| Trial of cannabidiol for drug-resistant seizures in the Dravet syndrome O Devinsky, JH Cross, L Laux, E Marsh, I Miller, R Nabbout, IE Scheffer, ... New England Journal of Medicine 376 (21), 2011-2020, 2017 | 1654 | 2017 |
| Tuberous sclerosis complex diagnostic criteria update: recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference H Northrup, DA Krueger, S Roberds, K Smith, J Sampson, B Korf, ... Pediatric neurology 49 (4), 243-254, 2013 | 1579 | 2013 |
| Tuberous sclerosis complex surveillance and management: recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference DA Krueger, H Northrup, S Roberds, K Smith, J Sampson, B Korf, ... Pediatric neurology 49 (4), 255-265, 2013 | 889 | 2013 |
| Adjunctive everolimus therapy for treatment-resistant focal-onset seizures associated with tuberous sclerosis (EXIST-3): a phase 3, randomised, double-blind, placebo-controlled … JA French, JA Lawson, Z Yapici, H Ikeda, T Polster, R Nabbout, ... The Lancet 388 (10056), 2153-2163, 2016 | 661 | 2016 |
| The right brain hemisphere is dominant in human infants. C Chiron, I Jambaque, R Nabbout, R Lounes, A Syrota, O Dulac Brain: a journal of neurology 120 (6), 1057-1065, 1997 | 610 | 1997 |
| Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1 YJ Crow, DS Chase, J Lowenstein Schmidt, M Szynkiewicz, GMA Forte, ... American journal of medical genetics Part A 167 (2), 296-312, 2015 | 559 | 2015 |
| De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy G Barcia, MR Fleming, A Deligniere, VR Gazula, MR Brown, M Langouet, ... Nature genetics 44 (11), 1255-1259, 2012 | 500 | 2012 |
| Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females C Depienne, D Bouteiller, B Keren, E Cheuret, K Poirier, O Trouillard, ... PLoS genetics 5 (2), e1000381, 2009 | 445 | 2009 |
| 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 | 394 | 2009 |
| Proposed consensus definitions for new‐onset refractory status epilepticus (NORSE), febrile infection‐related epilepsy syndrome (FIRES), and related conditions LJ Hirsch, N Gaspard, A van Baalen, R Nabbout, S Demeret, ... Epilepsia 59 (4), 739-744, 2018 | 380 | 2018 |
| Efficacy of ketogenic diet in severe refractory status epilepticus initiating fever induced refractory epileptic encephalopathy in school age children (FIRES) R Nabbout, M Mazzuca, P Hubert, S Peudennier, C Allaire, V Flurin, ... Epilepsia 51 (10), 2033-2037, 2010 | 371 | 2010 |
| International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood: Position paper by the ILAE Task Force on Nosology and Definitions N Specchio, EC Wirrell, IE Scheffer, R Nabbout, K Riney, P Samia, ... Epilepsia 63 (6), 1398-1442, 2022 | 347 | 2022 |
| Febrile infection–related epilepsy syndrome (FIRES): pathogenesis, treatment, and outcome: a multicenter study on 77 children U Kramer, CS Chi, KL Lin, N Specchio, M Sahin, H Olson, R Nabbout, ... Epilepsia 52 (11), 1956-1965, 2011 | 345 | 2011 |
| Reviews of evidence regarding interventions to reduce tobacco use and exposure to environmental tobacco smoke DP Hopkins, PA Briss, CJ Ricard, CG Husten, VG Carande-Kulis, ... American journal of preventive medicine 20 (2), 16-66, 2001 | 335 | 2001 |
| ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and Definitions SM Zuberi, E Wirrell, E Yozawitz, JM Wilmshurst, N Specchio, K Riney, ... Epilepsia 63 (6), 1349-1397, 2022 | 334 | 2022 |
| Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy R Nabbout, E Gennaro, B Dalla Bernardina, O Dulac, F Madia, E Bertini, ... Neurology 60 (12), 1961-1967, 2003 | 326 | 2003 |
| Updated international tuberous sclerosis complex diagnostic criteria and surveillance and management recommendations H Northrup, ME Aronow, EM Bebin, J Bissler, TN Darling, PJ de Vries, ... Pediatric Neurology 123, 50-66, 2021 | 308 | 2021 |
| Mutations in the neuronal β-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defects K Poirier, Y Saillour, N Bahi-Buisson, XH Jaglin, C Fallet-Bianco, ... Human molecular genetics 19 (22), 4462-4473, 2010 | 292 | 2010 |
| Fever, genes, and epilepsy S Baulac, I Gourfinkel-An, R Nabbout, G Huberfeld, J Serratosa, ... The lancet neurology 3 (7), 421-430, 2004 | 288 | 2004 |
| Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency) PB Mills, EJ Footitt, KA Mills, K Tuschl, S Aylett, S Varadkar, C Hemingway, ... Brain 133 (7), 2148-2159, 2010 | 281 | 2010 |
