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Neuromuscular disorders : NMD

Showing results (1-10 of 4,221) with videos related to

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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|July 19, 2003
102nd ENMC International Workshop on Schwartz-Jampel syndrome, 14-16 December, 2001, Naarden, The NetherlandsSophie Nicole, Haluk Topaloglu, Bertrand Fontaine
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.
Pageof 423

Showing results (1-10 of 4,221) with videos related to

Sort By:
Pageof 423
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|July 19, 2003
102nd ENMC International Workshop on Schwartz-Jampel syndrome, 14-16 December, 2001, Naarden, The NetherlandsSophie Nicole, Haluk Topaloglu, Bertrand Fontaine
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.
Pageof 423