Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2008-4-16
pubmed:abstractText
A majority of mutations within the beta-amyloid region of the amyloid precursor protein (APP) gene cause inherited forms of intracerebral hemorrhage. Most of these mutations may also cause cognitive impairment, but the Arctic APP mutation is the only known intra-beta-amyloid mutation to date causing the more typical clinical picture of Alzheimer disease.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-10720282, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-10735393, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-10922078, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-11004129, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-11409420, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-11528419, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-11932745, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-12058030, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-12391599, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-12395079, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-1302033, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-1303239, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-1415269, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-15037694, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-15984012, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-1925564, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-1944558, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-2011243, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-2111584, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-7596406, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-8310820, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-8705854, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-8737926, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-8938131, http://linkedlifedata.com/resource/pubmed/commentcorrection/18413473-9754958
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1538-3687
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
65
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
499-505
pubmed:dateRevised
2011-9-26
pubmed:meshHeading
pubmed-meshheading:18413473-Age Factors, pubmed-meshheading:18413473-Age of Onset, pubmed-meshheading:18413473-Aged, pubmed-meshheading:18413473-Alzheimer Disease, pubmed-meshheading:18413473-Amyloid beta-Protein Precursor, pubmed-meshheading:18413473-Atrophy, pubmed-meshheading:18413473-Brain, pubmed-meshheading:18413473-Child, pubmed-meshheading:18413473-Electroencephalography, pubmed-meshheading:18413473-Female, pubmed-meshheading:18413473-Genotype, pubmed-meshheading:18413473-Heterozygote Detection, pubmed-meshheading:18413473-Humans, pubmed-meshheading:18413473-Magnetic Resonance Imaging, pubmed-meshheading:18413473-Middle Aged, pubmed-meshheading:18413473-Neurologic Examination, pubmed-meshheading:18413473-Neuropsychological Tests, pubmed-meshheading:18413473-Parietal Lobe, pubmed-meshheading:18413473-Pedigree, pubmed-meshheading:18413473-Phenotype, pubmed-meshheading:18413473-Plaque, Amyloid, pubmed-meshheading:18413473-Protease Nexins, pubmed-meshheading:18413473-Receptors, Cell Surface, pubmed-meshheading:18413473-Regional Blood Flow, pubmed-meshheading:18413473-Sweden, pubmed-meshheading:18413473-Tomography, Emission-Computed, Single-Photon, pubmed-meshheading:18413473-United States
pubmed:year
2008
pubmed:articleTitle
Clinical and neuropathological features of the arctic APP gene mutation causing early-onset Alzheimer disease.
pubmed:affiliation
Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Huddinge, Sweden. hans.basun@pubcare.uu.se
pubmed:publicationType
Journal Article