11907964

Source:http://linkedlifedata.com/resource/pubmed/id/11907964

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0001125, umls-concept:C0162671, umls-concept:C1852373, umls-concept:C1857287
pubmed:issue	10 Pt 1
pubmed:dateCreated	2002-3-22
pubmed:abstractText	The MELAS syndrome (Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-like episodes) belongs to the category of mitochondrial disorders. The most common molecular etiology of the syndrome is a mutation A to G transition at base pair 3243 in the mitochondrial genome. The phenotype is varied and depends on the proportion of DNA muted and which organ on aerobic metabolism suffers most.
pubmed:language	fre
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7702013
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	0151-9638
pubmed:author	pubmed-author:CanapleSS, pubmed-author:CarmiEE, pubmed-author:DefossezCC, pubmed-author:DenoeuxJ PJP, pubmed-author:FraitagSS, pubmed-author:LoiMM, pubmed-author:MorinGG, pubmed-author:WesteelP FPF
pubmed:issnType	Print
pubmed:volume	128
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1031-5
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:11907964-Adolescent, pubmed-meshheading:11907964-Female, pubmed-meshheading:11907964-Humans, pubmed-meshheading:11907964-MELAS Syndrome
pubmed:year	2001
pubmed:articleTitle	[MELAS syndrome (mitochondrial encephalopathy with lactic acidosis and stroke-like episodes].
pubmed:affiliation	Service de Dermatologie et Vénéréologie, CHU Amiens.
pubmed:publicationType	Journal Article, English Abstract, Case Reports