Neuromuscular disorders : NMD - JoVE Visualize

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Neuromuscular Disorders : NMD|July 19, 2003

Cardiomyopathic features associated with muscular dystrophy are independent of dystrophin absence in cardiovasculatureT A Hainsey, S Senapati, D E Kuhn, et al.

Neuromuscular Disorders : NMD|July 19, 2003

Pathological characteristics of skeletal muscle in Ullrich's disease with collagen VI deficiencyItsuro Higuchi, Takashi Horikiri, Takahito Niiyama, et al.

Neuromuscular Disorders : NMD|July 19, 2003

Variability of disease progression in a family with autosomal recessive CMT associated with a S194X and new R310Q mutation in the GDAP1 geneH Azzedine, M Ruberg, D Ente, et al.

Neuromuscular Disorders : NMD|January 1, 1992

Polysaccharide storage myopathy associated with recurrent exertional rhabdomyolysis in horsesS J Valberg, G H Cardinet, G P Carlson, et al.

Neuromuscular Disorders : NMD|June 12, 2003

Correlated NOS-Imu and myf5 expression by satellite cells in mdx mouse muscle regeneration during NOS manipulation and deflazacort treatmentJudy E Anderson, Cinthya Vargas

Neuromuscular Disorders : NMD|June 12, 2003

Two pathogenic mutations in the mitochondrial DNA tRNA Leu(UUR) gene (T3258C and A3280G) resulting in variable clinical phenotypesY Campos, A García, P del Hoyo, et al.

Neuromuscular Disorders : NMD|August 19, 2003

Muscle disease caused by mutations in the skeletal muscle alpha-actin gene (ACTA1)John C Sparrow, Kristen J Nowak, Hayley J Durling, et al.

Neuromuscular Disorders : NMD|August 19, 2003

The 10 autosomal recessive limb-girdle muscular dystrophiesMayana Zatz, Flavia de Paula, Alessandra Starling, et al.

Neuromuscular Disorders : NMD|August 19, 2003

Muscle magnetic resonance imaging in patients with congenital muscular dystrophy and Ullrich phenotypeE Mercuri, C Cini, A Pichiecchio, et al.

Neuromuscular Disorders : NMD|January 1, 1992

Chronic myopathy in a patient suspected of carrying two malignant hyperthermia susceptibility (MHS) mutationsT Deufel, W Müller-Felber, D E Pongratz, et al.

Pageof 340

Showing results (1-10 of 3,394) with videos related to

Sort By:

Pageof 340

Neuromuscular Disorders : NMD|July 19, 2003

Cardiomyopathic features associated with muscular dystrophy are independent of dystrophin absence in cardiovasculatureT A Hainsey, S Senapati, D E Kuhn, et al.

Neuromuscular Disorders : NMD|July 19, 2003

Pathological characteristics of skeletal muscle in Ullrich's disease with collagen VI deficiencyItsuro Higuchi, Takashi Horikiri, Takahito Niiyama, et al.

Neuromuscular Disorders : NMD|July 19, 2003

Variability of disease progression in a family with autosomal recessive CMT associated with a S194X and new R310Q mutation in the GDAP1 geneH Azzedine, M Ruberg, D Ente, et al.

Neuromuscular Disorders : NMD|January 1, 1992

Polysaccharide storage myopathy associated with recurrent exertional rhabdomyolysis in horsesS J Valberg, G H Cardinet, G P Carlson, et al.

Neuromuscular Disorders : NMD|June 12, 2003

Correlated NOS-Imu and myf5 expression by satellite cells in mdx mouse muscle regeneration during NOS manipulation and deflazacort treatmentJudy E Anderson, Cinthya Vargas

Neuromuscular Disorders : NMD|June 12, 2003

Two pathogenic mutations in the mitochondrial DNA tRNA Leu(UUR) gene (T3258C and A3280G) resulting in variable clinical phenotypesY Campos, A García, P del Hoyo, et al.

Neuromuscular Disorders : NMD|August 19, 2003

Muscle disease caused by mutations in the skeletal muscle alpha-actin gene (ACTA1)John C Sparrow, Kristen J Nowak, Hayley J Durling, et al.

Neuromuscular Disorders : NMD|August 19, 2003

The 10 autosomal recessive limb-girdle muscular dystrophiesMayana Zatz, Flavia de Paula, Alessandra Starling, et al.

Neuromuscular Disorders : NMD|August 19, 2003

Muscle magnetic resonance imaging in patients with congenital muscular dystrophy and Ullrich phenotypeE Mercuri, C Cini, A Pichiecchio, et al.

Neuromuscular Disorders : NMD|January 1, 1992

Chronic myopathy in a patient suspected of carrying two malignant hyperthermia susceptibility (MHS) mutationsT Deufel, W Müller-Felber, D E Pongratz, et al.

Pageof 340