Autosomal Dominant Polycystic Kidney Disease in Children and Adolescents: Assessing and Managing Risk of Progression-Reference-Cited by-同舟云学术

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Autosomal Dominant Polycystic Kidney Disease in Children and Adolescents: Assessing and Managing Risk of Progression

Published:2023-05 Issue:3 Volume:30 Page:236-244
ISSN:2949-8139
Container-title:Advances in Kidney Disease and Health
language:en
Short-container-title:Advances in Kidney Disease and Health

Author:

Dachy Angélique^ORCID,Van Loo Liselotte^ORCID,Mekahli Djalila^ORCID

Publisher

Elsevier BV

Reference105 articles.

1. Prevalence estimates of polycystic kidney and liver disease by population sequencing;Lanktree;J Am Soc Nephrol,2018

2. Prevalence of autosomal dominant polycystic kidney disease in the European Union;Willey;Nephrol Dial Transplant,2017

3. Analysis of data from the ERA-EDTA Registry indicates that conventional treatments for chronic kidney disease do not reduce the need for renal replacement therapy in autosomal dominant polycystic kidney disease;Spithoven;Kidney Int,2014

4. Polycystic kidney disease at end-stage renal disease in the United States: patient characteristics and survival;Abbott;Clin Nephrol,2002

5. Autosomal dominant polycystic kidney disease;Torres;Lancet,2007

Cited by 1 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. Estimating risk of rapid disease progression in pediatric patients with autosomal dominant polycystic kidney disease: a randomized trial of tolvaptan;Pediatric Nephrology;2023-12-13

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