Citation Tools
PDF
Other content recommended for you
- CJD mimics and chameleons
- RT-QuIC: a new test for sporadic CJD
- 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
- Creutzfeldt-Jakob disease as a cause of dementia
- 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
- Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene
- Fatal insomnia: the elusive prion disease
- Diagnostic challenge of rapidly progressing sporadic Creutzfeldt-Jakob disease
- Heidenhain variant sporadic Creutzfeldt-Jakob disease diagnosed as an autoimmune encephalitis due to a false-positive GAD autoantibody
- Study protocol for enhanced CJD surveillance in the 65+ years population group in Scotland: an observational neuropathological screening study of banked brain tissue donations for evidence of prion disease