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Journal Article
02/2013
Objective:Beta thalassemia major is a prevalent hereditary disease in Mediterranean region especially Iran. Early blood transfusion is necessary for most of... 
Iran | Beta Thalassemia major | Complication | Hospitalization
Web Resource
Circulation: Cardiovascular Imaging, ISSN 1941-9651, 08/2015, Volume 8, Issue 8, p. e003230
Journal Article
Annals of the New York Academy of Sciences, ISSN 0077-8923, 12/2016, Volume 1386, Issue 1, pp. 16 - 29
Journal Article
Journal of Pediatric Hematology/Oncology, ISSN 1077-4114, 2018, p. 1
Beta thalassemia major (βTM) is the most common inherited hemoglobinopathy. Management essentially focuses on preventing and treating complications.... 
Osteoporosis | Hemochromatosis | Hypopituitarism | Thalassemia major | Alloimmunization
Journal Article