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Neuromuscular Disorders : NMD|August 30, 2001
Congenital myopathy with central cores and fingerprint bodies in association with malignant hyperthermia susceptibilityT Stojkovic, C A Maurage, A Moerman, et al.
Neuromuscular Disorders : NMD|August 30, 2001
Do immune cells promote the pathology of dystrophin-deficient myopathies?M J Spencer, J G Tidball
Neuromuscular Disorders : NMD|March 21, 2001
A standardized method for the evaluation of respiratory muscle endurance in patients with Duchenne muscular dystrophyS Matecki, N Topin, M Hayot, et al.
Neuromuscular Disorders : NMD|April 12, 2001
IGF-I treatment improves the functional properties of fast- and slow-twitch skeletal muscles from dystrophic miceG S Lynch, S A Cuffe, D R Plant, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Surplus protein myopathiesH H Goebel, I A Warlo
Neuromuscular Disorders : NMD|February 13, 2001
MNGIE: from nuclear DNA to mitochondrial DNAI Nishino, A Spinazzola, M Hirano
Neuromuscular Disorders : NMD|February 13, 2001
Use of magnetic resonance imaging for noninvasive characterization and follow-up of an experimental injury to normal mouse musclesA Wishnia, H Alameddine, S Tardif de Géry, et al.
Neuromuscular Disorders : NMD|July 19, 2000
Immunohistochemical staining of dystrophin on formalin-fixed paraffin-embedded sections in Duchenne/Becker muscular dystrophy and manifesting carriers of Duchenne muscular dystrophyS Hoshino, N Ohkoshi, M Watanabe, et al.
Neuromuscular Disorders : NMD|July 19, 2000
A homozygous missense mutation (A659D) in the myophosphorylase gene in a Spanish patient with McArdle's diseaseM A Martín, J C Rubio, Y Campos, et al.
Neuromuscular Disorders : NMD|July 19, 2000
Rhabdomyosarcoma rho(0) cells: isolation and characterization of a mitochondrial DNA depleted cell line with 'muscle-like' propertiesL Vergani, A R Prescott, I J Holt
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