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Variably protease‐sensitive prionopathy mimicking frontotemporal dementia
Sporadic prion diseases are fatal neurodegenerative disorders characterized clinically by rapidly progressive dementia and myoclonus. Variably protease‐sensitive prionopathy (VPSPr) is a recently identified sporadic human prion disorder that may present with a lengthy atypical clinical history. Here...
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| Vydáno v: | Neuropathology |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley & Sons Australia, Ltd
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6778052/ https://ncbi.nlm.nih.gov/pubmed/30847986 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/neup.12538 |
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