Showing results (31-40 of 3,394) with videos related to

Sort By:
Pageof 340
Neuromuscular Disorders : NMD|June 19, 2010
Reduction of abnormal behavioral response to brief restraint by information from other mice in dystrophin-deficient mdx miceKazuhiro Yamamoto, Daisuke Yamada, Tomohiro Kabuta, et al.
Neuromuscular Disorders : NMD|September 21, 2010
A new truncating MPZ mutation associated with a very mild CMT1 B phenotypeSelina Piazza, Fulvia Baldinotti, Antonella Fogli, et al.
Neuromuscular Disorders : NMD|July 13, 2010
Fukutin mutations in congenital muscular dystrophies with defective glycosylation of dystroglycan in KoreaBung Chan Lim, Chang-Seok Ki, Jong-Won Kim, et al.
Neuromuscular Disorders : NMD|January 23, 2009
Interfamilial phenotypic heterogeneity in SMARD1S Joseph, S A Robb, S Mohammed, et al.
Neuromuscular Disorders : NMD|August 10, 2010
Disorders of muscle lipid metabolism: diagnostic and therapeutic challengesPascal Laforêt, Christine Vianey-Saban
Neuromuscular Disorders : NMD|March 29, 2011
Impaired neuromuscular transmission and response to acetylcholinesterase inhibitors in centronuclear myopathiesStephanie A Robb, Caroline A Sewry, James J Dowling, et al.
Neuromuscular Disorders : NMD|May 28, 2019
Central drive and ventilatory failure in late-onset Pompe disease: At the gates of a new phenotypeE L De Vito, S C Arce, S G Monteiro, et al.
Neuromuscular Disorders : NMD|October 14, 2018
Enzyme replacement therapy with alglucosidase alfa in a late-onset Pompe disease patient during pregnancyMiguel Oliveira Santos, Teresinha Evangelista, Isabel Conceição
Neuromuscular Disorders : NMD|November 5, 1997
Oxidative stress as a potential pathogenic mechanism in an animal model of Duchenne muscular dystrophyR J Ragusa, C K Chow, J D Porter
Neuromuscular Disorders : NMD|November 5, 1997
Toxoplasmic polymyositis revisited: case report and review of literatureM Cuturic, G R Hayat, C A Vogler, et al.
Pageof 340