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Neuromuscular Disorders : NMD
|
July 19, 2003
Cardiomyopathic features associated with muscular dystrophy are independent of dystrophin absence in cardiovasculature
T 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 deficiency
Itsuro 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 gene
H 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 Netherlands
Sophie Nicole, Haluk Topaloglu, Bertrand Fontaine
Neuromuscular Disorders : NMD
|
January 1, 1992
Polysaccharide storage myopathy associated with recurrent exertional rhabdomyolysis in horses
S 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 treatment
Judy 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 phenotypes
Y 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 dystrophies
Mayana 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 phenotype
E Mercuri, C Cini, A Pichiecchio, et al.
Page
of 423
Search research articles
Search
Showing results (1-10 of 4,221) with videos related to
Sort By:
Page
of 423
Neuromuscular Disorders : NMD
|
July 19, 2003
Cardiomyopathic features associated with muscular dystrophy are independent of dystrophin absence in cardiovasculature
T 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 deficiency
Itsuro 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 gene
H 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 Netherlands
Sophie Nicole, Haluk Topaloglu, Bertrand Fontaine
Neuromuscular Disorders : NMD
|
January 1, 1992
Polysaccharide storage myopathy associated with recurrent exertional rhabdomyolysis in horses
S 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 treatment
Judy 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 phenotypes
Y 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 dystrophies
Mayana 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 phenotype
E Mercuri, C Cini, A Pichiecchio, et al.
Page
of 423