Hemochromatosis gene and nonalcoholic fatty liver disease: a systematic review and meta-analysis. (Q36727784)

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23 January 2020

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title

Hemochromatosis gene and nonalcoholic fatty liver disease: a systematic review and meta-analysis (English)

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23 January 2020

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metabolic dysfunction–associated steatotic liver disease

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1

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23 January 2020

Edwina Yeung

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Kris V Kowdley

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23 January 2020

author name string

Jeanne M Clark

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23 January 2020

Frederick L Brancati

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Wen Hong Linda Kao

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publication date

24 February 2011

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23 January 2020

published in

Journal of Hepatology

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volume

55

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issue

5

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23 January 2020

page(s)

1079-1085

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Nonalcoholic fatty liver disease and HFE gene mutations: a Polish study

23 January 2020

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Histological evaluation of iron in liver biopsies: relationship to HFE mutations.

30 September 2017

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Serum ferritin is a clinical biomarker in Japanese patients with nonalcoholic steatohepatitis (NASH) independent of HFE gene mutation.

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Iron overload alters glucose homeostasis, causes liver steatosis, and increases serum triacylglycerols in rats

5 September 2018

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5 September 2018

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5 September 2018

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5 September 2018

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5 September 2018

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5 September 2018

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5 September 2018

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5 September 2018

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5 September 2018

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5 September 2018

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The origin and spread of the HFE-C282Y haemochromatosis mutation

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HFE mutations, hepatic iron, and fibrosis: ethnic-specific association of NASH with C282Y but not with fibrotic severity

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Dietary iron overload and induced lipid peroxidation are associated with impaired plasma lipid transport and hepatic sterol metabolism in rats

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The clinical relevance of compound heterozygosity for the C282Y and H63D substitutions in hemochromatosis

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Hemochromatosis genotypes and risk of 31 disease endpoints: meta-analyses including 66,000 cases and 226,000 controls

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10.1016/J.JHEP.2011.02.013

Identifiers

DOI

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23 January 2020

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23 January 2020

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