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Showing articles 0 to 8 of 8 Filter Applied: familial (Click to remove) Essential Tremor NEJM 378:1802-1810, Haubenberger, D.,et al, 2018 MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study AJNR 29:1638-1643, Fulbright,R.K.,et al, 2008 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 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 Intracranial Hemorrhage in Patients with Polycystic Kidney Disease Stroke 21:291-294, Ryu,S.J., 1990 Showing articles 0 to 8 of 8