Electrophysiological characterization of a Cav3.2 calcium channel missense variant associated with epilepsy and hearing loss

Hearing Loss Related to Gene Mutations in Distal Renal Tubular Acidosis

(2023) Ezgi Ay et al.   AUDIOLOGY AND NEURO-OTOLOGY

CaV3.2 calcium channels contribute to trigeminal neuralgia

(2022) Eder Gambeta et al.   PAIN

Contribution of CACNA1H Variants in Autism Spectrum Disorder Susceptibility

(2022) Marta Viggiano et al.   Frontiers in Psychiatry

Investigation of CACNA1I Cav3.3 Dysfunction in Hemiplegic Migraine

(2022) Neven Maksemous et al.   Frontiers in Molecular Neuroscience

Electrophysiological and computational analysis of Cav3.2 channel variants associated with familial trigeminal neuralgia

(2022) Emilio R. Mustafá et al.   Molecular Brain

Alkaline brain pH shift in rodent lithium-pilocarpine model of epilepsy with chronic seizures

(2021) Dongshuang Lu et al.   BRAIN RESEARCH

A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Cav3.2 T-type channel activity

(2020) Robin N. Stringer et al.   Molecular Brain

Genetic T-type calcium channelopathies

(2019) Norbert Weiss et al.   JOURNAL OF MEDICAL GENETICS

Cav3.2 T-Type Calcium Channels Are Physiologically Mandatory for the Auditory System

(2019) Andreas Lundt et al.   NEUROSCIENCE

CACNA1Hmissense mutations associated with amyotrophic lateral sclerosis alter Cav3.2 T-type calcium channel activity and reticular thalamic neuron firing

(2016) Yuriy Rzhepetskyy et al.   Channels

CACNA1H Mutations Are Associated With Different Forms of Primary Aldosteronism

(2016) Georgios Daniil et al.   EBioMedicine

Brain alkalosis causes birth asphyxia seizures, suggesting therapeutic strategy

(2011) Mohamed M. Helmy et al.   ANNALS OF NEUROLOGY

Respiratory alkalosis in children with febrile seizures

(2011) Sebastian Schuchmann et al.   EPILEPSIA

Anti-epileptic drugs delay age-related loss of spiral ganglion neurons via T-type calcium channel

(2011) Debin Lei et al.   HEARING RESEARCH