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Showing articles 0 to 7 of 7 Filter Applied: seizure,familial (Click to remove) Absence Epilepsies With Widely Variable Onset are a Key Feature of Familial GLUT1 Deficiency Neurol 75:432-440, Mullen,S.A., et al, 2010 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 Juvenile Myoclonic Epilepsy, Underdiagnosed and Treatment May Have to be Life Long BMJ 305:4-5, Timmings,P.L.&Richens,A., 1992 Hereditary Long Q-T Syndrome Presenting as Epilepsy:Electroencephalography Laboratory Diagnosis Ann Neurol 25:514-516, Gospe,S.M.&Choy,M., 1989 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 7 of 7