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Genotype-phenotype correlation in NF1 : evidence for a more severe phenotype associated with missense mutations affecting NF1 codons 844–848
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Inborn errors in RNA polymerase III underlie severe varicella zoster virus infections
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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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Effect of Pycnogenol® on attention-deficit hyperactivity disorder (ADHD) : study protocol for a randomised controlled trial
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Severe congenital microcephaly with AP4M1 mutation, a case report
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Nusinersen versus sham control in infantile-onset spinal muscular atrophy
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RC3H1 mutation with increased ICOS expression causes an autoinflammatory syndrome
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EFFECTS : an expanded access program of everolimus for patients with subependymal giant cell astrocytoma associated with tuberous sclerosis complex
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Therapeutic plasma exchange in children with acute autoimmune central nervous system disorders