1 Ocak 2018 Dergi makalesi Açık Erişim

Trautmann, Agnes; Lipska-Zietkiewicz, Beata S.; Schaefer, Franz

Dublin Core

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  <dc:creator>Trautmann, Agnes</dc:creator>
  <dc:creator>Lipska-Zietkiewicz, Beata S.</dc:creator>
  <dc:creator>Schaefer, Franz</dc:creator>
  <dc:date>2018-01-01</dc:date>
  <dc:description>Background: Steroid resistant nephrotic syndrome (SRNS) is a rare condition, accounting for 10-15% of all children with idiopathic nephrotic syndrome. SRNS can be caused by genetic abnormalities or immune system dysfunction. The prognosis of SRNS varies from permanent remission to progression to end-stage kidney disease, and post-transplant recurrence is common.</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/29971</dc:identifier>
  <dc:identifier>oai:zenodo.org:29971</dc:identifier>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights>
  <dc:source>FRONTIERS IN PEDIATRICS 6</dc:source>
  <dc:title>Exploring the Clinical and Genetic Spectrum of Steroid Resistant Nephrotic Syndrome: The PodoNet Registry</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
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