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Associations between muscle morphology and spasticity in children with spastic cerebral palsy
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Is diffuse axonal injury on susceptibility weighted imaging a biomarker for executive functioning in adolescents with traumatic brain injury? (vol 23, pg 525, 2019)
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- Journal Article
- A1
- open access
Standardized motor assessments before the age of five predicting school-aged motor outcome including DCD : a systematic review
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Neurodevelopmental outcomes of very preterm and very-low-birthweight infants in a population-based clinical cohort with a definite perinatal treatment policy
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Motor outcome after perinatal stroke and early prediction of unilateral spastic cerebral palsy
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Recurrent arterial ischemic stroke with good response to mycophenolate mofetil
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Is diffuse axonal injury on susceptibility weighted imaging a biomarker for executive functioning in adolescents with traumatic brain injury?
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Spastic paraplegia with crystalline retinopathy : a recognisable phenotype?
(2017) EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY. In European Journal of Paediatric Neurology 21(Supplement 1). p.e139-e139 -
NR4A2 causes an autism spectrum disorder
(2017) EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY. In European Journal of Paediatric Neurology 21(Supplement 1). p.e49-e49 -
Multiple sclerosis in Belgian children : a multicentre retrospective study
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Imaging in cutis laxa syndrome caused by a dominant negative ALDH18A1 mutation, with hypotheses for intracranial vascular tortuosity and wide perivascular spaces
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Multiple symmetrical lipomatosis: an uncommon presentation of a mitochondrial disease
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Outcome of 12 antenatally diagnosed fetal arachnoid cysts: case series and review of the literature
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Lambert-Eaton myasthenic syndrome in a 13-year-old girl with Xp11.22-p11.23 duplication
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Quality of life in youngsters with cerebral palsy after single-event multilevel surgery
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Elaborating the phenotypic spectrum associated with mutations in ARFGEF2: case study and literature review
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Succinyl-CoA ligase deficiency : report on the first patient resulting from a combined defect in SUGL1 an SUGL2 genes
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Early myoclonic epilepsy, hypertrophic cardiomyopathy and subsequently a nephrotic syndrome in a patient with CoQ10 deficiency caused by mutations in para-hydroxybenzoate-polyprenyl transferase (COQ2)
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A homozygous mutation in IBA57 involved in intramitochondrial iron-sulfur cluster synthesis causes severe encephalopathy and mypathy in two neonates
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Polymerase gamma deficiency (POLG): clinical course in a child with two stage evolution from infantile myocerebrohepatopathy spectrum to an Alpers syndrome and neuropathological findings of Leigh’s encephalopathy