Prion dementia without characteristic pathology
- 1 July 1990
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 336 (8706), 7-9
- https://doi.org/10.1016/0140-6736(90)91518-f
Abstract
No abstract availableThis publication has 31 references indexed in Scilit:
- Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndromeExperimental Neurology, 1989
- Linkage of a prion protein missense variant to Gerstmann–Sträussler syndromeNature, 1989
- Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA PolymeraseScience, 1988
- Prions and Neurodegenerative DiseasesNew England Journal of Medicine, 1987
- Experimental transmission of an autosomal dominant spongiform encephalopathy: does the infectious agent originate in the human genome?BMJ, 1985
- Clinical diagnosis of Alzheimer's diseaseNeurology, 1984
- Creutzfeldt-Jakob Disease (Spongiform Encephalopathy): Transmission to the ChimpanzeeScience, 1968
- Experimental Transmission of a Kuru-like Syndrome to ChimpanzeesNature, 1966
- Encephalopathy of mink: I. Epizootiologic and clinical observationsThe Journal of Infectious Diseases, 1965
- A RARE PRESENILE DEMENTIA ASSOCIATED WITH CORTICAL BLINDNESS (HEIDENHAIN'S SYNDROME)Journal of Neurology, Neurosurgery & Psychiatry, 1954