Impact of H63D mutations, magnetic resonance and metabolic syndrome among outpatient referrals for elevated serum ferritin in the Basque Country-Reference-Cited by-同舟云学术

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Impact of H63D mutations, magnetic resonance and metabolic syndrome among outpatient referrals for elevated serum ferritin in the Basque Country

Published:2015-05 Issue:3 Volume:14 Page:333-339
ISSN:1665-2681
Container-title:Annals of Hepatology
language:en
Short-container-title:Annals of Hepatology

Author:

Castiella Agustin,Zapata Eva,Zubiaurre Leire,Alustiza Jose Ma.,Juan Ma. Dolores De,Iribarren Arantxa,Emparanza Jose I.,Otazua Pedro

Publisher

Elsevier BV

Subject

Hepatology,General Medicine

Reference31 articles.

1. The diversity of liver diseases among outpatient referrals for elevated serum ferritin;Wong;Can J Gastroenterol,2006

2. Phenotypic characteristics and diagnoses of patients referred to an iron overload clinic;Dever;Dig Dis Sci,2010

3. Hyperferritinemia is a risk factor for steatosis in chronic liver disease;Licata;World J Gastroenterol,2009

4. The epidemiology of hyperferritinemia;Hearnshaw;World J Gastroenterol,2006

5. Hyperferritinemia in the Chinese and Asian community: A retrospective review of the university of British Columbia experience;Yenson;Can J Gastroenterol,2008

Cited by 7 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. Prediction of liver iron overload in the Basque country (Spain) in patients referred for hyperferritinemia;Digestive and Liver Disease;2021-01

2. H63/H63D genotype and the H63D allele are associated in patients with hyperferritinemia to the development of metabolic syndrome;European Journal of Internal Medicine;2020-02

3. Herediter hemokromatozun nadir bir nedeni: homozigot H63D;Cukurova Medical Journal;2018-12-30

4. Liver Iron Concentration in Patients Referred to a Secondary Hospital for Hyperferritinemia: Analysis of the Different Groups According to HFE Mutations and the Transferrin Saturation Index;Hepatitis Monthly;2017-01-01

5. Proven: The causative role of homozygous H63D mutation in hereditary haemochromatosis;Gastroenterología y Hepatología;2016-08

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