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Neuromuscular Disorders : NMD|August 14, 2020
Lack of effect on ambulation of dalfampridine-ER (4-AP) treatment in adult SMA patientsClaudia A Chiriboga, Jonathan Marra, Nicole M LaMarca, et al.Neuromuscular Disorders : NMD|April 13, 2021
Clinical and genetic characteristics of Chinese patients with reducing body myopathyLei Chen, Hui-Xia Lin, Xin-Xia Yang, et al.Neuromuscular Disorders : NMD|March 29, 2023
Clinical characteristics and prognosis of very late-onset myasthenia gravis in ChinaYong-Lan Tang, Zhe Ruan, Yue Su, et al.Neuromuscular Disorders : NMD|September 5, 2002
A novel mitochondrial DNA tRNA(Ile) (A4267G) mutation in a sporadic patient with mitochondrial myopathyRobert W Taylor, Andrew M Schaefer, Robert McFarland, et al.Neuromuscular Disorders : NMD|September 5, 2002
Na(+)/Ca(2+) exchange in human myotubes: intracellular calcium rises in response to external sodium depletion are enhanced in DMDEmmanuel Deval, Dmitri O Levitsky, Eric Marchand, et al.Neuromuscular Disorders : NMD|September 5, 2002
Exclusion of serine palmitoyltransferase long chain base subunit 2 (SPTLC2) as a common cause for hereditary sensory neuropathyJennifer L Dawkins, Sonal Brahmbhatt, Michaela Auer-Grumbach, et al.Neuromuscular Disorders : NMD|September 11, 2002
Myogenic stem cells from the bone marrow: a therapeutic alternative for muscular dystrophy?Giuliana Ferrari, Fulvio MavilioNeuromuscular Disorders : NMD|September 11, 2002
Current protocol of a research phase I clinical trial of full-length dystrophin plasmid DNA in Duchenne/Becker muscular dystrophies. Part II: clinical protocolNorma Beatriz Romero, Olivier Benveniste, Christine Payan, et al.Neuromuscular Disorders : NMD|September 11, 2002
Oligonucleotide-mediated gene therapy for muscular dystrophiesThomas A RandoNeuromuscular Disorders : NMD|September 11, 2002
Screening for antisense modulation of dystrophin pre-mRNA splicingG Dickson, V Hill, I R GrahamPageof 340