Biochemical Status of Beta-Thalassemia Major Patients in Erbil City
Background and objectives: β -thalassemia major patient is one of the hereditary hemolytic diseases, which can cause many hematological and biochemical changes in the affected patient. And these changes can happen even when the patient is treated adequately. The objective was to study biochemical c...
Saved in:
Main Authors: | Omar Surchi, Sarkawt Ali |
---|---|
Format: | Article |
Language: | English |
Published: |
College Of Dentistry Hawler Medical University
2018-06-01
|
Series: | Erbil Dental Journal |
Subjects: | |
Online Access: | https://edj.hmu.edu.krd/index.php/journal/article/view/20 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Assessment of cardiac iron deposition and genotypic classification in pediatric beta-thalassemia major: the role of cardiac MRI
by: Siqi Zhang, et al.
Published: (2025-01-01) -
The effect of blood transfusion on serum hepcidin levels in chronically transfused patients of β-thalassemia major: An observational study in a tertiary care centre in Western Maharashtra
by: Sujay Bhowmik, et al.
Published: (2024-01-01) -
Association between Alpha- Klotho Protein, Calcium, and Phosphate concentrations in Adult Iraqi Patients with Beta-Thalassemia Major
by: Ahmed J. Kadhim, et al.
Published: (2024-12-01) -
A scoping review on the obstacles faced by beta thalassemia major patients in Pakistan- Matter of policy investment
by: Ali Hussain Ansari, et al.
Published: (2024-11-01) -
Assessment of the Nutritional Status, Bone Mineralization, and Anthropometrics of Children with Thalassemia Major
by: Serap Cevher Bulğurcu, et al.
Published: (2021-12-01)