BINDA, ANNA

BINDA, ANNA  

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

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Titolo Tipologia Data di pubblicazione Autori File
A novel de novo HCN2 loss-of-function variant causing developmental and epileptic encephalopathy treated with a ketogenic diet 01 - Articolo su rivista 2023 DiFrancesco, Jacopo CMurano, CarmenMelgari, DarioBinda, AnnaCalamaio, SerenaPrevostini, RacheleMauri, MarioBarbuti, AndreaRivolta, Ilaria +
Unravelling Novel SCN5A Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights 01 - Articolo su rivista 2023 Calamaio S.Melgari D.Prevostini R.Binda A.Rivolta I. +
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, ADifrancesco, J +
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
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.DiFrancesco J. C.Rivolta I. +
Effect of the ketogenic diet in excitable tissues 01 - Articolo su rivista 2021 Murano, CarmenBinda, AnnaPalestini, PaolaDiFrancesco, Jacopo CRivolta, Ilaria +
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 +
Cardiac and neuronal HCN channelopathies 01 - Articolo su rivista 2020 Rivolta, IlariaBinda, AnnaDiFrancesco, Jacopo C +
Gabapentin treatment in a patient with KCNQ2 developmental epileptic encephalopathy 01 - Articolo su rivista 2020 Rivolta, IlariaBinda, AnnaMurano, CarmenDiFrancesco, Jacopo C. +
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 +
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 +
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 DiFrancesco, Jacopo C.Ferrarese, CarloMagri, StefaniaBinda, AnnaRivolta, Ilaria +
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 +
A novel KCNJ2 mutation identified in an autistic proband affects the single channel properties of Kir2.1 01 - Articolo su rivista 2018 Binda, AnnaRivolta, IlariaVilla, ChiaraChisci, ElisaBeghi, MassimilianoCornaggia, Cesare M.Giovannoni, RobertoCombi, Romina
HCN1 mutation spectrum: From neonatal epileptic encephalopathy to benign generalized epilepsy and beyond 01 - Articolo su rivista 2018 Rivolta, IBinda, ADi Francesco, JC +
HCN1 novel mutations in familiar generalized epilepsy 02 - Intervento a convegno 2018 Binda, AMurano, CDiFrancesco, JCRivolta, I +
Modulation of the intrinsic neuronal excitability by multifunctional liposomes tailored for treatment of Alzheimer’s disease 01 - Articolo su rivista 2018 Binda, APanariti, AMURANO, CARMENDal Magro, RMasserini, MRe, FRivolta, I +
SCN4A as modifier gene in patients with myotonic dystrophy type 2 01 - Articolo su rivista 2018 Binda, AnnaBOSE', FRANCESCARivolta, Ilaria +