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M Fardeau

Showing results (151-160 of 289) with videos related to

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Journal of the Neurological Sciences|December 1, 1986
Immunocytochemical analysis of myosin heavy chains in human fetal skeletal musclesF Pons, J O Léger, M Chevallay, et al.
American Journal of Human Genetics|June 1, 1997
A mutation in the MTM1 gene invalidates a previous suggestion of nonallelic heterogeneity in X-linked myotubular myopathyC Guiraud-Chaumeil, M C Vincent, J Laporte, et al.
Revue D'Epidemiologie Et De Sante Publique|January 1, 1995
[Cost-benefit analysis of vaccinal prevention of hepatitis B policy]M Kerleau, Y A Flori, B Nalpas, et al.
La Nouvelle Presse Medicale|November 21, 1981
[First-line exploration: fiberoptic gastroscopy or barium meal? A pragmatic evaluation (author's transl)]E A Pariente, M Kerlau, J L Lanoe, et al.
Revue Neurologique|February 1, 1997
[Progressive external ophthalmoplegia of mitochondrial origin: contribution of morphological and molecular studies]P Laforêt, B Eymard, C Danan, et al.
Neuromuscular Disorders : NMD|September 1, 1995
Chronic progressive external ophthalmoplegia with ragged-red fibers: clinical, morphological and genetic investigations in 43 patientsP Laforêt, A Lombès, B Eymard, et al.
Neurology|November 18, 1998
Cardiac involvement in genetically confirmed facioscapulohumeral muscular dystrophyP Laforêt, C de Toma, B Eymard, et al.
Neuromuscular Disorders : NMD|November 1, 1995
Morphological and functional study of extensor digitorum longus muscle regeneration after iterative crush lesions in mdx mouseJ P Louboutin, V Fichter-Gagnepain, C Pastoret, et al.
Neurology|January 6, 2009
A new centronuclear myopathy phenotype due to a novel dynamin 2 mutationM Bitoun, J A Bevilacqua, B Eymard, et al.
Neurology|November 9, 2000
Juvenile and adult-onset acid maltase deficiency in France: genotype-phenotype correlationP Laforêt, M Nicolino, P B Eymard, et al.
Pageof 29

Showing results (151-160 of 289) with videos related to

Sort By:
Pageof 29
Journal of the Neurological Sciences|December 1, 1986
Immunocytochemical analysis of myosin heavy chains in human fetal skeletal musclesF Pons, J O Léger, M Chevallay, et al.
American Journal of Human Genetics|June 1, 1997
A mutation in the MTM1 gene invalidates a previous suggestion of nonallelic heterogeneity in X-linked myotubular myopathyC Guiraud-Chaumeil, M C Vincent, J Laporte, et al.
Revue D'Epidemiologie Et De Sante Publique|January 1, 1995
[Cost-benefit analysis of vaccinal prevention of hepatitis B policy]M Kerleau, Y A Flori, B Nalpas, et al.
La Nouvelle Presse Medicale|November 21, 1981
[First-line exploration: fiberoptic gastroscopy or barium meal? A pragmatic evaluation (author's transl)]E A Pariente, M Kerlau, J L Lanoe, et al.
Revue Neurologique|February 1, 1997
[Progressive external ophthalmoplegia of mitochondrial origin: contribution of morphological and molecular studies]P Laforêt, B Eymard, C Danan, et al.
Neuromuscular Disorders : NMD|September 1, 1995
Chronic progressive external ophthalmoplegia with ragged-red fibers: clinical, morphological and genetic investigations in 43 patientsP Laforêt, A Lombès, B Eymard, et al.
Neurology|November 18, 1998
Cardiac involvement in genetically confirmed facioscapulohumeral muscular dystrophyP Laforêt, C de Toma, B Eymard, et al.
Neuromuscular Disorders : NMD|November 1, 1995
Morphological and functional study of extensor digitorum longus muscle regeneration after iterative crush lesions in mdx mouseJ P Louboutin, V Fichter-Gagnepain, C Pastoret, et al.
Neurology|January 6, 2009
A new centronuclear myopathy phenotype due to a novel dynamin 2 mutationM Bitoun, J A Bevilacqua, B Eymard, et al.
Neurology|November 9, 2000
Juvenile and adult-onset acid maltase deficiency in France: genotype-phenotype correlationP Laforêt, M Nicolino, P B Eymard, et al.
Pageof 29