Dent-2 Disease: A Mild Variant of Lowe Syndrome
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference55 articles.
1. X-linked hypercalciuric nephrolithiasis: clinical syndromes and chloride channel mutations;Scheinman;Kidney Int,1998
2. Novel OCRL1 mutations in patients with the phenotype of Dent disease;Utsch;Am J Kidney Dis,2006
3. Dent disease with mutations in OCRL1;Hoopes;Am J Hum Genet,2005
4. OCRL1 mutations in patients with Dent disease phenotype in Japan;Sekine;Pediatr Nephrol,2007
5. Renal manifestations of Dent disease and Lowe syndrome;Cho;Pediatr Nephrol,2008
Cited by 103 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. Atypical phenotypes and novel OCRL variations in southern Chinese patients with Lowe syndrome;Pediatric Nephrology;2024-04-08
2. Ocular Manifestations of the Oculocerebrorenal Syndrome of Lowe;Essentials in Ophthalmology;2024
3. An overview of Dent disease;Childhood Kidney Diseases;2023-12-29
4. КЛИНИЧЕСКИЙ СЛУЧАЙ: БОЛЕЗНЬ ДЕНТА У РЕБЕНКА;Вестник Северо-Восточного федерального университета имени М.К. Аммосова. Серия: Медицинские науки;2023-10-09
5. Ocular manifestations of the genetic renal tubulopathies;Ophthalmic Genetics;2023-09-13
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