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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
1997-1-8
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pubmed:abstractText |
McArdle's disease (myophosphorylase deficiency) results in the inability to metabolise skeletal muscle glycogen to lactate. A patient with this condition developed angina and therefore offered a unique opportunity to explore the differential expression of the defective myophosphorylase gene in skeletal and cardiac muscle.
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
|
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1355-6037
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:volume |
76
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
372-3
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:8983689-Aged,
pubmed-meshheading:8983689-Angina Pectoris,
pubmed-meshheading:8983689-Cardiac Pacing, Artificial,
pubmed-meshheading:8983689-Electrophoresis, Polyacrylamide Gel,
pubmed-meshheading:8983689-Gene Expression,
pubmed-meshheading:8983689-Glycogen Storage Disease Type V,
pubmed-meshheading:8983689-Humans,
pubmed-meshheading:8983689-Isoenzymes,
pubmed-meshheading:8983689-Lactic Acid,
pubmed-meshheading:8983689-Male,
pubmed-meshheading:8983689-Muscle, Skeletal,
pubmed-meshheading:8983689-Myocardium,
pubmed-meshheading:8983689-Phosphorylases
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pubmed:year |
1996
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pubmed:articleTitle |
Angina in McArdle's disease.
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pubmed:affiliation |
Royal Victoria Hospital, Belfast Northern Ireland.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Case Reports
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