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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
Annals of the New York Academy of Sciences, ISSN 0077-8923, 12/2016, Volume 1386, Issue 1, pp. 16 - 29
Journal Article
Circulation: Cardiovascular Imaging, ISSN 1941-9651, 08/2015, Volume 8, Issue 8, pp. e003230 - e003230
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
Journal Article
Haematologica, ISSN 0390-6078, 06/2012, Volume 97, Issue 6, pp. 842 - 848
Journal Article
03/2013
Background: First and second-degree heart blocks are partly common rhythm disorders in thalassemic patients but complete heart block is a very rare... 
Iron overload | Arrhythmia | β-Thalassemia | Cardiomyopathy
Web Resource
Pediatric Blood & Cancer, ISSN 1545-5009, 05/2019, Volume 66, Issue 5, pp. e27643 - n/a
Background Regular blood transfusion therapy still remains the cornerstone in the management of beta-thalassemia. Although recommendations are clear for... 
transfusion | thalassemia | hemoglobinopathies | Beta‐thalassemia major | Beta-thalassemia major | ONCOLOGY | PEDIATRICS | HEMATOLOGY | ALPHA-GLOBIN | Blood transfusions | Medical personnel | Splenomegaly | Therapy | Patents | Transfusion | Thalassemia | Blood transfusion | Patients | Blood | Doctors | Hepatitis | Adequacy | Underweight | Hemoglobin | Determinants | Trends | Hepatitis C virus | Hepatitis C
Journal Article