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Showing articles 0 to 8 of 8 Filter Applied: prion disease (Click to remove) Clinicopathologic Conference, Creutzfeldt-Jakob Disease NEJM 381:1569-1578, Case 32-2019, 2019 Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies NEJM 339:1994-2004, Johnson,R.T. & Gibbs,Jr.,C.J., 1998 Sporadic Creutzfeldt-Jakob Disease in a Very Young Person Neurol 97:813-816,801, Appleby, B.S.,et al, 2021 A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms Neurol 94:e1213-e1218, Lima, J.E.E.,et al, 2020 Clinicopath conf., Human Prion Disease, Sporadic CJD Neurol 69:1881-1887, Geschwind,M.D., et al, 2007 New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests Lancet 350:903-907, Zeidler,M.,et al, 1997 A New Variant of Creutzfeldt-Jakob Disease in the UK Lancet 347:921-925, 915, 916, 91796., Will,R.G.,et al, 1996 Clinicopath Conf Spongiform Encephalopathy (Creutzfeldt-Jakob Disease) , with Amyloid (KURU) Plaques, Case 17-1993, N, JM 328:66,1993., 1993 Showing articles 0 to 8 of 8