Sarah Weckhuysen

Antwerpen, VLG, Belgium

Last Updated: 09/26/2026

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Found 166 publications

Add-on treatment with vinpocetine reduces seizure frequency and improves comorbidities in patients with loss-of-function γ-aminobutyric acid type A receptor variants.

Add-on treatment with vinpocetine reduces seizure frequency and improves comorbidities in patients with loss-of-function γ-aminobutyric acid type A receptor variants.

Journal: Epilepsia
Published: February 03, 2026

Correction: GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy.

Correction: GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy.

Journal: Molecular psychiatry
Published: January 07, 2026

Navigating Human Astrocyte Differentiation: Direct and Rapid One-Step Differentiation of Induced Pluripotent Stem Cells to Functional Astrocytes Supporting Neuronal Network Development.

Navigating Human Astrocyte Differentiation: Direct and Rapid One-Step Differentiation of Induced Pluripotent Stem Cells to Functional Astrocytes Supporting Neuronal Network Development.

Journal: Glia
Published: October 31, 2025

Early sodium channel blocker initiation is associated with better outcomes in KCNQ2 disorders.

Early sodium channel blocker initiation is associated with better outcomes in KCNQ2 disorders.

Journal: Brain : a journal of neurology
Published: October 17, 2025

Predictive value of seizure onset for gross motor dysfunction in individuals with pathogenic GABRB2 and GABRB3 variants.

Predictive value of seizure onset for gross motor dysfunction in individuals with pathogenic GABRB2 and GABRB3 variants.

Journal: Epilepsia
Published: October 02, 2025

Unperturbed dye-based imaging of spontaneous synchronized calcium activity in iPSC-derived neuronal cultures.

Unperturbed dye-based imaging of spontaneous synchronized calcium activity in iPSC-derived neuronal cultures.

Journal: iScience
Published: September 15, 2025

Bi-allelic variants in FSD1L cause a neurodevelopmental disorder overlapping with L1 syndrome.

Bi-allelic variants in FSD1L cause a neurodevelopmental disorder overlapping with L1 syndrome.

Journal: American journal of human genetics
Published: August 13, 2025

Kv7.2 loss-of-function causes early hyperexcitability and network remodelling.

Kv7.2 loss-of-function causes early hyperexcitability and network remodelling.

Journal: Brain : a journal of neurology
Published: July 24, 2025

KV7.2 channel dysfunction delays neuronal maturation and undermines early network development in a hiPSC model of KCNQ2-DEE.

KV7.2 channel dysfunction delays neuronal maturation and undermines early network development in a hiPSC model of KCNQ2-DEE.

Journal: Neurobiology of disease
Published: June 18, 2025

Budget impact analysis of cenobamate, a novel adjunctive therapy for the treatment of drug resistant focal onset seizures, from the Belgian healthcare payer perspective.

Budget impact analysis of cenobamate, a novel adjunctive therapy for the treatment of drug resistant focal onset seizures, from the Belgian healthcare payer perspective.

Journal: Journal of medical economics
Published: June 17, 2025

Imaging brain development in a KCNQ2-developmental and epileptic encephalopathy mouse model: identifying early biomarkers for functional and structural brain changes.

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

Precision medicine in epilepsy: Clinicians' perspectives from an international qualitative study.

Precision medicine in epilepsy: Clinicians' perspectives from an international qualitative study.

Journal: Epilepsia
Published: April 01, 2025
Showing 1-12 of 166

Last Updated: 09/26/2026