Blog

Prof. Jean-Louis Mandel, President of the Foundation For Rare Diseases and Prof. Daniel Scherman, Director of the Foundation For Rare Diseases will speak at the...

On December 8 will take place the 19th edition of the Walk of Rare Diseases as part of the Telethon 2018 and organized by the Alliance Maladies...

During its 62nd Magistral Chapter, the Guyenne-Occitan Commandery of the International Order of Anysetiers renewed for the 4th year...

To support its opening to e-health, the Foundation For Rare Diseases joins LeLabEsanté, a multidisciplinary think-tank for digital health. With...

The Innovation & Galien Meetings will take place on December 12, 2018 in Paris under the high patronage of Mr. Emmanuel Macron, President of the...

INFRAFRONTIER (Research Infrastructure) and IMPC (International Mouse Phenotyping Consortium) invite all the actors of the research...

The Square Foundation for Entrepreneurship, Children and Health is launching a call for projects dedicated to medical research for children...

Overcoming Cystic Fibrosis and SHS: the 2019 call for scientific research projects is open to Humanities and Social Sciences projects. All...

Philippe Mendels-Flandre presents and explains the partnership agreement between Lysogene, Dr. Hervé Moine and SATT Conectus Alsace thanks to the...

Since 2011, Orphanet has been providing access to massive datasets from its database, for the benefit of research, via the...

During its 35th Magistral Chapter of the Commanderie des Landes, the International Order of Anysetiers Commanderie des Landes handed over a check of...

The SATT Nord and the Foundation For Rare Diseases are combining their complementary expertise to promote the emergence and maturation of projects...