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01.06.2026

2 Am J Hematol
3 Ann Hematol
1 Blood
11 Hemoglobin
1 N Engl J Med
4 PLoS One


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Single Articles


    Am J Hematol

  1. BERNAUDIN F, Verlhac S, Ducros-Miralles E, Arnaud C, et al
    Better 10-Year Cerebrovascular Outcome After Transplant Than on Standard-Care in Sickle Cell Anemia: DREPAGREFFE Trial.
    Am J Hematol. 2026 May 28. doi: 10.1002/ajh.70336.
    PubMed         Abstract available


  2. Correction to "DNA Methylation Episignature as a Novel Diagnostic Tool for Diamond-Blackfan Anemia Syndrome".
    Am J Hematol. 2026 May 24. doi: 10.1002/ajh.70378.
    PubMed        


    Ann Hematol

  3. CHEN D, Mo W, Gao L, Liu W, et al
    Sarcopenia-associated CD8(+) T-cell reconstitution predicts poor outcomes in severe aplastic anemia after hematopoietic stem cell transplantation.
    Ann Hematol. 2026 May 29. doi: 10.1007/s00277-026-07093.
    PubMed         Abstract available

  4. AVCU G, Karadas N, Gadashova A, Onder C, et al
    Febrile neutropenia in pediatric acquired aplastic anemia: a 20-year analysis of infections and mortality.
    Ann Hematol. 2026 May 25. doi: 10.1007/s00277-026-06874.
    PubMed         Abstract available

  5. MANZ K, Kobrosly M, Crodel CC, Al-Ali H, et al
    Value of functional iron parameters in diagnostic re-assessment of MPN: refinement of iron-deficiency markers by zinc protoporphyrin (ZPP).
    Ann Hematol. 2026;105:294.
    PubMed         Abstract available


    Blood

  6. LING T, Bezavada L, Mehmood R, Zhang K, et al
    The GATA1 N terminus coordinates metabolic reprogramming in erythropoiesis.
    Blood. 2026;147:2666-2681.
    PubMed         Abstract available


    Hemoglobin

  7. KARAUNARATHNE J, Warnakulasuriya S, Perera C, Premathilaka H, et al
    Comparative Study of Ferritin Levels between Two Generic Formulations of Deferasirox in Sri Lankan Patients with Beta-Thalassemia Major.
    Hemoglobin. 2026;50:229-236.
    PubMed         Abstract available

  8. MISHRA V, Singh R, Halder R, Agarwal N, et al
    "Assessing Long-Term Health-Related Quality of Life in Children with beta-Thalassemia Major Following Hematopoietic Stem Cell Transplantation" - A Cross-Sectional Comparative Study.
    Hemoglobin. 2026;50:221-228.
    PubMed         Abstract available

  9. OUALI F, Sahli A, Yessine A, Dabboubi R, et al
    Inflammatory Biomarkers in Sickle Cell Disease: Understanding Their Role in Predicting the Disease-Related Complications.
    Hemoglobin. 2026;50:237-246.
    PubMed         Abstract available

  10. GAO J, Li Y, Li W, Li S, et al
    miR-192-5p as a Potential Diagnostic Biomarker for beta-Thalassemia and Its Regulatory Mechanism via Targeting BCL11A.
    Hemoglobin. 2026;50:213-220.
    PubMed         Abstract available

  11. ZHANG M, Liu X, Chen L, Yuan D, et al
    HBA2 Gene Conversion Disrupts Reverse Dot-Blot Hybridization Genotyping: A Prenatal Case of Non-Deletional alpha-Thalassemia Misdiagnosis.
    Hemoglobin. 2026;50:271-277.
    PubMed         Abstract available

  12. ALSHURAFA A, Abdulgayoom M, Wafi JR, Abouzeid T, et al
    Hyperbaric Oxygen Therapy in Sickle Cell Disease: A Narrative Review of Mechanisms, Clinical Applications, and Future Directions.
    Hemoglobin. 2026;50:256-263.
    PubMed         Abstract available

  13. RAVIOLA M, Maroni G, Pratti A, Detarsio GA, et al
    Hemoglobin Evans Associated with HBA1 Mutation: First Report from Rosario, Argentina.
    Hemoglobin. 2026;50:278-281.
    PubMed         Abstract available

  14. NASIRI A, Mohammed Saleh MF, Alshammari M, Alahmari A, et al
    Beyond Diagnosis: A Systematic Review of Artificial Intelligence and Deep Learning in Monitoring Iron Overload and Organ Toxicity in Beta-Thalassemia.
    Hemoglobin. 2026;50:247-255.
    PubMed         Abstract available

  15. CHENG AN, Cohen J, Lundberg RK, Sayani FA, et al
    Beyond Hypersplenism: Splenic Marginal Zone Lymphoma in an Older Adult with Hemoglobin E/Beta-Thalassemia.
    Hemoglobin. 2026;50:288-292.
    PubMed         Abstract available

  16. GUO J, Li T, Liang L, Huang J, et al
    Prenatal Counseling Conundrum: Unexpectedly Mild Phenotype in a Pregnant Woman with Homozygous CD41/42(-TTCT) beta-Thalassemia.
    Hemoglobin. 2026;50:282-287.
    PubMed         Abstract available

  17. SEN A, Dolai TK
    Detection of the Hb Hoshida (HBB: C. 130 G > C) Variant in the Indian Population.
    Hemoglobin. 2026;50:264-270.
    PubMed         Abstract available


    N Engl J Med

  18. WARE RE, Opoka RO, Latham T, Kasirye P, et al
    Ten Years of Hydroxyurea for Ugandan Children with Sickle Cell Anemia.
    N Engl J Med. 2026;394:2059-2061.
    PubMed        


    PLoS One

  19. NATTIMBA JP, Bakeera-Kitaka S, Rujumba J, Namazzi R, et al
    School absenteeism among children and adolescents aged 6-19 years with sickle cell disease in Uganda: A comparative cross-sectional study.
    PLoS One. 2026;21:e0350308.
    PubMed         Abstract available

  20. MENSAH J, Marfo AFA, Opare-Addo MNA, Obeng P, et al
    Challenges and opportunities in hydroxyurea access and adherence for sickle cell disease patients at Komfo Anokye Teaching Hospital: Insights from healthcare providers.
    PLoS One. 2026;21:e0347848.
    PubMed         Abstract available

  21. AL-SHAMI A, Al-Maktari LAS, Qasem L, Aldhorae K, et al
    Serum ferritin in Yemeni patients with sickle cell anemia: Association with sociodemographic factors and hematological profiles.
    PLoS One. 2026;21:e0350016.
    PubMed         Abstract available

  22. ARCHAMBEAUD A, Aumont C, Pouplard C, Agier MS, et al
    Dapsone and schistocytes: Thrombotic microangiopathy or not?
    PLoS One. 2026;21:e0349570.
    PubMed         Abstract available


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