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Maria Virginia Soldovieri

Observed names: M. V. Soldovieri, M.V. Soldovieri, Maria Soldovieri, Maria V. Soldovieri, SOLDOVIERI MV, Soldovieri M. V., Soldovieri Maria Virginia, Soldovieri, Maria Virginia, Virginia Soldovieri
Observed institutions: University of Messina, University of Copenhagen, University of Molise, University of Milan, University of Campania "Luigi Vanvitelli", IRCCS Eugenio Medea, University of Naples Federico II
ORCID: 0000-0002-3601-9374
Observed ORCID: 0000-0002-3601-9374
OpenAlex ID: A5031203360
Early-Onset Epileptic Encephalopathy Caused by Gain-of-Function Mutations in the Voltage Sensor of K v 7.2 and K v 7.3 Potassium Channel Subunits
2015 · Francesco Miceli, Maria Virginia Soldovieri, et al. · Journal of Neuroscience · 198
Genotype–phenotype correlations in neonatal epilepsies caused by mutations in the voltage sensor of K v 7.2 potassium channel subunits
2013 · Francesco Miceli, Maria Virginia Soldovieri, et al. · Proceedings of the National Academy of Sciences · 191
Driving With No Brakes: Molecular Pathophysiology of Kv7 Potassium Channels
2011 · Maria Virginia Soldovieri, Francesco Miceli, et al. · Physiology · 173
Molecular pharmacology and therapeutic potential of neuronal Kv7-modulating drugs
2007 · Francesco Miceli, Maria Virginia Soldovieri, et al. · Current Opinion in Pharmacology · 162
A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation
2004 · R. Borgatti, C. Zucca, et al. · Neurology · 157
Activation and desensitization of TRPV1 channels in sensory neurons by the PPARα agonist palmitoylethanolamide
2012 · Paolo Ambrosino, Maria Virginia Soldovieri, et al. · British Journal of Pharmacology · 146
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Effects of natural and synthetic isothiocyanate-based H 2 S-releasers against chemotherapy-induced neuropathic pain: Role of Kv7 potassium channels
2017 · Lorenzo Di Cesare Mannelli, Elena Lucarini, et al. · Neuropharmacology · 118
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Autism and developmental disability caused by KCNQ3 gain‐of‐function variants
2019 · Tristan T. Sands, Francesco Miceli, et al. · Annals of Neurology · 116
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Epileptic channelopathies caused by neuronal Kv7 (KCNQ) channel dysfunction
2020 · Piera Nappi, Francesco Miceli, et al. · Pflügers Archiv - European Journal of Physiology · 111
Characterization of two de novo KCNT1 mutations in children with malignant migrating partial seizures in infancy
2016 · Francesca Rizzo, Paolo Ambrosino, et al. · Molecular and Cellular Neuroscience · 110
Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain‐of‐function variant
2016 · John J. Millichap, Francesco Miceli, et al. · Epilepsia · 105
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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
2013 · Maria Virginia Soldovieri, Nadia Boutry-Kryza, et al. · Human Mutation · 100
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The Ever Changing Moods of Calmodulin: How Structural Plasticity Entails Transductional Adaptability
2014 · Alvaro Villarroel, Maurizio Taglialatela, et al. · Journal of Molecular Biology · 98
Early Treatment with Quinidine in 2 Patients with Epilepsy of Infancy with Migrating Focal Seizures (EIMFS) Due to Gain-of-Function KCNT1 Mutations: Functional Studies, Clinical Responses, and Critical Issues for Personalized Therapy
2018 · Robertino Dilena, Jacopo C. DiFrancesco, et al. · Neurotherapeutics · 90
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A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability
2014 · Francesco Miceli, Pasquale Striano, et al. · Epilepsia · 87
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Expression and function of Kv7.4 channels in rat cardiac mitochondria: possible targets for cardioprotection
2015 · Lara Testai, Vincenzo Barrese, et al. · Cardiovascular Research · 80
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Expression, Localization, and Pharmacological Role of Kv7 Potassium Channels in Skeletal Muscle Proliferation, Differentiation, and Survival after Myotoxic Insults
2009 · Fabio Arturo Iannotti, Elisabetta Panza, et al. · Journal of Pharmacology and Experimental Therapeutics · 73
Decreased Subunit Stability as a Novel Mechanism for Potassium Current Impairment by a KCNQ2 C Terminus Mutation Causing Benign Familial Neonatal Convulsions
2005 · Maria Virginia Soldovieri, Pasqualina Castaldo, et al. · Journal of Biological Chemistry · 69
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Human neoplastic mesothelial cells express voltage-gated sodium channels involved in cell motility
2006 · Gianluca Fulgenzi, Laura Graciotti, et al. · The International Journal of Biochemistry & Cell Biology · 64
A novel KCNQ2 K + channel mutation in benign neonatal convulsions and centrotemporal spikes
2003 · G. Coppola, P. Castaldo, et al. · Neurology · 64
Early-onset epileptic encephalopathy caused by a reduced sensitivity of Kv7.2 potassium channels to phosphatidylinositol 4,5-bisphosphate
2016 · Maria Virginia Soldovieri, Paolo Ambrosino, et al. · Scientific Reports · 51
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Atypical Gating Of M-Type Potassium Channels Conferred by Mutations in Uncharged Residues in the S4Region of KCNQ2 Causing Benign Familial Neonatal Convulsions
2007 · Maria Virginia Soldovieri, Maria Roberta Cilio, et al. · Journal of Neuroscience · 51
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Epilepsy-causing mutations in Kv7.2 C-terminus affect binding and functional modulation by calmodulin
2015 · Paolo Ambrosino, Alessandro Alaimo, et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 49
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Pharmacological Targeting of Neuronal Kv7.2/3 Channels: A Focus on Chemotypes and Receptor Sites
2017 · Francesco Miceli, Maria V. Soldovieri, et al. · Current Medicinal Chemistry · 48
De novo gain‐of‐function variants in KCNT2 as a novel cause of developmental and epileptic encephalopathy
2018 · Paolo Ambrosino, Maria Virginia Soldovieri, et al. · Annals of Neurology · 47
Works count: 102
Citation count: 3,589
H-index: 35
I10-index: 61
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