pubmed-article:18332256 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18332256 | lifeskim:mentions | umls-concept:C0015576 | lld:lifeskim |
pubmed-article:18332256 | lifeskim:mentions | umls-concept:C0948051 | lld:lifeskim |
pubmed-article:18332256 | lifeskim:mentions | umls-concept:C0228174 | lld:lifeskim |
pubmed-article:18332256 | lifeskim:mentions | umls-concept:C0521451 | lld:lifeskim |
pubmed-article:18332256 | lifeskim:mentions | umls-concept:C0039082 | lld:lifeskim |
pubmed-article:18332256 | lifeskim:mentions | umls-concept:C0004083 | lld:lifeskim |
pubmed-article:18332256 | lifeskim:mentions | umls-concept:C0439064 | lld:lifeskim |
pubmed-article:18332256 | lifeskim:mentions | umls-concept:C0596620 | lld:lifeskim |
pubmed-article:18332256 | lifeskim:mentions | umls-concept:C0205210 | lld:lifeskim |
pubmed-article:18332256 | lifeskim:mentions | umls-concept:C0205349 | lld:lifeskim |
pubmed-article:18332256 | lifeskim:mentions | umls-concept:C2348519 | lld:lifeskim |
pubmed-article:18332256 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:18332256 | pubmed:dateCreated | 2008-3-11 | lld:pubmed |
pubmed-article:18332256 | pubmed:abstractText | To determine the involvement of cerebral metabolism in 2 siblings with mitochondrial neurogastrointestinal encephalomyopathy syndrome (MNGIE)-like disease with multiple mitochondrial DNA (mtDNA) deletions. | lld:pubmed |
pubmed-article:18332256 | pubmed:language | eng | lld:pubmed |
pubmed-article:18332256 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18332256 | pubmed:citationSubset | AIM | lld:pubmed |
pubmed-article:18332256 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18332256 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18332256 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18332256 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18332256 | pubmed:month | Mar | lld:pubmed |
pubmed-article:18332256 | pubmed:issn | 0003-9942 | lld:pubmed |
pubmed-article:18332256 | pubmed:author | pubmed-author:Möller-Hartma... | lld:pubmed |
pubmed-article:18332256 | pubmed:author | pubmed-author:SobeskyJanJ | lld:pubmed |
pubmed-article:18332256 | pubmed:author | pubmed-author:JacobsAndreas... | lld:pubmed |
pubmed-article:18332256 | pubmed:author | pubmed-author:KrachtLutzL | lld:pubmed |
pubmed-article:18332256 | pubmed:author | pubmed-author:HorvathRitaR | lld:pubmed |
pubmed-article:18332256 | pubmed:author | pubmed-author:LehnhardtFrit... | lld:pubmed |
pubmed-article:18332256 | pubmed:author | pubmed-author:HauptWalter... | lld:pubmed |
pubmed-article:18332256 | pubmed:author | pubmed-author:UllrichRoland... | lld:pubmed |
pubmed-article:18332256 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:18332256 | pubmed:volume | 65 | lld:pubmed |
pubmed-article:18332256 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18332256 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18332256 | pubmed:pagination | 407-11 | lld:pubmed |
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pubmed-article:18332256 | pubmed:meshHeading | pubmed-meshheading:18332256... | lld:pubmed |
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pubmed-article:18332256 | pubmed:meshHeading | pubmed-meshheading:18332256... | lld:pubmed |
pubmed-article:18332256 | pubmed:year | 2008 | lld:pubmed |
pubmed-article:18332256 | pubmed:articleTitle | Altered cerebral glucose metabolism in a family with clinical features resembling mitochondrial neurogastrointestinal encephalomyopathy syndrome in association with multiple mitochondrial DNA deletions. | lld:pubmed |
pubmed-article:18332256 | pubmed:affiliation | Department of Neurology, University of Cologne, Köln, Germany. | lld:pubmed |
pubmed-article:18332256 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18332256 | pubmed:publicationType | Case Reports | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:18332256 | lld:pubmed |
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