SOLDOVIERI, Maria Virginia

SOLDOVIERI, Maria Virginia  

DIPARTIMENTO DI MEDICINA E DI SCIENZE DELLA SALUTE  

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Risultati 1 - 20 di 65 (tempo di esecuzione: 0.05 secondi).
Titolo Data di pubblicazione Autore(i) File
A new Italian FHM2 family: Clinical aspects and functional analysis of the disease-associated mutation 1-gen-2011 Santoro, L; Manganelli, F; Fortunato, Mr; Soldovieri, Maria Virginia; Ambrosino, P; Iodice, R; Pisciotta, C; Tessa, A; Santorelli, F; Taglialatela, M.
A novel homozygous KCNQ3 loss-of-function variant causes non-syndromic intellectual disability and neonatal-onset pharmacodependent epilepsy 1-gen-2019 Lauritano, A.; Moutton, S.; Longobardi, E.; Tran Mau-Them, F.; Laudati, G.; Nappi, P.; Soldovieri, M. V.; Ambrosino, P.; Cataldi, M.; Jouan, T.; Lehalle, D.; Maurey, H.; Philippe, C.; Miceli, F.; Vitobello, A.; Taglialatela, M.
A novel KCNC1 gain-of-function variant causing developmental and epileptic encephalopathy: "Precision medicine" approach with fluoxetine 1-gen-2023 Ambrosino, Paolo; Ragona, Francesca; Mosca, Ilaria; Vannicola, Chiara; Canafoglia, Laura; Solazzi, Roberta; Rivolta, Ilaria; Freri, Elena; Granata, Tiziana; Messina, Giuliana; Castellotti, Barbara; Gellera, Cinzia; Soldovieri, Maria Virginia; Difrancesco, Jacopo Cosimo; Taglialatela, Maurizio
A novel KCNQ2 K+ channel mutation in benign neonatal convulsions and centrotemporal spikes 1-gen-2003 Coppola, G; Castaldo, P; del Giudice, Em; Bellini, G; Galasso, F; Soldovieri, Maria Virginia; Anzalone, L; Sferro, C; Annuniziato, L; Taglialatela, Maurizio
A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability. 1-gen-2015 Miceli, F; Striano, P; Soldovieri, Maria Virginia; Fontana, A; Nardello, R; Robbiano, A; Bellini, G; Elia, M; Zara, F; Taglialatela, Maurizio; Mangano, S.
A Novel Kv7.3 Variant in the Voltage-Sensing S4 Segment in a Family With Benign Neonatal Epilepsy: Functional Characterization and in vitro Rescue by β-Hydroxybutyrate 1-gen-2020 Miceli, F.; Carotenuto, L.; Barrese, V.; Soldovieri, M. V.; Heinzen, E. L.; Mandel, A. M.; Lippa, N.; Bier, L.; Goldstein, D. B.; Cooper, E. C.; Cilio, M. R.; Taglialatela, M.; Sands, T. T.
A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation 1-gen-2004 Borgatti, R; Zucca, C; Cavallini, A; Ferrario, M; Panzeri, C; Castaldo, P; Soldovieri, Maria Virginia; Baschirotto, C; Bresolin, N; Dalla Bernardina, B; Taglialatela, Maurizio; Bassi, Mt
Activation and Desensitization of Trpv1 Channels in Sensory Neurons by the Peroxisome Proliferator-Activated Receptor α Agonist Palmitoylethanolamide 1-gen-2013 Ambrosino, P; Soldovieri, Maria Virginia; Russo, Claudio; Taglialatela, Maurizio
Activation of Kv7 potassium channels inhibits intracellular Ca2+ increases triggered by TRPV1-mediated pain-inducing stimuli in F11 immortalized sensory neurons 1-gen-2019 Ambrosino, P.; Soldovieri, M. V.; Di Zazzo, E.; Paventi, G.; Iannotti, F. A.; Mosca, I.; Miceli, F.; Franco, C.; Canzoniero, L. M. T.; Taglialatela, M.
Addressing the use of PDIF-CN(2) molecules in the development of n-type organic field-effect transistors for biosensing applications 1-gen-2013 Barra, M; Viggiano, Davide; Ambrosino, P; Bloisi, F; Di Girolamo, Fv; Soldovieri, Maria Virginia; Taglialatela, M; Cassinese, A.
Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S-4 region of KCNQ2 causing benign familial neonatal convulsions 1-gen-2007 Soldovieri, Maria Virginia; Cilio, Mr; Miceli, F; Bellini, G; del Giudice, Em; Castaldo, P; Hernandez, Cc; Shapiro, Ms; Pascotto, A; Annunziato, L; Taglialatela, Maurizio
Autism and developmental disability caused by KCNQ3 gain-of-function variants 1-gen-2019 Sands, T. T.; Miceli, F.; Lesca, G.; Beck, A. E.; Sadleir, L. G.; Arrington, D. K.; Schonewolf-Greulich, B.; Moutton, S.; Lauritano, A.; Nappi, P.; Soldovieri, M. V.; Scheffer, I. E.; Mefford, H. C.; Stong, N.; Heinzen, E. L.; Goldstein, D. B.; Perez, A. G.; Kossoff, E. H.; Stocco, A.; Sullivan, J. A.; Shashi, V.; Gerard, B.; Francannet, C.; Bisgaard, A. -M.; Tumer, Z.; Willems, M.; Rivier, F.; Vitobello, A.; Thakkar, K.; Rajan, D. S.; Barkovich, A. J.; Weckhuysen, S.; Cooper, E. C.; Taglialatela, M.; Cilio, M. R.
Calcium cytotoxicity sensitizes prostate cancer cells to standard-of-care treatments for locally advanced tumors 1-gen-2020 Alaimo, A.; Lorenzoni, M.; Ambrosino, P.; Bertossi, A.; Bisio, A.; Macchia, A.; Zoni, E.; Genovesi, S.; Cambuli, F.; Foletto, V.; De Felice, D.; Soldovieri, M. V.; Mosca, I.; Gandolfi, F.; Brunelli, M.; Petris, G.; Cereseto, A.; Villarroel, A.; Thalmann, G.; Carbone, F. G.; Kruithof-de Julio, M.; Barbareschi, M.; Romanel, A.; Taglialatela, M.; Lunardi, A.
Cardiotoxic effects of antihistamines: From basics to clinics (... and back) 1-gen-2008 Soldovieri, Maria Virginia; Miceli, F; Taglialatela, Maurizio
Case report: Marked electroclinical improvement by fluoxetine treatment in a patient with KCNT1-related drug-resistant focal epilepsy 1-gen-2024 Mosca, Ilaria; Freri, Elena; Ambrosino, Paolo; Belperio, Giorgio; Granata, Tiziana; Canafoglia, Laura; Ragona, Francesca; Solazzi, Roberta; Filareto, Ilaria; Castellotti, Barbara; Messina, Giuliana; Gellera, Cinzia; Difrancesco, Jacopo C; Soldovieri, Maria Virginia; Taglialatela, Maurizio
Characterization of two de novo KCNT1 mutations in children with malignant migrating partial seizures in infancy 1-gen-2016 Rizzo, F; Ambrosino, P; Guacci, A; Chetta, M; Marchese, G; Rocco, T; Soldovieri, Mv; Manocchio, L; Mosca, I; Casara, G; Vecchi, Paolo Maria; Taglialatela, M; Coppola, G; Weisz, A
CORRELATING THE CLINICAL AND GENETIC FEATURES OF BENIGN FAMILIAL NEONATAL SEIZURES (BFNS) WITH THE FUNCTIONAL CONSEQUENCES OF THE UNDERLYING MUTATIONS 1-gen-2007 Soldovieri, Maria Virginia; Francesco, Miceli; Giulia, Bellini; Giangennaro, Coppola; Antonio, Pascotto; Taglialatela, Maurizio
Critical role of large-conductance calcium- and voltage-activated potassium channels in leptin-induced neuroprotection of N-methyl-d-aspartate-exposed cortical neurons. 1-gen-2014 Mancini, M; Soldovieri, Maria Virginia; Gessner, G; Wissuwa, B; Barrese, V; Boscia, F; Secondo, A; Miceli, F; Franco, C; Ambrosino, P; Canzoniero, Lm; Bauer, M; Hoshi, T; Heinemann, Sh; Taglialatela, Maurizio
De novo gain-of-function variants in KCNT2 as a novel cause of developmental and epileptic encephalopathy 1-gen-2018 Ambrosino, Paolo; Soldovieri, Maria Virginia; Bast, Thomas; Turnpenny, Peter D.; Uhrig, Sabine; Biskup, Saskia; Döcker, Miriam; Fleck, Thilo; Mosca, Ilaria; Manocchio, Laura; Iraci, Nunzio; Taglialatela, Maurizio; Lemke, Johannes R.
De novo variants in KCNA3 cause developmental and epileptic encephalopathy 1-gen-2024 Soldovieri, Maria Virginia; Ambrosino, Paolo; Mosca, Ilaria; Servettini, Ilenio; Pietrunti, Francesca; Belperio, Giorgio; Syrbe, Steffen; Taglialatela, Maurizio; Lemke, Johannes R