Article metrics
PDF
Other content recommended for you
- Fatal insomnia: the elusive prion disease
- Systematic approach to diagnosing suspected Creutzfeldt-Jakob disease
- CJD mimics and chameleons
- An atypical case of sporadic fatal insomnia
- Diagnostic challenge of rapidly progressing sporadic Creutzfeldt-Jakob disease
- Genetic prion disease: D178N with 129MV disease modifying polymorphism—a clinical phenotype
- 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
- MM2-type sporadic Creutzfeldt-Jakob disease: new diagnostic criteria for MM2-cortical type
- Clinical profile of fatal familial insomnia: phenotypic variation in 129 polymorphisms and geographical regions