Temporal evolution of electroencephalographic abnormalities in Creutzfeldt-Jakob disease
✍ Scribed by G. K. Schlenska; G. F. Walter
- Publisher
- Springer
- Year
- 1989
- Tongue
- English
- Weight
- 499 KB
- Volume
- 236
- Category
- Article
- ISSN
- 0340-5354
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We report 3 patients with autopsy-proven Creutzfeldt-Jakob disease who, early in their course, developed abnormal eye movements that included periodic alternating nystagmus and slow vertical saccades. These findings suggested involvement of the cerebellar nodulus and uvula, and the brainstem reticul
## Abstract In 1996, our group published objective electroencephalogram (EEG) criteria to define periodic sharp‐wave complexes (PSWCs) suggestive for Creutzfeldt–Jakob disease (CJD). These criteria have since then been strictly applied in all cases reported to us as possible CJD in the course of th
## Abstract Movement disturbances are common in dementia disorders and are a central feature of the clinical classification criteria of Creutzfeldt‐Jakob disease (CJD). Polymorphism at codon 129 of the prion protein gene is known to determine the clinical picture of CJD. The frequency and character