Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:12221176rdf:typepubmed:Citationlld:pubmed
pubmed-article:12221176lifeskim:mentionsumls-concept:C0442874lld:lifeskim
pubmed-article:12221176lifeskim:mentionsumls-concept:C0071316lld:lifeskim
pubmed-article:12221176lifeskim:mentionsumls-concept:C1417248lld:lifeskim
pubmed-article:12221176lifeskim:mentionsumls-concept:C0596611lld:lifeskim
pubmed-article:12221176lifeskim:mentionsumls-concept:C0332514lld:lifeskim
pubmed-article:12221176pubmed:issue5lld:pubmed
pubmed-article:12221176pubmed:dateCreated2002-9-10lld:pubmed
pubmed-article:12221176pubmed:abstractTextA patient with hereditary neuropathy presented with asymmetric distal weakness. On nerve biopsy, there was demyelination and onion-bulb formation, and molecular analysis revealed that the patient was heterozygous for an MPZ mutation. The patient improved with corticosteroid treatment.lld:pubmed
pubmed-article:12221176pubmed:languageenglld:pubmed
pubmed-article:12221176pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:12221176pubmed:citationSubsetAIMlld:pubmed
pubmed-article:12221176pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:12221176pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:12221176pubmed:statusMEDLINElld:pubmed
pubmed-article:12221176pubmed:monthSeplld:pubmed
pubmed-article:12221176pubmed:issn0028-3878lld:pubmed
pubmed-article:12221176pubmed:authorpubmed-author:WatanabeMMlld:pubmed
pubmed-article:12221176pubmed:authorpubmed-author:KohnoYYlld:pubmed
pubmed-article:12221176pubmed:authorpubmed-author:HayashiAAlld:pubmed
pubmed-article:12221176pubmed:authorpubmed-author:NagataHHlld:pubmed
pubmed-article:12221176pubmed:authorpubmed-author:YamamotoNNlld:pubmed
pubmed-article:12221176pubmed:authorpubmed-author:ShojiSSlld:pubmed
pubmed-article:12221176pubmed:authorpubmed-author:OhkoshiNNlld:pubmed
pubmed-article:12221176pubmed:authorpubmed-author:TamaokaAAlld:pubmed
pubmed-article:12221176pubmed:issnTypePrintlld:pubmed
pubmed-article:12221176pubmed:day10lld:pubmed
pubmed-article:12221176pubmed:volume59lld:pubmed
pubmed-article:12221176pubmed:ownerNLMlld:pubmed
pubmed-article:12221176pubmed:authorsCompleteYlld:pubmed
pubmed-article:12221176pubmed:pagination767-9lld:pubmed
pubmed-article:12221176pubmed:dateRevised2009-11-19lld:pubmed
pubmed-article:12221176pubmed:meshHeadingpubmed-meshheading:12221176...lld:pubmed
pubmed-article:12221176pubmed:meshHeadingpubmed-meshheading:12221176...lld:pubmed
pubmed-article:12221176pubmed:meshHeadingpubmed-meshheading:12221176...lld:pubmed
pubmed-article:12221176pubmed:meshHeadingpubmed-meshheading:12221176...lld:pubmed
pubmed-article:12221176pubmed:meshHeadingpubmed-meshheading:12221176...lld:pubmed
pubmed-article:12221176pubmed:meshHeadingpubmed-meshheading:12221176...lld:pubmed
pubmed-article:12221176pubmed:meshHeadingpubmed-meshheading:12221176...lld:pubmed
pubmed-article:12221176pubmed:meshHeadingpubmed-meshheading:12221176...lld:pubmed
pubmed-article:12221176pubmed:meshHeadingpubmed-meshheading:12221176...lld:pubmed
pubmed-article:12221176pubmed:year2002lld:pubmed
pubmed-article:12221176pubmed:articleTitleCorticosteroid- responsive asymmetric neuropathy with a myelin protein zero gene mutation.lld:pubmed
pubmed-article:12221176pubmed:affiliationDepartment of Neurology, Institute of Clinical Medicine, University of Tsukuba, Ibaraki, Japan. masa.wat@igaku.md.tsukuba.ac.jplld:pubmed
pubmed-article:12221176pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12221176pubmed:publicationTypeReviewlld:pubmed
pubmed-article:12221176pubmed:publicationTypeCase Reportslld:pubmed
entrez-gene:4359entrezgene:pubmedpubmed-article:12221176lld:entrezgene