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Phenotypes and genotypes in non‐consanguineous and consanguineous primary microcephaly : high incidence of epilepsy
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Lessons learned from 40 novel PIGA patients and a review of the literature
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IQSEC2-related encephalopathy in males and females : a comparative study including 37 novel patients
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- 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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Multiple sclerosis in Belgian children : a multicentre retrospective study
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- Journal Article
- A1
- open access
Effect of Pycnogenol® on attention-deficit hyperactivity disorder (ADHD) : study protocol for a randomised controlled trial
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FOXP1-related intellectual disability syndrome : a recognisable entity
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- Journal Article
- A1
- open access
A restricted repertoire of de novo mutations in ITPR1 cause Gillespie syndrome with evidence for dominant-negative effect
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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
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- Journal Article
- A1
- open access
First line management of prolonged convulsive seizures in children and adults : good practice points
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Extending the KCNQ2 encephalopathy spectrum: clinical and neuroimaging findings in 17 patients
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KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy
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Development of an electronic decision tool to support appropriate treatment choice in adult patients with epilepsy: Epi-Scope®
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Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome
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Development of an electronic decision tool to support appropriate treatment choice in epilepsy
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Vagus nerve stimulation for refractory epilepsy: a Belgian multicenter study
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Prospective screening of migraine criteria in Belgian patients with epilepsy
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Steroids in intractable childhood epilepsy: clinical experience and review of the literature
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Anti-epileptogenesis research: the clinical relevance
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Reciprocal translocation between the proximal regions of the long arms of chromosomes 13 and 15 resulting in unbalanced offspring: characterization by fluorescence in situ hybridization and DNA analysis