Amyotrophic lateral sclerosis: a defect in autophagy responsible for the disease Read more about Amyotrophic lateral sclerosis: a defect in autophagy responsible for the disease
Incontinentia Pigmenti, a rare skin disease that also predisposes to viral infections Read more about Incontinentia Pigmenti, a rare skin disease that also predisposes to viral infections
The fifth HEROES auction for the benefit of Institut Imagine reaches €10 million Read more about The fifth HEROES auction for the benefit of Institut Imagine reaches €10 million
The first inherited TNF deficiency in human underlies susceptibility to tuberculosis Read more about 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. Read more about 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 Read more about 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) Read more about 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 Read more about 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 Read more about 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 Read more about A new mutation implicated in autoimmune lymphoproliferative syndrome