Evaluation of Erythroferrone, Hepcidin, and Iron Overload Status in Iraqi Transfusion-Dependent β-Thalassemia Major Patients
Author:
Affiliation:
1. Department of Chemistry, College of Science, University of Kufa, Kufa, Iraq
2. Protein Research Center, Shahid Beheshti University, G.C., Tehran, Iran
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
https://www.tandfonline.com/doi/pdf/10.1080/03630269.2020.1794888
Reference38 articles.
1. Optimal management of β thalassaemia intermedia
2. Genetic Epidemiology, Hematological and Clinical Features of Hemoglobinopathies in Iran
3. Major Depression in Children with Transfusion-Dependent Thalassemia Is Strongly Associated with the Combined Effects of Blood Transfusion Rate, Iron Overload, and Increased Pro-inflammatory Cytokines
4. Thalassemia Minor and Major: Current Management
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1. BIOCHEMICAL STUDY OF SERUM β-HYDROXYBUTYRATE DEHYDROGENASE IN β-THALASSEMIA;Military Medical Science Letters;2023-03-03
2. Correlation of Erythroferrone and Hepcidin Hormones with Iron Status Levels in Patients with Iron Deficiency;Journal of Applied Hematology;2023
3. Is the Role of Hepcidin and Erythroferrone in the Pathogenesis of Beta Thalassemia the Key to Developing Novel Treatment Strategies?;Thalassemia Reports;2022-09-09
4. Comparison between H63D and G71D gene mutation effects on iron overload in Iraqi patients with β-thalassemia major: A case–control study;Iraqi Journal of Hematology;2022
5. Improving Ineffective Erythropoiesis in Thalassemia: A Hope on the Horizon;Cureus;2021-10-05
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