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Showing articles 0 to 9 of 9 Filter Applied: hyperhidrosis (Click to remove) Morvan Syndrome: Clinical and Serological Observations in 29 Cases Ann Neurol 72:241-255, Irani, S.R.,et al, 2012 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 The Writing on the Wall Lancet 372:344, Wilder-Smith,E.P. &Ng,E.S., 2008 Acromegaly:Clinical and Biochemical Features in 500 Patients Medicine 73:233-240, Ezzat,S.,et al, 1994 Clinicopath Conf Pheochromocytoma with Hemorrhagic Infarct, Catecholamine-Induced Dilated Cardiomyopathy, Case Record, 15988,NEJM 318:970-981,1988., 1988 Autonomic Epilepsy:Clonidine Blockade of Paroxysmal Catecholamine Release & Flushing Ann Int Med 88:189, Metz,S.A.,et al, 1978 Blue Rubber Bleb Nevus Syndrome with CNS Involvement & Thrombosis of a Vein of Galen Malformation Ann Neurol 3:464, Waybright,E.A.,et al, 1978 The Neurologist's Experience with Pheochromocytoma JAMA 197:100, Thomas,J.E.,et al, 1966 Showing articles 0 to 9 of 9