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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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Hlavní autoři: | , , , , , , , |
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Médium: | Artigo |
Jazyk: | Inglês |
Vydáno: |
Karger Publishers
2014-04-01
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Edice: | Dementia and Geriatric Cognitive Disorders Extra |
Témata: | |
On-line přístup: | http://www.karger.com/Article/FullText/355428 |
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