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Muscle & Nerve|January 17, 2020
Brody myopathy demonstrates a pseudo-increment on repetitive nerve stimulationMarion Masingue, Marianne Arzel, Damien Sternberg, et al.Journal of the Peripheral Nervous System : JPNS|May 27, 2025
A Case Series of Unilateral Peripheral NeuropathyCaroline Kramarz, Marion Masingue, Françoise Bouhour, et al.Muscle & Nerve|April 12, 2019
Whole-Body Muscle Magnetic Resonance Imaging in Glycogen-Storage Disease Type IIIDavid Tobaly, Pascal Laforêt, Ariane Perry, et al.Annals of Neurology|January 30, 2020
Natural History of Adult Patients with GM2 GangliosidosisMarion Masingue, Louis Dufour, Timothée Lenglet, et al.Orphanet Journal of Rare Diseases|December 9, 2025
Transition from childhood to adulthood in neuromuscular disorders: results from the ERN EURO-NMD surveyTeresinha Evangelista, Houda Ali, Charlotte Handberg, et al.Journal of Neurology|May 4, 2026
Prospective gait analysis in patients from the French registry of glycogen storage disease type III: implications for clinical trialsJean-Yves Hogrel, Frédéric Fer, Isabelle Ledoux, et al.Journal of Neuromuscular Diseases|November 14, 2022
LAMA2-Related Muscular Dystrophy: The Importance of Accurate Phenotyping and Brain Imaging in the Diagnosis of LGMDTanya Stojkovic, Marion Masingue, Corinne Métay, et al.Neuromuscular Disorders : NMD|December 16, 2022
Diagnostic yield of a practical electrodiagnostic protocol discriminating between different congenital myasthenic syndromesTanya Stojkovic, Marion Masingue, Helène Turmel, et al.Journal of Neuromuscular Diseases|April 5, 2021
Improved Cardiac Outcomes by Early Treatment with Angiotensin-Converting Enzyme Inhibitors in Becker Muscular DystrophyCaroline Stalens, Leslie Motté, Anthony Béhin, et al.Scientific Reports|August 28, 2023
New mutation in the β1 propeller domain of LRP4 responsible for congenital myasthenic syndrome associated with Cenani-Lenz syndromeMarion Masingue, Olivia Cattaneo, Nicolas Wolff, et al.Pageof 4