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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
|
pubmed:dateCreated |
1978-9-25
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pubmed:abstractText |
We describe the clinical, pathologic, and ultrastructural findings in a case of juvenile onset neuronal ceroid-lipofuscinosis without visual symptoms or retinal abnormalities. The histochemical and ultrastructural characteristics of the neuronal lipopigment were similar to those in typical cases of neuronal ceroid-lipofuscinosis. Atypical neuronal ceroid-lipofuscinosis may be distinguished histochemically, ultrastructurally, and clinically from another disorder called juvenile dystonic lipidosis, with which it has been confused.
|
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jul
|
pubmed:issn |
0028-3878
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
28
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
710-7
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:566870-Adolescent,
pubmed-meshheading:566870-Brain,
pubmed-meshheading:566870-Ceroid,
pubmed-meshheading:566870-Female,
pubmed-meshheading:566870-Humans,
pubmed-meshheading:566870-Lipidoses,
pubmed-meshheading:566870-Lipofuscin,
pubmed-meshheading:566870-Nervous System Diseases,
pubmed-meshheading:566870-Neurons,
pubmed-meshheading:566870-Pigments, Biological
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pubmed:year |
1978
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pubmed:articleTitle |
Atypical neuronal ceroid-lipofuscinosis.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Case Reports
|