Article metrics
PDF
Other content recommended for you
- 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
- RT-QuIC: a new test for sporadic CJD
- Multicentre multiobserver study of diffusion-weighted and fluid-attenuated inversion recovery MRI for the diagnosis of sporadic Creutzfeldt–Jakob disease: a reliability and agreement study
- Rare histotype of sporadic Creutzfeldt-Jakob disease, clinically suspected as corticobasal degeneration
- CSF levels of SNAP-25 are increased early in Creutzfeldt-Jakob and Alzheimer’s disease
- Systematic approach to diagnosing suspected Creutzfeldt-Jakob disease
- Fatal insomnia: the elusive prion disease
- Heidenhain variant sporadic Creutzfeldt-Jakob disease diagnosed as an autoimmune encephalitis due to a false-positive GAD autoantibody
- 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