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Trautmann, Agnes; Lipska-Zietkiewicz, Beata S.; Schaefer, Franz
{ "@context": "https://schema.org/", "@id": 29971, "@type": "ScholarlyArticle", "creator": [ { "@type": "Person", "affiliation": "Univ Ctr Pediat & Adolescent Med, Div Pediat Nephrol, Heidelberg, Germany", "name": "Trautmann, Agnes" }, { "@type": "Person", "affiliation": "Med Univ Gdansk, Dept Biol & Med Genet, Clin Genet Unit, Gdansk, Poland", "name": "Lipska-Zietkiewicz, Beata S." }, { "@type": "Person", "affiliation": "Univ Ctr Pediat & Adolescent Med, Div Pediat Nephrol, Heidelberg, Germany", "name": "Schaefer, Franz" } ], "datePublished": "2018-01-01", "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.", "headline": "Exploring the Clinical and Genetic Spectrum of Steroid Resistant Nephrotic Syndrome: The PodoNet Registry", "identifier": 29971, "image": "https://aperta.ulakbim.gov.tr/static/img/logo/aperta_logo_with_icon.svg", "license": "http://www.opendefinition.org/licenses/cc-by", "name": "Exploring the Clinical and Genetic Spectrum of Steroid Resistant Nephrotic Syndrome: The PodoNet Registry", "url": "https://aperta.ulakbim.gov.tr/record/29971" }
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