Sfoglia per Autore
Progressive epileptic encephalopathy associated with a novel HCN2 mutation
2019 Binda, A; Murano, C; DI FRANCESCO, J; Castellotti, B; Milanesi, R; Ragona, F; Freri, E; Canafoglia, L; Franceschetti, S; Solazzi, R; Granata, T; Gellera, C; Rivolta, I
HCN ion channels and accessory proteins in epilepsy: genetic analysis of a large cohort of patients and review of the literature
2019 Difrancesco, J; Castellotti, B; Milanesi, R; Ragona, F; Freri, E; Canafoglia, L; Franceschetti, S; Ferrarese, C; Magri, S; Taroni, F; Costa, C; Labate, A; Gambardella, A; Solazzi, R; Binda, A; Rivolta, I; Di Gennaro, G; Casciato, S; D'Incerti, L; Barbuti, A; Difrancesco, D; Granata, T; Gellera, C
Two novel SCN5A loss-of-function mutations affect patients with severe arrhytmogenic syndromes
2019 Murano, C; Binda, A; Lucano, D; Micaglio, E; Ciconte, G; Ghiroldi, A; Anastasia, L; Pappone, C; Rivolta, I
HCN1 novel mutations in familiar generalized epilepsy
2018 Binda, A; Murano, C; Granata, T; Ragona, F; Freri, E; Franceschetti, S; Canafoglia, L; Castellotti, B; Gellere, C; Milanesi, R; Difrancesco, J; Rivolta, I
Functional studies of a novel copy number deletion in GSTM3 gene associated with increase of ventricular arrhythmia in patients with Brugada syndrome and ICD implantation
2018 Juang, J; Lu, T; Chen, C; Lin, L; Hwang, J; Lai, L; Rivolta, I; Chiang, F; Lin, J
Vander Fisiologia
2018 Imeri, L; Ricci, V; Rivolta, I
Fisiologia Medica - Terza Edizione
2018 Buccino, G; Colombini, B; Crnjar, R; D'Amelio, M; Filippi, G; Gennarini, G; Ghirardi, M; Poggesi, C; Possenti, R; Rivolta, I; Sardo, P; Silvani, A
Sangue
2018 Iannuzzi, C; Ippolito, D; Poltronieri, R; Rivolta, I; Sirangelo, I
Innovative and Efficient Oral Delivery Method of APOA-1Milano Muteins Which Retain Anti-Atherosclerotic and Anti-Inflammatory Properties
2018 Giovannoni, R; Facoetti, A; Chisci, E; Reggi, S; Kutryb-Zajac, B; Bombelli, S; Di Marzo, N; Farina, L; Bianchi, C; Perego, R; Avezza, F; Cadamuro, M; Crippa, L; Lavitrano, M; Bentivegna, A; Leone, B; Rivolta, I; Barisani, D; Smolenski, R; Romano, G
‘In Vitro’, ‘In Vivo’ and ‘In Silico’ Investigation of the Anticancer Effectiveness of Oxygen-Loaded Chitosan-Shelled Nanodroplets as Potential Drug Vector
2018 Khadjavi, A; Stura, I; Prato, M; Minero, V; Panariti, A; Rivolta, I; Gulino, G; Bessone, F; Giribaldi, G; Quaglino, E; Cavalli, R; Cavallo, F; Guiot, C
Modulation of the intrinsic neuronal excitability by multifunctional liposomes tailored for treatment of Alzheimer’s disease
2018 Binda, A; Panariti, A; Barbuti, A; Murano, C; Dal Magro, R; Masserini, M; Re, F; Rivolta, I
A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability
2018 Bonzanni, M; Difrancesco, J; Milanesi, R; Campostrini, G; Castellotti, B; Bucchi, A; Baruscotti, M; Ferrarese, C; Franceschetti, S; Canafoglia, L; Ragona, F; Freri, E; Labate, A; Gambardella, A; Costa, C; Rivolta, I; Gellera, C; Granata, T; Barbuti, A; Difrancesco, D
A novel KCNJ2 mutation identified in an autistic proband affects the single channel properties of Kir2.1
2018 Binda, A; Rivolta, I; Villa, C; Chisci, E; Beghi, M; Cornaggia, C; Giovannoni, R; Combi, R
SCN4A as modifier gene in patients with myotonic dystrophy type 2
2018 Binda, A; Renna, L; Bose', F; Brigonzi, E; Botta, A; Valaperta, R; Fossati, B; Rivolta, I; Meola, G; Cardani, R
Tissue specificity of mitochondrial adaptations in rats after 4 weeks of normobaric hypoxia
2018 Ferri, A; Panariti, A; Miserocchi, G; Rocchetti, M; Buoli Comani, G; Rivolta, I; Bishop, D
HCN1 mutation spectrum: From neonatal epileptic encephalopathy to benign generalized epilepsy and beyond
2018 Marini, C; Porro, A; Rastetter, A; Dalle, C; Rivolta, I; Bauer, D; Oegema, R; Nava, C; Parrini, E; Mei, D; Mercer, C; Dhamija, R; Chambers, C; Coubes, C; Thévenon, J; Kuentz, P; Julia, S; Pasquier, L; Dubourg, C; Carré, W; Rosati, A; Melani, F; Pisano, T; Giardino, M; Innes, A; Alembik, Y; Scheidecker, S; Santos, M; Figueiroa, S; Garrido, C; Fusco, C; Frattini, D; Spagnoli, C; Binda, A; Granata, T; Ragona, F; Freri, E; Franceschetti, S; Canafoglia, L; Castellotti, B; Gellera, C; Milanesi, R; Mancardi, M; Clark, D; Kok, F; Helbig, K; Ichikawa, S; Sadler, L; Neupauerová, J; Laššuthova, P; Šterbová, K; Laridon, A; Brilstra, E; Koeleman, B; Lemke, J; Zara, F; Striano, P; Soblet, J; Smits, G; Deconinck, N; Barbuti, A; Difrancesco, D; Leguern, E; Guerrini, R; Santoro, B; Hamacher, K; Thiel, G; Moroni, A; Di Francesco, J; Depienne, C
APOA-1Milano muteins, orally delivered via genetically modified rice, show anti-atherogenic and anti-inflammatory properties in vitro and in Apoe −/− atherosclerotic mice
2018 Romano, G; Reggi, S; Kutryb-Zajac, B; Facoetti, A; Chisci, E; Pettinato, M; Giuffrè, M; Vecchio, F; Leoni, S; De Giorgi, M; Avezza, F; Cadamuro, M; Crippa, L; Leone, B; Lavitrano, M; Rivolta, I; Barisani, D; Smolenski, R; Giovannoni, R
SCN4A as modifier gene in myotonic dystrophy type 2 (DM2) patients with early and severe myotonia
2017 Binda, A; Cardani, R; Renna, L; Fossati, B; Bosè, F; Botta, A; Valaperta, R; Meola, G; Rivolta, I
Pharmacological and Biochemical Characterization of TLQP-21 Activation of a Binding Site on CHO Cells
2017 Molteni, L; Rizzi, L; Bresciani, E; Possenti, R; Petrocchi Passeri, P; Ghè, C; Muccioli, G; Fehrentz, J; Verdié, P; Martinez, J; Omeljaniuk, R; Biagini, G; Binda, A; Rivolta, I; Locatelli, V; Torsello, A
The expression of the rare caveolin-3 variant T78M alters cardiac ion channels function and membrane excitability
2017 Campostrini, G; Bonzanni, M; Lissoni, A; Bazzini, C; Milanesi, R; Vezzoli, E; Francolini, M; Baruscotti, M; Bucchi, A; Rivolta, I; Fantini, M; Severi, S; Cappato, R; Crotti, L; Schwartz, P; Di Francesco, D; Barbuti, A
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