Background: Oxidative stress is the most common complication in Beta-thalassemia patients
due to iron over load that is resulted from long life blood transfusion leading to growth …

Amaç: Araştırma 2-17 yaş arası talasemi tanılı çocukların beslenme durumunu incelemek
amacıyla yapılmıştır. Yöntem: Araştırma, 86 talasemi hastasından dahil edilme kriterlerini …

Thalassemia is a well-known erythrocyte disorder characterized by low or defected
hemoglobin synthesis. β-Thalassemia is common in Jordan and classified into three types …

The aim of this study was to evaluate the plasma coenzyme Q10 (CoQ10) concentration, a
vitamin-like substance found in every cell, which is also viewed as the most effective …

Aim: In this study, the relationship between iron accumulation and blood lipid profile in TM
children was evaluated. Methods: In this study, blood hemoglobin, ferritin, and lipid levels of …

Background: Children with beta-thalassemia major may suffer from working memory
impairment. For a more refined understanding of this issue, we assessed working memory …

Background Ineffective erythropoiesis and multiple blood transfusions may cause iron
overload, leading to high level of ferritin in β-thalassemia patients. Iron has the ability to …

Abstract β-thalassemia major (β-TM) is an acute hereditary blood disorder that causes many
disorders such as bone dysfunction. Sixty five β-TM patients with β-thalassemia main …

Methods: This a cross–sectional study was carried out on 58 patients (34 males and 24
females) diagnosed β-thalassemia major on the base of the blood investigations (peripheral …

Background: Thalassemia is a genetic blood disorder caused by a mutation in the gene
encoding for the beta chains. In non-transfusiondependent-thalassemia, ocular involvement …