| LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy C Nobile, R Michelucci, S Andreazza, E Pasini, SCE Tosatto, P Striano Human mutation 30 (4), 530-536, 2009 | 172 | 2009 |
| Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy E Dazzo, M Fanciulli, E Serioli, G Minervini, P Pulitano, S Binelli, ... The American Journal of Human Genetics 96 (6), 992-1000, 2015 | 144 | 2015 |
| 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 |
| Lateral temporal lobe epilepsies: clinical and genetic features R Michelucci, E Pasini, C Nobile Epilepsia 50, 52-54, 2009 | 90 | 2009 |
| Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K+ channel properties KL Oliver, S Franceschetti, CJ Milligan, M Muona, SA Mandelstam, ... Annals of neurology 81 (5), 677-689, 2017 | 82 | 2017 |
| The prognostic roles of gender and O6-methylguanine-DNA methyltransferase methylation status in glioblastoma patients: the female power E Franceschi, A Tosoni, S Minichillo, R Depenni, A Paccapelo, S Bartolini, ... World neurosurgery 112, e342-e347, 2018 | 57 | 2018 |
| Myoclonus and seizures in progressive myoclonus epilepsies: pharmacology and therapeutic trials R Michelucci, E Pasini, P Riguzzi, E Andermann, R Kälviäinen, P Genton Epileptic Disorders 18 (s2), S145-S153, 2016 | 56 | 2016 |
| Epilepsy in primary cerebral tumors: The characteristics of epilepsy at the onset (results from the PERNO study–P roject of E milia R omagna R egion on N euro‐O ncology) R Michelucci, E Pasini, S Meletti, E Fallica, R Rizzi, I Florindo, A Chiari, ... Epilepsia 54, 86-91, 2013 | 55 | 2013 |
| Mild L afora disease: clinical, neurophysiologic, and genetic findings E Ferlazzo, L Canafoglia, R Michelucci, A Gambardella, E Gennaro, ... Epilepsia 55 (12), e129-e133, 2014 | 53 | 2014 |
| Aerosol drug delivery to spontaneously-breathing preterm neonates: lessons learned F Bianco, F Salomone, I Milesi, X Murgia, S Bonelli, E Pasini, R Dellacà, ... Respiratory Research 22, 1-31, 2021 | 52 | 2021 |
| From bench to bedside: in vitro and in vivo evaluation of a neonate-focused nebulized surfactant delivery strategy F Bianco, F Ricci, C Catozzi, X Murgia, M Schlun, A Bucholski, U Hetzer, ... Respiratory research 20, 1-11, 2019 | 52 | 2019 |
| EEG findings in COVID-19 related encephalopathy E Pasini, F Bisulli, L Volpi, I Minardi, M Tappatà, L Muccioli, U Pensato, ... Clinical Neurophysiology 131 (9), 2265, 2020 | 50 | 2020 |
| Intravenous immunoglobulin therapy in COVID-19-related encephalopathy L Muccioli, U Pensato, G Bernabè, L Ferri, M Tappatà, L Volpi, I Cani, ... Journal of neurology 268, 2671-2675, 2021 | 49 | 2021 |
| The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations R Michelucci, P Pulitano, C Di Bonaventura, S Binelli, C Luisi, E Pasini, ... Epilepsy & Behavior 68, 103-107, 2017 | 49 | 2017 |
| DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy P Striano, E Serioli, L Santulli, I Manna, A Labate, E Dazzo, E Pasini, ... Epilepsia 56 (10), e168-e171, 2015 | 48 | 2015 |
| Pattern of care and effectiveness of treatment for glioblastoma patients in the real world: Results from a prospective population-based registry. Could survival differ in a … AA Brandes, E Franceschi, M Ermani, A Tosoni, F Albani, R Depenni, ... Neuro-oncology practice 1 (4), 166-171, 2014 | 46 | 2014 |
| Multiple variants in families with amyotrophic lateral sclerosis and frontotemporal dementia related to C9orf72 repeat expansion: further observations on their … MP Giannoccaro, A Bartoletti-Stella, S Piras, A Pession, P De Massis, ... Journal of neurology 264, 1426-1433, 2017 | 45 | 2017 |
| Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1 G Rubboli, P Veggiotti, A Pini, A Berardinelli, G Cantalupo, E Bertini, ... Epilepsia 56 (5), 692-698, 2015 | 45 | 2015 |
| Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations R Michelucci, E Pasini, S Malacrida, P Striano, CD Bonaventura, ... Epilepsia 54 (7), 1288-1297, 2013 | 43 | 2013 |
| Genetics of epilepsy and relevance to current practice R Michelucci, E Pasini, P Riguzzi, L Volpi, E Dazzo, C Nobile Current neurology and neuroscience reports 12, 445-455, 2012 | 35 | 2012 |
