Résultat de recherche

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

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

Discover our web-conferences dedicated to rare diseases in replay

Research on nephronophthisis and renal ciliopathies at Imagine

Familial Hemophagocytic Lymphohystiocytosis and Digestive Malabsorption

Institut Imagine accelerates research on autism spectrum disorders

Discovery of a new genetic disease predisposing to mycobacterial infections

An innovative method to characterize each cell individually

Identification of a new genetic cause of intellectual disability

COVID-19 and multisystemic inflammatory syndrome in children: 75% of affected children have the same immune abnormality

Discovery of a new gene responsible of syndromes causing aortic aneurysms

Identification of a first genetic cause for tree-man syndrome (cutaneous papillomavirus)