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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
10
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pubmed:dateCreated |
2001-10-8
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pubmed:abstractText |
Hereditary hemochromatosis (HH) is a common genetic disease leading to accumulation of iron in several organs, most notably the liver. The C282Y/C282Y mutation in the HFE gene is found in most cases. In order to prevent clinical disease and to study the cost and feasibility of screening, a large population was screened.
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pubmed:commentsCorrections |
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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 |
Oct
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pubmed:issn |
0036-5521
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
36
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1108-15
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:11589387-Adult,
pubmed-meshheading:11589387-Aged,
pubmed-meshheading:11589387-Aged, 80 and over,
pubmed-meshheading:11589387-Biological Markers,
pubmed-meshheading:11589387-Biopsy,
pubmed-meshheading:11589387-Cost-Benefit Analysis,
pubmed-meshheading:11589387-Female,
pubmed-meshheading:11589387-Ferritins,
pubmed-meshheading:11589387-Hemochromatosis,
pubmed-meshheading:11589387-Humans,
pubmed-meshheading:11589387-Liver,
pubmed-meshheading:11589387-Liver Cirrhosis,
pubmed-meshheading:11589387-Male,
pubmed-meshheading:11589387-Mass Screening,
pubmed-meshheading:11589387-Middle Aged,
pubmed-meshheading:11589387-Norway,
pubmed-meshheading:11589387-Prevalence,
pubmed-meshheading:11589387-Transferrin
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pubmed:year |
2001
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pubmed:articleTitle |
Screening for hemochromatosis: high prevalence and low morbidity in an unselected population of 65,238 persons.
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pubmed:affiliation |
Dept. of Clinical Chemistry, Trondheim University Hospital, Norway. arne.asberg@rit.no
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pubmed:publicationType |
Journal Article
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