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SLC7A3 : in silico prediction of a potential new cause of childhood epilepsy
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- Journal Article
- A1
- open access
Use of zebrafish models to boost research in rare genetic diseases
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- Journal Article
- A1
- open access
Recommendations for the treatment of epilepsy in adult and pediatric patients in Belgium : 2020 update
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Absent population-level laterality for white matter asymmetries in specific language impairment
(2018) -
- Journal Article
- A1
- open access
Inborn errors in RNA polymerase III underlie severe varicella zoster virus infections
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Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders
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- Journal Article
- A1
- open access
Serotonergic modulation as effective treatment for Dravet syndrome in a zebrafish mutant model
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Interictal cardiorespiratory variability in temporal lobe and absence epilepsy in childhood
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Detecting rare events using extreme value statistics applied to epileptic convulsions in children
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Accelerometry-based home monitoring for detection of nocturnal hypermotor seizures based on novelty detection