Cerebral perfusion changes in presymptomatic genetic frontotemporal dementia: a GENFI study
Abstract
Genetic forms of frontotemporal dementia are most commonly due to mutations in three genes, C9orf72, GRN or MAPT, with presymptomatic carriers from families representing those at risk. While cerebral blood flow shows differences between frontotemporal dementia and other forms of dementia, there is limited evidence of its utility in presymptomatic stages of frontotemporal dementia. This study aimed to delineate the cerebral blood flow signature...
Paper Details
Title
Cerebral perfusion changes in presymptomatic genetic frontotemporal dementia: a GENFI study
Published Date
Mar 7, 2019
Journal
Volume
142
Issue
4
Pages
1108 - 1120
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