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Issue Date	Title	Author(s)
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
2003	Identification of a heteromeric interaction that influences the rectification, gating, and pH sensitivity of Kir4.1/Kir5.1 potassium channels	Casamassima, Maria; D'Adamo, Maria Cristina; Pessia, Mauro; Tucker, Stephen J.
1992	Different response of vascular fibrinolysis to adrenergic stimulation in young and aged rats	Iacoviello, Licia; D'Adamo, Maria Cristina; Curtis, Amalia de; Donati, Maria Benedetta
2015	Update on the implication of potassium channels in autism : K+ channelautism spectrum disorder	Luca, Giovanni; Ilenio, Servettini; Martino, Caramia; Luigi, Catacuzzeno; Fabio, Franciolini; D'Adamo, Maria Cristina; Mauro, Pessia
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
2002	Expression in E. coli and purification of recombinant fragments of wild type and mutant human prion protein	Corsaro, A.; Thellung, Stefano; Russo, Claudio; Villa, Valentina; Arena, Sara; D'Adamo, Maria Cristina; Paludi, Domenico; Rossi Principe, D.; Damonte, Gianluca L.; Benatti, Umberto; Aceto, Antonio; Tagliavini, Fabrizio; Schettini, Gennaro; Florio, Tullio
2000	Role of receptor protein tyrosine phosphatase α (RPTPα) and tyrosine phosphorylation in the serotonergic inhibition of voltage-dependent potassium channels	Imbrici, Paola; Tucker, Stephen J.; D'Adamo, Maria Cristina; Pessia, Mauro
2015	De novo point mutations in patients diagnosed with ataxic cerebral palsy	Parolin Schnekenberg, Ricardo; Perkins, Emma M.; Miller, Jack W.; Davies, Wayne L.; D'Adamo, Maria Cristina; Pessia, Mauro; Fawcett, Katherine A.; Sims, David; Gillard, Elodie; Hudspith, Karl A. Z.; Skehel, Paul A.; Williams, Jonathan; O'Regan, Mary E.; Jayawant, Sandeep S.; Jefferson, Rosalind J.; Hughes, Sarah M.; Lustenberger, Andrea; Ragoussis, Jiannis; Jackson, Mandy; Tucker, Stephen J.; Nemeth, Andrea H.
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