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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Neuroradiology 31 (1989), S. 16-18 
    ISSN: 1432-1920
    Keywords: MRI ; Hereditary cerebellar ataxia ; Cerebellum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Thirty-two patients with primary progressive cerebellar ataxia were studied using MRI. This technique is better than CT in demonstrating atrophy of cerebellar structures as well as of brainstem and spinal cord. The differential diagnosis from other diseases particularly with multiple sclerosis is easier. The degree of ataxia correlated well with the degree of atrophy of cerebellum. However we could not see any correlation between the degree of atrophy and the onset and duration of the disease and no certain specific aspects could be demonstrated in the different groups examined.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Neurological sciences 2 (1981), S. 237-242 
    ISSN: 1590-3478
    Keywords: ALS disease ; varieties ; prognosis ; life tables
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Sommario Sono stati considerati 210 casi di Sclerosi Laterale Amiotrofica nel periodo dal 1955 al 1979. Sono stati messi in relazione ai 4 tipi clinici della malattia: tipo convenzionale, pseudopolinevritico, piramidale e bulbare, vari parametri quali sesso, età, durata e decorso clinico. La distribuzione per età mostra un picco di incidenza nella 5a decade di vita. Il rapporto maschi/femmine è di 2,08∶1. La durata mediana di malattia per tutti i 4 tipi è di 27,05 mesi. La varietà bulbare ha la prognosi peggiore (19,6 mesi) mentre quella piramidale ha la prognosi migliore (37,59 mesi). Solamente in 3 casi è stata messa in evidenza una storia familiare. Tutti i nostri dati sono discussi e confrontati con quelli della letteraura.
    Notes: 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.
    Type of Medium: Electronic Resource
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