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Showing articles 0 to 15 of 15 Filter Applied: gene (Click to remove) Fibromuscular Dysplasia and Its Neurologic Manifestations JAMA Neurol 76:217-226, Touze, E.,et al, 2019 A Hereditary Moyamoya Syndrome With Multisystemic Manifestations Neurol 75:259-264, Herv�,D., et al, 2010 A Multidisciplinary Study of Patients with Early-Onset PD with and Without Parkin Mutations Neurol 72:110-116,106, Lohmann,E.,et al, 2009 Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease NEJM 360:1729-1739, Hara,K.,et al, 2009 Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts & Leukoencephalopathy (CADASIL) UpToDate (www.uptodate.com) Aug 21, Dichgans,M.,et al., 2007 The Tuberous Sclerosis Complex NEJM 355:1345-1356, Crino,P.B.,et al, 2006 Complete Genomic Screen in Parkinson Disease JAMA 286:2239-2244, Scott,W.K.,et al, 2001 Hereditary Hemorrhagic Telangiectasia NEJM 333:918-924, Guttmacher,A.E.,et al, 1995 The Neurogenetic Genie:Testing for Huntington's Disease Mutation Neurol 44:1369-1373, 1533-15361994., Hersch,S.,et al, 1994 A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats NEJM 330:1401-1406, 14501994., Kremer,B.,et al, 1994 Reduced Basal Ganglia Volume Associated with the Gene for Huntington's Disease in Asymptomatic at-Risk Persons Neurol 44:823-828, Aylward,E.H.,et al, 1994 Clinical Consequences of Isolating the Gene for Huntington's Disease BMJ 307:397-398, Harper,P.S., 1993 Predictive Testing for Huntington's Disease, Progress and Problems BMJ 298:404-405, 1989, Harper,P.S.&Morris,M.J., 1989 Predictive Testing for Huntington's Disease with Use of a Linked DNA Marker NEJM 318:535-542, Meissen,G.J.,et al, 1988 A Genetic Marker for Huntington's Chorea BMJ 287:1567-1568, Harper,P.S., 1983 Showing articles 0 to 15 of 15