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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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Detalles Bibliográficos
Autores principales:	Premi, Enrico, Garibotto, Valentina, Gazzina, Stefano, Formenti, Anna, Archetti, Silvana, Gasparotti, Roberto, Padovani, Alessandro, Borroni, Barbara
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	S. Karger AG 2014
Materias:	Original Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4036148/ https://www.ncbi.nlm.nih.gov/pubmed/24926307 http://dx.doi.org/10.1159/000355428

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