Diana Conte
Asl, 73100, Italy
Last Updated: 09/26/2026
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Found 18 publications
Bisphosphonates Targeting Ion Channels and Musculoskeletal Effects.
Journal: Frontiers in pharmacology
Published: December 16, 2021
Target Mutation-Driven Drug Discovery.
Journal: Current medicinal chemistry
Published: October 20, 2021
The impact of SARS-CoV-2 on skeletal muscles.
Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology
Published: October 06, 2020
Skeletal muscle ClC-1 chloride channels in health and diseases.
Journal: Pflugers Archiv : European journal of physiology
Published: February 20, 2020
Safinamide's potential in treating nondystrophic myotonias: Inhibition of skeletal muscle voltage-gated sodium channels and skeletal muscle hyperexcitability in vitro and in vivo.
Journal: Experimental neurology
Published: October 29, 2019
Pharmacogenetics of myotonic hNav1.4 sodium channel variants situated near the fast inactivation gate.
Journal: Pharmacological research
Published: October 03, 2018
Ion Channels in Drug Discovery and Safety Pharmacology.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: June 24, 2018
Bartter syndrome, severe rare orphan kidney disease: a step towards therapy through pharmacogenetic and epidemiological studies
Journal: Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia
Published: May 23, 2018
The analysis of myotonia congenita mutations discloses functional clusters of amino acids within the CBS2 domain and the C-terminal peptide of the ClC-1 channel.
Journal: Human mutation
Published: March 27, 2018
Mapping ligand binding pockets in chloride ClC-1 channels through an integrated in silico and experimental approach using anthracene-9-carboxylic acid and niflumic acid.
Journal: British journal of pharmacology
Published: October 16, 2017
Paving the way for Bartter syndrome type 3 drug discovery: a hope from basic research.
Journal: The Journal of physiology
Published: June 10, 2017
A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctions.
Journal: Molecular and cellular neurosciences
Published: December 22, 2016
Last Updated: 09/26/2026