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Showing articles 0 to 2 of 2 Filter Applied: pyramidal tract dysfunction (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 Clinical Correlates of Vascular Parkinsonism Arch Neurol 56:98-102, Winikates,J.&Jancovic,J., 1999 Showing articles 0 to 2 of 2