| Literature DB >> 19347022 |
Michael Weller1, Adriano Aguzzi.
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.Entities:
Mesh：
Year: 2009 PMID： 19347022 DOI： 10.1038/nrneurol.2009.32
Source DB: PubMed Journal: Nat Rev Neurol ISSN： 1759-4758 Impact factor: 42.937