V. González-Martínez

Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.

F. Pasquier, A. Durr, D. Hannequin, 2008, Brain : a journal of neurology.

A type I interferon signature identifies bilateral striatal necrosis due to mutations in ADAR1

A. Munnich, Y. Crow, Jean-Pierre Lin, 2013, Journal of Medical Genetics.

Immunological, Clinical, and Epidemiological Features of Guillain-Barré Syndrome Associated with SARS-CoV-2 Infection

J. Sotoca, A. Palasí, M. Salvadó, 2023, Acta Neurologica Scandinavica.

Staged implantation of multiple electrodes in the internal globus pallidus in the treatment of primary generalized dystonia.

L. Cif, P. Coubes, A. Bonafe, 2012, Journal of neurosurgery.