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Showing articles 0 to 4 of 4 Filter Applied: pyramidal tract dysfunction (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 Clinicopath Conf Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992 Chronic Meningitis Medicine 55:341, Ellner,J.J.,et al, 1976 Mollaret's Meningitis & Differential Diagnosis of Recurrent Meningitis Am J Med 52:128, Hermans,P.,et al, 1972 Showing articles 0 to 4 of 4