Am J Hematol

1. 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.
   

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   Ann Hematol

2. 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.
   Ann Hematol. 2024 Apr 24. doi: 10.1007/s00277-024-05756.
   

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3. 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.
   Ann Hematol. 2024 Apr 22. doi: 10.1007/s00277-024-05746.
   

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   Blood

4. MONTORO J, Eikema DJ, Tuffnell J, Potter V, et al
   Alternative donor transplantation for severe aplastic anemia: a comparative study of the SAAWP EBMT.
   Blood. 2024 Apr 21:blood.2024024173. doi: 10.1182/blood.2024024173.
   

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   Hemoglobin

5. LIU D, Nong X, Lai F, Nong C, et al
   Noninvasive Prenatal Diagnosis of SEA-Thalassemia by Combining 1000 Genomes Database and Relative Haplotype Dosage.
   Hemoglobin. 2024;48:71-78.
   

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6. VOUSVOUKI M, Delaki EE, Boutou E, Yfanti E, et al
   A New alpha1-Globin Variant, Hb Ormylia [HBA1:c.63C > G; p.His21Gln]. Report of Eleven Cases in Northern Greece.
   Hemoglobin. 2024;48:133-137.
   

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7. ASSAF N, El Zibaoui R, Monsef C, Abi Nassif T, et al
   Severe Transfusion-Dependent Thalassemia in Compound Heterozygote Palestinian Siblings with Two alpha-Globin Gene Defects, Hb Taybe D HBA1: C.119_121delCCA Mutation and HBA2: C.*94A > G Mutation.
   Hemoglobin. 2024;48:129-132.
   

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8. CHIN N, Asnani M
   Poor Sleep Quality in Jamaican Adults With Sickle Cell Disease: Prevalence, Risk Factors, and Association With Quality of Life.
   Hemoglobin. 2024;48:87-93.
   

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9. WAYE JS, Hanna M, Hohenadel BA, Nakamura L, et al
   Newborn Screening for beta-Thalassemia Identifies a Complex Genotype Involving a Novel beta-Globin Gene Mutation (HBB:c.336dup).
   Hemoglobin. 2024;48:113-115.
   

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10. AL-ALLAWI N, Atroshi SD, Sadullah RK, Eissa AA, et al
    A Population-Oriented Genetic Scoring System to Predict Phenotype: A Pathway to Personalized Medicine in Iraqis With beta-Thalassemia.
    Hemoglobin. 2024;48:94-100.
    

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11. WAYE JS, Hanna M, Nakamura L, Walker L, et al
    Splice Acceptor Mutation [HBB:c.93-2A > T] in a Patient with Hb S/beta(0)-Thalassemia.
    Hemoglobin. 2024;48:116-117.
    

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    J Pediatr Hematol Oncol

12. CREGO N, Douglas C, Bonnabeau E, Eason K, et al
    Opioid Use Among Children and Adults With Sickle Cell Disease in North Carolina Medicaid Enrollees in the Era of Opioid Harm Reduction.
    J Pediatr Hematol Oncol. 2024;46:181-187.
    

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    Kidney Int

13. CHE M, Moran SM, Smith RJ, Ren KYM, et al
    A case-based narrative review of pregnancy-associated atypical hemolytic uremic syndrome/complement-mediated thrombotic microangiopathy.
    Kidney Int. 2024;105:960-970.
    

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14. MAISONS V, Duval A, Mesnard L, Frimat M, et al
    Assessment of epidemiology and outcomes of adult patients with kidney-limited thrombotic microangiopathies.
    Kidney Int. 2024;105:1100-1112.
    

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    Minerva Pediatr (Torino)

15. RIBILOTTA A, Sergio M, Scarponi D
    Parental stress in the relationship with children affected by chronic hematologic disease.
    Minerva Pediatr (Torino). 2024;76:173-179.
    

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    Nephrol Dial Transplant

16. MACDOUGALL IC
    Anaemia in CKD-treatment standard.
    Nephrol Dial Transplant. 2024;39:770-777.
    

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    PLoS One

17. ADUGNA DG, Mengstie MA, Admasu FT, Teshome MG, et al
    Multilevel analysis of anemia and associated factors among women of reproductive age (15-49 years) in Liberia: Evidence from the 2019/20 Liberia demographic and health survey data.
    PLoS One. 2024;19:e0296747.
    

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18. KAREKEZI P, Nzabakiriraho JD, Gayawan E
    Modeling the shared risks of malaria and anemia in Rwanda.
    PLoS One. 2024;19:e0298259.
    

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19. RAZAZI K, Berti E, Cecchini J, Carteaux G, et al
    Decreased risk of underdosing with continuous infusion versus intermittent administration of cefotaxime in patients with sickle cell disease and acute chest syndrome.
    PLoS One. 2024;19:e0302298.
    

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