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Showing articles 0 to 8 of 8 Filter Applied: prion disease (Click to remove) Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease NEJM 386;674-687, Case 5-2022, 2022 Sporadic Creutzfeldt-Jakob Disease in a Very Young Person Neurol 97:813-816,801, Appleby, B.S.,et al, 2021 Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies NEJM 339:1994-2004, Johnson,R.T. & Gibbs,Jr.,C.J., 1998 Creutzfeldt-Jakob Disease in a Young Woman Lancet 347:945-948, Tabrizi,S.J.,et al, 1996 Inherited Prion Disease (PrP lysine 200) in Britain:Two Case Reports BMJ 306:301-302, 2881993., Collinge,J.,et al, 1993 Clinicopath Conf Spongiform Encephalopathy (Creutzfeldt-Jakob Disease) , with Amyloid (KURU) Plaques, Case 17-1993, N, JM 328:66,1993., 1993 Prion Dementia Without Characteristic Pathology Lancet 336:7-9, 21-221990., Collinge,J.,et al, 1990 Diagnosis of Gerstmann-Straussler Syndrome in Familial Dementia with Prion Protein Gene Analysis Lancet 2:15-17, Collinge,J.,et al, 1989 Showing articles 0 to 8 of 8