Showing results 28 to 47 of 48
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Issue Date | Title | Author(s) |
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 | KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability | Kaya, Namik; Alsagob, Maysoon; D'Adamo, Maria Cristina; Al-Bakheet, Albandary Bandary; Hasan, Sonia M.; Muccioli, Maria; Almutairi, Faten B.; Almass, Rawan; Aldosary, Mazhor S.; Monies, Dorota Marta; Mustafa, Osama M.; Alyounes, Banan; Kenana, Rosan; Al-Zahrani, Jawaher; Naim, Ewa A.; Binhumaid, Faisal S.; Qari, Alya A.; Almutairi, Fatema; Meyer, Brian Francis; Plageman, Timothy F.; Pessia, Mauro; Colak, Dilek; Al-Owain, Mohammed A. |
2011 | The Kir5.1 potassium channel is an important determinant of neuronal PCO2/pH sensitivity | D'Adamo, Maria Cristina; Shang, Lijun; Imbrici, Paola; Brown, Steve D. M.; Pessia, Mauro; Tucker, Stephen J. |
2012 | Kv1.1 knock-in ataxic mice exhibit spontaneous myokymic activity exacerbated by fatigue, ischemia and low temperature | Brunetti, Orazio; Imbrici, Paola; Botti, Fabio Massimo; Pettorossi, Vito Enrico; D'Adamo, Maria Cristina; Valentino, Mario; Zammit, Christian; Mora, Marina; Gibertini, Sara; Di Giovanni, Giuseppe; Muscat, Richard; Pessia, Mauro |
2017 | Lethal digenic mutations in the K+ 1 channels Kir4.1 (KCNJ10) and SLACK 2 (KCNT1) associated with severe-disabling seizures and neurodevelopmental delay | Hasan, Sonia M.; Balobaid, Ameera; Grottesi, Alessandro; Dabbagh, Omar; Cenciarini, Marta; Rawashdeh, Rifaat; Al-Sagheir, Afaf; Bove, Cecilia; Macchioni, Lara; Pessia, Mauro; Al-Owain, Mohammed A.; D'Adamo, Maria Cristina |
1999 | Localization and age-dependent expression of the inward rectifier K+ channel subunit Kir 5.1 in a mammalian reproductive system | Salvatore, Lorena; D'Adamo, Maria Cristina; Polishchuk, Roman S.; Salmona, Mario; Pessia, Mauro |
2014 | A method to identify tissue cell subpopulations with distinct multi-molecular profiles from data on co-localization of two markers at a time : the case of sensory ganglia | Catacuzzeno, Luigi; Sforna, Luigi; D'Adamo, Maria Cristina; Pessia, Mauro; Franciolini, Fabio |
1999 | Mutations in the KCNA1 gene associated with episodic ataxia type-1 syndrome impair heteromeric voltage-gated K+ channel function | D'Adamo, Maria Cristina; Imbrici, Paola; Sponcichetti, Fabio; Pessia, Mauro |
2008 | A novel KCNA1 mutation identified in an Italian family affected by episodic ataxia type 1 | Imbrici, Paola; Gualandi, Francesca; D'Adamo, Maria Cristina; Masieri, Marina Taddei; Cudia, Paola; De Grandis, Domenico; Mannucci, Roberta; Nicoletti, Ildo; Tucker, Stephen J.; Ferlini, Alessandra; Pessia, Mauro |
2017 | A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctions | Imbrici, Paola; Altamura, Concetta; Gualandi, Francesca; Felice Mangiatordi, Giuseppe; Neri, Marcella; De Maria, Giovanni; Ferlini, Alessandra; Padovani, Alessandro; D'Adamo, Maria Cristina; Nicolotti, Orazio; Pessia, Mauro; Conte, Diana; Filosto, Massimiliano; Desaphy, Jean-Francois |
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 | 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. |
2000 | pH dependence of the inwardly rectifying potassium channel, Kir5.1, and localization in renal tubular epithelia | Tucker, Stephen J.; Imbrici, Paola; Salvatore, Lorena; D'Adamo, Maria Cristina; Pessia, Mauro |
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 |
2012 | Redox sensitivity of tyrosine hydroxylase activity and expression in dopaminergic dysfunction | Di Giovanni, Giuseppe; Pessia, Mauro; Di Maio, Roberto |
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 |
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 |
2013 | The role of serotonergic system at the interface of aggression and suicide | Bortolato, Marco; Pivac, Nela; Muck-Seler, Dorotea; Nikolac Perkovic, Matea; Pessia, Mauro; Di Giovanni, Giuseppe |
2014 | Role(s) of the 5-HT2C receptor in the development of maximal dentate activation in the hippocampus of anesthetized rats | Orban, Gergely; Bombardi, Cristiano; Marino Gammazza, Antonella; Colangeli, Roberto; Pierucci, Massimo; Pomara, Cristoforo; Pessia, Mauro; Bucchieri, Fabio; Arcangelo, Benigno; Smolders, Ilse J.; De Deurwaerdère, Philippe; Di Giovanni, Giuseppe |
2012 | Serotonin-dopamine interaction in nicotine addiction: focus on 5-ht2c receptors | Esposito, Ennio; Di Matteo, Vincenzo; Pierucci, Massimo; Benigno, Arcangelo; Pessia, Mauro; Pitruzzella, Alessandro; Zammit, Christian; Valentino, Mario; Muscat, Richard; Di Giovanni, Giuseppe |