rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
10
|
pubmed:dateCreated |
2010-9-29
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pubmed:abstractText |
Familial hypercholesterolemia (FH) due to mutations in the low-density lipoprotein receptor (LDLR) gene exhibit severe, premature aortic calcification in a gene-dosage, age-dependent fashion. We sought to determine potential associations with mineral and skeletal indices.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
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pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
1530-8561
|
pubmed:author |
|
pubmed:issnType |
Electronic
|
pubmed:volume |
56
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1599-607
|
pubmed:dateRevised |
2010-11-18
|
pubmed:meshHeading |
pubmed-meshheading:20702785-Aortic Diseases,
pubmed-meshheading:20702785-Aortography,
pubmed-meshheading:20702785-Bone Density,
pubmed-meshheading:20702785-Bone and Bones,
pubmed-meshheading:20702785-Calcinosis,
pubmed-meshheading:20702785-Calcium,
pubmed-meshheading:20702785-Female,
pubmed-meshheading:20702785-Homeostasis,
pubmed-meshheading:20702785-Humans,
pubmed-meshheading:20702785-Hyperlipoproteinemia Type II,
pubmed-meshheading:20702785-Hypolipidemic Agents,
pubmed-meshheading:20702785-Lipoproteins, LDL,
pubmed-meshheading:20702785-Male,
pubmed-meshheading:20702785-Middle Aged,
pubmed-meshheading:20702785-Mutation,
pubmed-meshheading:20702785-Osteocalcin,
pubmed-meshheading:20702785-Receptors, LDL,
pubmed-meshheading:20702785-Tomography, X-Ray Computed
|
pubmed:year |
2010
|
pubmed:articleTitle |
Calcium homeostasis and skeletal integrity in individuals with familial hypercholesterolemia and aortic calcification.
|
pubmed:affiliation |
Cardiovascular Research Laboratories, McGill University Health Centre and McGill University, Montreal, Quebec, Canada.
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pubmed:publicationType |
Journal Article
|