Annals of neurology

Aberrant seizure-induced neurogenesis in experimental temporal lobe epilepsy.

Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromes.

Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation.

Linkage and association with the NOS2A locus on chromosome 17q11 in multiple sclerosis.

Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation.

Linkage and association with the NOS2A locus on chromosome 17q11 in multiple sclerosis.

Bilateral frontoparietal polymicrogyria: clinical and radiological features in 10 families with linkage to chromosome 16.

Potential of gene therapy for pediatric neurotransmitter diseases: lessons from Parkinson's disease.

Potential of gene therapy for pediatric neurotransmitter diseases: lessons from Parkinson's disease.

Mistaken treatment of anterior ischemic optic neuropathy with interferon beta-1a.

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