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Showing articles 0 to 7 of 7 Filter Applied: familial (Click to remove) Seizures on Hearing the Alarm Clock Lancet 370:2172, Vollmar,C.,et al, 2007 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 Familial Temporal Lobe Epilepsy with Febrile Seizures Neurol 58:1429-1433, Depondt,C.,et al, 2002 A Locus for Febrile Seizures (FEB3) Maps to Chromosome 2q23-24 Ann Neurol 46:671-678, Peiffer,A.,et al, 1999 Predictors of Recurrent Febrile Seizures Arch Pediatr Adolesc Med 151:371-378, Berg,A.T.,et al, 1997 Clinicopath Conf Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992 Showing articles 0 to 7 of 7