Showing results 29 to 44 of 44
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| Issue Date | Title | Author(s) |
| 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 |
| 1996 | Morphological and hemostatic changes in rats with abdominal arterial prosthesis | Chabielska, Ewa; Kolpakov, Valeri A.; D'Adamo, Maria Cristina; Curtis, Amalia de; Buczko, Wlodizimierz X.; Iacoviello, Licia; Donati, Maria Benedetta |
| 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 |
| 2015 | New insights into the pathogenesis and therapeutics of episodic ataxia type 1 | D'Adamo, Maria Cristina; Hasan, Sonia M.; Guglielmi, Luca; Servettini, Ilenio; Cenciarini, Marta; Catacuzzeno, Luigi; Franciolini, Fabio |
| 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 |
| 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 |
| 2017 | Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis | Romani, Luigina; Oikonomou, Vasilis; Moretti, Silvia; Iannitti, Rossana Giulietta; D'Adamo, Maria Cristina; Villella, Valeria Rachela; Pariano, Marilena; Sforna, Luigi; Borghi, Monica; Bellet, Marina M.; Fallarino, Francesca; Pallotta, Maria Teresa; Servillo, Giuseppe; Ferrari, Eleonora; Puccetti, P.; Kroemer, Guido; Pessia, Mauro; Maiuri, Luigi; Goldstein, Allan L.; Garaci, Enrico |
| 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 |
