Charissa Millevert
Antwerpen, VLG 2610, Belgium
Last Updated: 09/26/2026
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Found 13 publications
Early sodium channel blocker initiation is associated with better outcomes in KCNQ2 disorders.
Journal: Brain : a journal of neurology
Published: October 17, 2025
Imaging brain development in a KCNQ2-developmental and epileptic encephalopathy mouse model: identifying early biomarkers for functional and structural brain changes.
Journal: EBioMedicine
Published: June 13, 2025
ATP1A3 Variants, Variably Penetrant Short QT Intervals, and Lethal Ventricular Arrhythmias.
Journal: JAMA pediatrics
Published: March 03, 2025
The genetic and phenotypic spectrum of GABRB1-related disorders.
Journal: Brain : a journal of neurology
Published: December 19, 2024
Children and Adolescent Patients with Variants in the ATP1A3 -encoded Sodium-Potassium ATPase Alpha-3 Subunit Demonstrate an Impaired QT Response to Bradycardia and Predisposition to Sinus Node Dysfunction.
Journal: medRxiv : the preprint server for health sciences
Published: September 10, 2024
Resting-State Functional MRI and PET Imaging as Noninvasive Tools to Study (Ab)Normal Neurodevelopment in Humans and Rodents.
Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience
Published: June 09, 2023
ILAE Genetic Literacy Series: Self-limited familial epilepsy syndromes with onset in neonatal age and infancy.
Journal: Epileptic disorders : international epilepsy journal with videotape
Published: October 10, 2022
KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanism.
Journal: EBioMedicine
Published: January 22, 2022
Impact of COVID-19 on the lives and psychosocial well-being of persons with epilepsy during the third trimester of the pandemic: Results from an international, online survey.
Journal: Epilepsy & behavior : E&B
Published: December 18, 2020
Last Updated: 09/26/2026