A case report on the exceptional coincidence of two inherited renal disorders: ADPKD and Alport syndrome-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

A case report on the exceptional coincidence of two inherited renal disorders: ADPKD and Alport syndrome

Published:2017-07-01 Issue:07 Volume:88 Page:45-51
ISSN:0301-0430
Container-title:Clinical Nephrology
language:en
Short-container-title:CN

Author:

Ebner Kathrin,Reintjes Nadine,Feldkötter Markus,Körber Friederike,Nagel Mato,Dötsch Jörg,Hoppe Bernd,Weber Lutz,Beck Bodo,Liebau Max

Publisher

Dustri-Verlgag Dr. Karl Feistle

Subject

Nephrology,General Medicine

Cited by 6 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. Coexisting presentation of two rare genetic variants of autosomal dominant polycystic kidney disease and Alport syndrome;BMJ Case Reports;2024-05

2. Diagnosing Fabry nephropathy: the challenge of multiple kidney disease;BMC Nephrology;2023-11-21

3. Paget’s Disease of the Bone and Lynch Syndrome: An Exceptional Finding;Diagnostics;2023-06-17

4. Features of Autosomal Recessive Alport Syndrome: A Systematic Review;Journal of Clinical Medicine;2019-02-03

5. Digenic inheritance and genetic modifiers;Clinical Genetics;2018-01-25

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