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Showing articles 0 to 11 of 11 Filter Applied: gene mutation (Click to remove) Cranial Cavernous Malformations Stroke 49:1029-1035, Stapleton, C.J. & Barker, F.G., 2018 Intractable Epilepsy and Progressive Cognitive Decline in a Young Man JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017 Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency NEJM 375:1879-1890, Case 34-2016, 2016 A Case of Refractory Nocturnal Seizures Neurol 84:e134-e136, Pavlakis, P.P. & Douglass, L.M., 2015 Sturge-Weber Syndrome UptoDate , Nov, Bodensteiner, J.B., 2014 Extending the KCNQ2 encephalopathy Spectrum Neurol 81:1697-1703, Weckhuysen, S.,et al, 2013 Sturge-Weber Syndrome MedLink Neurology, July, Comi, A.M., 2013 Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006 Factor V Leiden Mutation is a Risk Factor for Cerebral Venous Thrombosis,A Case-Control Study of 55 Patients Stroke 29:2507-2510, Ludemann,P.,et al, 1998 Cerebral Venous Sinus Thrombosis Associated with Factor V Gene Mutation JNNP 61:204-205, Kimber,T.,et al, 1996 Cerebral Venous Thrombosis:Role of Activated Protein C Resistance and Factor V Gene Mutation Stroke 27:1719-1720, Brey,R.L.&Coull,B.M., 1996 Showing articles 0 to 11 of 11