Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's disease-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's disease

Published:2018-10 Issue: Volume:393 Page:27-30
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Jankovic M.Z.,Dobricic V.,Kresojevic N.,Markovic V.,Petrovic I.,Svetel M.,Pekmezovic T.,Novakovic I.,Kostic V.

Funder

Serbian Ministry of Science and Technological Development

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference38 articles.

1. Genetics in Parkinson disease: Mendelian versus non-Mendelian inheritance;Hernandez;J. Neurochem.,2016

2. Alternative splicing generates different parkin protein isoforms: evidences in human, rat, and mouse brain;Scuderi;Biomed. Res. Int.,2014

3. Parkin disease: a phenotypic study of a large case series;Khan;Brain,2003

4. Association between early-onset Parkinson's disease and mutations in the parkin gene;Lucking;N. Engl. J. Med.,2000

5. Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease;Kilarski;Mov. Disord.,2012

Cited by 8 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. Genetic Testing in Parkinson's Disease;Movement Disorders;2023-06-27

2. A multicenter study of genetic testing for Parkinson’s disease in the clinical setting;npj Parkinson's Disease;2022-11-04

3. Recent developments in nucleic acid-based therapies for Parkinson’s disease: Current status, clinical potential, and future strategies;Frontiers in Pharmacology;2022-10-20

4. Age Cutoff for Early‐Onset Parkinson's Disease: Recommendations from the International Parkinson and Movement Disorder Society Task Force on Early Onset Parkinson's Disease;Movement Disorders Clinical Practice;2022-09-10

5. Transcriptome datasets of neural progenitors and neurons differentiated from induced pluripotent stem cells of healthy donors and Parkinson's disease patients with mutations in the PARK2 gene;Data in Brief;2022-04

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