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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
6
|
| pubmed:dateCreated |
1988-6-17
|
| pubmed:abstractText |
We studied four patients with a focal epilepsy and bilateral occipital corticosubcortical calcifications without any sign of phakomatosis. The clinical course of the disease was similar in all the patients and evolved from a benign onset to a severe encephalopathy with progressive mental impairment. The question of whether these patients have an incomplete and atypical form of Sturge-Weber syndrome or a previously undescribed disorder is addressed.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
AIM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Jun
|
| pubmed:issn |
0028-3878
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
38
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
913-20
|
| pubmed:dateRevised |
2004-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:3368073-Adolescent,
pubmed-meshheading:3368073-Adult,
pubmed-meshheading:3368073-Brain Diseases,
pubmed-meshheading:3368073-Calcinosis,
pubmed-meshheading:3368073-Epilepsy,
pubmed-meshheading:3368073-Female,
pubmed-meshheading:3368073-Humans,
pubmed-meshheading:3368073-Male,
pubmed-meshheading:3368073-Occipital Lobe
|
| pubmed:year |
1988
|
| pubmed:articleTitle |
Epilepsy with bilateral occipital calcifications: a benign onset with progressive severity.
|
| pubmed:affiliation |
Department of Child Neurology, University of Bologna Medical School, Italy.
|
| pubmed:publicationType |
Journal Article
|