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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1993-7-29
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pubmed:abstractText |
Probable or possible multiple system atrophy (MSA) was diagnosed on strict clinical criteria in 42 patients: 20 with combined parkinsonism and cerebellar ataxia, 9 with striatonigral degeneration (SND) and 13 with olivopontocerebellar atrophy (OPCA). All patients were then studied with 0.5 and/or 1.5 Tesla magnetic resonance (MR) units. MR imaged putaminal abnormalities in all 9 patients with SND and posterior fossa abnormalities consistent with OPCA in all 13 patients with this diagnosis. Of the 20 patients with parkinsonism and cerebellar involvement, classified as probable MSA, 7 presented putaminal abnormalities only, 3 abnormalities consistent with OPCA only and 10 a combination of both. These findings show strong MRI support for the clinical diagnosis of MSA.
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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 |
Apr
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pubmed:issn |
0392-0461
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
14
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
211-6
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:8314674-Adult,
pubmed-meshheading:8314674-Aged,
pubmed-meshheading:8314674-Brain Diseases,
pubmed-meshheading:8314674-Corpus Striatum,
pubmed-meshheading:8314674-Female,
pubmed-meshheading:8314674-Humans,
pubmed-meshheading:8314674-Magnetic Resonance Imaging,
pubmed-meshheading:8314674-Male,
pubmed-meshheading:8314674-Middle Aged,
pubmed-meshheading:8314674-Nerve Degeneration,
pubmed-meshheading:8314674-Olivopontocerebellar Atrophies,
pubmed-meshheading:8314674-Parkinson Disease,
pubmed-meshheading:8314674-Shy-Drager Syndrome,
pubmed-meshheading:8314674-Substantia Nigra
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pubmed:year |
1993
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pubmed:articleTitle |
Multiple system atrophy. Clinical and MR observations on 42 cases.
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pubmed:affiliation |
Dipartimento di Neurologia, Istituto Nazionale Neurologico C. Besta, Milano.
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pubmed:publicationType |
Journal Article
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