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Showing articles 0 to 6 of 6 Filter Applied: myoclonus,epilepsy (Click to remove) Progressive Gait Deterioration in Adolescents with Dravet Syndrome Arch Neurol 69:873-878, Rodda, J.M.,et al, 2012 Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006 Epilepsy Syndromes in Infancy Pediatr Neurol 34:253-263, Korff,C.M. &Nordii,D.R.,Jr., 2006 Clinical Correlations of Mutations in the SCN1A Gene: From Febrile Seizures to Severe Myoclonic Epilepsy in Infancy Pediatr Neurol 30:236-243, Ceulemans,B.P.G.M.,et al, 2004 Nicotine-Sensitive Paresis Neurol 42:382-388, Yokota,T.,et al, 1992 Clinicopath Conf Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992 Showing articles 0 to 6 of 6