Oxidative DNA damage in β-thalassemic children-Reference-Cited by-同舟云学术

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Oxidative DNA damage in β-thalassemic children

Published:2015-12 Issue:2 Volume:14 Page:41-46
ISSN:2090-6242
Container-title:Medical Research Journal
language:en
Short-container-title:Medical Research Journal

Author:

El Gindi Hala D.,Hassanin Amal I.,Mostafa Naglaa O.,El Kassas Ghada M.,El Wakeel Maged A.,El Batal Wael H.,Galal Essam M.,Elmalt Heba A.,Amer Marwa F.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference26 articles.

1. β-Thalassemia mutations and hemoglobinopathies in Adana, Turkey: results from a single center study

2. Beta-thalassemia: from genotype to phenotype

3. BETA-GLOBIN GENE MUTATIONS IN TURKISH CHILDREN WITH BETA-THALASSEMIA: RESULTS FROM A SINGLE CENTER STUDY

4. Increased Oxidative Stress and Iron Overload in Jordanian β-Thalassemic Children

5. Oxidative stress and disturbance in antioxidant balance in beta thalassemia major

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Role of malonaldehyde as a surrogate biomarker for iron overload in the β-thalassemia patient: A systematic meta-analysis;Advances in Redox Research;2021-12

2. Clinical Laboratory Manifestation and Molecular Diagnosis of β-Thalassemia Patients in Iraq;Journal of Pediatric Hematology/Oncology;2019-11-08

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