| Lamotrigine and seizure aggravation in severe myoclonic epilepsy R Guerrini, C Dravet, P Genton, A Belmonte, A Kaminska, O Dulac Epilepsia 39 (5), 508-512, 1998 | 586 | 1998 |
| 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 | 536 | 2012 |
| Rapid cortical oscillations and early motor activity in premature human neonate M Milh, A Kaminska, C Huon, A Lapillonne, Y Ben-Ari, R Khazipov Cerebral cortex 17 (7), 1582-1594, 2007 | 320 | 2007 |
| A conserved switch in sensory processing prepares developing neocortex for vision MT Colonnese, A Kaminska, M Minlebaev, M Milh, B Bloem, S Lescure, ... Neuron 67 (3), 480-498, 2010 | 294 | 2010 |
| The three stages of epilepsy in patients with CDKL5 mutations N Bahi‐Buisson, A Kaminska, N Boddaert, M Rio, A Afenjar, M Gérard, ... Epilepsia 49 (6), 1027-1037, 2008 | 235 | 2008 |
| Genome search for susceptibility loci of common idiopathic generalised epilepsies T Sander, H Schulz, K Saar, E Gennaro, MC Riggio, A Bianchi, F Zara, ... Human molecular genetics 9 (10), 1465-1472, 2000 | 224 | 2000 |
| Delineation of cryptogenic Lennox–Gastaut syndrome and myoclonic astatic epilepsy using multiple correspondence analysis A Kaminska, A Ickowicz, P Plouin, MF Bru, G Dellatolas, O Dulac Epilepsy research 36 (1), 15-29, 1999 | 184 | 1999 |
| Mutations and deletions in PCDH19 account for various familial or isolated epilepsies in females C Depienne, O Trouillard, D Bouteiller, I Gourfinkel‐An, K Poirier, F Rivier, ... Human mutation 32 (1), E1959-E1975, 2011 | 165 | 2011 |
| Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations M Milh, N Villeneuve, M Chouchane, A Kaminska, C Laroche, MA Barthez, ... Epilepsia 52 (10), 1828-1834, 2011 | 160 | 2011 |
| 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 | 152 | 2017 |
| Mutations in the mitochondrial glutamate carrier SLC25A22 in neonatal epileptic encephalopathy with suppression bursts F Molinari, A Kaminska, G Fiermonte, N Boddaert, A Raas‐Rothschild, ... Clinical genetics 76 (2), 188-194, 2009 | 143 | 2009 |
| Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2 M Milh, N Boutry-Kryza, J Sutera-Sardo, C Mignot, S Auvin, C Lacoste, ... Orphanet journal of rare diseases 8, 1-8, 2013 | 116 | 2013 |
| Normal EEG in childhood: from neonates to adolescents M Eisermann, A Kaminska, ML Moutard, C Soufflet, P Plouin Neurophysiologie Clinique/Clinical Neurophysiology 43 (1), 35-65, 2013 | 110 | 2013 |
| Ictal SPECT in children with epilepsy: comparison with intracranial EEG and relation to postsurgical outcome A Kaminska, C Chiron, D Ville, G Dellatolas, A Hollo, C Cieuta, C Jalin, ... Brain 126 (1), 248-260, 2003 | 105 | 2003 |
| Mutations in the tricarboxylic acid cycle enzyme, aconitase 2, cause either isolated or syndromic optic neuropathy with encephalopathy and cerebellar atrophy MD Metodiev, S Gerber, L Hubert, A Delahodde, D Chretien, X Gérard, ... Journal of medical genetics 51 (12), 834-838, 2014 | 100 | 2014 |
| Early electro-clinical features may contribute to diagnosis of the anti-NMDA receptor encephalitis in children C Gitiaux, H Simonnet, M Eisermann, D Leunen, O Dulac, R Nabbout, ... Clinical Neurophysiology 124 (12), 2354-2361, 2013 | 98 | 2013 |
| Use of subtraction ictal SPECT co-registered to MRI for optimizing the localization of seizure foci in children P Véra, A Kaminska, C Cieuta, A Hollo, JL Stiévenart, I Gardin, D Ville, ... Journal of Nuclear Medicine 40 (5), 786-792, 1999 | 98 | 1999 |
| Epilepsy in Menkes disease: analysis of clinical stages N Bahi‐Buisson, A Kaminska, R Nabbout, C Barnerias, I Desguerre, ... Epilepsia 47 (2), 380-386, 2006 | 95 | 2006 |
| Cryptogenic late‐onset epileptic spasms: an overlooked syndrome of early childhood? MM Eisermann, D Ville, C Soufflet, P Plouin, C Chiron, O Dulac, ... Epilepsia 47 (6), 1035-1042, 2006 | 93 | 2006 |
| 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 2) M Koutroumanidis, A Arzimanoglou, R Caraballo, S Goyal, A Kaminska, ... Epileptic Disorders 19 (4), 385-437, 2017 | 89 | 2017 |
