Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:15711422rdf:typepubmed:Citationlld:pubmed
pubmed-article:15711422lifeskim:mentionsumls-concept:C0030705lld:lifeskim
pubmed-article:15711422lifeskim:mentionsumls-concept:C0152035lld:lifeskim
pubmed-article:15711422lifeskim:mentionsumls-concept:C0242692lld:lifeskim
pubmed-article:15711422lifeskim:mentionsumls-concept:C0006685lld:lifeskim
pubmed-article:15711422lifeskim:mentionsumls-concept:C0238358lld:lifeskim
pubmed-article:15711422lifeskim:mentionsumls-concept:C0596611lld:lifeskim
pubmed-article:15711422lifeskim:mentionsumls-concept:C1413064lld:lifeskim
pubmed-article:15711422pubmed:issue2lld:pubmed
pubmed-article:15711422pubmed:dateCreated2005-2-15lld:pubmed
pubmed-article:15711422pubmed:abstractTextThyrotoxic periodic paralysis (TPP), familial periodic paralysis (FPP), and sporadic periodic paralysis (SPP) are common causes of hypokalemic periodic paralysis and have similar clinical presentations, thus possibly sharing the identical mutations.lld:pubmed
pubmed-article:15711422pubmed:languageenglld:pubmed
pubmed-article:15711422pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15711422pubmed:citationSubsetAIMlld:pubmed
pubmed-article:15711422pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15711422pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15711422pubmed:statusMEDLINElld:pubmed
pubmed-article:15711422pubmed:monthFeblld:pubmed
pubmed-article:15711422pubmed:issn0002-9629lld:pubmed
pubmed-article:15711422pubmed:authorpubmed-author:KaoMing-Ching...lld:pubmed
pubmed-article:15711422pubmed:authorpubmed-author:LinShih-HuaSHlld:pubmed
pubmed-article:15711422pubmed:authorpubmed-author:HsuYaw-DonYDlld:pubmed
pubmed-article:15711422pubmed:authorpubmed-author:ChengNai-LinN...lld:pubmed
pubmed-article:15711422pubmed:issnTypePrintlld:pubmed
pubmed-article:15711422pubmed:volume329lld:pubmed
pubmed-article:15711422pubmed:ownerNLMlld:pubmed
pubmed-article:15711422pubmed:authorsCompleteYlld:pubmed
pubmed-article:15711422pubmed:pagination66-70lld:pubmed
pubmed-article:15711422pubmed:meshHeadingpubmed-meshheading:15711422...lld:pubmed
pubmed-article:15711422pubmed:meshHeadingpubmed-meshheading:15711422...lld:pubmed
pubmed-article:15711422pubmed:meshHeadingpubmed-meshheading:15711422...lld:pubmed
pubmed-article:15711422pubmed:meshHeadingpubmed-meshheading:15711422...lld:pubmed
pubmed-article:15711422pubmed:meshHeadingpubmed-meshheading:15711422...lld:pubmed
pubmed-article:15711422pubmed:meshHeadingpubmed-meshheading:15711422...lld:pubmed
pubmed-article:15711422pubmed:meshHeadingpubmed-meshheading:15711422...lld:pubmed
pubmed-article:15711422pubmed:meshHeadingpubmed-meshheading:15711422...lld:pubmed
pubmed-article:15711422pubmed:meshHeadingpubmed-meshheading:15711422...lld:pubmed
pubmed-article:15711422pubmed:meshHeadingpubmed-meshheading:15711422...lld:pubmed
pubmed-article:15711422pubmed:year2005lld:pubmed
pubmed-article:15711422pubmed:articleTitleSkeletal muscle dihydropyridine-sensitive calcium channel (CACNA1S) gene mutations in chinese patients with hypokalemic periodic paralysis.lld:pubmed
pubmed-article:15711422pubmed:affiliationDivision of Nephrology, Department of Medicine, Tri-Service General Hospital, 114 Taipei, Taiwan.lld:pubmed
pubmed-article:15711422pubmed:publicationTypeJournal Articlelld:pubmed
entrez-gene:779entrezgene:pubmedpubmed-article:15711422lld:entrezgene
http://linkedlifedata.com/r...entrezgene:pubmedpubmed-article:15711422lld:entrezgene
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:15711422lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:15711422lld:pubmed