Study of vascular endothelial dysfunction in children with beta-thalassemia major before and after quercetin therapy
Abstract Background Beta-thalassemia stands as an autosomal recessive disorder that occurs as a result of a defect in the beta-globin chain synthesis of hemoglobin. Oxidative stress has a crucial role in the β-thalassemia pathophysiology. It occurs due to erythroid expansion along with ineffective e...
Saved in:
| Main Authors: | Fatma Al Zahraa Sherai, Maaly Mabrouk, Ibrahim Badraia, Adel Hagag, Eman Elaskary |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
SpringerOpen
2025-02-01
|
| Series: | Egyptian Pediatric Association Gazette |
| Subjects: | |
| Online Access: | https://doi.org/10.1186/s43054-025-00347-w |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Comparative study of efficacy of different iron chelating agents in treatment of iron overload in children with Beta Thalassemia Major
by: adel abd elhaleim hagag
Published: (2014-08-01) -
Study of T lymphocyte Subsets in children with Beta Thalassemia Major: Correlation with iron overload Adel A. Hagag, Mokhtar A. Hussein, Enaam S. Abed Elbar* From Pediatrics and Clinical Pathology*departments, Faculty of Medicine, Tanta University, Egy
by: adel abd elhaleim hagag
Published: (2014-08-01) -
Prevalence of Candida albicans in the oral cavity of Beta Thalassemia Major and Thalassemia Minor Patients [version 1; peer review: 2 approved]
by: Maha Adel Mahmood, et al.
Published: (2025-06-01) -
Prevalence of Candida albicans in the oral cavity of Beta Thalassemia Major and Thalassemia Minor Patients [version 2; peer review: 2 approved]
by: Maha Adel Mahmood, et al.
Published: (2025-08-01) -
Therapeutic Value of Silymarin as Iron Chelator in Children with Beta Thalassemia with Iron Overload
by: adel abd elhaleim hagag
Published: (2014-08-01)