pubmed-article:8778602 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:8778602 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
pubmed-article:8778602 | lifeskim:mentions | umls-concept:C1867742 | lld:lifeskim |
pubmed-article:8778602 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
pubmed-article:8778602 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
pubmed-article:8778602 | lifeskim:mentions | umls-concept:C0023816 | lld:lifeskim |
pubmed-article:8778602 | lifeskim:mentions | umls-concept:C1314792 | lld:lifeskim |
pubmed-article:8778602 | lifeskim:mentions | umls-concept:C1706413 | lld:lifeskim |
pubmed-article:8778602 | pubmed:issue | 12 | lld:pubmed |
pubmed-article:8778602 | pubmed:dateCreated | 1996-9-19 | lld:pubmed |
pubmed-article:8778602 | 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. | lld:pubmed |
pubmed-article:8778602 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8778602 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8778602 | pubmed:language | eng | lld:pubmed |
pubmed-article:8778602 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8778602 | pubmed:citationSubset | AIM | lld:pubmed |
pubmed-article:8778602 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8778602 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8778602 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8778602 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:8778602 | pubmed:month | Sep | lld:pubmed |
pubmed-article:8778602 | pubmed:issn | 0028-4793 | lld:pubmed |
pubmed-article:8778602 | pubmed:author | pubmed-author:De GennesJ... | lld:pubmed |
pubmed-article:8778602 | pubmed:author | pubmed-author:HaydenMM | lld:pubmed |
pubmed-article:8778602 | pubmed:author | pubmed-author:ZhangHH | lld:pubmed |
pubmed-article:8778602 | pubmed:author | pubmed-author:BenlianPP | lld:pubmed |
pubmed-article:8778602 | pubmed:author | pubmed-author:FoubertLL | lld:pubmed |
pubmed-article:8778602 | pubmed:author | pubmed-author:GagnéS ESE | lld:pubmed |
pubmed-article:8778602 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:8778602 | pubmed:day | 19 | lld:pubmed |
pubmed-article:8778602 | pubmed:volume | 335 | lld:pubmed |
pubmed-article:8778602 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:8778602 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:8778602 | pubmed:pagination | 848-54 | lld:pubmed |
pubmed-article:8778602 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
pubmed-article:8778602 | pubmed:meshHeading | pubmed-meshheading:8778602-... | lld:pubmed |
pubmed-article:8778602 | pubmed:meshHeading | pubmed-meshheading:8778602-... | lld:pubmed |
pubmed-article:8778602 | pubmed:meshHeading | pubmed-meshheading:8778602-... | lld:pubmed |
pubmed-article:8778602 | pubmed:meshHeading | pubmed-meshheading:8778602-... | lld:pubmed |
pubmed-article:8778602 | pubmed:meshHeading | pubmed-meshheading:8778602-... | lld:pubmed |
pubmed-article:8778602 | pubmed:meshHeading | pubmed-meshheading:8778602-... | lld:pubmed |
pubmed-article:8778602 | pubmed:meshHeading | pubmed-meshheading:8778602-... | lld:pubmed |
pubmed-article:8778602 | pubmed:meshHeading | pubmed-meshheading:8778602-... | lld:pubmed |
pubmed-article:8778602 | pubmed:meshHeading | pubmed-meshheading:8778602-... | lld:pubmed |
pubmed-article:8778602 | pubmed:meshHeading | pubmed-meshheading:8778602-... | lld:pubmed |
pubmed-article:8778602 | pubmed:meshHeading | pubmed-meshheading:8778602-... | lld:pubmed |
pubmed-article:8778602 | pubmed:meshHeading | pubmed-meshheading:8778602-... | lld:pubmed |
pubmed-article:8778602 | pubmed:year | 1996 | lld:pubmed |
pubmed-article:8778602 | pubmed:articleTitle | Premature atherosclerosis in patients with familial chylomicronemia caused by mutations in the lipoprotein lipase gene. | lld:pubmed |
pubmed-article:8778602 | pubmed:affiliation | Department of Medical Genetics, University of British Columbia, Vancouver, Canada. | lld:pubmed |
pubmed-article:8778602 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:8778602 | pubmed:publicationType | Case Reports | lld:pubmed |
pubmed-article:8778602 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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