Literature DB >> 7341546

Prognosis and clinical varieties of ALS disease.

P Mortara, D Bardelli, M Leone, D Schiffer.   

Abstract

210 cases of ALS disease in the period 1955-1979 are considered. Different parameters such as sex, age, duration and clinical course have been correlated with four clinical types: conventional, pseudopolyneuritic, pyramidal and bulbar. The age distribution shows a peak in the fifth decade of life. The sex ratio is 2.08:1. Considering together all the clinical types, the mean duration of the disease is 27.05 months. The bulbar variety has the poorest prognosis (19.6 months) and the pyramidal variety the best (37.59 months). Familiarity is evidenced in only 3 cases. All our data are discussed and compared with those of the literature.

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Year:  1981        PMID: 7341546     DOI: 10.1007/bf02335403

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


  14 in total

1.  Amyotrophic lateral sclerosis in Finland. I: An epidemiologic study.

Authors:  M Jokelainen
Journal:  Acta Neurol Scand       Date:  1977-09       Impact factor: 3.209

2.  Epidemiologic study of amyotrophic lateral sclerosis in Hawaii. Identification of high incidence among Filipino men.

Authors:  N Matsumoto; R M Worth; L T Kurland; H Okazaki
Journal:  Neurology       Date:  1972-09       Impact factor: 9.910

3.  Mexican "resistance" to amyotrophic lateral sclerosis.

Authors:  L Olivares; E S Estéban; M Alter
Journal:  Arch Neurol       Date:  1972-11

4.  [Clinico-statistical findings on 150 cases of amyotrophic lateral sclerosis].

Authors:  P Dazzi; F S Finizio; A Mercuriali
Journal:  G Psichiatr Neuropatol       Date:  1969

5.  [Epidemiological analysis of amyotrophic lateral sclerosis in Poznan District in Western Poland].

Authors:  W Cendrowski; M Wender; M Owsianowski
Journal:  Acta Neurol Scand       Date:  1970       Impact factor: 3.209

6.  ALS in Rochester, Minnesota, 1925-1977.

Authors:  S M Juergens; L T Kurland; H Okazaki; D W Mulder
Journal:  Neurology       Date:  1980-05       Impact factor: 9.910

7.  The epidemiology of amyotrophic lateral sclerosis in Finland. A study based on the death certificates of 421 patients.

Authors:  M Jokelainen
Journal:  J Neurol Sci       Date:  1976-09       Impact factor: 3.181

8.  Patient resistance and prognosis in amyotrophic lateral sclerosis.

Authors:  D W Mulder; F M Howard
Journal:  Mayo Clin Proc       Date:  1976-09       Impact factor: 7.616

9.  Amyotrophic lateral sclerosis. Clinical features and prognosis.

Authors:  A D Rosen
Journal:  Arch Neurol       Date:  1978-10

10.  Studies on epidemiological, clinical, and etiological aspects of ALS disease in Sardinia, Southern Italy.

Authors:  G Rosati; L Pinna; E Granieri; I Aiello; R Tola; V Agnetti; A Pirisi; P de Bastiani
Journal:  Acta Neurol Scand       Date:  1977-03       Impact factor: 3.209

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  3 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

3.  Natural history and clinical features of the flail arm and flail leg ALS variants.

Authors:  L C Wijesekera; S Mathers; P Talman; C Galtrey; M H Parkinson; J Ganesalingam; E Willey; M A Ampong; C M Ellis; C E Shaw; A Al-Chalabi; P N Leigh
Journal:  Neurology       Date:  2009-03-24       Impact factor: 9.910

  3 in total

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