Clinical problems in hemodialysis patients with autosomal dominant polycystic kidney disease
Author:
Affiliation:
1. Department of Nephrology; Erciyes University Medical Faculty; Kayseri Turkey
2. Department of Nephrology; Sutcu Imam University Medical Faculty; Kahramanmaras Turkey
Publisher
Wiley
Subject
Nephrology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/sdi.12696/fullpdf
Reference136 articles.
1. Autosomal dominant polycystic kidney disease;Gabow;N Engl J Med,1993
2. Polycystic kidney disease;Wilson;N Engl J Med,2004
3. A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16;Reeders;Nature,1985
4. Autosomal dominant polycystic kidney disease: localization of the second gene to chromosome 4q13-q23;Kimberling;Genomics,1993
5. Coassembly of polycystin-1 and -2 produces unique cation permeable currents;Hanaoka;Nature,2000
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1. NOS3 gene intron 4 a/b polymorphism is associated with ESRD in autosomal dominant polycystic kidney disease patients;Brazilian Journal of Nephrology;2022-06
2. Atteintes cardiovasculaires associées à la polykystose rénale autosomique dominante;Néphrologie & Thérapeutique;2021-02
3. Peritoneal dialysis patient selection from a comorbidity perspective;Seminars in Dialysis;2020-10-22
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