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Neuromuscular Disorders : NMD|August 21, 2007
A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern ItalyF L Conforti, T Sprovieri, R Mazzei, et al.Neuromuscular Disorders : NMD|December 17, 2008
Rate of disease progression during long-term follow-up of patients with late-onset Pompe diseaseN A M E Van der Beek, M L C Hagemans, A J J Reuser, et al.Neuromuscular Disorders : NMD|December 17, 2008
Sensory-motor polyradiculoneuropathy as the first manifestation of sternum bone plasmacytoma only revealed by bone scintigraphyR Velasco, L Bau, M Povedano, et al.Neuromuscular Disorders : NMD|January 22, 2009
Absence of beta-tropomyosin is a new cause of Escobar syndrome associated with nemaline myopathyNicole Monnier, Joel Lunardi, Isabelle Marty, et al.Neuromuscular Disorders : NMD|August 8, 2008
Becker's muscular dystrophy aggravating facioscapulohumeral muscular dystrophy--double trouble as an explanation for an atypical phenotypeS Rudnik-Schöneborn, J Weis, W Kress, et al.Neuromuscular Disorders : NMD|July 8, 2008
Different clinical and magnetic resonance imaging features between Charcot-Marie-Tooth disease type 1A and 2AK W Chung, B C Suh, M E Shy, et al.Neuromuscular Disorders : NMD|June 28, 2008
Caveolinopathy--new mutations and additional symptomsAhmed Aboumousa, Jessica Hoogendijk, Richard Charlton, et al.Neuromuscular Disorders : NMD|July 1, 2008
Sensory ataxic neuropathy with ophthalmoparesis caused by POLG mutationsMargherita Milone, Nicola Brunetti-Pierri, Lin-Ya Tang, et al.Neuromuscular Disorders : NMD|July 27, 2007
Ciliary neurotrophic factor null alleles are not a risk factor for Charcot-Marie-Tooth disease, hereditary neuropathy with pressure palsies and amyotrophic lateral sclerosisPaul W J Van Vught, Joost Van Wijk, Ted E J Bradley, et al.Neuromuscular Disorders : NMD|December 6, 2008
Relationship between foot strength and motor function in preschool-age childrenKristy J Rose, Joshua Burns, Kathryn N NorthPageof 341