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Neuromuscular Disorders : NMD|April 3, 2012
Hand weakness in Charcot-Marie-Tooth disease 1XP J Arthur-Farraj, S M Murphy, M Laura, et al.Neuromuscular Disorders : NMD|June 17, 2011
Clinical and myopathological evaluation of early- and late-onset subtypes of myofibrillar myopathyMontse Olivé, Zagaa Odgerel, Amaia Martínez, et al.Neuromuscular Disorders : NMD|November 15, 2011
Flow cytometry analysis: a quantitative method for collagen VI deficiency screeningJ Kim, C Jimenez-Mallebrera, A R Foley, et al.Neuromuscular Disorders : NMD|November 11, 2011
Blood glutathione decrease in subjects carrying lamin A/C gene mutations is an early marker of cardiac involvementChristophe Meune, Lara Khouzami, Karim Wahbi, et al.Neuromuscular Disorders : NMD|November 1, 1995
Duplication of dystrophin gene and dissimilar clinical phenotype in the same familyA Toscano, L Vitiello, G P Comi, et al.Neuromuscular Disorders : NMD|May 1, 1996
Clinical heterogeneity of seronegative myasthenia gravisA Evoli, A P Batocchi, M Lo Monaco, et al.Neuromuscular Disorders : NMD|May 1, 1996
Prenatal diagnosis of limb-girdle muscular dystrophy type 2AG Restagno, N Romero, I Richard, et al.Neuromuscular Disorders : NMD|May 1, 1996
Application of in vitro Myo-differentiation of non-muscle cells to enhance gene expression and facilitate analysis of muscle proteinsP A Roest, A C van der Tuijn, H B Ginjaar, et al.Neuromuscular Disorders : NMD|May 1, 1996
Role of nicotinic acetylcholine receptors at the vertebrate myotendinous junction: a hypothesisL Bernheim, M Hamann, J H Liu, et al.Neuromuscular Disorders : NMD|August 1, 1996
DNA fragmentation and BCL-2 expression in infantile spinal muscular atrophyD S Tews, H H GoebelPageof 340