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

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

Mayo Clinic proceedings - 1 Mar 2004

Olynyk John K, Hagan Simone E, Cullen Digby J, Beilby John, Whittall Davina E

Abstract excerpt

OBJECTIVE: To describe the evolution of biochemical and clinical features during a 17-year period in untreated subjects homozygous for the C282Y mutation in the hemochromatosis gene. SUBJECTS AND METHODS: In 1998, 12 subjects from Busselton, Australia, were newly diagnosed as being homozygous for the C282Y mutation. We determined transferrin saturation and ferritin values and retrieved clinical information from...

Read the complete abstract on PubMed

Topics

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

Share to Australia
Share to Ferritins
Share to Hemochromatosis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hemochromatosis Protein

Share to Histocompatibility Antigens Class I

Share to Liver Cirrhosis

Share to Population Surveillance

Share to Transferrin

Source

Identifiers

PMID: 15008603
DOI: 10.4065/79.3.309

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

Evolution of untreated hereditary hemochromatosis in the Busselton population: a 17-year study.PMID 15008603Read ↗

The natural history of serum iron indices for HFE C282Y homozygosity associated with hereditary hemochromatosis.Semantic proximity Read ↗

A population-based study of the clinical expression of the hemochromatosis gene.Semantic proximity Read ↗

Serial serum ferritin measurements in untreated HFE C282Y homozygotes in the Hemochromatosis and Iron Overload Screening Study.Semantic proximity Read ↗

Automated measurement of unsaturated iron binding capacity is an effective screening strategy for C282Y homozygous haemochromatosis.Semantic proximity Read ↗

HFE p.C282Y homozygosity predisposes to rapid serum ferritin rise after menopause: A genotype-stratified cohort study of hemochromatosis in Australian women.Semantic proximity Read ↗

Patient-focused outcomes following detection in a hospital-based screening programme for C282Y haemochromatosis.Semantic proximity Read ↗

Iron overload in urban Africans in the 1990s.Semantic proximity Read ↗

Hepatic iron concentration, fibrosis and response to venesection associated with the A77D and V162del "loss of function" mutations in ferroportin disease.Semantic proximity Read ↗

The impact of population-based screening studies on hemochromatosis screening practices.Semantic proximity Read ↗

Inherited haemochromatosis with C282Y mutation in a patient with alpha-thalassaemia: a treatment dilemma.Semantic proximity Read ↗

Deferasirox in patients with iron overload secondary to hereditary hemochromatosis: results of a 1-yr Phase 2 study.Semantic proximity Read ↗

Screening for hemochromatosis by measuring ferritin levels: a more effective approachSemantic proximity Read ↗

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