Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

HFE gene mutations in Polish patients with disturbances of iron metabolism: an initial assessment.

International journal of molecular medicine - 1 Dec 2005

Sikorska Katarzyna, Bielawski Krzysztof Piotr, Stalke Piotr, Lakomy Elzbieta Anna, Michalska Zofia, Witczak-Malinowska Krystyna, Romanowski Tomasz

Abstract excerpt

Hereditary hemochromatosis is one of the most frequent genetic disorders in Europeans, but its prevalence in Poland is still unknown. The aim of the study was an initial assessment of the prevalence of C282Y and H62D HFE gene mutations and their influence on the course of chronic hepatitis C. For...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Blood Chemical Analysis
Share to Hemochromatosis Protein
Share to Hepacivirus

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Histocompatibility Antigens Class I

Share to Iron Metabolism Disorders

Share to Iron Overload

Share to Poland

Source

Identifiers

PMID: 16273299

Genes

HFE

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16273299-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

HFE gene mutations in Polish patients with disturbances of iron metabolism: an initial assessment.PMID 16273299Read ↗

Iron overload and HFE gene mutations in Czech patients with chronic liver diseases.Semantic proximity Read ↗

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

HFE gene mutations in patients with alcoholic liver disease. A prospective study from northwestern Poland.Semantic proximity Read ↗

Iron overload and HFE gene mutations in Polish patients with liver cirrhosis.Semantic proximity Read ↗

HFE Gene Mutations and Iron Status in 100 Healthy Polish Children.Semantic proximity Read ↗

HFE gene mutations in patients with altered iron metabolism in Argentina.Semantic proximity Read ↗

Prevalence and clinical significance of HFE gene mutations in patients with iron overload.Semantic proximity Read ↗

The prevalence of HFE C282Y gene mutation is increased in Spanish patients with porphyria cutanea tarda without hepatitis C virus infection.Semantic proximity Read ↗

Mutations in the HFE gene (C282Y, H63D, S65C) in a Brazilian populationSemantic proximity Read ↗

Hemochromatosis (HFE) gene mutations and hepatitis C virus infection as risk factors for porphyria cutanea tarda in Hungarian patients.Semantic proximity Read ↗

Analysis of HFE genes C282Y, H63D, and S65D in patients with hyperferritinemia from northeastern Brazil.Semantic proximity Read ↗

Analysis of HFE gene mutations and HLA-A alleles in Brazilian patients with iron overload.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.