Subcortical and Deep Cortical Atrophy in Frontotemporal Dementia due to Granulin Mutations

BACKGROUND/AIMS: Parkinsonism is often associated with symptoms of frontotemporal dementia (FTD), but its pathogenesis has been largely neglected. In genetic inherited FTD-related granulin (GRN) mutations, parkinsonism is an early sign, and it is more common than in sporadic disorders. Our aim was t...

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Библиографические подробности
Главные авторы: Premi, Enrico, Garibotto, Valentina, Gazzina, Stefano, Formenti, Anna, Archetti, Silvana, Gasparotti, Roberto, Padovani, Alessandro, Borroni, Barbara
Формат: Artigo
Язык:Inglês
Опубликовано: S. Karger AG 2014
Предметы:
Original Research Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC4036148/
https://ncbi.nlm.nih.gov/pubmed/24926307
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000355428
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