Association of hepcidin promoter c.-582 A>G variant and iron overload in thalassemia major-Reference-Cited by-同舟云学术

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Association of hepcidin promoter c.-582 A>G variant and iron overload in thalassemia major

Published:2009-09-01 Issue:9 Volume:94 Page:1293-1296
ISSN:0390-6078
Container-title:Haematologica
language:en
Short-container-title:Haematologica

Author:

Andreani M.,Radio F. C.,Testi M.,De Bernardo C.,Troiano M.,Majore S.,Bertucci P.,Polchi P.,Rosati R.,Grammatico P.

Publisher

Ferrata Storti Foundation (Haematologica)

Subject

Hematology

Cited by 29 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. Genetic Correlation of HBB, HFE and HAMP Genes to Endocrinal Complications in Egyptian Beta Thalassemia Major Patients;Biochemical Genetics;2024-07-02

2. Molecular characterization of HAMP rs10421768 gene and phenotypic expression of hepcidin; a case-control study among sickle cell anaemia patients in Ghana;PLOS ONE;2024-06-27

3. Correlation of Serum Ferritin Levels with Creatinine, Sgot and Sgpt Levels in Thalassemia Major Patients;Advances in Social Science, Education and Humanities Research;2023

4. 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

5. Hepcidin (rs10421768), Transferrin (rs3811647, rs1049296) and Transferrin Receptor 2 (rs7385804) Gene Polymorphism Might Be Associated with the Origin of Multiple Sclerosis;International Journal of Environmental Research and Public Health;2022-06-04

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