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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
1998-3-26
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pubmed:abstractText |
To evaluate the brain magnetic resonance (MR) imaging findings in patients with the "classic" form of congenital muscular dystrophy (patients with normal intelligence) in relation to the absence of merosin, a recently identified molecular component in the basement membrane of muscle fiber.
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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 |
Mar
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pubmed:issn |
0033-8419
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
206
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
811-6
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:9494506-Adult,
pubmed-meshheading:9494506-Biopsy,
pubmed-meshheading:9494506-Brain,
pubmed-meshheading:9494506-Child,
pubmed-meshheading:9494506-Female,
pubmed-meshheading:9494506-Humans,
pubmed-meshheading:9494506-Laminin,
pubmed-meshheading:9494506-Magnetic Resonance Imaging,
pubmed-meshheading:9494506-Male,
pubmed-meshheading:9494506-Muscle, Skeletal,
pubmed-meshheading:9494506-Muscle Fibers, Skeletal,
pubmed-meshheading:9494506-Muscular Dystrophies
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pubmed:year |
1998
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pubmed:articleTitle |
Congenital muscular dystrophy: use of brain MR imaging findings to predict merosin deficiency.
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pubmed:affiliation |
Department of Radiology, Hôpital Raymond Poincare, Garches, France.
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pubmed:publicationType |
Journal Article
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