Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Giuditta Pellino"'
Autor:
Roberto Grandinetti, Nicole Mussi, Simone Pilloni, Greta Ramundo, Angela Miniaci, Emanuela Turco, Benedetta Piccolo, Maria Elena Capra, Roberta Forestiero, Serena Laudisio, Giovanni Boscarino, Laura Pedretti, Martina Menoni, Giuditta Pellino, Silvia Tagliani, Andrea Bergomi, Francesco Antodaro, Maria Cristina Cantù, Maria Teresa Bersini, Sandra Mari, Franco Mazzini, Giacomo Biasucci, Agnese Suppiej, Susanna Esposito
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Pediatric Autoimmune Neuropsychiatric Disorder Associated with Streptococcal Infections (PANDAS) and Pediatric Acute-onset Neuropsychiatric Syndrome (PANS) are broad diagnoses that encompass a range of sudden-onset neuropsychiatric symptoms in childr
Externí odkaz:
https://doaj.org/article/964ea60d6db64994880bba20c7804cf9
Autor:
Cristina Forest, Michele Laudisi, Cristina Malaventura, Valeria Tugnoli, Giuditta Pellino, Elisabetta Marangoni, Eleonora Baldi, Luca Borgatti, Maura Pugliatti, Agnese Suppiej
Publikováno v:
European Journal of Paediatric Neurology. 42:117-121
Acute necrotizing encephalopathy (ANE) is a rare disease not yet described in children with Covid-19. RANBP2 gene variations are implicated in recurrences in the genetic form of ANE, the so called ANE1. We report the first case of pediatric ANE1 foll
Autor:
Angelo Russo, Jacopo Pruccoli, Carlo Alberto Cesaroni, Laura Maria Beatrice Belotti, Corrado Zenesini, Paolo Bonanni, Antonella Boni, Elisabetta Cesaroni, Giangennaro Coppola, Duccio Maria Cordelli, Alberto Danieli, Maria Margherita Mancardi, Francesca Marchese, Sara Matricardi, Tullio Messana, Giovanna Martina Nocera, Francesca Felicia Operto, Giuditta Pellino, Federica Reina, Francesca Vanadia, Alberto Verrotti, Pasquale Striano
Publikováno v:
Seizure. 102:120-124
To report the efficacy and tolerability of brivaracetam (BRV) in add-on therapy in pediatric patients with severe drug-resistant epilepsy. Prognostic factors of clinical outcome were also analyzed.This Italian multicenter retrospective observational
Autor:
Elisabetta Amadori, Giuditta Pellino, Lalit Bansal, Serena Mazzone, Rikke S. Møller, Guido Rubboli, Pasquale Striano, Angelo Russo
Publikováno v:
European journal of medical genetics. 65(12)
Publikováno v:
European Journal of Medical Case Reports. :223-225
Autor:
Valentina Gentile, Giuditta Pellino, Antonella Boni, Michael Duchowny, Daniela Chiarello, Antonella Pini, Angelo Russo, Corrado Zenesini, Matteo Martinoni, Mario Lima, Prasanna Jayakar, Duccio Maria Cordelli, Ian Miller, Ann Hyslop, John Ragheb
Objective: We describe a multicenter experience with VNS implantation in pediatric patients with epileptic encephalopathy. Our goal was to assess VNS efficacy and identify potential predictors of favorable outcome. Methods: This was a retrospective s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c6c3c1e0ff78c13a2f2945c1c203604
http://hdl.handle.net/11585/830907
http://hdl.handle.net/11585/830907
Autor:
Giuditta Pellino, Lucia Chiasso, Giulia Fiori, Serena Mazzone, Daniele Zama, Duccio Maria Cordelli, Angelo Russo
Publikováno v:
European Journal of Medical Genetics. 65:104457
Weiss-Kruszka syndrome is a recently described genetic disorder characterized by craniofacial features, ptosis, dysgenesis of the corpus callosum, and neurodevelopmental impairment. It is caused by heterozygous loss-of-function variantsin ZNF462 gene
Autor:
Elisabetta Amadori, Giuditta Pellino, Lalit Bansal, Serena Mazzone, Rikke S. Møller, Guido Rubboli, Pasquale Striano, Angelo Russo
Publikováno v:
Amadori, E, Pellino, G, Bansal, L, Mazzone, S, Møller, R S, Rubboli, G, Striano, P & Russo, A 2022, ' Genetic paroxysmal neurological disorders featuring episodic ataxia and epilepsy ', European Journal of Medical Genetics, vol. 65, no. 4, 104450 . https://doi.org/10.1016/j.ejmg.2022.104450
Objective: This review article focuses on clinical and genetic features of paroxysmal neurological disorders featuring episodic ataxia (EA) and epilepsy and help clinicians recognize, diagnose, and treat patients with co-existing EA and epilepsy. It
Publikováno v:
Epilepsy & Behavior. 127:108498
According to the operational epilepsy definition adopted by the International League Against Epilepsy (ILAE) in 2014, in patients with one unprovoked seizure, clinicians must stratify the recurrence risk to determine if the criteria for diagnosis of
Autor:
Giuditta Pellino, Raffaella Faggioli, Elisa Fiumana, Sara Bertelli, Angelo Russo, Jessica Gencarelli
Publikováno v:
Epilepsybehavior : EB. 107
Purpose Neurocutaneous melanosis (NCM) is a rare congenital syndrome characterized by giant melanocytic cutaneous nevi and melanosis within the central nervous system (CNS), often sparing leptomeninges and concentrated in the brain parenchyma. Epilep