[HTML][HTML] Hematological and biochemical status of Beta-thalassemia major patients in Bangladesh: A comparative analysis

MF Karim, M Ismail, AKMM Hasan… - International journal of …, 2016 - ncbi.nlm.nih.gov
Background: Thalassemia is one of the most common hereditary disorders and Beta-
thalassemia major is its severe form. The present study is concerned with the analysis of …

A study of the prevalence of thalassemia and its correlation with liver function test in different age and sex group in the Chittagong district of Bangladesh

S Palit, RH Bhuiyan, J Aklima, TB Emran… - Journal of basic and …, 2012 - ncbi.nlm.nih.gov
Thalassemia is the name of a group of genetic, inherited disorders of the blood. More
specifically, it is a disorder of the hemoglobin molecule inside the red blood cells. According …

[PDF][PDF] Effect of β-Thalassemia on Hematological and Biochemical Profiles of female Patients

B Munir, T Iqbal, A Jamil, F Muhammad - Pakistan Journal of life and …, 2013 - pjlss.edu.pk
Thalassemia is one of the most common monogenic disorders that affect synthesis of globin
chain in the patients. The disease is more prevalent in Mediterranean countries and …

[HTML][HTML] Hematological and biochemical evaluation of β-thalassemia major (βTM) patients in Gaza Strip: A cross-sectional study

H Ayyash, M Sirdah - International journal of health sciences, 2018 - ncbi.nlm.nih.gov
Objectives In Gaza Strip, Palestine, β-thalassemia is a major public health problem where
more than 300 β-thalassemia major (βTM) patients are currently being managed at …

[PDF][PDF] Thyroid hormone profile in beta-thalassemia major children

G Gathwala, K Das, N Agrawal - Bangladesh Medical Research …, 2009 - banglajol.info
Thalassemia is the most common genetic disorder worldwide1. The striking increase in
survival of these patients over the past decade has focused attention on abnormal endocrine …

A cross-sectional study of metabolic and endocrine complications in beta-thalassemia major

F Najafipour, A Aliasgarzadeh… - Annals of Saudi …, 2008 - annsaudimed.net
BACKGROUND AND OBJECTIVES: Iron overload is a major problem in patients with beta-
thalassemia major, and it has many structural and metabolic consequences. The aim of this …

[PDF][PDF] Molecular and biochemical study on β-thalassemia patients in Iraq

AM Saud - University of Baghdad, 2012 - researchgate.net
First, a special gratitude and thanks are due to “Allah” for his entire blessing during the
pursuit of my academic career goals. I would like to express my deepest appreciation and …

Biochemical Markers of Bone Turnover in Patients with β‐Thalassemia Major: A Single Center Study from Southern Pakistan

S Sultan, SM Irfan, SI Ahmed - Advances in hematology, 2016 - Wiley Online Library
Objectives. Skeletal complications in β‐homozygous thalassemic patients are uncommon
but often debilitating, even amongst children and adolescent patients with well maintained …

Study of thyroid function in Egyptian children with β-thalassemia major and β-thalassemia intermedia

ARA Abdel-Razek, A Abdel-Salam… - The Journal Of The …, 2013 - journals.lww.com
Background Thyroid dysfunction is a known complication of transfusion-dependent β-
thalassemia. However, information on its frequency and risk factors among Egyptian …

[HTML][HTML] Endocrine and metabolic disorders in β-thalassemiamajor patients

F Saffari, A Mahyar, S Jalilolgadr - Caspian journal of internal …, 2012 - ncbi.nlm.nih.gov
Background: Thalassemia is the most common hereditary anemia and beta thalassemia
major is its most severe form. Endocrine abnormalities in thalassemia major are common …