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Showing articles 0 to 8 of 8 Filter Applied: gene (Click to remove) A Hereditary Moyamoya Syndrome With Multisystemic Manifestations Neurol 75:259-264, Herv�,D., et al, 2010 RNF213 Polymorphisms in Intracranial Artery Dissection Genes doi.org/10.3390/genesis 15060725, Zedde,M.,et al, 2024 Fibromuscular Dysplasia and Its Neurologic Manifestations JAMA Neurol 76:217-226, Touze, E.,et al, 2019 Ehlers-Danlos Syndromes BMJ 366:I4966, Ghali, N.,et al, 2019 Muscular Dystrophies Lancet 394:2025-2038, Mercuri, E.,et al, 2019 Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease NEJM 360:1729-1739, Hara,K.,et al, 2009 Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene NEJM 354:2584-2592, Case 18-2006, 2006 Variable Presentation of Brugada Syndrome: Lessons from Three Generations with Syncope BMJ 326:1078-1079, Plunkett,A.,et al, 2003 Showing articles 0 to 8 of 8