Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism

Andrew Dwyer(University of Lausanne), Beatriz Lecumberri(Hospital Universitario La Paz), Magdalena Avbelj Stefanija(Ljubljana University Medical Centre), Nelly Pitteloud(University of Lausanne), Nicos Skordis(Archbishop Makarios III Hospital), Cristina Ghervan(Iuliu Hațieganu University of Medicine and Pharmacy), Vera Popović(University of Belgrade), Ivan Borshchevsky(Ghent University Hospital), Eli Hershkovitz(Soroka Medical Center), Anders Juul(University of Copenhagen), Richard Quinton(Newcastle upon Tyne Hospitals NHS Foundation Trust), Erik Hrabovszky(HUN-REN Institute of Experimental Medicine), Marco Bonomi(University of Milan), Manuel C. Lemos(University of Beira Interior), Sandra Pekić(University Clinical Centre), Marek Niedziela(Poznan University of Medical Sciences), Corin Badiu(Carol Davila University of Medicine and Pharmacy), Luca Persani(University of Milan), Duarte Pignatelli(Universidade do Porto), Vassos Neocleous(Poznan University of Medical Sciences), Jacques Young(Inserm), Franziska Phan-Hug(Hospital de São João), Soo‐Hyun Kim(CHA University Gangnam Medical Center), Cheng Xu(Bicêtre Hospital), Neil Smith(National Patient Safety Foundation), Martine Cools(Ghent University Hospital), Michael Hauschild(Ben-Gurion University of the Negev), Phillip Kumanov(Medical University of Sofia), Margarita Craen
Orphanet Journal of Rare Diseases
March 20, 2017
Cited by 68


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