1 Ocak 2014 Dergi makalesi Açık Erişim

Lipska-Zietkiewicz, Beata S.; Ranchin, Bruno; Iatropoulos, Paraskevas; Gellermann, Jutta; Melk, Anette; Ozaltin, Fatih; Caridi, Gianluca; Seeman, Tomas; Tory, Kalman; Jankauskiene, Augustina; Zurowska, Aleksandra; Szczepanska, Maria; Wasilewska, Anna; Harambat, Jerome; Trautmann, Agnes; Peco-Antic, Amira; Borzecka, Halina; Moczulska, Anna; Saeed, Bassam; Bogdanovic, Radovan; Bogdanovic, Radovan

Dublin Core

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  <dc:creator>Lipska-Zietkiewicz, Beata S.</dc:creator>
  <dc:creator>Ranchin, Bruno</dc:creator>
  <dc:creator>Iatropoulos, Paraskevas</dc:creator>
  <dc:creator>Gellermann, Jutta</dc:creator>
  <dc:creator>Melk, Anette</dc:creator>
  <dc:creator>Ozaltin, Fatih</dc:creator>
  <dc:creator>Caridi, Gianluca</dc:creator>
  <dc:creator>Seeman, Tomas</dc:creator>
  <dc:creator>Tory, Kalman</dc:creator>
  <dc:creator>Jankauskiene, Augustina</dc:creator>
  <dc:creator>Zurowska, Aleksandra</dc:creator>
  <dc:creator>Szczepanska, Maria</dc:creator>
  <dc:creator>Wasilewska, Anna</dc:creator>
  <dc:creator>Harambat, Jerome</dc:creator>
  <dc:creator>Trautmann, Agnes</dc:creator>
  <dc:creator>Peco-Antic, Amira</dc:creator>
  <dc:creator>Borzecka, Halina</dc:creator>
  <dc:creator>Moczulska, Anna</dc:creator>
  <dc:creator>Saeed, Bassam</dc:creator>
  <dc:creator>Bogdanovic, Radovan</dc:creator>
  <dc:creator>Bogdanovic, Radovan</dc:creator>
  <dc:date>2014-01-01</dc:date>
  <dc:description>WT1 mutations cause a wide spectrum of renal and extrarenal manifestations. Here we evaluated disease prevalence, phenotype spectrum, and genotype-phenotype correlations of 61 patients with WT1-related steroid-resistant nephrotic syndrome relative to 700 WT1-negative patients, all with steroid-resistant nephrotic syndrome. WT1 patients more frequently presented with chronic kidney disease and hypertension at diagnosis and exhibited more rapid disease progression. Focal segmental glomerulosclerosis was equally prevalent in both cohorts, but diffuse mesangial sclerosis was largely specific for WT1 disease and was present in 34% of cases. Sex reversal and/or urogenital abnormalities (52%), Wilms tumor (38%), and gonadoblastoma (5%) were almost exclusive to WT1 disease.</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/66453</dc:identifier>
  <dc:identifier>oai:zenodo.org:66453</dc:identifier>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights>
  <dc:source>KIDNEY INTERNATIONAL 85(5) 1169-1178</dc:source>
  <dc:title>Genotype-phenotype associations in WT1 glomerulopathy</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
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