(Q35859008)

English

Prevalence of HFE mutations and relation to serum iron status in patients with chronic hepatitis C and patients with nonalcoholic fatty liver disease in Taiwan

scientific article published in July 2005

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Prevalence of HFE mutations and relation to serum iron status in patients with chronic hepatitis C and patients with nonalcoholic fatty liver disease in Taiwan (English)

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

fatty liver disease

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

metabolic dysfunction–associated steatotic liver disease

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

chronic hepatitis C

1 reference

based on heuristic

inferred from title

chronic hepatitis

1 reference

based on heuristic

inferred from title

author name string

Tsung-Jung Lin

1

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Chih-Lin Lin

2

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Chaur-Shine Wang

3

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Shu-O Liu

4

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Li-Ying Liao

5

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

language of work or name

0 references

publication date

1 July 2005

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

World Journal of Gastroenterology

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

11

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

25

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

3905-3908

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4504894

11 July 2018

Heterozygosity for hereditary hemochromatosis is associated with more fibrosis in chronic hepatitis C.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4504894

11 July 2018

Global prevalence of putative haemochromatosis mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4504894

11 July 2018

Iron and chronic viral hepatitis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4504894

11 July 2018

Clinical and biochemical abnormalities in people heterozygous for hemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4504894

11 July 2018

Haemochromatosis and HLA-H.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4504894

11 July 2018

Iron in liver diseases other than hemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4504894

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4504894

11 July 2018

The pathology of hepatic iron overload: a free radical--mediated process?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4504894

11 July 2018

Measurements of iron status in patients with chronic hepatitis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4504894

11 July 2018

Relationship between serum ferritin and total body iron stores in idiopathic haemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4504894

11 July 2018

HFE mutations and chronic hepatitis C: H63D and C282Y heterozygosity are independent risk factors for liver fibrosis and cirrhosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4504894

24 September 2018

C282Y and H63D mutations in the HFE gene have no effect on iron overload disorders in Japan

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4504894

24 September 2018

Increased hepatic iron concentration in nonalcoholic steatohepatitis is associated with increased fibrosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4504894

24 September 2018

Iron overload in patients with chronic viral hepatitis: how common is it?

1 reference

https://pubmed.ncbi.nlm.nih.gov/15991291

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors

1 reference

https://pubmed.ncbi.nlm.nih.gov/15991291

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple genetic test identifies 90% of UK patients with haemochromatosis. The UK Haemochromatosis Consortium

1 reference

https://pubmed.ncbi.nlm.nih.gov/15991291

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid diagnosis of the HLA-H gene Cys 282 Tyr mutation in hemochromatosis by polymerase chain reaction--a very rare mutation in the Chinese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/15991291

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haemochromatosis and HLA-H

1 reference

https://pubmed.ncbi.nlm.nih.gov/15991291

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cheaper and more rapid polymerase chain reaction-restriction fragment length polymorphism method for the detection of the HLA-H gene mutations occurring in hereditary hemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15991291

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-term survival in patients with hereditary hemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15991291

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The relation of iron status and hemochromatosis gene mutations in patients with chronic hepatitis C

1 reference

https://pubmed.ncbi.nlm.nih.gov/15991291

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15991291

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HFE mutations, hepatic iron, and fibrosis: ethnic-specific association of NASH with C282Y but not with fibrotic severity

1 reference

https://pubmed.ncbi.nlm.nih.gov/15991291

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Non-alcoholic steatohepatitis and iron: increased prevalence of mutations of the HFE gene in non-alcoholic steatohepatitis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15991291

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Liver iron concentration in chronic viral hepatitis: a study of 98 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/15991291

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterogeneity of hemochromatosis in Italy

1 reference

https://pubmed.ncbi.nlm.nih.gov/15991291

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.3748/WJG.V11.I25.3905

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

ResearchGate publication ID

0 references

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