Compliance with Deferoxamine Therapy and Thyroid Dysfunction of Patients with β-Thalassemia Major in Syria
Author:
Affiliation:
1. Department of Biochemistry and Microbiology, Faculty of Pharmacy, Damascus University, Damascus, Syria;
2. Department of Endocrinology, Faculty of Medicine, Damascus University, Damascus, Syria;
3. Thalassemia Center, Damascus, Syria
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
https://www.tandfonline.com/doi/pdf/10.1080/03630269.2019.1639517
Reference15 articles.
1. Weatherall DJ. The thalassemias: disorders of globin synthesis. In: Kaushansky K, Lichman MA, Beutler E, et al., Editors. Williams Hematology, 8th ed. McGraw-Hill Professional (published online). 2010:675–707.
2. Molecular Update of β-Thalassemia Mutations in the Syrian Population: Identification of Rare β-Thalassemia Mutations
3. Prevention of Hemoglobinopathies in Syria
4. Study of the effect of iron overload on the function of endocrine glands in male thalassemia patients
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