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Current Opinion in Neurology|August 9, 2022
Therapeutic thoroughfares for adults living with Pompe diseaseBenedikt Schoser, Pascal Laforet
Annals of Translational Medicine|August 9, 2019
Progress and challenges of gene therapy for Pompe diseaseGiuseppe Ronzitti, Fanny Collaud, Pascal Laforet, et al.
European Journal of Pain (London, England)|December 24, 2003
Clinical study of chronic pain in hereditary myopathiesThierry Delorme, François Boureau, Bruno Eymard, et al.
Journal of Neuromuscular Diseases|August 7, 2023
Determinants and Characterization of Locomotion in Adults with Late-Onset Pompe Disease: New Clinical BiomarkersThéo Maulet, Thomas Cattagni, Fabien Dubois, et al.
Thorax|March 25, 2018
Effect and impact of mechanical ventilation in myotonic dystrophy type 1: a prospective cohort studyGhilas Boussaïd, Hélène Prigent, Pascal Laforet, et al.
Journal of Neurology|July 4, 2024
Real-world data of in-hospital administration of alglucosidase alfa in French patients with Pompe disease: results from the National Claims DatabaseShahram Attarian, Emmanuelle Salort Campana, Stanislas Perrier, et al.
Muscle & Nerve|March 20, 2015
Should patients with asymptomatic pompe disease be treated? A nationwide study in FranceAndoni Echaniz-Laguna, Robert-Yves Carlier, Kenza Laloui, et al.
Neuromuscular Disorders : NMD|November 13, 2018
Isokinetic assessment of trunk muscles in facioscapulohumeral muscular dystrophy type 1 patientsJulien Esnault, Besma Missaoui, Samy Bendaya, et al.
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