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Revue Neurologique|January 29, 2005
[Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations]R Ben Yaou, H-M Bécane, L Demay, et al.Journal of Neurology|December 17, 2009
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7A Ben Ammar, F Petit, N Alexandri, 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.Pageof 5