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Journal of Human Genetics|December 20, 2019
Identification of novel pathogenic copy number variations in Charcot-Marie-Tooth diseaseJ Mortreux, J Bacquet, A Boyer, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Towards the molecular elucidation of congenital myasthenic syndromes: identification of mutations in MuSKF Chevessier, B Faraut, A Ravel-Chapuis, et al.
Mitochondrion|December 15, 2007
Rapid identification of mitochondrial DNA (mtDNA) mutations in neuromuscular disorders by using surveyor strategyS Bannwarth, V Procaccio, C Rouzier, et al.
Revue Neurologique|September 7, 2015
Myofibrillar myopathies: State of the art, present and future challengesA Béhin, E Salort-Campana, K Wahbi, et al.
Muscle & Nerve|April 7, 2026
Limb Girdle Muscular Dystrophy Associated With TRIM32 Variants: A National Cohort StudyAlexandre Guérémy, V Morel, T Stojkovic, et al.
European Journal of Neurology|August 2, 2025
Prevalence of SOD1 and C9orf72 Variants Among French ALS Population: The GENIALS StudyP Corcia, D Erazo, M D M Amador, et al.
Revue Neurologique|April 20, 2024
Transthyretin amyloid polyneuropathy in France: A cross-sectional study with 413 patients and real-world tafamidis meglumine use (2009-2019)D Adams, P Cintas, G Solé, et al.
Neurophysiologie Clinique = Clinical Neurophysiology|May 11, 2015
Somatosensory evoked potentials in the assessment of peripheral neuropathies: Commented results of a survey among French-speaking practitioners and recommendations for practiceR Morizot-Koutlidis, N André-Obadia, J-C Antoine, et al.
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