Items where Author is "Hoppe, Bernd"

2010

Sullivan, Maren and Erlic, Zoran and Hoffmann, Michael M. and Arbeiter, Klaus and Patzer, Ludwig and Budde, Klemens and Hoppe, Bernd and Zeier, Martin and Lhotta, Karl and Rybicki, Lisa A. and Bock, Andreas and Berisha, Gani and Neumann, Hartmut P. H.. (2010) Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndrome. Annals of human genetics, Vol. 74, H. 1. pp. 17-26.

2008

Offner, Gisela and Toenshoff, Burkhard and Höcker, Britta and Krauss, Manuela and Bulla, Monika and Cochat, Pierre and Fehrenbach, Henry and Fischer, Wolfgang and Foulard, Michel and Hoppe, Bernd and Hoyer Peter, F. and Jungraithmayr Therese, C. and Klaus, Günter and Latta, Kay and Leichter, Heinz and Mihatsch Michael, J. and Misselwitz, Joachim and Montoya, Carmen and Müller-Wiefel Dirk, E. and Neuhaus Thomas, J. and Pape, Lars and Querfeld, Uwe and Plank, Christian and Schwarke, Dieter and Wygoda, Simone and Zimmerhackl Lothar, B.. (2008) Efficacy and safety of basiliximab in pediatric renal transplant patients receiving cyclosporine, mycophenolate mofetil, and steroids. Transplantation, Vol. 86. pp. 1241-1248.

2006

Sayer, John A. and Otto, Edgar A. and O'Toole, John F. and Nurnberg, Gudrun and Kennedy, Michael A. and Becker, Christian and Hennies, Hans Christian and Helou, Juliana and Attanasio, Massimo and Fausett, Blake V. and Utsch, Boris and Khanna, Hemant and Liu, Yan and Drummond, Iain and Kawakami, Isao and Kusakabe, Takehiro and Tsuda, Motoyuki and Ma, Li and Lee, Hwankyu and Larson, Ronald G. and Allen, Susan J. and Wilkinson, Christopher J. and Nigg, Erich A. and Shou, Chengchao and Lillo, Concepcion and Williams, David S. and Hoppe, Bernd and Kemper, Markus J. and Neuhaus, Thomas and Parisi, Melissa A. and Glass, Ian A. and Petry, Marianne and Kispert, Andreas and Gloy, Joachim and Ganner, Athina and Walz, Gerd and Zhu, Xueliang and Goldman, Daniel and Nurnberg, Peter and Swaroop, Anand and Leroux, Michel R. and Hildebrandt, Friedhelm. (2006) The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4. Nature genetics, Vol. 38, H. 6. pp. 674-681.