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Showing articles 0 to 12 of 12 Filter Applied: gene (Click to remove) Genes Associated With Adult Cerebral Venous Thrombosis Stroke 42:913-918, Marjot,T.,et al, 2011 RNF213 Polymorphisms in Intracranial Artery Dissection Genes doi.org/10.3390/genesis 15060725, Zedde,M.,et al, 2024 Recurrent Cerebral Ischemia During Pregnancies Neurol 95:e2453-e2457, Bulwa, Z.,et al, 2020 Fibromuscular Dysplasia and Its Neurologic Manifestations JAMA Neurol 76:217-226, Touze, E.,et al, 2019 Neurological Management of Von Hippel-Lindau Disease Neurologist 21:73-78, Hodgson, T.S.,et al, 2016 An unusual cause of stroke and hypoxia BMJ 342:c7200, Bell, S.L. & Eveson, D.J., 2011 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 Autosomal Dominant Moyamoya Disease Maps to Chromosome 17q25.3 Neurol 70:2357-2363, Mineharu,Y.,et al, 2008 Pulmonary Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia: A Series of 126 Patients Medicine 86:1-7, Cottin,V.,et al, 2007 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 12 of 12