| Literature DB >> 7333813 |
P David, M Lo Monaco, G Palieri, C Scoppetta, S Servidei, P Tonali, M L Vaccario.
Abstract
The clinical features and course of amyotrophic lateral sclerosis are discussed. The data on a series of 116 patients are compared with those of the literature. The following points emerge: 1) when the disease starts before the age of 50, the prognosis is often less poor than usual; 2) the forms with spinal, and especially cervical, onset appear to be less rapid than bulbar forms; 3) in 20% of the patients survival is over 5 years. There may be some unknown factor that increases the resistance of some subject to the disease.Entities:
Mesh:
Year: 1981 PMID: 7333813 DOI: 10.1007/bf02335430
Source DB: PubMed Journal: Ital J Neurol Sci ISSN: 0392-0461