COPPOLA, Giangennaro

COPPOLA, Giangennaro  

Dipartimento di Medicina, Chirurgia e Odontoiatria “Scuola Medica Salernitana”/DIPMED  

Mostra records
Risultati 1 - 20 di 215 (tempo di esecuzione: 0.02 secondi).
Titolo Data di pubblicazione Autore(i) File
[Electroencephalographic aspects of pediatric brain tumors. Considerations in 151 cases] 1-gen-1986 Pascotto, A; Liguori, G; Coppola, Giangennaro
[Marfan's syndrome: clinical diagnostic criteria with a case report] 1-gen-1981 Baione, Mt; Coppola, Giangennaro; Gugliucci, N; Cupo, G; Sacco, R.
A 12-month longitudinal study of calcium metabolism and bone turnover during valproate monotherapy. 1-gen-2010 Verrotti, A; Agostinelli, S; Coppola, Giangennaro; Parisi, P; Chiarelli, F.
A calorie-restricted ketogenic diet reduces cerebral cortex vascularization in prepubertal rats 1-gen-2019 Viggiano, A.; Meccariello, R.; Santoro, A.; Secondulfo, C.; Operto, F. F.; Monda, M.; Coppola, G.
A Low Cost Amplifier And Acquisition System For Cortical-Electroncephalography In Non-Human Applications 1-gen-2014 Viggiano, Andrea; Coppola, Giangennaro
A multicenter, randomized, placebo-controlled trial of levetiracetam in children and adolescents with newly diagnosed absence epilepsy. 1-gen-2011 Fattore, C; Boniver, C; Capovilla, G; Cerminara, C; Citterio, A; Coppola, Giangennaro; Costa, P; Darra, F; Vecchi, M; Perucca, E.
A mutation (V260M) in the middle of the M2 pore-lining domain of the glycine receptor causes hereditary hyperekplexia. 1-gen-2001 DEL GIUDICE, Em; Coppola, Giangennaro; Bellini, G; Cirillo, G; Scuccimarra, G; Pascotto, A.
A novel hyperekplexia-causing mutation in the pre-transmembrane segment 1 of the human glycine receptor alpha1 subunit reduces membrane expression and impairs gating by agonists 1-gen-2004 Castaldo, P; Stefanoni, P; Miceli, F; Coppola, Giangennaro; DEL GIUDICE, Em; Bellini, G; Pascotto, A.; Trudell, Jr; Harrison, Nl; Annunziato, L; Taglialatela, M.
A novel KCNQ2 K+ channel mutation in benign neonatal convulsions and centrotemporal spikes. 1-gen-2003 Coppola, Giangennaro; Castaldo, P; MIRAGLIA DEL GIUDICE, E; Bellini, G; Galasso, F; Soldovieri, Mv; Anzalone, L; Sferro, C; Annunziato, L; Pascotto, A; Taglialatela, M.
A novel mutation (R218Q) at the boundary between the N-terminal and the first transmembrane domain of the glycine receptor in a case of sporadic hyperekplexia. 1-gen-2003 MIRAGLIA DEL GIUDICE, E; Coppola, Giangennaro; Bellini, G; Ledaal, P; Hertz, Jm; Pascotto, A.
Afebrile benign convulsions with mildgastroenteritis: a new entity? 1-gen-2009 Verrotti, A; Tocco, Am; Coppola, Giangennaro; Altobelli, E; Chiarelli, F.
An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy. 1-gen-2007 Striano, P; Coppola, A; Pezzella, M; Ciampa, C; Specchio, N; Ragona, F; Mancardi, Mm; Gennaro, E; Beccaria, F; Capovilla, G; Rasmini, P; Besana, D; Coppola, Giangennaro; Elia, M; Granata, T; Vecchi, M; Vigevano, F; Viri, M; Gaggero, R; Striano, S; Zara, F.
Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy. 1-gen-2008 Bovo, G; Diani, E; Bisulli, F; DI BONAVENTURA, C; Striano, P; Gambardella, A; Ferlazzo, E; Egeo, G; Mecarelli, O; Elia, M; Bianchi, A; Bortoluzzi, S; Vettori, A; Aguglia, U; Binelli, S; DE FALCO, A; Coppola, Giangennaro; Gobbi, G; Sofia, V; Striano, S; Tinuper, P; Giallonardo, At; Michelucci, R; Nobile, C.
Anticonvulsant drugs for generalized tonic-clonic epilepsy 1-gen-2017 Coppola, Giangennaro; Piccorossi, Alessandra; Operto, Francesca Felicia; Verrotti, Alberto
Anticonvulsant properties of an oral ketone ester in a pentylenetetrazole-model of seizure 1-gen-2015 Viggiano, Andrea; Pilla, Raffaele; Arnold, Patrick; Monda, Marcellino; D׳agostino, Dominic; Coppola, Giangennaro
Antiepileptic drug withdrawal in childhood epilepsy: What are the riskfactors associated with seizure relapse? 1-gen-2012 Verrotti, A; D'Egidio, C; Agostinelli, S; Parisi, P; Spalice, A; Chiarelli, F; Coppola, Giangennaro
Antiepileptic drugs, sex hormones, and PCOS 1-gen-2011 Verrotti, A; D'Egidio, C; Mohn, A; Coppola, Giangennaro; Parisi, P; Chiarelli, F.
Argomenti di Neuropsichiatria Infantile. 1-gen-2008 Coppola, Giangennaro
Association between SCN1A gene polymorphisms and drug resistant epilepsy in pediatric patients 1-gen-2018 Margari, Lucia; Legrottaglie, Anna R.; Vincenti, Alessandra; Coppola, Giangennaro; Operto, FRANCESCA FELICIA; Buttiglione, Maura; Cassano, Amalia; Bartolomeo, Nicola; Mariggiò, Maria A.
Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy. 1-gen-2011 Busolin, G; Malacrida, S; Bisulli, F; Striano, P; Di Bonaventura, C; Egeo, G; Pasini, E; Cianci, V; Ferlazzo, E; Bianchi, A; Coppola, Giangennaro; Elia, M; Mecarelli, O; Gobbi, G; Casellato, S; Marchini, M; Binelli, S; Freri, E; Granata, T; Posar, A; Parmeggiani, A; Vigliano, P; Boniver, C; Aguglia, U; Striano, S; Tinuper, P; Giallonardo, At; Michelucci, R; Nobile, C.