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Showing articles 0 to 6 of 6 Filter Applied: seizure,familial (Click to remove) Delayed Diagnosis of Juvenile Myoclonic Epilepsy JNNP 55:497-499, Grunewald,R.A.,et al, 1992 Absence Epilepsies With Widely Variable Onset are a Key Feature of Familial GLUT1 Deficiency Neurol 75:432-440, Mullen,S.A., et al, 2010 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 Benign Versive or Circling Epilepsy with Bilateral 3-Cps Spike- & -Wave Discharges in Late Childhood Ann Neurol 19:301-303, Gastaut,H.,et al, 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