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Showing articles 0 to 6 of 6 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 Juvenile Myoclonic Epilepsy, Underdiagnosed and Treatment May Have to be Life Long BMJ 305:4-5, Timmings,P.L.&Richens,A., 1992 Delayed Diagnosis of Juvenile Myoclonic Epilepsy JNNP 55:497-499, Grunewald,R.A.,et al, 1992 Clinicopath Conf Tuberous Sclerosis, Case 41-1986, NEJM 315:1013-1022986., , 1986 Neurological Findings in Patients with the Fragile-X Syndrome JNNP 48:150-153, Finelli,P.F.,et al, 1985 Showing articles 0 to 6 of 6