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Volumn 249, Issue 7, 2002, Pages 847-854

Longitudinal MRI study of multiple system atrophy - When do the findings appear, and what is the course?

Author keywords

Magnetic resonance imaging (MRI); Multiple system atrophy; Pontine "cross sign"

Indexed keywords

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DIFFERENTIAL DIAGNOSIS; DISEASE COURSE; DISEASE DURATION; DISEASE SEVERITY; DOMINANT INHERITANCE; FEMALE; HUMAN; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; ONSET AGE; PONS; PRIORITY JOURNAL; PUTAMEN; SHY DRAGER SYNDROME;

EID: 0036305705     PISSN: 03405354     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00415-002-0734-0     Document Type: Article
Times cited : (120)

References (16)
  • 10
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    • Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy-Drager syndrome)
    • (1989) J Neurol Sci , vol.94 , pp. 79-100
    • Papp, M.I.1    Kahn, J.E.2    Lantos, P.L.3
  • 11
    • 0028339722 scopus 로고
    • The distribution of oligodendroglial inclusions in multiple system atrophy and its relevance to clinical symptomatology
    • (1994) Brain , vol.117 , pp. 235-243
    • Papp, M.I.1    Lantos, P.L.2
  • 16
    • 0029904204 scopus 로고    scopus 로고
    • Consensus statement on the definition of orthostatic hypotension, pure autonomic failure, and multiple system atrophy
    • (1996) Neurology , vol.46 , pp. 1470


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.