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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1980-5-14
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pubmed:abstractText |
The authors present results of histological and electron-microscopical investigations of muscular tissue obtained by biopsy from a 20-year-old man, who showed typical features of Marfan's syndrome associated with slowly progressive muscular weakness. The muscle showed a peculiar combination of centronuclear myopathy with hypotrophy of type I fibres and the so called "fingerprint myopathy". The combination of such myopathic phenomena with Marfan's syndrome presents a unique and hitherto undescribed condition.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0022-510X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
45
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
43-56
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:6244371-Adult,
pubmed-meshheading:6244371-Cell Nucleus,
pubmed-meshheading:6244371-Humans,
pubmed-meshheading:6244371-Inclusion Bodies,
pubmed-meshheading:6244371-Male,
pubmed-meshheading:6244371-Marfan Syndrome,
pubmed-meshheading:6244371-Muscle Hypotonia,
pubmed-meshheading:6244371-Muscles,
pubmed-meshheading:6244371-Muscular Atrophy
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pubmed:year |
1980
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pubmed:articleTitle |
Centronuclear myopathy with type I fibre hypotrophy and "fingerprint" inclusions associated with Marfan's syndrome.
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pubmed:publicationType |
Journal Article,
Case Reports
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