Peritoneal Dialysis in Special Situations
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-030-70897-9_20
Reference74 articles.
1. Torres VE, Harris PC, Pirson Y. Autosomal dominant polycystic kidney disease. Lancet. 2007;369:1287–301. https://doi.org/10.1016/S0140-6736(07)60601-1.
2. Spithoven EM, et al. Renal replacement therapy for autosomal dominant polycystic kidney disease (ADPKD) in Europe: prevalence and survival--an analysis of data from the ERA-EDTA Registry. Nephrol Dial Transplant. 2014;29 Suppl 4:iv15–25. https://doi.org/10.1093/ndt/gfu017.
3. Hadimeri H, Johansson AC, Haraldsson B, Nyberg G. CAPD in patients with autosomal dominant polycystic kidney disease. Perit Dial Int. 1998;18:429–32.
4. Abbott KC, Agodoa LY. Polycystic kidney disease at end-stage renal disease in the United States: patient characteristics and survival. Clin Nephrol. 2002;57:208–14. https://doi.org/10.5414/cnp57208.
5. Koc Y, et al. Is peritoneal dialysis a therapeutic option for polycystic kidney disease? 15 years’ experience in a single center. Nephrol Ther. 2016;12:215–20. https://doi.org/10.1016/j.nephro.2015.12.006.
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