Berten P. Ceulemans

Edegem, VLG, Belgium

Last Updated: 09/26/2026

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Found 118 publications

Cerebral, spinal, ophthalmological and skeletal findings associated with abusive and non-abusive head injury in children under 2 years old: A systematic review.

Cerebral, spinal, ophthalmological and skeletal findings associated with abusive and non-abusive head injury in children under 2 years old: A systematic review.

Journal: Child abuse & neglect

Published: April 22, 2026

CMIP as a novel candidate gene for neurodevelopmental and neuropsychiatric disorders.

CMIP as a novel candidate gene for neurodevelopmental and neuropsychiatric disorders.

Journal: European journal of human genetics : EJHG

Published: December 09, 2025

Breaking the seizure cycle: Belgian expert consensus on the diagnostics and treatment of acute convulsive seizures in children.

Breaking the seizure cycle: Belgian expert consensus on the diagnostics and treatment of acute convulsive seizures in children.

Journal: Acta neurologica Belgica

Published: November 26, 2025

Monoallelic and biallelic KDM5A variants identified in patients with autism spectrum disorder.

Monoallelic and biallelic KDM5A variants identified in patients with autism spectrum disorder.

Journal: HGG advances

Published: November 26, 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

Clinical features associated with abusive and non-abusive head injury in children under 2 years old: A systematic review.

Clinical features associated with abusive and non-abusive head injury in children under 2 years old: A systematic review.

Journal: Child abuse & neglect

Published: June 26, 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

Amitriptyline use in individuals with KCNQ2/3 gain-of-function variants: A retrospective cohort study.

Amitriptyline use in individuals with KCNQ2/3 gain-of-function variants: A retrospective cohort study.

Journal: Epilepsia

Published: October 22, 2024

Comprehensive scoping review of fenfluramine's role in managing generalized tonic-clonic seizures in developmental and epileptic encephalopathies.

Comprehensive scoping review of fenfluramine's role in managing generalized tonic-clonic seizures in developmental and epileptic encephalopathies.

Journal: Epilepsia

Published: February 09, 2024

Burden re-analysis of neurodevelopmental disorder cohorts for prioritization of candidate genes.

Burden re-analysis of neurodevelopmental disorder cohorts for prioritization of candidate genes.

Journal: European journal of human genetics : EJHG

Published: January 17, 2024

The Genetic Puzzle of Cerebral Palsy: Results of a Monocentric Study.

The Genetic Puzzle of Cerebral Palsy: Results of a Monocentric Study.

Journal: Pediatric neurology

Published: December 01, 2023

Genotype-phenotype associations in 1018 individuals with SCN1A-related epilepsies.

Genotype-phenotype associations in 1018 individuals with SCN1A-related epilepsies.

Journal: Epilepsia

Published: September 17, 2023

Showing 1-12 of 118

Last Updated: 09/26/2026