| Neonatal status epilepticus vs recurrent neonatal seizures: clinical findings and outcome F Pisani, C Cerminara, C Fusco, L Sisti Neurology 69 (23), 2177-2185, 2007 | 218 | 2007 |
| Diagnostic targeted resequencing in 349 patients with drug‐resistant pediatric epilepsies identifies causative mutations in 30 different genes E Parrini, C Marini, D Mei, A Galuppi, E Cellini, D Pucatti, L Chiti, ... Human mutation 38 (2), 216-225, 2017 | 173 | 2017 |
| Immunohistochemical study of muscle biopsy in children with cerebral palsy A Marbini, A Ferrari, G Cioni, MF Bellanova, C Fusco, F Gemignani Brain and Development 24 (2), 63-66, 2002 | 139 | 2002 |
| HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond C Marini, A Porro, A Rastetter, C Dalle, I Rivolta, D Bauer, R Oegema, ... Brain 141 (11), 3160-3178, 2018 | 116 | 2018 |
| Neonatal seizures and postneonatal epilepsy: a 7-y follow-up study F Pisani, B Piccolo, G Cantalupo, C Copioli, C Fusco, A Pelosi, ... Pediatric research 72 (2), 186-193, 2012 | 99 | 2012 |
| ADCY5-related movement disorders: Frequency, disease course and phenotypic variability in a cohort of paediatric patients M Carecchio, NE Mencacci, A Iodice, R Pons, C Panteghini, G Zorzi, ... Parkinsonism & related disorders 41, 37-43, 2017 | 83 | 2017 |
| Idiopathic stabbing headache: clinical characteristics of children and adolescents C Fusco, F Pisani, C Faienza Brain and Development 25 (4), 237-240, 2003 | 68 | 2003 |
| 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 |
| The hyperkinetic movement disorder of FOXG1‐related epileptic–dyskinetic encephalopathy E Cellini, A Vignoli, T Pisano, M Falchi, A Molinaro, P Accorsi, ... Developmental Medicine & Child Neurology 58 (1), 93-97, 2016 | 41 | 2016 |
| Infantile neuroaxonal dystrophy and PLA2G6-associated neurodegeneration: an update for the diagnosis A Iodice, C Spagnoli, GG Salerno, D Frattini, G Bertani, P Bergonzini, ... Brain and Development 39 (2), 93-100, 2017 | 37 | 2017 |
| Syndromic intellectual disability: A new phenotype caused by an aromatic amino acid decarboxylase gene (DDC) variant C Graziano, A Wischmeijer, T Pippucci, C Fusco, C Diquigiovanni, ... Gene 559 (2), 144-148, 2015 | 37 | 2015 |
| Early onset methylmalonic aciduria and homocystinuria cblC type with demyelinating neuropathy D Frattini, C Fusco, V Ucchino, B Tavazzi, E Della Giustina Pediatric neurology 43 (2), 135-138, 2010 | 33 | 2010 |
| Neuroimaging changes in menkes disease, part 2 R Manara, MC Rocco, L D'agata, R Cusmai, E Freri, L Giordano, F Darra, ... American Journal of Neuroradiology 38 (10), 1858-1865, 2017 | 32 | 2017 |
| Acute and chronic corticosteroid treatment of ten patients with paralytic form of Sydenham’s chorea C Fusco, V Ucchino, D Frattini, F Pisani, E Della Giustina european journal of paediatric neurology 16 (4), 373-378, 2012 | 30 | 2012 |
| Hereditary spastic paraplegia and axonal motor neuropathy caused by a novel SPG3A de novo mutation C Fusco, D Frattini, E Farnetti, D Nicoli, B Casali, F Fiorentino, A Nuccitelli, ... Brain and Development 32 (7), 592-594, 2010 | 29 | 2010 |
| Expanding phenotype of PRRT2 gene mutations: A new case with epilepsy and benign myoclonus of early infancy I Maini, A Iodice, C Spagnoli, GG Salerno, G Bertani, D Frattini, C Fusco european journal of paediatric neurology 20 (3), 454-456, 2016 | 27 | 2016 |
| Coexistent central and peripheral nervous system involvement in a Charcot-Marie-Tooth syndrome X-linked patient C Fusco, D Frattini, F Pisani, F Spaggiari, A Ferlini, E Della Giustina Journal of child neurology 25 (6), 759-763, 2010 | 27 | 2010 |
| Clinical features in aromatic L-amino acid decarboxylase (AADC) deficiency: a systematic review S Rizzi, C Spagnoli, D Frattini, F Pisani, C Fusco Behavioural Neurology 2022, 2022 | 24 | 2022 |
| Stress fracture of the peroneal bone secondary to a complex tic C Fusco, G Bertani, G Caricati, E Della Giustina Brain and Development 28 (1), 52-54, 2006 | 24 | 2006 |
| KCNQ2 encephalopathy: A case due to a de novo deletion C Spagnoli, GG Salerno, A Iodice, D Frattini, F Pisani, C Fusco Brain and Development 40 (1), 65-68, 2018 | 23 | 2018 |
Barbara GaravagliaPhD Istituto Neurologico Carlo BestaEmail verificata su istituto-besta.it
