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Balciuniene J, DeChene ET, Akgumus G, Romasko EJ, Cao K, Dubbs HA, Mulchandani S, Spinner NB, Conlin LK, Marsh ED, Goldberg E, Helbig I, Sarmady M, Abou Tayoun A. “Use of a Dynamic Genetic Testing Approach for Childhood-Onset Epilepsy.” JAMA
Netw Open. 2019 Apr 5;2(4): e192129. Fulltext: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6481455/

Muriel V, Garcia-Molina A, Aparicio-Lopez C, Ensenat A, Roig-Rovira T. “Neuropsychological Deficits in Alternating Hemiplegia of Childhood: A Case Study.” Rev Neurol. (July 2015): 25-28. (In Spanish)

Bartolini E, Campostrini R, Kiferle L, Pradella S, Rosati E, Chinthapalli K, Palumbo P. “Epilepsy and Brain Channelopathies from Infancy to Adulthood.” Neurol Sci. 2019 Dec 14. Abstract: https://www.ncbi.nlm.nih.gov/pubmed/31838630

Neville B.G., Ninan M. “The Treatment and Management of Alternating Hemiplegia of Childhood.” Developmental Medicine and Child Neurology (2007): 777–780.

Dhakar MB, Bamford NS. “Pearls & Oysters: Alternating Hemiplegia of Childhood Mimics Focal Epilepsy and Paroxysmal Dyskinesia in Infancy.” Neurology. 2018 Jul 3; 91(1): 47-49. Fulltext: http://n.neurology.org/content/91/1/47.long

Rinalduzzi S, Valeriani M, Vigevano F. “Brainstem Dysfunction in Alternating Hemiplegia of Childhood: A Neurophysiological Study.” Cephalalgia 26, no. 5(May 2006): 511-519.

Shafer ME, Mayfield JW, McDonald F. “Alternating Hemiplegia of Childhood: A Study of Neuropsychological Functioning.” Applied Neuropsychology 12, no. 1 (2005): 49-56.

Smedemark-Margulies N, Brownstein CA, Vargas S, Tembulkar SK, Towne, MC, Shi J, et. al. “A Novel de Novo Mutation in ATP1A3 and Childhood-onset Schizophrenia.” Cold Spring Harb Mol Case Studies 2, no. 5 (Setptember 2016): 1008-.

Sugimoto H, Ikeda K, Kawakami K. “Atp1a3-deficient Heterozygous Mice Show Lower Rank in the Hierarchy and Altered Social Behavior.” Genes Brain Behav. 2017 Oct 23.

Sweney M, Newcomb T, Swoboda K. “The Expanding Spectrum of Neurological Phenotypes in Children with ATP1A3 Mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and Beyond.” Pediatric Neurolog (January 2015): 56-64.