Liddle syndrome in a Turkish family with heterogeneous phenotypes-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Liddle syndrome in a Turkish family with heterogeneous phenotypes

Published:2016-06-21 Issue:8 Volume:58 Page:801-804
ISSN:1328-8067
Container-title:Pediatrics International
language:en
Short-container-title:Pediatrics International

Author:

Büyükkaragöz Bahar¹,Yilmaz Aysun Caltik¹,Karcaaltincaba Deniz²,Ozdemir Osman³,Ludwig Michael⁴

Affiliation:

1. Department of Pediatric Nephrology; Keciören Research and Training Hospital; Ankara Turkey

2. Department of Obstetrics and Gynecology; Gazi University; Ankara Turkey

3. Department of Pediatric Cardiology; Keciören Research and Training Hospital; Ankara Turkey

4. Department of Clinical Biochemistry and Clinical Pharmacology; University of Bonn; Bonn Germany

Publisher

Wiley

Subject

Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ped.12985/fullpdf

Reference11 articles.

1. Hypertension in the teenager;Anyaegbu;Pediatr. Clin. North Am.,2014

2. A case of Liddle syndrome;Sinha;Indian J. Pediatr.,2013

3. Genetic diagnosis of Liddle's syndrome by mutation analysis of SCNN1B and SCNN1G in a Chinese family;Wang;Chin. Med. J. (Engl.),2012

4. Liddle syndrome in a Serbian family and literature review of underlying mutations;Bogdanovic;Eur. J. Pediatr.,2012

5. Molecular genetics of Liddle's syndrome;Yang;Clin. Chim. Acta,2014

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. Clinical Features and Mutations in Children with Liddle Syndrome: A Systematic Review of Case Reports;Indian Pediatrics Case Reports;2024-01

2. Neonatal presentation of a patient with Liddle syndrome, South Africa;African Journal of Laboratory Medicine;2023-04-14

3. Clinical and genetic characteristics of the patients with hypertension and hypokalemia carrying a novel SCNN1A mutation;Scandinavian Journal of Clinical and Laboratory Investigation;2022-11-06

4. Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family;Frontiers in Pediatrics;2022-05-24

5. Late-onset hypertension in a child with growth retardation: Answers;Pediatric Nephrology;2022-03-14

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