Background: Iron overload is a common complication in β-thalassemia that induces intracellular oxidative stress producing lesions in the DNA including double strand breaks. Objectives: The aim of this study was to evaluate DNA damage in peripheral leukocytes of β -thalassemic children and to investigate its association with the iron overload and the role of L-carnitine therapy upon this damage. Subjects and Methods: Fifty β-thalassemic children (25 TM and 25 TI) with 20 age and sex matched apparently healthy children (control group) were included. Serum ferritin level was measured by ELISA. DNA damage was evaluated by the Gel electrophoresis to determine the total DNA genomic damage (TGD). The intensity of DNA nucleoprotein w...
Thalassaemia is a group of genetic diseases where haemoglobin synthesis is impaired. This chronic an...
To study the effect of iron overload due to continuous blood transfusions on peroxidation products, ...
Background: HFE gene mutations have been shown to be responsible for hereditaryhemochromatosis. Thei...
Objectives: Thalassemia with frequent blood transfusion was considered under oxidative stress becaus...
Objective: Thalassemia is a group of genetic diseases where hemoglobin synthesis is impaired. Chroni...
Iron deficiency is frequently associated with anemia. Iron is a transition-metal ion, and it can ind...
Introduction: Iron overload is the main cause of morbidity and mortality in patients with β-tha...
Objective: The objective of this research was to evaluate oxidative stress status in children with Î...
Redox imbalance and genotoxic damage are commonly observed in β thalassaemic patients. The aim of th...
Background:"thalassaemia" refers to a group of blood diseases characterized by low or absent synthes...
Impairment of haemoglobin synthesis occurs in the genetic diseases known as thalassaemia. The conseq...
This research include studying the oxidative stress state and measuring some biochemical parameters ...
It has been projected that ferritin and iron yoke in homozygous thalassemic children is coupled with...
Impairment of haemoglobin synthesis occurs in the genetic diseases known as thalassaemia. The conseq...
Iron overload is the primary cause of morbidity in transfusion-dependent thalassemia. Increase in ir...
Thalassaemia is a group of genetic diseases where haemoglobin synthesis is impaired. This chronic an...
To study the effect of iron overload due to continuous blood transfusions on peroxidation products, ...
Background: HFE gene mutations have been shown to be responsible for hereditaryhemochromatosis. Thei...
Objectives: Thalassemia with frequent blood transfusion was considered under oxidative stress becaus...
Objective: Thalassemia is a group of genetic diseases where hemoglobin synthesis is impaired. Chroni...
Iron deficiency is frequently associated with anemia. Iron is a transition-metal ion, and it can ind...
Introduction: Iron overload is the main cause of morbidity and mortality in patients with β-tha...
Objective: The objective of this research was to evaluate oxidative stress status in children with Î...
Redox imbalance and genotoxic damage are commonly observed in β thalassaemic patients. The aim of th...
Background:"thalassaemia" refers to a group of blood diseases characterized by low or absent synthes...
Impairment of haemoglobin synthesis occurs in the genetic diseases known as thalassaemia. The conseq...
This research include studying the oxidative stress state and measuring some biochemical parameters ...
It has been projected that ferritin and iron yoke in homozygous thalassemic children is coupled with...
Impairment of haemoglobin synthesis occurs in the genetic diseases known as thalassaemia. The conseq...
Iron overload is the primary cause of morbidity in transfusion-dependent thalassemia. Increase in ir...
Thalassaemia is a group of genetic diseases where haemoglobin synthesis is impaired. This chronic an...
To study the effect of iron overload due to continuous blood transfusions on peroxidation products, ...
Background: HFE gene mutations have been shown to be responsible for hereditaryhemochromatosis. Thei...