pubmed-article:21458901 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:21458901 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
pubmed-article:21458901 | lifeskim:mentions | umls-concept:C0085413 | lld:lifeskim |
pubmed-article:21458901 | lifeskim:mentions | umls-concept:C0206074 | lld:lifeskim |
pubmed-article:21458901 | lifeskim:mentions | umls-concept:C0031139 | lld:lifeskim |
pubmed-article:21458901 | pubmed:issue | 6 | lld:pubmed |
pubmed-article:21458901 | pubmed:dateCreated | 2011-5-23 | lld:pubmed |
pubmed-article:21458901 | pubmed:abstractText | Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary cause of kidney failure. Peritoneal dialysis (PD) often is avoided because of concerns about hernias and peritonitis. | lld:pubmed |
pubmed-article:21458901 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21458901 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21458901 | pubmed:language | eng | lld:pubmed |
pubmed-article:21458901 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21458901 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:21458901 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:21458901 | pubmed:month | Jun | lld:pubmed |
pubmed-article:21458901 | pubmed:issn | 1523-6838 | lld:pubmed |
pubmed-article:21458901 | pubmed:author | pubmed-author:JooFF | lld:pubmed |
pubmed-article:21458901 | pubmed:author | pubmed-author:SzetoCheuk-Ch... | lld:pubmed |
pubmed-article:21458901 | pubmed:author | pubmed-author:ChowKai-MingK... | lld:pubmed |
pubmed-article:21458901 | pubmed:author | pubmed-author:LeungChi-BonC... | lld:pubmed |
pubmed-article:21458901 | pubmed:author | pubmed-author:KwanBonnie... | lld:pubmed |
pubmed-article:21458901 | pubmed:author | pubmed-author:Kam-Tao... | lld:pubmed |
pubmed-article:21458901 | pubmed:copyrightInfo | Copyright © 2011 National Kidney Foundation, Inc. Published by Elsevier Inc. All rights reserved. | lld:pubmed |
pubmed-article:21458901 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:21458901 | pubmed:volume | 57 | lld:pubmed |
pubmed-article:21458901 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:21458901 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:21458901 | pubmed:pagination | 903-7 | lld:pubmed |
pubmed-article:21458901 | pubmed:dateRevised | 2011-9-30 | lld:pubmed |
pubmed-article:21458901 | pubmed:meshHeading | pubmed-meshheading:21458901... | lld:pubmed |
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pubmed-article:21458901 | pubmed:meshHeading | pubmed-meshheading:21458901... | lld:pubmed |
pubmed-article:21458901 | pubmed:meshHeading | pubmed-meshheading:21458901... | lld:pubmed |
pubmed-article:21458901 | pubmed:meshHeading | pubmed-meshheading:21458901... | lld:pubmed |
pubmed-article:21458901 | pubmed:meshHeading | pubmed-meshheading:21458901... | lld:pubmed |
pubmed-article:21458901 | pubmed:meshHeading | pubmed-meshheading:21458901... | lld:pubmed |
pubmed-article:21458901 | pubmed:meshHeading | pubmed-meshheading:21458901... | lld:pubmed |
pubmed-article:21458901 | pubmed:year | 2011 | lld:pubmed |
pubmed-article:21458901 | pubmed:articleTitle | Peritoneal dialysis as the first-line renal replacement therapy in patients with autosomal dominant polycystic kidney disease. | lld:pubmed |
pubmed-article:21458901 | pubmed:affiliation | Department of Nephrology, Shanghai Changzheng Hospital, Second Military Medical University, Shanghai, China. lilin_616@163.com | lld:pubmed |
pubmed-article:21458901 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:21458901 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:21458901 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:21458901 | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:21458901 | lld:pubmed |