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M Fardeau

Showing results (181-190 of 289) with videos related to

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The New England Journal of Medicine|June 25, 1987
NADH measured by laser fluorimetry in skeletal muscle in McArdle's diseaseD Duboc, G Renault, J Polianski, et al.
Histochemistry and Cell Biology|January 1, 1995
Immunohistochemical analysis of muscle cytochrome c oxidase deficiency in childrenS Possekel, A Lombes, H Ogier de Baulny, et al.
Human Genetics|October 1, 1996
Human desmin gene: cDNA sequence, regional localization and exclusion of the locus in a familial desmin-related myopathyP Vicart, J M Dupret, J Hazan, et al.
Neurology|September 17, 2008
Fine-mapping the gene for X-linked myopathy with excessive autophagyI Munteanu, N Ramachandran, G N Mnatzakanian, et al.
Nature|September 24, 1992
Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophyK Matsumura, F M Tomé, H Collin, et al.
Revue Neurologique|March 1, 1997
[Juvenile GM2 gangliosidosis with progressive spinal muscular atrophy onset]P Rondot, R Navon, B Eymard, et al.
Developmental Biology|January 12, 1999
Expression of matrix metalloproteinases 2 and 9 in regenerating skeletal muscle: a study in experimentally injured and mdx musclesS Kherif, C Lafuma, M Dehaupas, et al.
Neuromuscular Disorders : NMD|March 1, 1994
Expression of dystrophin-associated proteins in dystrophin-positive muscle fibers (revertants) in Duchenne muscular dystrophyK Matsumura, F M Tomé, H Collin, et al.
Digestive Diseases and Sciences|March 1, 1992
Chronic intestinal pseudoobstruction with myopathy and ophthalmoplegia. A muscular biochemical study of a mitochondrial disorderV Li, J Hostein, N B Romero, et al.
Neurology|August 1, 1987
Extracts of muscle biopsies from patients with spinal muscular atrophies inhibit neurite outgrowth from spinal neuronsC E Henderson, S L Hauser, M Huchet, et al.
Pageof 29

Showing results (181-190 of 289) with videos related to

Sort By:
Pageof 29
The New England Journal of Medicine|June 25, 1987
NADH measured by laser fluorimetry in skeletal muscle in McArdle's diseaseD Duboc, G Renault, J Polianski, et al.
Histochemistry and Cell Biology|January 1, 1995
Immunohistochemical analysis of muscle cytochrome c oxidase deficiency in childrenS Possekel, A Lombes, H Ogier de Baulny, et al.
Human Genetics|October 1, 1996
Human desmin gene: cDNA sequence, regional localization and exclusion of the locus in a familial desmin-related myopathyP Vicart, J M Dupret, J Hazan, et al.
Neurology|September 17, 2008
Fine-mapping the gene for X-linked myopathy with excessive autophagyI Munteanu, N Ramachandran, G N Mnatzakanian, et al.
Nature|September 24, 1992
Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophyK Matsumura, F M Tomé, H Collin, et al.
Revue Neurologique|March 1, 1997
[Juvenile GM2 gangliosidosis with progressive spinal muscular atrophy onset]P Rondot, R Navon, B Eymard, et al.
Developmental Biology|January 12, 1999
Expression of matrix metalloproteinases 2 and 9 in regenerating skeletal muscle: a study in experimentally injured and mdx musclesS Kherif, C Lafuma, M Dehaupas, et al.
Neuromuscular Disorders : NMD|March 1, 1994
Expression of dystrophin-associated proteins in dystrophin-positive muscle fibers (revertants) in Duchenne muscular dystrophyK Matsumura, F M Tomé, H Collin, et al.
Digestive Diseases and Sciences|March 1, 1992
Chronic intestinal pseudoobstruction with myopathy and ophthalmoplegia. A muscular biochemical study of a mitochondrial disorderV Li, J Hostein, N B Romero, et al.
Neurology|August 1, 1987
Extracts of muscle biopsies from patients with spinal muscular atrophies inhibit neurite outgrowth from spinal neuronsC E Henderson, S L Hauser, M Huchet, et al.
Pageof 29