Emmanuel Fournier

New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis

P. Laforêt, B. Eymard, T. Kuntzer, 2004, Neurology.

Pregnancy in congenital myasthenic syndrome

L. Servais, B. Eymard, T. Stojkovic, 2013, Journal of Neurology.

Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutations

B. Eymard, T. Stojkovic, T. Kuntzer, 2012, Neuromuscular Disorders.

Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7

D. Orlikowski, L. Viollet, B. Eymard, 2010, Journal of Neurology.

Hypokalemic periodic paralysis

M. Hallett, J. Grafman, I. Litvan, 2014, Definitions.

[Congenital myasthenic syndromes: difficulties in the diagnosis, course and prognosis, and therapy--The French National Congenital Myasthenic Syndrome Network experience].

A. Béhin, D. Hantaı̈, T. Stojkovic, 2013, Revue neurologique.