Prof. Dr. Michael Wiesener

Professur für Innere Medizin (Nephrologie)

Experience with belatacept rescue therapy in kidney transplant recipients (2016) Brakemeier S, Kannenkeril D, Duerr M, Braun T, Bachmann F, Schmidt D, Wiesener M, Budde K Journal article Complement Factor H-Related 5-Hybrid Proteins Anchor Properdin and Activate Complement at Self-Surfaces (2016) Chen Q, Manzke M, Hartmann A, Büttner M, Amann KU, Pauly D, Wiesener M, et al. Journal article Hypoxia inhibits nephrogenesis through paracrine Vegfa despite the ability to enhance tubulogenesis (2015) Schley G, Scholz H, Kraus A, Hackenbeck T, Klanke B, Willam C, Wiesener M, et al. Journal article Association of a coding polymorphism in Fc gamma receptor 2A and graft survival in re-transplant candidates (2015) Fuernrohr BG, Weiss KM, Harre U, Wiesener M, Spriewald BM, Arnold M Journal article Discordant Clinical Course of Vitamin-D-Hydroxylase (CYP24A1) Associated Hypercalcemia in Two Adult Brothers With Nephrocalcinosis (2015) Jobst-Schwan T, Pannes A, Schlingmann KP, Eckardt KU, Beck BB, Wiesener M Journal article Depression, Anxiety, Resilience and Coping Pre and Post Kidney Transplantation - Initial Findings from the Psychiatric Impairments in Kidney Transplantation (PI-KT)-Study (2015) Mueller HH, Englbrecht M, Wiesener M, Titze S, Heller K, Groemer TW, Schett G, et al. Journal article Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management-A KDIGO consensus report (2015) Eckardt KU, Alper SL, Antignac C, Bleyer AJ, Chauveau D, Dahan K, Deltas C, et al. Journal article Complement factor H-related hybrid protein deregulates complement in dense deposit disease (2014) Chen Q, Wiesener M, Eberhardt HU, Hartmann A, Uzonyi B, Kirschfink M, Amann KU, et al. Journal article Hypoxia regulates the sperm associated antigen 4 (SPAG4) via HIF, which is expressed in renal clear cell carcinoma and promotes migration and invasion in vitro (2014) Knaup K, Monti J, Hackenbeck T, Jobst-Schwan T, Klanke B, Schietke RE, Wacker I, et al. Journal article Renal fibrosis is the common feature of autosomal dominant tubulointerstitial kidney diseases caused by mutations in mucin 1 or uromodulin (2014) Ekici AB, Hackenbeck T, Moriniere V, Panness A, Büttner M, Uebe S, Janka RM, et al. Journal article