3 Einträge gefunden

1. Twenty-one additional cases of familial renal glucosuria: absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletion.

   1. Calado, Joaquim
   2. Sznajer, Yves
   3. Metzger, Daniel
   4. Rita, Ana
   5. Hogan, Marie C
   6. Kattamis, Antonis
   7. Scharf, Mauro

   2008 - Forschungsinformationssystem des UKE
2. Rituximab: is replacement of cyclophosphamide and calcineurin inhibitors in steroid-dependent nephrotic syndrome possible?

   1. Dötsch, Jörg
   2. Müller-Wiefel, Dirk E.
   3. Kemper, Markus J.

   2008 - Forschungsinformationssystem des UKE
3. The clinical course of steroid-sensitive childhood nephrotic syndrome is associated with a functional IL12B promoter polymorphism.

   1. Müller-Berghaus, Jan
   2. Kemper, Markus J.
   3. Hoppe, Bernd
   4. Querfeld, Uwe
   5. Müller-Wiefel, Dirk E.
   6. Morahan, Grant
   7. Schadendorf, Dirk

   2008 - Forschungsinformationssystem des UKE