The objectives of the European Reference Networks (ERN) are to:

  • share expertise,
  • improve diagnosis,
  • educate and train patients, care providers and doctors,
  • produce guidelines,
  • build databases,
  • develop connections to facilitate research,
  • perform clinical trials on rare endocrine conditions,
  • disseminate results to patients, health care providers (HCPs) and public health organisations,
  • link up with other ERNs.
ESPE in collaboration with the European Society for Endocrinology (ESE) have worked together to establish a European Reference Network for Rare Endocrine Disorders (EndoERN).  If you are interested in any aspect of the EndoERN are advised to contact Olaf Hiort or Alberto Pereira.

EndoERN Updates