Enter your terms above and click the 'Search' button.

Showing articles 0 to 11 of 11 Filter Applied: autonomic dysfunction (Click to remove) A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia Neurol 105:e213993, Shen,F.,et al, 2025 Antibody-Mediated Encephalitis NEJM 378:840-851, Dalmau, J.,et al, 2018 Neuroimaging and Clinical Features in Type II (late-onset) Alexander Disease Neurol 82:49-56, Graff-Radford, J.,et al, 2014 Serotonin Syndrome BMJ 348:g1626, Buckley, N.A.,et al, 2014 GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease Neurol 77:1287-1294, Prust, M.,et al, 2011 The Serotonin Syndrome NEMJ 352:1112-20, Boyer, E.W. & Shannon, M., 2005 Clinicopath Conf, Multiple-System Atrophy NEJM 351:912-921, Case 27-2004, 2004 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 11 of 11