Mutational and phenotypic expansion of ATP1A3-related disorders: Report of nine cases
Author:
Funder
DAAD
Medical Genomic Cluster
Thailand Research Fund
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference34 articles.
1. More Than a Decade of Misdiagnosis of Alternating Hemiplegia of Childhood with Catastrophic Outcome;Algahtani;Case Rep Med,2017
2. Hemiconvulsion-hemiplegia-epilepsy syndrome: current understandings;Auvin;Eur J Paediatr Neurol,2012
3. Psychiatric disorders in rapid-onset dystonia-parkinsonism;Brashear;Neurology,2012
4. The phenotypic spectrum of rapid-onset dystonia–parkinsonism (RDP) and mutations in the ATP1A3 gene;Brashear;Brain,2007
5. Sporadic rapid-onset dystonia-parkinsonism syndrome: failure of bilateral pallidal stimulation;Deutschlander;Mov Disord,2005
Cited by 10 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Dystonia;Movement Disorders Phenomenology;2024
2. Molecular Mimicry between Meningococcal B Factor H-Binding Protein and Human Proteins;Global Medical Genetics;2023-11-16
3. Hemidystonia with polymicrogyria is part of ATP1A3-related disorders;Brain and Development;2022-09
4. ATP1A3 mutation in rapid-onset dystonia parkinsonism: New data and genotype-phenotype correlation analysis;Frontiers in Aging Neuroscience;2022-08-01
5. Molecular and clinical characteristics of ATP1A3-related diseases;Frontiers in Neurology;2022-07-26
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3