Abstract α-Thalassemia is an inherited blood disorder characterized by decreased synthesis
of α-globin chains that results in an imbalance of α and β globin and thus varying degrees of …

This systematic literature review assessed the global prevalence and birth prevalence of
clinically significant forms of alpha‐and beta‐thalassemia. Embase, MEDLINE, and the …

Epilepsy constitutes a global health concern, affecting millions of individuals and
approximately one-third of patients exhibit drug resistance. Recent investigations have …

Thalassemia is a genetics syndrome which lead to abnormal hemoglobin protein and this
produce hemolysis, inefficient erythropoiesis, and moderate to severe anemia. Very few …

Aim: To assess the frequency of nutritional status of the children with thalassemia major by
BMI at Bahawal Victoria Hospital Bahawalpur. Methods: This cross sectional study was …

Background: Hypothyroidism is one of the common complications among beta thalasemia.
Objective: To determine the frequency of hypothyroidism in patients of beta thalassemia …

Yisui Shengxue granules, which is a Chinese traditional medicine, can increase
hemoglobin, red blood cells, and Ret of thalassemia patients with mild, moderate, and …

Background: Beta thalassemia is one of the major hemolytic diseases of childhood. Multiple
blood transfusions can lead to transmitted infections. Hepatitis C infection is relatively more …

Objective: To assess the nutritional status of the children with thalassemia major by WHO
based BMI classification at Bahawal Victoria Hospital Bahawalpur. Study Design: Cross …

Precise control over the intracellular free Ca2+ level is of key importance for any cell, red
blood cells (RBCs) included. Cell fate of erythroid precursor cells, as well as volume, redox …