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24. The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease. Brown P; Goldfarb LG; Gibbs CJ; Gajdusek DC Eur J Epidemiol; 1991 Sep; 7(5):469-76. PubMed ID: 1684754 [TBL] [Abstract][Full Text] [Related]
25. New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred. Goldfarb LG; Haltia M; Brown P; Nieto A; Kovanen J; McCombie WR; Trapp S; Gajdusek DC Lancet; 1991 Feb; 337(8738):425. PubMed ID: 1671440 [No Abstract] [Full Text] [Related]
26. Ultrastructural characteristics (or evaluation) of Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies or prion diseases. Liberski PP; Sikorska B; Hauw JJ; Kopp N; Streichenberger N; Giraud P; Boellaard J; Budka H; Kovacs GG; Ironside J; Brown P Ultrastruct Pathol; 2010 Dec; 34(6):351-61. PubMed ID: 21070167 [TBL] [Abstract][Full Text] [Related]
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29. Genetic analysis of Creutzfeldt-Jakob disease and related disorders. Goldfarb LG; Brown P; Cervenakova L; Gajdusek DC Philos Trans R Soc Lond B Biol Sci; 1994 Mar; 343(1306):379-84. PubMed ID: 8041803 [TBL] [Abstract][Full Text] [Related]
30. [Prions, epidemic of Creutzfeldt-Jakob variant disease and global emergency]. Bratosiewicz J; Liberski PP Neurol Neurochir Pol; 2001; 35(4 Suppl):25-44. PubMed ID: 11873615 [TBL] [Abstract][Full Text] [Related]
31. A three-sister sibship of Gerstmann-Sträussler-Scheinker disease with a CJD phenotype. Majtényi C; Brown P; Cervenáková L; Goldfarb LG; Tateishi J Neurology; 2000 Jun; 54(11):2133-7. PubMed ID: 10851377 [TBL] [Abstract][Full Text] [Related]
32. Molecular genetic studies of Creutzfeldt-Jakob disease. Goldfarb LG; Brown P; Cervenakova L; Gajdusek DC Mol Neurobiol; 1994; 8(2-3):89-97. PubMed ID: 7999318 [TBL] [Abstract][Full Text] [Related]
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34. Experimental transmission of human subacute spongiform encephalopathy to small rodents. IV. Positive transmission from a typical case of Gerstmann-Sträussler-Scheinker's disease. Tateishi J; Sato Y; Nagara H; Boellaard JW Acta Neuropathol; 1984; 64(1):85-8. PubMed ID: 6382907 [TBL] [Abstract][Full Text] [Related]
35. Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome. Kitamoto T; Ohta M; Doh-ura K; Hitoshi S; Terao Y; Tateishi J Biochem Biophys Res Commun; 1993 Mar; 191(2):709-14. PubMed ID: 8461023 [TBL] [Abstract][Full Text] [Related]
37. [Genetic markers in four Chilean families with familial Creutzfeldt-Jakob disease]. Cartier R L; Fernández O J; Ramírez V E Rev Med Chil; 2006 Sep; 134(9):1116-22. PubMed ID: 17171212 [TBL] [Abstract][Full Text] [Related]