Actualités

COVID-19: Institut Imagine and Cerba HealthCare are partnering to test for patients likely to develop severe symptoms

Familial Hemophagocytic Lymphohystiocytosis and Digestive Malabsorption

Research on nephronophthisis and renal ciliopathies at Imagine

Medetia : towards a first treatment of severe ciliopathy in children

International Women's Day: They are looking for Imagine

Discover our web-conferences dedicated to rare diseases in replay

Genetic deafness: an update on these pathologies, research and care

Genetic deafness, which path of research and care for patients?

Understanding genetic deafness

Two type 1 interferopathies where the lung becomes inflamed

Erminia Rubino, business developer at Institut Imagine

6 new rare disease reference centers affiliated to the Institut Imagine

From rare to frequent: the importance of conducting research on genetic diseases

February 27 and 28, 2021: a weekend dedicated to rare diseases

Science for children: Covid-19 and genetics