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
Study of the effects of nanoliposomes engineered for the treatment of Alzheimer's disease on the electrical activity of cortical neurons 02 - Intervento a convegno 2013 BINDA, ANNABANA, LAURAPANARITI, ALICE LUCIAMINNITI, STEFANIAMASSERINI, MASSIMO ERNESTORE, FRANCESCARIVOLTA, ILARIA
Acetylation mediates Cx43 reduction caused by electrical stimulation 01 - Articolo su rivista 2015 BINDA, ANNAPANARITI, ALICE LUCIARIVOLTA, ILARIA +
SCN4A mutation as modifying factor of Myotonic Dystrophy Type 2 phenotype 01 - Articolo su rivista 2015 RIVOLTA, ILARIABINDA, ANNACINTI, ALESSANDROGIOVANNONI, ROBERTO +
SCN4A as modifier gene in myotonic dystrophy type 2 (DM2) patients with early and severe myotonia 02 - Intervento a convegno 2017 BINDA, ANNARIVOLTA, ILARIA +
JMV5656, a novel derivative of TLQP-21, triggers the activation of a calcium-dependent potassium outward current in microglial cells 01 - Articolo su rivista 2017 RIVOLTA, ILARIABINDA, ANNAMOLTENI, LAURARIZZI, LAURABRESCIANI, ELENALOCATELLI, VITTORIOTORSELLO, ANTONIO BIAGIO +
Pharmacological and Biochemical Characterization of TLQP-21 Activation of a Binding Site on CHO Cells 01 - Articolo su rivista 2017 MOLTENI, LAURARIZZI, LAURABRESCIANI, ELENABINDA, ANNARIVOLTA, ILARIALOCATELLI, VITTORIOTORSELLO, ANTONIO BIAGIO +
Relevance of electrolytic balance in channelopathies. 07 - Tesi di dottorato Bicocca post 2009 2017 BINDA, ANNA
HCN1 novel mutations in familiar generalized epilepsy 02 - Intervento a convegno 2018 Binda, AMurano, CRivolta, 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
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 +
HCN1 mutation spectrum: From neonatal epileptic encephalopathy to benign generalized epilepsy and beyond 01 - Articolo su rivista 2018 Rivolta, IBinda, A +
Two novel SCN5A loss-of-function mutations affect patients with severe arrhytmogenic syndromes 02 - Intervento a convegno 2019 Murano CBinda ARivolta I +
Progressive epileptic encephalopathy associated with a novel HCN2 mutation 02 - Intervento a convegno 2019 Binda AMURANO, CARMENDi Francesco JCRivolta 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 +
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 +
Gabapentin treatment in a patient with KCNQ2 developmental epileptic encephalopathy 01 - Articolo su rivista 2020 Rivolta, IlariaBinda, AnnaMurano, Carmen +
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
Cardiac and neuronal HCN channelopathies 01 - Articolo su rivista 2020 Rivolta, IlariaBinda, Anna +
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 +