| The CDKL5 disorder is an independent clinical entity associated with early-onset encephalopathy S Fehr, M Wilson, J Downs, S Williams, A Murgia, S Sartori, M Vecchi, ... European Journal of Human Genetics 21 (3), 266-273, 2013 | 301 | 2013 |
| Antibiotic treatment for pyelonephritis in children: multicentre randomised controlled non-inferiority trial G Montini, A Toffolo, P Zucchetta, R Dall'Amico, D Gobber, A Calderan, ... Bmj 335 (7616), 386, 2007 | 264 | 2007 |
| Herpes simplex virus‐induced anti‐N‐methyl‐d‐aspartate receptor encephalitis: a systematic literature review with analysis of 43 cases M Nosadini, SS Mohammad, F Corazza, EM Ruga, K Kothur, G Perilongo, ... Developmental Medicine & Child Neurology 59 (8), 796-805, 2017 | 170 | 2017 |
| Comorbidity between headache and epilepsy in a pediatric headache center I Toldo, E Perissinotto, F Menegazzo, C Boniver, S Sartori, L Salviati, ... The journal of headache and pain 11, 235-240, 2010 | 111 | 2010 |
| Early-onset seizure variant of Rett syndrome: definition of the clinical diagnostic criteria R Artuso, MA Mencarelli, R Polli, S Sartori, F Ariani, M Pollazzon, ... Brain and Development 32 (1), 17-24, 2010 | 110 | 2010 |
| Use and safety of immunotherapeutic management of N-methyl-d-aspartate receptor antibody encephalitis: a meta-analysis M Nosadini, M Eyre, E Molteni, T Thomas, SR Irani, J Dalmau, RC Dale, ... JAMA neurology 78 (11), 1333-1344, 2021 | 105 | 2021 |
| Treatment of convulsive status epilepticus in childhood: Recommendations of the I talian L eague A gainst E pilepsy G Capovilla, F Beccaria, E Beghi, F Minicucci, S Sartori, M Vecchi Epilepsia 54, 23-34, 2013 | 104 | 2013 |
| Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications KM Johannesen, Y Liu, M Koko, CE Gjerulfsen, L Sonnenberg, J Schubert, ... Brain 145 (9), 2991-3009, 2022 | 84 | 2022 |
| Plasma exchange in pediatric anti-NMDAR encephalitis: a systematic review A Suppiej, M Nosadini, L Zuliani, MF Pelizza, I Toldo, C Bertossi, T Tison, ... Brain and Development 38 (7), 613-622, 2016 | 84 | 2016 |
| Management of antibody-mediated autoimmune encephalitis in adults and children: literature review and consensus-based practical recommendations L Zuliani, M Nosadini, M Gastaldi, M Spatola, R Iorio, M Zoccarato, ... Neurological Sciences 40, 2017-2030, 2019 | 70 | 2019 |
| Paediatric anti-N-methyl-D-aspartate receptor encephalitis: the first Italian multicenter case series S Sartori, M Nosadini, E Cesaroni, R Falsaperla, G Capovilla, F Beccaria, ... European Journal of Paediatric Neurology 19 (4), 453-463, 2015 | 69 | 2015 |
| Characterization of intellectual disability and autism comorbidity through gene panel sequencing MC Aspromonte, M Bellini, A Gasparini, M Carraro, E Bettella, R Polli, ... Human mutation 40 (9), 1346-1363, 2019 | 68 | 2019 |
| Pontocerebellar hypoplasia: clinical, pathologic, and genetic studies D Cassandrini, R Biancheri, A Tessa, M Di Rocco, M Di Capua, C Bruno, ... Neurology 75 (16), 1459-1464, 2010 | 68 | 2010 |
| Long-term neurocognitive outcome and quality of life in pediatric acute disseminated encephalomyelitis A Suppiej, E Cainelli, G Casara, A Cappellari, M Nosadini, S Sartori Pediatric Neurology 50 (4), 363-367, 2014 | 63 | 2014 |
| Intrathecal synthesis of oligoclonal bands in rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation syndrome: new evidence supporting … S Sartori, E Priante, A Pettenazzo, P Marson, A Suppiej, F Benini, ... Journal of child neurology 29 (3), 421-425, 2014 | 57 | 2014 |
| Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders H Guo, E Bettella, PC Marcogliese, R Zhao, JC Andrews, TJ Nowakowski, ... Nature communications 10 (1), 4679, 2019 | 56 | 2019 |
| Longitudinal Electroencephalographic (EEG) Findings in Pediatric Anti-N-Methyl-d-Aspartate (Anti-NMDA) Receptor Encephalitis: The Padua Experience M Nosadini, C Boniver, L Zuliani, L de Palma, E Cainelli, PA Battistella, ... Journal of child neurology 30 (2), 238-245, 2015 | 56 | 2015 |
| Neuroimaging changes in Menkes disease, part 1 R Manara, L D'Agata, MC Rocco, R Cusmai, E Freri, L Pinelli, F Darra, ... American Journal of Neuroradiology 38 (10), 1850-1857, 2017 | 55 | 2017 |
| Molecular epidemiology of childhood neuronal ceroid-lipofuscinosis in Italy FM Santorelli, B Garavaglia, F Cardona, N Nardocci, BD Bernardina, ... Orphanet Journal of Rare Diseases 8, 1-7, 2013 | 55 | 2013 |
| A novel deletion in the GJA12 gene causes Pelizaeus–Merzbacher-like disease L Salviati, E Trevisson, MC Baldoin, I Toldo, S Sartori, M Calderone, ... Neurogenetics 8, 57-60, 2007 | 55 | 2007 |
