Screening for hemochromatosis: patients with liver disease, families, and populations. (Q35628117)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14720453%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

review article

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title

Screening for hemochromatosis: patients with liver disease, families, and populations (English)

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17 November 2019

3

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17 November 2019

author name string

Sumedha P Galhenage

series ordinal

1

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17 November 2019

Charlie H Viiala

series ordinal

2

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17 November 2019

publication date

1 February 2004

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Current gastroenterology reports

17 November 2019

published in

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17 November 2019

volume

6

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17 November 2019

issue

1

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17 November 2019

page(s)

44-51

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https://scigraph.springernature.com/pub.10.1007/s11894-004-0025-2

17 November 2019

exact match

0 references

cites work

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Underdiagnosis of hereditary haemochromatosis: lack of presentation or penetration?

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

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

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Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis

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Histological evaluation of iron in liver biopsies: relationship to HFE mutations.

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Hereditary haemochromatosis: only 1% of adult HFEC282Y homozygotes in South Wales have a clinical diagnosis of iron overload

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

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Genetics of haemochromatosis

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Disrupted hepcidin regulation in HFE-associated haemochromatosis and the liver as a regulator of body iron homoeostasis.

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Expression of HLA-linked hemochromatosis in subjects homozygous or heterozygous for the C282Y mutation.

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Distribution of transferrin saturation in an Australian population: relevance to the early diagnosis of hemochromatosis.

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Noninvasive prediction of fibrosis in C282Y homozygous hemochromatosis

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Hereditary haemochromatosis: diagnosis and management in the gene era.

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

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Prevalence of hereditary haemochromatosis in late-onset type 1 diabetes mellitus: a retrospective study

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Prevalence of genetic haemochromatosis among diabetic patients

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Prevalence of hemochromatosis-related symptoms among individuals with mutations in the HFE gene

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Automated measurement of unsaturated iron binding capacity is an effective screening strategy for C282Y homozygous haemochromatosis

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Genetic testing for haemochromatosis in patients with chondrocalcinosis

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Constitutive hepcidin expression prevents iron overload in a mouse model of hemochromatosis

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Hepatic iron concentration as a predictor of response to interferon alfa therapy in chronic hepatitis C.

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

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Genetic polymorphisms and the progression of liver fibrosis: a critical appraisal

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Expression of hepcidin in hereditary hemochromatosis: evidence for a regulation in response to the serum transferrin saturation and to non-transferrin-bound iron

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Long-term survival in patients with hereditary hemochromatosis

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Haptoglobin phenotype 2-2 overrepresentation in Cys282Tyr hemochromatotic patients.

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Haptoglobin type neither influences iron accumulation in normal subjects nor predicts clinical presentation in HFE C282Y haemochromatosis: phenotype and genotype analysis.

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

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Lack of hepcidin gene expression and severe tissue iron overload in upstream stimulatory factor 2 (USF2) knockout mice

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Hereditary hemochromatosis. Detecting and correcting iron overload

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Seeking candidate mutations that affect iron homeostasis

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

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Evolution of untreated hereditary hemochromatosis in the Busselton population: a 17-year study.

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A mutation, in the iron-responsive element of H ferritin mRNA, causing autosomal dominant iron overload

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A population-based study of the biochemical and clinical expression of the H63D hemochromatosis mutation

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HFE mutations in an inflammatory arthritis population

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Hemochromatosis: diagnosis and management

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Molecular pathogenesis of iron overload.

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Heterogeneity of hemochromatosis in Italy

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

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Tumor necrosis factor alpha promoter polymorphisms influence the phenotypic expression of hereditary hemochromatosis

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Long-term survival analysis in hereditary hemochromatosis

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Estimating the efficacy and efficiency of cascade genetic screening

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

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Diagnosis and management of hemochromatosis.

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12 December 2020

10.1007/S11894-004-0025-2

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14720453%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

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