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Articles published in Ann Hematol

Retrieve available abstracts of 226 articles:
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Single Articles


    May 2026
  1. WANG T, Chen Q, Ma Y, Wang B, et al
    Eltrombopag restores T-cell homeostasis in aplastic anemia by regulating oxidative metabolism and reactive oxygen species levels.
    Ann Hematol. 2026 May 18. doi: 10.1007/s00277-026-07060.
    PubMed     Abstract available


  2. MOHAMMED SALEH MF, Nasiri A, Kotb A, Alfadil H, et al
    Romiplostim in the management of severe aplastic anemia: a comprehensive clinical review.
    Ann Hematol. 2026 May 9. doi: 10.1007/s00277-026-07057.
    PubMed     Abstract available


  3. NASR NM, Ghaffar NKAE, El Asmar SM, Saber YM, et al
    The role of interleukin-1 beta as an early biomarker for renal dysfunction in Egyptian sickle cell disease patients.
    Ann Hematol. 2026;105:287.
    PubMed     Abstract available


  4. BI JY, Zhang YY, Fu HX, He Y, et al
    Haploidentical allogeneic haematopoietic stem cell transplantation for paroxysmal nocturnal haemoglobinuria: a retrospective analysis.
    Ann Hematol. 2026;105:285.
    PubMed     Abstract available


  5. SUH K, Newman TV, Yang J, Haubner A, et al
    Real-world use of pharmacologic therapy and chronic blood transfusion in sickle cell disease, 2014-2021.
    Ann Hematol. 2026;105:282.
    PubMed     Abstract available


    April 2026
  6. CHEN ZX, Yang LY, Wang LT, Chen BY, et al
    A case report of congenital sideroblastic anemia caused by a novel ALAS2 mutation in conjunction with thalassemia.
    Ann Hematol. 2026;105:237.
    PubMed     Abstract available


    March 2026
  7. ZHANG M, Zhang R, Tian Y, Wang H, et al
    Association of CBC-derived inflammatory biomarkers with overall anemia in U.S. youth: NHANES study.
    Ann Hematol. 2026;105:217.
    PubMed     Abstract available


  8. YANG L, Chen Y, Wu Y
    Integrated transcriptome-proteome analysis in patients with myelofibrosis-related anemia.
    Ann Hematol. 2026;105:211.
    PubMed     Abstract available


  9. TAN Z, Zhao Y, Hu H, Yu Q, et al
    Comparison of clinical outcomes between early and delayed allogeneic hematopoietic stem cell transplantation for severe aplastic anemia: a single-center retrospective study.
    Ann Hematol. 2026;105:186.
    PubMed     Abstract available


  10. YE QQ, Zhou XG, Yang G, Xie WT, et al
    Correction to: Overcoming transfusion-refractory anemia: partial splenic embolization to facilitate orthopedic surgery in beta-thalassemia.
    Ann Hematol. 2026;105:165.
    PubMed    


  11. CORDELLA S, Gilioli A, Pioli V, Messerotti A, et al
    Hemopoietic stem cell transplantation for infectious mononucleosis-related aplastic anemia.
    Ann Hematol. 2026;105:160.
    PubMed     Abstract available


  12. WANG Y, Yuan X, Xiao W, Lu Y, et al
    Comparison of the diagnostic performance of machine learning algorithms for differentiating iron deficiency anemia and thalassemia.
    Ann Hematol. 2026;105:159.
    PubMed     Abstract available


    February 2026
  13. HASANI E, Naghinejad M, Kohkalani M, Mansoori Derakhshan S, et al
    A novel frameshift deletion in SLC25A38 and its role in mitochondrial dysfunction: A case study of sideroblastic anemia in a child from Iran.
    Ann Hematol. 2026;105:128.
    PubMed    


  14. GUNDUZ E, Ulas T, Ozkalemkas F, Toprak SK, et al
    Assessment of characteristics and treatment patterns of adult patients with acquired aplastic anemia in Turkiye (PLANE-TR).
    Ann Hematol. 2026;105:130.
    PubMed     Abstract available


  15. YE QQ, Zhou XG, Yang G, Xie WT, et al
    Overcoming transfusion-refractory anemia: partial splenic embolization to facilitate orthopedic surgery in beta-thalassemia.
    Ann Hematol. 2026;105:101.
    PubMed     Abstract available


  16. MALAEB F, Mobarak N, Alshahrani D, Almanjomi F, et al
    Neurofibromatosis type I -related severe aplastic anemia: an unusual association with a complicated bone marrow transplantation course.
    Ann Hematol. 2026;105:83.
    PubMed     Abstract available


  17. TAN Z, Hu J, Zhao Y, Hu H, et al
    Plasma exchange combined with anti-B-cell therapy enables comparable outcomes between DSA-positive and DSA-negative aplastic anemia after haplo-HSCT: a propensity-score-matched cohort study.
    Ann Hematol. 2026;105:73.
    PubMed     Abstract available


  18. BAI Z, Hu J, Jin Y, Li X, et al
    Activated partial thromboplastin time prolongation without hemorrhagic dienhesis: a study of a chinese family coexisting with hereditary KNG1 p.Arg240 mutation and --SEA/alphaalpha genotype thalassemia.
    Ann Hematol. 2026;105:72.
    PubMed     Abstract available


  19. GAMEEL AM, Abdelsattar S, Kasemy ZA, El-Hamid MEA, et al
    The impact of the expression signatures of LncRNAs HBBP1 and XIST on the diagnostic significance of patients with beta-Thalassemia.
    Ann Hematol. 2026;105:75.
    PubMed     Abstract available


  20. KOMVILAISAK P, Laoaroon N, Paopongsawan P, Jirapradittha J, et al
    Many faces of non?deletional alpha?thalassaemia variants in neonate and early childhood.
    Ann Hematol. 2026;105:80.
    PubMed     Abstract available


    January 2026
  21. WEN X, Xiao L, Li D, Liao M, et al
    Machine learning mortality prediction model for cyclosporine therapy in pediatric aplastic anemia.
    Ann Hematol. 2026;105:69.
    PubMed     Abstract available


  22. GEORGE B, Ross CR, Damodar S, Seth T, et al
    A meta-analysis of immunosuppressive and Pharmacological therapies in aplastic anaemia with and without Indigenous equine antithymocyte globulin (eATG).
    Ann Hematol. 2026;105:52.
    PubMed     Abstract available


  23. HALKES CJM, Koster EAS, Bogers EJM, Heubel-Moenen FCJI, et al
    Anti-thymocyte globulin-based treatment frequently leads to enduring treatment success in both old and young adult patients with aplastic anaemia: a real-world analysis from the Dutch aplastic anaemia registry.
    Ann Hematol. 2026;105:51.
    PubMed     Abstract available


  24. IORI AP, De Vivo A, Di Bona E, Caocci G, et al
    Real life use of ravulizumab in Italian patients with paroxysmal nocturnal hemoglobinuria: evidence from the REACTION observational study.
    Ann Hematol. 2026;105:50.
    PubMed     Abstract available


  25. ALLARD PN, Kulozik AE, Kunz JB
    Case series: a rare dominant form of beta-thalassemia successfully treated by luspatercept.
    Ann Hematol. 2026;105:45.
    PubMed     Abstract available


  26. HU K, Cheng Y, Xiao G, Shen X, et al
    Mendelian randomization analysis of immune cell subsets and inflammatory cytokines in aplastic anaemia.
    Ann Hematol. 2026;105:36.
    PubMed     Abstract available


  27. BISIOU S, Lobbes H, Palassin P, Allouchery M, et al
    Immune checkpoint inhibitor-induced pure red cell aplasia: a nationwide retrospective case series and literature review.
    Ann Hematol. 2026;105:38.
    PubMed     Abstract available


  28. XING L, Yang W, Fan H, Li J, et al
    Cyclosporine related adverse events in aplastic anemia patients treated with immunosuppressive therapy.
    Ann Hematol. 2026;105:27.
    PubMed     Abstract available


  29. JIA X, Zheng R, Hong Y, Ge H, et al
    Luspatercept for the treatment of transfusion-dependent non-severe aplastic anemia.
    Ann Hematol. 2026;105:6.
    PubMed    


  30. OTHMANI M, Amri Y, Jouini Y, Ouali F, et al
    Vitamin D deficiency in sickle cell disease: a neglected comorbidity in Tunisia.
    Ann Hematol. 2026;105:2.
    PubMed     Abstract available


    December 2025
  31. BENITO SF, Abio M, Bardon-Cancho EJ, Nieto JM, et al
    Importance of the 3'UTR region in globin synthesis: identification of two novel HBA1 mutations causing alpha-Thalassemia.
    Ann Hematol. 2025;104:6169-6174.
    PubMed     Abstract available


  32. CHIBUIFE EC, Chisom Adaobi NE, Odini F, Deepika HD, et al
    Can platelet to neutrophil ratio (PNR) serve as a viable alternative tool for monitoring sickle cell disease patients on hydroxyurea in low income countries?
    Ann Hematol. 2025;104:6161-6168.
    PubMed     Abstract available


  33. LIU HL, Huang WT
    Hemoglobin suresnes combined with alpha(0)-thalassemia: Diagnostic challenges and insights from trio-based whole exome sequencing.
    Ann Hematol. 2025;104:6391-6394.
    PubMed     Abstract available


  34. YE C, Zhou X, Wei Y, Zhao Y, et al
    A direct multiplex isothermal amplification-reverse dot blot hybridization system for beta-thalassemia diagnosis.
    Ann Hematol. 2025;104:6147-6159.
    PubMed     Abstract available


    November 2025
  35. GE Y, Yang Y, Luo Y, Xian L, et al
    Characterization and risk assessment of HbF elevation in non-thalassemia hematologic disease patients in Guangdong region.
    Ann Hematol. 2025;104:5647-5654.
    PubMed     Abstract available


  36. FARES R, Bakr S, El-Hamid RGA, Abdelaleem OO, et al
    Circulating miR-145-5p and miR-133a-3p in pediatric sickle cell disease: biomarker potential for vaso-occlusive crises and disease activity.
    Ann Hematol. 2025;104:5625-5633.
    PubMed     Abstract available


  37. FUREDER W, Granser S, Repa A, Farr A, et al
    Ravulizumab exposure in early pregnancy.
    Ann Hematol. 2025;104:6081-6084.
    PubMed     Abstract available


    October 2025
  38. 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.
    PubMed     Abstract available


  39. WANG Z, Yu XH, Liang JL, Lai BR, et al
    Establishment of reference interval (RI) for G6PD/6PGD ratio in adults from Yangjiang, China.
    Ann Hematol. 2025;104:4959-4968.
    PubMed     Abstract available


  40. KOTILA T, Aworanti O, Akunwata C, Ogundeji P, et al
    Haemoglobin variants in nigeria: real-world data from a point-of-care device.
    Ann Hematol. 2025;104:5055-5061.
    PubMed     Abstract available


  41. NKYA S, Mahawi I, Shungu R, Nzunda C, et al
    Early-life clinical and hematological profiles: a comparative study of children with and without sickle cell disease in the first three years of life.
    Ann Hematol. 2025;104:4949-4957.
    PubMed     Abstract available


  42. WU J, Wang L, Jin Z, Ren L, et al
    Epidemiological study of thalassemia in the Buyi population of Qiannan Prefecture, Guizhou Province, China based on third-generation sequencing.
    Ann Hematol. 2025;104:5037-5045.
    PubMed     Abstract available


  43. KOFFI JFK, Botti RP, Ayemou R, N'dri AAC, et al
    Morbidity and mortality of sickle cell disease in Cote d'Ivoire.
    Ann Hematol. 2025;104:5019-5025.
    PubMed     Abstract available


  44. WANG X, Ding Y, Huang Z, Huang J, et al
    The diagnosis and clinical characterization of -alpha3.7/--SEA thalassemia patients: two cases report.
    Ann Hematol. 2025;104:5501-5506.
    PubMed     Abstract available


  45. WIRAHMADI A, Rahmartani LD, Wahidiyat PA
    Revisiting hepatitis B vaccination in children with transfusion-dependent thalassemia.
    Ann Hematol. 2025;104:5011-5017.
    PubMed     Abstract available


    September 2025
  46. 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.
    PubMed     Abstract available


  47. 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.
    PubMed     Abstract available


  48. 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.
    PubMed    


  49. MAKALO L, Manka M, Perez OR, Joof S, et al
    Severity patterns and predictors of sickle cell anaemia among Gambian children: A cross-sectional analysis.
    Ann Hematol. 2025;104:4429-4436.
    PubMed     Abstract available


  50. GONG Y, Chai X, Liu X, Zhang Y, et al
    Comprehensive analysis of the clinical feature, myeloid neoplasm-related gene mutation profiles and T cell diversity acquired pure red cell aplasia.
    Ann Hematol. 2025;104:4411-4427.
    PubMed     Abstract available


  51. ABBAS S, Khan MO, Arif A, Majid H, et al
    Framework for the comprehensive screening for endocrine disorders in patients with transfusion-dependent thalassemia in low-resource settings.
    Ann Hematol. 2025;104:4391-4409.
    PubMed     Abstract available


  52. YU L, Xu G, Chen Z, Lin K, et al
    Genetic analysis of thalassemia in putian: comparative insights into mutation spectra with other global regions.
    Ann Hematol. 2025;104:4465-4476.
    PubMed     Abstract available


  53. WEI R, Qiu D, Zeng X
    Genetic biomarkers and crucial cell subsets of iron metabolism in Beta-Thalassemia: insights from bioinformatics and experimental validation.
    Ann Hematol. 2025;104:4369-4384.
    PubMed     Abstract available


  54. BROGHAMMER S, Gagesch M, Wieczorek M, Kressig RW, et al
    Hemoglobin levels and frailty status in generally healthy and active community-dwelling adults age 70 years and older in the three-year DO-HEALTH study.
    Ann Hematol. 2025;104:4437-4445.
    PubMed     Abstract available


  55. BEZIRGIANNIDOU Z, Stamatiou I, Theodoridis TM, Kontekaki E, et al
    Ravulizumab stabilizes life-threating intravascular hemolysis following delayed hemolytic transfusion reaction due to alloantibodies anti-e and anti-Jka: the first successful administration.
    Ann Hematol. 2025;104:4849-4854.
    PubMed     Abstract available


  56. D'ADDIO A, Rondoni M, Salvucci M, Marconi G, et al
    PNH clones prevalence study in ph-negative myeloproliferative neoplasms: a multicenter Italian study.
    Ann Hematol. 2025;104:4487-4494.
    PubMed     Abstract available


  57. HUANG L, Li M, Niu T, Chang H, et al
    Anti-plasma cell therapy in patients with monoclonal gammopathy-associated refractory pure red cell aplasia: A report of three cases and literature review.
    Ann Hematol. 2025;104:4837-4841.
    PubMed     Abstract available


  58. ALKINDI S, Al Subhi A, Pathare A
    Rapid withdrawal of voxelotor can precipitate sickle cell disease related crisis.
    Ann Hematol. 2025;104:4855-4857.
    PubMed     Abstract available


    August 2025
  59. 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.
    PubMed     Abstract available


  60. 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.
    PubMed     Abstract available


  61. 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.
    PubMed     Abstract available


  62. 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.
    PubMed     Abstract available


  63. 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.
    PubMed     Abstract available


  64. 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.
    PubMed     Abstract available


  65. 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.
    PubMed     Abstract available


  66. 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.
    PubMed     Abstract available


  67. 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.
    PubMed     Abstract available


    July 2025
  68. 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.
    PubMed     Abstract available


  69. 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.
    PubMed     Abstract available


  70. 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.
    PubMed     Abstract available


  71. 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.
    PubMed     Abstract available


  72. LI Y, Jiang H, Luo L, Mei H, et al
    Immunotherapy-associated hemostatic abnormalities: bleeding and thrombotic complications.
    Ann Hematol. 2025;104:3537-3551.
    PubMed     Abstract available


  73. 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.
    PubMed     Abstract available


  74. 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.
    PubMed     Abstract available


    June 2025
  75. 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.
    PubMed     Abstract available


  76. CHAIPOKAM J, Rojnuckarin P
    Good response to oxymetholone in adult aplastic anemia.
    Ann Hematol. 2025 Jun 14. doi: 10.1007/s00277-025-06460.
    PubMed     Abstract available


  77. 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.
    PubMed     Abstract available


  78. 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.
    PubMed     Abstract available


    May 2025
  79. 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.
    PubMed     Abstract available


  80. 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.
    PubMed     Abstract available


  81. 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.
    PubMed     Abstract available


  82. 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.
    PubMed     Abstract available


  83. AN N, Bian K, Li C
    Alemtuzumab for haematological malignancies.
    Ann Hematol. 2025;104:2593-2603.
    PubMed     Abstract available


    April 2025
  84. 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    


  85. 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


  86. 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


  87. 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


  88. 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


  89. 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


  90. 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


  91. 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


  92. 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


  93. 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
  94. 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


  95. 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


  96. 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


  97. 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


  98. 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


  99. 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


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