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Showing articles 0 to 3 of 3 Filter Applied: seizure,familial (Click to remove) Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006 X-Linked Malformation of Neuronal Migration Neurol 47:331-339, Dobyns,W.B.,et al, 1996 Periventricular Heterotopia and Epilepsy Neurol 44:51-55, Huttenlocher,P.R.,et al, 1994 Showing articles 0 to 3 of 3