scholarly journals Induced pluripotent stem cells derived from an autosomal dominant polycystic kidney disease patient carrying a PKD1 Q533X mutation

2017 ◽  
Vol 25 ◽  
pp. 83-87 ◽  
Author(s):  
Jia-Jung Lee ◽  
Ming-Ching Ho ◽  
Ching-Ying Huang ◽  
Cheng-Hao Wen ◽  
Yu-Che Cheng ◽  
...  
2020 ◽  
Vol 9 (4) ◽  
pp. 478-490 ◽  
Author(s):  
Annegien T. Kenter ◽  
Eveline Rentmeester ◽  
Job Riet ◽  
Ruben Boers ◽  
Joachim Boers ◽  
...  

2013 ◽  
Vol 24 (10) ◽  
pp. 1571-1586 ◽  
Author(s):  
Benjamin S. Freedman ◽  
Albert Q. Lam ◽  
Jamie L. Sundsbak ◽  
Rossella Iatrino ◽  
Xuefeng Su ◽  
...  

2017 ◽  
Vol 37 (4) ◽  
pp. 384-388 ◽  
Author(s):  
Sana Khan ◽  
Anna Giuliani ◽  
Carlo Crepaldi ◽  
Claudio Ronco ◽  
Mitchell H. Rosner

End-stage renal disease secondary to autosomal dominant poly-cystic kidney (ADPKD) is a common issue worldwide. Peritoneal dialysis (PD) is a reasonable option for renal replacement therapy for these patients and should not be withheld due to concerns that the patient may not tolerate the fluid volumes in the peritoneal cavity. This review covers the existing data on the outcomes and complications associated with the use of PD in the polycystic kidney disease patient. In general, PD is well tolerated and outcomes in ADPKD patients are equivalent to or better than other patient groups.


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