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Neuromuscular Disorders : NMD|October 22, 2017
Molecular characterization of congenital myasthenic syndromes in SpainD Natera-de Benito, A Töpf, J J Vilchez, et al.
Neuromuscular Disorders : NMD|August 30, 2017
A novel mutation in FGD4 causes Charcot-Marie-Tooth disease type 4H with cranial nerve involvementDaisuke Kondo, Koji Shinoda, Ken-Ichiro Yamashita, et al.
Neuromuscular Disorders : NMD|September 2, 2014
Comparing clinical data and muscle imaging of DYSF and ANO5 related muscular dystrophiesLeroy Ten Dam, Anneke J van der Kooi, Fleur Rövekamp, et al.
Neuromuscular Disorders : NMD|May 24, 2016
TMEM5-associated dystroglycanopathy presenting with CMD and mild limb-girdle muscle involvementGuja Astrea, Ilaria Pezzini, Ester Picillo, et al.
Neuromuscular Disorders : NMD|May 31, 2016
Idebenone reduces respiratory complications in patients with Duchenne muscular dystrophyCraig M McDonald, Thomas Meier, Thomas Voit, et al.
Neuromuscular Disorders : NMD|August 17, 2014
Congenital myopathies with secondary neuromuscular transmission defects; a case report and review of the literaturePedro M Rodríguez Cruz, Caroline Sewry, David Beeson, et al.
Neuromuscular Disorders : NMD|June 28, 2016
A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1bL Corrado, S Magri, A Bagarotti, et al.
Neuromuscular Disorders : NMD|March 2, 2016
Thrombospondin-1 levels correlate with macrophage activity and disease progression in dysferlin deficient miceNorifumi Urao, Rita E Mirza, Ahlke Heydemann, et al.
Neuromuscular Disorders : NMD|February 27, 2016
Health-related quality of life and functional changes in DMD: A 12-month longitudinal cohort studySonia Messina, Gian Luca Vita, Maria Sframeli, et al.
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