Causal and putative pathogenic mutations identified in 39% of children with primary steroid-resistant nephrotic syndrome in South Africa-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Causal and putative pathogenic mutations identified in 39% of children with primary steroid-resistant nephrotic syndrome in South Africa

Published:2022-08-03 Issue:10 Volume:181 Page:3595-3606
ISSN:1432-1076
Container-title:European Journal of Pediatrics
language:en
Short-container-title:Eur J Pediatr

Author:

Nandlal Louansha,Winkler Cheryl A.,Bhimma Rajendra,Cho Sungkweon,Nelson George W.,Haripershad Sudesh,Naicker Thajasvarie

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Link

https://link.springer.com/content/pdf/10.1007/s00431-022-04581-x.pdf

Reference67 articles.

1. Eddy AA, Symons JM (2003) Nephrotic syndrome in childhood. Lancet 362(9384):629–39. https://doi.org/10.1016/S0140-6736(03)14184-0

2. Sinha A, Bagga A (2012) Nephrotic syndrome. Indian J Pediatr 79(8):1045–55. https://doi.org/10.1007/s12098-012-0776-y

3. Yu Z, Ding J, Huang J, Yao Y, Xiao H, Zhang J et al (2005) Mutations in NPHS2 in sporadic steroid-resistant nephrotic syndrome in Chinese children. Nephrol Dial Transplant 20(5):902–908. https://doi.org/10.1093/ndt/gfh769

4. Gipson DS, Massengill SF, Yao L, Nagaraj S, Smoyer WE, Mahan JD et al (2009) Management of childhood onset nephrotic syndrome. Pediatrics 124(2):747–57. https://doi.org/10.1542/peds.2008-1559

5. Levey AS, Eckardt K-U, Dorman NM, Christiansen SL, Cheung M, Jadoul M et al (2020) Nomenclature for kidney function and disease: executive summary and glossary from a Kidney Disease: Improving Global Outcomes (KDIGO) consensus conference. Kidney Dis 6(5):309–317. https://doi.org/10.1159/000509359

Cited by 5 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. Estimation of the Age of the Kashubian-Specific Pathogenic NPHS2 Variant Responsible for Hereditary Steroid-Resistant Nephrotic Syndrome Points to Its Recent Local Origin;Human Mutation;2024-03-21

2. Effects of a novel ANLN E841K mutation associated with SRNS on podocytes and its mechanism;Cell Communication and Signaling;2023-11-13

3. The Alzheimer’s disease risk gene CD2AP functions in dendritic spines by remodelling F-actin;2023-09-01

4. When steroid-resistant nephrotic syndrome runs out of breath;Die Nephrologie;2023-04-28

5. Therapeutic Potential Targeting Podocyte Mitochondrial Dysfunction in Focal Segmental Glomerulosclerosis;Kidney Diseases;2023

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