Share
Other content recommended for you
- CJD mimics and chameleons
- Systematic approach to diagnosing suspected Creutzfeldt-Jakob disease
- Intensity of human prion disease surveillance predicts observed disease incidence
- Clinicopathological case: rapid cognitive decline in an older man
- RT-QuIC: a new test for sporadic CJD
- The clinical assessment of the patient with early dementia
- 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
- Imaging and CSF analyses effectively distinguish CJD from its mimics
- Comparison between plasma and cerebrospinal fluid biomarkers for the early diagnosis and association with survival in prion disease
- MM2-type sporadic Creutzfeldt-Jakob disease: new diagnostic criteria for MM2-cortical type