Cortical and hippocampal atrophy in patients with autosomal dominant familial Alzheimer's disease

Dementia and Geriatric Cognitive Disorders

Volumn 32, Issue 2, 2011, Pages 118-125

  Apostolova, Liana G ^a,b   Hwang, Kristy S ^a,b   Medina, Luis D ^a   Green, Amity E ^e   Braskie, Meredith N ^a,b   Dutton, Rebecca A ^c   Lai, Jeffrey ^d   Geschwind, Daniel H ^a   Cummings, Jeffrey L ^a   Thompson, Paul M ^a,b   Ringman, John M ^a  

^a Mary S Easton Center for Alzheimer's Disease Research   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^e MONASH UNIVERSITY   (Australia)

Author keywords

Amyloid precursor protein; Cortical atrophy; Familial Alzheimer's disease; Familial autosomal dominant Alzheimer's disease; Hippocampal atrophy; Mutation carriers; Presenilin

Indexed keywords

PRESENILIN 1;

AGED; ALZHEIMER DISEASE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRAIN ATROPHY; BRAIN CORTEX ATROPHY; CINGULATE GYRUS; CLINICAL ARTICLE; CONTROLLED STUDY; FAMILIAL DISEASE; FEMALE; FRONTAL CORTEX; GENE MUTATION; HETEROZYGOTE; HIPPOCAMPUS; HIPPOCAMPUS ATROPHY; HUMAN; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PARIETAL LOBE; PRIORITY JOURNAL;

ADULT; ALZHEIMER DISEASE; ATROPHY; CASE-CONTROL STUDIES; CEREBRAL CORTEX; FEMALE; GENES, DOMINANT; HETEROZYGOTE; HIPPOCAMPUS; HUMANS; MALE; MIDDLE AGED; REFERENCE VALUES;

EID: 80054856707     PISSN: 14208008     EISSN: 14219824     Source Type: Journal    
DOI: 10.1159/000330471     Document Type: Article

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