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Gianluca D'Onofrio
Gianluca D'Onofrio
PhD Student, Università di Genova
在 ssss.gouv.qc.ca 的电子邮件经过验证
标题
引用次数
引用次数
年份
An accelerated shift in the use of remote systems in epilepsy due to the COVID-19 pandemic
M Kuchenbuch, G d'Onofrio, E Wirrell, Y Jiang, S Dupont, ZM Grinspan, ...
Epilepsy & Behavior 112, 107376, 2020
422020
Slow titration of cannabidiol add-on in drug-resistant epilepsies can improve safety with maintained efficacy in an open-label study
G D'Onofrio, M Kuchenbuch, C Hachon-Le Camus, B Desnous, V Staath, ...
Frontiers in Neurology 11, 829, 2020
262020
Add‐on cannabidiol significantly decreases seizures in 3 patients with SYNGAP1 developmental and epileptic encephalopathy
M Kuchenbuch, G D'Onofrio, N Chemaly, G Barcia, T Teng, R Nabbout
Epilepsia Open 5 (3), 496-500, 2020
182020
Impact and management of drooling in children with neurological disorders: an Italian Delphi consensus
A Riva, E Amadori, MS Vari, A Spalice, V Belcastro, M Viri, D Capodiferro, ...
Italian Journal of Pediatrics 48 (1), 118, 2022
152022
A European pilot study in Dravet Syndrome to delineate what really matters for the patients and families
N Chemaly, M Kuchenbuch, T Teng, E Marie, G D'Onofrio, T Lo Barco, ...
Epilepsia Open 9 (1), 388-396, 2024
102024
Current and promising therapeutic options for Dravet syndrome
A Riva, G D’Onofrio, E Amadori, D Tripodi, G Balagura, V Iurilli, MS Vari, ...
Expert Opinion on Pharmacotherapy 23 (15), 1727-1736, 2022
102022
Urinary metabotypes of newborns with perinatal asphyxia undergoing therapeutic hypothermia
E Valerio, V Mardegan, M Stocchero, ME Cavicchiolo, P Pirillo, ...
Plos one 17 (8), e0273175, 2022
82022
A real‐life pilot study of the clinical application of pharmacogenomics testing on saliva in epilepsy
A Riva, R Roberti, G D'Onofrio, MS Vari, E Amadori, V De Giorgis, ...
Epilepsia Open 8 (3), 1142-1150, 2023
62023
Clinical and Neurophysiologic Phenotypes in Neonates With BRAT1 Encephalopathy
E Carapancea, MC Cornet, M Milh, L De Cosmo, EJ Huang, T Granata, ...
Neurology 100 (12), e1234-e1247, 2023
62023
Novel biallelic variants expand the phenotype of NAA20‐related syndrome
G D'Onofrio, C Cuccurullo, SK Larsen, M Severino, A D'Amico, K Brønstad, ...
Clinical Genetics 104 (3), 371-376, 2023
52023
Genotype–phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorder
G D’Onofrio, A Accogli, M Severino, H Caliskan, T Kokotović, A Blazekovic, ...
Human Genetics 142 (7), 909-925, 2023
52023
Influenza-associated hemolytic uremic syndrome: The pathogenic role of the virus
V Silecchia, G D’Onofrio, E Valerio, G Rubin, E Vidal, L Murer
Clinical nephrology. Case Studies 9, 45, 2021
52021
Treatment of refractory epilepsy with MEK inhibitor in patients with RASopathy
G D'Onofrio, MA Delrue, A Lortie, C Marquis, P Striano, M Jaworski, ...
Pediatric Neurology 148, 148-151, 2023
42023
Pharmacokinetic considerations surrounding the use of levetiracetam for seizure prophylaxis in neurocritical care–an overview
G D’Onofrio, A Riva, E Amadori, S Lattanzi, K Rose, A Verrotti, P Striano
Expert Opinion on Drug Metabolism & Toxicology 18 (9), 575-585, 2022
42022
Cannabidiol add-on in glycosylphosphatidylinositol-related drug-resistant epilepsy
A Riva, G D'Onofrio, A Pisati, R Roberti, E Amadori, F Bosch, ...
Cannabis and Cannabinoid Research 9 (4), 990-995, 2024
32024
Myoclonus: Differential diagnosis and current management
A Riva, G D'Onofrio, E Ferlazzo, A Pascarella, E Pasini, S Franceschetti, ...
Epilepsia Open 9 (2), 486-500, 2024
32024
A PAK1 mutational hotspot within the regulatory CRIPaK domain is associated with severe neurodevelopmental disorders in children
G Scorrano, G D'Onofrio, A Accogli, M Severino, R Buchert, U Kotzaeridou, ...
Pediatric Neurology 149, 84-92, 2023
32023
Paroxysmal limb dystonias associated with GABBR2 pathogenic variant: A case-based literature review
G D'Onofrio, A Riva, G Di Rosa, S Efthymiou, E Gitto, F Madia, A Accogli, ...
Brain and Development 44 (7), 469-473, 2022
32022
Sleep exacerbations and facial twitching: diagnostic clues for ADCY5-related dyskinesias
M Nosadini, G D'Onofrio, MF Pelizza, C Luisi, D Padrin, L Baggio, ...
Neuropediatrics 52 (03), 208-211, 2021
32021
Genotype–phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders
P Borgia, S Baldassari, N Pedemonte, E Alkhunaizi, G D’Onofrio, ...
Orphanet Journal of Rare Diseases 17 (1), 286, 2022
22022
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