Judith S. Verhoeven
Heeze, NB 5590AB, Netherlands
Last Updated: 09/26/2026
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Found 21 publications
Quality of life in SCN1A-related seizure disorders across the lifespan.
Journal: Brain communications
Published: May 13, 2024
Understanding neurodevelopmental trajectories and behavioral profiles in SCN1A-related epilepsy syndromes.
Journal: Epilepsy & behavior : E&B
Published: December 13, 2023
Gastrointestinal and eating problems in SCN1A-related seizure disorders.
Journal: Epilepsy & behavior : E&B
Published: May 25, 2023
SCN1A-deficient excitatory neuronal networks display mutation-specific phenotypes.
Journal: Brain : a journal of neurology
Published: January 18, 2023
Human KCNQ5 de novo mutations underlie epilepsy and intellectual disability.
Journal: Journal of neurophysiology
Published: May 18, 2022
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications.
Journal: Brain : a journal of neurology
Published: March 12, 2021
NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 08, 2020
Cardiac arrhythmias in Dravet syndrome: an observational multicenter study.
Journal: Annals of clinical and translational neurology
Published: February 23, 2020
Epilepsy phenotype in individuals with chromosomal duplication encompassing FGF12.
Journal: Epilepsia open
Published: October 31, 2019
Failure of ketogenic diet therapy in GLUT1 deficiency syndrome.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: January 10, 2019
Last Updated: 09/26/2026