Endothelin-1 gene polymorphism (G8002A) and endothelial monocyte-activating polypeptide II: Role in vascular dysfunction in pediatric patients with β-thalassemia …
AAG Tantawy, MAR Tadros, AAM Adly, EAR Ismail… - Cytokine, 2023 - Elsevier
Abstract Background: Endothelin-1 (ET-1), a potent endogenous vasoconstrictor, stimulates
production of reactive oxygen species. Endothelial monocyte-activating polypeptide-II …
production of reactive oxygen species. Endothelial monocyte-activating polypeptide-II …
Protein antioxidants in thalassemia
S Awadallah - Advances in clinical chemistry, 2013 - Elsevier
It is common knowledge that thalassemic patients are under significant oxidative stress.
Chronic hemolysis, frequent blood transfusion, and increased intestinal absorption of iron …
Chronic hemolysis, frequent blood transfusion, and increased intestinal absorption of iron …
[HTML][HTML] Lipids profile in children and adolescents with β-thalassemia major
HK Jabbar, MK Hassan, LM Al-Naama - Hematology, Transfusion and …, 2023 - SciELO Brasil
Introduction: Patients with β-thalassemia major (β-TM) are at risk of developing abnormal
lipid profiles. Lipid abnormalities, in turn, have a potential role in the pathogenesis of some …
lipid profiles. Lipid abnormalities, in turn, have a potential role in the pathogenesis of some …
Ferric citrate CYP2E1-independently promotes alcohol-induced apoptosis in HepG2 cells via oxidative/nitrative stress which is attenuated by pretreatment with …
Y Xu, Y Feng, H Li, Z Gao - Food and chemical toxicology, 2012 - Elsevier
In the case of alcoholic liver injury, an iron overload is always present. Both alcohol and iron
can individually induce oxidative stress in liver. However, the combined effect of …
can individually induce oxidative stress in liver. However, the combined effect of …
[HTML][HTML] Role of malonaldehyde as a surrogate biomarker for iron overload in the β-thalassemia patient: A systematic meta-analysis
D Basu, DG Adhya, R Sinha, N Chakravorty - Advances in Redox Research, 2021 - Elsevier
Malonaldehyde (MDA), a biomarker of oxidative stress is found to be increased in many
individuals suffering from β-thalassemia. This may possibly be attributed to iron overload …
individuals suffering from β-thalassemia. This may possibly be attributed to iron overload …
[HTML][HTML] Status of superoxide dismutase in transfusion dependent thalassaemia
Background: Thalassemia is a collection of genetic impairments in beta and alpha genes
causing various states of anemia. Severe types of the disease need lifelong transfusions …
causing various states of anemia. Severe types of the disease need lifelong transfusions …
Effect of antioxidant therapy on hepatic fibrosis and liver iron concentrations in β-thalassemia major patients
To assess the effects of combined vitamin therapy on oxidant-antioxidant hepatic status and
hemoglobin (Hb) derivatives on β-thalassemia major (β-TM), a prospective study of 60 β-TM …
hemoglobin (Hb) derivatives on β-thalassemia major (β-TM), a prospective study of 60 β-TM …
Zinc improved erythrocyte deformability and aggregation in patients with beta-thalassemia: An in vitro study
BACKGROUND: Thalassemia patients have reduced red cell deformability and decreased
plasma zinc levels in their blood. OBJECTIVE: This study aimed to evaluate the effects of …
plasma zinc levels in their blood. OBJECTIVE: This study aimed to evaluate the effects of …
[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 …
pursuit of my academic career goals. I would like to express my deepest appreciation and …