Objective: Thalassemia along with hematopoietic stem cell transplantation (HSCT) can lead to major oxidative stress. Vitamins A and E are antioxidants which protect membrane from lipid peroxidation. We sought to determine for the first time, whether vitamins A and E supplementation is efficacious in maintaining or increasing plasma level of these vitamins in thalassemic children undergoing HSCT. Methods: A cross-sectional study was performed on 50 children with β-thalassemia major hospitalized for HSCT. Patients took a daily multivitamin. Plasma vitamins A and E levels were measured at four different times: on admission, HSCT day (day 0), day 7 and day 14 after HSCT. Findings: Plasma vitamin A and E were abnormal on admission in most patien...
Copyright © 2014 Laila M. Sherief et al.This is an open access article distributed under the Creativ...
BACKGROUND: Disturbed oxidant/antioxidant status is involved in pathogenesis of anemia in end stage...
Background: Vitamin C may be of benefit to sickle cell disease sufferers. In the steady state, sickl...
Objective: Thalassemia along with hematopoietic stem cell transplantation (HSCT) can lead to major o...
<p><strong><em>Background: </em></strong>Thalassemic patients undergoing Hematopoietic Stem Cell Tra...
Background β−Thalassemic children have oxidative stress and antioxidant deficiency even without iron...
Background: Vitamin C is a well-known powerful water soluble antioxidant and very powerful iron abso...
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 ...
Background: Traditionally, lipids used in parenteral nutrition (PN) are based on ω-6 fatty acid-rich...
Background and Objective: In pathogenesis of beta major thalassemia, tissue damage is occurring due ...
<strong>BACKGROUND</strong>: Thalassemia is the most common hereditary disease in the wo...
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...
To study the effect of iron overload due to continuous blood transfusions on peroxidation products, ...
Copyright © 2014 Laila M. Sherief et al.This is an open access article distributed under the Creativ...
BACKGROUND: Disturbed oxidant/antioxidant status is involved in pathogenesis of anemia in end stage...
Background: Vitamin C may be of benefit to sickle cell disease sufferers. In the steady state, sickl...
Objective: Thalassemia along with hematopoietic stem cell transplantation (HSCT) can lead to major o...
<p><strong><em>Background: </em></strong>Thalassemic patients undergoing Hematopoietic Stem Cell Tra...
Background β−Thalassemic children have oxidative stress and antioxidant deficiency even without iron...
Background: Vitamin C is a well-known powerful water soluble antioxidant and very powerful iron abso...
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 ...
Background: Traditionally, lipids used in parenteral nutrition (PN) are based on ω-6 fatty acid-rich...
Background and Objective: In pathogenesis of beta major thalassemia, tissue damage is occurring due ...
<strong>BACKGROUND</strong>: Thalassemia is the most common hereditary disease in the wo...
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...
To study the effect of iron overload due to continuous blood transfusions on peroxidation products, ...
Copyright © 2014 Laila M. Sherief et al.This is an open access article distributed under the Creativ...
BACKGROUND: Disturbed oxidant/antioxidant status is involved in pathogenesis of anemia in end stage...
Background: Vitamin C may be of benefit to sickle cell disease sufferers. In the steady state, sickl...