Background β−Thalassemic children have oxidative stress and antioxidant deficiency even without iron overload status. In these patients, tissue damage due to oxidative stress may be occurred. Also, it seems that thalassemic patients have higher levels of ALT, AST therefore, the main aim of the present study was to determine the benefits of vitamin E as an antioxidant supplements in β-Thalassemia children. Materials and Methods This clinical trial was carried out on 45 beta-thalassemic patients undergoing occasional transfusions (24 males, 21 females), mean age 16 ± 8 years, admitted to Yazd and Shahid Sadoughi hospital in 2011. Fallowing three months treatment of vitaminE (vitamin E 400-600 unit/day),liver function test and hemopoitic syste...
There are several reports that increased oxidative stress and DNA damage were found in beta-thalasse...
Background: Thalassemia is the most common genetic disorder in humans; they are encountered among al...
Copyright © 2014 Laila M. Sherief et al.This is an open access article distributed under the Creativ...
Objective: Thalassemia along with hematopoietic stem cell transplantation (HSCT) can lead to major o...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Ci...
Thalassemia is a hereditary form of anemia that affects the synthesis of hemoglobin. The management ...
Objective: In beta thalassemic patients, tissue damage occurs due to oxidative stress and it happens...
Background and Objective: In pathogenesis of beta major thalassemia, tissue damage is occurring due ...
Objective: In beta thalassemic patients, tissue damage occurs due to oxidative stress and it happens...
Background: Vitamin C is a well-known powerful water soluble antioxidant and very powerful iron abso...
Objective: In beta thalassemic patients, tissue damage occurs due to oxidative stress and it happen...
<strong>BACKGROUND</strong>: Thalassemia is the most common hereditary disease in the wo...
To study the effect of iron overload due to continuous blood transfusions on peroxidation products, ...
Accelerated oxidative damage is one of the hallmarks in both sickle cell disease (SCD) and thalassem...
In beta-thalassemic homozygotes, low plasma levels of tocopherols may induce a red blood cell (RBC) ...
There are several reports that increased oxidative stress and DNA damage were found in beta-thalasse...
Background: Thalassemia is the most common genetic disorder in humans; they are encountered among al...
Copyright © 2014 Laila M. Sherief et al.This is an open access article distributed under the Creativ...
Objective: Thalassemia along with hematopoietic stem cell transplantation (HSCT) can lead to major o...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Ci...
Thalassemia is a hereditary form of anemia that affects the synthesis of hemoglobin. The management ...
Objective: In beta thalassemic patients, tissue damage occurs due to oxidative stress and it happens...
Background and Objective: In pathogenesis of beta major thalassemia, tissue damage is occurring due ...
Objective: In beta thalassemic patients, tissue damage occurs due to oxidative stress and it happens...
Background: Vitamin C is a well-known powerful water soluble antioxidant and very powerful iron abso...
Objective: In beta thalassemic patients, tissue damage occurs due to oxidative stress and it happen...
<strong>BACKGROUND</strong>: Thalassemia is the most common hereditary disease in the wo...
To study the effect of iron overload due to continuous blood transfusions on peroxidation products, ...
Accelerated oxidative damage is one of the hallmarks in both sickle cell disease (SCD) and thalassem...
In beta-thalassemic homozygotes, low plasma levels of tocopherols may induce a red blood cell (RBC) ...
There are several reports that increased oxidative stress and DNA damage were found in beta-thalasse...
Background: Thalassemia is the most common genetic disorder in humans; they are encountered among al...
Copyright © 2014 Laila M. Sherief et al.This is an open access article distributed under the Creativ...