Immunohistochemical verification of senile and kuru plaques in Creutzfeldt-Jakob disease and the allied disease
✍ Scribed by Dr. Tetsuyuki Kitamoto; June Tateishi; Yuji Sato
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 718 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0364-5134
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## 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
## Abstract Movement disorders and epilepsy rarely occur in the early stage of Creutzfeldt–Jakob disease (CJD) but have not been reported concurrently. We report on a 47‐year‐old patient with probable CJD who presented with generalized chorea and focal dystonia with myoclonic jerks on the right han