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Titolo:
Cerebellar diseases
Autore:
Shill, HA; Hallett, M;
Indirizzi:
NINCDS, Human Motor Control Sect, Med Neurol Branch, NIH, Bethesda, MD 20892 USA NINCDS Bethesda MD USA 20892 d Neurol Branch, NIH, Bethesda, MD 20892 USA
Titolo Testata:
INTERNATIONAL REVIEW OF PSYCHIATRY
fascicolo: 4, volume: 13, anno: 2001,
pagine: 261 - 267
SICI:
0954-0261(200111)13:4<261:CD>2.0.ZU;2-K
Fonte:
ISI
Lingua:
ENG
Soggetto:
MULTIPLE SYSTEM ATROPHY; FRIEDREICHS ATAXIA; ABNORMALITIES; DEGENERATION;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Social & Behavioral Sciences
Citazioni:
34
Recensione:
Indirizzi per estratti:
Indirizzo: Hallett, M NINCDS, Human Motor Control Sect, Med Neurol Branch, NIH, Bldg 10,Rm 5N226,10 Ctr Dr,MSC 1428, Bethesda, MD 20892 USA NINCDS Bldg 10,Rm 5N226,10 Ctr Dr,MSC 1428 Bethesda MD USA 20892
Citazione:
H.A. Shill e M. Hallett, "Cerebellar diseases", INT R PSYC, 13(4), 2001, pp. 261-267

Abstract

Cerebellar diseases are recognized by a combination of clinical findings consisting of gait ataxia, dysarthria, incoordination and eye movement abnormalities. The patient with a cerebellar syndrome can be classified by age of onset of symptoms and course of illness. In general, an acute presentation is more likely to have a symptomatic cause whereas a chronic, progressivecourse is likely to represent a neurodegenerative condition. Increasingly,the spectrum of cerebellar degeneration is being elucidated as molecular techniques identify genetic causes. This review synthesizes the clinical features of cerebellar dysfunction and presents a method for classifying the cerebellar disorders. Evaluation would then follow according to this classification and prognosis and treatment based on specific etiology determined.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 09/04/20 alle ore 06:57:58