(Q36516216)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21959608%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

title

Low frequency of HFE gene mutations in Croatian patients suspected of having hereditary hemochromatosis (English)

1 reference

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13 February 2020

8

1 reference

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13 February 2020

7

Borut Peterlin

1 reference

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13 February 2020

author name string

Sandra Milić

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21959608%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

Smiljana Ristić

2

1 reference

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13 February 2020

Nada Starčević-Čizmarević

3

1 reference

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13 February 2020

Bojana Brajenović-Milić

4

1 reference

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13 February 2020

Marija Crnić-Martinović

5

1 reference

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13 February 2020

Miljenko Kapović

6

1 reference

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13 February 2020

publication date

1 October 2011

1 reference

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13 February 2020

published in

Medical Science Monitor

1 reference

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13 February 2020

volume

17

1 reference

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13 February 2020

issue

10

1 reference

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13 February 2020

page(s)

CR552-6

1 reference

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Clinical manifestations of hemochromatosis in HFE C282Y homozygotes identified by screening

13 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3539475

Iron storage disease: facts, fiction and progress

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3539475

Frequency of the HFE C282Y and H63D mutations in Danish patients with clinical haemochromatosis initially diagnosed by phenotypic methods

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3539475

HFE gene and hereditary hemochromatosis: a HuGE review. Human Genome Epidemiology

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3539475

Geography of HFE C282Y and H63D mutations

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3539475

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3539475

Hemochromatosis in Ireland and HFE

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3539475

Global prevalence of putative haemochromatosis mutations

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3539475

Mutation analysis of the HLA-H gene in Italian hemochromatosis patients

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3539475

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3539475

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3539475

The role of iron overload and HFE gene mutations in the era of pegylated interferon and ribavirin treatment of chronic hepatitis C.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3539475

Mutant HFE genotype leads to significant iron overload in patients with liver diseases from western Romania.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3539475

Genetic screening for HFE hemochromatosis in 6,020 Danish men: penetrance of C282Y, H63D, and S65C variants.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3539475

Hereditary hemochromatosis: HFE mutation analysis in Greeks reveals genetic heterogeneity

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3539475

Prevalence of the C282Y and H63D mutations in the HFE gene in patients with hereditary haemochromatosis and in control subjects from Northern Germany.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3539475

Screening for hemochromatosis: high prevalence and low morbidity in an unselected population of 65,238 persons

21 September 2018

1 reference

12 December 2020

Hemochromatosis gene mutations in the Croatian and Slovenian populations

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

Heterogeneity of hemochromatosis in Italy

1 reference

12 December 2020

HFEmutations in patients with hereditary haemochromatosis in Sweden

1 reference

12 December 2020

HFE mutations analysis in 711 hemochromatosis probands: evidence for S65C implication in mild form of hemochromatosis

1 reference

12 December 2020

Inherited HFE-unrelated hemochromatosis in Italian families

1 reference

12 December 2020

Frequency of HFE H63D, S65C, and C282Y mutations in patients with iron overload and controls from Toledo, Spain

1 reference

12 December 2020

Frequency and clinical expression of HFE gene mutations in a Spanish population of subjects with abnormal iron metabolism

1 reference

12 December 2020

Hemochromatosis genotypes and risk of 31 disease endpoints: meta-analyses including 66,000 cases and 226,000 controls

1 reference

12 December 2020

Abdominal ultrasound for diagnosis of nonalcoholic fatty liver disease (NAFLD)

1 reference

12 December 2020

Distribution of HFE gene mutations in Slovenian patients with hereditary hemochromatosis

1 reference

12 December 2020

Identifiers

DOI

10.12659/MSM.881980

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21959608%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21959608%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

PubMed publication ID

21959608

1 reference