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B Eymard

Showing results (81-90 of 160) 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.
Neurology|February 21, 2012
Adult cases of mitochondrial DNA depletion due to TK2 defect: an expanding spectrumA Béhin, C Jardel, K G Claeys, et al.
Revue Neurologique|January 1, 1989
[Myasthenia and pregnancy: a clinical and immunologic study of 42 cases (21 neonatal myasthenia cases)]B Eymard, E Morel, O Dulac, 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.
Neurology|May 12, 2004
Clinical and histologic findings in autosomal centronuclear myopathyP-Y Jeannet, G Bassez, B Eymard, et al.
The Journal of Clinical Endocrinology and Metabolism|August 6, 2002
A comprehensive endocrine description of Kennedy's disease revealing androgen insensitivity linked to CAG repeat lengthS Dejager, H Bry-Gauillard, E Bruckert, et al.
Endocrinology|April 1, 1995
Quantitative analysis by polymerase chain reaction of growth hormone receptor gene expression in human liver and muscleJ F Martini, S M Villares, M Nagano, et al.
Presse Medicale (Paris, France : 1983)|June 25, 1994
[Severe cardiomyopathy revealing amylopectinosis. Two cases in adolescents from the same family]A de La Blanchardière, C Vayssier, D Duboc, et al.
Pageof 16

Showing results (81-90 of 160) with videos related to

Sort By:
Pageof 16
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.
Neurology|February 21, 2012
Adult cases of mitochondrial DNA depletion due to TK2 defect: an expanding spectrumA Béhin, C Jardel, K G Claeys, et al.
Revue Neurologique|January 1, 1989
[Myasthenia and pregnancy: a clinical and immunologic study of 42 cases (21 neonatal myasthenia cases)]B Eymard, E Morel, O Dulac, 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.
Neurology|May 12, 2004
Clinical and histologic findings in autosomal centronuclear myopathyP-Y Jeannet, G Bassez, B Eymard, et al.
The Journal of Clinical Endocrinology and Metabolism|August 6, 2002
A comprehensive endocrine description of Kennedy's disease revealing androgen insensitivity linked to CAG repeat lengthS Dejager, H Bry-Gauillard, E Bruckert, et al.
Endocrinology|April 1, 1995
Quantitative analysis by polymerase chain reaction of growth hormone receptor gene expression in human liver and muscleJ F Martini, S M Villares, M Nagano, et al.
Presse Medicale (Paris, France : 1983)|June 25, 1994
[Severe cardiomyopathy revealing amylopectinosis. Two cases in adolescents from the same family]A de La Blanchardière, C Vayssier, D Duboc, et al.
Pageof 16