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Showing articles 0 to 7 of 7 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 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 A Locus for Febrile Seizures (FEB3) Maps to Chromosome 2q23-24 Ann Neurol 46:671-678, Peiffer,A.,et al, 1999 Seizure Characteristics in Chromosome 20 Benign Familial Neonatal Convulsions Neurol 43:1355-1360, Ronen,G.M.,et al, 1993 Benign Familial Neonatal Convulsions:Evidence for Clinical and Genetic Heterogeneity Ann Neurol 29:469-473, Ryan,S.G.,et al, 1991 Benign Versive or Circling Epilepsy with Bilateral 3-Cps Spike- & -Wave Discharges in Late Childhood Ann Neurol 19:301-303, Gastaut,H.,et al, 1986 Benign Familial Neonatal Seizures E. , Arch Neurol 37:47-48980., Pettit,R., 1980 Showing articles 0 to 7 of 7