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Showing articles 0 to 7 of 7 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 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 Showing articles 0 to 7 of 7