Sfoglia per Titolo
PROYECTO SOCIOPOLIS, eco-viviendas sociales.
2003-01-01 GAUSA NAVARRO, Manuel
Proyectos para la diagonal: una reflexión critica 1989
1989-01-01 GAUSA NAVARRO, Manuel; Marta, Cervelló
Pròtesis Parcial Removible
2000-01-01 G., Preti; Pera, Paolo
Prólogo
2013-01-01 Guastini, Riccardo
Prólogo
2017-01-01 Grondona, M.; Benedetti, A. M.
Prólogo
2019-01-01 Scudieri, Laura; Guaglianone, Luciana; Escudero, Ricardo
Prólogo a la setima edición
2013-01-01 Grondona, Mauro
Prólogo a la sexta edición
2012-01-01 Ferrando, Gilda
PRRT2 controls neuronal excitability by negatively modulating Na+ channel 1.2/1.6 activity
2018-01-01 Fruscione, F; Valente, P; Sterlini, B; Romei, A; Baldassari, S; Fadda, M; Prestigio, C; Giansante, G; Sartorelli, J; Rossi, P; Rubio, A; Gambardella, A; Nieus, T; Broccoli, V; Fassio, A; Baldelli, P; Corradi, A; Zara, F; Benfenati, F.
PRRT2 Is a Key Component of the Ca2+-Dependent Neurotransmitter Release Machinery
2016-01-01 Valente, Pierluigi; Castroflorio, Enrico; Rossi, Pia; Fadda, Manuela; Sterlini, Bruno; Cervigni, Romina Ines; Prestigio, Cosimo; Giovedi', Silvia; Onofri, Franco; Mura, Elisa; Guarnieri, Fabrizia C.; Marte, Antonella; Orlando, Marta; Zara, Federico; Fassio, Anna; Valtorta, Flavia; Baldelli, Pietro; Corradi, ANNA MARGHERITA; Benfenati, Fabio
PRRT2 is mutated in familial and non-familial benign infantile seizures
2013-01-01 Specchio, N.; Terracciano, A.; Trivisano, M.; Cappelletti, S.; Claps, D.; Travaglini, L.; Cusmai, R.; Marras, C. E.; Zara, F.; Fusco, L.; Bertini, E.; Vigevano, F.
The PRRT2 knockout mouse recapitulates the neurological diseases associated with PRRT2 mutations.
2017-01-01 Michetti, C; Castroflorio, Enrico; Marchionni, I; Forte, N; Sterlini, Bruno; Binda, F; Fruscione, F; Baldelli, Pietro; Valtorta, F; Zara, F; Corradi, ANNA MARGHERITA; Benfenati, Fabio
PRRT2 modulates presynaptic Ca2+ influx by interacting with P/Q-type channels
2021-01-01 Ferrante, D.; Sterlini, B.; Prestigio, C.; Marte, A.; Corradi, A.; Onofri, F.; Tortarolo, G.; Vicidomini, G.; Petretto, A.; Muia, J.; Thalhammer, A.; Valente, P.; Cingolani, L. A.; Benfenati, F.; Baldelli, P.
PRRT2 Mutations are the major cause of benign familial infantile seizures
2012-01-01 Schubert, J; Paravidino, R; Becker, F; Berger, A; Bebek, N; Bianchi, A; Brockmann, K; Capovilla, G; Bernardina, Bd; Fukuyama, Y; Hoffmann, Gf; Jurkat Rott, K; Antonnen, Ak; Kurlemann, G; Lehesjoki, Ae; Lehmann Horn, F; Mastrangelo, M; Mause, U; Müller, S; Neubauer, B; Püst, B; Rating, D; Robbiano, A; Ruf, S; Schroeder, C; Seidel, A; Specchio, N; Stephani, U; Striano, Pasquale; Teichler, J; Turkdogan, D; Vigevano, F; Viri, M; Bauer, P; Zara, F; Lerche, H; Weber, Y. G.
PRRT2 Regulates Synaptic Fusion by Directly Modulating SNARE Complex Assembly
2018-01-01 Coleman, J.; Jouannot, O.; Ramakrishnan, S. K.; Zanetti, M. N.; Wang, J.; Salpietro, V.; Houlden, H.; Rothman, J. E.; Krishnakumar, S. S.
PRRT2, a network stability gene
2017-01-01 Michetti, C; Corradi, ANNA MARGHERITA; Benfenati, Fabio
PRRT2-Na+ CHANNELS INTERACTION: PATHOGENETIC BASIS OF PRRT2-ASSOCIATED PAROXYSMAL DISORDERS AND NEW THERAPEUTIC STRATEGIES
2023-04-26 Franchi, Francesca
PRRT2-related disorders: further PKD and ICCA cases and review of the literature.
2013-01-01 Becker, F; Schubert, J; Striano, Pasquale; Anttonen, Ak; Liukkonen, E; Gaily, E; Gerloff, C; Müller, S; Heußinger, N; Kellinghaus, C; Robbiano, A; Polvi, A; Zittel, S; von Oertzen, Tj; Rostasy, K; Schöls, L; Warner, T; Münchau, A; Lehesjoki, Ae; Zara, F; Lerche, H; Weber, Yg
PRRT2: A major cause of infantile epilepsy and other paroxysmal disorders of childhood
2014-01-01 Nobile, Carlo; Striano, Pasquale
PRRT2: from Paroxysmal Disorders to Regulation of Synaptic Function.
2016-01-01 Valtorta, F; Benfenati, F; Zara, F; Meldolesi, J
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| PROYECTO SOCIOPOLIS, eco-viviendas sociales. | 1-gen-2003 | GAUSA NAVARRO, Manuel | |
| Proyectos para la diagonal: una reflexión critica 1989 | 1-gen-1989 | GAUSA NAVARRO, Manuel; Marta, Cervelló | |
| Pròtesis Parcial Removible | 1-gen-2000 | G., Preti; Pera, Paolo | |
| Prólogo | 1-gen-2013 | Guastini, Riccardo | |
| Prólogo | 1-gen-2017 | Grondona, M.; Benedetti, A. M. | |
| Prólogo | 1-gen-2019 | Scudieri, Laura; Guaglianone, Luciana; Escudero, Ricardo | |
| Prólogo a la setima edición | 1-gen-2013 | Grondona, Mauro | |
| Prólogo a la sexta edición | 1-gen-2012 | Ferrando, Gilda | |
| PRRT2 controls neuronal excitability by negatively modulating Na+ channel 1.2/1.6 activity | 1-gen-2018 | Fruscione, F; Valente, P; Sterlini, B; Romei, A; Baldassari, S; Fadda, M; Prestigio, C; Giansante, G; Sartorelli, J; Rossi, P; Rubio, A; Gambardella, A; Nieus, T; Broccoli, V; Fassio, A; Baldelli, P; Corradi, A; Zara, F; Benfenati, F. | |
| PRRT2 Is a Key Component of the Ca2+-Dependent Neurotransmitter Release Machinery | 1-gen-2016 | Valente, Pierluigi; Castroflorio, Enrico; Rossi, Pia; Fadda, Manuela; Sterlini, Bruno; Cervigni, Romina Ines; Prestigio, Cosimo; Giovedi', Silvia; Onofri, Franco; Mura, Elisa; Guarnieri, Fabrizia C.; Marte, Antonella; Orlando, Marta; Zara, Federico; Fassio, Anna; Valtorta, Flavia; Baldelli, Pietro; Corradi, ANNA MARGHERITA; Benfenati, Fabio | |
| PRRT2 is mutated in familial and non-familial benign infantile seizures | 1-gen-2013 | Specchio, N.; Terracciano, A.; Trivisano, M.; Cappelletti, S.; Claps, D.; Travaglini, L.; Cusmai, R.; Marras, C. E.; Zara, F.; Fusco, L.; Bertini, E.; Vigevano, F. | |
| The PRRT2 knockout mouse recapitulates the neurological diseases associated with PRRT2 mutations. | 1-gen-2017 | Michetti, C; Castroflorio, Enrico; Marchionni, I; Forte, N; Sterlini, Bruno; Binda, F; Fruscione, F; Baldelli, Pietro; Valtorta, F; Zara, F; Corradi, ANNA MARGHERITA; Benfenati, Fabio | |
| PRRT2 modulates presynaptic Ca2+ influx by interacting with P/Q-type channels | 1-gen-2021 | Ferrante, D.; Sterlini, B.; Prestigio, C.; Marte, A.; Corradi, A.; Onofri, F.; Tortarolo, G.; Vicidomini, G.; Petretto, A.; Muia, J.; Thalhammer, A.; Valente, P.; Cingolani, L. A.; Benfenati, F.; Baldelli, P. | |
| PRRT2 Mutations are the major cause of benign familial infantile seizures | 1-gen-2012 | Schubert, J; Paravidino, R; Becker, F; Berger, A; Bebek, N; Bianchi, A; Brockmann, K; Capovilla, G; Bernardina, Bd; Fukuyama, Y; Hoffmann, Gf; Jurkat Rott, K; Antonnen, Ak; Kurlemann, G; Lehesjoki, Ae; Lehmann Horn, F; Mastrangelo, M; Mause, U; Müller, S; Neubauer, B; Püst, B; Rating, D; Robbiano, A; Ruf, S; Schroeder, C; Seidel, A; Specchio, N; Stephani, U; Striano, Pasquale; Teichler, J; Turkdogan, D; Vigevano, F; Viri, M; Bauer, P; Zara, F; Lerche, H; Weber, Y. G. | |
| PRRT2 Regulates Synaptic Fusion by Directly Modulating SNARE Complex Assembly | 1-gen-2018 | Coleman, J.; Jouannot, O.; Ramakrishnan, S. K.; Zanetti, M. N.; Wang, J.; Salpietro, V.; Houlden, H.; Rothman, J. E.; Krishnakumar, S. S. | |
| PRRT2, a network stability gene | 1-gen-2017 | Michetti, C; Corradi, ANNA MARGHERITA; Benfenati, Fabio | |
| PRRT2-Na+ CHANNELS INTERACTION: PATHOGENETIC BASIS OF PRRT2-ASSOCIATED PAROXYSMAL DISORDERS AND NEW THERAPEUTIC STRATEGIES | 26-apr-2023 | Franchi, Francesca | |
| PRRT2-related disorders: further PKD and ICCA cases and review of the literature. | 1-gen-2013 | Becker, F; Schubert, J; Striano, Pasquale; Anttonen, Ak; Liukkonen, E; Gaily, E; Gerloff, C; Müller, S; Heußinger, N; Kellinghaus, C; Robbiano, A; Polvi, A; Zittel, S; von Oertzen, Tj; Rostasy, K; Schöls, L; Warner, T; Münchau, A; Lehesjoki, Ae; Zara, F; Lerche, H; Weber, Yg | |
| PRRT2: A major cause of infantile epilepsy and other paroxysmal disorders of childhood | 1-gen-2014 | Nobile, Carlo; Striano, Pasquale | |
| PRRT2: from Paroxysmal Disorders to Regulation of Synaptic Function. | 1-gen-2016 | Valtorta, F; Benfenati, F; Zara, F; Meldolesi, J |
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