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Neuromuscular Disorders : NMD|March 11, 2000
Single large-scale mitochondrial DNA deletion in a patient with encephalopathy, cardiomyopathy, and prominent intestinal pseudo-obstructionY Campos, M A Martín, C Caballero, et al.Neuromuscular Disorders : NMD|July 10, 1999
Muscle ultrasound in the assessment of suspected neuromuscular disease in childhoodS M Zuberi, N Matta, S Nawaz, et al.Neuromuscular Disorders : NMD|June 26, 1999
McArdle's disease associated with homozygosity for the missense mutation Gly204Ser of the myophosphorylase gene in a Spanish patientJ C Rubio, M A Martín, A García, et al.Neuromuscular Disorders : NMD|July 17, 1999
Behavioral characterization of mdx3cv mice deficient in C-terminal dystrophinsC Vaillend, A UngererNeuromuscular Disorders : NMD|July 17, 1999
Infantile lipid storage myopathy with nocturnal hypoventilation shows abnormal low-affinity muscle carnitine uptake in vitroL Vergani, C AngeliniNeuromuscular Disorders : NMD|July 17, 1999
Decreased expression of laminin beta 1 in chromosome 21-linked Bethlem myopathyL Merlini, M Villanova, P Sabatelli, et al.Neuromuscular Disorders : NMD|November 2, 1999
Peripheral myelin modification in CMT1B correlates with MPZ gene mutationsA Lagueny, P Latour, A Vital, et al.Neuromuscular Disorders : NMD|November 2, 1999
The relationship of plasma catecholamine and lactate during anaerobic threshold exercise in mitochondrial myopathiesG Siciliano, M Renna, M L Manca, et al.Neuromuscular Disorders : NMD|January 5, 2000
A diagnostic fluorescent marker kit for six limb girdle muscular dystrophiesI Richard, N Bourg, S Marchand, et al.Pageof 340