Epilepsias benignas del niño

Guerrini, 2012, Benign childhood focal epilepsies, Epilepsia, 53, 9, 10.1111/j.1528-1167.2012.03609.x Kramer, 2008, Atypical presentations of benign childhood epilepsy with centrotemporal spikes: a review, J Child Neurol, 23, 785, 10.1177/0883073808316363 Tovia, 2011, The prevalence of atypical presentations and comorbidities of benign childhood epilepsy with centrotemporal spikes, Epilepsia, 52, 1483, 10.1111/j.1528-1167.2011.03136.x Japaridze, 2014, Risk factors of cognitive outcome in patients with atypical benign partial epilepsy/pseudo-Lennox syndrome (ABPE/PLS) and continues spike and wave during sleep (CSWS), Eur J Paediatr Neurol, 18, 368, 10.1016/j.ejpn.2014.01.012 Kanemura, 2012, Do sequential EEG changes predict atypical clinical features in rolandic epilepsy?, Dev Med Child Neurol, 54, 912, 10.1111/j.1469-8749.2012.04358.x Metz-Lutz, 2006, Neuropsychological findings in rolandic epilepsy and Landau-Kleffner syndrome, Epilepsia, 47, 71, 10.1111/j.1528-1167.2006.00695.x Pinton, 2006, Cognitive functions in children with benign childhood epilepsy with centrotemporal spikes (BECTS), Epileptic Disord, 8, 11 Vannest, 2015, Cognitive and behavioral outcomes in benign childhood epilepsy with centro temporal spikes, Epilepsy Behav, 45, 85, 10.1016/j.yebeh.2015.01.041 Danielson, 2009, Cognitive deficits in children with benign rolandic epilepsy of childhood or rolandic discharges: a study of children between 4 and 7 years of age with or without seizures compared with healthy controls, Epilepsy Behav, 16, 646, 10.1016/j.yebeh.2009.08.012 Hommet, 2001, Cognitive function in adolescent and young adults in complete remission from benign childhood epilepsy with centrotemporal spikes, Epileptic Disord, 3, 207 Goldberg-Stern, 2010, Neuropsychological aspects of benign childhood epilepsy with centrotemporal spikes, Seizure, 19, 12, 10.1016/j.seizure.2009.10.004 Ma, 2015, Language dysfunction is associated with age of onset of benign epilepsy with centrotemporal spikes in children, Eur Neurol, 73, 179, 10.1159/000371417 Schneebaum-Sender, 2012, Does a normalizing electroencephalogram in benign childhood epilepsy with centrotemporal spikes abort attention deficit hyperactivity disorder?, Pediatr Neurol, 47, 279, 10.1016/j.pediatrneurol.2012.06.009 Ebus, 2011, Reading performance in children with rolandic epilepsy correlates with nocturnal epileptiform activity, but not with epileptiform activity while awake, Epilepsy Behav, 22, 518, 10.1016/j.yebeh.2011.08.008 Filippini, 2013, Neuropsychological development in children belonging to BECTS spectrum: long-term effect of epileptiform activity, Epilepsy Behav, 28, 504, 10.1016/j.yebeh.2013.06.016 Massa, 2001, EEG criteria predictive of complicated evolution in idiopathic rolandic epilepsy, Neurology, 57, 1071, 10.1212/WNL.57.6.1071 You, 2006, Benign childhood epilepsy with centrotemporal spikes (BECTS): early onset of seizures is associated with poorer response to initial treatment, Epileptic Disord, 8, 285 Mellish, 2013, Antiepileptic drug treatment of rolandic epilepsy and Panayiotopoulos syndrome: clinical practice survey and clinical trial feasibility, Arch Dis Child, 100, 62, 10.1136/archdischild-2013-304211 Incerik, 2015, Prognostic significance of failure of the initial antiepileptic drug in children with benign childhood epilepsy with centrotemporal spikes, Brain Dev, 37, 66, 10.1016/j.braindev.2014.02.008 Xia, 2014, Evaluation of levetiracetam and valproic acid as low dose monotherapies for children with typical benign childhood epilepsy with centrotemporal spikes (BECTS), Seizure, 23, 756, 10.1016/j.seizure.2014.06.006 Lesca, 2013, GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction, Nat Genet, 45, 1061, 10.1038/ng.2726 Carvill, 2013, Mutations in GRIN2A cause epilepsy-aphasia spectrum disorders, Nat Genet, 45, 1073, 10.1038/ng.2727 Pal, 2016, Idiopathic focal epilepsies: the “lost tribe”, Epileptic Disord, 18, 252, 10.1684/epd.2016.0839 Dura-Trave, 2008, Panayiotopoulos syndrome: epidemiological and clinical characteristics and outcome, Eur J Neurol, 18, 336, 10.1111/j.1468-1331.2008.02074.x Specchio, 2010, Panayiotopoulos syndrome: a clinical, EEG, and neuropsychological study of 93 consecutive patients, Epilepsia, 51, 2098, 10.1111/j.1528-1167.2010.02639.x Carabello, 2007, Panayiotopoulos syndrome: a prospective study of 192 patients, Epilepsia, 48, 1054, 10.1111/j.1528-1167.2007.01085.x Dirani, 2015, Panayiotopoulos syndrome presenting with arrest: a case report and literature review, Epilepsy Behav Case Rep, 3, 12, 10.1016/j.ebcr.2014.11.002 Verrotti, 2014, Panayiotopoulos syndrome with convulsive status epilepticus at the onset: a long-term study, Seizure, 23, 728, 10.1016/j.seizure.2014.05.013 Hodges, 2016, Neuropsychological findings associated with Panayiotopoulos syndrome in three children, Epilepsy Behav, 54, 158, 10.1016/j.yebeh.2015.11.012 Taylor, 2008, Benign occipital epilepsies of childhood: clinical features and genetics, Brain, 131, 2287, 10.1093/brain/awn138 Garcia, 2009, Efficacy and safety of levetiracetam in the treatment of Panayiotopoulos syndrome, Epilepsy Res, 85, 318, 10.1016/j.eplepsyres.2009.03.024 Parisi, 2007, Panayiotopoulos syndrome: diagnosis and management, Neurol Sci, 28, 72, 10.1007/s10072-007-0790-4 Ferrie, 2006, Panayiotopoulos syndrome: a consensus view, Dev Med Child Neurol, 48, 236, 10.1017/S0012162206000508 Caraballo, 2008, Childhood occipital epilepsy of Gastaut: a study of 33 patients, Epilepsia, 49, 288, 10.1111/j.1528-1167.2007.01322.x Wakamoto, 2011, Idiopathic childhood occipital epilepsy of Gastaut: report of 12 patients, Pediatr Neurol, 44, 183, 10.1016/j.pediatrneurol.2010.10.005 Ferrari-Marinho, 2013, Gastaut type idiopathic childhood occipital epilepsy, Epileptic Disord, 15, 80, 10.1684/epd.2013.0551 Mei Shu, 2013, The characterization of childhood occipital epilepsy of Gastaut: a study of seven patients, Cell Biochm Biophys, 67, 991, 10.1007/s12013-013-9594-8 Funata, 2018, Respiratory arrest at the onset of idiopathic childhood occipital epilepsy of Gastaut, Brain Dev, 40, 74, 10.1016/j.braindev.2017.06.009 Caraballo, 2009, Idiopathic childhood occipital epilepsy of Gastaut: a review and differentiation from migraine and other epilepsies, J Child Neurol, 24, 1536, 10.1177/0883073809332395 Verrotti, 2009, Levetiracetam monotherapy for childhood occipital epilepsy of Gastaut, Acta Neurol Scand, 120, 342, 10.1111/j.1600-0404.2009.01264.x Berg, 1999, Newly diagnosed epilepsy in children: presentation at diagnosis, Epilepsia, 40, 445, 10.1111/j.1528-1157.1999.tb00739.x Sadleir, 2006, Electroclinical features of absence seizures in childhood absence epilepsy, Neurology, 67, 413, 10.1212/01.wnl.0000228257.60184.82 Watemberg, 2015, Hyperventilation during routine electroencephalography: are three minutes really necessary?, Pediatr Neurol, 52, 410, 10.1016/j.pediatrneurol.2014.12.003 Dlugos, 2013, Childhood Absence Epilepsy S. Pretreatment EEG in childhood absence epilepsy associations with attention and treatment outcome, Neurology, 81, 150, 10.1212/WNL.0b013e31829a3373 Wirrell, 1996, Long-term prognosis of typical childhood absence epilepsy: remission or progression to juvenile myoclonic epilepsy, Neurology, 47, 912, 10.1212/WNL.47.4.912 Grosso, 2005, Childhood absence epilepsy: evolution and prognosis factors, Epilepsia, 46, 1796, 10.1111/j.1528-1167.2005.00277.x Callenbach, 2009, Long-term outcome of childhood absence epilepsy: Dutch study of epilepsy in childhood, Epilepsy Res, 83, 249, 10.1016/j.eplepsyres.2008.11.011 Shahar, 2007, Typical absence epilepsy presenting prior to age of 3 years: an uncommon form of idiopathic generalized epilepsy, Eur J Paediatr Neurol, 6, 346, 10.1016/j.ejpn.2007.02.015 Verrotti, 2015, Neuropsychological impairment in childhood absence epilepsy: review of the literature, J Neurol Sci, 359, 59, 10.1016/j.jns.2015.10.035 Caplan, 2008, Childhood absence epilepsy: behavioral, cognitive, and linguistic comorbidities, Epilepsia, 49, 1838, 10.1111/j.1528-1167.2008.01680.x Kernan, 2012, Neurocognitive profiles in children with epilepsy, Epilepsia, 53, 2156, 10.1111/j.1528-1167.2012.03706.x Masur, 2013, Pretreatment cognitive deficits and treatment effects on attention in childhood absence epilepsy, Neurology, 81, 1572, 10.1212/WNL.0b013e3182a9f3ca D’Agati, 2012, Attention and executive functions profile in childhood absence epilepsy, Brain Dev, 34, 812, 10.1016/j.braindev.2012.03.001 Glauser, 2013, Childhood Absence Epilepsy S. Ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy: Initial monotherapy outcomes at 12 months, Epilepsia, 54, 141, 10.1111/epi.12028 Siren, 2007, Beneficial effects of antiepileptic medication on absence seizures and cognitive functioning in children, Epilepsy Behav, 11, 85, 10.1016/j.yebeh.2007.04.009 Matricardi, 2014, Current advance in childhood absence epilepsy, Pediatr Neurol, 50, 205, 10.1016/j.pediatrneurol.2013.10.009 Verrotti, 2011, Long-term outcome in children affected by absence epilepsy with onset before the age of 3 years, Epilepsy Behav, 20, 366, 10.1016/j.yebeh.2010.12.015 Glauser, 2010, Childhood Absence Epilepsy S. Ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy, N Engl J Med, 362, 790, 10.1056/NEJMoa0902014 Berg, 2014, Long term seizure remission in childhood absence epilepsy: might initial treatment matter?, Epilepsia, 55, 551, 10.1111/epi.12551 Fattore, 2011, A multicenter, randomized, placebo-controlled trial of levetiracetam in children and adolescents with newly diagnosed absence epilepsy, Epilepsia, 52, 802, 10.1111/j.1528-1167.2010.02976.x Shinnar, 2015, Long-term outcomes of generalized tonic-clonic seizures in a childhood absence epilepsy trial, Neurology, 85, 1108, 10.1212/WNL.0000000000001971