Yves-Olivier Guettard

A Rare Motor Neuron Deleterious Missense Mutation in the DPYSL3 (CRMP4) Gene is Associated with ALS

B. Pettmann, P. Andersen, V. Meininger, 2013, Human mutation.

Brain imaging determinants of functional prognosis after severe endocarditis: a multicenter observational study

B. Souweine, J. Reignier, R. Robert, 2022, Neurological Sciences.

Association between divalent metal transport 1 encoding gene (SLC11A2) and disease duration in amyotrophic lateral sclerosis

V. Meininger, P. Vourc'h, C. Andres, 2011, Journal of the Neurological Sciences.

Homozygous SMN2 deletion is a protective factor in the Swedish ALS population

P. Andersen, P. Vourc'h, C. Andres, 2012, European Journal of Human Genetics.

Critically ill patients with infective endocarditis, neurological complications and indication for cardiac surgery: a multicenter propensity-adjusted study

R. Prével, A. Orieux, D. Gruson, 2024, Annals of intensive care.