39 Einträge gefunden

1. Pathogenesis, diagnosis and management of hyperkalemia.

   1. Lehnhardt, Anja
   2. Kemper, Markus J.

   2011 - Forschungsinformationssystem des UKE
2. High prevalence of renal dysfunction in children after liver transplantation: non-invasive diagnosis using a cystatin C-based equation.

   1. Brinkert, Florian
   2. Kemper, Markus J.
   3. Briem-Richter, Andrea
   4. Van Husen, Michel
   5. Treszl, András
   6. Ganschow, Rainer

   2011 - Forschungsinformationssystem des UKE
3. New therapies in steroid-sensitive and steroid-resistant idiopathic nephrotic syndrome.

   1. Van Husen, Michel
   2. Kemper, Markus J.

   2011 - Forschungsinformationssystem des UKE
4. Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome.

   1. Büscher, Anja K
   2. Kranz, Birgitta
   3. Büscher, Rainer
   4. Hildebrandt, Friedhelm
   5. Dworniczak, Bernd
   6. Pennekamp, Petra
   7. Kuwertz-Bröking, Eberhard

   2010 - Forschungsinformationssystem des UKE
5. Diagnostic examination of the child with urolithiasis or nephrocalcinosis.

   1. Hoppe, Bernd
   2. Kemper, Markus J.

   2010 - Forschungsinformationssystem des UKE
6. Nephronophthisis

   1. Kemper, Markus J.

   2010 - Forschungsinformationssystem des UKE
7. Fibroblast growth factor 23 and bone metabolism in children with chronic kidney disease.

   1. Van Husen, Michel
   2. Fischer, Ann-Katrin
   3. Lehnhardt, Anja
   4. Klaassen, Ilka
   5. Möller, Kristina
   6. Müller-Wiefel, Dirk E.
   7. Kemper, Markus J.

   2010 - Forschungsinformationssystem des UKE
8. Das nephrotische Syndrom im Kindesalter Das nephrotische Syndrom im Kindesalter

   1. Klaassen, Ilka
   2. Kemper, Markus J.

   2010 - Forschungsinformationssystem des UKE
9. Acute renal failure

   1. Kemper, Markus J.

   2010 - Forschungsinformationssystem des UKE
10. Nephrotic Syndrome

    1. Kemper, Markus J.

    2010 - Forschungsinformationssystem des UKE
11. Second-line Options for Refractory Steroid-sensitive and -resistant Nephrotic Syndrome

    1. Oh, Jun
    2. Kemper, Markus J.

    2010 - Forschungsinformationssystem des UKE
12. Biologika in der Therapie des nephrotischen Syndroms.(Biologicals in the treatment of childhood nephrotic syndrome)

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

    2009 - Forschungsinformationssystem des UKE
13. Prevalence of polyomavirus viruria (JC virus/BK virus) in children following liver transplantation.

    1. Brinkert, Florian
    2. Briem-Richter, Andrea
    3. Ilchmann, Corina
    4. Kemper, Markus J.
    5. Ganschow, Rainer

    2009 - Forschungsinformationssystem des UKE
14. Urinary tract infections in children after renal transplantation.

    1. John, Ulrike
    2. Kemper, Markus J.

    2009 - Forschungsinformationssystem des UKE
15. Characterization of the transcriptional regulation of the human MT1-MMP gene and association of risk reduction for focal-segmental glomerulosclerosis with two functional promoter SNPs.

    1. Munkert, Astrid
    2. Helmchen, Udo
    3. Kemper, Markus J.
    4. Bubenheim, Michael
    5. Stahl, Rolf A.K.
    6. Harendza, Sigrid

    2009 - Forschungsinformationssystem des UKE
16. Urinary proteome pattern in children with renal Fanconi syndrome.

    1. Drube, Jens
    2. Schiffer, Eric
    3. Mischak, Harald
    4. Kemper, Markus J.
    5. Neuhaus, Thomas
    6. Pape, Lars
    7. Lichtinghagen, Ralf

    2009 - Forschungsinformationssystem des UKE
17. Transplantation procedures in children with primary hyperoxaluria type 1: outcome and longitudinal growth.

    1. Brinkert, Florian
    2. Ganschow, Rainer
    3. Helmke, Knut
    4. Harps, Egmond
    5. Fischer, Lutz
    6. Nashan, Björn
    7. Hoppe, Bernd

    2009 - Forschungsinformationssystem des UKE
18. Proteomic analysis of mononuclear cells of patients with minimal-change nephrotic syndrome of childhood.

    1. González, Elsa
    2. Neuhaus, Thomas
    3. Kemper, Markus J.
    4. Girardin, Eric

    2009 - Forschungsinformationssystem des UKE
19. 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
20. 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