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Showing articles 0 to 2 of 2 Filter Applied: developmental retardation (Click to remove) A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever Neurol 102:e209358, Barbosa,A.R.,et al, 2024 Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006 Showing articles 0 to 2 of 2