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

Hemochromatosis gene mutations and iron metabolism in celiac disease.

Haematologica - 1 Nov 2004

Barisani Donatella, Ceroni Stefano, Del Bianco Silvia, Meneveri Raffaella, Bardella Maria Teresa

Abstract excerpt

BACKGROUND AND OBJECTIVES: Iron deficiency anemia is a common manifestation of celiac disease, which may be due to genetic and environmental factors. HFE mutations, frequent in Caucasian populations, can cause increased intestinal iron absorption and thus could protect against the development of iron deficiency. The aim of this study was to evaluate the prevalence of HFE mutations and their effect on iron...

Read the complete abstract on PubMed

Topics

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

Share to Celiac Disease
Share to Ferritins
Share to Glutens

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hemochromatosis

Share to Hemochromatosis Protein

Share to Hemoglobins

Share to Histocompatibility Antigens Class I

Source

Identifiers

PMID: 15531451

Genes

HFE

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hemochromatosis gene mutations and iron metabolism in celiac disease.PMID 15531451Read ↗

The role of hemochromatosis susceptibility gene mutations in protecting against iron deficiency in celiac disease.Semantic proximity Read ↗

The role of TMPRSS6 and HFE variants in iron deficiency anemia in celiac disease.Semantic proximity Read ↗

Haptoglobin polymorphism: a novel genetic risk factor for celiac disease development and its clinical manifestations.Semantic proximity Read ↗

HLA-DQB1*0201 homozygosis predisposes to severe intestinal damage in celiac disease.Semantic proximity Read ↗

Haemochromatosis gene mutations in a clustered Italian population: evidence of high prevalence in people of Celtic ancestry.Semantic proximity Read ↗

Hemochromatosis in Ireland and HFE.Semantic proximity Read ↗

Absence of hemochromatosis associated Cys282Tyr HFE gene mutation and low frequency of hemochromatosis phenotype in nonalcoholic chronic liver disease patients in India.Semantic proximity Read ↗

Hemochromatosis (HFE) gene mutations and risk of gastric cancer in the European Prospective Investigation into Cancer and Nutrition (EPIC) study.Semantic proximity Read ↗

Effects of C282Y, H63D, and S65C HFE gene mutations, diet, and life-style factors on iron status in a general Mediterranean population from Tarragona, Spain.Semantic proximity Read ↗

Hemochromatosis gene (HFE) mutations and cancer riskSemantic proximity Read ↗

Iron biomarkers in plasma, HFE genotypes, and the risk for colorectal cancer in a prospective setting.Semantic proximity Read ↗

The influence of hemochromatosis mutations on iron overload of thalassemia major.Semantic proximity Read ↗

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