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Showing articles 0 to 8 of 8 Filter Applied: gene (Click to remove) Fibromuscular Dysplasia and Its Neurologic Manifestations JAMA Neurol 76:217-226, Touze, E.,et al, 2019 An unusual cause of stroke and hypoxia BMJ 342:c7200, Bell, S.L. & Eveson, D.J., 2011 Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder Brain 133:655-670, Leen,W.G., et al, 2010 A Hereditary Moyamoya Syndrome With Multisystemic Manifestations Neurol 75:259-264, Herv�,D., et al, 2010 Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease NEJM 360:1729-1739, Hara,K.,et al, 2009 Aicardi-Gouti�res Syndrome Br Med Bull 89:183-201, Orcesi, S.,et al, 2009 Variable Presentation of Brugada Syndrome: Lessons from Three Generations with Syncope BMJ 326:1078-1079, Plunkett,A.,et al, 2003 Hereditary Hemorrhagic Telangiectasia NEJM 333:918-924, Guttmacher,A.E.,et al, 1995 Showing articles 0 to 8 of 8