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rdf:type |
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|
lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
2011-3-29
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pubmed:abstractText |
Wolfram syndrome (WS) is a rare neurodegenerative disorder characterized by juvenile-onset diabetes mellitus and optic atrophy. Our aim was to describe the nature and the frequency of the neurologic manifestations, which had been poorly studied until now.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
|
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1531-8249
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pubmed:author |
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pubmed:copyrightInfo |
Copyright © 2010 American Neurological Association.
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pubmed:issnType |
Electronic
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pubmed:volume |
69
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
501-8
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pubmed:meshHeading |
pubmed-meshheading:21446023-Adolescent,
pubmed-meshheading:21446023-Adult,
pubmed-meshheading:21446023-Age Factors,
pubmed-meshheading:21446023-Alleles,
pubmed-meshheading:21446023-Child,
pubmed-meshheading:21446023-Cognition Disorders,
pubmed-meshheading:21446023-Epilepsy,
pubmed-meshheading:21446023-Female,
pubmed-meshheading:21446023-Genetic Association Studies,
pubmed-meshheading:21446023-Humans,
pubmed-meshheading:21446023-Male,
pubmed-meshheading:21446023-Membrane Proteins,
pubmed-meshheading:21446023-Mutation,
pubmed-meshheading:21446023-Nervous System Diseases,
pubmed-meshheading:21446023-Wolfram Syndrome
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pubmed:year |
2011
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pubmed:articleTitle |
Neurologic features and genotype-phenotype correlation in Wolfram syndrome.
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pubmed:affiliation |
Department of Medical Genetics, Archet 2 Hospital, CHU of Nice, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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