Literature DB >> 7333813

Clinical features of amyotrophic amyotrophic lateral sclerosis.

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.

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Year:  1981        PMID: 7333813     DOI: 10.1007/bf02335430

Source DB:  PubMed          Journal:  Ital J Neurol Sci        ISSN: 0392-0461


  2 in total

1.  Clinical features and associations of 560 cases of motor neuron disease.

Authors:  T M Li; E Alberman; M Swash
Journal:  J Neurol Neurosurg Psychiatry       Date:  1990-12       Impact factor: 10.154

2.  The prognosis of adult-onset motor neuron disease: a prospective study based on the Scottish Motor Neuron Disease Register.

Authors:  A M Chancellor; J M Slattery; H Fraser; R J Swingler; S M Holloway; C P Warlow
Journal:  J Neurol       Date:  1993-06       Impact factor: 4.849

  2 in total

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