RIVOLTA, ILARIA

RIVOLTA, ILARIA  

DIPARTIMENTO DI MEDICINA E CHIRURGIA (SCHOOL OF MEDICINE AND SURGERY)  

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Risultati 1 - 20 di 100 (tempo di esecuzione: 0.019 secondi).
Titolo Tipologia Data di pubblicazione Autori File
Functional Characterization of Two Variants at the Intron 6-Exon 7 Boundary of the KCNQ2 Potassium Channel Gene Causing Distinct Epileptic Phenotypes 01 - Articolo su rivista 2022 Rivolta, IBinda, A +
T-Type Calcium Channels: A Mixed Blessing 01 - Articolo su rivista 2022 Melgari, DarioCalamaio, SerenaRivolta, Ilaria +
Alterations of the Sialylation Machinery in Brugada Syndrome 01 - Articolo su rivista 2022 Creo, PMelgari, DRivolta, I +
Role of the Air-Blood Barrier Phenotype in Lung Oxygen Uptake and Control of Extravascular Water 01 - Articolo su rivista 2022 Miserocchi, GiuseppeBeretta, EgidioRivolta, IlariaBartesaghi, Manuela
Binary biocompatible CNCs-Gelatine hydrogel as 3D scaffolds suitable for cell culture adhesion and growth 01 - Articolo su rivista 2021 Zoia, LBinda, ACipolla, LRivolta, ILa Ferla, B
Effect of the ketogenic diet in excitable tissues 01 - Articolo su rivista 2021 Murano, CarmenBinda, AnnaPalestini, PaolaRivolta, Ilaria +
Do the functional properties of HCN1 mutants correlate with the clinical features in epileptic patients? 01 - Articolo su rivista 2021 Veronesi V.Binda A.Antolini L.Rivolta I. +
Dietary nanoparticles interact with gluten peptides and alter the intestinal homeostasis increasing the risk of celiac disease 01 - Articolo su rivista 2021 Mancuso, CRe, FRivolta, IGnodi, EBarisani, D +
Novel SCN5A p.Val1667Asp Missense Variant Segregation and Characterization in a Family with Severe Brugada Syndrome and Multiple Sudden Deaths 01 - Articolo su rivista 2021 Rivolta, IlariaBinda, Anna +
Brugada syndrome genetics is associated with phenotype severity 01 - Articolo su rivista 2021 Di Resta, ChiaraRivolta, Ilaria +
Innovative therapies and nanomedicine applications for the treatment of alzheimer’s disease: A state-of-the-art (2017–2020) 01 - Articolo su rivista 2020 Binda, AMurano, CRivolta, I
Rational design of a mutation to investigate the role of the brain protein TRIP8b in limiting the cAMP response of HCN channels in neurons 01 - Articolo su rivista 2020 Binda, AnnaRivolta, Ilaria +
GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death 01 - Articolo su rivista 2020 Binda, AnnaRivolta, Ilaria +
Gabapentin treatment in a patient with KCNQ2 developmental epileptic encephalopathy 01 - Articolo su rivista 2020 Rivolta, IlariaBinda, AnnaMurano, Carmen +
Cardiac and neuronal HCN channelopathies 01 - Articolo su rivista 2020 Rivolta, IlariaBinda, Anna +
Progressive epileptic encephalopathy associated with a novel HCN2 mutation 02 - Intervento a convegno 2019 Binda AMURANO, CARMENDi Francesco JCRivolta I +
Two novel SCN5A loss-of-function mutations affect patients with severe arrhytmogenic syndromes 02 - Intervento a convegno 2019 Murano CBinda ARivolta I +
HCN ion channels and accessory proteins in epilepsy: genetic analysis of a large cohort of patients and review of the literature 01 - Articolo su rivista 2019 Ferrarese, CarloMagri, StefaniaBinda, AnnaRivolta, Ilaria +
Fisiologia Medica - Terza Edizione 05 - Curatele 2018 Rivolta, I +
Vander Fisiologia 05 - Curatele 2018 Rivolta, I +