Review of disease-related complications and management in adult patients with thalassemia: A multi-center study in Thailand
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference28 articles.
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1. Disease burden, management strategies, and unmet needs in α‐thalassemia due to hemoglobin H disease;American Journal of Hematology;2024-07-22
2. Adipocyte fatty acid-binding protein (FABP4) as a potential biomarker for predicting metabolically driven low-grade and organ damage in thalassemia syndromes;Annals of Hematology;2024-07-19
3. De-novo ATR-16 syndrome associated with inherited hemoglobin Evanston causing HbH phenotype: a rare occurrence;Annals of Hematology;2024-07-11
4. Evaluation of microstructural changes in the brain in transfusion dependent thalassemia patients with advanced magnetic resonance imaging techniques;Neuroradiology;2024-07-08
5. De-novo ATR-16 syndrome associated with inherited hemoglobin Evanston causing HbH phenotype: a rare occurrence;2024-06-17
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