Philippe Lory

Montpellier, France

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 41 publications

An improved electrophysiological cellular assay to unlock the pharmacological modulation of the NALCN channelosome.

An improved electrophysiological cellular assay to unlock the pharmacological modulation of the NALCN channelosome.

Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

Published: February 24, 2026

Clinic-to-Mechanism: Unraveling in-depth molecular dysfunctions caused by a GluN2B C-Terminal deletion in developmental and epileptic encephalopathies.

Clinic-to-Mechanism: Unraveling in-depth molecular dysfunctions caused by a GluN2B C-Terminal deletion in developmental and epileptic encephalopathies.

Journal: Translational psychiatry

Published: September 15, 2025

The sodium leak channel NALCN in Drd2+ striatal neurons regulates neuronal excitability, locomotion and food-seeking in a sex-dependent manner.

The sodium leak channel NALCN in Drd2+ striatal neurons regulates neuronal excitability, locomotion and food-seeking in a sex-dependent manner.

Journal: Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology

Published: July 08, 2025

The 33rd Ion Channels Meeting, September 2024, Sète, France.

The 33rd Ion Channels Meeting, September 2024, Sète, France.

Journal: Bioelectricity

Published: May 09, 2025

Electrophysiological classification of CACNA1G gene variants associated with neurodevelopmental and neurological disorders.

Electrophysiological classification of CACNA1G gene variants associated with neurodevelopmental and neurological disorders.

Journal: Frontiers in pharmacology

Published: April 16, 2025

Zebrafish fast muscle contractions avoid the mammalian requirement for voltage-gated Na+ channels.

Zebrafish fast muscle contractions avoid the mammalian requirement for voltage-gated Na+ channels.

Journal: PLoS biology

Published: December 23, 2024

The characterization of new de novo CACNA1G variants affecting the intracellular gate of Cav3.1 channel broadens the spectrum of neurodevelopmental phenotypes in SCA42ND.

The characterization of new de novo CACNA1G variants affecting the intracellular gate of Cav3.1 channel broadens the spectrum of neurodevelopmental phenotypes in SCA42ND.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: August 07, 2024

NALCN/Cch1 channelosome subunits originated in early eukaryotes.

NALCN/Cch1 channelosome subunits originated in early eukaryotes.

Journal: The Journal of general physiology

Published: July 08, 2024

Structural basis for human Cav3.2 inhibition by selective antagonists.

Structural basis for human Cav3.2 inhibition by selective antagonists.

Journal: Cell research

Published: December 21, 2023

The good company of T-type calcium channels : Commentary on: "T-type calcium channelosome," a review by N. Weiss and G. W. Zamponi.

The good company of T-type calcium channels : Commentary on: "T-type calcium channelosome," a review by N. Weiss and G. W. Zamponi.

Journal: Pflugers Archiv : European journal of physiology

Published: December 18, 2023

New insights into the physiology and pathophysiology of the atypical sodium leak channel NALCN.

New insights into the physiology and pathophysiology of the atypical sodium leak channel NALCN.

Journal: Physiological reviews

Published: August 24, 2023

New Challenges Resulting From the Loss of Function of Nav1.4 in Neuromuscular Diseases.

New Challenges Resulting From the Loss of Function of Nav1.4 in Neuromuscular Diseases.

Journal: Frontiers in pharmacology

Published: July 31, 2021

Showing 1-12 of 41

Last Updated: 09/26/2026