| 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 | 196 | 2013 |
| Driving with no brakes: molecular pathophysiology of Kv7 potassium channels MV Soldovieri, F Miceli, M Taglialatela Physiology 26 (5), 365-376, 2011 | 185 | 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 | 180 | 2015 |
| 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 | 176 | 2008 |
| Vasorelaxation by hydrogen sulphide involves activation of Kv7 potassium channels A Martelli, L Testai, MC Breschi, K Lawson, NG McKay, F Miceli, ... Pharmacological research 70 (1), 27-34, 2013 | 140 | 2013 |
| 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 | 118 | 2014 |
| KCNQ2-related disorders F Miceli, MV Soldovieri, S Weckhuysen, E Cooper, M Taglialatela | 97 | 2022 |
| 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 | 94 | 2017 |
| 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 | 92 | 2015 |
| Autism and developmental disability caused by KCNQ3 gain‐of‐function variants TT Sands, F Miceli, G Lesca, AE Beck, LG Sadleir, DK Arrington, ... Annals of neurology 86 (2), 181-192, 2019 | 88 | 2019 |
| 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 | 88 | 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 | 83 | 2006 |
| 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 | 81 | 2016 |
| Coupling between the voltage-sensing and phosphatase domains of Ci-VSP CA Villalba-Galea, F Miceli, M Taglialatela, F Bezanilla Journal of General Physiology 134 (1), 5-14, 2009 | 76 | 2009 |
| Epileptic channelopathies caused by neuronal Kv7 (KCNQ) channel dysfunction P Nappi, F Miceli, MV Soldovieri, P Ambrosino, V Barrese, M Taglialatela Pflügers Archiv-European Journal of Physiology 472, 881-898, 2020 | 73 | 2020 |
| IKs channels open slowly because KCNE1 accessory subunits slow the movement of S4 voltage sensors in KCNQ1 pore-forming subunits KJ Ruscic, F Miceli, CA Villalba-Galea, H Dai, Y Mishina, F Bezanilla, ... Proceedings of the National Academy of Sciences 110 (7), E559-E566, 2013 | 68 | 2013 |
| 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, 225-236, 2010 | 68 | 2010 |
| 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 | 66 | 2007 |
| A novel hyperekplexia-causing mutation in the pre-transmembrane segment 1 of the human glycine receptor α1 subunit reduces membrane expression and impairs gating by agonists P Castaldo, P Stefanoni, F Miceli, G Coppola, EM Del Giudice, G Bellini, ... Journal of Biological Chemistry 279 (24), 25598-25604, 2004 | 63 | 2004 |
| Involvement of KCNQ2 subunits in [3H]dopamine release triggered by depolarization and pre‐synaptic muscarinic receptor activation from rat striatal synaptosomes M Martire, M D’Amico, E Panza, F Miceli, D Viggiano, F Lavergata, ... Journal of neurochemistry 102 (1), 179-193, 2007 | 62 | 2007 |
