Hepcidin in hemochromatosis: The message or the messenger?
Author:
Affiliation:
1. Department of Medicine; University Hospital; London Ontario Canada
Publisher
Wiley
Subject
Hepatology
Reference21 articles.
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2. The hemochromatosis founder mutation in HLA-H disrupts beta-2-microglobulin interaction and cell surface expression;Feder;J Biol Chem,1997
3. Hepcidin, a key regulator of iron metabolism and mediator of anemia of inflammation;Ganz;Blood,2003
4. Disrupted hepcidin regulation in HFE-associated haemochromatosis and the liver as a regulator of body iron homeostasis;Bridle;Lancet,2003
5. Liver transplantation normalizes serum hepcidin level and cures iron metabolism alterations in HFE hemochromatosis;Bardou-Jacquet;Hepatology,2014
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2. Penetrance of HFE haemochromatosis variants to clinical disease: polygenic risk score associations in UK Biobank;2022-03-09
3. A farewell to phlebotomy—use of placenta-derived drugs Laennec and Porcine for improving hereditary hemochromatosis without phlebotomy: a case report;Journal of Medical Case Reports;2022-01-23
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