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Titolo:
Multiple system atrophy
Autore:
Wenning, GK; Seppi, K; Scherfler, C; Stefanova, N; Puschban, Z;
Indirizzi:
Univ Klin Neurol, Innsbruck, Austria Univ Klin Neurol Innsbruck AustriaUniv Klin Neurol, Innsbruck, Austria
Titolo Testata:
SEMINARS IN NEUROLOGY
fascicolo: 1, volume: 21, anno: 2001,
pagine: 33 - 40
SICI:
0271-8235(2001)21:1<33:MSA>2.0.ZU;2-6
Fonte:
ISI
Lingua:
ENG
Soggetto:
PROGRESSIVE SUPRANUCLEAR PALSY; POSITRON-EMISSION-TOMOGRAPHY; GLIAL CYTOPLASMIC INCLUSIONS; RICHARDSON-OLSZEWSKI SYNDROME; CLINICAL FOLLOW-UP; PARKINSONS-DISEASE; STRIATONIGRAL DEGENERATION; ALPHA-SYNUCLEIN; NATURAL-HISTORY; OLIVOPONTOCEREBELLAR ATROPHY;
Keywords:
multiple system atrophy; differential diagnosis; therapy;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Clinical Medicine
Citazioni:
68
Recensione:
Indirizzi per estratti:
Indirizzo: Wenning, GK Univ Innsbruck Hosp, Dept Neurol, Anichstr 35, A-6020 Innsbruck, Austria Univ Innsbruck Hosp Anichstr 35 Innsbruck Austria A-6020 tria
Citazione:
G.K. Wenning et al., "Multiple system atrophy", SEM NEUROL, 21(1), 2001, pp. 33-40

Abstract

Multiple system atrophy (MSA) is an adult-onset sporadic progressive neurodegenerative disorder of unknown etiology. It is clinically characterized by the variable combination of autonomic failure, parkinsonism, cerebellar ataxia, and pyramidal signs. The present review summarizes up-to-date knowledge on the clinical diagnosis and molecular pathology of MSA. We also review the role of additional investigations that may support a clinical diagnosis of MSA. Finally, we briefly discuss the management of MSA, focusing on possible future therapeutic strategies.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/01/20 alle ore 22:14:20