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Naslov | Phenotypic and genotypic spectrum of familial cases with congenital anomalies of the kidney and urinary tract (CAKUT) (Meeting Abstract) |
Autori | Schniedermeier Timo Goldammer Stephanie Tasic Velibor Vollhardt Anne Abazi Emini Nora Gessner Michaela Putnik Jovana Stavileci Valbona Mueller Dominik Specht Sabine Stajic Natasa Braunisch Matthias C Riedhammer Korbinian Maria Weber Stefanie Hoefele Julia |
Info | PEDIATRIC NEPHROLOGY, (2024), vol. 39 br. 1, Suppl. S, str. S11-S12 |
Ispravka | Web of Science Elečas Rang časopisa |
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Naslov | CLDN16 genotype predicts renal decline in familial hypomagnesemia with hypercalciuria and nephrocalcinosis (Article) |
Autori | Konrad Martin Hou Jianghui Weber Stefanie Doetsch Joerg Kari Jameela A Seeman Tomas Kuwertz-Broeking Eberhard Peco-Antic Amira E Tasic Velibor Dittrich Katalin Alshaya Hammad O von Vigier Rodo O Gallati Sabina Goodenough Daniel A Schaller Andre |
Info | JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, (2008), vol. 19 br. 1 , Suppl. , str. 171 -181 |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: Results of the ESCAPE study (Article) |
Autori | Weber Stefanie Moriniere V Knuppel T Charbit M Dusek J Ghiggeri GM Jankauskiene A Mir S Montini G Peco-Antic Amira E Wuhl E Zurowska AM Mehls O Antignac C Schaefer F Salomon R |
Info | JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, (2006), vol. 17 br. 10, str. 2864-2870 |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Mutations in uroplakin IIIA are a rare cause of renal hypodysplasia in humans (Article) |
Autori | Schonfelder EM Knuppel T Tasic Velibor Miljkovic Predrag Konrad Martin Wuhl E Antignac C Bakkaloglu A Schaefer F Weber Stefanie |
Info | AMERICAN JOURNAL OF KIDNEY DISEASES, (2006), vol. 47 br. 6, str. 1004-1012 |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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