Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology (clinical)
Reference288 articles.
1. National CJD Research & Surveillance Unit. 28th Annual Report 2019. Creutzfeldt-Jakob Disease Surveillance in the UK https://www.cjd.ed.ac.uk/sites/default/files/Report28.pdf (2020).
2. Uttley, L., Carroll, C., Wong, R., Hilton, D. A. & Stevenson, M. Creutzfeldt-Jakob disease: a systematic review of global incidence, prevalence, infectivity, and incubation. Lancet Infect. Dis. 20, e2–e10 (2020).
3. Kovacs, G. G. et al. Genetic prion disease: the EUROCJD experience. Hum. Genet. 118, 166–174 (2005). An international study on the epidemiology of genetic prion diseases in the Euro-CJD network nations.
4. Masters, C. L. et al. Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering. Ann. Neurol. 5, 177–188 (1979).
5. Brown, P. et al. Iatrogenic Creutzfeldt-Jakob disease, final assessment. Emerg. Infect. Dis. 18, 901–907 (2012). A detailed summary of the iCJD epidemic worldwide.
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