Sfoglia per Autore
How ketogenic diet may be beneficial in controlling neuronal excitability?
2023 Prevostini, R; Frosio, A; Melgari, D; Calamaio, S; Rivolta, I
A novel KCNC1 gain-of-function variant causing developmental and epileptic encephalopathy: "Precision medicine" approach with fluoxetine
2023 Ambrosino, P; Ragona, F; Mosca, I; Vannicola, C; Canafoglia, L; Solazzi, R; Rivolta, I; Freri, E; Granata, T; Messina, G; Castellotti, B; Gellera, C; Soldovieri, M; Difrancesco, J; Taglialatela, M
Unravelling Novel SCN5A Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights
2023 Frosio, A; Micaglio, E; Polsinelli, I; Calamaio, S; Melgari, D; Prevostini, R; Ghiroldi, A; Binda, A; Carrera, P; Villa, M; Mastrocinque, F; Presi, S; Salerno, R; Boccellino, A; Anastasia, L; Ciconte, G; Ricagno, S; Pappone, C; Rivolta, I
Automated Patch-Clamp and Induced Pluripotent Stem Cell-Derived Cardiomyocytes: A Synergistic Approach in the Study of Brugada Syndrome
2023 Melgari, D; Calamaio, S; Frosio, A; Prevostini, R; Anastasia, L; Pappone, C; Rivolta, I
A novel de novo HCN2 loss-of-function variant causing developmental and epileptic encephalopathy treated with a ketogenic diet
2023 Difrancesco, J; Ragona, F; Murano, C; Frosio, A; Melgari, D; Binda, A; Calamaio, S; Prevostini, R; Mauri, M; Canafoglia, L; Castellotti, B; Messina, G; Gellera, C; Previtali, R; Veggiotti, P; Milanesi, R; Barbuti, A; Solazzi, R; Freri, E; Granata, T; Rivolta, I
Alterations of the Sialylation Machinery in Brugada Syndrome
2022 Ghiroldi, A; Ciconte, G; Creo, P; Tarantino, A; Melgari, D; D'Imperio, S; Piccoli, M; Cirillo, F; Micaglio, E; Monasky, M; Frosio, A; Locati, E; Vicedomini, G; Rivolta, I; Pappone, C; Anastasia, L
T-Type Calcium Channels: A Mixed Blessing
2022 Melgari, D; Frosio, A; Calamaio, S; Marzi, G; Pappone, C; Rivolta, I
Role of the Air-Blood Barrier Phenotype in Lung Oxygen Uptake and Control of Extravascular Water
2022 Miserocchi, G; Beretta, E; Rivolta, I; Bartesaghi, M
Functional Characterization of Two Variants at the Intron 6-Exon 7 Boundary of the KCNQ2 Potassium Channel Gene Causing Distinct Epileptic Phenotypes
2022 Mosca, I; Rivolta, I; Labalme, A; Ambrosino, P; Castellotti, B; Gellera, C; Granata, T; Freri, E; Binda, A; Lesca, G; Difrancesco, J; Soldovieri, M; Taglialatela, M
Dietary nanoparticles interact with gluten peptides and alter the intestinal homeostasis increasing the risk of celiac disease
2021 Mancuso, C; Re, F; Rivolta, I; Elli, L; Gnodi, E; Beaulieu, J; Barisani, D
Effect of the ketogenic diet in excitable tissues
2021 Murano, C; Binda, A; Palestini, P; Baruscotti, M; Difrancesco, J; Rivolta, I
Brugada syndrome genetics is associated with phenotype severity
2021 Ciconte, G; Monasky, M; Santinelli, V; Micaglio, E; Vicedomini, G; Anastasia, L; Negro, G; Borrelli, V; Giannelli, L; Santini, F; de Innocentiis, C; Rondine, R; Locati, E; Bernardini, A; Mazza, B; Mecarocci, V; Ćalović, Ž; Ghiroldi, A; D'Imperio, S; Benedetti, S; Di Resta, C; Rivolta, I; Casari, G; Petretto, E; Pappone, C
Novel SCN5A p.Val1667Asp Missense Variant Segregation and Characterization in a Family with Severe Brugada Syndrome and Multiple Sudden Deaths
2021 Monasky, M; Micaglio, E; Ciconte, G; Rivolta, I; Borrelli, V; Ghiroldi, A; D'Imperio, S; Binda, A; Melgari, D; Benedetti, S; Mitrovic, P; Anastasia, L; Mecarocci, V; Ćalović, Ž; Casari, G; Pappone, C
Do the functional properties of HCN1 mutants correlate with the clinical features in epileptic patients?
2021 Porro, A; Abbandonato, G; Veronesi, V; Russo, A; Binda, A; Antolini, L; Granata, T; Castellotti, B; Marini, C; Moroni, A; Difrancesco, J; Rivolta, I
Binary biocompatible CNCs-Gelatine hydrogel as 3D scaffolds suitable for cell culture adhesion and growth
2021 Zoia, L; Binda, A; Cipolla, L; Rivolta, I; La Ferla, B
Cardiac and neuronal HCN channelopathies
2020 Rivolta, I; Binda, A; Masi, A; Difrancesco, J
Rational design of a mutation to investigate the role of the brain protein TRIP8b in limiting the cAMP response of HCN channels in neurons
2020 Porro, A; Binda, A; Pisoni, M; Donadoni, C; Rivolta, I; Saponaro, A
GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death
2020 Juang, J; Binda, A; Lee, S; Hwang, J; Chen, W; Liu, Y; Lin, L; Yu, C; Ho, L; Huang, H; Chen, C; Lu, T; Lai, L; Yeh, S; Lai, L; Chuang, E; Rivolta, I; Antzelevitch, C
Gabapentin treatment in a patient with KCNQ2 developmental epileptic encephalopathy
2020 Soldovieri, M; Freri, E; Ambrosino, P; Rivolta, I; Mosca, I; Binda, A; Murano, C; Ragona, F; Canafoglia, L; Vannicola, C; Solazzi, R; Granata, T; Castellotti, B; Messina, G; Gellera, C; Labalme, A; Lesca, G; Difrancesco, J; Taglialatela, M
Innovative therapies and nanomedicine applications for the treatment of alzheimer’s disease: A state-of-the-art (2017–2020)
2020 Binda, A; Murano, C; Rivolta, I
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