OPA1-related disorders: Diversity of clinical expression, modes of inheritance and pathophysiology

International audience

A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family

International audience

Mutation in NDUFA13/GRIM19 leads to early onset hypotonia, dyskinesia and sensorial deficiencies, and mitochondrial complex I instability

International audience

In vivo time-lapse imaging of mitochondria in healthy and diseased peripheral myelin sheath

International audience

Remote Ischemic Conditioning Influences Mitochondrial Dynamics

International audience

A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disability

International audience

Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies

International audience

Neuroradiological findings expand the phenotype of OPA1-related mitochondrial dysfunction

International audience