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Author/Creator Waldegger, Siegfried

1. Deficiency of the sphingosine‐1‐phosphate lyase SGPL1 is associated with congenital nephrotic syndrome and congenital adrenal calcifications. Issue 4 (6th March 2017)

Authors:
Janecke, Andreas R.; Xu, Ruijuan; Steichen‐Gersdorf, Elisabeth; Waldegger, Siegfried; Entenmann, Andreas; Giner, Thomas; Krainer, Iris; Huber, Lukas A; Hess, Michael W; Frishberg, Yaacov; Barash, Hila; Tzur, Shay; Schreyer‐Shafir, Nira; Sukenik–Halevy, Rivka; Zehavi, Tania; Raas‐Rothschild, Annic...
Journal:
Human mutation
Issue:
Volume 38:Issue 4(2017)
Page Start:
365
Record Type:
Journal Article
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2. Successful management of recurrent focal segmental glomerulosclerosis. Issue 11 (13th August 2018)

Authors:
Kienzl‐Wagner, Katrin; Rosales, Alejandra; Scheidl, Stefan; Giner, Thomas; Bösmüller, Claudia; Rudnicki, Michael; Oberhuber, Rupert; Margreiter, Christian; Soleiman, Afschin; Öfner, Dietmar; Waldegger, Siegfried; Schneeberger, Stefan
Journal:
American journal of transplantation
Issue:
Volume 18:Issue 11(2018)
Page Start:
2818
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗