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| Issue Date | Title | Author(s) |
| 2013 | 5-HT2 receptors-mediated modulation of voltage-gated K+ channels and neurophysiopathological correlates | D'Adamo, Maria Cristina; Servettini, Ilenio; Guglielmi, Luca; Di Matteo, Vincenzo; Di Maio, Roberto; Di Giovanni, Giuseppe; Pessia, Mauro |
| 2023 | An activator of voltage-gated K+ channels Kv1.1 as a therapeutic candidate for episodic ataxia type 1 | Servettini, Ilenio; Talani, Giuseppe; Megaro, Alfredo; Setzu, Maria Dolores; Biggio, Francesca; Briffa, Michelle; Guglielmi, Luca; Savalli, Nicoletta; Binda, Francesca; Delicata, Francis; Bru–Mercier, Gilles; Vassallo, Neville; Maglione, Vittorio; Cauchi, Ruben J.; Di Pardo, Alba; Colluc, Maria; Imbrici, Paola; Catacuzzeno, Luigi; D’Adamo, Maria Cristina; Olcese, Riccardo; Pessia, Mauro |
| 2015 | Animal models of episodic ataxia type 1 (EA1) | D'Adamo, Maria Cristina; Di Giovanni, Giuseppe; Pessia, Mauro |
| 2020-12 | Autism spectrum disorder | Mubashir, Sana; Farrugia, Matthias; Coretti, Lorena; Pessia, Mauro; D’Adamo, Maria Cristina |
| 2011 | Autism with seizures and intellectual disability : possible causative role of gain-of-function of the inwardly-rectifying K + channel Kir4.1 | Sicca, Federico; Imbrici, Paola; D'Adamo, Maria Cristina; Moro, Francesca; Bonatti, Fabrizia; Brovedani, Paola; Grottesi, Alessandro; Guerrini, Renzo; Masi, Gabriele; Santorelli, Filippo Maria; Pessia, Mauro |
| 2016 | A Calsequestrin-1 mutation associated with a skeletal muscle disease alters sarcoplasmic Ca2+ release | D'Adamo, Maria Cristina; Sforna, Luigi; Visentin, Sergio; Grottesi, Alessandro; Servettini, Ilenio; Guglielmi, Luca; Macchioni, Lara; Saredi, Simona; Curcio, Maurizio; Nuccio, Chiara de; Hasan, Sonia M.; Corazzi, L.; Franciolini, Fabio; Mora, Marina; Catacuzzeno, Luigi; Pessia, Mauro |
| 2017 | A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia | Hasan, Sonia M.; Bove, Cecilia; Silvestri, Gabriella; Mantuano, Elide; Modoni, Anna; Veneziano, Liana; Macchioni, Lara; Hunter, Therese; Hunter, Gary J.; Pessia, Mauro; D'Adamo, Maria Cristina |
| 2018 | Commentary : a channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia | Hasan, Sonia; Hunter, Therese; Hunter, Gary; Pessia, Mauro; D'Adamo, Maria Cristina |
| 2009 | Contributions of the central hydrophobic residue in the PXP motif of voltage-dependent K+ channels to S6 flexibility and gating properties | Imbrici, Paola; Grottesi, Alessandro; D'Adamo, Maria Cristina; Tucker, Stephen J.; Pessia, Mauro |
| 2019 | Dexamethasone in glioblastoma multiforme therapy : mechanisms and controversies | Cenciarini, Marta; Valentino, Mario; Belia, Silvia; Sforna, Luigi; Rosa, Paolo; Ronchetti, Simona; D’Adamo, Maria Cristina; Pessia, Mauro |
| 2021 | Dexamethasone in Glioblastoma multiforme therapy : mechanisms and controversies | Cenciarini, Marta; Valentino, Mario; Belia, Silvia; Sforna, Luigi; Rosa, Paolo; Ronchetti, Simona; D’Adamo, Maria Cristina; Pessia, Mauro |
| 2001 | Differential pH sensitivity of Kir4.1 and Kir4.2 potassium channels and their modulation by heteropolymerisation with Kir5.1 | Pessia, Mauro; Imbrici, Paola; D'Adamo, Maria Cristina; Salvatore, Lorena; Tucker, Stephen J. |
| 2012 | Dysfunction of voltage-gated K + Channels Kv1.1 in sciatic nerve causes spontaneous and stress-induced neuromuscular hyperexcitability | Brunetti, Orazio; Imbrici, Paola; Botti, Fabio Massimo; Pettorossi, Vito Enrico; D’Adamo, Maria Cristina; Valentino, Mario; Zammit, Christian; Mora, Marina; Di Giovanni, Giuseppe; Muscat, Richard; Pessia, Mauro |
| 2020 | Electromechanical coupling of the Kv1.1 voltage-gated K+ channel is fine-tuned by the simplest amino acid residue in the S4-S5 linker | Hasan, Sonia; Megaro, Alfredo; Cenciarini, Marta; Coretti, Lorena; Botti, Fabio Massimo; Imbrici, Paola; Steinbusch, Harry W. M.; Hunter, Therese; Hunter, Gary; Pessia, Mauro; D’Adamo, Maria Cristina |
| 2011 | The emerging role of the inwardly rectifying K+ channels in autism spectrum disorders and epilepsy | D’Adamo, Maria Cristina; Moro, Francesca; Imbrici, Paola; Martino, Dianda; Roscini, Mauro; Santorelli, Filippo Maria; Sicca, Federico; Pessia, Mauro |
| 2012 | Episodic ataxia type 1 | D'Adamo, Maria Cristina; Hanna, Michael G.; Di Giovanni, Giuseppe; Pessia, Mauro |
| 2007 | Episodic ataxia type 1 mutation F184C alters Zn2+-induced modulation of the human K+ channel Kv1.4-Kv1.1/Kvβ1.1 | Imbrici, Paola; D'Adamo, Maria Cristina; Cusimano, Antonella; Pessia, Mauro |
| 2011 | Episodic ataxia type 1 mutations affect fast inactivation of K + channels by a reduction in either subunit surface expression or affinity for inactivation domain | Imbrici, Paola; D'Adamo, Maria Cristina; Grottesi, Alessandro; Biscarini, Andrea; Pessia, Mauro |
| 2006 | Episodic ataxia type 1 mutations in the KCNA1 gene impair the fast inactivation properties of the human potassium channels Kv1.4-1.1/Kvβ1.1 and Kv1.4-1.1/Kvβ1.2 | Imbrici, Paola; D'Adamo, Maria Cristina; Kullmann, Dimitri M.; Pessia, Mauro |
| 2004 | An episodic ataxia type-1 mutation in the S1 segment sensitises the hKv1.1 potassium channel to extracellular Zn2+ | Cusimano, Antonella; D'Adamo, Maria Cristina; Pessia, Mauro |
