21288980

Source:http://linkedlifedata.com/resource/pubmed/id/21288980

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008059, umls-concept:C0011304, umls-concept:C0012929, umls-concept:C0026882, umls-concept:C0205099, umls-concept:C0439661
pubmed:issue	9
pubmed:dateCreated	2011-3-1
pubmed:abstractText	We investigated mitochondrial DNA (mtDNA) variants in children with a first episode of acquired demyelinating syndromes (PD-ADS) of the CNS and their relationship to disease phenotype, including subsequent diagnosis of multiple sclerosis (MS).
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/R01NS058988
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/21288980-21288985
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA, Mitochondrial
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	1526-632X
pubmed:author	pubmed-author:ArnoldD LDL, pubmed-author:BanwellBB, pubmed-author:Bar-OrAA, pubmed-author:Canadian Pediatric Demyelinating Disease Network, pubmed-author:GagneDD, pubmed-author:SacchettiMM, pubmed-author:SadovnickA DAD, pubmed-author:SchererS WSW, pubmed-author:SimonD KDK, pubmed-author:VenkateswaranSS, pubmed-author:ZhengKK
pubmed:issnType	Electronic
pubmed:day	1
pubmed:volume	76
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	774-80
pubmed:meshHeading	pubmed-meshheading:21288980-Adolescent, pubmed-meshheading:21288980-Adult, pubmed-meshheading:21288980-Child, pubmed-meshheading:21288980-Child, Preschool, pubmed-meshheading:21288980-Cohort Studies, pubmed-meshheading:21288980-DNA, Mitochondrial, pubmed-meshheading:21288980-Demyelinating Diseases, pubmed-meshheading:21288980-Female, pubmed-meshheading:21288980-Follow-Up Studies, pubmed-meshheading:21288980-Genetic Variation, pubmed-meshheading:21288980-Haplotypes, pubmed-meshheading:21288980-Humans, pubmed-meshheading:21288980-Infant, pubmed-meshheading:21288980-Male, pubmed-meshheading:21288980-Mutation, pubmed-meshheading:21288980-Polymorphism, Single Nucleotide, pubmed-meshheading:21288980-Prospective Studies, pubmed-meshheading:21288980-Young Adult
pubmed:year	2011
pubmed:articleTitle	Mitochondrial DNA haplogroups and mutations in children with acquired central demyelination.
pubmed:affiliation	Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA 02215, USA.
pubmed:publicationType	Journal Article, Comparative Study, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural