Weller, M; Aguzzi, A (2009). Movement disorders reveal Creutzfeldt-Jakob disease. Nature Reviews. Neurology, 5(4):185-186.
Human prion diseases are sometimes difficult to diagnose because few clinical features distinguish them reliably from other neurological disorders. A new study suggests that analysis of movement disorders might contribute to the clinical differentiation of sporadic Creutzfeldt-Jakob disease from Alzheimer disease and dementia with Lewy bodies.
Human prion diseases are sometimes difficult to diagnose because few clinical features distinguish them reliably from other neurological disorders. A new study suggests that analysis of movement disorders might contribute to the clinical differentiation of sporadic Creutzfeldt-Jakob disease from Alzheimer disease and dementia with Lewy bodies.
| Item Type: | Journal Article, refereed, further contribution |
|---|---|
| Communities & Collections: | 04 Faculty of Medicine > University Hospital Zurich > Institute of Neuropathology
04 Faculty of Medicine > University Hospital Zurich > Clinic for Neurology |
| Dewey Decimal Classification: | 570 Life sciences; biology
610 Medicine & health |
| Scopus Subject Areas: | Health Sciences > Neurology (clinical)
Life Sciences > Cellular and Molecular Neuroscience |
| Language: | English |
| Date: | April 2009 |
| Deposited On: | 17 Nov 2009 11:10 |
| Last Modified: | 29 Jun 2022 08:45 |
| Publisher: | Nature Publishing Group |
| ISSN: | 1759-4758 |
| OA Status: | Green |
| Publisher DOI: | https://doi.org/10.1038/nrneurol.2009.32 |
| PubMed ID: | 19347022 |
Weller, M