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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1978-11-18
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pubmed:abstractText |
Leukocyte glycerolipid fatty acid compositions were determined in four patients of juvenile form of neuronal ceroid-lipofuscinosis (Battens disease), their parents and age-matched controls. A 54 to 93% reduction in docosahexaenoic acid (22:6, n-3) was noted in patient leukocytes. The parents also showed reduction in docosahexaenoic acid content, but to a lesser degree. The levels of linolenic family (n-6) polyunsaturated fatty acids were unchanged suggesting that the metabolic defect in this disease is specific to the linolenic family (n-3) of fatty acids.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0028-3797
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
9
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
127-30
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:581217-Adolescent,
pubmed-meshheading:581217-Child,
pubmed-meshheading:581217-Fatty Acids, Unsaturated,
pubmed-meshheading:581217-Female,
pubmed-meshheading:581217-Glycerides,
pubmed-meshheading:581217-Humans,
pubmed-meshheading:581217-Leukocytes,
pubmed-meshheading:581217-Lipidoses,
pubmed-meshheading:581217-Male
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pubmed:year |
1978
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pubmed:articleTitle |
Leukocyte docosahexaenoic acid in juvenile form of ceroid-lipofuscinosis.
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pubmed:publicationType |
Journal Article
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