Benign Epilepsy in Children

Capovilla, 2009, Workshop report: conceptual dichotomies in classifying epilepsies: partial versus generalized and idiopathic versus symptomatic, Epilepsia, 50, 1648 Willmore, 2001, Treatment of benign epilepsy syndromes throughout life, Epilepsia, 42, 6, 10.1046/j.1528-1157.2001.0420s8006.x Fukuyama, 1963, Borderland of epilepsy with special reference with special reference to febrile convulsions and so-called infantile convulsion, Seishin Igaku (Clin Psychiatry), 5, 211 IY, 2010, Benign familial and non-familial infantile seizures (Fukuyama-Watanabe- Vigevano syndrome): a study of 14 cases from Saudi Arabia, Brain Dev, 32, 378, 10.1016/j.braindev.2009.04.014 Espeche, 2010, Benign infantile seizures: a prospective study, Epilepsy Res, 89, 96, 10.1016/j.eplepsyres.2009.10.017 Xiao, 2005, Clinical and genetic study on a new Chinese family with benign familial infantile seizures, Eur J Neurol, 12, 344, 10.1111/j.1468-1331.2004.00989.x Striano, 2006, A novel SCN2A mutation in family with benign familial infantile seizures, Epilepsia, 47, 218, 10.1111/j.1528-1167.2006.00392.x Weber, 2008, A BFIS-like syndrome with late onset and febrile seizures: suggestive linkage to chromosome 16p11.2-16q12.1, Epilepsia, 49, 1959, 10.1111/j.1528-1167.2008.01646.x Herlenius, 2007, SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrum, Epilepsia, 48, 1138, 10.1111/j.1528-1167.2007.01049.x Panayiotoupoulos, 2005, 296 Valentin, 2007, Idiopathic generalized epilepsy with absences: syndrome classification, Epilepsia, 48, 2187, 10.1111/j.1528-1167.2007.01226.x Rubboli, 2009, Idiopathic generalized epilepsy (IGE) syndromes in development: IGE with absences of early childhood, IGE with phantom absences, and perioral myoclonia with absences, Epilepsia, 50, 24, 10.1111/j.1528-1167.2009.02116.x Caplan, 2008, Childhood absence epilepsy: behavioral, cognitive, and linguistic co morbidities, Epilepsia, 49, 1838, 10.1111/j.1528-1167.2008.01680.x Caplan, 2009, Language in pediatric epilepsy, Epilepsia, 50, 2397, 10.1111/j.1528-1167.2009.02199.x Duncan, 2005, Brain imaging in idiopathic generalized epilepsies, Epilepsia, 46, 108, 10.1111/j.1528-1167.2005.00321.x Caplan, 2009, Frontal and temporal volumes in childhood absence epilepsy, Epilepsia, 50, 2466, 10.1111/j.1528-1167.2009.02198.x Moeller, 2008, Simultaneous EEG-fMRI in drug-naive children with newly diagnosed absence epilepsy, Epilepsia, 49, 1510, 10.1111/j.1528-1167.2008.01626.x Penovich, 2009, Use of a new antiepileptic drug or an old one as first drug for treatment of absence epilepsy, Epilepsia, 50, 37, 10.1111/j.1528-1167.2009.02234.x Coppola, 2004, Lamotrigine versus valproic acid as first-line monotherapy in newly diagnosed typical absence seizures: an open-label, randomized, parallel-group study, Epilepsia, 45, 1049, 10.1111/j.0013-9580.2004.40903.x Noachtar, 2008, Levetiracetam for the treatment of idiopathic generalized epilepsy with myoclonic seizures, Neurology, 70, 607, 10.1212/01.wnl.0000297512.18364.40 Cross, 2002, Topiramate monotherapy for childhood absence seizures: an open label pilot study, Seizure, 11, 406, 10.1053/seiz.2001.0655 Savic, 2000, MR spectroscopy shows reduced frontal lobe concentrations of N-acetyl aspartate in patients with juvenile myoclonic epilepsy, Epilepsia, 41, 290, 10.1111/j.1528-1157.2000.tb00158.x Lin, 2009, Magnetic resonance spectroscopy reveals an epileptic network in juvenile myoclonic epilepsy, Epilepsia, 50, 1191, 10.1111/j.1528-1167.2008.01948.x Piazzini, 2007, Frontal cognitive dysfunction in juvenile myoclonic epilepsy, Epilepsia, 49, 657, 10.1111/j.1528-1167.2007.01482.x Betting, 2006, Voxel-based morphometry in patients with idiopathic generalized epilepsies, NeuroImage, 32, 498, 10.1016/j.neuroimage.2006.04.174 Pascalicchio, 2007, Neuropsychological profile of patients with juvenile myoclonic epilepsy: a controlled study of 50 patients, Epilepsy Behav, 10, 263, 10.1016/j.yebeh.2006.11.012 Swartz, 1996, Visual working memory in primary generalized epilepsy: an 18FDG-PET study, Neurology, 47, 1203, 10.1212/WNL.47.5.1203 Roebling, 2009, Evaluation of cognition, structural, and functional MRI in juvenile myoclonic epilepsy, Epilepsia, 50, 2456, 10.1111/j.1528-1167.2009.02127.x Panayiotopoulos, 2008, Benign childhood focal epilepsies: assessment of established and newly recognized syndromes, Brain, 131, 2264, 10.1093/brain/awn162 Shields, 2009, Benign epilepsy with centrotemporal spikes, Epilepsia, 50, 10, 10.1111/j.1528-1167.2009.02229.x Fejerman, 2009, Atypical rolandic epilepsy, Epilepsia, 50, 9, 10.1111/j.1528-1167.2009.02210.x Bourgeois, 2000, Drug treatment of benign focal epilepsies of childhood, Epilepsia, 41, 1057, 10.1111/j.1528-1157.2000.tb00297.x Ambrosetto, 1990, Antiepileptic drug treatment of benign childhood epilepsy with rolandic spikes: is it necessary?, Epilepsia, 31, 802, 10.1111/j.1528-1157.1990.tb05522.x Ambrosetto, 1987, Predictive factors of seizure frequency and duration of antiepileptic treatment in rolandic epilepsy: a retrospective study, Brain Dev, 9, 300, 10.1016/S0387-7604(87)80049-9 Bouma, 1997, The course of benign partial epilepsy of childhood with centrotemporal spikes: a meta-analysis, Neurology, 48, 430, 10.1212/WNL.48.2.430 Kossoff, 2007, A pilot study transitioning children onto levetiracetam monotherapy to improve language dysfunction associated with benign rolandic epilepsy, Epilepsy Behav, 11, 514, 10.1016/j.yebeh.2007.07.011 Bali, 2007, Autosomal dominant inheritance of centrotemporal sharp waves in rolandic epilepsy families, Epilepsia, 48, 2266 Kugler, 2008, An autosomal dominant genetically heterogeneous variant of rolandic epilepsy and speech disorder, Epilepsia, 49, 1086, 10.1111/j.1528-1167.2007.01517.x Vadlamudi, 2006, Analyzing the etiology of benign rolandic epilepsy: a multicenter twin collaboration, Epilepsia, 47, 550, 10.1111/j.1528-1167.2006.00466.x Neubauer, 1998, Centrotemporal spikes with rolandic epilepsy: linkage to chromosome 15q14, Neurology, 51, 1608, 10.1212/WNL.51.6.1608 Strug, 2009, Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4), Eur J Hum Genet, 17, 1171, 10.1038/ejhg.2008.267 Roll, 2006, SRPX2 mutations in disorders of language cortex and cognition, Hum Mol Genet, 15, 1195, 10.1093/hmg/ddl035 B, 2008, Epileptic and developmental disorders of the speech cortex: ligand/receptor interaction of wild-type and mutant SRPX2 with the plasminogen activator receptor uPAR, Hum Mol Genet, 17, 3617, 10.1093/hmg/ddn256 Rudolf, 2009, From rolandic epilepsy to continuous spike-and-waves during sleep and Landau-Kleffner syndromes: insights into possible genetic factors, Epilepsia, 50, 25, 10.1111/j.1528-1167.2009.02214.x Riva, 2007, Intellectual and language findings and their relationship to EEG characteristics in benign childhood epilepsy with centrotemporal spikes, Epilepsy Behav, 10, 278, 10.1016/j.yebeh.2006.12.003 Kavros, 2008, Attention impairment in rolandic epilepsy: systematic review, Epilepsia, 49, 1570, 10.1111/j.1528-1167.2008.01610.x Clarke, 2007, High risk of reading disability and speech sound disorder in rolandic epilepsy families: case-control study, Epilepsia, 48, 2258 Baglietto, 2001, Neuropsychological disorders related to interictal epileptic discharges during sleep in benign epilepsy of childhood with centrotemporal or Rolandic spikes, Dev Med Child Neurol, 43, 407, 10.1017/S0012162201000755 Wolff, 2005, Benign partial epilepsy in childhood: selective cognitive deficits are related to the location of focal spikes determined by combined EEG/MEG, Epilepsia, 46, 1661, 10.1111/j.1528-1167.2005.00255.x Deonna, 1993, Speech and oromotor deficits of epileptic origin in benign partial epilepsy of childhood with rolandic spikes (BPERS). Relationship to the acquired aphasia epilepsy syndrome, Neuropediatrics, 24, 83, 10.1055/s-2008-1071519 Monjauze, 2005, Language in benign childhood epilepsy with centro-temporal spikes abbreviated form: rolandic epilepsy and language, Brain Lang, 92, 300, 10.1016/j.bandl.2004.07.001 Lillywhite, 2009, Neuropsychological and functional MRI studies provide converging evidence of anterior language dysfunction in BECTS, Epilepsia, 50, 2276, 10.1111/j.1528-1167.2009.02065.x Boatman, 2008, Cortical auditory dysfunction in benign rolandic epilepsy, Epilepsia, 49, 1018, 10.1111/j.1528-1167.2007.01519.x J, 2006, Report of the ILAE classification core group, Epilepsia, 47, 1558, 10.1111/j.1528-1167.2006.00215.x Panayiotopoulos, 2007, The birth and evolution of the concept of Panayiotopoulos syndrome, Epilepsia, 48, 1041, 10.1111/j.1528-1167.2006.01092.x Capovilla, 2009, Changes in Panayiotopoulos syndrome over time, Epilepsia, 50, 45, 10.1111/j.1528-1167.2009.02120.x Koutroumanidis, 2007, Panayiotopoulos syndrome: an important electroclinical example of benign childhood system epilepsy, Epilepsia, 48, 1044, 10.1111/j.1528-1167.2007.01096.x Taylor, 2008, Benign occipital epilepsies of childhood: clinical features and genetics, Brain, 131, 2287, 10.1093/brain/awn138 Ferrie, 2007, Autonomic status epilepticus in Panayiotopoulos syndrome and other childhood and adult epilepsies: a consensus view, Epilepsia, 48, 1165, 10.1111/j.1528-1167.2007.01087.x Caraballo, 2007, Panayiotopoulos syndrome: a prospective study of 192 patients, Epilepsia, 48, 1054, 10.1111/j.1528-1167.2007.01085.x T, 2008, Panayiotopoulos syndrome: epidemiological and clinical characteristics and outcome, Eur J Neurol, 15, 336, 10.1111/j.1468-1331.2008.02074.x Du, 2007, Clinical analysis of childhood occipital lobe epilepsy in 43 Taiwanese patients, Pediatr Neurol, 36, 387, 10.1016/j.pediatrneurol.2007.02.004 Schuele, 2008, Ictal asystole: a benign condition?, Epilepsia, 49, 168, 10.1111/j.1528-1167.2007.01330.x Covanis, 2006, Panayiotopoulos syndrome: a benign childhood autonomic epilepsy frequently imitating encephalitis, syncope, migraine, sleep disorder, or gastroenteritis, Pediatrics, 118, e1237, 10.1542/peds.2006-0623 Yoshinaga, 2006, EEG dipole characteristics in Panayiotopoulos syndrome, Epilepsia, 47, 781, 10.1111/j.1528-1167.2006.00519.x Hirano, 2009, Neurobehavioral abnormalities may correlate with increased seizure burden in children with Panayiotopoulos syndrome, Pediatr Neurol, 40, 443, 10.1016/j.pediatrneurol.2008.12.005 Ferrie, 2006, Panayiotopoulos syndrome: a consensus view, Dev Med Child Neurol, 48, 236, 10.1017/S0012162206000508 Gastaut, 1982, A new type of epilepsy: benign partial epilepsy of childhood with occipital spike-waves, Clin Electroencephalogr, 13, 13, 10.1177/155005948201300102 Carabello, 2008, Childhood occipital epilepsy of Gastaut: a study of 33 patients, Epilepsia, 49, 288, 10.1111/j.1528-1167.2007.01322.x Verrotti, 2009, Levetiracetam monotherapy for childhood occipital epilepsy of Gastaut, Acta Neurol Scand, 120, 342, 10.1111/j.1600-0404.2009.01264.x