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2020
- April 2020. D’Genes y otras organizaciones elaboran un decálogo de necesidades de personas sin diagnóstico. 20 minutos
- March 20 2020. Global Rare Disease Group’s Focus: 1,000 New Therapies by 2027, Despite COVID-19. ALS News
- March 10 2020. Malattie rare: «e ora non dimentichiamo la ricerca di base». Vita
- February 28 2020. Q&A: ‘We can diagnose more than 4,000 rare diseases but there’s still a long way to go’. Horizon Magazine
2019
- December 2019. Orientations towards the first Strategic Plan for Horizon Europe. EU Commission
- July 18 2019 The fight for equal access to rare disease treatment. Raconteur by The Times – The Sunday Times
2018
- December 21 2018 El IRDiRC espera aprobar 1.000 nuevas terapias para enfermedades raras (AELMHU)
- December 21 2018 Dr Lucia Monaco succeeds Dr Austin as IRDiRC Chair (OrphaNews)
- November 28 2018 Lucia Monaco eletta nuova presidentessa dell’assemblea di IRDiRC (Fondazione Telethon)
- November 15 2018 Medical mystery program takes a global approach to disease sleuthing (Nan-Byo Research)
- October 26 2018 Malattie rare. Domenica Taruscio Chair del Comitato scientifico dell’International Rare Diseases Research Consortium (Quotidiano Sanita)
- August 31 2018 Findings and recommendations of the Privacy-Preserving Record Linkage Task Force (OrphaNews)
- August 31 2018 Findings and recommendations of the Privacy-Preserving Record Linkage Task Force (OrphaNews)
- August 31 2018 New IRDiRC Recognized Resource: Exomiser (OrphaNews)
- June 14 2018 The Matchmaker Exchange connects researchers and clinicians to identify novel Mendelian disease genes (Health Europa)
- April 19 2018 Ángel Carracedo: «La vida no es “House”, no siempre es posible diagnosticarlo todo» (La Voz de Galicia)
- April 12 2018 RD-Connect Genome-Phenome Analysis Platform is an IRDiRC Recommended Resources (ERN Euro NMD newsletter)
- April 8 2018 Challenges and opportunities for rare diseases in India : Prasanna Kumar B Shirol (Healthworld)
- April 8 2018 RD-Connect Genome-Phenome Analysis Platform is an IRDiRC Recommended Resources (Catalunyapress)
- March 22 2018 Over 70 million people in India are affected by rare diseases : Prasanna Kumar B Shirol (Healthworld)
- March 13 2018 El 40% d’afectats per malalties rares triguen més de 4 anys a obtenir diagnòstic (Catalunyapress)
- March 13 2018 Un programa de entrenamiento mejora la capacidad física de pacientes con enfermedades mitocondriales (Gaceta Medica)
- February 23 2018 2017 retrospective: highlights of the year (OrphaNews)
- February 23 2018 Rare genetic diseases and how international cooperation can change research (OrphaNews)
- February 22 2018 Especialistas en enfermedades raras ven posible alcanzar un diagnóstico en menos de un año (Acta Sanitaria)
- February 10 2018 La importancia de tener nombre propio (El Nacional.cat)
- January 30 2018 Epidemiología de las Enfermedades Raras: Actualización y Revisión (Acta Sanitaria)
- January 22 2018 The future of rare diseases research – IRDiRC’s perspective published in Clinical and Translational Science (European Commission)
- January 22 2018 IRDiRC recognized resources (OrphaNews)
- January 8 2018 Enfermedades raras: camino de las 200 terapias en los próximos dos años (La Razon)
Archives
IRDiRC in the news before 2017 can be found here.