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Showing articles 0 to 9 of 9 Filter Applied: fatal familial insomnia (Click to remove) A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms Neurol 94:e1213-e1218, Lima, J.E.E.,et al, 2020 Transmissible Spongiform Encephalopathies Lancet 363:51-61, Collins,S.J.,et al, 2004 Fatal Insomnia in a Case of Familial Creutzfeldt-Jakob Disease with the Codon 200Lys Mutation Neurol 46:758-761, Chapman,J.,et al, 1996 Clinical and Genetic Studies of Fatal Familial Insomnia Neurol 45:1068-1075, Reder,A.T.,et al, 1995 Human Prion Diseases Ann Neurol 35:385-395, Prusiner,S.B.&Hsiao,K.K., 1994 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 Fatal Familial Insomnia:A Second Kindred with Mutation of Prion Protein Gene at Codon 178 Neurol 42:669-670, 1992, Medori,R.,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 9 of 9