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Guillaume Bassez

Showing results (41-50 of 92) with videos related to

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Journal of Neuropathology and Experimental Neurology|July 2, 2020
A Heterozygous Mutation in the Filamin C Gene Causes an Unusual Nemaline Myopathy With Ring FibersTeresinha Evangelista, Xavière Lornage, Pierre G Carlier, et al.
Acta Neuropathologica Communications|October 24, 2014
Myofiber HLA-DR expression is a distinctive biomarker for antisynthetase-associated myopathyJessie Aouizerate, Marie De Antonio, Guillaume Bassez, et al.
Neuromuscular Disorders : NMD|May 29, 2016
Relationship between muscle impairments, postural stability, and gait parameters assessed with lower-trunk accelerometry in myotonic dystrophy type 1Damien Bachasson, Amélie Moraux, Gwenn Ollivier, et al.
Archives of Neurology|August 19, 2007
Phenotypic study in 40 patients with dysferlin gene mutations: high frequency of atypical phenotypesKarine Nguyen, Guillaume Bassez, Martin Krahn, et al.
Molecular Therapy. Nucleic Acids|June 19, 2017
Targeting DMPK with Antisense Oligonucleotide Improves Muscle Strength in Myotonic Dystrophy Type 1 MiceDominic Jauvin, Jessina Chrétien, Sanjay K Pandey, et al.
Molecular Genetics and Metabolism|June 7, 2023
Hypersensitivity infusion-associated reactions induced by enzyme replacement therapy in a cohort of patients with late-onset Pompe disease: An experience from the French Pompe RegistryLola E R Lessard, Céline Tard, Emmanuelle Salort-Campana, 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.
Neurology|August 10, 2019
Genetic determinants of disease severity in the myotonic dystrophy type 1 OPTIMISTIC cohortSarah A Cumming, Cecilia Jimenez-Moreno, Kees Okkersen, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|July 28, 2010
Excess of neuromuscular spindles in a fetus with Costello syndrome: a clinicopathological reportMartine Sinico, Guillaume Bassez, Claudine Touboul, et al.
Trials|January 20, 2018
The benefits and tolerance of exercise in myasthenia gravis (MGEX): study protocol for a randomised controlled trialSimone Birnbaum, Jean-Yves Hogrel, Raphael Porcher, et al.
Pageof 10

Showing results (41-50 of 92) with videos related to

Sort By:
Pageof 10
Journal of Neuropathology and Experimental Neurology|July 2, 2020
A Heterozygous Mutation in the Filamin C Gene Causes an Unusual Nemaline Myopathy With Ring FibersTeresinha Evangelista, Xavière Lornage, Pierre G Carlier, et al.
Acta Neuropathologica Communications|October 24, 2014
Myofiber HLA-DR expression is a distinctive biomarker for antisynthetase-associated myopathyJessie Aouizerate, Marie De Antonio, Guillaume Bassez, et al.
Neuromuscular Disorders : NMD|May 29, 2016
Relationship between muscle impairments, postural stability, and gait parameters assessed with lower-trunk accelerometry in myotonic dystrophy type 1Damien Bachasson, Amélie Moraux, Gwenn Ollivier, et al.
Archives of Neurology|August 19, 2007
Phenotypic study in 40 patients with dysferlin gene mutations: high frequency of atypical phenotypesKarine Nguyen, Guillaume Bassez, Martin Krahn, et al.
Molecular Therapy. Nucleic Acids|June 19, 2017
Targeting DMPK with Antisense Oligonucleotide Improves Muscle Strength in Myotonic Dystrophy Type 1 MiceDominic Jauvin, Jessina Chrétien, Sanjay K Pandey, et al.
Molecular Genetics and Metabolism|June 7, 2023
Hypersensitivity infusion-associated reactions induced by enzyme replacement therapy in a cohort of patients with late-onset Pompe disease: An experience from the French Pompe RegistryLola E R Lessard, Céline Tard, Emmanuelle Salort-Campana, 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.
Neurology|August 10, 2019
Genetic determinants of disease severity in the myotonic dystrophy type 1 OPTIMISTIC cohortSarah A Cumming, Cecilia Jimenez-Moreno, Kees Okkersen, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|July 28, 2010
Excess of neuromuscular spindles in a fetus with Costello syndrome: a clinicopathological reportMartine Sinico, Guillaume Bassez, Claudine Touboul, et al.
Trials|January 20, 2018
The benefits and tolerance of exercise in myasthenia gravis (MGEX): study protocol for a randomised controlled trialSimone Birnbaum, Jean-Yves Hogrel, Raphael Porcher, et al.
Pageof 10