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Showing articles 0 to 4 of 4 Filter Applied: status epilepticus (Click to remove) The Phenotypic Continuum of ATP1A3-Related Disorders Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022 Clinicopath Conf Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992 Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006 New Research in Tuberous Sclerosis, Probably More Common with More Adult Complications BMJ 304:1647-1648, Mitchell,S.&Bradbeer,C., 1992 Showing articles 0 to 4 of 4