|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
12
|
|
pubmed:dateCreated |
1996-9-19
|
|
pubmed:abstractText |
Patients with lipoprotein lipase deficiency usually present with chylomicronemia in childhood. The syndrome has been considered nonatherogenic primarily because of the low levels of low-density lipoprotein (LDL) cholesterol. We prospectively evaluated patients with lipoprotein lipase deficiency for atherosclerosis.
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|
pubmed:commentsCorrections |
|
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pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
AIM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Sep
|
|
pubmed:issn |
0028-4793
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:day |
19
|
|
pubmed:volume |
335
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
848-54
|
|
pubmed:dateRevised |
2006-11-15
|
|
pubmed:meshHeading |
pubmed-meshheading:8778602-Aged,
pubmed-meshheading:8778602-Arteriosclerosis,
pubmed-meshheading:8778602-Cholesterol,
pubmed-meshheading:8778602-Female,
pubmed-meshheading:8778602-Humans,
pubmed-meshheading:8778602-Hyperlipoproteinemia Type I,
pubmed-meshheading:8778602-Lipoprotein Lipase,
pubmed-meshheading:8778602-Male,
pubmed-meshheading:8778602-Middle Aged,
pubmed-meshheading:8778602-Mutation,
pubmed-meshheading:8778602-Pedigree,
pubmed-meshheading:8778602-Triglycerides
|
|
pubmed:year |
1996
|
|
pubmed:articleTitle |
Premature atherosclerosis in patients with familial chylomicronemia caused by mutations in the lipoprotein lipase gene.
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|
pubmed:affiliation |
Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
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|
pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
|
