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eNauka >  Rezultati >  Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism
Naziv: Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism
Autori : Badiu, Corin; Bonomi, Marco; Borshchevsky, Ivan; Cools, Martine; Craen, Margarita; Ghervan, Cristina; Hauschild, Michael; Hershkovitz, Eli; Hrabovszky, Erik; Juul, Anders;
Kim, Soo-Hyun; Kumanov, Phillip; Lecumberri, Beatriz; Lemos, Manuel C.; Neocleous, Vassos; Niedziela, Marek; Djurdjevic, Sandra Pekic; Persani, Luca; Phan-Hug, Franziska; Pignatelli, Duarte; Pitteloud, Nelly; Popović, Vera ; Quinton, Richard; Skordis, Nicos; Smith, Neil; Stefanija, Magdalena Avbelj; Xu, Cheng; Young, Jacques; Dwyer, Andrew A.;
Godina: 2017
Publikacija: Orphanet Journal of Rare Diseases
ISSN: 1750-1172 Orphanet Journal of Rare Diseases Pretraži identifikator
Tip rezultata: Naučni članak
Kolacija: vol. 12 br. 1
DOI: 10.1186/s13023-017-0608-2
WoS-ID: 000397669000002
Scopus-ID: 2-s2.0-85015737361
PMID: 28320476
PMCID: PMC5359990
URI: https://enauka.gov.rs/handle/123456789/219692
Izvor metapodataka: Migrirano iz RIS podataka
M-kategorija: 
21M21 - Vodeći međunarodni časopis kategorije M21

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