Correlation of Oxidative Stress with Serum Trace Element Levels and Antioxidant Enzyme Status in Beta Thalassemia Major Patients: A Review of the Literature
Beta thalassemia major is an inherited disease resulting from reduction or total lack of beta globin chains. Patients with this disease need repeated blood transfusion for survival. This may cause oxidative stress and tissue injury due to iron overload, altered antioxidant enzymes, and other essenti...
Saved in:
Main Authors: | Q. Shazia, Z. H. Mohammad, Taibur Rahman, Hossain Uddin Shekhar |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2012-01-01
|
Series: | Anemia |
Online Access: | http://dx.doi.org/10.1155/2012/270923 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Nutritional Status of Children with Beta Thalassemia Major
by: Dhara Bipin Joshi, et al.
Published: (2023-12-01) -
Biochemical Status of Beta-Thalassemia Major Patients in Erbil City
by: Omar Surchi, et al.
Published: (2018-06-01) -
Investigating Oxidative Stress and Antioxidant Dynamics in Beta-thalassemia Major: A Comparative Study from Al-Diwaniyah, Iraq
by: Hadeer Hayder Inteek, et al.
Published: (2024-12-01) -
Beta-Thalassemia Major and Female Fertility: The Role of Iron and Iron-Induced Oxidative Stress
by: Paraskevi Roussou, et al.
Published: (2013-01-01) -
Relation of Left Ventricular Diastolic Dysfunction to Serum Ferritin in Thalassemia Major
by: Aso Faeq Salih, et al.
Published: (2019-11-01)