1. Zou, Shuang, Lan, Yu-Long, Gong, Yiwei, Chen, Zhong, Xu, Cenglin. 2023. The role of ATP1A3 gene in epilepsy: We need to know more. In Frontiers in cellular neuroscience, 17, 1143956. doi:10.3389/fncel.2023.1143956. https://pubmed.ncbi.nlm.nih.gov/36866063/
2. Vezyroglou, Aikaterini, Akilapa, Rhoda, Barwick, Katy, Cross, J Helen, Balasubramanian, Meena. 2022. The Phenotypic Continuum of ATP1A3-Related Disorders. In Neurology, 99, e1511-e1526. doi:10.1212/WNL.0000000000200927. https://pubmed.ncbi.nlm.nih.gov/36192182/
3. Kostopoulou, E, Avgeri, A, Apostolou, M I, Tzifas, S, Dimitriou, G. . A novel presentation of an ATP1A3 gene mutation - case report and literature review. In European review for medical and pharmacological sciences, 26, 1108-1113. doi:10.26355/eurrev_202202_28100. https://pubmed.ncbi.nlm.nih.gov/35253165/
4. Ananthavarathan, Piriyankan, Kamourieh, Salwa. . Alternating hemiplegia of childhood. In Handbook of clinical neurology, 198, 221-227. doi:10.1016/B978-0-12-823356-6.00005-6. https://pubmed.ncbi.nlm.nih.gov/38043964/
5. Samanta, Debopam. 2019. Management of Alternating Hemiplegia of Childhood: A Review. In Pediatric neurology, 103, 12-20. doi:10.1016/j.pediatrneurol.2019.10.003. https://pubmed.ncbi.nlm.nih.gov/31836335/
6. Salles, Philippe A, Mata, Ignacio F, Brünger, Tobias, Lal, Dennis, Fernandez, Hubert H. 2021. ATP1A3-Related Disorders: An Ever-Expanding Clinical Spectrum. In Frontiers in neurology, 12, 637890. doi:10.3389/fneur.2021.637890. https://pubmed.ncbi.nlm.nih.gov/33868146/
7. Heinzen, Erin L, Arzimanoglou, Alexis, Brashear, Allison, van den Maagdenberg, Arn, Vilsen, Bente. . Distinct neurological disorders with ATP1A3 mutations. In The Lancet. Neurology, 13, 503-14. doi:10.1016/S1474-4422(14)70011-0. https://pubmed.ncbi.nlm.nih.gov/24739246/
8. Geyer, Howard L, Bressman, Susan B. . Rapid-onset dystonia-parkinsonism. In Handbook of clinical neurology, 100, 559-62. doi:10.1016/B978-0-444-52014-2.00040-9. https://pubmed.ncbi.nlm.nih.gov/21496607/
9. Ledoux, Mark S. 2024. ATP1A3-Associated Paroxysmal Dystonia. In Tremor and other hyperkinetic movements (New York, N.Y.), 14, 61. doi:10.5334/tohm.975. https://pubmed.ncbi.nlm.nih.gov/39712145/
10. Muthaffar, Osama Y, Alqarni, Asma, Shafei, Jumana A, Alyazidi, Anas S, Naseer, Muhammad Imran. 2024. Childhood-related neural genotype-phenotype in ATP1A3 mutations: comprehensive analysis. In Genes & genomics, 46, 475-487. doi:10.1007/s13258-023-01481-8. https://pubmed.ncbi.nlm.nih.gov/38243045/
智鼠故事 
