Načítá se...
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...
Uloženo v:
| Hlavní autoři: | , , , , , , , |
|---|---|
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
S. Karger AG
2014
|
| Témata: | |
| On-line přístup: | 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 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|