Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Proteinuria and CLCN5[original query] |
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Screening for CLCN5 mutation in renal calcium stone formers patients. Anais da Academia Brasileira de Ciências 2005 Mar 77 (1): 95-101. Rebelo Maria Alice P, Tostes Vera, Araújo Nordeval C, Martini Sabrina V, Botelho Bruno F, Guggino William B, Morales Marcelo |
Prevalence of low molecular weight proteinuria and Dent disease 1 CLCN5 mutations in proteinuric cohorts. Pediatric nephrology (Berlin, Germany) 2019 3 35 (4): 633-640. Beara-Lasic Lada, Cogal Andrea, Mara Kristin, Enders Felicity, Mehta Ramila A, Haskic Zejfa, Furth Susan L, Trachtman Howard, Scheinman Steven J, Milliner Dawn S, Goldfarb David S, Harris Peter C, Lieske John C, |
Phenotypic spectrum and antialbuminuric response to angiotensin converting enzyme inhibitor and angiotensin receptor blocker therapy in pediatric Dent disease. Molecular genetics & genomic medicine 2020 6 8 (8): e1306. Deng Haiyue, Zhang Yanqin, Xiao Huijie, Yao Yong, Zhang Hongwen, Liu Xiaoyu, Su Baige, Guan Na, Zhong Xuhui, Wang Suxia, Ding Jie, Wang Fa |
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- Page last updated:Sep 25, 2023
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