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B Eymard

Showing results (61-70 of 160) with videos related to

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Journal of Neurology|October 31, 2012
Pregnancy in congenital myasthenic syndromeL Servais, H Baudoin, K Zehrouni, et al.
Revue Neurologique|February 10, 2023
Congenital myasthenic syndrome by mutation of the ColQ gene: Phenotypic and evolutionary profile of three Algerian familiesM I Kediha, M Tazir, C Magnouche, et al.
Neurology|November 14, 2001
Linkage of HLA to myasthenia gravis and genetic heterogeneity depending on anti-titin antibodiesM Giraud, G Beaurain, A M Yamamoto, et al.
The European Respiratory Journal|December 2, 2005
Respiratory insufficiency and limb muscle weakness in adults with Pompe's diseaseN Pellegrini, P Laforet, D Orlikowski, et al.
Neuroradiology|March 1, 1997
Cranial MRI findings in myotonic dystrophyY Miaux, J Chiras, B Eymard, et al.
Revue Neurologique|September 26, 2016
Unravelling the myotonic dystrophy type 1 clinical spectrum: A systematic registry-based study with implications for disease classificationM De Antonio, C Dogan, D Hamroun, et al.
Neuromuscular Disorders : NMD|January 24, 2018
Childhood-onset form of myotonic dystrophy type 1 and autism spectrum disorder: Is there comorbidity?N Angeard, E Huerta, A Jacquette, et al.
Revue Neurologique|February 24, 2004
[Myopathy-lipomatosis associated with A8344G mitochondrial DNA mutation]K Auré, D Sternberg, T Maisonobe, et al.
Journal of the Neurological Sciences|November 1, 1989
Immunocytological and histochemical correlation in Kearns-Sayre syndrome with mtDNA deletion and partial cytochrome c oxidase deficiency in skeletal muscleN B Romero, P Lestienne, C Marsac, et al.
The European Journal of Neuroscience|September 29, 1998
Accumulation of acetylcholine receptors is a necessary condition for normal accumulation of acetylcholinesterase during in vitro neuromuscular synaptogenesisS De La Porte, E Chaubourt, F Fabre, et al.
Pageof 16

Showing results (61-70 of 160) with videos related to

Sort By:
Pageof 16
Journal of Neurology|October 31, 2012
Pregnancy in congenital myasthenic syndromeL Servais, H Baudoin, K Zehrouni, et al.
Revue Neurologique|February 10, 2023
Congenital myasthenic syndrome by mutation of the ColQ gene: Phenotypic and evolutionary profile of three Algerian familiesM I Kediha, M Tazir, C Magnouche, et al.
Neurology|November 14, 2001
Linkage of HLA to myasthenia gravis and genetic heterogeneity depending on anti-titin antibodiesM Giraud, G Beaurain, A M Yamamoto, et al.
The European Respiratory Journal|December 2, 2005
Respiratory insufficiency and limb muscle weakness in adults with Pompe's diseaseN Pellegrini, P Laforet, D Orlikowski, et al.
Neuroradiology|March 1, 1997
Cranial MRI findings in myotonic dystrophyY Miaux, J Chiras, B Eymard, et al.
Revue Neurologique|September 26, 2016
Unravelling the myotonic dystrophy type 1 clinical spectrum: A systematic registry-based study with implications for disease classificationM De Antonio, C Dogan, D Hamroun, et al.
Neuromuscular Disorders : NMD|January 24, 2018
Childhood-onset form of myotonic dystrophy type 1 and autism spectrum disorder: Is there comorbidity?N Angeard, E Huerta, A Jacquette, et al.
Revue Neurologique|February 24, 2004
[Myopathy-lipomatosis associated with A8344G mitochondrial DNA mutation]K Auré, D Sternberg, T Maisonobe, et al.
Journal of the Neurological Sciences|November 1, 1989
Immunocytological and histochemical correlation in Kearns-Sayre syndrome with mtDNA deletion and partial cytochrome c oxidase deficiency in skeletal muscleN B Romero, P Lestienne, C Marsac, et al.
The European Journal of Neuroscience|September 29, 1998
Accumulation of acetylcholine receptors is a necessary condition for normal accumulation of acetylcholinesterase during in vitro neuromuscular synaptogenesisS De La Porte, E Chaubourt, F Fabre, et al.
Pageof 16