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V Allamand

Showing results (21-30 of 33) with videos related to

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Human Molecular Genetics|February 1, 1994
Mapping of a chromosome 15 region involved in limb girdle muscular dystrophyF Fougerousse, O Broux, I Richard, et al.
American Journal of Human Genetics|June 1, 1995
Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 intervalV Allamand, O Broux, I Richard, et al.
Human Molecular Genetics|December 1, 1994
Adhalin gene polymorphismV Allamand, F Leturcq, F Piccolo, et al.
Human Molecular Genetics|March 1, 1995
Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locusV Allamand, O Broux, N Bourg, et al.
Cell|August 26, 1994
Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophyS L Roberds, F Leturcq, V Allamand, et al.
Neuromuscular Disorders : NMD|June 26, 2010
Differentiating Emery-Dreifuss muscular dystrophy and collagen VI-related myopathies using a specific CT scanner patternN Deconinck, E Dion, R Ben Yaou, et al.
Neuromuscular Disorders : NMD|December 10, 2013
Diaphragmatic dysfunction in Collagen VI myopathiesS Quijano-Roy, S Khirani, M Colella, et al.
Brain : a Journal of Neurology|November 19, 2008
Cyclosporine A treatment for Ullrich congenital muscular dystrophy: a cellular study of mitochondrial dysfunction and its rescueD Hicks, A K Lampe, S H Laval, et al.
Genomics|March 15, 1996
Low-molecular-weight, calcium-dependent phospholipase A2 genes are linked and map to homologous chromosome regions in mouse and humanJ A Tischfield, Y R Xia, D M Shih, et al.
Human Molecular Genetics|May 1, 1997
Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chainV Allamand, Y Sunada, M A Salih, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Human Molecular Genetics|February 1, 1994
Mapping of a chromosome 15 region involved in limb girdle muscular dystrophyF Fougerousse, O Broux, I Richard, et al.
American Journal of Human Genetics|June 1, 1995
Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 intervalV Allamand, O Broux, I Richard, et al.
Human Molecular Genetics|December 1, 1994
Adhalin gene polymorphismV Allamand, F Leturcq, F Piccolo, et al.
Human Molecular Genetics|March 1, 1995
Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locusV Allamand, O Broux, N Bourg, et al.
Cell|August 26, 1994
Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophyS L Roberds, F Leturcq, V Allamand, et al.
Neuromuscular Disorders : NMD|June 26, 2010
Differentiating Emery-Dreifuss muscular dystrophy and collagen VI-related myopathies using a specific CT scanner patternN Deconinck, E Dion, R Ben Yaou, et al.
Neuromuscular Disorders : NMD|December 10, 2013
Diaphragmatic dysfunction in Collagen VI myopathiesS Quijano-Roy, S Khirani, M Colella, et al.
Brain : a Journal of Neurology|November 19, 2008
Cyclosporine A treatment for Ullrich congenital muscular dystrophy: a cellular study of mitochondrial dysfunction and its rescueD Hicks, A K Lampe, S H Laval, et al.
Genomics|March 15, 1996
Low-molecular-weight, calcium-dependent phospholipase A2 genes are linked and map to homologous chromosome regions in mouse and humanJ A Tischfield, Y R Xia, D M Shih, et al.
Human Molecular Genetics|May 1, 1997
Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chainV Allamand, Y Sunada, M A Salih, et al.
Pageof 4