Hepcidin mutation in a β-thalassemia major patient with persistent severe iron overload despite chelation therapy-Reference-Cited by-同舟云学术

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Hepcidin mutation in a β-thalassemia major patient with persistent severe iron overload despite chelation therapy

Published:2009-09-12 Issue:1 Volume:5 Page:83-85
ISSN:1828-0447
Container-title:Internal and Emergency Medicine
language:en
Short-container-title:Intern Emerg Med

Author:

Duca Lorena,Delbini Paola,Nava Isabella,Cappellini Maria Domenica,Meo Anna

Publisher

Springer Science and Business Media LLC

Subject

Emergency Medicine,Internal Medicine

Link

http://link.springer.com/content/pdf/10.1007/s11739-009-0306-8.pdf

Reference5 articles.

1. Darshan D, Anderson GJ (2009) Interacting signals in the control hepcidin expression. Biometals 22:77–87

2. Adamsky K, Weizer O, Amariglio N et al (2004) Decreased hepcidin mRNA expression in thalassemic mice. Br J Haematol 124:123–124

3. Porter JB, Abeysinghe RD, Marshall L et al (1996) Kinetics of removal and reappearance of non-transferrin-bound plasma iron with deferoxamine therapy. Blood 88:705–713

4. Biasiotto G, Roetto A, Daraio F et al (2004) Identification of new mutations of hepcidin and hemojuvelin in patients with HFE C282Y allele. Blood Cells Mol Dis 33:338–343

5. De Diego C, Opazo S, Murga MJ et al (2006) H63D homozygotes with hyperferritinaemia: is this genotype, the primary cause of iron overload? Eur J Haematol 78:66–71

Cited by 4 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. 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

3. Risk factors for heart disease in transfusion-dependent thalassemia: serum ferritin revisited;Internal and Emergency Medicine;2018-06-12

4. Genetic modifiers of secondary iron overload in beta thalassemia major;Blood Cells, Molecules, and Diseases;2015-03

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