18362280

Source:http://linkedlifedata.com/resource/pubmed/id/18362280

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0205210, umls-concept:C0439849, umls-concept:C0445223, umls-concept:C0449774, umls-concept:C1420008, umls-concept:C1552599, umls-concept:C1704787
pubmed:issue	13
pubmed:dateCreated	2008-3-25
pubmed:abstractText	To clarify the clinical and neurophysiologic spectrum of myoclonus-dystonia patients with mutations of the SGCE gene.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Genetic Markers, http://linkedlifedata.com/resource/pubmed/chemical/SGCE protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Sarcoglycans
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	1526-632X
pubmed:author	pubmed-author:André-ObadiaNN, pubmed-author:ApartisEE, pubmed-author:Bahi-BuissonNN, pubmed-author:BeaugendreYY, pubmed-author:BriceAA, pubmed-author:ClotFF, pubmed-author:DürrAA, pubmed-author:DamierPP, pubmed-author:De GreslanTT, pubmed-author:DorisonNN, pubmed-author:DoummarDD, pubmed-author:DupontSS, pubmed-author:DussauleJ CJC, pubmed-author:Echaniz-LagunaAA, pubmed-author:Guyant-MarechalLL, pubmed-author:JedynakC PCP, pubmed-author:MalteteDD, pubmed-author:PereonYY, pubmed-author:PonsotGG, pubmed-author:RozeEE, pubmed-author:ThoboisSS, pubmed-author:TranchantCC, pubmed-author:VidailhetMM
pubmed:issnType	Electronic
pubmed:day	25
pubmed:volume	70
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1010-6
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:18362280-Adolescent, pubmed-meshheading:18362280-Adult, pubmed-meshheading:18362280-Aged, pubmed-meshheading:18362280-Brain, pubmed-meshheading:18362280-Child, pubmed-meshheading:18362280-Child, Preschool, pubmed-meshheading:18362280-DNA Mutational Analysis, pubmed-meshheading:18362280-Disease Progression, pubmed-meshheading:18362280-Dystonia, pubmed-meshheading:18362280-Electroencephalography, pubmed-meshheading:18362280-Female, pubmed-meshheading:18362280-Genetic Markers, pubmed-meshheading:18362280-Genetic Predisposition to Disease, pubmed-meshheading:18362280-Genetic Testing, pubmed-meshheading:18362280-Genotype, pubmed-meshheading:18362280-Humans, pubmed-meshheading:18362280-Male, pubmed-meshheading:18362280-Middle Aged, pubmed-meshheading:18362280-Muscle, Skeletal, pubmed-meshheading:18362280-Mutation, pubmed-meshheading:18362280-Myoclonus, pubmed-meshheading:18362280-Prospective Studies, pubmed-meshheading:18362280-Reflex, Abnormal, pubmed-meshheading:18362280-Remission, Spontaneous, pubmed-meshheading:18362280-Sarcoglycans
pubmed:year	2008
pubmed:articleTitle	Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutations.
pubmed:affiliation	Service de Neurologie, Hôpital Saint Antoine, 184 rue du Faubourg Saint-Antoine, 75571 Paris cedex 12, France. emmanuel.roze@sat.aphp.fr
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't