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Articles published in
Ann Hematol
    October 2025
  1. BOSQUES L, Modepalli S, Nagarajan A, Tang C, et al
    Codanin-1, defective in congenital dyserythropoietic anemia I (CDA-I), regulates erythroid differentiation.
    Ann Hematol. 2025 Oct 1. doi: 10.1007/s00277-025-06540.
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    September 2025
  2. YANG C, Huang J, Yang K, Wei C, et al
    Haploidentical hematopoietic stem cell transplantation for the treatment of congenital dyserythropoietic anemia combined with thalassemia: a report of two cases.
    Ann Hematol. 2025 Sep 26. doi: 10.1007/s00277-025-06615.
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  3. BIRSIN Z, Salihoglu A, Tokdil KO, Pirdal BZ, et al
    Is splenectomy one of the contributory factors to pulmonary hypertension? An analysis of splenectomized hemolytic anemia and immune thrombocytopenia patients.
    Ann Hematol. 2025 Sep 9. doi: 10.1007/s00277-025-06583.
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  4. NAGEL SN, Brintrup J, Ghannam Y, Stallmach A, et al
    Combined heterozygosity for the highly unstable variant hemoglobin Taybe, and alpha-thalassemia as a rare cause of hemolytic anemia.
    Ann Hematol. 2025 Sep 9. doi: 10.1007/s00277-025-06578.
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    August 2025
  5. ZHANG X, Xie J, Wang H, Li J, et al
    Analysis of fecal microbiome in Chinese patients with non-severe aplastic anemia.
    Ann Hematol. 2025 Aug 19. doi: 10.1007/s00277-025-06459.
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  6. YE L, Zhang L, Zhang D, Zhao X, et al
    Somatic mutations and the efficacy of immunosuppressive therapy in severe/very severe aplastic anemia and transfusion-dependent nonsevere aplastic anemia.
    Ann Hematol. 2025 Aug 7. doi: 10.1007/s00277-025-06393.
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  7. SHI L, Yan X, Xia Y, Zhao Y, et al
    Beyond transfusions and transplants: genomic innovations rewriting the narrative of thalassemia.
    Ann Hematol. 2025;104:3963-3980.
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  8. OZAHATA MC, Gomes I, Oliveira BA, Park M, et al
    Genetic modifiers of frequent vaso-occlusive hospitalizations among individuals with sickle cell disease (SCD).
    Ann Hematol. 2025;104:4029-4035.
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  9. LI H, Gu Y, Zhao X, Ding G, et al
    Comparative longitudinal analysis of pulmonary function post-pediatric Allo-HSCT: benign vs. malignant diseases and early predictors.
    Ann Hematol. 2025;104:4201-4211.
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  10. WARNCKE K, Nero A, Sarode R, Adkins BD, et al
    Hyperhemolysis in a sickle cell disease patient in pregnancy.
    Ann Hematol. 2025;104:4245-4249.
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  11. PEDERSEN TH, Tjonnfjord E, Korkama ES, Vikman M, et al
    The incidence of paroxysmal nocturnal hemoglobinuria cell clones in the Nordic countries.
    Ann Hematol. 2025;104:4277-4283.
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  12. NIKOLAIDIS CG, Gyriki D, Gogos DG, Stavropoulou E, et al
    Sickle cell beta-thalassemia diagnosed at age 40: a case report.
    Ann Hematol. 2025;104:4229-4236.
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  13. WANG Y, Liu T, Wang W, Li Y, et al
    Three novel heterozygous ANK1 loss-of-function variants cause hereditary spherocytosis in Chinese families.
    Ann Hematol. 2025;104:4045-4056.
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    July 2025
  14. JANG JH, Mitani K, Tomiyama Y, Miyazaki K, et al
    Predictive factors of romiplostim response in patients with refractory aplastic anemia: data from two clinical trials.
    Ann Hematol. 2025 Jul 1. doi: 10.1007/s00277-025-06337.
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  15. CHEN R, Zhang R, He X, Zhang Q, et al
    Factors influencing prenatal diagnosis of deletional hemoglobin H disease in thalassemia prevention and control program, Southern China.
    Ann Hematol. 2025;104:3567-3574.
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  16. UEDA Y, Obara N, Ueno S, Sakurai M, et al
    Treatment burden in patients with paroxysmal nocturnal hemoglobinuria: an in-depth interview survey.
    Ann Hematol. 2025;104:3575-3584.
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  17. LIU H, Du Y, Yang Y, Cui D, et al
    Identification of a novel complex variant in a patient involving the alpha-globin gene cluster by third-generation sequencing.
    Ann Hematol. 2025;104:3619-3629.
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  18. LI Y, Jiang H, Luo L, Mei H, et al
    Immunotherapy-associated hemostatic abnormalities: bleeding and thrombotic complications.
    Ann Hematol. 2025;104:3537-3551.
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  19. ENGOLE YM, Makulo JRR, Bukabau JB, Nlandu YM, et al
    Genotype-dependent albuminuria in adult sickle cell disease in Kinshasa.
    Ann Hematol. 2025;104:3585-3595.
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  20. ZHU G, Ren Y, Wang L, Wang S, et al
    Assessing serum thrombopoietin for enhanced diagnosis of ITP, AA, and MDS using machine learning: A retrospective cohort study.
    Ann Hematol. 2025;104:3631-3645.
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    June 2025
  21. ZHANG S, Ji Q, Gao L, Wang Q, et al
    Efficacy and safety of rabbit ATLG and ATG in allogeneic hematopoietic stem cell transplantation for children with acquired severe aplastic anemia.
    Ann Hematol. 2025 Jun 19. doi: 10.1007/s00277-025-06461.
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  22. CHAIPOKAM J, Rojnuckarin P
    Good response to oxymetholone in adult aplastic anemia.
    Ann Hematol. 2025 Jun 14. doi: 10.1007/s00277-025-06460.
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  23. AMRI Y, Fredj SH, Dabboubi R, Othmani R, et al
    Revealing silent alpha-thalassemia: characterization of novel HBA1 deletion and missense mutation in Tunisian families.
    Ann Hematol. 2025;104:3173-3182.
    >> Share

  24. LIN MH, Wang YJ, Zhang YY, Cheng YF, et al
    The outcomes of second haploidentical donor transplantation for graft failure in patients with severe aplastic anaemia.
    Ann Hematol. 2025;104:3469-3476.
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    May 2025
  25. PARK S, Kim HK
    Epidemiologic sequential analysis of pure red blood cell aplasia and T-cell large granular lymphocyte leukemia in Korea.
    Ann Hematol. 2025 May 22. doi: 10.1007/s00277-025-06406.
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  26. EFOBI C, Ukpai N, Eze OE, Basil B, et al
    Platelet-to-Neutrophil ratio as a predictor of risk of complications in sickle cell disease: a valuable insight for resource-limited settings.
    Ann Hematol. 2025;104:2663-2669.
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  27. MAHABHOL C, Yothindamrongkul L, Nuntanajaroenkul N, Nawasod P, et al
    Genetic polymorphism of novel SNP rs5006884 in OR51B6 and SNP rs4499252 in AHSP among transfusion-dependent and non-transfusion-dependent beta-thalassemia/Hb E patients in Thailand: a multivariate analysis of clinical and genetic polymorphism.
    Ann Hematol. 2025;104:2653-2661.
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  28. KWON YD, Hong KT, Lee J, Sunwoo Y, et al
    Clinical usefulness of next-generation sequencing-based target gene sequencing in diagnosis of inherited bone marrow failure syndrome.
    Ann Hematol. 2025;104:2693-2706.
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  29. AN N, Bian K, Li C
    Alemtuzumab for haematological malignancies.
    Ann Hematol. 2025;104:2593-2603.
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    April 2025
  30. 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.
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  31. 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.
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  32. 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.
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  33. 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.
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  34. 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.
    >> Share

  35. 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.
    >> Share

  36. 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.
    >> Share

  37. 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.
    >> Share

  38. 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.
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  39. 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.
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    March 2025
  40. 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.
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  41. 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.
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  42. 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.
    >> Share

  43. 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.
    >> Share

  44. 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.
    >> Share

  45. 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.
    >> Share

  46. 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.
    >> Share

  47. 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.
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  48. 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.
    >> Share

  49. 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.
    >> Share

  50. 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.
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  51. 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.
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  52. 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.
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  53. 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.
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    February 2025
  54. 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.
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  55. 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.
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  56. 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.
    >> Share

  57. 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.
    >> Share

  58. 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.
    >> Share

  59. 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.
    >> Share

  60. 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.
    >> Share

  61. 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.
    >> Share

  62. 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.
    >> Share

  63. 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.
    >> Share

  64. 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.
    >> Share

  65. 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.
    >> Share

    January 2025
  66. 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.
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  67. 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.
    >> Share

  68. 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.
    >> Share

    December 2024
  69. 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.
    >> Share

  70. 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.
    >> Share

  71. 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.
    >> Share

  72. 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.
    >> Share

  73. 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.
    >> Share

  74. 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.
    >> Share

  75. 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.
    >> Share

  76. 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.
    >> Share

    November 2024
  77. 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.
    >> Share

  78. 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.
    >> Share

    October 2024
  79. 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.
    >> Share

  80. 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.
    >> Share

  81. 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.
    >> Share

    September 2024
  82. 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.
    >> Share

  83. 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.
    >> Share

  84. 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.
    >> Share

  85. 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.
    >> Share

  86. 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.
    >> Share

    August 2024
  87. 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.
    >> Share

  88. 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.
    >> Share

  89. 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.
    >> Share

  90. 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.
    >> Share

  91. 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.
    >> Share

  92. 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.
    >> Share

  93. 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.
    >> Share

  94. 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.
    >> Share

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

  96. KIRTHAN JPA, Somannavar MS
    Pathophysiology and management of iron deficiency anaemia in pregnancy: a review.
    Ann Hematol. 2024;103:2637-2646.
    >> Share

    July 2024
  97. 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.
    >> Share

  98. 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.
    >> Share

    June 2024
  99. 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.
    >> Share

  100. 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.
    >> Share

  101. 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.
    >> Share

  102. 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.
    >> Share

  103. 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.
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  104. 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.
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  105. 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.
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    May 2024
  106. 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.
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  107. 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.
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  108. 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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  109. AL-KURAISHY HM, Mazhar Ashour MH, Saad HM, Batiha GE, et al
    COVID-19 and beta-thalassemia: in lieu of evidence and vague nexus.
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    April 2024
  110. 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.
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  111. 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.
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  112. LOMMERSE IN, Hinnen C, van Vliet LM, Schubert B, et al
    Quality of life after immune suppressive therapy in aplastic anemia.
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  113. DE CASTRO JNP, da Silva Costa SM, Camargo ACL, Ito MT, et al
    Comparative transcriptomic analysis of circulating endothelial cells in sickle cell stroke.
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  114. 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.
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  115. 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
  116. 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).
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  117. 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.
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    February 2024
  118. SECK M, Manal B, Toure SA, Keita M, et al
    Challenges in the management of iron-deficiency anemia in Senegal, West Africa.
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  119. ZHA Q, Shi Y, Shi Z, Huang F, et al
    Loeys-Dietz syndrome with concomitant aplastic anemia.
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  120. 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.
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  121. GARCIA-MORIN M, Bardon-Cancho EJ, Belendez C, Dulin E, et al
    Madrid Newborn Sickle Cell Disease Cohort: clinical outcomes, stroke prevention and survival.
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  122. 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.
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    January 2024
  123. 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.
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  124. 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.
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  125. 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.
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  126. 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.
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    December 2023
  127. 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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  128. 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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  129. 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.
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    November 2023
  130. 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.
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  131. 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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  132. 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.
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  133. 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.
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  134. 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.
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  135. 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.
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  136. VALLEE T, Schmid I, Gloning L, Bacova M, et al
    Excellent outcome of stem cell transplantation for sickle cell disease.
    Ann Hematol. 2023;102:3217-3227.
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  137. HOCHSMANN B, Peffault de Latour R, Hill A, Roth A, et al
    Risk factors for thromboembolic events in patients with paroxysmal nocturnal hemoglobinuria (PNH): a nested case-control study in the International PNH Registry.
    Ann Hematol. 2023;102:2979-2988.
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    October 2023
  138. 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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  139. 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.
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  140. 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.
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  141. 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.
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  142. 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
  143. 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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  144. 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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  145. 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.
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  146. 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.
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  147. 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
  148. 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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  149. 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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  150. 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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  151. 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.
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    July 2023
  152. 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.
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  153. 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.
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  154. 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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  155. 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.
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  156. 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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  157. 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.
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  158. 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
  159. 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.
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    May 2023
  160. 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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  161. 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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  162. 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.
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  163. 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.
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  164. 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.
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    April 2023
  165. 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.
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  166. 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.
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  167. 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.
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  168. 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.
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  169. 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
  170. 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.
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  171. 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.
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  172. 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.
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