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Frontiers in Neuroscience|March 19, 2011
Fitting neuron models to spike trainsCyrille Rossant, Dan F M Goodman, Bertrand Fontaine, et al.The Journal of Physiology|April 28, 2011
Mechanisms underlying a life-threatening skeletal muscle Na+ channel disorderDina Simkin, Isabelle Léna, Pierre Landrieu, et al.The Journal of Physiology|November 18, 2003
Functional characterization and cold sensitivity of T1313A, a new mutation of the skeletal muscle sodium channel causing paramyotonia congenita in humansMagali Bouhours, Damien Sternberg, Claire-Sophie Davoine, et al.Muscle & Nerve|April 16, 2009
Electrophysiological studies in a mouse model of Schwartz-Jampel syndrome demonstrate muscle fiber hyperactivity of peripheral nerve originAndoni Echaniz-Laguna, Frédérique Rene, Christophe Marcel, et al.Journal of Neurophysiology|May 3, 2014
Emergence of band-pass filtering through adaptive spiking in the owl's cochlear nucleusBertrand Fontaine, Katrina M MacLeod, Susan T Lubejko, et al.Muscle & Nerve|November 3, 2009
Homozygosity for dominant mutations increases severity of muscle channelopathiesMarianne Arzel-Hézode, Damien Sternberg, Nacira Tabti, et al.Annals of Neurology|September 25, 2004
Electromyography guides toward subgroups of mutations in muscle channelopathiesEmmanuel Fournier, Marianne Arzel, Damien Sternberg, et al.Muscle & Nerve|July 27, 2007
Comparative efficacy of repetitive nerve stimulation, exercise, and cold in differentiating myotonic disordersPatrik Michel, Damien Sternberg, Pierre-Yves Jeannet, et al.Journal of Neurology|March 3, 2006
A new phenotype linked to SPG27 and refinement of the critical region on chromosomePascale Ribai, Giovanni Stevanin, Naima Bouslam, et al.Scientific Reports|November 14, 2018
A204E mutation in Nav1.4 DIS3 exerts gain- and loss-of-function effects that lead to periodic paralysis combining hyper- with hypo-kalaemic signsYosuke Kokunai, Carine Dalle, Savine Vicart, et al.Pageof 15