UBE3A reinstatement as a disease‐modifying therapy for Angelman syndrome-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

UBE3A reinstatement as a disease‐modifying therapy for Angelman syndrome

Published:2021-02-04 Issue:7 Volume:63 Page:802-807
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:Dev Med Child Neurol

Author:

Elgersma Ype¹²³^ORCID,Sonzogni Monica¹³^ORCID

Affiliation:

1. Department of Neuroscience Erasmus University Medical Center Rotterdamthe Netherlands

2. Deptartment of Clinical Genetics Erasmus University Medical Center Rotterdamthe Netherlands

3. The ENCORE Expertise Center for Neurodevelopmental Disorders Erasmus MC Rotterdam the Netherlands

Publisher

Wiley

Subject

Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/dmcn.14831

Reference68 articles.

1. ‘Puppet’ Children A Report on Three Cases

2. Angelman syndrome in Denmark. Birth incidence, genetic findings, and age at diagnosis

3. The behavioral phenotype of the Angelman syndrome

4. An overview of health issues and development in a large clinical cohort of children with Angelman syndrome

5. Clinical aspects of a large group of adults with Angelman syndrome

Cited by 32 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. Association between sleep disturbances and challenging behavior in children and adolescents with Angelman syndrome;Sleep Medicine;2024-11

2. 1H-NMR-based metabolomics reveals metabolic alterations in early development of a mouse model of Angelman syndrome;Molecular Autism;2024-07-24

3. The ubiquitin E3 ligase UBE3A regulates GRIPAP1 and PACSIN1 proteins linked to the endocytic recycling of AMPA receptors;2024-06-20

4. Cobalamins Function as Allosteric Activators of an Angelman Syndrome‐Associated UBE3A/E6AP Variant;ChemBioChem;2024-05-02

5. Undiagnosed rare disease clinic identifies a novel UBE3A variant in two sisters with Angelman syndrome: The end of a diagnostic odyssey;Congenital Anomalies;2024-03-23

同舟云学术

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