Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:3122068rdf:typepubmed:Citationlld:pubmed
pubmed-article:3122068lifeskim:mentionsumls-concept:C1304649lld:lifeskim
pubmed-article:3122068lifeskim:mentionsumls-concept:C0684224lld:lifeskim
pubmed-article:3122068lifeskim:mentionsumls-concept:C0014550lld:lifeskim
pubmed-article:3122068lifeskim:mentionsumls-concept:C1857276lld:lifeskim
pubmed-article:3122068lifeskim:mentionsumls-concept:C0023866lld:lifeskim
pubmed-article:3122068lifeskim:mentionsumls-concept:C1552617lld:lifeskim
pubmed-article:3122068lifeskim:mentionsumls-concept:C0282443lld:lifeskim
pubmed-article:3122068lifeskim:mentionsumls-concept:C1533148lld:lifeskim
pubmed-article:3122068pubmed:issue4lld:pubmed
pubmed-article:3122068pubmed:dateCreated1988-2-25lld:pubmed
pubmed-article:3122068pubmed:abstractTextA patient with intention and action myoclonus, epilepsy, ataxia, and mental deterioration in association with ragged-red fibers in striated muscle is described. This patient demonstrated a unique form of erratic myoclonus with continuous EEG spike activity during eye closure. Both the myoclonus and the EEG spiking disappeared on opening the eyes. A defect in the activity of complex I in the respiratory chain was demonstrated.lld:pubmed
pubmed-article:3122068pubmed:languageenglld:pubmed
pubmed-article:3122068pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:3122068pubmed:citationSubsetIMlld:pubmed
pubmed-article:3122068pubmed:statusMEDLINElld:pubmed
pubmed-article:3122068pubmed:monthNovlld:pubmed
pubmed-article:3122068pubmed:issn0174-304Xlld:pubmed
pubmed-article:3122068pubmed:authorpubmed-author:AicardiJJlld:pubmed
pubmed-article:3122068pubmed:authorpubmed-author:GoutièresFFlld:pubmed
pubmed-article:3122068pubmed:authorpubmed-author:ChevrieJ JJJlld:pubmed
pubmed-article:3122068pubmed:authorpubmed-author:Garcia...lld:pubmed
pubmed-article:3122068pubmed:issnTypePrintlld:pubmed
pubmed-article:3122068pubmed:volume18lld:pubmed
pubmed-article:3122068pubmed:ownerNLMlld:pubmed
pubmed-article:3122068pubmed:authorsCompleteYlld:pubmed
pubmed-article:3122068pubmed:pagination200-4lld:pubmed
pubmed-article:3122068pubmed:dateRevised2011-11-17lld:pubmed
pubmed-article:3122068pubmed:meshHeadingpubmed-meshheading:3122068-...lld:pubmed
pubmed-article:3122068pubmed:meshHeadingpubmed-meshheading:3122068-...lld:pubmed
pubmed-article:3122068pubmed:meshHeadingpubmed-meshheading:3122068-...lld:pubmed
pubmed-article:3122068pubmed:meshHeadingpubmed-meshheading:3122068-...lld:pubmed
pubmed-article:3122068pubmed:meshHeadingpubmed-meshheading:3122068-...lld:pubmed
pubmed-article:3122068pubmed:meshHeadingpubmed-meshheading:3122068-...lld:pubmed
pubmed-article:3122068pubmed:meshHeadingpubmed-meshheading:3122068-...lld:pubmed
pubmed-article:3122068pubmed:meshHeadingpubmed-meshheading:3122068-...lld:pubmed
pubmed-article:3122068pubmed:meshHeadingpubmed-meshheading:3122068-...lld:pubmed
pubmed-article:3122068pubmed:meshHeadingpubmed-meshheading:3122068-...lld:pubmed
pubmed-article:3122068pubmed:meshHeadingpubmed-meshheading:3122068-...lld:pubmed
pubmed-article:3122068pubmed:year1987lld:pubmed
pubmed-article:3122068pubmed:articleTitleThe syndrome of myoclonic epilepsy with ragged-red fibers. Report of a case and review of the literature.lld:pubmed
pubmed-article:3122068pubmed:affiliationHôpital des Enfants Malades, Paris, France.lld:pubmed
pubmed-article:3122068pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:3122068pubmed:publicationTypeReviewlld:pubmed