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Showing articles 0 to 10 of 10 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 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 Localization of Idiopathic Generalized Epilepsy on Chromosome 6p in Families of Juvenile Myoclonic epilepsy patients Neurol 41:1651-1655, Durner,M.,et al, 1991 Monozygotic Twins with Seizures, Shared Characteristics Arch Neurol 48:1041-1045, Segal,R.A.,et al, 1991 Hereditary Long Q-T Syndrome Presenting as Epilepsy:Electroencephalography Laboratory Diagnosis Ann Neurol 25:514-516, Gospe,S.M.&Choy,M., 1989 Juvenile Myoclonic Epilepsy:An Autosomal Recessive Disease Ann Neurol 25:440-443, Panayiotopoulos,C.P.&Obeid,T., 1989 Neurological Findings in Patients with the Fragile-X Syndrome JNNP 48:150-153, Finelli,P.F.,et al, 1985 Benign Familial Neonatal Seizures E. , Arch Neurol 37:47-48980., Pettit,R., 1980 Showing articles 0 to 10 of 10