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7. [Creutzfeldt-Jakob encephalopathy with mutation E200K. Report of a "sporadic" case]. Cosacov RM; Taratuto AL; Ghiraridi G; Barrionuevo P; Diaz A; Begué C; Martinetto H Rev Fac Cien Med Univ Nac Cordoba; 2004; 61(1):48-53. PubMed ID: 15366237 [TBL] [Abstract][Full Text] [Related]
8. Familial Creutzfeldt-Jakob disease homozygous to the E200K mutation: clinical characteristics and disease course. Nitsan Z; Cohen OS; Chapman J; Kahana E; Korczyn AD; Appel S; Osherov M; Rosenmann H; Milo R J Neurol; 2020 Aug; 267(8):2455-2458. PubMed ID: 32367297 [TBL] [Abstract][Full Text] [Related]
9. Movement disturbances in the differential diagnosis of Creutzfeldt-Jakob disease. Edler J; Mollenhauer B; Heinemann U; Varges D; Werner C; Zerr I; Schulz-Schaeffer WJ Mov Disord; 2009 Feb; 24(3):350-6. PubMed ID: 19053051 [TBL] [Abstract][Full Text] [Related]
10. Familial Creutzfeldt-Jakob disease with the E200K mutation: longitudinal neuroimaging from asymptomatic to symptomatic CJD. Cohen OS; Chapman J; Korczyn AD; Nitsan Z; Appel S; Hoffmann C; Rosenmann H; Kahana E; Lee H J Neurol; 2015 Mar; 262(3):604-13. PubMed ID: 25522698 [TBL] [Abstract][Full Text] [Related]
11. Mutation and polymorphism of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease (CJD). Gabizon R; Rosenmann H; Meiner Z; Kahana I; Kahana E; Shugart Y; Ott J; Prusiner SB Am J Hum Genet; 1993 Oct; 53(4):828-35. PubMed ID: 8105682 [TBL] [Abstract][Full Text] [Related]
12. Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development. Mitrová E; Belay G Acta Virol; 2002; 46(1):31-9. PubMed ID: 12197632 [TBL] [Abstract][Full Text] [Related]
13. The Libyan Creutzfeldt-Jakob disease focus in Israel: an epidemiologic evaluation. Zilber N; Kahana E; Abraham M Neurology; 1991 Sep; 41(9):1385-9. PubMed ID: 1891086 [TBL] [Abstract][Full Text] [Related]
14. Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy. Kovacs GG; Seguin J; Quadrio I; Höftberger R; Kapás I; Streichenberger N; Biacabe AG; Meyronet D; Sciot R; Vandenberghe R; Majtenyi K; László L; Ströbel T; Budka H; Perret-Liaudet A Acta Neuropathol; 2011 Jan; 121(1):39-57. PubMed ID: 20593190 [TBL] [Abstract][Full Text] [Related]
15. Genetics and biochemistry of Creutzfeldt-Jakob disease in Libyan Jews. Gabizon R; Halimi M; Meiner Z Biomed Pharmacother; 1994; 48(8-9):385-90. PubMed ID: 7858176 [TBL] [Abstract][Full Text] [Related]
16. A mutation in the prion protein gene in Creutzfeldt-Jakob disease in Jewish patients of Libyan, Greek, and Tunisian origin. Korczyn AD; Chapman J; Goldfarb LG; Brown P; Gajdusek DC Ann N Y Acad Sci; 1991; 640():171-6. PubMed ID: 1685643 [TBL] [Abstract][Full Text] [Related]
17. Mutation in codon 200 and polymorphism in codon 129 of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease. Gabizon R; Rosenman H; Meiner Z; Kahana I; Kahana E; Shugart Y; Ott J; Prusiner SB Philos Trans R Soc Lond B Biol Sci; 1994 Mar; 343(1306):385-90. PubMed ID: 7913755 [TBL] [Abstract][Full Text] [Related]