| Phenomenology and clinical course of movement disorder in GNAO1 variants: results from an analytical review T Schirinzi, G Garone, L Travaglini, G Vasco, S Galosi, L Rios, ... Parkinsonism & Related Disorders 61, 19-25, 2019 | 77 | 2019 |
| Clinical and genetic overview of paroxysmal movement disorders and episodic ataxias G Garone, A Capuano, L Travaglini, F Graziola, F Stregapede, G Zanni, ... International Journal of Molecular Sciences 21 (10), 3603, 2020 | 63 | 2020 |
| Acute ataxia in paediatric emergency departments: a multicentre Italian study G Garone, A Reale, N Vanacore, P Parisi, C Bondone, A Suppiej, ... Archives of Disease in Childhood 104 (8), 768-774, 2019 | 46 | 2019 |
| Epilepsy is a possible feature in Williams‐Beuren syndrome patients harboring typical deletions of the 7q11. 23 critical region F Nicita, G Garone, A Spalice, S Savasta, P Striano, C Pantaleoni, ... American Journal of Medical Genetics Part A 170 (1), 148-155, 2016 | 45 | 2016 |
| Highlighting the Dystonic Phenotype Related to GNAO1 T Wirth, G Garone, MA Kurian, A Piton, F Millan, A Telegrafi, N Drouot, ... Movement Disorders 37 (7), 1547-1554, 2022 | 42 | 2022 |
| Diagnostic yield of a targeted next-generation sequencing gene panel for pediatric-onset movement disorders: a 3-year cohort study F Graziola, G Garone, F Stregapede, L Bosco, F Vigevano, P Curatolo, ... Frontiers in genetics 10, 1026, 2019 | 36 | 2019 |
| Alternating hemiplegia of childhood: understanding the genotype–phenotype relationship of ATP1A3 variations A Capuano, G Garone, G Tiralongo, F Graziola The Application of Clinical Genetics, 71-81, 2020 | 34 | 2020 |
| Infantile-onset syndromic cerebellar ataxia and CACNA1G mutations S Barresi, ML Dentici, F Manzoni, E Bellacchio, E Agolini, S Pizzi, A Ciolfi, ... Pediatric neurology 104, 40-45, 2020 | 28 | 2020 |
| A novel KCTD17 mutation is associated with childhood early-onset hyperkinetic movement disorder F Graziola, F Stregapede, L Travaglini, G Garone, M Verardo, L Bosco, ... Parkinsonism & related disorders 61, 4-6, 2019 | 28 | 2019 |
| Early Myoclonic Encephalopathy in 9q33‐q34 Deletion Encompassing STXBP1 and SPTAN1 F Nicita, F Ulgiati, L Bernardini, G Garone, L Papetti, A Novelli, A Spalice Annals of human genetics 79 (3), 209-217, 2015 | 26 | 2015 |
| Impact of Italian lockdown on Tourette's syndrome patients at the time of the COVID‐19 pandemic F Graziola, G Garone, L Di Criscio, M Grasso, P Curatolo, F Vigevano, ... Psychiatry and Clinical Neurosciences 74 (11), 610, 2020 | 20 | 2020 |
| Acute hyperkinetic movement disorders in Italian paediatric emergency departments U Raucci, P Parisi, N Vanacore, G Garone, C Bondone, A Palmieri, ... Archives of disease in childhood 103 (8), 790-794, 2018 | 18 | 2018 |
| Severe early onset ethylmalonic encephalopathy with West syndrome L Papetti, G Garone, L Schettini, C Giordano, F Nicita, P Papoff, M Zeviani, ... Metabolic brain disease 30, 1537-1545, 2015 | 17 | 2015 |
| Prestatus and status dystonicus in children and adolescents G Garone, F Graziola, F Nicita, F Frascarelli, F Randi, M Zazza, ... Developmental Medicine & Child Neurology 62 (6), 742-749, 2020 | 16 | 2020 |
| Cognitive Assessment in GNAO1 Neurodevelopmental Disorder Using an Eye Tracking System F Graziola, G Garone, M Grasso, A Capuano Journal of Clinical Medicine 10 (16), 3541, 2021 | 15 | 2021 |
| Could Rolandic spikes be a prognostic factor of the neurocognitive outcome of children with BECTS? I Tristano, F Nicita, G Garone, F Ursitti, C Nardone, V Rocchi, CA Guido, ... Epilepsy & Behavior 86, 157-162, 2018 | 12 | 2018 |
| Acute movement disorders in childhood G Garone, F Graziola, M Grasso, A Capuano Journal of Clinical Medicine 10 (12), 2671, 2021 | 11 | 2021 |
| Characteristics of acute nystagmus in the pediatric emergency department G Garone, A Suppiej, N Vanacore, F La Penna, P Parisi, L Calistri, ... Pediatrics 146 (2), 2020 | 11 | 2020 |
| Movement disorders in patients with genetic developmental and epileptic encephalopathies S Van Der Veen, GTW Tse, A Ferretti, G Garone, B Post, N Specchio, ... Neurology 101 (19), e1884-e1892, 2023 | 8 | 2023 |
| Working memory, attention and planning abilities in NKX2. 1-related chorea F Graziola, G Garone, M Grasso, T Schirinzi, A Capuano Parkinsonism & Related Disorders 88, 24-27, 2021 | 6 | 2021 |
