Linked Life Data

20697050

Source:http://linkedlifedata.com/resource/pubmed/id/20697050

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2010-8-10
pubmed:abstractText
To report the clinical, genetic, neuroimaging, and neuropathologic studies of patients with the hereditary cerebral hemorrhage with amyloidosis linked to the APP E693K mutation.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1538-3687
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
67
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
987-95
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:20697050-Aged, pubmed-meshheading:20697050-Amyloid beta-Peptides, pubmed-meshheading:20697050-Amyloid beta-Protein Precursor, pubmed-meshheading:20697050-Amyloidosis, Familial, pubmed-meshheading:20697050-Apolipoprotein E4, pubmed-meshheading:20697050-Cerebral Hemorrhage, pubmed-meshheading:20697050-Family Health, pubmed-meshheading:20697050-Female, pubmed-meshheading:20697050-Gene Frequency, pubmed-meshheading:20697050-Genetic Predisposition to Disease, pubmed-meshheading:20697050-Genome-Wide Association Study, pubmed-meshheading:20697050-Genotype, pubmed-meshheading:20697050-Glutamic Acid, pubmed-meshheading:20697050-Humans, pubmed-meshheading:20697050-Italy, pubmed-meshheading:20697050-Lysine, pubmed-meshheading:20697050-Magnetic Resonance Imaging, pubmed-meshheading:20697050-Male, pubmed-meshheading:20697050-Middle Aged, pubmed-meshheading:20697050-Mutation, pubmed-meshheading:20697050-Peptide Fragments
pubmed:year
2010
pubmed:articleTitle
Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP.
pubmed:affiliation
Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Celoria 11-20133, Milan, Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't