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Showing articles 0 to 9 of 9 Filter Applied: myoclonus,epilepsy (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 Progressive Gait Deterioration in Adolescents with Dravet Syndrome Arch Neurol 69:873-878, Rodda, J.M.,et al, 2012 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 Stiripentol in Severe Myoclinic Epilepsy in Infancy: A Randomised Placebo-Controlled Syndrome-Dedicated Trial Lancet 356:1638-1642,1623, Chiron,C.,et al, 2000 Clinicopath Conf Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992 Mitochondril Encephalopathies:Molecular Genetic Diagnosis from Blood Samples Lancet 337:1311-1313, Hammans,S.R.,et al, 1991 Neonatal Seizures:Current Concepts and Revised Classification Pediatrics 84:422-428, Volpe,J.J., 1989 Chronic Progressive Panencephalitis due to Rubella Virus Simulating Subacute Sclerosing Panencephalitis NEJM 292:994-998,1023, Weil, M.L.,et al, 1975 Showing articles 0 to 9 of 9