(Q83155337)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16615007%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

title

Individuals homozygous for the H63D mutation have significantly elevated iron indexes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16615007%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference

Jason Samarasena

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16615007%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Wendy Winsor

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16615007%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Richard Lush

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16615007%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Peter Duggan

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16615007%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Yagang Xie

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16615007%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Mark Borgaonkar

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16615007%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

publication date

1 April 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16615007%20AND%20SRC:MED&resulttype=core&format=json

Digestive Diseases and Sciences

19 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16615007%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

volume

51

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16615007%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16615007%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

page(s)

803-807

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16615007%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s10620-006-3210-3

19 January 2020

exact match

0 references

cites work

HFE genotype in patients with hemochromatosis and other liver diseases.

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10620-006-3210-3

Is genetic screening for hemochromatosis worthwhile?

21 January 2018

1 reference

12 December 2020

Diagnosis and management of hemochromatosis

1 reference

12 December 2020

Hereditary hemochromatosis: update for 2003.

1 reference

12 December 2020

H63D is an haemochromatosis associated allele

1 reference

12 December 2020

Genotypic/phenotypic correlations in genetic hemochromatosis: evolution of diagnostic criteria.

1 reference

12 December 2020

A European allele map of the C282Y mutation of hemochromatosis: Celtic versus Viking origin of the mutation?

1 reference

12 December 2020

Frequency and biochemical expression of C282Y/H63D hemochromatosis (HFE) gene mutations in the healthy adult population in Italy

1 reference

12 December 2020

Contribution of the H63D mutation in HFE to murine hereditary hemochromatosis

1 reference

12 December 2020

A population-based study of the clinical expression of the hemochromatosis gene

1 reference

12 December 2020

The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding

1 reference

12 December 2020

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

1 reference

12 December 2020

EASL International Consensus Conference on Haemochromatosis

1 reference

12 December 2020

Prevalence of hereditary hemochromatosis in a Massachusetts corporation: is Celtic origin a risk factor?

1 reference

12 December 2020

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

1 reference

12 December 2020

Molecular medicine and hemochromatosis: at the crossroads

1 reference

12 December 2020

Long-term survival in patients with hereditary hemochromatosis

1 reference

12 December 2020

Prevalence and clinical significance of HFE gene mutations in patients with iron overload.

1 reference

12 December 2020

Hereditary Hemochromatosis and Its Elusive Natural History

1 reference

12 December 2020

Biochemical liver profile in hemochromatosis. A survey of 100 patients

1 reference

12 December 2020

Hereditary hemochromatosis--a new look at an old disease

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

Screening for genetic haemochromatosis in blood samples with raised alanine aminotransferase.

1 reference

12 December 2020

Prevalence of C282Y and H63D mutations in the hemochromatosis (HFE) gene in the United States

1 reference

12 December 2020

Hereditary hemochromatosis: gene discovery and its implications for population-based screening

1 reference

12 December 2020

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

1 reference

12 December 2020