myoclonic

Severe myoclonic epilepsy in infancy: Dravet syndromeJuvenile Myoclonic Epilepsy: A 5-Year Prospective StudySevere myoclonic epilepsy of infancy: extended spectrum of GEFS+?Mutations in EFHC1 cause juvenile myoclonic epilepsyLamotrigine and seizure aggravation in severe myoclonic epilepsyMyoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy.De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.Shoffner, J. M. et al. Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALYS mutati...Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy