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Showing articles 0 to 13 of 13 Filter Applied: familial (Click to remove) Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease NEJM 386;674-687, Case 5-2022, 2022 More Than a Little Unsteady NEJM 387:e9, Kraft, A.W.,et al, 2022 MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study AJNR 29:1638-1643, Fulbright,R.K.,et al, 2008 Creutzfeldt-Jacob Disease in a Husband and Wife Neurol 50:684-688, Brown,P.,et al, 1998 Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies NEJM 339:1994-2004, Johnson,R.T. & Gibbs,Jr.,C.J., 1998 Fatal Insomnia in a Case of Familial Creutzfeldt-Jakob Disease with the Codon 200Lys Mutation Neurol 46:758-761, Chapman,J.,et al, 1996 Risk Factors for Creutzfeldt-Jakob Disease:A Reanalysis of Case-Control Studies Neurol 46:1287-1291, Wientjens,D.P.W.M.,et al, 1996 Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992 Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease NEJM 324:1091-1097, Hsiao,K.,et al, 1991 The Spongiform Encephalopathies, Editorial JNNP 54:761-763, Will,R.G., 1991 Inherited Human Prion Diseases Neurol 40:1820-1827, Hsiao,K.&Prusiner,S.B., 1990 Familial Creutzfeldt-Jakob Disease without Periodic EEG Activity Ann Neurol 28:585-588, Tietjen,G.E.&Drury,I., 1990 Supranuclear Gaze Palsy in Familial Creutzfeldt-Jakob Disease Arch Neurol 40:618-622, Bertoni,J.M.,et al, 1983 Showing articles 0 to 13 of 13