Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:930489rdf:typepubmed:Citationlld:pubmed
pubmed-article:930489lifeskim:mentionsumls-concept:C0008059lld:lifeskim
pubmed-article:930489lifeskim:mentionsumls-concept:C0439660lld:lifeskim
pubmed-article:930489lifeskim:mentionsumls-concept:C0015371lld:lifeskim
pubmed-article:930489lifeskim:mentionsumls-concept:C0441469lld:lifeskim
pubmed-article:930489lifeskim:mentionsumls-concept:C0205210lld:lifeskim
pubmed-article:930489lifeskim:mentionsumls-concept:C0750729lld:lifeskim
pubmed-article:930489pubmed:issue10lld:pubmed
pubmed-article:930489pubmed:dateCreated1978-1-27lld:pubmed
pubmed-article:930489pubmed:abstractTextThe report contains a description of the clinical development of hepato-cerebral dystrophy in 11 children and of deformans muscular dystrophy in 7 children. The authors indicate to expressed visceral disorders in patients with hepato-cerebral dystrophy and to positive results in the treatment by thiol preparations. The paper also contains an observation with an inheritance of deformans muscular dystonia of a dominant type. Due to a clinical polymorphism of hepato-cerebral dystrophy and deformans muscular dystrophy in children a possibility of a wide phenocopy of this pathology should be taken into consideration.lld:pubmed
pubmed-article:930489pubmed:languageruslld:pubmed
pubmed-article:930489pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:930489pubmed:citationSubsetIMlld:pubmed
pubmed-article:930489pubmed:statusMEDLINElld:pubmed
pubmed-article:930489pubmed:issn0044-4588lld:pubmed
pubmed-article:930489pubmed:authorpubmed-author:MalyshevIu...lld:pubmed
pubmed-article:930489pubmed:authorpubmed-author:BondarenkoE...lld:pubmed
pubmed-article:930489pubmed:issnTypePrintlld:pubmed
pubmed-article:930489pubmed:volume77lld:pubmed
pubmed-article:930489pubmed:ownerNLMlld:pubmed
pubmed-article:930489pubmed:authorsCompleteYlld:pubmed
pubmed-article:930489pubmed:pagination1458-63lld:pubmed
pubmed-article:930489pubmed:dateRevised2006-11-15lld:pubmed
pubmed-article:930489pubmed:meshHeadingpubmed-meshheading:930489-H...lld:pubmed
pubmed-article:930489pubmed:meshHeadingpubmed-meshheading:930489-A...lld:pubmed
pubmed-article:930489pubmed:meshHeadingpubmed-meshheading:930489-C...lld:pubmed
pubmed-article:930489pubmed:meshHeadingpubmed-meshheading:930489-H...lld:pubmed
pubmed-article:930489pubmed:meshHeadingpubmed-meshheading:930489-F...lld:pubmed
pubmed-article:930489pubmed:meshHeadingpubmed-meshheading:930489-M...lld:pubmed
pubmed-article:930489pubmed:meshHeadingpubmed-meshheading:930489-D...lld:pubmed
pubmed-article:930489pubmed:meshHeadingpubmed-meshheading:930489-B...lld:pubmed
pubmed-article:930489pubmed:year1977lld:pubmed
pubmed-article:930489pubmed:articleTitle[Clinical picture and course of hereditary extrapyramidal diseases in children].lld:pubmed
pubmed-article:930489pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:930489pubmed:publicationTypeEnglish Abstractlld:pubmed
pubmed-article:930489pubmed:publicationTypeCase Reportslld:pubmed