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ATP1A3mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia

机译：婴儿ATP1A3媒体：一种新的快速发病肌瘤 - 帕金森主义表型，其特征是运动延迟和共济失调

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ALLISON BRASHEAR; JONATHAN W MINK; DEBORAH F HILL; NIKI BOGGS; W VAUGHN MCCALL; MARK A STACY; BEVERLY SNIVELY; LANEY S LIGHT; KATHLEEN J SWEADNER; LAURIE J OZELIUS; LESLIE MORRISON;
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1. ATP1A3 mutations in infants: A new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia [J] . BrashearA., MinkJ.W., HillD.F., Developmental Medicine and Child Neurology . 2012,第11期

机译：婴儿的ATP1A3突变：一种以运动迟缓和共济失调为特征的快速发作的肌张力障碍-帕金森病新表型
2. Rapid-Onset Dystonia-Parkinsonism Phenotype Consistency for a Novel Variant of ATP1A3 in Patients Across 3 Global Populations [J] . Kyoko Hoshino, Kathleen J. Sweadner, Toshitaka Kawarai, Neurology: Genetics . 2021,第2期

机译：快速发作肌瘤 - 帕金森主义表型一致性ATP1A3在3个全球群体患者中的新变种
3. Rapid-onset dystonia-parkinsonism preceded by a single episode of subacute persisting hemiparesis: Expanding the ATP1A3-related disorders phenotype [J] . Mariano Marrodan, Malco Rossi, Marcelo Merello Journal of the Neurological Sciences: Official Bulletin of the World Federation of Neurology . 2018,第期

机译：快速发作的肌瘤毒素 - 帕金森表明亚急性持续血清的一集：扩张ATP1A3相关疾病表型
4. Ailu: An Affordable Sensorized Toy for Detection of Neuro and Motor Delays in Infants [C] . Elaine S. Ho, Wilson Torres, Laura Prosser, IEEE International Conference on Rehabilitation Robotics . 2019

机译：艾露（Ailu）：一种价格合理的感测玩具，可检测婴儿的神经和运动延迟
5. Infant Onset Spinocerebellar Ataxia Type 13 Mutation Leads to Developmental and Rapid Degenerative Phenotypes Related to Hyperexcitability in Purkinje Cells [D] . Ulrich, Brittany Nicole. 2017

机译：婴儿起病的脊髓小脑共济失调13型突变导致发展和快速退化的表型与浦肯野细胞过度兴奋有关。
6. ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia [O] . ALLISON BRASHEAR, JONATHAN MINK, DEBORAH F HILL, -1

机译：婴幼儿aTp1a3基因突变：一种新的快速起效的肌张力障碍帕金森表型特征是运动延迟和共济失调
7. Rapid-Onset Dystonia-Parkinsonism Phenotype Consistency for a Novel Variant of ATP1A3 in Patients Across 3 Global Populations [O] . Kyoko Hoshino, Kathleen J. Sweadner, Toshitaka Kawarai, 2021

机译：快速发作逐步 - 帕金森主义在3个全球群体患者患者ATP1A3新变种的表型一致性

ATP1A3mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia

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