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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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| Hauptverfasser: | , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
S. Karger AG
2014
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| Schlagworte: | |
| Online Zugang: | 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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