Study of Serum Hepcidin in Hereditary Hemolytic Anemias-Reference-Cited by-同舟云学术

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Study of Serum Hepcidin in Hereditary Hemolytic Anemias

Published:2012-08 Issue:6 Volume:36 Page:555-570
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

El Beshlawy Amal,Alaraby Ibrahim,Abdel Kader Mohamed S.E.M.,Ahmed Dina H.,Abdelrahman Hossam E.M.

Publisher

Informa UK Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2012.721151

Reference30 articles.

1. Iron chelation in thalassemia: combined or monotherapy? The Egyptian experience

2. Advances in management of Thalassemia

3. Hepcidin, a Urinary Antimicrobial Peptide Synthesized in the Liver

4. Regulation of hepcidin: Insights from biochemical analyses on human serum samples

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1. Mitapivat reprograms the RBC metabolome and improves anemia in a mouse model of hereditary spherocytosis;JCI Insight;2023-10-23

2. Luspatercept stimulates erythropoiesis, increases iron utilization, and redistributes body iron in transfusion‐dependent thalassemia;American Journal of Hematology;2023-10-02

3. Effect of HFE Gene Mutations on Iron Metabolism of Beta-Thalassemia Carriers;Thalassemia Reports;2023-03-17

4. Molecular mechanisms of hepatic dysfunction in sickle cell disease: lessons from Townes mouse model;American Journal of Physiology-Cell Physiology;2022-08-01

5. Iron Status in Newly Diagnosed β-Thalassemia Major: High Rate of Iron Status due to Erythropoiesis Drive;BioMed Research International;2021-04-16

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