Abstract β-Thalassemia (β-thal) is a genetic disorder, representing a major health problem in
Algeria. It is associated with altered lipid levels and a state of oxidative stress that can lead …

Background: In beta-thalassemia major impaired biosynthesis of beta globin leads to
accumulation of unpaired alpha globin chain. An iron overload, usually observed, generates …

β-Thalassemia (β-thal) is associated with abnormal synthesis of hemoglobin (Hb). Repeated
blood transfusions in patients with β-thal major (β-TM) leads to an enhanced generation of …

Abstract β-Thalassemia (β-thal), especially β-thalassemia major (β-TM), is reported to be
related to reactive oxygen species (ROS) and enhanced oxidation status. It is reflected by …

Beta thalassemia major (BT) is an inherited blood disorder caused by reduced or absent
synthesis of the hemoglobin beta chains, associated with profound anemia, jaundice …

Objective Beta-thalassemia major is an autosomal recessive disease causing severe and
hemolytic anemia, which begins about 2-6 months after birth. Iron overload, which arises …

Objective: Evaluation serum lipids, lipoprotein (a), apolipoprotein A1, apolipoprotein B and
total antioxidant status (TAS) in syrian patients with β-thalassemia major. Methods: This …

Non‐alcoholic fatty liver disease (NAFLD) is a global health problem. Iron is the leading
cause of liver damage in patients with transfusion‐dependent thalassaemia (TDT), and data …

Reduction or total lack of beta-globin chains caused by a congenital disease called ß-
thalassemia major is one of the lives threatening diseases. Patients who suffer from ß …

Because of continuous blood transfusions, thalassemia patients are subjected to
peroxidative tissue injury by the secondary iron overload. In accordance, analysis of serum …