| Challenges and management of neurological and psychiatric manifestations in SARS-CoV-2 (COVID-19) patients A Orsini, M Corsi, A Santangelo, A Riva, D Peroni, T Foiadelli, S Savasta, ... Neurological Sciences 41, 2353-2366, 2020 | 112 | 2020 |
| Recent advances in epilepsy genetics A Orsini, F Zara, P Striano Neuroscience letters 667, 4-9, 2018 | 105 | 2018 |
| The AMS-02 lead-scintillating fibres Electromagnetic Calorimeter C Adloff, L Basara, G Bigongiari, F Bosi, P Brun, F Cadoux, F Cervelli, ... Nuclear Instruments and Methods in Physics Research Section A: Accelerators …, 2013 | 91 | 2013 |
| The spectrum of intermediate SCN8A‐related epilepsy KM Johannesen, E Gardella, AC Encinas, AE Lehesjoki, T Linnankivi, ... Epilepsia 60 (5), 830-844, 2019 | 82 | 2019 |
| The best evidence for progressive myoclonic epilepsy: a pathway to precision therapy A Orsini, A Valetto, V Bertini, M Esposito, N Carli, BA Minassian, ... Seizure 71, 247-257, 2019 | 72 | 2019 |
| Mothers and fathers of children with epilepsy: gender differences in post-traumatic stress symptoms and correlations with mood spectrum symptoms C Carmassi, M Corsi, CA Bertelloni, B Carpita, C Gesi, V Pedrinelli, ... Neuropsychiatric disease and treatment, 1371-1379, 2018 | 57 | 2018 |
| Autosomal dominant SCN8A mutation with an unusually mild phenotype JS Anand G, Collett-White F, Orsini A, Thomas S, Jayapal S, Trump N, Zaiwalla Z Europena Journal Paediatric Neurology, 761-765, 2016 | 55* | 2016 |
| 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 |
| The brain–heart interaction in epilepsy: implications for diagnosis, therapy, and SUDEP prevention G Costagliola, A Orsini, M Coll, R Brugada, P Parisi, P Striano Annals of Clinical and Translational neurology 8 (7), 1557-1568, 2021 | 46 | 2021 |
| Case of Myhre syndrome with autism and peculiar skin histological findings L Titomanlio, MG Marzano, E Rossi, M D'Armiento, D De Brasi, GR Vega, ... American journal of medical genetics 103 (2), 163-165, 2001 | 45 | 2001 |
| Molecular cytogenetic characterization of an interstitial deletion of chromosome 21 (21q22. 13q22. 3) in a patient with dysmorphic features, intellectual disability and severe … A Valetto, A Orsini, V Bertini, B Toschi, A Bonuccelli, F Simi, I Sammartino, ... European journal of medical genetics 55 (5), 362-366, 2012 | 42 | 2012 |
| Post-traumatic stress, anxiety, and depressive symptoms in caregivers of children tested for COVID-19 in the acute phase of the Italian outbreak A Orsini, M Corsi, V Pedrinelli, A Santangelo, C Bertelloni, V Dell’Oste, ... Journal of Psychiatric Research 135, 256-263, 2021 | 41 | 2021 |
| Pitt-Hopkins syndrome: report of a case with a TCF4 gene mutation G Taddeucci, A Bonuccelli, I Mantellassi, A Orsini, E Tarantino Italian journal of pediatrics 36, 1-5, 2010 | 31 | 2010 |
| Post-traumatic stress and major depressive disorders in parent caregivers of children with a chronic disorder C Carmassi, M Corsi, CA Bertelloni, V Pedrinelli, G Massimetti, DG Peroni, ... Psychiatry research 279, 195-200, 2019 | 29 | 2019 |
| Trait impulsivity in juvenile myoclonic epilepsy A Shakeshaft, N Panjwani, R McDowall, H Crudgington, J Peña Ceballos, ... Annals of clinical and translational neurology 8 (1), 138-152, 2021 | 28 | 2021 |
| Personalized medicine in epilepsy patients A Orsini, M Esposito, D Perna, A Bonuccelli, D Peroni, P Striano J Transl Genet Genom 2, 16, 2018 | 28 | 2018 |
| Sex-specific disease modifiers in juvenile myoclonic epilepsy A Shakeshaft, N Panjwani, A Collingwood, H Crudgington, A Hall, ... Scientific reports 12 (1), 2785, 2022 | 26 | 2022 |
| Rasmussen's encephalitis: from immune pathogenesis towards targeted-therapy A Orsini, T Foiadelli, N Carli, G Costagliola, B Masini, A Bonuccelli, ... Seizure 81, 76-83, 2020 | 26 | 2020 |
| Targeted re-sequencing for early diagnosis of genetic causes of childhood epilepsy: the Italian experience from the ‘beyond epilepsy’project E Amadori, M Scala, GS Cereda, MS Vari, F Marchese, V Di Pisa, ... Italian Journal of Pediatrics 46, 1-9, 2020 | 25 | 2020 |
| Novel AMPD2 mutation in pontocerebellar hypoplasia, dysmorphisms, and teeth abnormalities A Accogli, M Iacomino, F Pinto, A Orsini, MS Vari, R Selmi, A Torella, ... Neurology: Genetics 3 (5), e179, 2017 | 25 | 2017 |
Pasquale Striano, MD, PhDPediatric neurologist, IRCCS 'G. Gaslini'; Professor of Paediatrics, University of GenovaGeverifieerd e-mailadres voor gaslini.org
