(Q41758975)

8 October 2017

1 reference

title

Hemochromatosis after the gene discovery: revisiting the diagnostic strategy (English)

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8 October 2017

P Brissot

1

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8 October 2017

R Moirand

2

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8 October 2017

D Guyader

3

1 reference

8 October 2017

O Loréal

4

1 reference

8 October 2017

B Turlin

5

1 reference

8 October 2017

Y Deugnier

6

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8 October 2017

publication date

1 January 1998

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8 October 2017

published in

Journal of Hepatology

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8 October 2017

volume

28 Suppl 1

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8 October 2017

page(s)

14-18

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

8 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

Haemochromatosis and HLA-H

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

Global prevalence of putative haemochromatosis mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

Haemochromatosis and HLA-H.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

Mutations in the MHC class I-like candidate gene for hemochromatosis in French patients

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

Genetic and clinical description of hemochromatosis probands and heterozygotes: evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

1 reference

7 January 2021

Clinical features of genetic hemochromatosis in women compared with men.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

The relationship between iron overload, clinical symptoms, and age in 410 patients with genetic hemochromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

Screening for hemochromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

Twenty-four hour variation of transferrin saturation in treated and untreated haemochromatosis homozygotes

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

Clinical and biochemical abnormalities in people heterozygous for hemochromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

Ascorbic acid status in idiopathic hemochromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

A new syndrome of liver iron overload with normal transferrin saturation.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

Increase in glycosylated and nonglycosylated serum ferritin in chronic alcoholism and their evolution during alcohol withdrawal

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

Regulation of ferritin expression by alcohol in a human hepatoblastoma cell line and in rat hepatocyte cultures

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

1 reference

7 January 2021

A linkage between hereditary hyperferritinaemia not related to iron overload and autosomal dominant congenital cataract

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

Mutation in the iron responsive element of the L ferritin mRNA in a family with dominant hyperferritinaemia and cataract

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

Liver pathology in genetic hemochromatosis: a review of 135 homozygous cases and their bioclinical correlations

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

Determination of hepatic iron concentration in fresh and paraffin-embedded tissue: diagnostic implications

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

Variability in hepatic iron concentration measurement from needle-biopsy specimens

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

Hemosiderosis in cirrhosis: a study of 447 native livers

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

A reappraisal of hepatic siderosis in patients with end-stage cirrhosis: practical implications for the diagnosis of hemochromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

Liver fibrosis in genetic hemochromatosis. Respective roles of iron and non-iron-related factors in 127 homozygous patients

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

Clinical and family studies in genetic hemochromatosis: microsatellite and HFE studies in five atypical families

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980369-3

7 January 2021

10.1016/S0168-8278(98)80369-3

Identifiers

DOI

1 reference

8 October 2017

1 reference