
    PubMed     Abstract available


  60. IQBAL N, Meghani MA, Khalid W, Ansari AH, et al
    Transcobalamin deficiency - a rare genetic defect in transportation of cobalamin; case report.
    Ann Hematol. 2024;103:3243-3246.
    PubMed     Abstract available


  61. FUREDER W, Valent P
    Stable responses to danicopan as add-on to ravulizumab in two patients with paroxysmal nocturnal hemoglobinuria.
    Ann Hematol. 2024;103:3235-3238.
    PubMed    


  62. MARCO SANCHEZ JM, Bardon Cancho EJ, Beneitez D, Payan-Pernia S, et al
    Haemoglobinopathies and other rare anemias in Spain: ten years of a nationwide registry (REHem-AR).
    Ann Hematol. 2024;103:2743-2755.
    PubMed     Abstract available


  63. YANG J, Shi X, Liu X, Qiao X, et al
    STK10 mutations block erythropoiesis in acquired pure red cell aplasia via impairing ribosome biogenesis.
    Ann Hematol. 2024;103:2711-2720.
    PubMed     Abstract available


  64. BHANGU G, Uminski K, Roessner C, Goodyear D, et al
    Dry gangrene in a patient with sickle cell disease on hydroxyurea: a case report.
    Ann Hematol. 2024;103:3277-3279.
    PubMed    


  65. LI J, Lv A, Chen M, Xu L, et al
    Activating transcription factor 4 in erythroid development and beta -thalassemia: a powerful regulator with therapeutic potential.
    Ann Hematol. 2024;103:2659-2670.
    PubMed     Abstract available


  66. YOUSSRY I, Ayad N
    Sickle cell disease: combination new therapies vs. CRISPR-Cas9 potential and challenges - review article.
    Ann Hematol. 2024;103:2613-2619.
    PubMed     Abstract available


  67. KIRTHAN JPA, Somannavar MS
    Pathophysiology and management of iron deficiency anaemia in pregnancy: a review.
    Ann Hematol. 2024;103:2637-2646.
    PubMed     Abstract available


    July 2024
  68. MUSALLAM KM, Barella S, Origa R, Ferrero GB, et al
    Revisiting iron overload status and change thresholds as predictors of mortality in transfusion-dependent beta-thalassemia: a 10-year cohort study.
    Ann Hematol. 2024;103:2283-2297.
    PubMed     Abstract available


  69. TER AVEST M, Langemeijer SMC, Blijlevens NMA, van de Kar NCAJ, et al
    Development of a target concentration intervention to individualize paroxysmal nocturnal hemoglobinuria treatment with pegcetacoplan.
    Ann Hematol. 2024;103:2267-2272.
    PubMed     Abstract available


    June 2024
  70. GONG Y, Li Y, Chen X, Yang H, et al
    Refractory pure red cell aplasia associated with T-cell large granular lymphocyte leukemia treated by ruxolitinib.
    Ann Hematol. 2024 Jun 27. doi: 10.1007/s00277-024-05856.
    PubMed     Abstract available


  71. WANG L, Fang L, Shi H, Liu Y, et al
    Treatment of myelofibrosis with refractory anemia with luspatercept: a multicenter Chinese study.
    Ann Hematol. 2024 Jun 22. doi: 10.1007/s00277-024-05847.
    PubMed     Abstract available


  72. KANTER J, Ataga KI, Bhasin N, Guarino S, et al
    Expert consensus on the management of infusion-related reactions (IRRs) in patients with sickle cell disease (SCD) receiving crizanlizumab: a RAND/UCLA modified Delphi panel.
    Ann Hematol. 2024;103:1909-1917.
    PubMed     Abstract available


  73. ZHANG Z, Hu Q, Yang C, Chen M, et al
    Comparison of human leukocyte antigen in patients with paroxysmal nocturnal hemoglobinuria of different clone sizes.
    Ann Hematol. 2024;103:1897-1907.
    PubMed     Abstract available


  74. MELONI A, Pistoia L, Ricchi P, Bagnato S, et al
    Impact of genotype on multi-organ iron and complications in patients with non-transfusion-dependent beta-thalassemia intermedia.
    Ann Hematol. 2024;103:1887-1896.
    PubMed     Abstract available


  75. YANG L, Niu H, Zhang T, Cao Q, et al
    A nomogram model for predicting the efficacy of cyclosporine in patients with pure red cell aplasia.
    Ann Hematol. 2024;103:1877-1885.
    PubMed     Abstract available


  76. ALAYOUBI AM, Khawaji ZY, Mohammed MA, Mercier FE, et al
    CRISPR-Cas9 system: a novel and promising era of genotherapy for beta-hemoglobinopathies, hematological malignancy, and hemophilia.
    Ann Hematol. 2024;103:1805-1817.
    PubMed     Abstract available


    May 2024
  77. SHI Y, Zhao Y, Liang W, Zhang B, et al
    A preliminary study of roxadustat in the treatment of aplastic anemia patients with inadequate erythroid responses.
    Ann Hematol. 2024 May 22. doi: 10.1007/s00277-024-05799.
    PubMed     Abstract available


  78. NAKAMURA Y, Zaimoku Y, Yamaguchi H, Yamazaki H, et al
    Significance of absolute neutrophil count before allogeneic hematopoietic stem cell transplantation in adult patients with aplastic anemia.
    Ann Hematol. 2024 May 16. doi: 10.1007/s00277-024-05800.
    PubMed     Abstract available


  79. 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.
    PubMed     Abstract available


  80. 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.
    PubMed     Abstract available


    April 2024
  81. HU M, Li J, Liu R, Zhang Z, et al
    Unrelated umbilical cord blood transplantation with low-dose anti-thymocyte globulin for children with severe aplastic anemia: A case series.
    Ann Hematol. 2024 Apr 24. doi: 10.1007/s00277-024-05756.
    PubMed     Abstract available


  82. QIN S, Jiang Y, Ou Y, Zhan Y, et al
    Mendelian randomization of circulating proteome identifies IFN-gamma as a druggable target in aplastic anemia.
    Ann Hematol. 2024 Apr 22. doi: 10.1007/s00277-024-05746.
    PubMed     Abstract available


  83. 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.
    PubMed     Abstract available


  84. 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.
    PubMed     Abstract available


  85. 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.
    PubMed     Abstract available


  86. 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.
    PubMed     Abstract available


    March 2024
  87. 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.
    PubMed     Abstract available


  88. 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.
    PubMed    


    February 2024
  89. 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.
    PubMed    


  90. 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.
    PubMed    


  91. 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.
    PubMed     Abstract available


  92. 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.
    PubMed     Abstract available


  93. 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.
    PubMed     Abstract available


    January 2024
  94. 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.
    PubMed     Abstract available


  95. 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.
    PubMed     Abstract available


  96. 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.
    PubMed     Abstract available


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    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.
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    December 2023
  98. DELGADINHO M, Veiga L, Ginete C, Santos B, et al
    Differential expression of adhesion molecules in sickle cell anemia and gut microbiome effect.
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  99. FU L, Zhang J, Wang R, Yang B, et al
    Clinical characteristics of hepatitis-associated aplastic anemia in children.
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    Functional similarity of ABP 959 and eculizumab in simulated serum models of aHUS and NMOSD.
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    November 2023
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    Warm autoimmune hemolytic anemia associated with SARS-CoV-2 infection responsive to eculizumab.
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  102. 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.
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    Cold agglutinin-induced acrocyanosis without hemolytic anemia.
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  104. POPE V, Hsia CC
    Safe utilization of ruxolitinib in simultaneous primary myelofibrosis and warm autoimmune hemolytic anemia.
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    Successful use of thrombopoietin analogs in thrombocytopenia associated with MYH-9 mutation.
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    Cytopenia: a report of haplo-cord transplantation in twin brothers caused by a novel germline GATA1 mutation and family survey.
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    Excellent outcome of stem cell transplantation for sickle cell disease.
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    Risk factors for thromboembolic events in patients with paroxysmal nocturnal hemoglobinuria (PNH): a nested case-control study in the International PNH Registry.
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    October 2023
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    Comment on: Association between anemia and depression: results from NHANES 2005-2018 and Mendelian randomization analyses.
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    Real-life experience with luspatercept in transfusion-dependent beta-thalassemia.
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    Comparison of different intravenous iron preparations in terms of total oxidant and total antioxidant status, single center data.
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    September 2023
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    Alternative treatment modality for severe aplastic anemia in a resource-limited setting: a single-institution prospective cohort study from Upper Egypt.
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    Age-related differences in risks and outcomes of 30-day readmission in adults with sickle cell disease.
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    Molecular insights into hereditary elliptocytosis and pyropoikilocytosis: NGS uncovers multiple potential candidate genes.
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    August 2023
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    Real-life use of mTOR inhibitor-based therapy in adults with autoimmune cytopenia highlights strong efficacy in relapsing/refractory multi-lineage autoimmune cytopenia.
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    Patient preference for deferasirox film-coated versus dispersible tablet formulation: a sequential-design phase 2 study in patients with thalassemia.
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    Successful treatment with cyclosporine of pure red cell aplasia induced by obinutuzumab bendamustine therapy.
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    July 2023
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    June 2023
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    May 2023
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    March 2023
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    Hematopoietic cell transplantation for congenital dyserythropoietic anemia IV caused by compound heterozygous KLF1 mutations.
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    Use of roxadustat (FG-4592) in ruxolitinib-treatment-related anemia of two myelofibrosis patients.
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