|
rdf:type |
|
|
lifeskim:mentions |
umls-concept:C0004083,
umls-concept:C0015576,
umls-concept:C0039082,
umls-concept:C0205210,
umls-concept:C0205349,
umls-concept:C0228174,
umls-concept:C0439064,
umls-concept:C0521451,
umls-concept:C0596620,
umls-concept:C0948051,
umls-concept:C2348519
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|
pubmed:issue |
3
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|
pubmed:dateCreated |
2008-3-11
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|
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.
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pubmed:language |
eng
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|
pubmed:journal |
|
|
pubmed:citationSubset |
AIM
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pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Mar
|
|
pubmed:issn |
0003-9942
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pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:volume |
65
|
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pubmed:owner |
NLM
|
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pubmed:authorsComplete |
Y
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pubmed:pagination |
407-11
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pubmed:meshHeading |
pubmed-meshheading:18332256-Adult,
pubmed-meshheading:18332256-Cerebral Cortex,
pubmed-meshheading:18332256-DNA, Mitochondrial,
pubmed-meshheading:18332256-Gene Deletion,
pubmed-meshheading:18332256-Glucose,
pubmed-meshheading:18332256-Glucose Metabolism Disorders,
pubmed-meshheading:18332256-Humans,
pubmed-meshheading:18332256-Magnetic Resonance Imaging,
pubmed-meshheading:18332256-Magnetic Resonance Spectroscopy,
pubmed-meshheading:18332256-Male,
pubmed-meshheading:18332256-Mitochondrial Encephalomyopathies,
pubmed-meshheading:18332256-Positron-Emission Tomography,
pubmed-meshheading:18332256-Protons,
pubmed-meshheading:18332256-Siblings
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|
pubmed:year |
2008
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|
pubmed:articleTitle |
Altered cerebral glucose metabolism in a family with clinical features resembling mitochondrial neurogastrointestinal encephalomyopathy syndrome in association with multiple mitochondrial DNA deletions.
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|
pubmed:affiliation |
Department of Neurology, University of Cologne, Köln, Germany.
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pubmed:publicationType |
Journal Article,
Case Reports
|
