The Swiss National Registry for Primary Immunodeficiencies: report on the first 6 years' activity from 2008 to 2014.

@article{Marschall2015TheSN,
  title={The Swiss National Registry for Primary Immunodeficiencies: report on the first 6 years' activity from 2008 to 2014.},
  author={K Marschall and Miriam Hoernes and M Bitzenhofer-Gr{\"u}ber and Peter Jandus and Andrea Duppenthaler and Walter A. Wuillemin and Johannes R Rischewski and Onur Boyman and Ulrich Heininger and Thomas Hauser and U C Steiner and Klara M Posfay-Barbe and J{\"o}rg D Seebach and Mike Recher and Christoph Hess and Arthur Helbling and Janine Reichenbach},
  journal={Clinical and experimental immunology},
  year={2015},
  volume={182 1},
  pages={45-50}
}
The Swiss National Registry for Primary Immunodeficiency Disorders (PID) was established in 2008, constituting a nationwide network of paediatric and adult departments involved in the care of patients with PID at university medical centres, affiliated teaching hospitals and medical institutions. The registry collects anonymized clinical and genetic information on PID patients and is set up within the framework of the European database for PID, run by the European Society of Immunodeficiency… CONTINUE READING
Recent Discussions
This paper has been referenced on Twitter 5 times over the past 90 days. VIEW TWEETS
7 Citations
10 References
Similar Papers

Citations

Publications citing this paper.
Showing 1-7 of 7 extracted citations

References

Publications referenced by this paper.
Showing 1-10 of 10 references

Similar Papers

Loading similar papers…