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Showing articles 0 to 11 of 11 Filter Applied: prion disease (Click to remove) Rapidly Progressive Dementia Ann Neurol 64:97-108, Geschwind,M.D.,et al., 2008 Neuroimaging Findings in Human Prion Disease JNNP 78:664-670, Macfarlane,R.G.,et al, 2007 Neurodegenerative Diseases and Prions NEJM 344:1516-1526,1548, Prusiner,S.B., 2001 Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease BMJ 315:856-857, Fox,N.C.,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 Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease NEJM 324:1091-1097, Hsiao,K.,et al, 1991 Rapid Detection of Creutzfeldt-Jakob Disease and Scrapie Prion Porteins Neurol 40:110-117, Serban,D.,et al, 1990 Inherited Human Prion Diseases Neurol 40:1820-1827, Hsiao,K.&Prusiner,S.B., 1990 Prions & Neurodegenerative Diseases NEJM 317:1571-1581, 15971987., Prusiner,S.B., 1987 Clinicopath conf., Human Prion Disease, Sporadic CJD Neurol 69:1881-1887, Geschwind,M.D., et al, 2007 Diagnosis of Creutzfeldt-Jakob Disease in Two-Dimensional Gel Electrophoresis of Cerebrospinal Fluid Lancet 348:846-849, Zerr,I.,et al, 1996 Showing articles 0 to 11 of 11