Maria Virginia Soldovieri
Maria Virginia Soldovieri
Universitą degli Studi del Molise, Dipartimento di Medicina e di Scienze della Salute, Campobasso
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A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation
R Borgatti, C Zucca, A Cavallini, M Ferrario, C Panzeri, P Castaldo, ...
Neurology 63 (1), 57-65, 2004
Molecular pharmacology and therapeutic potential of neuronal Kv7-modulating drugs
F Miceli, MV Soldovieri, M Martire, M Taglialatela
Current opinion in pharmacology 8 (1), 65-74, 2008
Genotype–phenotype correlations in neonatal epilepsies caused by mutations in the voltage sensor of Kv7. 2 potassium channel subunits
F Miceli, MV Soldovieri, P Ambrosino, V Barrese, M Migliore, MR Cilio, ...
Proceedings of the National Academy of Sciences 110 (11), 4386-4391, 2013
Driving with no brakes: molecular pathophysiology of Kv7 potassium channels
MV Soldovieri, F Miceli, M Taglialatela
Physiology 26 (5), 365-376, 2011
Early-onset epileptic encephalopathy caused by gain-of-function mutations in the voltage sensor of Kv7. 2 and Kv7. 3 potassium channel subunits
F Miceli, MV Soldovieri, P Ambrosino, M De Maria, M Migliore, R Migliore, ...
Journal of Neuroscience 35 (9), 3782-3793, 2015
Activation and Desensitization of Trpv1 Channels in Sensory Neurons by the Peroxisome Proliferator-Activated Receptor α Agonist Palmitoylethanolamide.
P Ambrosino, M Soldovieri, C Russo, M Taglialatela
British journal of pharmacology, 2012
The ever changing moods of calmodulin: how structural plasticity entails transductional adaptability
A Villarroel, M Taglialatela, G Bernardo-Seisdedos, A Alaimo, J Agirre, ...
Journal of molecular biology 426 (15), 2717-2735, 2014
Novel KCNQ2 and KCNQ3 Mutations in a Large Cohort of Families with Benign Neonatal Epilepsy: First Evidence for an Altered Channel Regulation by Syntaxin‐1A
MV Soldovieri, N Boutry‐Kryza, M Milh, D Doummar, B Heron, E Bourel, ...
Human mutation 35 (3), 356-367, 2014
Human neoplastic mesothelial cells express voltage-gated sodium channels involved in cell motility
G Fulgenzi, L Graciotti, M Faronato, MV Soldovieri, F Miceli, S Amoroso, ...
The international journal of biochemistry & cell biology 38 (7), 1146-1159, 2006
Decreased subunit stability as a novel mechanism for potassium current impairment by a KCNQ2 C terminus mutation causing benign familial neonatal convulsions
MV Soldovieri, P Castaldo, L Iodice, F Miceli, V Barrese, G Bellini, ...
Journal of Biological Chemistry 281 (1), 418-428, 2006
A novel KCNQ2 K+ channel mutation in benign neonatal convulsions and centrotemporal spikes
G Coppola, P Castaldo, EM Del Giudice, G Bellini, F Galasso, ...
Neurology 61 (1), 131-134, 2003
Effects of natural and synthetic isothiocyanate-based H2S-releasers against chemotherapy-induced neuropathic pain: Role of Kv7 potassium channels
LDC Mannelli, E Lucarini, L Micheli, I Mosca, P Ambrosino, MV Soldovieri, ...
Neuropharmacology 121, 49-59, 2017
KCNQ2-related disorders
F Miceli, MV Soldovieri, N Joshi, S Weckhuysen, E Cooper, M Taglialatela
GeneReviews®[Internet], 2018
Expression, localization, and pharmacological role of Kv7 potassium channels in skeletal muscle proliferation, differentiation, and survival after myotoxic insults
FA Iannotti, E Panza, V Barrese, D Viggiano, MV Soldovieri, ...
Journal of Pharmacology and Experimental Therapeutics 332 (3), 811-820, 2010
A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability
F Miceli, P Striano, MV Soldovieri, A Fontana, R Nardello, A Robbiano, ...
Epilepsia 56 (2), e15-e20, 2015
Neuronal potassium channel openers in the management of epilepsy: role and potential of retigabine
V Barrese, F Miceli, MV Soldovieri, P Ambrosino, FA Iannotti, MR Cilio, ...
Clinical pharmacology: advances and applications 2, 225, 2010
Expression and function of Kv7. 4 channels in rat cardiac mitochondria: possible targets for cardioprotection
L Testai, V Barrese, MV Soldovieri, P Ambrosino, A Martelli, I Vinciguerra, ...
Cardiovascular research 110 (1), 40-50, 2016
Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S4 region of KCNQ2 causing benign familial neonatal convulsions
MV Soldovieri, MR Cilio, F Miceli, G Bellini, EM Del Giudice, P Castaldo, ...
Journal of Neuroscience 27 (18), 4919-4928, 2007
Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain‐of‐function variant
JJ Millichap, F Miceli, M De Maria, C Keator, N Joshi, B Tran, ...
Epilepsia 58 (1), e10-e15, 2017
Characterization of two de novo KCNT1 mutations in children with malignant migrating partial seizures in infancy
F Rizzo, P Ambrosino, A Guacci, M Chetta, G Marchese, T Rocco, ...
Molecular and Cellular Neuroscience 72, 54-63, 2016
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