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Childhood epilepsy with occipital paroxysms: clinical variants in 134 patients.

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Reversible cortical atrophy and cognitive decline induced by valproic acid.

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Absence of mutations in ATM, the gene responsible for ataxia telangiectasia in patients with cerebellar ataxia.

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Incidence, Prevalence, Risk Factors, and Outcomes of ICU-Acquired Weakness Among Critically Ill Children: A Systematic Review and Meta-Analysis.

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Familial infantile bilateral striatal necrosis: clinical features and response to biotin treatment.

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