15q13. 3 microdeletions increase risk of idiopathic generalized epilepsy I Helbig, HC Mefford, AJ Sharp, M Guipponi, M Fichera, A Franke, ... Nature genetics 41 (2), 160-162, 2009 | 681 | 2009 |
Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies HC Mefford, H Muhle, P Ostertag, S von Spiczak, K Buysse, C Baker, ... PLoS genetics 6 (5), e1000962, 2010 | 521 | 2010 |
'De novo'absence status of late onset: Report of 11 cases P Thomas, A Beaumanoir, P Genton, C Dolisi, M Chatel Neurology 42 (1), 104-104, 1992 | 300 | 1992 |
Absence and myoclonic status epilepticus precipitated by antiepileptic drugs in idiopathic generalized epilepsy P Thomas, L Valton, P Genton Brain 129 (5), 1281-1292, 2006 | 295 | 2006 |
Mutations of DEPDC5 cause autosomal dominant focal epilepsies S Ishida, F Picard, G Rudolf, E Noé, G Achaz, P Thomas, P Genton, ... Nature genetics 45 (5), 552-555, 2013 | 274 | 2013 |
Do carbamazepine and phenytoin aggravate juvenile myoclonic epilepsy? P Genton, P Gelisse, P Thomas, C Dravet Neurology 55 (8), 1106-1109, 2000 | 262 | 2000 |
Clinical factors of drug resistance in juvenile myoclonic epilepsy P Gelisse, P Genton, P Thomas, M Rey, JC Samuelian, C Dravet Journal of Neurology, Neurosurgery & Psychiatry 70 (2), 240-243, 2001 | 237 | 2001 |
Fear as the main feature of epileptic seizures A Biraben, D Taussig, P Thomas, C Even, JP Vignal, JM Scarabin, ... Journal of Neurology, Neurosurgery & Psychiatry 70 (2), 186-191, 2001 | 216 | 2001 |
Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome VL Sheen, A Jansen, MH Chen, E Parrini, T Morgan, R Ravenscroft, ... Neurology 64 (2), 254-262, 2005 | 211 | 2005 |
Epileptic syndromes in infancy, childhood and adolescence B Michelle, G Pierre, D Charlotte John Libbey Eurotext, 2012 | 204 | 2012 |
Consensus on diagnosis and management of JME: from founder's observations to current trends DGAKN Trenité, B Schmitz, D Janz, AV Delgado-Escueta, P Thomas, ... Epilepsy & Behavior 28, S87-S90, 2013 | 189 | 2013 |
The role of EEG in the diagnosis and classification of the epilepsy syndromes: a tool for clinical practice by the ILAE Neurophysiology Task Force (Part 1) M Koutroumanidis, A Arzimanoglou, R Caraballo, S Goyal, A Kaminska, ... Epileptic Disorders 19 (3), 233-298, 2017 | 188 | 2017 |
Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasia S Weckhuysen, E Marsan, V Lambrecq, C Marchal, M Morin‐Brureau, ... Epilepsia 57 (6), 994-1003, 2016 | 184 | 2016 |
Nonconvulsive status epilepticus of frontal origin P Thomas, B Zifkin, O Migneco, C Lebrun, J Darcourt, F Andermann Neurology 52 (6), 1174-1174, 1999 | 172 | 1999 |
Cortical myoclonus in Angelman syndrome R Guerrini, P Bonanni, TM de Lorey, JM Serratosa, A Moncla, P Malzac, ... Annals of Neurology: Official Journal of the American Neurological …, 1996 | 170 | 1996 |
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16. 1, 2q22. 3 and 17q21. 32 Epicure Consortium, EMINet Consortium, M Steffens, C Leu, AK Ruppert, ... Human molecular genetics 21 (24), 5359-5372, 2012 | 155 | 2012 |
Epilepsy with myoclonic absences CA Tassinari, M Bureau, P Thomas Epileptic syndromes in infancy, childhood and adolescence 2, 151-160, 1992 | 133 | 1992 |
Juvenile myoclonic epilepsy P Thomas Epileptic syndromes in infancy, childhood and adolescence, 2005 | 130 | 2005 |
Successful treatment of refractory generalized myasthenia gravis with rituximab C Lebrun, V Bourg, N Tieulie, P Thomas European journal of neurology 16 (2), 246-250, 2009 | 126 | 2009 |
Nitroso-urea–cisplatin-based chemotherapy associated with valproate: Increase of haematologic toxicity V Bourg, C Lebrun, RM Chichmanian, P Thomas, M Frenay Annals of oncology 12 (2), 217-220, 2001 | 124 | 2001 |