1. Ritchie DL, Ironside JW. Neuropathology of human prion diseases. Prog Mol Biol Transl Sci. 2017;150:319–39.
2. Zerr I, Kallenberg K, Summers DM, Romero C, Taratuto A, Heinemann U, et al. Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease. Brain. 2009;132(10):2659–68.
3. Delasnerie-Laupretre N, Alperovitch A. Epidemiology of Creutzfeldt-Jakob disease. Pathol Biol. 1995;43(1):22–4.
4. Yao Y, Dong X, Guan H, Lu Q. Cerebrospinal fluid real-time quaking-induced conversion test for sporadic Creutzfeldt-Jakob disease in an 18-year-old woman: a case report. Medicine. 2017;96(48):e8699.
5. Collins S, Boyd A, Lee JS, Lewis V, Fletcher A, McLean CA, et al. Creutzfeldt-Jakob disease in Australia 1970–1999. Neurology. 2002 Nov 12;59(9):1365–71.