Nicole Monnier

Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization

K. Claeys, A. Laquérriere, N. Romero, 2011, Neuropathology and applied neurobiology.

Muscle imaging in dominant core myopathies linked or unlinked to the ryanodine receptor 1 gene

N. Romero, J. Chiras, L. Viollet, 2006, Neurology.

Comparative analysis of in vitro contracture tests with ryanodine and a combination of ryanodine with either halothane or caffeine: a comparative investigation in malignant hyperthermia

P. Cozzone, N. Monnier, J. Lunardi, 2004, Acta anaesthesiologica Scandinavica.

Mutation screening of the RYR1 gene in malignant hyperthermia: detection of a novel Tyr to Ser mutation in a pedigree with associated central cores.

N. Monnier, J. Lunardi, K. Keating, 1994, Genomics.