Items where Author is "Skordis, N."
Group by: Item Type | No Grouping Number of items: 1. Badiu, C. and Bonomi, M. and Borshchevsky, I. and Cools, M. and Craen, M. and Ghervan, C. and Hauschild, M. and Hershkovitz, E. and Hrabovszky, E. and Juul, A. and Kim, S. H. and Kumanov, P. and Lecumberri, B. and Lemos, M. C. and Neocleous, V. and Niedziela, M. and Djurdjevic, S. P. and Persani, L. and Phan-Hug, F. and Pignatelli, D. and Pitteloud, N. and Popovic, V. and Quinton, R. and Skordis, N. and Smith, N. and Stefanija, M. A. and Xu, C. and Young, J. and Dwyer, A. A. (2017) Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism. Orphanet Journal of Rare Diseases. pp. 1-9. ISSN 1750-1172 |