Article Text
PDFClinicopathological conference
31st Advanced Clinical Neurology Course, Edinburgh 2009: progressive cognitive impairment, behavioural change and upper motor neuron signs in a 57-year-old woman
Statistics from Altmetric.com
Footnotes
Competing interests None.
Patient consent Obtained.
Provenance and peer review Commissioned, not externally peer reviewed.
Read the full text or download the PDF:
Other content recommended for you
- Variably protease-sensitive prionopathy with methionine homozygosity at codon 129 in the prion protein gene
- Molecular pathology of neurodegenerative diseases: principles and practice
- Molecular neurology of prion disease
- CJD mimics and chameleons
- Presenile dementia syndromes: an update on taxonomy and diagnosis
- Palliative care in Creutzfeldt-Jakob disease: looking back, thinking ahead
- Intensity of human prion disease surveillance predicts observed disease incidence
- Rare histotype of sporadic Creutzfeldt-Jakob disease, clinically suspected as corticobasal degeneration
- Methionine homozygosity for PRNP polymorphism and susceptibility to human prion diseases
- 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