Premature atherosclerosis in children with beta-thalassemia major: New diagnostic marker

LM Sherief, O Dawood, A Ali, HS Sherbiny, NM Kamal… - BMC pediatrics, 2017 - Springer
Background Early vascular alteration, atherosclerosis and coronary artery disease have
emerged as important cardiovascular complications among beta-thalassemia major (B-TM) …

The effects of iron overload, insulin resistance and oxidative stress on metabolic disorders in patients with β-thalassemia major

S Setoodeh, M Khorsand, MA Takhshid - Journal of Diabetes & Metabolic …, 2020 - Springer
Background Serum lipids and glycemic dysregulation are the known characteristics of β-
thalassemia major (β-TM). Here, we evaluated the association of these disorders with insulin …

[HTML][HTML] Correlation between 25-hydroxyvitamin D and lipid profile among children with beta thalassemia major

C Nasir, N Rosdiana, AD Lubis - Open Access Macedonian …, 2018 - ncbi.nlm.nih.gov
BACKGROUND: Beta thalassemia major is associated with lipid profile abnormalities,
presented as a lower level of total cholesterol (TC), low-density lipoproteins (LDL), high …

Serum fasting lipid profile in children and adolescents with β-thalassaemia major in southern Pakistan.

S Ashar, S Sultan, SM Irfan… - Malaysian Journal of …, 2015 - search.ebscohost.com
Objective: Serum fasting lipid profile has been studied in various clinical spectrum of Beta
(β)-thalassaemia syndrome. Premature cardiac impairment in thalassaemia major appears …

[PDF][PDF] Lipid profile in?-thalassemia major children and its correlation with various parameters

P Daswani, K Garg - Indian Journal of Child Health, 2021 - academia.edu
Background: Beta-thalassemia is considered to be the most frequent hereditary blood
disorder worldwide. Lipid abnormalities have been detected in different types of beta …

[PDF][PDF] Molecular, biochemical and hematological investigations of β-thalassemic children in gaza governorate

RM Al Haddad - The Islamic University-Gaza, 2012 - academia.edu
Background: Thalassemias are hereditary anemias mostly common in the Mediterranean,
the equatorial, or near equatorial regions of Africa and Asia. They are classified according to …

Reflection of treatment proficiency of hydroxyurea treated β-thalassemia serum samples through nuclear magnetic resonance based metabonomics

A Khalid, AJ Siddiqui, SH Ansari, SG Musharraf - Scientific Reports, 2019 - nature.com
Abstract β-Thalassemia is a widespread autosomal recessive blood disorder found in most
parts of the world. Fetal hemoglobin (HbF), a form of hemoglobin is found in infants …

[PDF][PDF] Study of serological parameters in thalassemic patients of GMC Jammu

S Singh, R Singh, KK Kaul, M Kour - IOSR J Dent Med Sci, 2016 - academia.edu
The present study was conducted in the Post-Graduate Department of Pathology in
collaboration with department of biochemistry, Government Medical College, Jammu. This …

[PDF][PDF] Diagnosis dan tata laksana intoksikasi asam jengkolat

RA Jesslin, VND Pauta - Cermin Dunia Kedokt, 2023 - academia.edu
Diagnosis dan Tata Laksana Intoksikasi Asam Jengkolat Page 1 426 CDK-319/ vol. 50 no. 8
th. 2023 Alamat Korespondensi email: Diagnosis dan Tata Laksana Intoksikasi Asam …

Ascertaining Genetics of β—Thalassemia and Sickle Cell Disease Using Machine Learning Heuristics

P Aswathi, SR Anjana, S Kumar, G Singh, S Kapoor… - 2024 - preprints.org
Hemoglobinopathies are a group of disorders in which the hemoglobin molecule has
abnormal production or structure. The hemoglobin molecules in red blood cells (RBC) are …