| ILAE official report: a practical clinical definition of epilepsy RS Fisher, C Acevedo, A Arzimanoglou, A Bogacz, JH Cross, CE Elger, ... Epilepsia 55 (4), 475-482, 2014 | 7326 | 2014 |
| Definition of drug resistant epilepsy: consensus proposal by the ad hoc Task Force of the ILAE Commission on Therapeutic Strategies P Kwan, A Arzimanoglou, AT Berg, MJ Brodie, W Allen Hauser, G Mathern, ... Epilepsia 51 (6), 1069-1077, 2010 | 5469 | 2010 |
| Is the underlying cause of epilepsy a major prognostic factor for recurrence? F Semah, MC Picot, C Adam, D Broglin, A Arzimanoglou, B Bazin, ... Neurology 51 (5), 1256-1262, 1998 | 1410 | 1998 |
| Histopathological findings in brain tissue obtained during epilepsy surgery I Blumcke, R Spreafico, G Haaker, R Coras, K Kobow, CG Bien, M Pfäfflin, ... New England Journal of Medicine 377 (17), 1648-1656, 2017 | 876 | 2017 |
| Lennox-Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology A Arzimanoglou, J French, WT Blume, JH Cross, JP Ernst, M Feucht, ... The Lancet Neurology 8 (1), 82-93, 2009 | 579 | 2009 |
| GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction G Lesca, G Rudolf, N Bruneau, N Lozovaya, A Labalme, N Boutry-Kryza, ... Nature genetics 45 (9), 1061-1066, 2013 | 507 | 2013 |
| Treatment of pediatric epilepsy: European expert opinion, 2007 JW Wheless, DF Clarke, A Arzimanoglou, D Carpenter Epileptic disorders 9 (4), 353-412, 2007 | 470 | 2007 |
| De novo mutations in ATP1A3 cause alternating hemiplegia of childhood EL Heinzen, KJ Swoboda, Y Hitomi, F Gurrieri, S Nicole, B de Vries, ... Nature genetics 44 (9), 1030-1034, 2012 | 427 | 2012 |
| Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients C Depienne, O Trouillard, C Saint-Martin, I Gourfinkel-An, D Bouteiller, ... Journal of medical genetics 46 (3), 183-191, 2009 | 408 | 2009 |
| MECP2 mutations account for most cases of typical forms of Rett syndrome T Bienvenu, A Carrié, N De Roux, MC Vinet, P Jonveaux, P Couvert, ... Human molecular genetics 9 (9), 1377-1384, 2000 | 361 | 2000 |
| Key clinical features to identify girls with CDKL5 mutations N Bahi-Buisson, J Nectoux, H Rosas-Vargas, M Milh, N Boddaert, ... Brain 131 (10), 2647-2661, 2008 | 349 | 2008 |
| Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q FV Elmslie, M Rees, MP Williamson, M Kerr, MJ Kjeldsen, K An Pang, ... Human Molecular Genetics 6 (8), 1329-1334, 1997 | 342 | 1997 |
| Aicardi's epilepsy in children A Arzimanoglou, R Guerrini, J Aicardi (No Title), 2004 | 300 | 2004 |
| Nocturnal hypermotor seizures, suggesting frontal lobe epilepsy, can originate in the insula P Ryvlin, L Minotti, G Demarquay, E Hirsch, A Arzimanoglou, D Hoffman, ... Epilepsia 47 (4), 755-765, 2006 | 291 | 2006 |
| Vagus nerve stimulation for drug‐resistant epilepsy: a European long‐term study up to 24 months in 347 children I Orosz, D McCormick, N Zamponi, S Varadkar, M Feucht, D Parain, ... Epilepsia 55 (10), 1576-1584, 2014 | 272 | 2014 |
| Seizure outcome and use of antiepileptic drugs after epilepsy surgery according to histopathological diagnosis: a retrospective multicentre cohort study HJ Lamberink, WM Otte, I Blümcke, KPJ Braun, M Aichholzer, I Amorim, ... The Lancet Neurology 19 (9), 748-757, 2020 | 268 | 2020 |
| Distinct neurological disorders with ATP1A3 mutations EL Heinzen, A Arzimanoglou, A Brashear, SJ Clapcote, F Gurrieri, ... The Lancet Neurology 13 (5), 503-514, 2014 | 247 | 2014 |
| Hypothalamic hamartoma and seizures: a treatable epileptic encephalopathy SF Berkovic, A Arzimanoglou, R Kuzniecky, AS Harvey, A Palmini, ... Epilepsia 44 (7), 969-973, 2003 | 228 | 2003 |
| Epileptic encephalopathies of the Landau‐Kleffner and continuous spike and waves during slow‐wave sleep types: Genomic dissection makes the link with autism G Lesca, G Rudolf, A Labalme, E Hirsch, A Arzimanoglou, P Genton, ... Epilepsia 53 (9), 1526-1538, 2012 | 205 | 2012 |
| Expert opinion on the management of Lennox–Gastaut syndrome: treatment algorithms and practical considerations JH Cross, S Auvin, M Falip, P Striano, A Arzimanoglou Frontiers in neurology 8, 505, 2017 | 199 | 2017 |
Jacqueline FrenchProfessor of Neurology, NYUAdresse e-mail validée de nyumc.org