Beta-thalassemia (BTH), a recessively inherited haemoglobin (Hb) disorder, causes iron
overload (IO), extra-medullary haematopoiesis and bone marrow expansion with major …

Malaria is a dangerous disease that contributes to millions of hospital visits and hundreds of
thousands of deaths, especially in children residing in sub-Saharan Africa. Although several …

The issue of lipid changes in muscle foods under the action of atmospheric oxygen has
captured the attention of researchers for over a century. Lipid oxidative processes initiate …

Objectives: Thalassemia, the most common global monogenetic disorder, is highly prevalent
in southern China. Epidemiological and molecular characterization of thalassemia is …

Iron in blood cells has several physiological functions like transporting oxygen to cells and
maintaining iron homeostasis. Iron is primarily contained in red blood cells (RBCs), but …

Purpose Our study aims to describe the mortality trends and disparities among individuals
with thalassemia in the United States (US). Patients and Methods We used CDC WONDER …

(1) Background: Alpha (α)-thalassaemia is a genetic disorder that affects 5% of the world
population. Deletional or nondeletional mutations of one or both HBA1 and HBA2 on …

Thalassaemia constitutes an especially prevalent human monogenic illness caused by a
lack of synthesis of the α-or β-globin chains. The clinical impact of β-thalassaemia is worse …

Background Transfusion-dependent thalassemia (TDT) is a severe form of betathalassemia,
characterized by defective-globin production, resulting in a buildup of unpaired alpha globin …

Introduction: The circulatory system is highly complex, and any dysfunction within the blood
circulatory system can lead to blood diseases. Hemoglobinopathies are among the most …