Phenotypic expression of HFE mutations: a French study of 1110 unrelated iron-overloaded patients and relatives (Q77917919)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9922318%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

title

Phenotypic expression of HFE mutations: a French study of 1110 unrelated iron-overloaded patients and relatives (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9922318%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

author name string

R Moirand

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9922318%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

A M Jouanolle

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9922318%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

P Brissot

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9922318%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

J Y Le Gall

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9922318%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

V David

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9922318%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

Y Deugnier

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9922318%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

language of work or name

English

0 references

publication date

1 February 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9922318%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9922318%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

volume

116

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9922318%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

page(s)

372-377

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9922318%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9922318%20AND%20SRC:MED&resulttype=core&format=json

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

9 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

Putting a hold on "HLA-H'. The WHO Nomenclature Committee for Factors of the HLA System.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

Haemochromatosis and HLA-H.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

Haemochromatosis and HLA-H

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

The significance of the 187G (H63D) mutation in hemochromatosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

Measurement of liver-iron concentration in needle-biopsy specimens

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

Hemochromatosis: diagnosis and quantification of liver iron with gradient-echo MR imaging

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

Value of hepatic iron measurements in early hemochromatosis and determination of the critical iron level associated with fibrosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

Association between alcoholism and increased hepatic iron stores

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

Variability in hepatic iron concentration measurement from needle-biopsy specimens

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

Hemosiderosis in cirrhosis: a study of 447 native livers

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

Clinical and biochemical abnormalities in people heterozygous for hemochromatosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

Long-term survival analysis in hereditary hemochromatosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

Survival and prognostic factors in 212 Italian patients with genetic hemochromatosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

Survival and causes of death in cirrhotic and in noncirrhotic patients with primary hemochromatosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2899%2970134-4

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0016-5085(99)70134-4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9922318%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

1 reference