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Showing articles 0 to 7 of 7 Filter Applied: seizure,familial (Click to remove) Delayed Diagnosis of Juvenile Myoclonic Epilepsy JNNP 55:497-499, Grunewald,R.A.,et al, 1992 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 Genetic Localization of the Familial Adult Myoclonic Epilepsy (FAME) Gene to Chromosome 8q24 Neurol 53:1180-1183, Plaster,N.M.,et al, 1999 Juvenile Myoclonic Epilepsy, Underdiagnosed and Treatment May Have to be Life Long BMJ 305:4-5, Timmings,P.L.&Richens,A., 1992 Localization of Idiopathic Generalized Epilepsy on Chromosome 6p in Families of Juvenile Myoclonic epilepsy patients Neurol 41:1651-1655, Durner,M.,et al, 1991 Juvenile Myoclonic Epilepsy:An Autosomal Recessive Disease Ann Neurol 25:440-443, Panayiotopoulos,C.P.&Obeid,T., 1989 Showing articles 0 to 7 of 7