CACNA1S Arg528Cys mutation in a young Chinese man with thyrotoxic hypokalemic periodic paralysis-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

CACNA1S Arg528Cys mutation in a young Chinese man with thyrotoxic hypokalemic periodic paralysis

Published:2020-07 Issue:10 Volume:8 Page:1962-1964
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Rezkalla Nader¹^ORCID,Imam Kamran²^ORCID,Marti Miriam²,Ip Karen²,Mashhadian Ardavan³,Liu Antonio²⁴^ORCID

Affiliation:

1. Ross University School of Medicine Miramar Florida USA

2. Department of Neurology Adventist Health White Memorial Los Angeles California USA

3. Department of Nephrology California Hospital Medical Center Los Angeles California USA

4. Department of Neurology California Hospital Medical Center Los Angeles California USA

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.3054

Reference21 articles.

1. Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

2. Genotype-phenotype correlations of DHP receptor α1-subunit gene mutations causing hypokalemic periodic paralysis

3. Periodic paralysis complicating thyrotoxicosis in Chinese.

4. Propranolol rapidly reverses paralysis, hypokalemia, and hypophosphatemia in thyrotoxic periodic paralysis

5. McKusickVA HamoshA.Online Mendelian Inheritance in Man[Internet] Calcium Channel Voltage‐Dependent L Type Alpha‐1S Subunit; CACNA1S. Published 14 Jan. 1993 (Updated 2016 Feb 17; Cited 2019 Sep 7)www.omim.org/entry/114208

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