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B Eymard

Showing results (131-140 of 160) with videos related to

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Pacing and Clinical Electrophysiology : PACE|January 4, 2001
High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutationH M Bécane, G Bonne, S Varnous, et al.
Clinical Pharmacology and Therapeutics|May 28, 2010
Long-term follow-up of bezafibrate treatment in patients with the myopathic form of carnitine palmitoyltransferase 2 deficiencyJ P Bonnefont, J Bastin, P Laforêt, et al.
Annals of Neurology|October 8, 1999
Prevention of autoimmune attack by targeting specific T-cell receptors in a severe combined immunodeficiency mouse model of myasthenia gravisA Aissaoui, I Klingel-Schmitt, J Couderc, et al.
Journal of Neuromuscular Diseases|January 2, 2023
Dystrophic Myopathy of the Diaphragm with Recurrent Severe Respiratory Failure is Congenital Myasthenic Syndrome 11J J Kramer, H T M Boon, Q H Leijten, et al.
Neurology|June 11, 2003
Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2A Vihola, G Bassez, G Meola, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Clinical and histopathological aspects of central core disease associated and non-associated with RYR1 locusN B Romero, M Herasse, N Monnier, et al.
Neuromuscular Disorders : NMD|July 26, 2008
Electron microscopy in myofibrillar myopathies reveals clues to the mutated geneK G Claeys, M Fardeau, R Schröder, et al.
Neuromuscular Disorders : NMD|January 5, 2000
A diagnostic fluorescent marker kit for six limb girdle muscular dystrophiesI Richard, N Bourg, S Marchand, et al.
Journal of Neurology|December 14, 2011
The association of systemic lupus erythematosus and myasthenia gravis: a series of 17 cases, with a special focus on hydroxychloroquine use and a review of the literatureM Jallouli, D Saadoun, B Eymard, et al.
Neuropathology and Applied Neurobiology|November 11, 2010
Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganizationJ A Bevilacqua, N Monnier, M Bitoun, et al.
Pageof 16

Showing results (131-140 of 160) with videos related to

Sort By:
Pageof 16
Pacing and Clinical Electrophysiology : PACE|January 4, 2001
High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutationH M Bécane, G Bonne, S Varnous, et al.
Clinical Pharmacology and Therapeutics|May 28, 2010
Long-term follow-up of bezafibrate treatment in patients with the myopathic form of carnitine palmitoyltransferase 2 deficiencyJ P Bonnefont, J Bastin, P Laforêt, et al.
Annals of Neurology|October 8, 1999
Prevention of autoimmune attack by targeting specific T-cell receptors in a severe combined immunodeficiency mouse model of myasthenia gravisA Aissaoui, I Klingel-Schmitt, J Couderc, et al.
Journal of Neuromuscular Diseases|January 2, 2023
Dystrophic Myopathy of the Diaphragm with Recurrent Severe Respiratory Failure is Congenital Myasthenic Syndrome 11J J Kramer, H T M Boon, Q H Leijten, et al.
Neurology|June 11, 2003
Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2A Vihola, G Bassez, G Meola, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Clinical and histopathological aspects of central core disease associated and non-associated with RYR1 locusN B Romero, M Herasse, N Monnier, et al.
Neuromuscular Disorders : NMD|July 26, 2008
Electron microscopy in myofibrillar myopathies reveals clues to the mutated geneK G Claeys, M Fardeau, R Schröder, et al.
Neuromuscular Disorders : NMD|January 5, 2000
A diagnostic fluorescent marker kit for six limb girdle muscular dystrophiesI Richard, N Bourg, S Marchand, et al.
Journal of Neurology|December 14, 2011
The association of systemic lupus erythematosus and myasthenia gravis: a series of 17 cases, with a special focus on hydroxychloroquine use and a review of the literatureM Jallouli, D Saadoun, B Eymard, et al.
Neuropathology and Applied Neurobiology|November 11, 2010
Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganizationJ A Bevilacqua, N Monnier, M Bitoun, et al.
Pageof 16