The European Registry on Cushing's syndrome: 2-year experience. Baseline demographic and clinical characteristics.

@article{Valassi2011TheER,
  title={The European Registry on Cushing's syndrome: 2-year experience. Baseline demographic and clinical characteristics.},
  author={Elena Valassi and Alicia de los Santos and Maria Yaneva and Mikl{\'o}s T{\'o}th and Christian Joseph Strasburger and Philippe Chanson and John A. H. Wass and Olivier Chabre and Marija Pfeifer and Richard A. Feelders and Stylianos Tsagarakis and Peter J. Trainer and Holger Franz and Kathrin Zopf and Sabina Z Zacharieva and Steven W. J. Lamberts and Antoine Tabarin and Susan M Webb},
  journal={European journal of endocrinology},
  year={2011},
  volume={165 3},
  pages={
          383-92
        }
}
OBJECTIVE The European Registry on Cushing's syndrome (ERCUSYN) is designed to collect prospective and follow-up data at EU level on Cushing's syndrome (CS). DESIGN AND METHODS Baseline data on 481 CS patients (390 females, 91 males; mean age (±s.d.): 44±14 years) collected from 36 centres in 23 countries, including new patients from 2008 and retrospective cases since 2000. Patients were divided into four major aetiologic groups: pituitary-dependent CS (PIT-CS) (66%), adrenal-dependent CS… CONTINUE READING

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