V. Robin

Efficient SMN Rescue following Subcutaneous Tricyclo-DNA Antisense Oligonucleotide Treatment

C. Leumann, A. Goyenvalle, L. García, 2017, Molecular therapy. Nucleic acids.

A rare recessive distal hereditary motor neuropathy with HSJ1 chaperone mutation

S. Blumen, R. Carasso, N. Blumen, 2012, Annals of neurology.

Can malondialdehyde be used as a biological marker of progression in neurodegenerative disease?

A. Favier, C. Desnuelle, C. Garrel, 2002, Journal of Neurology.

Gene and splicing therapies for neuromuscular diseases.

A. Goyenvalle, V. Robin, R. Benchaouir, 2015, Frontiers in bioscience.