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Movement disorders reveal Creutzfeldt-Jakob disease


Weller, M; Aguzzi, A (2009). Movement disorders reveal Creutzfeldt-Jakob disease. Nature Reviews. Neurology, 5(4):185-186.

Abstract

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.

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Additional indexing

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
Language:English
Date:April 2009
Deposited On:17 Nov 2009 11:10
Last Modified:05 Apr 2016 13:33
Publisher:Nature Publishing Group
ISSN:1759-4758
Publisher DOI:10.1038/nrneurol.2009.32
PubMed ID:19347022
Permanent URL: http://doi.org/10.5167/uzh-24078

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