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3. Insertions in the prion protein gene in atypical dementias. Owen F; Poulter M; Collinge J; Leach M; Shah T; Lofthouse R; Chen YF; Crow TJ; Harding AE; Hardy J Exp Neurol; 1991 May; 112(2):240-2. PubMed ID: 1674696 [TBL] [Abstract][Full Text] [Related]
4. Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome. Goldgaber D; Goldfarb LG; Brown P; Asher DM; Brown WT; Lin S; Teener JW; Feinstone SM; Rubenstein R; Kascsak RJ Exp Neurol; 1989 Nov; 106(2):204-6. PubMed ID: 2572450 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome. Doh-ura K; Tateishi J; Sasaki H; Kitamoto T; Sakaki Y Biochem Biophys Res Commun; 1989 Sep; 163(2):974-9. PubMed ID: 2783132 [TBL] [Abstract][Full Text] [Related]
7. Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome. Hsiao K; Baker HF; Crow TJ; Poulter M; Owen F; Terwilliger JD; Westaway D; Ott J; Prusiner SB Nature; 1989 Mar; 338(6213):342-5. PubMed ID: 2564168 [TBL] [Abstract][Full Text] [Related]
8. Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene. Medori R; Tritschler HJ; LeBlanc A; Villare F; Manetto V; Chen HY; Xue R; Leal S; Montagna P; Cortelli P N Engl J Med; 1992 Feb; 326(7):444-9. PubMed ID: 1346338 [TBL] [Abstract][Full Text] [Related]
9. Familial spongiform encephalopathy associated with a novel prion protein gene mutation. Nitrini R; Rosemberg S; Passos-Bueno MR; da Silva LS; Iughetti P; Papadopoulos M; Carrilho PM; Caramelli P; Albrecht S; Zatz M; LeBlanc A Ann Neurol; 1997 Aug; 42(2):138-46. PubMed ID: 9266722 [TBL] [Abstract][Full Text] [Related]
17. Prion encephalopathies of animals and humans. Prusiner SB Dev Biol Stand; 1993; 80():31-44. PubMed ID: 8270114 [TBL] [Abstract][Full Text] [Related]
18. Molecular biology of prions causing infectious and genetic encephalopathies of humans as well as scrapie of sheep and BSE of cattle. Prusiner SB Dev Biol Stand; 1991; 75():55-74. PubMed ID: 1686599 [TBL] [Abstract][Full Text] [Related]
19. [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]
20. Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred. Giaccone G; Verga L; Bugiani O; Frangione B; Serban D; Prusiner SB; Farlow MR; Ghetti B; Tagliavini F Proc Natl Acad Sci U S A; 1992 Oct; 89(19):9349-53. PubMed ID: 1357663 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]