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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 Neuroimaging Findings in Human Prion Disease JNNP 78:664-670, Macfarlane,R.G.,et al, 2007 Clinical Presentation and Pre-Mortem Diagnosis of Variant Creutzfeldt-Jakob Disease Associated With Blood Transfusion: A Case Report Lancet 368:2061-2067, Wroe,S.J.,et al, 2006 Creutzfeldt-Jakob Disease in a Young Woman Lancet 347:945-948, Tabrizi,S.J.,et al, 1996 Clinical and Genetic Studies of Fatal Familial Insomnia Neurol 45:1068-1075, Reder,A.T.,et al, 1995 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 Analysis of the Prion Protein Gene in Thalamic Dementia Neurol 42:1859-1863, Petersen,R.B.,et al, 1992 Showing articles 0 to 8 of 8