Actualités

Discovery of DOCK11 mutations responsible for a new X-linked autoimmune disease

Identification of a new gene involved in severe allergies and eczema

Identification of a whole new type of mutation in immune deficiencie

Covid-19: inborn errors responsible for multisystemic inflammatory syndrome in children

A new tool to correct a mutation in beta-thalassemia

A look at the latest advances in gene therapy

A look back at the Dravet Syndrome Alliance Days

A new gene therapy strategy for sickle cell disease and beta thalassemia

"The systematic screening of sickle cell disease extended to the entire French population is a real victory".

A key mechanism of inflammation in sickle cell disease identified for the first time

Institut Imagine, Hôpital Necker-Enfants malades AP-HP and HELEBOR collaborate in a clinical and fundamental research partnership on children's pain

Genetics and immunology of rare infections, a powerful tool for understanding common infections

Les causes génétiques des infections graves à staphylocoques

Scientists discover novel mutation associated with alternating hemiplegia of childhood

Institut Imagine (Paris) will coordinate a Horizon Europe-granted project on genome editing approaches to treat sickle cell disease