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Showing articles 0 to 9 of 9 Filter Applied: sleep pathology and physiology (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 Diagnosis and Management of Motor Neurone Disease BMJ 336:658-662, McDermott,C.J. &Shaw,P.J., 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 Congenital Central Hypoventilation Syndrome:Diagnosis, Management, and Long-Term Outcome in Thirty-Two Children J Pediatr 120:381-387, Weese-Mayer,D.E.,et al, 1992 Risk of Sudden Death During Sleep in Syringomyelia and Syringobulbia JNNP 55:585-589, Nogues,M.A.,et al, 1992 Obstructive Sleep Apnea in Family Members NEJM 299:969-973, Strohl,K.P.,et al, 1978 Showing articles 0 to 9 of 9