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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
12
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pubmed:dateCreated |
2000-12-14
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pubmed:abstractText |
Serum ferritin and heterozygosity for the C282Y mutation of the hemochromatosis gene have both been associated with an increased risk of cardiovascular events. The purpose of the study was to test whether either is a risk predictor for asymptomatic carotid atherosclerosis.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1524-4628
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
31
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3015-20
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11108765-Adult,
pubmed-meshheading:11108765-Aged,
pubmed-meshheading:11108765-Australia,
pubmed-meshheading:11108765-Carotid Artery Diseases,
pubmed-meshheading:11108765-Carotid Stenosis,
pubmed-meshheading:11108765-Female,
pubmed-meshheading:11108765-Ferritins,
pubmed-meshheading:11108765-Genotype,
pubmed-meshheading:11108765-Hemochromatosis,
pubmed-meshheading:11108765-Humans,
pubmed-meshheading:11108765-Male,
pubmed-meshheading:11108765-Middle Aged,
pubmed-meshheading:11108765-Mutation,
pubmed-meshheading:11108765-Prevalence,
pubmed-meshheading:11108765-Risk Factors,
pubmed-meshheading:11108765-Sampling Studies,
pubmed-meshheading:11108765-Ultrasonography, Doppler, Transcranial
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pubmed:year |
2000
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pubmed:articleTitle |
Serum ferritin and C282Y mutation of the hemochromatosis gene as predictors of asymptomatic carotid atherosclerosis in a community population.
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pubmed:affiliation |
Department of Clinical Biochemistry, PathCentre, Queen Elizabeth II Medical Centre, Nedlands, Western Australia. ric.rossi@health.wa.gov.au
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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