Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
1
|
| pubmed:dateCreated |
1978-8-28
|
| pubmed:abstractText |
Four patients with infantile familial sudanophilic leucodystrophy confirmed histologically and biochemically were investigated by E.E.G. and E.M.G. The E.E.G. showed a severe, non-specific slow wave abnormality, of moderate voltage and disorganized in 2 cases, with some critical' tonic' discharge. E.M.G. study was normal in relaxed muscle; peripheral nerve stimulation, however, revealed marked slowing of motor conduction velocities favouring a segmental demyelinisation process, which was ultimately confirmed histologically. This study underlines the value of investigation of infantile encephalopathies.
|
| pubmed:language |
fre
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:issn |
0370-4475
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
8
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
167-74
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:208121-Cerebral Cortex,
pubmed-meshheading:208121-Child, Preschool,
pubmed-meshheading:208121-Diffuse Cerebral Sclerosis of Schilder,
pubmed-meshheading:208121-Electroencephalography,
pubmed-meshheading:208121-Electromyography,
pubmed-meshheading:208121-Female,
pubmed-meshheading:208121-Humans,
pubmed-meshheading:208121-Infant,
pubmed-meshheading:208121-Infant, Newborn,
pubmed-meshheading:208121-Male,
pubmed-meshheading:208121-Neuromuscular Junction,
pubmed-meshheading:208121-Peripheral Nerves,
pubmed-meshheading:208121-Synaptic Transmission
|
| pubmed:articleTitle |
[The E.E.G. and E.M.G. findings in sudanophilic leucodystrophy (author's transl)].
|
| pubmed:publicationType |
Journal Article,
English Abstract
|