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B Eymard

Showing results (121-130 of 160) with videos related to

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Neuropathology and Applied Neurobiology|May 11, 2017
Diagnostic anoctamin-5 protein defect in patients with ANO5-mutated muscular dystrophyA Vihola, H Luque, M Savarese, et al.
Heart (British Cardiac Society)|July 16, 2004
Danon's disease as a cause of hypertrophic cardiomyopathy: a systematic surveyP Charron, E Villard, P Sébillon, et al.
Neurology|November 24, 2004
Severe cardiac arrhythmias in young patients with myotonic dystrophy type 1G Bassez, A Lazarus, I Desguerre, et al.
European Journal of Neurology|October 12, 2013
Antibodies to clustered acetylcholine receptor: expanding the phenotypeP Devic, P Petiot, T Simonet, et al.
Revue Neurologique|April 3, 2001
[Proximal myotonial myopathy (PROMM): clinical and histology study]G Bassez, S Attarian, P Laforêt, et al.
Neuromuscular Disorders : NMD|June 26, 2010
Differentiating Emery-Dreifuss muscular dystrophy and collagen VI-related myopathies using a specific CT scanner patternN Deconinck, E Dion, R Ben Yaou, et al.
International Journal of Cardiology|October 9, 2012
Dilated cardiomyopathy in patients with mutations in anoctamin 5K Wahbi, A Béhin, H M Bécane, et al.
Revue Neurologique|June 9, 2000
[Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material with mutation of the alphaB-cristallin gene]M Fardeau, P Vicart, A Caron, et al.
Revue Neurologique|July 23, 2004
[Congenital myasthenic syndromes due to mutations in the rapsyn gene]B Eymard, C Ioos, A Barois, et al.
Neuromuscular Disorders : NMD|July 26, 2021
Home-based exercise in autoimmune myasthenia gravis: A randomized controlled trialS Birnbaum, R Porcher, P Portero, et al.
Pageof 16

Showing results (121-130 of 160) with videos related to

Sort By:
Pageof 16
Neuropathology and Applied Neurobiology|May 11, 2017
Diagnostic anoctamin-5 protein defect in patients with ANO5-mutated muscular dystrophyA Vihola, H Luque, M Savarese, et al.
Heart (British Cardiac Society)|July 16, 2004
Danon's disease as a cause of hypertrophic cardiomyopathy: a systematic surveyP Charron, E Villard, P Sébillon, et al.
Neurology|November 24, 2004
Severe cardiac arrhythmias in young patients with myotonic dystrophy type 1G Bassez, A Lazarus, I Desguerre, et al.
European Journal of Neurology|October 12, 2013
Antibodies to clustered acetylcholine receptor: expanding the phenotypeP Devic, P Petiot, T Simonet, et al.
Revue Neurologique|April 3, 2001
[Proximal myotonial myopathy (PROMM): clinical and histology study]G Bassez, S Attarian, P Laforêt, et al.
Neuromuscular Disorders : NMD|June 26, 2010
Differentiating Emery-Dreifuss muscular dystrophy and collagen VI-related myopathies using a specific CT scanner patternN Deconinck, E Dion, R Ben Yaou, et al.
International Journal of Cardiology|October 9, 2012
Dilated cardiomyopathy in patients with mutations in anoctamin 5K Wahbi, A Béhin, H M Bécane, et al.
Revue Neurologique|June 9, 2000
[Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material with mutation of the alphaB-cristallin gene]M Fardeau, P Vicart, A Caron, et al.
Revue Neurologique|July 23, 2004
[Congenital myasthenic syndromes due to mutations in the rapsyn gene]B Eymard, C Ioos, A Barois, et al.
Neuromuscular Disorders : NMD|July 26, 2021
Home-based exercise in autoimmune myasthenia gravis: A randomized controlled trialS Birnbaum, R Porcher, P Portero, et al.
Pageof 16