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2015 Top Stories in Neurology: Child Neurology
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- Heimer G, Sadaka Y, Israelian L, et al. CAOS-episodic cerebellar ataxia, areflexia, optic atrophy, and sensorineural hearing loss: A third allelic disorder of the ATP1A3 gene. J Child Neurol. 2015;30(13):1749-1756.
- Ng J, Heales SJR, Kurian MA. Clinical features and pharmacotherapy of childhood monoamine neurotransmitter disorders. Pediatr Drugs. 2014;16(4):275-291.
- Pearl PL. Monoamine neurotransmitter disorders. Handb Clin Neurol. 2013;113:1819-1825.
- Viollet L, Glusman G, Murphy KJ, et al. Alternating hemiplegia of childhood: Retrospective genetic study and genotype-phenotype correlations in 187 subjects from the US AHCF Registry. PLoS One. 2015;10(8):e0127045.