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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
9
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pubmed:dateCreated |
2004-11-9
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pubmed:abstractText |
Most mutations in the amyloid precursor protein (APP) gene have been associated with familial Alzheimer disease (AD); however, some mutations within the Abeta-coding sequence have been described in families with recurrent cerebral hemorrhage. The APPAla692Gly (Flemish) mutation was reported in a family in which affected members developed hemorrhagic stroke, progressive dementia, or both.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1526-632X
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:day |
9
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pubmed:volume |
63
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1613-7
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15534244-Alzheimer Disease,
pubmed-meshheading:15534244-Amyloid beta-Protein Precursor,
pubmed-meshheading:15534244-Brain,
pubmed-meshheading:15534244-Cerebral Hemorrhage,
pubmed-meshheading:15534244-European Continental Ancestry Group,
pubmed-meshheading:15534244-Female,
pubmed-meshheading:15534244-Humans,
pubmed-meshheading:15534244-Magnetic Resonance Imaging,
pubmed-meshheading:15534244-Male,
pubmed-meshheading:15534244-Middle Aged,
pubmed-meshheading:15534244-Mutation,
pubmed-meshheading:15534244-Pedigree,
pubmed-meshheading:15534244-Tomography, X-Ray Computed
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pubmed:year |
2004
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pubmed:articleTitle |
Hemorrhage is uncommon in new Alzheimer family with Flemish amyloid precursor protein mutation.
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pubmed:affiliation |
Prince of Wales Medical Research Institute, University of New South Wales, Barker Street, Randwick, Sydney, NSW 2031, Australia. w.brooks@unsw.edu.au
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pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
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