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M Fardeau

Showing results (231-240 of 289) with videos related to

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Neurology|October 27, 2004
Charcot-Marie-Tooth features and maculopathy in a patient with Danon diseaseP Laforêt, P Charron, T Maisonobe, et al.
FEBS Letters|April 22, 1991
A homologue of dystrophin is expressed at the neuromuscular junctions of normal individuals and DMD patients, and of normal and mdx mice. Immunological evidenceF Pons, N Augier, J O Léger, et al.
Brain : a Journal of Neurology|February 1, 1996
Juvenile limb-girdle muscular dystrophy. Clinical, histopathological and genetic data from a small community living in the Reunion IslandM Fardeau, D Hillaire, C Mignard, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Morphological studies of skeletal muscle in lactic acidosisN B Romero, A Lombès, G Touati, et al.
The Journal of Clinical Investigation|August 1, 1993
Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophinK Matsumura, F M Tomé, V Ionasescu, et al.
Neuromuscular Disorders : NMD|September 1, 1993
The role of the dystrophin-glycoprotein complex in the molecular pathogenesis of muscular dystrophiesK Matsumura, K Ohlendieck, V V Ionasescu, 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.
Neurology|December 1, 1990
Presence of normal dystrophin in Tunisian severe childhood autosomal recessive muscular dystrophyS Ben Jelloun-Dellagi, P Chaffey, F Hentati, et al.
Human Molecular Genetics|March 1, 1995
The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac alpha and beta myosin heavy chain genes on chromosome 14q11.2-q13B Brais, Y G Xie, M Sanson, et al.
Neurology|August 28, 2002
Narrowing in on the causative defect of an intriguing X-linked myopathy with excessive autophagyB A Minassian, R Aiyar, S Alic, et al.
Pageof 29

Showing results (231-240 of 289) with videos related to

Sort By:
Pageof 29
Neurology|October 27, 2004
Charcot-Marie-Tooth features and maculopathy in a patient with Danon diseaseP Laforêt, P Charron, T Maisonobe, et al.
FEBS Letters|April 22, 1991
A homologue of dystrophin is expressed at the neuromuscular junctions of normal individuals and DMD patients, and of normal and mdx mice. Immunological evidenceF Pons, N Augier, J O Léger, et al.
Brain : a Journal of Neurology|February 1, 1996
Juvenile limb-girdle muscular dystrophy. Clinical, histopathological and genetic data from a small community living in the Reunion IslandM Fardeau, D Hillaire, C Mignard, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Morphological studies of skeletal muscle in lactic acidosisN B Romero, A Lombès, G Touati, et al.
The Journal of Clinical Investigation|August 1, 1993
Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophinK Matsumura, F M Tomé, V Ionasescu, et al.
Neuromuscular Disorders : NMD|September 1, 1993
The role of the dystrophin-glycoprotein complex in the molecular pathogenesis of muscular dystrophiesK Matsumura, K Ohlendieck, V V Ionasescu, 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.
Neurology|December 1, 1990
Presence of normal dystrophin in Tunisian severe childhood autosomal recessive muscular dystrophyS Ben Jelloun-Dellagi, P Chaffey, F Hentati, et al.
Human Molecular Genetics|March 1, 1995
The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac alpha and beta myosin heavy chain genes on chromosome 14q11.2-q13B Brais, Y G Xie, M Sanson, et al.
Neurology|August 28, 2002
Narrowing in on the causative defect of an intriguing X-linked myopathy with excessive autophagyB A Minassian, R Aiyar, S Alic, et al.
Pageof 29