Am J Hematol

1. 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.
   

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2. 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.
   

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   Blood

3. 
   Transplant outcome in pediatric Fanconi anemia.
   Blood. 2024;144:1350.
   

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4. SATTY AM
   Fanconi anemia: realizing hematopoietic cure.
   Blood. 2024;144:1245-1246.
   

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5. VADIVELAN A, Doyle EK, Carson S, Denton C, et al
   Significant pituitary siderosis is common in transfusion-dependent sickle cell disease.
   Blood. 2024;144:1457-1459.
   

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6. DUCAMP S, Sendamarai AK, Campagna DR, Chin DWL, et al
   Murine models of erythroid 5ALA synthesis disorders and their conditional synthetic lethal dependency on pyridoxine.
   Blood. 2024;144:1418-1432.
   

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   Br J Haematol

7. CATELLA J, Turpin E, Connes P, Nader E, et al
   Impaired microvascular function in patients with sickle cell anemia and leg ulcers improved with healing.
   Br J Haematol. 2024 Sep 24. doi: 10.1111/bjh.19785.
   

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   Hemoglobin

8. PAN L, Wang Y, Lin H, Zhang X, et al
   A Novel Frameshift Mutation(HBA2:C.337delC) Associated With alpha-Thalassemia Trait Detected by Next-Generation Sequencing in Southern China.
   Hemoglobin. 2024;48:200-202.
   

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9. HE X, Tian P, Zhong L, Peng S, et al
   A Novel 165 Kb Duplication Involving the alpha-Globin Gene Cluster Is Identified by Low-Pass Whole Genome Sequencing in a Chinese Thalassemia Intermedia Patient.
   Hemoglobin. 2024;48:203-208.
   

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10. IBRAHIM L, Gwarzo DH, Yusuf AA
    Secretory Phospholipase A2 Levels Are High in Women with Sickle Cell Disease and Menstruation-Induced Vaso-Occlusive Crises.
    Hemoglobin. 2024;48:175-181.
    

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11. RAVICHANDRAN S, Hoffmann M, Petersen J, Sjo L, et al
    A Rare Case of De Novo Beta-Thalassemia Diagnosed by Whole-Genome Sequencing in an Ethnically Danish Newborn.
    Hemoglobin. 2024;48:196-199.
    

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12. ADEGOKE SA, Makalo L, Sallah A, Saine H, et al
    Point-of-Care Newborn Screening for Sickle Cell Disease at Selected Health Facilities in the Gambia.
    Hemoglobin. 2024;48:169-174.
    

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13. BHATTACHARJEE S, Ghosh S, Shaw J, Bhattacharjee S, et al
    Thalidomide and Hydroxyurea in Transfusion-Dependent Thalassemia: Efficacy, Safety Profile and Impact on Quality of Life.
    Hemoglobin. 2024;48:161-168.
    

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14. YAO C, Chen L, Ma J, Li N, et al
    A Novel Frameshift Mutation of HBB Causing Dominant beta-Thalassemia in a Chinese Individual.
    Hemoglobin. 2024;48:182-185.
    

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15. SINGH R, Halder R, Hemant Gupta V, Rainchwar S, et al
    ATG-Thymoglobulin Versus ATG-Fresenius for Conditioning in Thalassemia Patients Who Underwent Allogenic Stem Cell Transplantation from Matched-Sibling Donor: A Tertiary Cancer Care Center Short-Term Experience.
    Hemoglobin. 2024;48:186-191.
    

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16. ASRI AS, Samsuddin MH, Jalil N, Mohamad Tahir N, et al
    Characterization of Hemoglobin Malay Phenotypes in Tertiary Hospitals.
    Hemoglobin. 2024;48:153-160.
    

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17. RAO E, Patel D, Saxena N, Saha KB, et al
    Ameliorating Mental Health Issues in Sickle Cell Disease Patients: A Viewpoint.
    Hemoglobin. 2024;48:212-213.
    

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    J Pediatr Hematol Oncol

18. AGARWALA S, Kalra M, Sachdeva A, Anand K, et al
    Paroxysmal Cold Hemoglobinuria: Mild to Catastrophic-Spectrum of a Rare Hemolytic Anemia of Childhood.
    J Pediatr Hematol Oncol. 2024 Sep 25. doi: 10.1097/MPH.0000000000002953.
    

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19. ABDELKADER S, Shah R, Crawford D, Baker A, et al
    Haploidentical Stem Cell Transplants in Children With Sickle Cell Disease: A Single Center Real-world Experience.
    J Pediatr Hematol Oncol. 2024;46:e556-e557.
    

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20. RAFFA EH, Raffa L, Almadani S, Murad W, et al
    Optical Coherence Tomography Angiography of Macular Microangiopathy in Children With Sickle Cell Disease.
    J Pediatr Hematol Oncol. 2024;46:349-355.
    

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    Nephrol Dial Transplant

21. STOUMPOS S, Crowe K, Sarafidis P, Barratt J, et al
    Hypoxia-inducible factor prolyl hydroxylase inhibitors for anaemia in chronic kidney disease: a document by the European Renal Best Practice board of the European Renal Association.
    Nephrol Dial Transplant. 2024 Apr 4:gfae075. doi: 10.1093.
    

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22. KOROTCHAEVA Y, Kozlovskaya N, Shifman E, Kudlay D, et al
    Eculizumab for pregnancy-related atypical hemolytic uremic syndrome.
    Nephrol Dial Transplant. 2024;39:1731-1733.
    

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