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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3-4
|
pubmed:dateCreated |
1982-9-24
|
pubmed:abstractText |
Some results of a follow-up study concerning 103 observations of chronic and transitory Lennox-Gastaut syndrome (SLG) are presented. The full-blown syndrome in the chronic SLG (mean duration 21 years and 2 months) is in 100% of the cases characterized by tonic seizures and 'complex absences', mental retardation and abnormal EEG with slow spike-waves and 10 c/sec recruiting bursts. Slow spike-waves are not the most specific EEG pattern of SLG with chronic outcome. The statement is discussed.
|
pubmed:language |
fre
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
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pubmed:month |
Dec
|
pubmed:issn |
0370-4475
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
11
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
468-73
|
pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:7345503-Child, Preschool,
pubmed-meshheading:7345503-Electroencephalography,
pubmed-meshheading:7345503-Follow-Up Studies,
pubmed-meshheading:7345503-Hemiplegia,
pubmed-meshheading:7345503-Humans,
pubmed-meshheading:7345503-Infant, Newborn,
pubmed-meshheading:7345503-Intellectual Disability,
pubmed-meshheading:7345503-Prognosis,
pubmed-meshheading:7345503-Spasms, Infantile,
pubmed-meshheading:7345503-Syndrome
|
pubmed:year |
1981
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pubmed:articleTitle |
[Nosological limits of the Lennox-Gastaut syndrome (author's transl)].
|
pubmed:publicationType |
Journal Article,
English Abstract
|