Clinical course of young patients with Dravet syndrome after vagal nerve stimulation

European Journal of Paediatric Neurology - Tập 15 - Trang 8-14 - 2011
Nelia Zamponi1, Claudia Passamonti1, Silvia Cappanera1, Cristina Petrelli1
1Pediatric Neurology Department, Ospedali Riuniti, Ancona, Italy

Tài liệu tham khảo

Dravet, 2002, Severe myoclonic epilepsy in infancy (Dravet syndrome), 81 Claes, 2001, De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy, Am J Hum Genet, 68, 1327, 10.1086/320609 Ohki, 1997, Severe myoclonic epilepsy in infancy: evolution of seizures, Seizure, 6, 219, 10.1016/S1059-1311(97)80009-X Ogino, 1989, The epileptic syndrome sharing common characteristics during early childhood with severe myoclonic epilepsy of infancy, Jpn J Psychiatry Neurol, 43, 479 Wallace, 1998, Myoclonus and epilepsy in childhood: a review of treatment with valproate, ethosuximide, lamotrigine and zonisamide, Epilepsy Res, 29, 147, 10.1016/S0920-1211(97)00080-6 Chiron, 2000, Stiripentol in severe myoclonic epilepsy in infancy: a randomized placebo-controlled syndrome-dedicated trial. STICLO study group, Lancet, 356, 1638, 10.1016/S0140-6736(00)03157-3 Coppola, 2002, Topiramate as add-on drug in severe myoclonic epilepsy in infancy: an Italian multicenter open trial, Epilepsy Res, 49, 45, 10.1016/S0920-1211(02)00010-4 Villeneuve, 2002, Topiramate (TPM) in severe myoclonic epilepsy in infancy, Epilepsia, 43, 155 Handforth, 1998, Vagus nerve stimulation therapy for partial onset seizures: a randomises active-control trial, Neurology, 51, 48, 10.1212/WNL.51.1.48 Wheless, 2002, Vagus nerve stimulation therapy in patients younger than 18 years, Neurology, 59, 21, 10.1212/WNL.59.6_suppl_4.S21 Dravet, 1992, Severe myoclonic epilepsy, 75 Wolff, 2006, Severe myoclonic epilepsy of infants (Dravet Syndrome): natural history and neuropsychological findings, Epilepsia, 47, 45, 10.1111/j.1528-1167.2006.00688.x Hallböök, 2005, Vagus nerve stimulation in 15 children with therapy resistant epilepsy; its impact on cognition, quality of life, behaviour and mood, Seizure, 14, 504, 10.1016/j.seizure.2005.08.007 Rossignol, 2009, Vagus nerve stimulation in pediatric epileptic syndromes, Seizure, 18, 34, 10.1016/j.seizure.2008.06.010 Shahwan, 2009, Vagus nerve stimulation for refractory epilepsy in children: more to VNS than seizure frequency reduction, Epilepsia, 50, 1220, 10.1111/j.1528-1167.2008.01940.x Commission on Classification and Terminology of the International League Against Epilepsy, 1989, Proposal for revised classification of epilepsies and epileptic syndromes, Epilepsia, 30, 289 Mc Intosh, 2010, Effects of vaccination onset and outcome of Dravet syndrome: a retrospective study, Lancet Neurol, 9, 559 Rychlicki, 2006, Vagus nerve stimulation: clinical experience in drug-resistant pediatric epileptic patients, Seizure, 15, 483, 10.1016/j.seizure.2006.06.001 McHugh, 2007, Outcome after vagal nerve stimulation therapy: proposal of a new classification, Epilepsia, 48, 375, 10.1111/j.1528-1167.2006.00931.x Bozzo, 1968, Adattamento Italiano della Scala d’Intelligenza Stanford-Binet Forma L-M nella Revisione Terman-Merril, vol. 14, 1 Wechsler, 1949 Balboni, 2003, Adattamento italiano delle Vineland adaptive behavior scales Lundgren, 1998, Vagus nerve stimulation in 16 children with refractory epilepsy, Epilepsia, 39, 809, 10.1111/j.1528-1157.1998.tb01173.x Vonck, 2004, Vagus nerve stimulation for refractory epilepsy: a transatlantic experience, J Clin Neurophysiol, 21, 283, 10.1097/01.WNP.0000139654.32974.4E Kostov, 2007, Is vagus nerve stimulation a treatment option for patients with drug-resistant idiopathic generalized epilepsy?, Acta Neurol Scand Suppl, 187, 55, 10.1111/j.1600-0404.2007.00848.x Zamponi, 2009, Vagal nerve stimulation in intractable epilepsy: clinical experience on 100 patients and review of the literature, J Pediatr Sci, 1, e17 Labar, 1818, Persistent antiepileptic effects after vagus nerve stimulation ends?, Neurology, 2003, 61 Nabbout, 2008, Nabbout. An unexpected EEG course in Dravet syndrome, Epilepsy Res, 81, 90, 10.1016/j.eplepsyres.2008.04.015 Nei, 2006, Refractory generalized seizures: response to corpus callosotomy and vagal nerve stimulation, Epilepsia, 47, 115, 10.1111/j.1528-1167.2006.00377.x Cukiert, 2006, One stage callosal section for treatment of refractory secondarily generalizad epilepsy in patients with Lennox-Gastaut and lennox-like syndromes, Epilepsia, 47, 371, 10.1111/j.1528-1167.2006.00430.x Caraballo, 2005, Ketogenic diet in patients with Dravet Syndrome, Epilepsia, 46, 1539, 10.1111/j.1528-1167.2005.05705.x Kang, 2005, Efficacy and safety of the ketogenic diet for intractable childhood epilepsy: Korean multicentric experience, Epilepsia, 46, 272, 10.1111/j.0013-9580.2005.48504.x Coppola, 2010, Ketogenic diet for the treatment of catastrophic epileptic encephalopathies in childhood, Eur J Paediatric Neurol, 14, 229, 10.1016/j.ejpn.2009.06.006 Chabardès, 2002, Deep brain stimulation in epilepsy with particular reference to the subthalamic nucleus, Epileptic Disord, 4, 83 Andrade, 2009, Dravet syndrome and deep brain stimulation: seizure control after 10 years of treatment, Epilepsia, 51, 1, 10.1111/j.1528-1167.2009.02408.x