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M Fardeau

Showing results (171-180 of 289) with videos related to

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Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|August 1, 1993
Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countriesM Fardeau, K Matsumura, F M Tomé, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Distinct contractile protein profile in congenital myotonic dystrophy and X-linked myotubular myopathyN Soussi-Yanicostas, M Chevallay, C Laurent-Winter, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Using the full power of linkage analysis in 11 French Canadian families to fine map the oculopharyngeal muscular dystrophy geneB Brais, J P Bouchard, F Gosselin, et al.
The Journal of Cell Biology|April 1, 1996
Partial laminin alpha2 chain restoration in alpha2 chain-deficient dy/dy mouse by primary muscle cell culture transplantationJ T Vilquin, I Kinoshita, B Roy, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1979
[Lipidic myopathy with severe cardiomyopathy caused by a generalized carnitine deficiency. Favourable course during carnitine hydrochloride treatment]P Morand, F Despert, H N Carrier, et al.
Human Molecular Genetics|November 7, 2000
An autosomal dominant congenital myopathy with cores and rods is associated with a neomutation in the RYR1 gene encoding the skeletal muscle ryanodine receptorN Monnier, N B Romero, J Lerale, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Expression of myosin heavy chain isoforms in Duchenne muscular dystrophy patients and carriersJ F Marini, F Pons, J Leger, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1993
[Cardiac involvement in certain muscular diseases. Apropos of 216 cases]J Monségu, D Duboc, L Freychet, et al.
Neuromuscular Disorders : NMD|January 5, 2000
Adult onset reducing body myopathyD Figarella-Branger, G A Putzu, C Bouvier-Labit, et al.
Journal of the Neurological Sciences|November 1, 1989
Immunocytological and histochemical correlation in Kearns-Sayre syndrome with mtDNA deletion and partial cytochrome c oxidase deficiency in skeletal muscleN B Romero, P Lestienne, C Marsac, et al.
Pageof 29

Showing results (171-180 of 289) with videos related to

Sort By:
Pageof 29
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|August 1, 1993
Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countriesM Fardeau, K Matsumura, F M Tomé, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Distinct contractile protein profile in congenital myotonic dystrophy and X-linked myotubular myopathyN Soussi-Yanicostas, M Chevallay, C Laurent-Winter, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Using the full power of linkage analysis in 11 French Canadian families to fine map the oculopharyngeal muscular dystrophy geneB Brais, J P Bouchard, F Gosselin, et al.
The Journal of Cell Biology|April 1, 1996
Partial laminin alpha2 chain restoration in alpha2 chain-deficient dy/dy mouse by primary muscle cell culture transplantationJ T Vilquin, I Kinoshita, B Roy, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1979
[Lipidic myopathy with severe cardiomyopathy caused by a generalized carnitine deficiency. Favourable course during carnitine hydrochloride treatment]P Morand, F Despert, H N Carrier, et al.
Human Molecular Genetics|November 7, 2000
An autosomal dominant congenital myopathy with cores and rods is associated with a neomutation in the RYR1 gene encoding the skeletal muscle ryanodine receptorN Monnier, N B Romero, J Lerale, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Expression of myosin heavy chain isoforms in Duchenne muscular dystrophy patients and carriersJ F Marini, F Pons, J Leger, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1993
[Cardiac involvement in certain muscular diseases. Apropos of 216 cases]J Monségu, D Duboc, L Freychet, et al.
Neuromuscular Disorders : NMD|January 5, 2000
Adult onset reducing body myopathyD Figarella-Branger, G A Putzu, C Bouvier-Labit, et al.
Journal of the Neurological Sciences|November 1, 1989
Immunocytological and histochemical correlation in Kearns-Sayre syndrome with mtDNA deletion and partial cytochrome c oxidase deficiency in skeletal muscleN B Romero, P Lestienne, C Marsac, et al.
Pageof 29