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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
1992-10-22
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pubmed:abstractText |
The adrenoleukodystrophies refer to three genetically distinct disorders all characterized by the accumulation of very long-chain fatty acids. In this paper we will review the biochemical aspects of these leukodystrophies with particular emphasis on the methods used to measure very long-chain fatty acid levels in plasma and their reliability. Furthermore, we will concentrate on the primary defect in the X-linked form of adrenoleukodystrophy.
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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:issn |
0141-8955
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
15
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
634-44
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pubmed:dateRevised |
2007-3-21
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pubmed:meshHeading |
pubmed-meshheading:1528022-Adrenoleukodystrophy,
pubmed-meshheading:1528022-Coenzyme A Ligases,
pubmed-meshheading:1528022-Fatty Acids,
pubmed-meshheading:1528022-Humans,
pubmed-meshheading:1528022-Microbodies,
pubmed-meshheading:1528022-Mitochondria,
pubmed-meshheading:1528022-Oxidation-Reduction,
pubmed-meshheading:1528022-X Chromosome
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pubmed:year |
1992
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pubmed:articleTitle |
X-linked adrenoleukodystrophy: biochemical diagnosis and enzyme defect.
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pubmed:affiliation |
Department of Pediatrics, University Hospital of Amsterdam, The Netherlands.
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pubmed:publicationType |
Journal Article,
Review
|