Meeting Abstracts from the XVI International Collaboration on Rare Diseases and Orphan Drugs (ICORD): Incentivizing Science and a Comprehensive Program for Rare Diseases
Year: 2026
Type: article
Abstract: prioritize based on local health conditions and to be developed in alignment with the social and economic conditions of each country; (2) Suggest working models and incentives for local scientists and the health industry to generate orphan diagnoses and treatments in collaboration with other countries worldwide and at the highest standard possible. Fostering multisectoral collaboration in rare diseases: perspectives from Argentina and CERyDH
Authors: Emilio J. A. Roldan, Rumen Stefanov, Cynthia J. Tifft, Pablo Andres Evelson, Manuel Posada, Silvia Lucangioli, Domenica Taruscio, Gabriela Berg, Patricia Sonia Demianczuk, Alberto Mantovani, Mireia del Toro, Micaela Tamar Calógero, Eva Bermejo-Sánchez, Bianca Raíces, Claudio Carta, Fabiana Estebenet, Ramaiah Muthyala, Luis Alejandro Barrera, Guadalupe Velia Pacciarini
Institutions: National Institutes of Health, Universidad de Buenos Aires, National Human Genome Research Institute, Consejo Nacional de Investigaciones Científicas y Técnicas, Fundación Estatal, Salud, Infancia y Bienestar Social, F.S.P., Vall d'Hebron Hospital Universitari, Instituto de Salud Carlos III, Instituto de Investigación de Enfermedades Raras, Istituto Superiore di Sanità, University of Minnesota, Hospital Universitario San Ignacio
Language: English
Topic: Genomics and Rare Diseases
Subfield: Genetics
Domain: Life Sciences
Open Access status: hybrid
OpenAlex ID: W7128047281