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Get Free AccessERKReg is a rapidly growing source of epidemiological information and patient cohorts for clinical research, and an innovative tool to monitor management quality and patient outcomes.
Giulia Bassanese, Tanja Wlodkowski, Aude Servais, Laurence Heidet, Dario Roccatello, Francesco Emma, Elena Levtchenko, Gema Ariceta, Justine Bacchetta, Giovambattista Capasso, Augustina Jankauskienė, Marius Miglinas, Pietro Manuel Ferraro, Giovanni Montini, Jun Oh, Stéphane Decramer, Tanja Kersnik Levart, Jack F.M. Wetzels, Elisabeth A. M. Cornelissen, Olivier Devuyst, Aleksandra Żurowska, Lars Pape, Anja Buescher, Dieter Haffner, Nataša Marčun Varda, Gian Marco Ghiggeri, Giuseppe Remuzzi, Martin Konrad, Germana Longo, Detlef Böckenhauer, Atif Awan, Ilze Andersone, Jaap W. Groothoff, Franz Schaefer (2021). The European Rare Kidney Disease Registry (ERKReg): objectives, design and initial results. , 16(1), DOI: https://doi.org/10.1186/s13023-021-01872-8.
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Type
Article
Year
2021
Authors
34
Datasets
0
Total Files
0
Language
en
DOI
https://doi.org/10.1186/s13023-021-01872-8
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