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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1
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pubmed:dateCreated |
1999-2-25
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pubmed:abstractText |
Salla disease is an autosomal recessive lysosomal free sialic acid storage disorder characterized by psychomotor retardation and ataxia. MRI studies have revealed evidence of dysmyelination, but the biological mechanism of the brain dysfunction is unknown.
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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 |
Jan
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pubmed:issn |
0161-5505
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pubmed:author |
pubmed-author:AärimaaTT,
pubmed-author:AulaPP,
pubmed-author:BergmanJJ,
pubmed-author:HaaparantaMM,
pubmed-author:HaatajaLL,
pubmed-author:HolopainenII,
pubmed-author:JääskeläinenSS,
pubmed-author:MannerTT,
pubmed-author:MetsähonkalaLL,
pubmed-author:RenlundMM,
pubmed-author:RuotsalainenUU,
pubmed-author:SillanpääMM,
pubmed-author:SolinOO,
pubmed-author:Suhonen-PolviHH,
pubmed-author:VainionpääLL,
pubmed-author:VatslIaIa
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pubmed:issnType |
Print
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pubmed:volume |
40
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
12-8
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9935050-Adolescent,
pubmed-meshheading:9935050-Adult,
pubmed-meshheading:9935050-Brain,
pubmed-meshheading:9935050-Child,
pubmed-meshheading:9935050-Child, Preschool,
pubmed-meshheading:9935050-Fluorodeoxyglucose F18,
pubmed-meshheading:9935050-Glucose,
pubmed-meshheading:9935050-Humans,
pubmed-meshheading:9935050-Infant,
pubmed-meshheading:9935050-Lysosomal Storage Diseases,
pubmed-meshheading:9935050-Magnetic Resonance Imaging,
pubmed-meshheading:9935050-Radiopharmaceuticals,
pubmed-meshheading:9935050-Sialic Acids,
pubmed-meshheading:9935050-Tomography, Emission-Computed
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pubmed:year |
1999
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pubmed:articleTitle |
Increased brain glucose utilization in Salla disease (free sialic acid storage disorder).
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pubmed:affiliation |
Department of Pediatric Neurology, University of Turku, Finland.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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