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Neuromuscular Disorders : NMD|December 16, 2014
New disease allele and de novo mutation indicate mutational vulnerability of titin exon 343 in hereditary myopathy with early respiratory failureDongyue Yue, Mingshi Gao, Wenhua Zhu, et al.Neuromuscular Disorders : NMD|December 16, 2014
Hip flexion weakness is associated with impaired mobility in oculopharyngeal muscular dystrophy: a retrospective study with implications for trial designSarah Youssof, Ronald Schrader, David Bear, et al.Neuromuscular Disorders : NMD|October 24, 2015
Positive effects of bisphosphonates on bone and muscle in a mouse model of Duchenne muscular dystrophySung-Hee Yoon, Kim S Sugamori, Marc D Grynpas, et al.Neuromuscular Disorders : NMD|October 3, 2015
Sparing of the extraocular muscles in mdx mice with absent or reduced utrophin expression: A life span analysisAbby A McDonald, Sadie L Hebert, Linda K McLoonNeuromuscular Disorders : NMD|October 3, 2015
A CHRNE frameshift mutation causes congenital myasthenic syndrome in young Jack Russell TerriersCaitlin J Rinz, Vanda A Lennon, Fiona James, et al.Neuromuscular Disorders : NMD|October 21, 2015
Fast-twitch skeletal muscle fiber adaptation to SERCA1 deficiency in a Dutch Improved Red and White calf pseudomyotonia caseTiziano Dorotea, Walter Grünberg, Leonardo Murgiano, et al.Neuromuscular Disorders : NMD|October 1, 2015
Molecular combing compared to Southern blot for measuring D4Z4 contractions in FSHDJessica Vasale, Fatih Boyar, Michael Jocson, et al.Neuromuscular Disorders : NMD|August 24, 2015
Spinal and bulbar muscular atrophy and Charcot-Marie-Tooth type 1A: Co-existence of two rare neuromuscular genetic diseases in the same patientAnna Sagnelli, Vidmer Scaioli, Giuseppe Piscosquito, et al.Neuromuscular Disorders : NMD|September 14, 2015
Congenital myasthenic syndrome due to mutation in CHRNE gene with clinical worsening and thymic hyperplasia attributed to association with autoimmune-myasthenia gravisErnestina Santos, Isabel Moreira, Ester Coutinho, et al.Neuromuscular Disorders : NMD|August 8, 2015
Atypical nuclear abnormalities in a patient with Brody diseaseJean-Marie Mussini, Armelle Magot, Daniel Hantaï, et al.Pageof 341