I. Rivolta

A. Aliverti, G. Miserocchi, I. Rivolta, 2014, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

Nav1.5 E1053K mutation causing Brugada syndrome blocks binding to ankyrin-G and expression of Nav1.5 on the surface of cardiomyocytes.

Carlo Napolitano, Silvia G Priori, Vann Bennett, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Changes in the mechanical properties of the respiratory system during the development of interstitial lung edema

Antonio Pedotti, Giulio Sancini, Ilaria Rivolta, 2008, Respiratory research.

The effect of exogenous surfactant on alveolar interdependence

A. Aliverti, G. Miserocchi, I. Rivolta, 2015, Respiratory Physiology & Neurobiology.

CHAPTER 63 – Ion Channels in the Heart

R. Kass, I. Rivolta, Hugues Abriel, 2001 .

HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond

K. Hamacher, C. Mercer, P. Striano, 2018, Brain : a journal of neurology.

SCN4A as modifier gene in patients with myotonic dystrophy type 2

G. Meola, I. Rivolta, A. Botta, 2018, Scientific Reports.

SCN4A mutation as modifying factor of Myotonic Dystrophy Type 2 phenotype

G. Meola, I. Rivolta, E. Bugiardini, 2015, Neuromuscular Disorders.

Acetylation mediates Cx43 reduction caused by electrical stimulation.

P. Pramstaller, F. Recchia, M. Capogrossi, 2015, Journal of molecular and cellular cardiology.

Remodelling of Membrane Rafts Expression in Lung Cells as an Early Sign of Mechanotransduction-Signalling in Pulmonary Edema

G. Miserocchi, I. Rivolta, P. Palestini, 2011, Journal of lipids.

Cardiac and neuronal HCN channelopathies

I. Rivolta, A. Masi, J. DiFrancesco, 2020, Pflügers Archiv - European Journal of Physiology.

Effect of nanoparticles binding β-amyloid peptide on nitric oxide production by cultured endothelial cells and macrophages

M. Masserini, P. Couvreur, F. Re, 2013, International journal of nanomedicine.

mRNA expression profile of selected oxygen sensing genes in the lung during recovery from chronic hypoxia.

G. Miserocchi, A. Panariti, I. Rivolta, 2013, Biological research.

A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability

B. Castellotti, C. Gellera, S. Franceschetti, 2018, Neurobiology of Disease.

In Vitro–In Vivo Fluctuation Spectroscopies

Michele Caccia, Giuseppe Chirico, Maddalena Collini, 2011 .

A Novel KCNJ2 Mutation Identified in an Autistic Proband Affects the Single Channel Properties of Kir2.1

I. Rivolta, M. Beghi, C. Cornaggia, 2018, Front. Cell. Neurosci..

GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death

C. Antzelevitch, E. Chuang, L. Lai, 2020, EBioMedicine.

Dynamic investigation of interaction of biocompatible iron oxide nanoparticles with epithelial cells for biomedical applications.

G. Miserocchi, C. Bucci, L. Sironi, 2013, Journal of biomedical nanotechnology.

Tissue specificity of mitochondrial adaptations in rats after 4 weeks of normobaric hypoxia

G. Miserocchi, A. Panariti, I. Rivolta, 2018, European Journal of Applied Physiology.

Characterization of Sodium Channel α- and β-Subunits in Rat and Mouse Cardiac Myocytes

R. Kass, I. Rivolta, J. Malhotra, 2001 .

Oxygen-Loaded Nanodroplets Effectively Abrogate Hypoxia Dysregulating Effects on Secretion of MMP-9 and TIMP-1 by Human Monocytes

R. Cavalli, A. Panariti, I. Rivolta, 2015, Mediators of inflammation.

Automated Patch-Clamp and Induced Pluripotent Stem Cell-Derived Cardiomyocytes: A Synergistic Approach in the Study of Brugada Syndrome

C. Pappone, I. Rivolta, Dario Melgari, 2023, International journal of molecular sciences.

From morphological heterogeneity at alveolar level to the overall mechanical lung behavior: an in vivo microscopic imaging study

A. Aliverti, G. Miserocchi, I. Rivolta, 2014, Physiological reports.

Erratum: Hypoxia‐induced modifications in plasma membranes and lipid microdomains in A549 cells and primary human alveolar cells. L. Botto, E. Beretta, A. Bulbarelli, I. Rivolta, B. Lettiero, B.E. Leone, G. Miserocchi, and P. Palestini

G. Miserocchi, I. Rivolta, P. Palestini, 2009 .

Gold Branched Nanoparticles for Cellular Treatments

L. Sironi, G. Chirico, M. Collini, 2012 .

Modulation of Cardiac Sodium Channel Gating by Protein Kinase A Can Be Altered by Disease-linked Mutation*

R. Kass, I. Rivolta, C. Clancy, 2003, Journal of Biological Chemistry.

Secondary Structure of the Human Cardiac Na+ Channel C Terminus

A. Yang, R. Kass, I. Rivolta, 2002, The Journal of Biological Chemistry.

Innovative Therapies and Nanomedicine Applications for the Treatment of Alzheimer’s Disease: A State-of-the-Art (2017–2020)

I. Rivolta, A. Binda, C. Murano, 2020, International journal of nanomedicine.

An outlook on the potential of Si nanocrystals as luminescent probes for bioimaging

A. Panariti, I. Rivolta, E. Trave, 2013 .

Rational design of a mutation to investigate the role of the brain protein TRIP8b in limiting the cAMP response of HCN channels in neurons

C. Donadoni, I. Rivolta, A. Saponaro, 2020, The Journal of general physiology.

Dextran-shelled oxygen-loaded nanodroplets reestablish a normoxia-like pro-angiogenic phenotype and behavior in hypoxic human dermal microvascular endothelium.

R. Cavalli, A. Panariti, I. Rivolta, 2015, Toxicology and applied pharmacology.

A novel SCN5A mutation associated with long QT-3: altered inactivation kinetics and channel dysfunction.

Silvia G Priori, Colleen E Clancy, Ilaria Rivolta, 2002, Physiological genomics.

Iron oxide nanoparticles surface coating and cell uptake affect biocompatibility and inflammatory responses of endothelial cells and macrophages

M. Masserini, A. Panariti, I. Rivolta, 2015, Journal of Nanoparticle Research.

Mechanistic Considerations on the Development of Lung Edema: Vascular, Perivascular and Molecular Aspects from Early Stage to Tissue and Vascular Remodeling Stage

G. Miserocchi, I. Rivolta, 2012 .

Alterations of the Sialylation Machinery in Brugada Syndrome

C. Pappone, G. Vicedomini, E. Locati, 2022, International journal of molecular sciences.

In silico assessment of Y1795C and Y1795H SCN5A mutations: implication for inherited arrhythmogenic syndromes.

S. Severi, S. Vecchietti, S. Cavalcanti, 2007, American journal of physiology. Heart and circulatory physiology.

Computer simulation of wild-type and mutant human cardiac Na+ current

Stefano Severi, Carlo Napolitano, Silvia G. Priori, 2006, Medical and Biological Engineering and Computing.

Nanodroplets: New Perspectives for Oxygen Delivery to Hypoxic Cutaneous Tissues

R. Cavalli, A. Panariti, I. Rivolta, 2022 .

Unravelling Novel SCN5A Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights

I. Rivolta, I. Polsinelli, S. Ricagno, 2023, International journal of molecular sciences.

Cardiac Sodium Channel Diseases

S. Priori, C. Napolitano, I. Rivolta, 2003, Clinical chemistry and laboratory medicine.

A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability

B. Castellotti, C. Gellera, S. Franceschetti, 2018, Neurobiology of Disease.

The effect of nanoparticle uptake on cellular behavior: disrupting or enabling functions?

G. Miserocchi, A. Panariti, I. Rivolta, 2012, Nanotechnology, science and applications.

Minireview: Effect of the ketogenic diet in excitable tissues.

I. Rivolta, P. Palestini, M. Baruscotti, 2021, American journal of physiology. Cell physiology.