Blog

The Rare Disease Foundation is pleased to announce the launch of its new call for research projects 'GenOmics: high throughput sequencing'.

Mutations in the MDH2 genes have been identified as being associated with severe clinical manifestations in children.

The 5th radiz Rare Diseases Summer School will focus on a wide variety of subjects in the arena of rare diseases, from disease mechanisms and animal...

Three publications, relayed in the news of the Institute of Genetics and Molecular and Cellular Biology (IGBMC), are the results of the...

2017 marks the 20th anniversary of EURORDIS - Rare Diseases Europe

SOS DESMOIDE launches its annual call for research projects on desmoid tumors, financed by the generosity of donors who are often...

A DYRK1-A, related kinases & human diseases conference will be held from March 28 to April 1, 2017 at the Palais du Grand Large in Saint Malo.

As part of its partnership with the Eliane and Gérard Pauthier Foundation, the Rare Disease Foundation was received yesterday by Professor Marc...

The Rare Disease Foundation filmed the UTMB© like you've never seen it before!

The "Medicine France Genomics 2025" plan is taking shape with a national call for projects to begin funding the first two platforms...

The Filière DéfiScience organized in collaboration with the Rare Disease Foundation, an international and interdisciplinary workshop on 5 and 6...

The Rare Diseases Foundation, in collaboration with the national infrastructure Phenomin, is launching its third call for research projects for the...