Familial Creutzfeldt-Jakob disease without periodic EEG activity
✍ Scribed by Gretchen E. Tietjen; Dr Ivo Drury
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 402 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0364-5134
No coin nor oath required. For personal study only.
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## 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 ## Objective Based on the current criteria, the diagnosis of “possible” or “probable” variant Creutzfeldt–Jakob disease (vCJD) implies the absence of periodic sharp wave complexes (PSWCs) in the electroencephalogram (EEG). To verify this point, we investigated the development of the EE
Creutzfeldt-Jakob disease (CJD) belongs to a group of chronic, progressive, neurodegenerative disorders that may be hereditary, infectious, or sporadic. Hereditary CJDs are associated with mutations in the PRNP gene on chromosome 20p12-pter. We report a family in which four patients developed classi
## Abstract A systematic search for cases of Creutzfeldt‐Jakob disease occurring in the ten‐year period 1968 through 1977 was conducted in the city of Paris and surrounding departments which comprise the greater Paris area. Fifty‐six cases were found among the total population of approximately 10 m