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Neuromuscular Disorders : NMD|September 21, 2000
Hyperparathyroidism in a patient with proximal myotonic myopathy (PROMM)C Schneider, T Grimm, W Kress, et al.Neuromuscular Disorders : NMD|June 6, 2000
Regenerative capacity and the number of satellite cells in soleus muscles of normal and mdx miceJ Reimann, A Irintchev, A WernigNeuromuscular Disorders : NMD|June 6, 2000
High resolution magnetic resonance imaging of the brain in the dy/dy mouse with merosin-deficient congenital muscular dystrophyD J Dubowitz, J M Tyszka, C A Sewry, et al.Neuromuscular Disorders : NMD|June 6, 2000
Pre-clinical screening of drugs using the mdx mouseJ A Granchelli, C Pollina, M S HudeckiNeuromuscular Disorders : NMD|March 14, 2000
Clinical and neuropathological parameters affecting the diagnostic yield of nerve biopsyM Deprez, C C de Groote, L Gollogly, et al.Neuromuscular Disorders : NMD|March 14, 2000
Severe gamma-sarcoglycanopathy caused by a novel missense mutation and a large deletionK J Nowak, P Walsh, R L Jacob, et al.Neuromuscular Disorders : NMD|March 14, 2000
Integrin and dystrophin associated adhesion protein complexes during regeneration of shearing-type muscle injuryM Kääriäinen, J Kääriäinen, T L Järvinen, et al.Neuromuscular Disorders : NMD|March 14, 2000
A missense mutation T487N in the myophosphorylase gene in a Spanish patient with McArdle's diseaseJ C Rubio, M A Martín, Y Campos, et al.Neuromuscular Disorders : NMD|March 14, 2000
A family with PROMM not linked to the recently mapped PROMM locus DM2T Wieser, D Bönsch, K Eger, et al.Neuromuscular Disorders : NMD|July 19, 2000
Phenotypic manifestations associated with CAG-repeat expansion in the androgen receptor gene in male patients and heterozygous females: a clinical and molecular study of 30 familiesC Mariotti, B Castellotti, D Pareyson, et al.Pageof 340