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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1992-9-10
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pubmed:abstractText |
Natural abundance 13C NMR (nuclear magnetic resonance) spectroscopy was used to distinguish patients suffering from muscle glycogenosis type V (McArdle's disease) from normal subjects by measuring their muscle glycogen content at rest. Proton-decoupled 13C spectra were obtained in 10-15 min from calf muscles at rest. The ratio of the glycogen/creatine signal areas was 12.9 +/- 1.7 in four McArdle's disease patients and 2.0 +/- 0.7 in seven normal subjects. This technique thus allows the non-invasive diagnosis of muscle glycogenosis.
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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 |
0960-8966
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
1
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
99-101
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:1822788-Adult,
pubmed-meshheading:1822788-Creatine,
pubmed-meshheading:1822788-Glycogen,
pubmed-meshheading:1822788-Glycogen Storage Disease Type V,
pubmed-meshheading:1822788-Humans,
pubmed-meshheading:1822788-Magnetic Resonance Spectroscopy,
pubmed-meshheading:1822788-Middle Aged,
pubmed-meshheading:1822788-Muscles
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pubmed:year |
1991
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pubmed:articleTitle |
Diagnosis of muscular glycogenosis by in vivo natural abundance 13C NMR spectroscopy.
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pubmed:affiliation |
Service Hospitalier Frederic Joliot, CEA, Orsay, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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