Challenges in Clinicogenetic Correlations: One Phenotype – Many Genes-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Challenges in Clinicogenetic Correlations: One Phenotype – Many Genes

Published:2021-03-02 Issue:3 Volume:8 Page:311-321
ISSN:2330-1619
Container-title:Movement Disorders Clinical Practice
language:en
Short-container-title:Mov Disord Clin Pract

Author:

Gannamani Rahul¹²³^ORCID,Veen Sterre¹³^ORCID,Egmond Martje¹³^ORCID,Koning Tom J.²³⁴^ORCID,Tijssen Marina A.J.¹³^ORCID

Affiliation:

1. Department of Neurology University of Groningen, University Medical Centre Groningen Groningen The Netherlands

2. Department of Genetics University of Groningen, University Medical Centre Groningen Groningen The Netherlands

3. Expertise Centre Movement Disorders Groningen University Medical Centre Groningen Groningen The Netherlands

4. Pediatrics, Department of Clinical Sciences Lund University Lund Sweden

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mdc3.13163

Reference81 articles.

1. Twenty years on: Myoclonus‐dystonia and ε‐sarcoglycan — neurodevelopment, channel, and signaling dysfunction

2. Recent advances in genetics of chorea

3. Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force

4. Dystonia in children and adolescents: a systematic review and a new diagnostic algorithm

5. The Classification of Autosomal Recessive Cerebellar Ataxias: a Consensus Statement from the Society for Research on the Cerebellum and Ataxias Task Force

Cited by 14 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. The natural history of progressive myoclonus ataxia;Neurobiology of Disease;2024-09

2. Next-generation sequencing and bioinformatics in rare movement disorders;Nature Reviews Neurology;2024-01-03

3. Involuntary movements and postures (Dystonia);Neurogenetics for the Practitioner;2024

4. Clinical and genetic analyses of a Swedish patient series diagnosed with ataxia;Journal of Neurology;2023-10-03

5. Editorial: Genetic advances and translational applications in movement disorders;Frontiers in Neurology;2023-09-20

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