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Neuromuscular Disorders : NMD|December 30, 2015
3D analysis of the chest wall motion for monitoring late-onset Pompe disease patientsHenri Meric, Line Falaize, Didier Pradon, et al.
Neuromuscular Disorders : NMD|January 19, 2016
Patterns of disease progression in type 2 and 3 SMA: Implications for clinical trialsEugenio Mercuri, Richard Finkel, Jacqueline Montes, et al.
Neuromuscular Disorders : NMD|November 4, 2015
Acid ceramidase deficiency associated with spinal muscular atrophy with progressive myoclonic epilepsyJoanna J Gan, Virginie Garcia, Jane Tian, et al.
Neuromuscular Disorders : NMD|October 24, 2015
Dropped-head in recessive oculopharyngeal muscular dystrophyMatteo Garibaldi, Elena Maria Pennisi, Mirella Bruttini, et al.
Neuromuscular Disorders : NMD|January 26, 2016
Erythromelalgia-like presentation of chronic acquired demyelinating polyneuropathy in a setting of past alcohol abuseMiguel Chuquilin, Upinder K Dhand
Neuromuscular Disorders : NMD|January 20, 2016
De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportionSander Pajusalu, Inga Talvik, Klari Noormets, et al.
Neuromuscular Disorders : NMD|March 8, 2016
Atrial flutter in myotonic dystrophy type 1: Patient characteristics and clinical outcomeKarim Wahbi, Frederic A Sebag, Nicolas Lellouche, et al.
Neuromuscular Disorders : NMD|December 16, 2014
Upper limb module in non-ambulant patients with spinal muscular atrophy: 12 month changesSerena Sivo, Elena Mazzone, Laura Antonaci, et al.
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