The essential of 2012 results from the French Renal Epidemiology and Information Network (REIN) ESRD registry.

@article{Lassalle2015TheEO,
  title={The essential of 2012 results from the French Renal Epidemiology and Information Network (REIN) ESRD registry.},
  author={Mathilde Lassalle and Carole Ayav and Luc Frimat and Christian Jacquelinet and C. Couchoud},
  journal={Nephrologie & therapeutique},
  year={2015},
  volume={11 2},
  pages={
          78-87
        }
}
The French Renal Epidemiology and Information Network (REIN) registry began in 2002 to provide a tool for public health decision support, evaluation and research related to renal replacement therapies (RRT) for end-stage renal disease (ESRD). It is relying on a network of nephrologists, epidemiologists, patients and public health representatives. Continuous registration covers all dialysis and transplanted patients. In 2012, in France, 10,048 patients started a RRT (154 per million inhabitants… CONTINUE READING
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