Actualités

Amyotrophic lateral sclerosis: a defect in autophagy responsible for the disease

Incontinentia Pigmenti, a rare skin disease that also predisposes to viral infections

The first inherited TNF deficiency in human underlies susceptibility to tuberculosis

Innov4-ePiK: Innovative diagnostic and therapeutic approaches in potassium channel developmental and epileptic encephalopathies (K-DEEs) using 4P for medicine.

The role of dendritic cells in papillomavirus infections: from the FLT3LG gene to therapeutic perspectives

From the probability of being born left-handed to Rare Diseases: The Mysteries of Tubulin Beta 4B Variations (TUBB4B)

Identification of a new key player in the immune control of Epstein-Barr virus infection

Discovery of a frequent genetic cause of autoimmunity From rare to frequent variants: the case of pre-TCRα deficiency

A new mutation implicated in autoimmune lymphoproliferative syndrome

CENTOGENE and the Laboratory of Human Genetics of Infectious Diseases at Institut Imagine Announce Rare Disease Research Collaboration

Identification of a new genetic disease responsible for pulmonary alveolar proteinosis and mycobacterial infections

Autoantibodies against type I interferon : detected and active in childhood

A link established between brain plasticity and improved social skills in children with autism spectrum disorders

A new genetic disease linked to the X chromosome explains immunity problems in the face of mycobacteria

Criss-cross heart : how a shortage of cells affects the shape of the heart