Mutations in DEPDC5 cause familial focal epilepsy with variable foci LM Dibbens, B De Vries, S Donatello, SE Heron, BL Hodgson, ... Nature genetics 45 (5), 546-551, 2013 | 389 | 2013 |
Determinants of health‐related quality of life in pharmacoresistant epilepsy: results from a large multicenter study of consecutively enrolled patients using validated … C Luoni, F Bisulli, MP Canevini, G De Sarro, C Fattore, CA Galimberti, ... Epilepsia 52 (12), 2181-2191, 2011 | 311 | 2011 |
Definition and diagnostic criteria of sleep-related hypermotor epilepsy P Tinuper, F Bisulli, JH Cross, D Hesdorffer, P Kahane, L Nobili, F Provini, ... Neurology 86 (19), 1834-1842, 2016 | 309 | 2016 |
Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations IE Scheffer, SE Heron, BM Regan, S Mandelstam, DE Crompton, ... Annals of neurology 75 (5), 782-787, 2014 | 264 | 2014 |
Ictal bradycardia in partial epileptic seizures: autonomic investigation in three cases and literature review P Tinuper, F Bisulli, A Cerullo, R Carcangiu, C Marini, G Pierangeli, ... Brain 124 (12), 2361-2371, 2001 | 251 | 2001 |
Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals YCA Feng, DP Howrigan, LE Abbott, K Tashman, F Cerrato, T Singh, ... The American Journal of Human Genetics 105 (2), 267-282, 2019 | 248 | 2019 |
Movement disorders in sleep: guidelines for differentiating epileptic from non-epileptic motor phenomena arising from sleep P Tinuper, F Provini, F Bisulli, L Vignatelli, G Plazzi, R Vetrugno, ... Sleep medicine reviews 11 (4), 255-267, 2007 | 223 | 2007 |
Mutations in the mammalian target of rapamycin pathway regulators NPRL2 and NPRL3 cause focal epilepsy MG Ricos, BL Hodgson, T Pippucci, A Saidin, YS Ong, SE Heron, ... Annals of neurology 79 (1), 120-131, 2016 | 218 | 2016 |
The landscape of epilepsy-related GATOR1 variants S Baldassari, F Picard, NE Verbeek, M van Kempen, EH Brilstra, G Lesca, ... Genetics in Medicine 21 (2), 398-408, 2019 | 203 | 2019 |
Autosomal dominant lateral temporal epilepsy: clinical spectrum, new epitempin mutations, and genetic heterogeneity in seven European families R Michelucci, JJ Poza, V Sofia, MR Feo, S Binelli, F Bisulli, E Scudellaro, ... Epilepsia 44 (10), 1289-1297, 2003 | 181 | 2003 |
Increased frequency of arousal parasomnias in families with nocturnal frontal lobe epilepsy: a common mechanism? F Bisulli, L Vignatelli, I Naldi, L Licchetta, F Provini, G Plazzi, L Di Vito, ... Epilepsia 51 (9), 1852-1860, 2010 | 147 | 2010 |
Non-paraneoplastic limbic encephalitis associated with anti-glutamic acid decarboxylase antibodies S Matà, GC Muscas, I Naldi, E Rosati, S Paladini, B Cruciatti, F Bisulli, ... Journal of neuroimmunology 199 (1-2), 155-159, 2008 | 139 | 2008 |
Seizure outcome of epilepsy surgery in focal epilepsies associated with temporomesial glioneuronal tumors: lesionectomy compared with tailored resection M Giulioni, G Rubboli, G Marucci, M Martinoni, L Volpi, R Michelucci, ... Journal of neurosurgery 111 (6), 1275-1282, 2009 | 129 | 2009 |
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2 MA Corbett, T Kroes, L Veneziano, MF Bennett, R Florian, AL Schneider, ... Nature communications 10 (1), 4920, 2019 | 127 | 2019 |
Expression of 19 microRNAs in glioblastoma and comparison with other brain neoplasia of grades I–III M Visani, D De Biase, G Marucci, S Cerasoli, E Nigrisoli, MLB Reggiani, ... Molecular oncology 8 (2), 417-430, 2014 | 118 | 2014 |
Epilepsy associated tumors M Giulioni, G Marucci, M Martinoni, AF Marliani, F Toni, F Bartiromo, ... World Journal of Clinical Cases: WJCC 2 (11), 623, 2014 | 108 | 2014 |
Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic cases F Bisulli, P Tinuper, P Avoni, P Striano, S Striano, G d’Orsi, L Vignatelli, ... Brain 127 (6), 1343-1352, 2004 | 99 | 2004 |
Nocturnal frontal lobe epilepsy L Nobili, P Proserpio, R Combi, F Provini, G Plazzi, F Bisulli, L Tassi, ... Current neurology and neuroscience reports 14, 1-11, 2014 | 94 | 2014 |
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study P May, S Girard, M Harrer, DR Bobbili, J Schubert, S Wolking, F Becker, ... The Lancet Neurology 17 (8), 699-708, 2018 | 92 | 2018 |
Videopolygraphic and functional MRI study of musicogenic epilepsy. A case report and literature review F Pittau, P Tinuper, F Bisulli, I Naldi, P Cortelli, A Bisulli, C Stipa, ... Epilepsy & Behavior 13 (4), 685-692, 2008 | 90 | 2008 |