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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
|
| pubmed:dateCreated |
1982-5-12
|
| pubmed:abstractText |
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.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
May
|
| pubmed:issn |
0392-0461
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
2
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
113-7
|
| pubmed:dateRevised |
2004-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:7333813-Adult,
pubmed-meshheading:7333813-Amyotrophic Lateral Sclerosis,
pubmed-meshheading:7333813-Diagnosis, Differential,
pubmed-meshheading:7333813-Female,
pubmed-meshheading:7333813-Humans,
pubmed-meshheading:7333813-Male,
pubmed-meshheading:7333813-Middle Aged,
pubmed-meshheading:7333813-Prognosis
|
| pubmed:year |
1981
|
| pubmed:articleTitle |
Clinical features of amyotrophic amyotrophic lateral sclerosis.
|
| pubmed:publicationType |
Journal Article
|