| Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders M Wolff, KM Johannesen, UBS Hedrich, S Masnada, G Rubboli, ... Brain 140 (5), 1316-1336, 2017 | 513 | 2017 |
| STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy H Stamberger, M Nikanorova, MH Willemsen, P Accorsi, M Angriman, ... Neurology 86 (10), 954-962, 2016 | 311 | 2016 |
| Therapeutic effect of Anakinra in the relapsing chronic phase of febrile infection–related epilepsy syndrome R Dilena, E Mauri, E Aronica, P Bernasconi, C Bana, C Cappelletti, ... Epilepsia open 4 (2), 344-350, 2019 | 97 | 2019 |
| Anakinra usage in febrile infection related epilepsy syndrome: an international cohort YC Lai, E Muscal, E Wells, N Shukla, K Eschbach, K Hyeong Lee, ... Annals of clinical and translational neurology 7 (12), 2467-2474, 2020 | 84 | 2020 |
| Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis A Citterio, A Arnoldi, E Panzeri, MG D’Angelo, M Filosto, R Dilena, ... Journal of neurology 261, 373-381, 2014 | 84 | 2014 |
| International consensus recommendations for management of new onset refractory status epilepticus including febrile infection‐related epilepsy syndrome: Statements and … R Wickstrom, O Taraschenko, R Dilena, ET Payne, N Specchio, ... Epilepsia 63 (11), 2840-2864, 2022 | 83* | 2022 |
| Spinal direct current stimulation modulates the activity of gracile nucleus and primary somatosensory cortex in anaesthetized rats J Aguilar, F Pulecchi, R Dilena, A Oliviero, A Priori, G Foffani The Journal of physiology 589 (20), 4981-4996, 2011 | 81 | 2011 |
| Efficacy of sodium channel blockers in SCN2A early infantile epileptic encephalopathy R Dilena, P Striano, E Gennaro, L Bassi, S Olivotto, L Tadini, F Mosca, ... Brain and Development 39 (4), 345-348, 2017 | 74 | 2017 |
| 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 |
| Dramatic effect of levetiracetam in early-onset epileptic encephalopathy due to STXBP1 mutation R Dilena, P Striano, M Traverso, M Viri, G Cristofori, L Tadini, S Barbieri, ... Brain and Development 38 (1), 128-131, 2016 | 61 | 2016 |
| Early treatment with quinidine in 2 patients with epilepsy of infancy with migrating focal seizures (EIMFS) due to gain-of-function KCNT1 mutations: functional studies … R Dilena, JC DiFrancesco, MV Soldovieri, A Giacobbe, P Ambrosino, ... Neurotherapeutics 15 (4), 1112-1126, 2018 | 55 | 2018 |
| Fetal acetylcholine receptor inactivation syndrome: a myopathy due to maternal antibodies Y Hacohen, LW Jacobson, S Byrne, F Norwood, A Lall, S Robb, R Dilena, ... Neuroimmunology & Neuroinflammation 2 (1), e57, 2014 | 49 | 2014 |
| Relapse risk factors in anti‐N‐methyl‐D‐aspartate receptor encephalitis M Nosadini, T Granata, S Matricardi, E Freri, F Ragona, L Papetti, ... Developmental Medicine & Child Neurology 61 (9), 1101-1107, 2019 | 48 | 2019 |
| Consensus protocol for EEG and amplitude-integrated EEG assessment and monitoring in neonates R Dilena, F Raviglione, G Cantalupo, DM Cordelli, P De Liso, M Di Capua, ... Clinical Neurophysiology 132 (4), 886-903, 2021 | 42 | 2021 |
| Transcranial direct current stimulation in two patients with Tourette syndrome S Mrakic-Sposta, S Marceglia, F Mameli, R Dilena, L Tadini, A Priori | 41 | 2008 |
| Epilepsy Course and Developmental Trajectories in STXBP1-DEE G Balagura, J Xian, A Riva, F Marchese, B Ben Zeev, L Rios, D Sirsi, ... Neurology: Genetics 8 (3), e676, 2022 | 25 | 2022 |
| Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy E Monfrini, L Straniero, S Bonato, GM Compagnoni, A Bordoni, R Dilena, ... Parkinsonism & Related Disorders 63, 66-72, 2019 | 24 | 2019 |
| Posterior reversible encephalopathy syndrome after kidney transplantation in pediatric recipients: two cases A Giussani, G Ardissino, M Belingheri, R Dilena, M Raiteri, A Pasciucco, ... Pediatric Transplantation 20 (1), 68-71, 2016 | 23 | 2016 |
| A de novo C19orf12 heterozygous mutation in a patient with MPAN E Monfrini, V Melzi, G Buongarzone, G Franco, D Ronchi, R Dilena, ... Parkinsonism & related disorders 48, 109-111, 2018 | 17 | 2018 |
| Congenital myasthenic syndrome due to choline acetyltransferase mutations in infants: clinical suspicion and comprehensive electrophysiological assessment are important for … R Dilena, A Abicht, P Sergi, GP Comi, AD Fonzo, G Chidini, F Natacci, ... Journal of child neurology 29 (3), 389-393, 2014 | 16 | 2014 |
