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Titolo:
A case of amyotrophic lateral sclerosis with a very slow progression over 44 years
Autore:
Grohme, K; von Maravic, M; Gasser, T; Borasio, GD;
Indirizzi:
Univ Munich, Klinikum Grosshadern, Dept Neurol, D-81366 Munich, Germany Univ Munich Munich Germany D-81366 Dept Neurol, D-81366 Munich, Germany Klinikum Erfurt, Dept Neurol, D-99089 Erfurt, Germany Klinikum Erfurt Erfurt Germany D-99089 t Neurol, D-99089 Erfurt, Germany
Titolo Testata:
NEUROMUSCULAR DISORDERS
fascicolo: 4, volume: 11, anno: 2001,
pagine: 414 - 416
SICI:
0960-8966(200105)11:4<414:ACOALS>2.0.ZU;2-R
Fonte:
ISI
Lingua:
ENG
Soggetto:
LINKAGE; GENE; FORM;
Keywords:
amyotrophic lateral sclerosis; motor neuron disease; long-term survival;
Tipo documento:
Editorial Material
Natura:
Periodico
Settore Disciplinare:
Life Sciences
Citazioni:
11
Recensione:
Indirizzi per estratti:
Indirizzo: Borasio, GD Univ Munich, Klinikum Grosshadern, Dept Neurol, D-81366 Munich, Germany Univ Munich Munich Germany D-81366 , D-81366 Munich, Germany
Citazione:
K. Grohme et al., "A case of amyotrophic lateral sclerosis with a very slow progression over 44 years", NEUROMUSC D, 11(4), 2001, pp. 414-416

Abstract

We report on a patient whose neurological and neurophysiological findings fulfil the El Escorial criteria for definite amyotrophic lateral sclerosis (ALS). and who is still alive 44 years after the initial diagnosis. Pertinent differential diagnoses were excluded on clinical and/or genetic grounds. Our patient has no afflicted relatives and her SOD1 testing was negative, thus allowing us to classify her form of ALS as sporadic. Informing ALS patients of the existence of documented cases with long-term survival can he ameans of fostering hope when delivering the diagnosis. (C) 2001 Elsevier Science B.V. All rights reserved.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 30/11/20 alle ore 00:44:28