Fatty liver in H63D homozygotes with hyperferritinemia (Q34012873)

30 July 2017

title

Fatty liver in H63D homozygotes with hyperferritinemia (English)

1 reference

30 July 2017

Giada Sebastiani

1

1 reference

30 July 2017

Daniel F Wallace

2

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30 July 2017

Susan E Davies

3

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30 July 2017

Vasu Kulhalli

4

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30 July 2017

Ann P Walker

5

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30 July 2017

James S Dooley

6

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30 July 2017

language of work or name

English

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publication date

1 March 2006

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World Journal of Gastroenterology

30 July 2017

published in

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30 July 2017

volume

12

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30 July 2017

issue

11

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30 July 2017

page(s)

1788-1792

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Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization

30 July 2017

cites work

1 reference

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5 July 2018

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Contribution of the H63D mutation in HFE to murine hereditary hemochromatosis

5 July 2018

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Variable phenotypic presentation of iron overload in H63D homozygotes: are genetic modifiers the cause?

5 July 2018

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5 July 2018

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Nonalcoholic steatohepatitis: a proposal for grading and staging the histological lesions

5 July 2018

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Multicentric origin of hemochromatosis gene (HFE) mutations

5 July 2018

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Steatohepatitis: a tale of two "hits"?

5 July 2018

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Global prevalence of putative haemochromatosis mutations

5 July 2018

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Haemochromatosis and HLA-H.

5 July 2018

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A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

5 July 2018

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Experimental liver cirrhosis induced by alcohol and iron

5 July 2018

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The natural history of nonalcoholic fatty liver: a follow-up study

5 July 2018

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5 July 2018

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H63D is an haemochromatosis associated allele

5 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.3748%2FWJG.V12.I11.1788

Banting lecture 1988. Role of insulin resistance in human disease

21 January 2018

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https://api.crossref.org/works/10.3748%2FWJG.V12.I11.1788

A new syndrome of liver iron overload with normal transferrin saturation

21 January 2018

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Screening selected blood donors with biochemical iron overload for hemochromatosis: a regional experience.

21 January 2018

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Non-alcoholic fatty liver disease: a multicentre clinical study by the Italian Association for the Study of the Liver

29 October 2018

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Nonalcoholic steatohepatitis: An expanded clinical entity

29 October 2018

1 reference

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HFE mutations, iron deficiency and overload in 10,500 blood donors

29 October 2018

1 reference

12 December 2020

A population-based study of the biochemical and clinical expression of the H63D hemochromatosis mutation

1 reference

12 December 2020

Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors

1 reference

12 December 2020

Compound heterozygotes for hemochromatosis gene mutations: may they help to understand the pathophysiology of the disease?

1 reference

12 December 2020

A simple genetic test identifies 90% of UK patients with haemochromatosis. The UK Haemochromatosis Consortium

1 reference

12 December 2020

Steatohepatitis-inducing drugs cause mitochondrial dysfunction and lipid peroxidation in rat hepatocytes

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12 December 2020

Molecular medicine and hemochromatosis: at the crossroads

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12 December 2020

Non-alcoholic steatohepatitis and iron: increased prevalence of mutations of the HFE gene in non-alcoholic steatohepatitis

1 reference

12 December 2020

Identifiers

DOI

10.3748/WJG.V12.I11.1788

1 reference

30 July 2017

1 reference

30 July 2017

1 reference