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Anemia

Free Subscription Articles published in Ann Hematol Retrieve available abstracts of 172 articles: HTML format

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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.
   PubMed     Abstract available
   
   
   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.
   PubMed     Abstract available
   
   
   
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.
   PubMed     Abstract available
   
   
   
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.
   PubMed    
   
   
   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.
   PubMed     Abstract available
   
   
   
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.
   PubMed     Abstract available
   
   
   
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.
   PubMed     Abstract available
   
   
   
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.
   PubMed     Abstract available
   
   
   
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.
   PubMed     Abstract available
   
   
   
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    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.
    PubMed     Abstract available
    
    
    
22. 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
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
29. AN N, Bian K, Li C
    Alemtuzumab for haematological malignancies.
    Ann Hematol. 2025;104:2593-2603.
    PubMed     Abstract available
    
    
    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.
    PubMed    
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    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.
    PubMed    
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed     Abstract available
    
    
    
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.
    PubMed    
    
    
    
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.
    PubMed     Abstract available
    
    
    
92. YANG J, Shi X, Liu X, Qiao X, et al
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