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10. [Recent advances in the research of Creutzfeldt-Jakob disease (CJD) and Gerstmann-Strüssler syndrome (GSS)]. Tateishi J Rinsho Shinkeigaku; 1991 Dec; 31(12):1306-8. PubMed ID: 1687809 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Sporadic Creutzfeldt-Jakob Disease in a Woman Married Into a Gerstmann-Sträussler-Scheinker Family: An Investigation of Prions Transmission via Microchimerism. Areškeviciute A; Melchior LC; Broholm H; Krarup LH; Lindquist SG; Johansen P; McKenzie N; Green A; Nielsen JE; Laursen H; Lund EL J Neuropathol Exp Neurol; 2018 Aug; 77(8):673-684. PubMed ID: 29889261 [TBL] [Abstract][Full Text] [Related]
13. [Creutzfeldt-Jakob disease(CJD) and Gerstmann-Sträussler-Scheinker syndrome(GSS)]. Udaka F; Fujisawa M; Kameyama M Nihon Rinsho; 1997 Apr; 55(4):972-7. PubMed ID: 9103904 [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. Dominantly inherited prion protein cerebral amyloidoses - a modern view of Gerstmann-Sträussler-Scheinker. Ghetti B; Piccardo P; Zanusso G Handb Clin Neurol; 2018; 153():243-269. PubMed ID: 29887140 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. A case of sporadic Creutzfeldt-Jakob disease with a Gerstmann-Sträussler-Scheinker phenotype but no alterations in the PRNP gene. Liberski PP; Barcikowska M; Cervenakova L; Bratosiewicz J; Marczewska M; Brown P; Gajdusek DC Acta Neuropathol; 1998 Oct; 96(4):425-30. PubMed ID: 9797009 [TBL] [Abstract][Full Text] [Related]
18. The primary structure of the prion protein influences the distribution of abnormal prion protein in the central nervous system. Kitamoto T; Doh-ura K; Muramoto T; Miyazono M; Tateishi J Am J Pathol; 1992 Aug; 141(2):271-7. PubMed ID: 1353945 [TBL] [Abstract][Full Text] [Related]
19. Presymptomatic detection or exclusion of prion protein gene defects in families with inherited prion diseases. Collinge J; Poulter M; Davis MB; Baraitser M; Owen F; Crow TJ; Harding AE Am J Hum Genet; 1991 Dec; 49(6):1351-4. PubMed ID: 1684089 [TBL] [Abstract][Full Text] [Related]
20. Prion protein mutation at codon 102 in an Italian family with Gerstmann-Sträussler-Scheinker syndrome. Kretzschmar HA; Kufer P; Riethmüller G; DeArmond S; Prusiner SB; Schiffer D Neurology; 1992 Apr; 42(4):809-10. PubMed ID: 1348851 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]