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Anemia

Free Subscription Articles published in Am J Hematol Retrieve available abstracts of 167 articles: HTML format

Single Articles

December 2025
1. LIANG P, Wan YS, Shan KZ, Chou R, et al
   Targeting PIEZO1-TMEM16F Coupling to Mitigate Sickle Cell Disease Complications.
   Am J Hematol. 2025;100:2261-2275.
   PubMed     Abstract available
   
   
   
2. HEMMER M, Moinard S, Lambotte O, Malphettes M, et al
   Pure Red Cell Aplasia Associated With Thymic Tumors, a Nationwide Retrospective Study.
   Am J Hematol. 2025;100:2230-2237.
   PubMed     Abstract available
   
   
   November 2025
3. QUARELLO P, Karimi K, Trajkova S, Garelli E, et al
   DNA Methylation Episignature as a Novel Diagnostic Tool for Diamond-Blackfan Anemia Syndrome.
   Am J Hematol. 2025 Nov 17. doi: 10.1002/ajh.70141.
   PubMed     Abstract available
   
   
   
4. KAPHAN E, Walter-Petrich A, Larcher L, Leblanc T, et al
   Recursive Partitioning to Differentiate Acquired From Inherited Bone Marrow Failure Syndromes.
   Am J Hematol. 2025;100:1983-1992.
   PubMed     Abstract available
   
   
   
5. FATTIZZO B, Pedone GL, Metafuni E, Beggiato E, et al
   Characterization of Breakthrough Hemolysis in Patients With Paroxysmal Nocturnal Hemoglobinuria: An International Multicenter Experience.
   Am J Hematol. 2025;100:1963-1971.
   PubMed     Abstract available
   
   
   
6. SIMON T, Savale L, Grundtvig Skaarup K, Breillat P, et al
   Sickle Cell Diastolic Cardiomyopathy and Mortality Risk: A Novel Echocardiographic Framework for Prognostic Stratification.
   Am J Hematol. 2025;100:1940-1951.
   PubMed     Abstract available
   
   
   October 2025
7. MABERRY MD, Smith CJ, Go RS
   Clinical Utility of Monoclonal Gammopathy Testing in the Evaluation of Anemia.
   Am J Hematol. 2025 Oct 23. doi: 10.1002/ajh.70102.
   PubMed     Abstract available
   
   
   
8. GANGAT N, Tefferi A
   The Hemojuvelin-Hepcidin Axis as a Target for the Treatment of Anemia or Conversely Polycythemia.
   Am J Hematol. 2025 Oct 21. doi: 10.1002/ajh.70120.
   PubMed     Abstract available
   
   
   
9. AL-SAMKARI H, Mayne TJ, Troutt M, Patle H, et al
   Characterizing the Healthcare Utilization and Costs of Hereditary Hemorrhagic Telangiectasia.
   Am J Hematol. 2025;100:1722-1735.
   PubMed     Abstract available
   
   
   September 2025
10. COATES TD
    Early Detection of Diastolic Dysfunction in Sickle Cell Anemia: Can It Help the Patient and Let Us See the Elephant in the Room?
    Am J Hematol. 2025 Sep 24. doi: 10.1002/ajh.70073.
    PubMed    
    
    
    
11. ZAIMOKU Y, Yamazaki H, Kanaya M, Hiramoto N, et al
    Loss-Prone HLA Class I Alleles Inform Outcomes of Early Hematopoietic Cell Transplantation in Acquired Aplastic Anemia.
    Am J Hematol. 2025 Sep 5. doi: 10.1002/ajh.70054.
    PubMed     Abstract available
    
    
    
12. CHEVALIER K, Holub M, Palich R, Blanckaert K, et al
    Cold Agglutinin Syndrome Secondary to Mycoplasma pneumoniae Infection in Adults: Results From a Large French Observational Study (MyCOLD Study).
    Am J Hematol. 2025;100:1557-1565.
    PubMed     Abstract available
    
    
    
13. ZADRO Y, Lusque A, Rey H, Cougoul P, et al
    Durable Responses With Front-Line Rituximab in Autoimmune Cytopenias Associated With Indolent B-Cell Clones.
    Am J Hematol. 2025;100:1670-1674.
    PubMed     Abstract available
    
    
    August 2025
14. ANDERSON JR, Hollenhorst MA
    Double Bite Cells in Oxidative Hemolytic Anemia.
    Am J Hematol. 2025 Aug 13. doi: 10.1002/ajh.70035.
    PubMed     Abstract available
    
    
    July 2025
15. AMARU R, Prchal J, Carrasco M, Mancilla S, et al
    History of Thrombosis at High Altitude Associates With Increased Erythropoietin.
    Am J Hematol. 2025 Jul 30. doi: 10.1002/ajh.70025.
    PubMed     Abstract available
    
    
    
16. HUET S, Kamdem A, Beaufront V, Yakouben K, et al
    Reversal of Glomerular Hyperfiltration Following Hematopoietic Stem Cell Transplantation in Children With Sickle-Cell Anemia.
    Am J Hematol. 2025 Jul 16. doi: 10.1002/ajh.70004.
    PubMed    
    
    
    
17. BOULARES A, Bragazzi NL, Gonzales GF, Robach P, et al
    Addressing Anemia in High-Altitude Populations: Global Impact, Prevalence, Challenges, and Potential Solutions.
    Am J Hematol. 2025 Jul 2. doi: 10.1002/ajh.27761.
    PubMed     Abstract available
    
    
    
18. MORRIS CR, Hatabah D, Korman R, Gillespie S, et al
    Arginine Therapy for Pain in Sickle Cell Disease: A Phase-2 Randomized, Placebo-Controlled Trial.
    Am J Hematol. 2025;100:1119-1131.
    PubMed     Abstract available
    
    
    
19. WANG D, Sra M, Glaeser-Khan S, Wang DY, et al
    Cost-Effectiveness of Ferritin Screening Thresholds for Iron Deficiency in Reproductive-Age Women.
    Am J Hematol. 2025;100:1132-1140.
    PubMed     Abstract available
    
    
    June 2025
20. BREWIN J, Clark B, Smith F, Parkin N, et al
    Loss of Function SPTA1 Variants Causes Neonatal Liver Failure and Fetal Anemia.
    Am J Hematol. 2025 Jun 26. doi: 10.1002/ajh.27751.
    PubMed    
    
    
    
21. MAFFIOLI M, Mora B, Iurlo A, Elli EM, et al
    The 2024 Three-Strata Baseline Anemia Definition of the Revised IWG-ELN Criteria Dissects Survival in Ruxolitinib-Treated Myelofibrosis Patients.
    Am J Hematol. 2025 Jun 6. doi: 10.1002/ajh.27734.
    PubMed    
    
    
    
22. RICCI E, Bagnasco F, Pierri F, Risitano A, et al
    Long-Term Outcome of Fanconi Anemia Patients From the Italian Registry on Behalf of the Marrow Failure Study Group of the AIEOP (Italian Association for Pediatric Haematology-Oncology).
    Am J Hematol. 2025 Jun 6. doi: 10.1002/ajh.27724.
    PubMed     Abstract available
    
    
    May 2025
23. JACOBS JW, Raza S, Clark LM, Stephens LD, et al
    Mixed Autoimmune Hemolytic Anemia: A Systematic Review of Epidemiology, Clinical Characteristics, Therapies, and Outcomes.
    Am J Hematol. 2025 May 20. doi: 10.1002/ajh.27721.
    PubMed     Abstract available
    
    
    
24. MEJIAS-FIGUEROA JA, Rodeghier M, DeBaun MR
    Impact of Switching From Race-Based to Race-Neutral Spirometry Reference Equations in Children With Sickle Cell Anemia.
    Am J Hematol. 2025 May 12. doi: 10.1002/ajh.27704.
    PubMed    
    
    
    
25. BESHAI M, Alhomsi N, Warkentin TE
    Thrombocytopenia and Anemia After Cardiac Surgery.
    Am J Hematol. 2025 May 2. doi: 10.1002/ajh.27696.
    PubMed    
    
    
    
26. TRAETS MJM, Bos JF, van der Veen S, van Pelt L, et al
    Pyruvate Kinase Function Correlates With Red Blood Cell Properties and Clinical Manifestations in Sickle Cell Disease.
    Am J Hematol. 2025;100:785-796.
    PubMed     Abstract available
    
    
    
27. MAGAGNOLI J, Knopf K, Hrushesky WJ, Carson KR, et al
    Ferric Carboxymaltose (FCM)-Associated Hypophosphatemia (HPP): A Systematic Review.
    Am J Hematol. 2025;100:840-846.
    PubMed     Abstract available
    
    
    April 2025
28. ZAHR RS, Kang G, Zhang X, Rashkin SR, et al
    Development of Polygenic Risk Score for Persistent Albuminuria in Children and Adults With Sickle Cell Anemia.
    Am J Hematol. 2025 Apr 5. doi: 10.1002/ajh.27678.
    PubMed     Abstract available
    
    
    March 2025
29. GANGAT N, Tefferi A
    Emerging Pathogenetic Mechanisms and New Drugs for Anemia in Myelofibrosis and Myelodysplastic Syndromes.
    Am J Hematol. 2025 Mar 8. doi: 10.1002/ajh.27659.
    PubMed     Abstract available
    
    
    
30. JIANG D, Sampino EV, Rosenlind K, Campagna DR, et al
    Expanding the Phenotype of DNA Ligase 1 Deficiency: First Report of Macrocytic Sideroblastic Anemia.
    Am J Hematol. 2025 Mar 7. doi: 10.1002/ajh.27649.
    PubMed    
    
    
    February 2025
31. NAAMANSEN AB, Hansen DL, Petersen J, Glenthoj A, et al
    10-Year Risk of Gallstones in Congenital Red Blood Cell Disorder Patients: A Nationwide Cohort Study.
    Am J Hematol. 2025;100:229-235.
    PubMed     Abstract available
    
    
    January 2025
32. FATTIZZO B, Gurnari C, Giammarco S, Ricchiuti A, et al
    Elderly Patients With Aplastic Anemia: Treatment Patterns and Outcomes in the Real World.
    Am J Hematol. 2025 Jan 29. doi: 10.1002/ajh.27611.
    PubMed     Abstract available
    
    
    
33. WANG CY, Melgar-Bermudez E, Welch D, Dagbay KB, et al
    A Recombinant Antibody Against ALK2 Promotes Tissue Iron Redistribution and Contributes to Anemia Resolution in a Mouse Model of Anemia of Inflammation.
    Am J Hematol. 2025 Jan 10. doi: 10.1002/ajh.27578.
    PubMed     Abstract available
    
    
    
34. KONTE K, Afzali-Hashemi L, Baas KPA, Schrantee A, et al
    Effect of voxelotor on cerebral perfusion and cerebral oxygen metabolism and cardiac stress in adult patients with sickle cell disease.
    Am J Hematol. 2025;100:78-84.
    PubMed     Abstract available
    
    
    
35. ROSATO BE, D'Onofrio V, Marra R, Nostroso A, et al
    RAS signaling pathway is essential in regulating PIEZO1-mediated hepatic iron overload in dehydrated hereditary stomatocytosis.
    Am J Hematol. 2025;100:52-65.
    PubMed     Abstract available
    
    
    
36. BOU-FAKHREDIN R, Cappellini MD, Taher AT, De Franceschi L, et al
    Hypercoagulability in hemoglobinopathies: Decoding the thrombotic threat.
    Am J Hematol. 2025;100:103-115.
    PubMed     Abstract available
    
    
    December 2024
37. LIN X, Yang C, Zhuang J, Li J, et al
    Rituximab Plus Bortezomib for Relapsed and Refractory Warm Autoimmune Hemolytic Anemia: A Prospective Phase 2 Trial.
    Am J Hematol. 2024 Dec 21. doi: 10.1002/ajh.27540.
    PubMed    
    
    
    
38. STUTE P, Akpan IJ, Breymann C, Murji A, et al
    Effect of Ferric Derisomaltose on Fatigue in Iron Deficiency Anemia Associated With Abnormal Uterine Bleeding.
    Am J Hematol. 2024 Dec 12. doi: 10.1002/ajh.27555.
    PubMed    
    
    
    
39. SISSOKO A, Cisse A, Duverdier C, Marin M, et al
    Clearance of pathogenic erythrocytes is maintained despite spleen dysfunction in children with sickle cell disease.
    Am J Hematol. 2024;99:2267-2278.
    PubMed     Abstract available
    
    
    November 2024
40. RAMIREZ MJ, Pujol R, Minguillon J, Bogliolo M, et al
    Prognostic significance of mutation type and chromosome fragility in Fanconi anemia.
    Am J Hematol. 2024 Nov 19. doi: 10.1002/ajh.27520.
    PubMed     Abstract available
    
    
    
41. MOSTAFA MA, Zand M, Taylor J, Kouides P, et al
    Successful 13-year ongoing remission with C5 inhibitor therapy following renal transplant in atypical hemolytic uremic syndrome.
    Am J Hematol. 2024;99:2241-2243.
    PubMed    
    
    
    
42. KULASEKARARAJ A, Lanza F, Arvanitakis A, Langemeijer S, et al
    Comparative clinical efficacy and safety of biosimilar ABP 959 and eculizumab reference product in patients with paroxysmal nocturnal hemoglobinuria.
    Am J Hematol. 2024;99:2108-2117.
    PubMed     Abstract available
    
    
    
43. VAN DOREN L, Brugnara C
    Self-pay laboratory charges for iron deficiency diagnosis in the Boston and New Haven metropolitan areas.
    Am J Hematol. 2024;99:2233-2235.
    PubMed    
    
    
    
44. CUMMINGS OW, Rahman S, Fletcher L, Scott AW, et al
    Advances in sickle cell retinopathy screening techniques, tests, and practices: A systematic review.
    Am J Hematol. 2024;99:2152-2163.
    PubMed     Abstract available
    
    
    
45. LAL A, Viprakasit V, Vichinsky E, Lai Y, et al
    Disease burden, management strategies, and unmet needs in alpha-thalassemia due to hemoglobin H disease.
    Am J Hematol. 2024;99:2164-2177.
    PubMed     Abstract available
    
    
    October 2024
46. BARCELLINI W, Pane F, Patriarca A, Murakhovskaya I, et al
    Parsaclisib for the treatment of primary autoimmune hemolytic anemia: Results from a phase 2, open-label study.
    Am J Hematol. 2024 Oct 22. doi: 10.1002/ajh.27493.
    PubMed     Abstract available
    
    
    
47. CONNES P, Stauffer E, Liem RI, Nader E, et al
    Exercise and training in sickle cell disease: Safety, potential benefits, and recommendations.
    Am J Hematol. 2024;99:1988-2001.
    PubMed     Abstract available
    
    
    
48. ARNOLD SD, Bakshi N, Ross D, Smith C, et al
    Long-term quality of life after hematopoietic cell transplant for sickle cell disease in childhood: A STELLAR interim analysis.
    Am J Hematol. 2024;99:2037-2040.
    PubMed     Abstract available
    
    
    
49. CASELLA JF, Furstenau DK, Adams RJ, Brambilla DJ, et al
    Hydroxyurea to prevent brain injury in children with sickle cell disease (HU Prevent)-A randomized, placebo-controlled phase II feasibility/pilot study.
    Am J Hematol. 2024;99:1906-1916.
    PubMed     Abstract available
    
    
    September 2024
50. BOUCHER AA, Dayton VJ, Pratt AR, Nassar NN, et al
    Three-generation female cohort with macrocytic anemia and iron overload.
    Am J Hematol. 2024 Sep 27. doi: 10.1002/ajh.27489.
    PubMed    
    
    
    
51. DELAFOY M, Dalle JH, Pondarre C, Andrieu GP, et al
    Assessing acute toxicity profiles of HLA-identical hematopoietic stem cell transplantation in pediatric patients with sickle cell anemia: A comprehensive analysis on behalf of the SFGM-TC.
    Am J Hematol. 2024 Sep 24. doi: 10.1002/ajh.27486.
    PubMed    
    
    
    
52. YOUNG DJ
    A growing panoply of options for patients with paroxysmal nocturnal hemoglobinuria.
    Am J Hematol. 2024;99:1667-1669.
    PubMed    
    
    
    
53. SCHEINBERG P, Cle DV, Kim JS, Nur E, et al
    Phase 3 randomized COMMODORE 1 trial: Crovalimab versus eculizumab in complement inhibitor-experienced patients with paroxysmal nocturnal hemoglobinuria.
    Am J Hematol. 2024;99:1757-1767.
    PubMed     Abstract available
    
    
    
54. TORRES C, Galadanci N, Osborn J, Kanter J, et al
    Real-world implementation of the David-Carroll buprenorphine protocol for pain management in sickle cell disease.
    Am J Hematol. 2024;99:1834-1836.
    PubMed    
    
    
    
55. ROTH A, He G, Tong H, Lin Z, et al
    Phase 3 randomized COMMODORE 2 trial: Crovalimab versus eculizumab in patients with paroxysmal nocturnal hemoglobinuria naive to complement inhibition.
    Am J Hematol. 2024;99:1768-1777.
    PubMed     Abstract available
    
    
    August 2024
56. MEANS RT JR, Bi C, Wong ECC, Bare LA, et al
    Ferritin reference intervals in a population of working-age adults without anemia.
    Am J Hematol. 2024 Aug 5. doi: 10.1002/ajh.27444.
    PubMed    
    
    
    
57. ACHOUR A, Knijnenburg J, Koopmann T, Raz A, et al
    Moderate-severe beta-thalassemia intermedia phenotype caused by sextuplicated alpha-globin gene allele in two beta-thalassemia carriers.
    Am J Hematol. 2024;99:1655-1658.
    PubMed    
    
    
    
58. YU EA, Zacharias HU, Kelly S, Vichinsky E, et al
    Improving healthspan among people with sickle cell disease: Leveraging precision health in an era of treatments with curative intent.
    Am J Hematol. 2024;99:1456-1458.
    PubMed    
    
    
    
59. BORTOLOTTI M, Trikha R, Salter S, Large J, et al
    Pregnancy in acquired bone marrow failure syndromes: Antenatal management and maternal and fetal outcomes.
    Am J Hematol. 2024;99:1647-1650.
    PubMed    
    
    
    
60. ITO S, Wang D, Purcell A, Chetlapalli K, et al
    Cost-effectiveness of sutimlimab in cold agglutinin disease.
    Am J Hematol. 2024;99:1475-1484.
    PubMed     Abstract available
    
    
    
61. DOVERN E, Aydin M, Hazenberg MD, Tang MW, et al
    Azathioprine/hydroxyurea preconditioning prior to nonmyeloablative matched sibling donor hematopoietic stem cell transplantation in adults with sickle cell disease: A prospective observational cohort study.
    Am J Hematol. 2024;99:1523-1531.
    PubMed     Abstract available
    
    
    
62. WEN S, Nisenbaum R, Weyand AC, Tang GH, et al
    High prevalence of iron deficiency and socioeconomic disparities in laboratory screening of non-pregnant females of reproductive age: A retrospective cohort study.
    Am J Hematol. 2024;99:1492-1499.
    PubMed     Abstract available
    
    
    
63. BORGEY M, Genty I, Habibi A, Arlet JB, et al
    High risk of progression for chronic major organ complications of sickle cell disease in adolescents and young adults: A long-term neonatal cohort study.
    Am J Hematol. 2024;99:1601-1605.
    PubMed    
    
    
    
64. VUONG C, Eckhardt CL, Heijboer H, Suijker MH, et al
    Long-term follow-up of children with sickle cell disease diagnosed by newborn screening in the Netherlands: Overview of morbidity and mortality.
    Am J Hematol. 2024;99:1606-1609.
    PubMed    
    
    
    
65. SUN R, Srivastava A, Derebail VK, Han J, et al
    GLP-1 agonists and SGLT-2 inhibitors in adults with sickle cell disease.
    Am J Hematol. 2024;99:1610-1612.
    PubMed    
    
    
    
66. LUGTHART G, Verweij EJT, Harteveld CL, Tan RNGB, et al
    Suppression of Hb Bart's to improve tissue oxygenation and fetal development in homozygous alpha-thalassemia.
    Am J Hematol. 2024;99:1613-1615.
    PubMed     Abstract available
    
    
    July 2024
67. VINCHI F
    New partners for Luspatercept in beta-thalassemia.
    Am J Hematol. 2024;99:1217-1219.
    PubMed    
    
    
    
68. KUO KHM, Grace RF, van Beers EJ, Barcellini W, et al
    Clinically meaningful improvements in patient-reported outcomes in mitapivat-treated patients with pyruvate kinase deficiency.
    Am J Hematol. 2024;99:1415-1419.
    PubMed     Abstract available
    
    
    
69. GUERRA A, Hamilton N, Rivera A, Demsko P, et al
    Combination of a TGF-beta ligand trap (RAP-GRL) and TMPRSS6-ASO is superior for correcting beta-thalassemia.
    Am J Hematol. 2024;99:1300-1312.
    PubMed     Abstract available
    
    
    
70. PLACAIS M, Laparra A, Maria ATJ, Kramkimel N, et al
    Drug-induced autoimmune hemolytic anemias related to immune checkpoint inhibitors, therapeutic management, and outcome.
    Am J Hematol. 2024;99:1427-1430.
    PubMed    
    
    
    
71. TANZI E, Di Modica SM, Bordini J, Olivari V, et al
    Bone marrow Tfr2 deletion improves the therapeutic efficacy of the activin-receptor ligand trap RAP-536 in beta-thalassemic mice.
    Am J Hematol. 2024;99:1313-1325.
    PubMed     Abstract available
    
    
    
72. WANG Z, Jiang B, Song L, Sun M, et al
    Patients with acquired pure red cell aplasia respond to PI3Kdelta inhibitor rapidly.
    Am J Hematol. 2024;99:1431-1433.
    PubMed    
    
    
    
73. CASTRO OL, De Franceschi L, Ganz T, Kanter J, et al
    Iron restriction in sickle cell disease: When less is more.
    Am J Hematol. 2024;99:1349-1359.
    PubMed     Abstract available
    
    
    
74. VAN DOREN L, Steinheiser M, Boykin K, Taylor KJ, et al
    Expert consensus guidelines: Intravenous iron uses, formulations, administration, and management of reactions.
    Am J Hematol. 2024;99:1338-1348.
    PubMed     Abstract available
    
    
    June 2024
75. GANGAT N, Tefferi A
    Targeting anemia in myeloid neoplasms.
    Am J Hematol. 2024 Jun 5. doi: 10.1002/ajh.27408.
    PubMed     Abstract available
    
    
    
76. TUBMAN VN, Maysonet D, Estrada N, Halder T, et al
    Unswitched memory B cell deficiency in children with sickle cell disease and response to pneumococcal polysaccharide vaccine.
    Am J Hematol. 2024;99:1084-1094.
    PubMed     Abstract available
    
    
    
77. RONDELLI D
    Non-myeloablative allogeneic HSCT in adult patients with sickle cell disease: Multiple take-home points from the Saudi Arabia experience.
    Am J Hematol. 2024;99:1021-1022.
    PubMed    
    
    
    
78. MINNITI CP
    Let's get "real" in sickle cell disease: Real-world data and long-term patients' registries.
    Am J Hematol. 2024;99:1019-1020.
    PubMed    
    
    
    
79. DOVERN E, Aydin M, DeBaun MR, Alizade K, et al
    Effect of allogeneic hematopoietic stem cell transplantation on sickle cell disease-related organ complications: A systematic review and meta-analysis.
    Am J Hematol. 2024;99:1129-1141.
    PubMed     Abstract available
    
    
    
80. DAMLAJ M, Alahmari B, Alaskar A, Alhejazi A, et al
    Favorable outcome of non-myeloablative allogeneic transplantation in adult patients with severe sickle cell disease: A single center experience of 200 patients.
    Am J Hematol. 2024;99:1023-1030.
    PubMed     Abstract available
    
    
    
81. KWIATKOWSKI JL, Thompson AA, Tricta F, Temin NT, et al
    Real-world evidence: Long-term safety of deferiprone in a large cohort of patients with sickle cell disease enrolled in a registry for up to 10 years.
    Am J Hematol. 2024;99:1031-1039.
    PubMed     Abstract available
    
    
    
82. JACOBS JW, Stephens LD, Chooljian DM, Sharma D, et al
    Crizanlizumab and sickle cell disease: When should medications have their approval status revoked?
    Am J Hematol. 2024;99:1016-1018.
    PubMed    
    
    
    
83. DE LIGT LA, Gaartman AE, Biemond BJ, Fijnvandraat K, et al
    Neutrophils in sickle cell disease: Exploring their potential role as a therapeutic target.
    Am J Hematol. 2024;99:1119-1128.
    PubMed     Abstract available
    
    
    May 2024
84. BROUSSE V, El Hoss S, Isnard P, Laurance S, et al
    Comparative histological analysis of spleens in pediatric patients with hemolytic anemias: Insights into the pathophysiological mechanisms of spleen destruction in sickle cell anemia.
    Am J Hematol. 2024 May 22. doi: 10.1002/ajh.27374.
    PubMed     Abstract available
    
    
    
85. MICHEL M, Sair M, Riviere E, Moulis G, et al
    Intravenous immunoglobulin as a rescue therapy for severe adult autoimmune hemolytic anemia: Results from a French multicenter observational study.
    Am J Hematol. 2024 May 14. doi: 10.1002/ajh.27361.
    PubMed    
    
    
    
86. NJOKU F, Pugh N, Brambilla D, Kroner B, et al
    Mortality in adults with sickle cell disease: Results from the sickle cell disease implementation consortium (SCDIC) registry.
    Am J Hematol. 2024;99:900-909.
    PubMed     Abstract available
    
    
    
87. GRIFFIN M, Kelly R, Brindel I, Maafa L, et al
    Real-world experience of pegcetacoplan in paroxysmal nocturnal hemoglobinuria.
    Am J Hematol. 2024;99:816-823.
    PubMed     Abstract available
    
    
    April 2024
88. MARRA R, Nostroso A, Rosato BE, Esposito FM, et al
    Unveiling the genetic landscape of suspected congenital dyserythropoietic anemia type I: A retrospective cohort study of 36 patients.
    Am J Hematol. 2024 Apr 26. doi: 10.1002/ajh.27350.
    PubMed     Abstract available
    
    
    
89. YOSHIMI A, Noellke P, Stary J, Kallay K, et al
    Comparison of outcomes of immunosuppressive therapy with rabbit versus horse antithymocyte globulin and cyclosporine a in children with acquired severe aplastic anemia.
    Am J Hematol. 2024 Apr 15. doi: 10.1002/ajh.27334.
    PubMed    
    
    
    
90. JACKSON TA, Buscetta AJ, Ramirez HC, Bonham VL Jr, et al
    Leg ulcers are indicators of systemic dysfunction in individuals with sickle cell disease.
    Am J Hematol. 2024;99:767-769.
    PubMed     Abstract available
    
    
    
91. FATTIZZO B, Roth A, Broome CM, Khan U, et al
    COVID-19 vaccine safety and immunogenicity in patients with cold agglutinin disease receiving concomitant sutimlimab.
    Am J Hematol. 2024;99:789-791.
    PubMed     Abstract available
    
    
    
92. EAPEN M, Kou J, Andreansky M, Bhatia M, et al
    Long-term outcomes after unrelated donor transplantation for severe sickle cell disease on the BMT CTN 0601 trial.
    Am J Hematol. 2024;99:785-788.
    PubMed    
    
    
    
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94. ALLALI S, Galacteros F, Oevermann L, Cannas G, et al
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    March 2024
95. GIARDINO S, Eikema DJ, Piepenbroek B, Algeri M, et al
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    A randomized double-blind pilot study to evaluate the efficacy, safety, and tolerability of intravenous iron versus oral iron for the treatment of restless legs syndrome in patients with iron deficiency anemia.
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97. SICA M, Notaro R
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98. MUSALLAM KM, Barella S, Origa R, Ferrero GB, et al
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99. JACOBS JW, Booth GS, Woo JS, Adkins BD, et al
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100. CORBACIOGLU S, Frangoul H, Locatelli F, Hobbs W, et al
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101. LOCATELLI F, Corbacioglu S, Hobbs W, Frangoul H, et al
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103. ABDULLAHI SU, Sunusi S, Aminu H, Umar R, et al
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104. TEFFERI A, Pardanani A, Gangat N
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105. SOUISSI M, Daliphard S, Picard V, Lebigot E, et al
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106. CHEN M, Hankins JS, Zhang M, Ataga KI, et al
     Comparative pharmacovigilance assessment of adverse events associated with the use of hydroxyurea, L-glutamine, voxelotor, and crizanlizumab in sickle cell disease.
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107. AFZALI-HASHEMI L, Dovern E, Baas KPA, Schrantee A, et al
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108. GARBOWSKI MW, Ugidos M, Risueno A, Shetty JK, et al
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     January 2024
109. SHAGIDOV D, Guttmann-Raviv N, Cunat S, Frech L, et al
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110. SEIDL E, Wilson D, Odame I, Kirby-Allen M, et al
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112. SOULIE A, Kamdem A, Neumann F, Hau I, et al
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113. HATEM A, Esperti S, Murciano N, Qiao M, et al
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114. BARAKAT A, Jasuja R, Tomlinson L, Wenzel Z, et al
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     November 2023
115. KHO S, Siregar NC, Qotrunnada L, Fricot A, et al
     Retention of uninfected red blood cells causing congestive splenomegaly is the major mechanism of anemia in malaria.
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116. HONG HG, Gouveia MH, Ogwang MD, Kerchan P, et al
     Sickle cell allele HBB-rs334(T) is associated with decreased risk of childhood Burkitt lymphoma in East Africa.
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117. KUTER DJ, Piatek C, Roth A, Siddiqui A, et al
     Fostamatinib for warm antibody autoimmune hemolytic anemia: Phase 3, randomized, double-blind, placebo-controlled, global study (FORWARD).
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118. PINCEZ T, Lettre G
     Re-assessing the effect of fetal hemoglobin on stroke in the Cooperative Study of Sickle Cell Disease.
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119. THOMAS B, Visanica S, Poussing S, Gerard D, et al
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121. DI MAURO M, El Hoss S, Nardo-Marino A, Stuart-Smith S, et al
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     October 2023
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123. ARCHER NM, Gnangnon B, Mikdar M, Ciuculescu MF, et al
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124. STEINBERG MH, Gladwin MT
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125. WALSH PS, Brousseau DC, Coleman KD
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126. VAN DIJK MJ, van Oirschot BA, Harrison AN, Recktenwald SM, et al
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127. PORTER JB, Scrimgeour A, Martinez A, James L, et al
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128. LIU H, Xia L, Weng J, Zhang F, et al
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129. ELALFY MS, Hamdy M, Adly A, Ebeid FSE, et al
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130. MUSALLAM KM, Lombard L, Kistler KD, Arregui M, et al
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131. VON SIEBENTHAL HK, Moretti D, Zimmermann MB, Stoffel NU, et al
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132. NYANGASA S, Solomon D, Njiro B, Faisal A, et al
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133. PIRAN S, Alhomsi N, Warkentin TE
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135. AGARWAL S, Stanek JR, Vesely SK, Creary SE, et al
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136. PATNAIK MM, Tefferi A
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137. SACHDEV V, Limerick E, Nguyen ML, Li W, et al
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138. ROTH A, Barcellini W, D'Sa S, Miyakawa Y, et al
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139. LANINO L, Restuccia F, Perego A, Ubezio M, et al
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140. GROS M, Pondarre C, Arnaud C, Kamdem A, et al
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143. MCGLOTHLIN J, Abeykoon J, Al-Hattab E, Ashrani AA, et al
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144. POWERS JM, Auerbach M
     When taking iron, a glass of orange juice a day keeps anemia away.
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145. RIBEIL JA, Pollock G, Frangoul H, Steinberg MH, et al
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146. ALLALI S, Elie J, Mayrand L, de Montalembert M, et al
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147. D'ALESSANDRO A, Nouraie SM, Zhang Y, Cendali F, et al
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     June 2023
148. URIO F, Nkya S, Mgaya J, Rooks H, et al
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149. PINTO VM, Russo R, Quintino S, Rosato BE, et al
     Coinheritance of PIEZO1 variants and multi-locus red blood cell defects account for the symptomatic phenotype in beta-thalassemia carriers.
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150. BORDONI V, Casale M, Pinto VM, Carsetti R, et al
     Inflammatory and senescence-associated mediators affect the persistence of humoral response to COVID-19 mRNA vaccination in transfusion-dependent beta-thalassemic patients.
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151. CHEN PH, Gorshein E, Tormey C, Siddon AJ, et al
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     May 2023
152. PEFFAULT DE LATOUR R, Risitano AM
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153. KULASEKARARAJ AG, Lazana I
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154. DUVAL A, Fremeaux-Bacchi V
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155. LEON J, LeStang MB, Sberro-Soussan R, Servais A, et al
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156. PANSE J
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157. DIAMANTOPOULOS PT, Solomou E, Symeonidis A, Pappa V, et al
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158. POURDIEU C, El Hoss S, Le Roux E, Pages J, et al
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     April 2023
160. TEFFERI A, Vannucchi AM
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161. AGGARWAL N, Manley AL, Shalhoub R, Durrani J, et al
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162. ONI MO, Archer NM
     Intranasal fentanyl works-Why are we not using it more to treat acute pain in sickle cell disease?
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163. REES CA, Brousseau DC, Ahmad FA, Bennett J, et al
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164. REDJOUL R, Beckerich F, de Luna G, Leclerc M, et al
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     March 2023
165. RISINGER M, Kim PS, Rodriguez RX, Narvaez Rivas M, et al
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167. LANSER L, Plaikner M, Schroll A, Burkert FR, et al
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