H63/H63D genotype and the H63D allele are associated in patients with hyperferritinemia to the development of metabolic syndrome-Reference-Cited by-同舟云学术

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H63/H63D genotype and the H63D allele are associated in patients with hyperferritinemia to the development of metabolic syndrome

Published:2020-02 Issue: Volume:72 Page:106-107
ISSN:0953-6205
Container-title:European Journal of Internal Medicine
language:en
Short-container-title:European Journal of Internal Medicine

Author:

Castiella Agustin^ORCID,Urreta Iratxe,Zapata Eva,de Juan M Dolores,Emparanza Jose I.

Publisher

Elsevier BV

Subject

Internal Medicine

Reference8 articles.

1. Prevalence of the metabolic syndrome in Luxembourg according to the Joint Interim Statement definition estimated from the Oriscav-Lux study;Alkerwi;BMC Public Health,2011

2. Impact of H63D mutations, magnetic resonance and metabolic syndrome among outpatient referrals for elevated serum ferritin in the Basque Country;Castiella;Ann Hepatol,2015

3. How should hyperferritinemia be investigated and managed?;Ong;Eur J Intern Med,2016

4. Diagnostic algorithm for high iron overload: results from a prospective study of 312 patients with hyperferritinemia;Zapata;J Hepatol,2016

5. Harmonizing the Metabolic Syndrome

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