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M Fardeau

Showing results (241-250 of 289) with videos related to

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Neuromuscular Disorders : NMD|June 3, 1998
Myoblast transplantation in non-dystrophic dogH Ito, J T Vilquin, D Skuk, et al.
Lancet (London, England)|August 26, 1998
Macrophagic myofasciitis: an emerging entity. Groupe d'Etudes et Recherche sur les Maladies Musculaires Acquises et Dysimmunitaires (GERMMAD) de l'Association Française contre les Myopathies (AFM)R K Gherardi, M Coquet, P Chérin, et al.
American Journal of Human Genetics|June 1, 1996
Substitution of a conserved cysteine-996 in a cysteine-rich motif of the laminin alpha2-chain in congenital muscular dystrophy with partial deficiency of the proteinM Nissinen, A Helbling-Leclerc, X Zhang, et al.
Neuroscience|June 1, 1992
Localization of dystrophin and dystrophin-related protein at the electromotor synapse and neuromuscular junction in Torpedo marmorataA Cartaud, M A Ludosky, F M Tomé, et al.
Neuromuscular Disorders : NMD|May 5, 1998
Impaired cerebral glucose metabolism in myotonic dystrophy: a triplet-size dependent phenomenonD Annane, M Fiorelli, B Mazoyer, et al.
Nature Genetics|September 10, 1998
A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopathyP Vicart, A Caron, P Guicheney, et al.
Revue Neurologique|January 1, 1996
[Congenital muscular dystrophy with merosin deficiency: clinical, histopathological, immunocytochemical and genetic analysis]M Fardeau, F M Tomé, A Helbling-Leclerc, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 1, 1994
Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiencyN B Romero, F M Tomé, F Leturcq, et al.
Revue Neurologique|April 3, 2001
[Proximal myotonial myopathy (PROMM): clinical and histology study]G Bassez, S Attarian, P Laforêt, et al.
Human Molecular Genetics|January 1, 1996
Deletions in Xq28 in two boys with myotubular myopathy and abnormal genital development define a new contiguous gene syndrome in a 430 kb regionL J Hu, J Laporte, W Kress, et al.
Pageof 29

Showing results (241-250 of 289) with videos related to

Sort By:
Pageof 29
Neuromuscular Disorders : NMD|June 3, 1998
Myoblast transplantation in non-dystrophic dogH Ito, J T Vilquin, D Skuk, et al.
Lancet (London, England)|August 26, 1998
Macrophagic myofasciitis: an emerging entity. Groupe d'Etudes et Recherche sur les Maladies Musculaires Acquises et Dysimmunitaires (GERMMAD) de l'Association Française contre les Myopathies (AFM)R K Gherardi, M Coquet, P Chérin, et al.
American Journal of Human Genetics|June 1, 1996
Substitution of a conserved cysteine-996 in a cysteine-rich motif of the laminin alpha2-chain in congenital muscular dystrophy with partial deficiency of the proteinM Nissinen, A Helbling-Leclerc, X Zhang, et al.
Neuroscience|June 1, 1992
Localization of dystrophin and dystrophin-related protein at the electromotor synapse and neuromuscular junction in Torpedo marmorataA Cartaud, M A Ludosky, F M Tomé, et al.
Neuromuscular Disorders : NMD|May 5, 1998
Impaired cerebral glucose metabolism in myotonic dystrophy: a triplet-size dependent phenomenonD Annane, M Fiorelli, B Mazoyer, et al.
Nature Genetics|September 10, 1998
A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopathyP Vicart, A Caron, P Guicheney, et al.
Revue Neurologique|January 1, 1996
[Congenital muscular dystrophy with merosin deficiency: clinical, histopathological, immunocytochemical and genetic analysis]M Fardeau, F M Tomé, A Helbling-Leclerc, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 1, 1994
Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiencyN B Romero, F M Tomé, F Leturcq, et al.
Revue Neurologique|April 3, 2001
[Proximal myotonial myopathy (PROMM): clinical and histology study]G Bassez, S Attarian, P Laforêt, et al.
Human Molecular Genetics|January 1, 1996
Deletions in Xq28 in two boys with myotubular myopathy and abnormal genital development define a new contiguous gene syndrome in a 430 kb regionL J Hu, J Laporte, W Kress, et al.
Pageof 29