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M Fardeau

Showing results (251-260 of 289) with videos related to

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American Journal of Human Genetics|August 1, 1992
Linkage studies in facioscapulohumeral muscular dystrophy (FSHD)J R Gilbert, J M Stajich, M C Speer, et al.
Revue Neurologique|June 9, 2000
[Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material with mutation of the alphaB-cristallin gene]M Fardeau, P Vicart, A Caron, et al.
Pacing and Clinical Electrophysiology : PACE|January 4, 2001
High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutationH M Bécane, G Bonne, S Varnous, et al.
FEBS Letters|February 26, 1996
Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12D Jung, F Leturcq, Y Sunada, et al.
The Journal of Cell Biology|January 3, 2001
Loss of calpain 3 proteolytic activity leads to muscular dystrophy and to apoptosis-associated IkappaBalpha/nuclear factor kappaB pathway perturbation in miceI Richard, C Roudaut, S Marchand, et al.
Annals of Neurology|July 13, 1999
Homozygotes for oculopharyngeal muscular dystrophy have a severe form of the diseaseS C Blumen, B Brais, A D Korczyn, et al.
Neurology|July 20, 2007
New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutationA Yanagisawa, C Bouchet, P Y K Van den Bergh, et al.
American Journal of Human Genetics|January 13, 2000
Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31G Feldman, M Li, S Martin, et al.
Neurology|December 28, 2006
Muscle imaging in dominant core myopathies linked or unlinked to the ryanodine receptor 1 geneD Fischer, M Herasse, A Ferreiro, et al.
Clinical Genetics|November 15, 2000
Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP)M Q Xu, G Feldman, M Le Merrer, et al.
Pageof 29

Showing results (251-260 of 289) with videos related to

Sort By:
Pageof 29
American Journal of Human Genetics|August 1, 1992
Linkage studies in facioscapulohumeral muscular dystrophy (FSHD)J R Gilbert, J M Stajich, M C Speer, et al.
Revue Neurologique|June 9, 2000
[Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material with mutation of the alphaB-cristallin gene]M Fardeau, P Vicart, A Caron, et al.
Pacing and Clinical Electrophysiology : PACE|January 4, 2001
High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutationH M Bécane, G Bonne, S Varnous, et al.
FEBS Letters|February 26, 1996
Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12D Jung, F Leturcq, Y Sunada, et al.
The Journal of Cell Biology|January 3, 2001
Loss of calpain 3 proteolytic activity leads to muscular dystrophy and to apoptosis-associated IkappaBalpha/nuclear factor kappaB pathway perturbation in miceI Richard, C Roudaut, S Marchand, et al.
Annals of Neurology|July 13, 1999
Homozygotes for oculopharyngeal muscular dystrophy have a severe form of the diseaseS C Blumen, B Brais, A D Korczyn, et al.
Neurology|July 20, 2007
New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutationA Yanagisawa, C Bouchet, P Y K Van den Bergh, et al.
American Journal of Human Genetics|January 13, 2000
Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31G Feldman, M Li, S Martin, et al.
Neurology|December 28, 2006
Muscle imaging in dominant core myopathies linked or unlinked to the ryanodine receptor 1 geneD Fischer, M Herasse, A Ferreiro, et al.
Clinical Genetics|November 15, 2000
Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP)M Q Xu, G Feldman, M Le Merrer, et al.
Pageof 29