MovDisordV3, PascalFrancis, Corpus, bibRecord, 002B33

The pathogenesis of multiple system atrophy : Past, present, and future

Identifieur interne : 002B33 ( PascalFrancis/Corpus ); précédent : 002B32; suivant : 002B34

The pathogenesis of multiple system atrophy : Past, present, and future

Auteurs : Evelyn Jaros ; David J. Burn

Source :

Movement disorders [ 0885-3185 ] ; 2000.

RBID : Pascal:00-0481440

Descripteurs français

Pascal (Inist)
- Atrophie multisystématisée, Inclusion cellulaire, Facteur trophique, Pathogénie, Evolution, Homme, α-Synucléine.

English descriptors

KwdEn :
- Cell inclusion, Evolution, Human, Multiple system atrophy, Pathogenesis, Trophic factor.

Abstract

Multiple system atrophy is a sporadic, adult-onset neurodegenerative disease of unknown etiology. The condition may be unique among neurodegenerative diseases by the prominent, if not primary, role played by the oligodendroglial cell in the pathogenetic process. Recent developments in our understanding of multiple system atrophy have included the detection of glial cytoplasmic inclusions and α-synuclein accumulation in these inclusions. The latter finding links multiple system atrophy as an "a-synucleinopathy" to Parkinson's disease and dementia with Lewy bodies. This article reviews recent important findings of potential relevance to the pathogenesis of multiple system atrophy. We also speculate on areas in which further advances may be made to progress our understanding of this devastating condition.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A11	`02`	`1`		`@1 BURN (David J.)`
A14	`01`			`@1 Department of Neuropathology, Newcastle General Hospital @2 Newcastle upon Tyne @3 GBR @Z 1 aut.`
A14	`02`			`@1 Department of Neurology, Royal Victoria Infirmary @2 Newcastle upon Tyne @3 GBR @Z 2 aut.`
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Format Inist (serveur)

NO :	PASCAL 00-0481440 INIST
ET :	The pathogenesis of multiple system atrophy : Past, present, and future
AU :	JAROS (Evelyn); BURN (David J.)
AF :	Department of Neuropathology, Newcastle General Hospital/Newcastle upon Tyne/Royaume-Uni (1 aut.); Department of Neurology, Royal Victoria Infirmary/Newcastle upon Tyne/Royaume-Uni (2 aut.)
DT :	Publication en série; Niveau analytique
SO :	Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2000; Vol. 15; No. 5; Pp. 784-788; Bibl. 61 ref.
LA :	Anglais
EA :	Multiple system atrophy is a sporadic, adult-onset neurodegenerative disease of unknown etiology. The condition may be unique among neurodegenerative diseases by the prominent, if not primary, role played by the oligodendroglial cell in the pathogenetic process. Recent developments in our understanding of multiple system atrophy have included the detection of glial cytoplasmic inclusions and α-synuclein accumulation in these inclusions. The latter finding links multiple system atrophy as an "a-synucleinopathy" to Parkinson's disease and dementia with Lewy bodies. This article reviews recent important findings of potential relevance to the pathogenesis of multiple system atrophy. We also speculate on areas in which further advances may be made to progress our understanding of this devastating condition.
CC :	002B17G
FD :	Atrophie multisystématisée; Inclusion cellulaire; Facteur trophique; Pathogénie; Evolution; Homme; α-Synucléine
FG :	Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Maladie dégénérative
ED :	Multiple system atrophy; Cell inclusion; Trophic factor; Pathogenesis; Evolution; Human
EG :	Nervous system diseases; Central nervous system disease; Cerebral disorder; Degenerative disease
SD :	Atrofia multisistematizada; Inclusión celular; Factor trófico; Patogenia; Evolución; Hombre
LO :	INIST-20953.354000091356830030
ID :	00-0481440

Links to Exploration step

Pascal:00-0481440

Le document en format XML

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	Movement Disorders (revue)
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Movement Disorders (revue)

The pathogenesis of multiple system atrophy : Past, present, and future

The pathogenesis of multiple system atrophy : Past, present, and future

Source :

Descripteurs français

English descriptors

Abstract

Notice en format standard (ISO 2709)

Format Inist (serveur)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri