Ilenio Servettini
Campobasso, Italy
Last Updated: 09/26/2026
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Found 15 publications
EA1-linked Kv1.1 dysfunction enhances susceptibility to cerebellar spreading depression and a transient cerebellar refractory state.
Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: January 14, 2026
Editorial: Pathogenic potassium channel variants in neurological disorders: from functional analysis to personalized pharmacological approaches.
Journal: Frontiers in cellular neuroscience
Published: April 18, 2025
Constitutive opening of the Kv7.2 pore activation gate causes KCNQ2-developmental encephalopathy.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: November 27, 2024
An activator of voltage-gated K+ channels Kv1.1 as a therapeutic candidate for episodic ataxia type 1.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: July 24, 2023
De novo variants in KCNA3 cause developmental and epileptic encephalopathy.
Journal: Annals of neurology
Published: January 16, 2023
Kv7.4 channels regulate potassium permeability in neuronal mitochondria.
Journal: Biochemical pharmacology
Published: October 21, 2021
New insights into the pathogenesis and therapeutics of episodic ataxia type 1.
Journal: Frontiers in cellular neuroscience
Published: May 29, 2015
Update on the implication of potassium channels in autism: K(+) channelautism spectrum disorder.
Journal: Frontiers in cellular neuroscience
Published: November 30, 2014
Novel phenotype associated with a mutation in the KCNA1(Kv1.1) gene.
Journal: Frontiers in physiology
Published: October 21, 2014
Expression and function of a CP339,818-sensitive K⁺ current in a subpopulation of putative nociceptive neurons from adult mouse trigeminal ganglia.
Journal: Journal of neurophysiology
Published: May 20, 2014
Last Updated: 09/26/2026