3rd Annual NephCure Kidney Network Data Report

We are pleased to provide you with the 3rd Annual Data Report of the NephCure Kidney Network Patient Registry. This report summarizes the data provided by 666 registry participants collected from March 2016 to March 2017.




Terms and Conditions | Privacy Policy
Established in collaboration with the Office of Rare Diseases Research (ORDR), National Center National Center for Advancing Translational Sciences (NCATS), National Institutes of Health as part of the Global Rare Diseases Patient Registry and Data Repository (GRDR) pilot project, partially funded through a Patient-Centered Outcomes Research Institute (PCORI) Award (1306-04903) for development of the National Patient-Centered Clinical Research Network, known as PCORnet.

Copyright © 2017 Arbor Research Collaborative for Health - All Rights Reserved