Citation Tools
PDF
Other content recommended for you
- CJD mimics and chameleons
- Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene
- Characteristics of Chinese patients with genetic CJD who have E196A or E196K mutation in PRNP: comparative analysis of patients identified in the Chinese National CJD Surveillance System
- Evaluation of the impact of CSF prion RT-QuIC and amended criteria on the clinical diagnosis of Creutzfeldt-Jakob disease: a 10-year study in Italy
- MM2-type sporadic Creutzfeldt-Jakob disease: new diagnostic criteria for MM2-cortical type
- Systematic approach to diagnosing suspected Creutzfeldt-Jakob disease
- Imaging and CSF analyses effectively distinguish CJD from its mimics
- Intensity of human prion disease surveillance predicts observed disease incidence
- Comparison between plasma and cerebrospinal fluid biomarkers for the early diagnosis and association with survival in prion disease
- Molecular pathology of neurodegenerative diseases: principles and practice