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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2007-6-7
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pubmed:abstractText |
To determine the occurrence of neuroradiological abnormalities and to perform genotype-phenotype correlations in severe myoclonic epilepsy of infancy (SMEI, Dravet syndrome).
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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 |
Jun
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pubmed:issn |
0013-9580
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pubmed:author |
pubmed-author:BeccariaFrancescaF,
pubmed-author:BiancheriRobertaR,
pubmed-author:CapovillaGiuseppeG,
pubmed-author:Dalla BernardinaBernardoB,
pubmed-author:DarraFrancescaF,
pubmed-author:DravetCharlotteC,
pubmed-author:EliaMaurizioM,
pubmed-author:GaggeroRobertoR,
pubmed-author:GennaroElenaE,
pubmed-author:GiordanoLucioL,
pubmed-author:GobbiGiuseppeG,
pubmed-author:GranataTizianaT,
pubmed-author:GuerriniRenzoR,
pubmed-author:LongarettiFrancescaF,
pubmed-author:MadiaFrancescaF,
pubmed-author:MancardiMaria MargheritaMM,
pubmed-author:MariniCarlaC,
pubmed-author:MeiDavideD,
pubmed-author:MinettiCarloC,
pubmed-author:ParavidinoRobertaR,
pubmed-author:RagonaFrancescaF,
pubmed-author:RomeoAntoninoA,
pubmed-author:RossiAndreaA,
pubmed-author:SiriLauraL,
pubmed-author:SpecchioNicolaN,
pubmed-author:StrianoPasqualeP,
pubmed-author:StrianoSalvatoreS,
pubmed-author:TortoraFabioF,
pubmed-author:VigevanoFedericoF,
pubmed-author:ZaraFedericoF
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pubmed:issnType |
Print
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pubmed:volume |
48
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1092-6
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pubmed:meshHeading |
pubmed-meshheading:17381446-Adolescent,
pubmed-meshheading:17381446-Adult,
pubmed-meshheading:17381446-Brain,
pubmed-meshheading:17381446-Child,
pubmed-meshheading:17381446-Child, Preschool,
pubmed-meshheading:17381446-Chromatography, High Pressure Liquid,
pubmed-meshheading:17381446-Epilepsies, Myoclonic,
pubmed-meshheading:17381446-Female,
pubmed-meshheading:17381446-Genotype,
pubmed-meshheading:17381446-Hippocampus,
pubmed-meshheading:17381446-Humans,
pubmed-meshheading:17381446-Infant,
pubmed-meshheading:17381446-Magnetic Resonance Imaging,
pubmed-meshheading:17381446-Male,
pubmed-meshheading:17381446-Mutation,
pubmed-meshheading:17381446-Nerve Tissue Proteins,
pubmed-meshheading:17381446-Phenotype,
pubmed-meshheading:17381446-Retrospective Studies,
pubmed-meshheading:17381446-Severity of Illness Index,
pubmed-meshheading:17381446-Sodium Channels,
pubmed-meshheading:17381446-Syndrome
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pubmed:year |
2007
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pubmed:articleTitle |
Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations.
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pubmed:affiliation |
Muscular and Neurodegenerative Disease Unit, Institute G. Gaslini, University of Genova, Italy. pstriano@email.it
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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