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dc.contributor.authorIscaife, Alexandre [UNIFESP]
dc.contributor.authorBarbosa, Mauro [UNIFESP]
dc.contributor.authorOrtiz, Valdemar [UNIFESP]
dc.contributor.authorMacedo, Antonio [UNIFESP]
dc.date.accessioned2016-01-24T14:17:03Z
dc.date.available2016-01-24T14:17:03Z
dc.date.issued2011-08-01
dc.identifierhttp://dx.doi.org/10.1016/j.jpurol.2010.12.005
dc.identifier.citationJournal of Pediatric Urology. Oxford: Elsevier B.V., v. 7, n. 4, p. 491-494, 2011.
dc.identifier.issn1477-5131
dc.identifier.urihttp://repositorio.unifesp.br/handle/11600/33925
dc.description.abstractSegmental multicystic dysplastic kidney is a rare subtype, found in only about 4% of children diagnosed with MCDK. To the best of our knowledge, we describe the 36th reported case of segmental multicystic kidney disease. (C) 2010 Journal of Pediatric Urology Company. Published by Elsevier B.V. All rights reserved.en
dc.format.extent491-494
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofJournal of Pediatric Urology
dc.rightsAcesso restrito
dc.subjectMulticystic dysplastic kidneyen
dc.titleSegmental multicystic dysplastic kidney: A rare situationen
dc.typeArtigo
dc.rights.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.description.affiliationUniversidade Federal de São Paulo, Dept Urol, BR-01323000 São Paulo, Brazil
dc.description.affiliationUnifespUniversidade Federal de São Paulo, Dept Urol, BR-01323000 São Paulo, Brazil
dc.identifier.doi10.1016/j.jpurol.2010.12.005
dc.description.sourceWeb of Science
dc.identifier.wosWOS:000292665400025


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