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2. Prions and prion diseases of the central nervous system. Tyler KL Curr Clin Top Infect Dis; 1999; 19():226-51. PubMed ID: 10472489 [No Abstract] [Full Text] [Related]
3. The molecular biology of the transmissible dementias. Owen F Mol Cell Biol Hum Dis Ser; 1994; 4():110-32. PubMed ID: 9439746 [No Abstract] [Full Text] [Related]
4. "Life, Jim, but not as we know it"? Transmissible dementias and the prion protein. Harrison PJ; Roberts GW Br J Psychiatry; 1991 Apr; 158():457-70. PubMed ID: 2054560 [TBL] [Abstract][Full Text] [Related]
5. An overview of human prion diseases. Imran M; Mahmood S Virol J; 2011 Dec; 8():559. PubMed ID: 22196171 [TBL] [Abstract][Full Text] [Related]
6. A case of sporadic Creutzfeldt-Jakob disease with a Gerstmann-Sträussler-Scheinker phenotype but no alterations in the PRNP gene. Liberski PP; Bratosiewicz J; Barcikowska M; Cervenakova L; Marczewska M; Brown P; Gajdusek DC Acta Neuropathol; 2000 Aug; 100(2):233-4. PubMed ID: 10963373 [No Abstract] [Full Text] [Related]
7. Aminoacid polymorphism in human prion protein and age at death in inherited prion disease. Baker HE; Poulter M; Crow TJ; Frith CD; Lofthouse R; Ridley RM Lancet; 1991 May; 337(8752):1286. PubMed ID: 1674080 [No Abstract] [Full Text] [Related]
8. Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndrome. Goldfarb LG; Brown P; Goldgaber D; Asher DM; Rubenstein R; Brown WT; Piccardo P; Kascsak RJ; Boellaard JW; Gajdusek DC Exp Neurol; 1990 Jun; 108(3):247-50. PubMed ID: 2190844 [TBL] [Abstract][Full Text] [Related]
9. [Prion diseases in humans]. Zavalishin IA; Roĭkhel' VM; Zhuchenko TD; Shitikova IE Zh Nevrol Psikhiatr Im S S Korsakova; 1998; 98(1):61-6. PubMed ID: 9505410 [No Abstract] [Full Text] [Related]
10. The prion diseases. Brown K; Mastrianni JA J Geriatr Psychiatry Neurol; 2010 Dec; 23(4):277-98. PubMed ID: 20938044 [TBL] [Abstract][Full Text] [Related]
11. Transmissible spongiform encephalopathies and human neurodegenerative disease. Esmonde TF; Will RG Br J Hosp Med; 1993 Mar 17-Apr 6; 49(6):400-4, 406. PubMed ID: 8472098 [TBL] [Abstract][Full Text] [Related]
12. [A trend of molecular genetics on prion diseases and prion protein]. Muramatsu Y; Shinagawa M Nihon Rinsho; 1993 Sep; 51(9):2494-502. PubMed ID: 8411733 [TBL] [Abstract][Full Text] [Related]
13. The evolution of views on the nosological position of transmissible spongiform encephalopathies. Liberski PP; Brown P; Gajdusek CD Folia Neuropathol; 1997; 35(4):214-25. PubMed ID: 9833398 [TBL] [Abstract][Full Text] [Related]
14. The prion diseases: Creutzfeldt-Jakob, Gerstmann-Sträussler-Scheinker, and related disorders. Mastrianni JA J Geriatr Psychiatry Neurol; 1998; 11(2):78-97. PubMed ID: 9877529 [TBL] [Abstract][Full Text] [Related]
15. [Gene mutation and pathology in human prion disease]. Tashiro H; Doh-ura K No To Shinkei; 1997 Aug; 49(8):681-7. PubMed ID: 9282361 [No Abstract] [Full Text] [Related]
17. The human spongiform encephalopathies: kuru, Creutzfeldt-Jakob disease, and the Gerstmann-Sträussler-Scheinker syndrome. Brown P; Gajdusek DC Curr Top Microbiol Immunol; 1991; 172():1-20. PubMed ID: 1687378 [No Abstract] [Full Text] [Related]
18. Creutzfeldt-Jakob disease patients with congophilic kuru plaques have the missense variant prion protein common to Gerstmann-Sträussler syndrome. Doh-ura K; Tateishi J; Kitamoto T; Sasaki H; Sakaki Y Ann Neurol; 1990 Feb; 27(2):121-6. PubMed ID: 2180366 [TBL] [Abstract][Full Text] [Related]
19. [Genetic background of human prion diseases]. Kovács GG Ideggyogy Sz; 2007 Nov; 60(11-12):438-46. PubMed ID: 18198790 [TBL] [Abstract][Full Text] [Related]