Filip Roelens
Roeselare, VLG, Belgium
Last Updated: 09/26/2026
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Found 17 publications
Seizure quantification in sunflower syndrome by a wrist-worn device.
Journal: Epileptic disorders : international epilepsy journal with videotape
Published: June 14, 2024
The Genetic Puzzle of Cerebral Palsy: Results of a Monocentric Study.
Journal: Pediatric neurology
Published: December 01, 2023
Mutations in RNU7-1 Weaken Secondary RNA Structure, Induce MCP-1 and CXCL10 in CSF, and Result in Aicardi-Goutières Syndrome with Severe End-Organ Involvement.
Journal: Journal of clinical immunology
Published: October 06, 2021
De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathies.
Journal: Brain : a journal of neurology
Published: June 14, 2021
Harlequin syndrome in a pediatric population: a case series.
Journal: Acta neurologica Belgica
Published: October 10, 2020
Delineating the neurological phenotype in children with defects in the ECHS1 or HIBCH gene.
Journal: Journal of inherited metabolic disease
Published: April 03, 2020
De Novo Variants in LMNB1 Cause Pronounced Syndromic Microcephaly and Disruption of Nuclear Envelope Integrity.
Journal: American journal of human genetics
Published: March 27, 2020
Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1.
Journal: JAMA neurology
Published: January 23, 2018
Bi-allelic variants in COL3A1 encoding the ligand to GPR56 are associated with cobblestone-like cortical malformation, white matter changes and cerebellar cysts.
Journal: Journal of medical genetics
Published: November 01, 2016
SPG20 mutation in three siblings with familial hereditary spastic paraplegia.
Journal: Cold Spring Harbor molecular case studies
Published: October 14, 2016
Redefining the MED13L syndrome.
Journal: European journal of human genetics : EJHG
Published: July 23, 2014
Last Updated: 09/26/2026