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Titolo:
Classification and clinical features of motor neurone diseases and motor neuropathies in adults
Autore:
Donaghy, M;
Indirizzi:
Univ Oxford, Radcliffe Infirm, Dept Clin Neurol, Oxford OX2 6HE, England Univ Oxford Oxford England OX2 6HE Clin Neurol, Oxford OX2 6HE, England
Titolo Testata:
JOURNAL OF NEUROLOGY
fascicolo: 5, volume: 246, anno: 1999,
pagine: 331 - 333
SICI:
0340-5354(199905)246:5<331:CACFOM>2.0.ZU;2-0
Fonte:
ISI
Lingua:
ENG
Soggetto:
AMYOTROPHIC-LATERAL-SCLEROSIS; MUSCULAR-ATROPHY; MUTATIONS; DISTAL; GENE;
Keywords:
motor neurone disease; amyotrophic lateral sclerosis; multifocal motor neuropathy;
Tipo documento:
Review
Natura:
Periodico
Settore Disciplinare:
Life Sciences
Citazioni:
13
Recensione:
Indirizzi per estratti:
Indirizzo: Donaghy, M UnivHE,ford, Radcliffe Infirm, Dept Clin Neurol, Woodstock Rd, Oxford OX2 6 Univ Oxford Woodstock Rd Oxford England OX2 6HE , Oxford OX2 6
Citazione:
M. Donaghy, "Classification and clinical features of motor neurone diseases and motor neuropathies in adults", J NEUROL, 246(5), 1999, pp. 331-333

Abstract

The term motor neurone disease encompasses combined upper and lower motor neurone disorders (amyotrophic lateral sclerosis), pure lower motor neuronedisorders (spinal muscular atrophies, multifocal motor neuropathies, post irradiation lumbosacral radiculopathy, postpolio syndrome, hereditary bulbar palsy) and pure upper motor neurone disorders (primary lateral sclerosis,hereditary spastic paraplegia, neuro-lathyrism, Konzo). The chief clinicaland electrophysiological criteria for these different disorders are discussed, with particular attention to diagnostically distinctive characteristics of each. Age of onset, and inheritance are considered as additional diagnostic features.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 28/11/20 alle ore 04:05:29