Occult celiac disease prevents penetrance of hemochromatosis (Q35045685)

6 August 2017

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Occult celiac disease prevents penetrance of hemochromatosis (English)

1 reference

6 August 2017

Ralf Weiskirchen

7

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Guenter Weiss

4

object named as

Guenter Weiss

1 reference

6 August 2017

Andreas Geier

1

1 reference

6 August 2017

Carsten Gartung

2

1 reference

6 August 2017

Igor Theurl

3

1 reference

6 August 2017

Frank Lammert

5

1 reference

6 August 2017

Christoph-G Dietrich

6

1 reference

6 August 2017

Heinz Zoller

8

1 reference

6 August 2017

Benita Hermanns

9

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6 August 2017

Siegfried Matern

10

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6 August 2017

language of work or name

English

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publication date

1 June 2005

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World Journal of Gastroenterology

6 August 2017

published in

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6 August 2017

volume

11

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6 August 2017

issue

21

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6 August 2017

page(s)

3323-3326

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Molecular aspects of iron absorption: Insights into the role of HFE in hemochromatosis

6 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4316075

Intestinal expression of genes involved in iron absorption in humans

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4316075

Physiology of iron transport and the hemochromatosis gene.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4316075

Penetrance of 845G--> A (C282Y) HFE hereditary haemochromatosis mutation in the USA.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4316075

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4316075

Molecular aspects of iron absorption and HFE expression

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4316075

Hemochromatosis: diagnosis and management

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4316075

Current approaches to diagnosis and treatment of celiac disease: an evolving spectrum

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4316075

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4316075

Diagnosis of coeliac disease at open-access endoscopy

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4316075

An autosomal screen for genes that predispose to celiac disease in the western counties of Ireland

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4316075

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4316075

Subclinical coeliac disease is a frequent cause of iron-deficiency anaemia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4316075

Evidence for a primary association of celiac disease to a particular HLA-DQ alpha/beta heterodimer

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4316075

Association of HLA-A3 and HLA-B14 antigens with idiopathic haemochromatosis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4316075

Expression of the duodenal iron transporters divalent-metal transporter 1 and ferroportin 1 in iron deficiency and iron overload

8 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.3748%2FWJG.V11.I21.3323

The role of hemochromatosis susceptibility gene mutations in protecting against iron deficiency in celiac disease.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.3748%2FWJG.V11.I21.3323

High prevalence of celiac disease in Italian general population

21 January 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4316075

25 October 2018

https://api.crossref.org/works/10.3748%2FWJG.V11.I21.3323

Genetics of Hemochromatosis

21 January 2018

1 reference

12 December 2020

Duodenal metal-transporter (DMT-1, NRAMP-2) expression in patients with hereditary haemochromatosis

1 reference

12 December 2020

Precipitation of iron overload and hereditary hemochromatosis after successful treatment of celiac disease

1 reference

12 December 2020

Efficacy of gluten-free diet alone on recovery from iron deficiency anemia in adult celiac patients

1 reference

12 December 2020

Hemochromatosis and celiac sprue. Case report

1 reference

12 December 2020

Adult celiac disease and hemochromatosis

1 reference

12 December 2020

Idiopathic hemochromatosis. Demonstration of recessive transmission and early detection by family HLA typing

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.3748/WJG.V11.I21.3323

1 reference

6 August 2017

1 reference

6 August 2017

1 reference