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M Fardeau

Showing results (131-140 of 289) with videos related to

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Neuromuscular Disorders : NMD|September 1, 1993
Late-onset rod myopathy associated with monoclonal gammopathyB Eymard, J C Brouet, H Collin, et al.
Neurology|April 1, 1987
Phosphorus NMR spectroscopy study of muscular enzyme deficiencies involving glycogenolysis and glycolysisD Duboc, P Jehenson, S Tran Dinh, et al.
Blood|July 1, 1982
A new case of phosphoglycerate kinase deficiency: PGK Creteil associated with rhabdomyolysis and lacking hemolytic anemiaR Rosa, C George, M Fardeau, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Dysphagia in oculopharyngeal muscular dystrophy: a series of 22 French casesS Périé, B Eymard, L Laccourreye, et al.
La Nouvelle Presse Medicale|December 18, 1982
[Acid maltase deficiency with diaphragmatic paralysis and respiratory insufficiency in adults]J Lissac, M Fardeau, F Contamin, et al.
Lancet (London, England)|September 8, 1990
Secondary metabolic defects in spinal muscular atrophy type IIJ P Harpey, C Charpentier, M Paturneau-Jouas, et al.
Neuromuscular Disorders : NMD|December 1, 1996
Chromosome 15-linked limb-girdle muscular dystrophy: clinical phenotypes in Reunion Island and French metropolitan communitiesM Fardeau, B Eymard, C Mignard, et al.
Neuromuscular Disorders : NMD|May 1, 1994
Expression of a recombinant dystrophin in mdx mice using adenovirus vectorH S Alameddine, B Quantin, A Cartaud, et al.
Applied and Environmental Microbiology|May 1, 1995
Thiosulfate reduction, an important physiological feature shared by members of the order thermotogalesG Ravot, B Ollivier, M Magot, et al.
Muscle & Nerve|June 17, 1998
X-linked vacuolated myopathy: membrane attack complex deposition on the surface membrane of injured muscle fibers is not accompanied by S-proteinJ P Louboutin, J M Navenot, M Villanova, et al.
Pageof 29

Showing results (131-140 of 289) with videos related to

Sort By:
Pageof 29
Neuromuscular Disorders : NMD|September 1, 1993
Late-onset rod myopathy associated with monoclonal gammopathyB Eymard, J C Brouet, H Collin, et al.
Neurology|April 1, 1987
Phosphorus NMR spectroscopy study of muscular enzyme deficiencies involving glycogenolysis and glycolysisD Duboc, P Jehenson, S Tran Dinh, et al.
Blood|July 1, 1982
A new case of phosphoglycerate kinase deficiency: PGK Creteil associated with rhabdomyolysis and lacking hemolytic anemiaR Rosa, C George, M Fardeau, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Dysphagia in oculopharyngeal muscular dystrophy: a series of 22 French casesS Périé, B Eymard, L Laccourreye, et al.
La Nouvelle Presse Medicale|December 18, 1982
[Acid maltase deficiency with diaphragmatic paralysis and respiratory insufficiency in adults]J Lissac, M Fardeau, F Contamin, et al.
Lancet (London, England)|September 8, 1990
Secondary metabolic defects in spinal muscular atrophy type IIJ P Harpey, C Charpentier, M Paturneau-Jouas, et al.
Neuromuscular Disorders : NMD|December 1, 1996
Chromosome 15-linked limb-girdle muscular dystrophy: clinical phenotypes in Reunion Island and French metropolitan communitiesM Fardeau, B Eymard, C Mignard, et al.
Neuromuscular Disorders : NMD|May 1, 1994
Expression of a recombinant dystrophin in mdx mice using adenovirus vectorH S Alameddine, B Quantin, A Cartaud, et al.
Applied and Environmental Microbiology|May 1, 1995
Thiosulfate reduction, an important physiological feature shared by members of the order thermotogalesG Ravot, B Ollivier, M Magot, et al.
Muscle & Nerve|June 17, 1998
X-linked vacuolated myopathy: membrane attack complex deposition on the surface membrane of injured muscle fibers is not accompanied by S-proteinJ P Louboutin, J M Navenot, M Villanova, et al.
Pageof 29