Dent's disease: can we slow its progression?
Author:
Publisher
Oxford University Press (OUP)
Subject
Transplantation,Nephrology
Link
http://academic.oup.com/ndt/article-pdf/16/7/1512/23370932/161512.pdf
Reference10 articles.
1. Dent CE, Friedman M. Hypercalciuric rickets associated with renal tubular damage. Arch Dis Child1964; 39: 240–249
2. Wrong OM, Norden AGW, Feest TG. Dent's Disease; a familial proximal renal tubular syndrome with low molecular weight proteinuria, hypercalciuria, nephrocalcinosis, metabolic bone disease, progressive renal failure and a marked male predominance. Q J Med1994; 87: 473–493
3. Pearce SHS. Straightening out the renal tubule: advances in the molecular basis of the inherited tubulopathies. Q J Med1998; 91: 5–12
4. Norden AGW, Scheinman SJ, Deschodt‐Lanckman MM et al. Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases. Kidney Int2000; 57: 240–249
5. Thakker RV. Pathogenesis of Dent's Disease and related syndromes of X‐linked tubular nephrolithiasis. Kidney Int2000; 57: 787–793
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. Dent-2 disease with a Bartter-like phenotype caused by the Asp631Glu mutation in the OCRL gene;BMC Nephrology;2022-05-12
2. Two brothers with identical variants of the CLCN5 gene—one developing Dent’s disease;Clinical Kidney Journal;2017-10-16
3. Le syndrome de Dent. Suivi néphrologique de quatre cas de la même famille;Néphrologie & Thérapeutique;2012-04
4. Growth Hormone Improves Growth Rate and Preserves Renal Function in Dent Disease;Journal of Pediatric Endocrinology and Metabolism;2008-01
5. Phenotype and genotype of Dent?s disease in three Korean boys;Pediatric Nephrology;2005-02-18
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