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March 23, 2024Annals of HematologyOpen Access

Spanish registry of hemoglobinopathies and rare anemias (REHem-AR): demographics, complications, and management of patients with β-thalassemia

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Authors

EBEduardo J. Bardón-CanchoUniversidad Complutense de MadridJMJosé Manuel Marco-SánchezHospital General Universitario Gregorio MarañónDBDavid Benéitez-PastorUniversitat Autònoma de Barcelona

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Bardón-Cancho et al. (2024) studied this question.

synapsesocial.com/papers/68e72a7db6db6435876a48b6https://doi.org/10.1007/s00277-024-05694-z
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Also Consider

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  1. 1Serum Ferritin Levels Correlation With Heart and Liver MRI and LIC in Patients With Transfusion-Dependent Thalassemia2015 · 51 citations
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  3. 3Deferiprone for transfusional iron overload in sickle cell disease and other anemias: open-label study of up to 3 years2022 · 26 citations
  4. 4Osteopenia–Osteoporosis Syndrome in Patients with Thalassemia: Understanding of Type of Bone Disease and Response to Treatment2009 · 25 citations
  5. 5Common Complications in Beta-Thalassemia Patients.2013 · 25 citations