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Phenotypes and genotypes in non‐consanguineous and consanguineous primary microcephaly : high incidence of epilepsy
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Recurrent arterial ischemic stroke with good response to mycophenolate mofetil
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The clinical heterogeneity of the NARS2 c.822G>C mutation clearly illustrated in two siblings : epilepsy and myopathy
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Multiple sclerosis in Belgian children : a multicentre retrospective study
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Nusinersen versus sham control in infantile-onset spinal muscular atrophy