Promoting Adherence to Iron Chelation Treatment in Beta-Thalassemia Patients
Author:
Publisher
Informa UK Limited
Subject
Health Policy,Pharmacology, Toxicology and Pharmaceutics (miscellaneous),Social Sciences (miscellaneous),Medicine (miscellaneous)
Reference100 articles.
1. Iron overload in thalassemia: different organs at different rates
2. HYPERTRANSFUSION REGIMEN IN PATIENTS WITH Cooley's ANEMIA
3. Relationship between transfusion regimen and suppression of erythropoiesis in β-thalassaemia major
4. Ineffective erythropoiesis in β-thalassemia is characterized by increased iron absorption mediated by down-regulation of hepcidin and up-regulation of ferroportin
5. Effect of transfusional iron intake on response to chelation therapy in β-thalassemia major
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2. Deferasirox adherence in patients with thalassemia: Exploring the association with patient knowledge and ferritin levels;Pharmacia;2024-07-30
3. Health-Related Quality-of-Life Impacts Associated with Transfusion-Dependent β-Thalassemia in the USA and UK: A Qualitative Assessment;The Patient - Patient-Centered Outcomes Research;2024-03-26
4. Beta thalassemia: Looking to the future, addressing unmet needs and challenges;Annals of the New York Academy of Sciences;2024-01-13
5. Assessment of Iron Chelation Therapy Adherence in Patients with Thalassemia Major in Babylon Province;Journal of Applied Hematology;2023
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