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Showing articles 0 to 10 of 10 Filter Applied: insomnia (Click to remove) Clinicopathologic Conference, Creutzfeldt-Jakob Disease NEJM 381:1569-1578, Case 32-2019, 2019 Clinical Manifestations of the anti-IgLON5 Disease Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017 Paraneoplastic and Autoimmune Encephalitis UptoDate July, Dalmau, J.,et al, 2017 N-Methyl-D-Aspartate Receptor Antibodies in Pediatric Dyskinetic Encephalitis Lethargica Ann Neurol 66:704-709, Dale,R.,et al, 2009 Transient Insomnia Induced by High-Frequency Deep Brain Stimulation in Parkinson Disease Neurol 62:1232-1233, Monaca,C.,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 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 & Dysautonomia with Selective Degeneration of Thalamic Nuclei NEJM 315:997-1003, Lugaresi,E.,et al, 1986 Showing articles 0 to 10 of 10