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M Fardeau

Showing results (191-200 of 289) with videos related to

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Revue Neurologique|June 1, 1996
[Exercise intolerance caused by muscular phosphorylase kinase deficiency. Contribution of in vivo metabolic studies]P Laforêt, B Eymard, A Lombès, et al.
Circulation|December 1, 1994
Correlation between decreased myocardial glucose phosphorylation and the DNA mutation size in myotonic dystrophyD Annane, D Duboc, B Mazoyer, et al.
Brain : a Journal of Neurology|May 4, 2001
Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disordersD Sternberg, E Chatzoglou, P Laforêt, et al.
Journal of the Neurological Sciences|August 1, 1988
Effect of myasthenic patient sera on the number and distribution of acetylcholine receptors in muscle and nerve-muscle cultures from rat. Correlations with clinical stateB Eymard, S de la Porte, C Pannier, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|April 1, 1994
Congenital muscular dystrophy with merosin deficiencyF M Tomé, T Evangelista, A Leclerc, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Cognitive functions in Duchenne muscular dystrophy: a reappraisal and comparison with spinal muscular atrophyC Billard, P Gillet, J L Signoret, et al.
American Journal of Medical Genetics|August 15, 1994
Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X-chromosome inactivationN Abbadi, C Philippe, M Chery, et al.
Neurology|December 3, 2008
New morphologic and genetic findings in cap disease associated with beta-tropomyosin (TPM2) mutationsM Ohlsson, S Quijano-Roy, N Darin, et al.
Journal of Medical Genetics|September 1, 1995
The myotubular myopathies: differential diagnosis of the X linked recessive, autosomal dominant, and autosomal recessive forms and present state of DNA studiesC Wallgren-Pettersson, A Clarke, F Samson, et al.
Revue Neurologique|January 1, 1991
[Mitochondrial function and mitochondrial DNA in a series of 64 patients suspected of having mitochondrial myopathy]C Marsac, F Degoul, G Bonne, et al.
Pageof 29

Showing results (191-200 of 289) with videos related to

Sort By:
Pageof 29
Revue Neurologique|June 1, 1996
[Exercise intolerance caused by muscular phosphorylase kinase deficiency. Contribution of in vivo metabolic studies]P Laforêt, B Eymard, A Lombès, et al.
Circulation|December 1, 1994
Correlation between decreased myocardial glucose phosphorylation and the DNA mutation size in myotonic dystrophyD Annane, D Duboc, B Mazoyer, et al.
Brain : a Journal of Neurology|May 4, 2001
Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disordersD Sternberg, E Chatzoglou, P Laforêt, et al.
Journal of the Neurological Sciences|August 1, 1988
Effect of myasthenic patient sera on the number and distribution of acetylcholine receptors in muscle and nerve-muscle cultures from rat. Correlations with clinical stateB Eymard, S de la Porte, C Pannier, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|April 1, 1994
Congenital muscular dystrophy with merosin deficiencyF M Tomé, T Evangelista, A Leclerc, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Cognitive functions in Duchenne muscular dystrophy: a reappraisal and comparison with spinal muscular atrophyC Billard, P Gillet, J L Signoret, et al.
American Journal of Medical Genetics|August 15, 1994
Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X-chromosome inactivationN Abbadi, C Philippe, M Chery, et al.
Neurology|December 3, 2008
New morphologic and genetic findings in cap disease associated with beta-tropomyosin (TPM2) mutationsM Ohlsson, S Quijano-Roy, N Darin, et al.
Journal of Medical Genetics|September 1, 1995
The myotubular myopathies: differential diagnosis of the X linked recessive, autosomal dominant, and autosomal recessive forms and present state of DNA studiesC Wallgren-Pettersson, A Clarke, F Samson, et al.
Revue Neurologique|January 1, 1991
[Mitochondrial function and mitochondrial DNA in a series of 64 patients suspected of having mitochondrial myopathy]C Marsac, F Degoul, G Bonne, et al.
Pageof 29