Linked Life Data

15981641

Source:http://linkedlifedata.com/resource/pubmed/id/15981641

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2005-6-28
pubmed:abstractText
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a rare hereditary disease characterized by recurrent transient ischemic attacks (TIA) and strokes, and vascular dementia caused by point mutations of the Notch 3 gene. Here, we report a Japanese CADASIL case who displayed limited dementia and had the Notch 3 R141C mutation. The relationship between pathogenesis and the mutation site in Notch 3 is discussed based on the case presented here.
pubmed:language
jpn
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0006-8969
pubmed:author
pubmed:issnType
Print
pubmed:volume
57
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
415-8
pubmed:dateRevised
2007-2-22
pubmed:meshHeading
pubmed:year
2005
pubmed:articleTitle
[Japanese CADASIL case with limited dementia who had the Notch 3 R141C mutation].
pubmed:affiliation
Department of Neurosurgery, Graduate School of Medicine, Osaka City University.
pubmed:publicationType
Journal Article, English Abstract, Case Reports