Aims: The aim of this study was to find a harmless, cost effective and easy available iron chelating agent for blood transfusion dependent thalassemia patients who developed iron overload due to repeated blood transfusions and subsequent failure of vital organs and need a concomi...
Open access
Research Article10.9734/AJMAH/2017/29569
The overall prognosis of beta thalassemia patients has improved considerably during the pastdecades mainly due to regular blood transfusions, improvements in the iron chelation therapy, and also enhanced surveillance with imaging studies examining the iron overload and other clin...
Open access
Research Article10.9734/IJMPCR/2016/29558
Aims: Hemoglobinopathies including HbE β thalassemia are associated with significant cardiac and pulmonary compromise in affected persons. The aim of this study was to evaluate the cardiac and pulmonary health of transfusion dependent 50 HbE β thalassemia patients of West Bengal....
Open access
Research Article10.9734/BBJ/2016/26529