Zobrazeno 1 - 10
of 412
pro vyhledávání: '"Federico, Vigevano"'
Autor:
Mattia Mercier, Chiara Pepi, Giusy Carfi-Pavia, Alessandro De Benedictis, Maria Camilla Rossi Espagnet, Greta Pirani, Federico Vigevano, Carlo Efisio Marras, Nicola Specchio, Luca De Palma
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract Epilepsy surgery is effective for patients with medication-resistant seizures, however 20–40% of them are not seizure free after surgery. Aim of this study is to evaluate the role of linear and non-linear EEG features to predict post-surgi
Externí odkaz:
https://doaj.org/article/ed4209e5482f4b9eaaf8a748a6258e1f
Autor:
Louise Gallagher, Michael Absoud, Miguel Castelo-Branco, Tony Charman, Maja Hempel, Richard Delorme, Guiomar Oliveira, Roberta Battini, Sven Bölte, Claire S Leblond, Thomas Bourgeron, Alexandra Lautarescu, Mercedes Serrano, Federico Vigevano, Christian P Schaaf, Bethany Oakley, Julian Tillmann, Pierre Violland, Declan G M Murphy, Sarah Douglas, Paolo Bonanni, Grainne McAlonan, Roberta Milone, Josefina Castro-Fornieles, Madeleine Bloomfield, Síofra Heraty, Roderik Plas, Anjuli Ghosh, Katrien Van den Bosch, Eliza Eaton, Ana Blázquez Hinojosa, Nadia Bolshakova, Jacqueline Borg, Sara Calderoni, Rosa Calvo Escalona, Pilar Caro, Freddy Cliquet, Alberto Danieli, Maurizio Elia, Nuno Madeira, Ciara J Molloy, Susana Mouga, Virginia Montiel, Ana Pina Rodrigues, Kristiina Tammimies, Charlotte Tye, Beatrice Mazzone, Cara O’Neill, Julie Pender, Verena Romero, Christopher Chatham
Publikováno v:
BMJ Open, Vol 14, Iss 6 (2024)
Introduction Autism is a common neurodevelopmental condition with a complex genetic aetiology that includes contributions from monogenic and polygenic factors. Many autistic people have unmet healthcare needs that could be served by genomics-informed
Externí odkaz:
https://doaj.org/article/815fdc95324e48c4ab0f1f29dd80968c
Autor:
Mattia Mercier, Chiara Pepi, Giusy Carf-Pavia, Alessandro De Benedictis, Maria Camilla Rossi Espagnet, Greta Pirani, Federico Vigevano, Carlo Efsio Marras, Nicola Specchio, Luca De Palma
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-1 (2024)
Externí odkaz:
https://doaj.org/article/ac7e57d2522c483db2916863243ae9d3
Autor:
Nicola Pietrafusa, Giovanni Falcicchio, Emilio Russo, Simona Lattanzi, Bianca Goffredo, Raffaele Simeoli, Sara Cairoli, Tiziana Corsetti, Roberta Roberti, Marina De Tommaso, Federico Vigevano, Angela La Neve, Nicola Specchio
Publikováno v:
Frontiers in Pharmacology, Vol 14 (2023)
Background: Cenobamate (CNB) is an anti-seizure medication (ASM) approved in 2021 in Europe for adjunctive treatment of focal-onset seizures in adults who were not adequately controlled with at least two previous ASMs.Methods: seizure outcome, treatm
Externí odkaz:
https://doaj.org/article/9c5993e6d1dd47cba23648716cd6dd48
Autor:
Marina Trivisano, Ambra Butera, Chiara Quintavalle, Angela De Dominicis, Costanza Calabrese, Simona Cappelletti, Federico Vigevano, Antonio Novelli, Nicola Specchio
Publikováno v:
Frontiers in Neuroscience, Vol 17 (2023)
IntroductionSLC6A1 pathogenic variants have been associated with epilepsy and neurodevelopmental disorders. The clinical phenotype includes different seizure types, intellectual disability, and psychiatric symptoms affecting mood and behavior. Few da
Externí odkaz:
https://doaj.org/article/b143ad6aadad4f88b87f954dee18bc40
Autor:
Anna Rosati, Manuela L’Erario, Roberto Bianchi, Sara Olivotto, Domenica Immacolata Battaglia, Francesca Darra, Paolo Biban, Annibale Biggeri, Dolores Catelan, Giacomo Danieli, Maria Cristina Mondardini, Duccio Maria Cordelli, Angela Amigoni, Elisabetta Cesaroni, Alessandra Conio, Paola Costa, Martina Lombardini, Rosanna Meleleo, Alessandra Pugi, Elena Eve Tornaboni, Marta Elena Santarone, Roberta Vittorini, Stefano Sartori, Carla Marini, Federico Vigevano, Massimo Mastrangelo, Silvia Maria Pulitanò, Francesca Izzo, Lucia Fusco
Publikováno v:
Epilepsia Open, Vol 7, Iss 3, Pp 532-540 (2022)
Abstract Objective To discuss the results of the KETASER01 trial and the reasons for its failure, particularly in view of future studies. Methods KETASER01 is a multicenter, randomized, controlled, open‐label, sequentially designed, non‐profit It
Externí odkaz:
https://doaj.org/article/4d10adf3a45b464680f5ae51665dca45
Autor:
Michela Giustizieri, Sara Petrillo, Jessica D’Amico, Caterina Torda, Andrea Quatrana, Federico Vigevano, Nicola Specchio, Fiorella Piemonte, Enrico Cherubini
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 17 (2023)
Epilepsy is a neurological disorder characterized by recurrent seizures, which result from excessive, synchronous discharges of neurons in different brain areas. In about 30% of cases, epileptic discharges, which vary in their etiology and symptomato
Externí odkaz:
https://doaj.org/article/97378ddfac9a42ff987fdfacc0f1a07b
Autor:
Gabriele Monte, Laura Papetti, Michela Ada Noris Ferilli, Fabiana Ursitti, Romina Moavero, Giorgia Sforza, Elena Panella, Samuela Tarantino, Martina Proietti Checchi, Federico Vigevano, Paolo Palma, Massimiliano Valeriani
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
IntroductionConcern of a correlation between disease relapse in patients with acquired demyelinating disorders of central nervous system (CNS) and SARS-CoV2 vaccines has been raised. In this single center study, we retrospectively evaluated safety of
Externí odkaz:
https://doaj.org/article/11ae6922760e45f58a30b6e9382a04fd
Publikováno v:
Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-3 (2022)
Abstract Background Goldenhar syndrome (GS) is a rare congenital disease characterized by impaired development of different facial structures and deformations of the teeth structures. Sialorrhea, which can cause difficulties in breathing and language
Externí odkaz:
https://doaj.org/article/07f13830b2ec4abcae8af29cd35b18db
Autor:
Nicola Specchio, Giusy Carfi Pavia, Luca dePalma, Alessandro De Benedictis, Chiara Pepi, Marta Conti, Carlo Efisio Marras, Federico Vigevano, Paolo Curatolo
Publikováno v:
Pediatric Investigation, Vol 6, Iss 1, Pp 16-22 (2022)
ABSTRACT Tuberous sclerosis complex (TSC) is a rare multisystem, autosomal dominant neurocutaneous syndrome in which epilepsy is the most common of several neurological and psychiatric manifestations. Around two thirds of patients develop drug‐resi
Externí odkaz:
https://doaj.org/article/1dd382c338884530a6ad75c652c0256a