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See Latest ArticlesHemiconvulsion–hemiplegia syndrome in a patient with severe myoclonic epilepsy in infancy
Epilepsia, 07/01/09
Sakakibara T et al. - A 2-year-old girl who had repeated febrile or afebrile seizures since infancy is reported. Prolonged left/right hemiconvulsions and myoclonus of the eyelids/extremities with generalization to tonic–clonic seizures, were refractory to antiepileptic agents. SCN1A mutations may need to be further explored in patients with HH syndrome without features of SME.
Today in Pediatric Neurology...keeping you current
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Today in Seizure...keeping you current
Receive free subspecialty "5-minute updates" via email
Effectiveness of the ketogenic diet in a broad range of seizure types and EEG features for severe childhood epilepsies
Acta Neurologica Scandinavica, 12/03/09
Cost-utility analysis of rufinamide versus topiramate and lamotrigine for the treatment of children with Lennox–Gastaut Syndrome in the United Kingdom
Seizure - European Journal of Epilepsy, 12/03/09
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