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

Internet

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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