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Article: Autosomal-dominant polycystic kidney disease (ADPKD): Executive summary from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference

TitleAutosomal-dominant polycystic kidney disease (ADPKD): Executive summary from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference
Authors
KeywordsDiagnosis
End-stage renal disease
Management
Patient support
Polycystic kidney disease
Issue Date2015
Citation
Kidney International, 2015, v. 88, n. 1, p. 17-27 How to Cite?
AbstractAutosomal-dominant polycystic kidney disease (ADPKD) affects up to 12 million individuals and is the fourth most common cause for renal replacement therapy worldwide. There have been many recent advances in the understanding of its molecular genetics and biology, and in the diagnosis and management of its manifestations. Yet, diagnosis, evaluation, prevention, and treatment vary widely and there are no broadly accepted practice guidelines. Barriers to translation of basic science breakthroughs to clinical care exist, with considerable heterogeneity across countries. The Kidney Disease: Improving Global Outcomes Controversies Conference on ADPKD brought together a panel of multidisciplinary clinical expertise and engaged patients to identify areas of consensus, gaps in knowledge, and research and health-care priorities related to diagnosis; monitoring of kidney disease progression; management of hypertension, renal function decline and complications; end-stage renal disease; extrarenal complications; and practical integrated patient support. These are summarized in this review.
Persistent Identifierhttp://hdl.handle.net/10722/316110
ISSN
2023 Impact Factor: 14.8
2023 SCImago Journal Rankings: 3.886
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChapman, Arlene B.-
dc.contributor.authorDevuyst, Olivier-
dc.contributor.authorEckardt, Kai Uwe-
dc.contributor.authorGansevoort, Ron T.-
dc.contributor.authorHarris, Tess-
dc.contributor.authorHorie, Shigeo-
dc.contributor.authorKasiske, Bertram L.-
dc.contributor.authorOdland, Dwight-
dc.contributor.authorPei, York-
dc.contributor.authorPerrone, Ronald D.-
dc.contributor.authorPirson, Yves-
dc.contributor.authorSchrier, Robert W.-
dc.contributor.authorTorra, Roser-
dc.contributor.authorTorres, Vicente E.-
dc.contributor.authorWatnick, Terry-
dc.contributor.authorWheeler, David C.-
dc.contributor.authorAhn, Curie-
dc.contributor.authorAlam, Ahsan-
dc.contributor.authorAussilhou, Beatrice-
dc.contributor.authorBae, Kyongtae T.-
dc.contributor.authorBennett, William M.-
dc.contributor.authorBergmann, Carsten-
dc.contributor.authorBichet, Daniel G.-
dc.contributor.authorBudde, Klemens-
dc.contributor.authorChauveau, Dominique-
dc.contributor.authorCowley, Benjamin-
dc.contributor.authorDe Coninck, Brenda-
dc.contributor.authorDell, Katherine M.-
dc.contributor.authorDrenth, Joost P.H.-
dc.contributor.authorEcder, Tevfik-
dc.contributor.authorEmma, Francesco-
dc.contributor.authorFérec, Claude-
dc.contributor.authorFlamion, Bruno-
dc.contributor.authorGalletti, Flavia-
dc.contributor.authorGitomer, Bernice-
dc.contributor.authorGrantham, Jared J.-
dc.contributor.authorHarr, Nicole-
dc.contributor.authorHarris, Peter C.-
dc.contributor.authorHigashihara, Eiji-
dc.contributor.authorHodouchi, Eiko-
dc.contributor.authorHogan, Marie C.-
dc.contributor.authorJha, Vivek-
dc.contributor.authorKorst, Uwe-
dc.contributor.authorLagrafeuil, Corinne-
dc.contributor.authorMartin, Rodolfo S.-
dc.contributor.authorMei, Changlin-
dc.contributor.authorMrug, Michal-
dc.contributor.authorObrador, Gregorio T.-
dc.contributor.authorOng, Albert C.M.-
dc.contributor.authorOnuchic, Luiz F.-
dc.contributor.authorPavia, Luisa Sternfeld-
dc.contributor.authorRangan, Gopala K.-
dc.contributor.authorSandford, Richard-
dc.contributor.authorSerra, Andreas L.-
dc.contributor.authorSteinman, Theodore I.-
dc.contributor.authorStrandgaard, Svend-
dc.contributor.authorWalz, Gerd-
dc.contributor.authorWinearls, Christopher G.-
dc.contributor.authorWinston, Kaori Yamane-
dc.date.accessioned2022-08-24T15:49:16Z-
dc.date.available2022-08-24T15:49:16Z-
dc.date.issued2015-
dc.identifier.citationKidney International, 2015, v. 88, n. 1, p. 17-27-
dc.identifier.issn0085-2538-
dc.identifier.urihttp://hdl.handle.net/10722/316110-
dc.description.abstractAutosomal-dominant polycystic kidney disease (ADPKD) affects up to 12 million individuals and is the fourth most common cause for renal replacement therapy worldwide. There have been many recent advances in the understanding of its molecular genetics and biology, and in the diagnosis and management of its manifestations. Yet, diagnosis, evaluation, prevention, and treatment vary widely and there are no broadly accepted practice guidelines. Barriers to translation of basic science breakthroughs to clinical care exist, with considerable heterogeneity across countries. The Kidney Disease: Improving Global Outcomes Controversies Conference on ADPKD brought together a panel of multidisciplinary clinical expertise and engaged patients to identify areas of consensus, gaps in knowledge, and research and health-care priorities related to diagnosis; monitoring of kidney disease progression; management of hypertension, renal function decline and complications; end-stage renal disease; extrarenal complications; and practical integrated patient support. These are summarized in this review.-
dc.languageeng-
dc.relation.ispartofKidney International-
dc.subjectDiagnosis-
dc.subjectEnd-stage renal disease-
dc.subjectManagement-
dc.subjectPatient support-
dc.subjectPolycystic kidney disease-
dc.titleAutosomal-dominant polycystic kidney disease (ADPKD): Executive summary from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1038/ki.2015.59-
dc.identifier.pmid25786098-
dc.identifier.scopuseid_2-s2.0-84934441161-
dc.identifier.volume88-
dc.identifier.issue1-
dc.identifier.spage17-
dc.identifier.epage27-
dc.identifier.eissn1523-1755-
dc.identifier.isiWOS:000357138000006-
dc.identifier.f1000725394119-

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