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B Eymard

Showing results (31-40 of 160) with videos related to

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Neuromuscular Disorders : NMD|September 1, 1993
Late-onset rod myopathy associated with monoclonal gammopathyB Eymard, J C Brouet, H Collin, et al.
Neuroradiology|January 1, 1991
Intracranial arachnoid cysts in myotonic dystrophyM Fiorelli, D Duboc, S Pappatà, et al.
Archives of Neurology|February 15, 2001
Missense CACNA1A mutation causing episodic ataxia type 2C Denier, A Ducros, A Durr, et al.
Neuropediatrics|August 26, 2004
Congenital myasthenic syndrome due to rapsyn deficiency: three cases with arthrogryposis and bulbar symptomsC Ioos, A Barois, P Richard, et al.
Neurology|June 27, 2001
A non-ischemic forearm exercise test for the screening of patients with exercise intoleranceJ Y Hogrel, P Laforêt, R Ben Yaou, et al.
Journal of Neuroimmunology|October 23, 1997
No evidence for an association of AChR beta-subunit gene (CHRNB1) with myasthenia gravisF Djabiri, P Gajdos, B Eymard, et al.
Journal of the Neurological Sciences|July 1, 1993
Effect of sera from myasthenia gravis patients and of alpha-bungarotoxin on acetylcholinesterase during in vitro neuromuscular synaptogenesisS de la Porte, F Ragueh, B Eymard, et al.
Presse Medicale (Paris, France : 1983)|May 31, 1986
[Assay of anti-acetylcholine receptor antibodies in myasthenic syndromes of newborn infants]B Eymard, E Morel, J P Harpey, et al.
Revue Neurologique|June 17, 2008
[Distal myopathy due to mutations of GNE gene: clinical spectrum and diagnosis]A Béhin, O Dubourg, P Laforêt, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Dysphagia in oculopharyngeal muscular dystrophy: a series of 22 French casesS Périé, B Eymard, L Laccourreye, et al.
Pageof 16

Showing results (31-40 of 160) with videos related to

Sort By:
Pageof 16
Neuromuscular Disorders : NMD|September 1, 1993
Late-onset rod myopathy associated with monoclonal gammopathyB Eymard, J C Brouet, H Collin, et al.
Neuroradiology|January 1, 1991
Intracranial arachnoid cysts in myotonic dystrophyM Fiorelli, D Duboc, S Pappatà, et al.
Archives of Neurology|February 15, 2001
Missense CACNA1A mutation causing episodic ataxia type 2C Denier, A Ducros, A Durr, et al.
Neuropediatrics|August 26, 2004
Congenital myasthenic syndrome due to rapsyn deficiency: three cases with arthrogryposis and bulbar symptomsC Ioos, A Barois, P Richard, et al.
Neurology|June 27, 2001
A non-ischemic forearm exercise test for the screening of patients with exercise intoleranceJ Y Hogrel, P Laforêt, R Ben Yaou, et al.
Journal of Neuroimmunology|October 23, 1997
No evidence for an association of AChR beta-subunit gene (CHRNB1) with myasthenia gravisF Djabiri, P Gajdos, B Eymard, et al.
Journal of the Neurological Sciences|July 1, 1993
Effect of sera from myasthenia gravis patients and of alpha-bungarotoxin on acetylcholinesterase during in vitro neuromuscular synaptogenesisS de la Porte, F Ragueh, B Eymard, et al.
Presse Medicale (Paris, France : 1983)|May 31, 1986
[Assay of anti-acetylcholine receptor antibodies in myasthenic syndromes of newborn infants]B Eymard, E Morel, J P Harpey, et al.
Revue Neurologique|June 17, 2008
[Distal myopathy due to mutations of GNE gene: clinical spectrum and diagnosis]A Béhin, O Dubourg, P Laforêt, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Dysphagia in oculopharyngeal muscular dystrophy: a series of 22 French casesS Périé, B Eymard, L Laccourreye, et al.
Pageof 16