Résultat de recherche

Evaluation of an innovative support programme for young patients with rare genetic epilepsies

Deciphering the genetic origin of language development disorders in children without intellectual disabilities, autism or apraxia of speech

Jean-Laurent Casanova’s pioneering genetic discoveries earn him the 2025 Novo Nordisk Prize

A genetic cause of an inherited bone marrow failure identified

Enhanced bone repair with FGFR antagonists in a model of hypochondroplasia

Notch3, a new player in heart development and asymmetry

Sickle cell disease: gene therapy efficacy depends on degree of host inflammation

A new MEDopathy caused by biallelic mutations of MED16

Discovery of a new genetic cause of brain inflammation

InFlaMe project: addressing virus-host interactions and defense strategies to design new therapeutics against flaviviruses

A new molecule to correct growth defects?

Cajal-Retzius cells at the heart of brain development during embryogenesis