- Abstract:
-
Polycystic liver disease is a well-described manifestation of autosomal dominant polycystic kidney disease (ADPKD). Biliary tract complications are less well-recognised. We report a 50-year single-centre experience of 1,007 patients, which raised a hypothesis that ADPKD is associated with biliary tract disease. This was then tested using all-England Hospital Episode Statistics data (1998-2012) within which 23,454 people recorded as having ADPKD and 6,412,754 hospital controls were identifi...
Expand abstract - Publication status:
- Published
- Peer review status:
- Peer reviewed
- Version:
- Accepted manuscript
- Files:
-
-
(pdf, 368.5kb)
-
- Publisher copy:
- 10.1681/ASN.2017010084
-
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- Publisher:
- American Society for Nephrology Publisher's website
- Journal:
- Journal of the American Society of Nephrology Journal website
- Volume:
- 28
- Issue:
- 9
- Pages:
- 2738-2748
- Publication date:
- 2017-05-02
- Acceptance date:
- 2017-03-25
- DOI:
- EISSN:
-
1533-3450
- ISSN:
-
1046-6673
- Pubs id:
-
pubs:690244
- URN:
-
uri:f372e8cb-91ad-4fff-b4dd-045397c08053
- UUID:
-
uuid:f372e8cb-91ad-4fff-b4dd-045397c08053
- Local pid:
- pubs:690244
- Copyright holder:
- American Society of Nephrology
- Copyright date:
- 2017
- Notes:
- Copyright © 2017 by the American Society of Nephrology. This is the accepted manuscript version of the article. The final version is available online from American Society of Nephrology at: http://dx.doi.org/10.1681/ASN.2017010084
Journal article
Biliary tract and liver complications in polycystic kidney disease
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