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Showing articles 0 to 8 of 8 Filter Applied: prion disease (Click to remove) Diagnosing variant Creutzfeldt-Jakob disease: a retrospective analysis of the first 150 cases in the UK JNNP 82:646-651, Heath, C.A.,et al, 2011 Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene NEJM 326:444-449, Medori,R.,et al, 1992 Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases Neurol 42:312-319, Manetto,V.,et al, 1992 Sporadic Creutzfeldt-Jakob Disease in a Very Young Person Neurol 97:813-816,801, Appleby, B.S.,et al, 2021 Variant Creutzfeldt-Jakob Disease Diagnosed 7.5 Years after Occupational Exposure NEJM 383:83-85, Brandel, J.P.,et al, 2020 New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests Lancet 350:903-907, Zeidler,M.,et al, 1997 BSE Linked to New Variant of CJD in Humans BMJ 312:795, 791, 843, 85496., , 1996 A New Variant of Creutzfeldt-Jakob Disease in the UK Lancet 347:921-925, 915, 916, 91796., Will,R.G.,et al, 1996 Showing articles 0 to 8 of 8