Background and Objective: In pathogenesis of beta major thalassemia, tissue damage is occurring due to oxidative stress. The present study was designed to evaluate the effects of vitamin E supplementation on serum Paraoxonase, SOD, GPX enzyme activity and lipid profiles in beta major thalassemia patients. Materials and Methods: In this clinical tiral study, Sixty (25 males, 35 females) beta major thalassemia patients with age≥18 years who had criterias to enter the study, were selected randomely in two groups. The patients in interventional group, vitamin E at a dose of 400 mg/day were given for three months, with no supplementations in control group. The enzyme activities of paraoxonase, SOD, GPX and lipid profiles (LDL-c, HDL-c, triglycer...
Smith-Lemli-Opitz syndrome (SLOS) is a severe monogenic disorder resulting in low cholesterol and hi...
BACKGROUND: Neutropenia and/or neutrophil dysfunction are part of glycogen storage disease type 1b (...
Neutropenia and/or neutrophil dysfunction are part of glycogen storage disease type 1b (GSD1b) pheno...
Objective: In beta thalassemic patients, tissue damage occurs due to oxidative stress and it happens...
Objective: In beta thalassemic patients, tissue damage occurs due to oxidative stress and it happen...
Objective: In beta thalassemic patients, tissue damage occurs due to oxidative stress and it happens...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Ci...
<strong>BACKGROUND</strong>: Thalassemia is the most common hereditary disease in the wo...
In beta-thalassemic homozygotes, low plasma levels of tocopherols may induce a red blood cell (RBC) ...
Thalassemia is a hereditary form of anemia that affects the synthesis of hemoglobin. The management ...
Background β−Thalassemic children have oxidative stress and antioxidant deficiency even without iron...
Autoxidation of globin chains and iron overload are the suggested mechanisms for the increased oxida...
Objective: Thalassemia along with hematopoietic stem cell transplantation (HSCT) can lead to major o...
There are several reports that increased oxidative stress and DNA damage were found in beta-thalasse...
To study the effect of iron overload due to continuous blood transfusions on peroxidation products, ...
Smith-Lemli-Opitz syndrome (SLOS) is a severe monogenic disorder resulting in low cholesterol and hi...
BACKGROUND: Neutropenia and/or neutrophil dysfunction are part of glycogen storage disease type 1b (...
Neutropenia and/or neutrophil dysfunction are part of glycogen storage disease type 1b (GSD1b) pheno...
Objective: In beta thalassemic patients, tissue damage occurs due to oxidative stress and it happens...
Objective: In beta thalassemic patients, tissue damage occurs due to oxidative stress and it happen...
Objective: In beta thalassemic patients, tissue damage occurs due to oxidative stress and it happens...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Ci...
<strong>BACKGROUND</strong>: Thalassemia is the most common hereditary disease in the wo...
In beta-thalassemic homozygotes, low plasma levels of tocopherols may induce a red blood cell (RBC) ...
Thalassemia is a hereditary form of anemia that affects the synthesis of hemoglobin. The management ...
Background β−Thalassemic children have oxidative stress and antioxidant deficiency even without iron...
Autoxidation of globin chains and iron overload are the suggested mechanisms for the increased oxida...
Objective: Thalassemia along with hematopoietic stem cell transplantation (HSCT) can lead to major o...
There are several reports that increased oxidative stress and DNA damage were found in beta-thalasse...
To study the effect of iron overload due to continuous blood transfusions on peroxidation products, ...
Smith-Lemli-Opitz syndrome (SLOS) is a severe monogenic disorder resulting in low cholesterol and hi...
BACKGROUND: Neutropenia and/or neutrophil dysfunction are part of glycogen storage disease type 1b (...
Neutropenia and/or neutrophil dysfunction are part of glycogen storage disease type 1b (GSD1b) pheno...