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Issue Date	Title	Author(s)
2014	Genetically induced dysfunctions of Kir2.1 channels : implications for short QT3 syndrome and autism-epilepsy phenotype	Ambrosini, Elena; Sicca, Federico; Brignone, Maria Stefania; D'Adamo, Maria Cristina; Napolitano, Carlo; Servettini, Ilenio; Moro, Francesca; Ruan, Yanfei; Guglielmi, Luca; Pieroni, Stefania; Servillo, Giuseppe; Lanciotti, Angela; Valvo, Giulia; Catacuzzeno, Luigi; Franciolini, Fabio; Molinari, Paola; Marchese, Maria; Grottesi, Alessandro; Guerrini, Renzo; Santorelli, Filippo Maria; Priori, Silvia Giuliana; Pessia, Mauro
2015	The role of ion channels in the hypoxia-induced aggressiveness of glioblastoma	Sforna, Luigi; Cenciarini, Marta; Belia, Silvia; D'Adamo, Maria Cristina; Pessia, Mauro; Franciolini, Fabio; Catacuzzeno, Luigi
2015	Novel phenotype associated with a mutation in the KCNA1(Kv1.1) gene	D'Adamo, Maria Cristina; Gallenmuller, Constanze; Servettini, Ilenio; Hartl, Elisabeth; Tucker, Stephen J.; Arning, Larissa; Biskup, Saskia; Grottesi, Alessandro; Guglielmi, Luca; Imbrici, Paola; Bernasconi, Pia; Di Giovanni, Giuseppe; Franciolini, Fabio; Catacuzzeno, Luigi; Pessia, Mauro; Klopstock, Thomas
2015	Reconciling the discrepancies on the involvement of large-conductance Ca2+-activated K channels in glioblastoma cell migration	Catacuzzeno, Luigi; Caramia, Martino; Sforna, Luigi; Belia, Silvia; Guglielmi, Luca; D'Adamo, Maria Cristina; Pessia, Mauro; Franciolini, Fabio
2016	Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy	Sicca, Federico; Ambrosini, Elena; Marchese, Maria; Sforna, Luigi; Servettini, Ilenio; Valvo, Giulia; Brignone, Maria Stefania; Lanciotti, Angela; Moro, Francesca; Grottesi, Alessandro; Catacuzzeno, Luigi; Baldini, Sara; Hasan, Sonia M.; D'Adamo, Maria Cristina; Franciolini, Fabio; Molinari, Paola; Santorelli, Filippo Maria; Pessia, Mauro
2013	K+ channelepsy : progress in the neurobiology of potassium channels and epilepsy	D'Adamo, Maria Cristina; Catacuzzeno, Luigi; Di Giovanni, Giuseppe; Franciolini, Fabio; 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