Showing results (731-740 of 3,396) with videos related to
Sort By:
Pageof 340
Neuromuscular Disorders : NMD|March 15, 2006
'Cap myopathy': case report of a familyJ M Cuisset, C A Maurage, J F Pellissier, et al.Neuromuscular Disorders : NMD|November 20, 2016
Knowledge of carrier status and barriers to testing among mothers of sons with Duchenne or Becker muscular dystrophyLauren Bogue, Holly Peay, Ann Martin, et al.Neuromuscular Disorders : NMD|October 19, 2016
A case of congenital spinal muscular atrophy with pain due to a mutation in TRPV4Jason Fleming, Dianna QuanNeuromuscular Disorders : NMD|October 30, 2016
Recurrent de novo BICD2 mutation associated with arthrogryposis multiplex congenita and bilateral perisylvian polymicrogyriaGianina Ravenscroft, Nataliya Di Donato, Gabriele Hahn, et al.Neuromuscular Disorders : NMD|March 12, 2014
Quantitative MRI and strength measurements in the assessment of muscle quality in Duchenne muscular dystrophyB H Wokke, J C van den Bergen, M J Versluis, et al.Neuromuscular Disorders : NMD|February 5, 2014
Longitudinal measurements of MRI-T2 in boys with Duchenne muscular dystrophy: effects of age and disease progressionR J Willcocks, I A Arpan, S C Forbes, et al.Neuromuscular Disorders : NMD|February 5, 2014
A novel missense mutation in POMT1 modulates the severe congenital muscular dystrophy phenotype associated with POMT1 nonsense mutationsStephanie E Wallace, Jessie H Conta, Thomas L Winder, et al.Neuromuscular Disorders : NMD|February 1, 2014
6th Dysferlin Conference, 3-6 April 2013, Arlington, Virginia, USADouglas E Albrecht, Laura E Rufibach, Bradley A Williams, et al.Neuromuscular Disorders : NMD|January 14, 2017
Prevalence of myotonic dystrophy type 1 in adults in western SwedenChristopher Lindberg, Fredrik BjerkneNeuromuscular Disorders : NMD|January 14, 2017
Resistant myasthenia gravis and rituximab: A monocentric retrospective study of 28 patientsVadim Afanasiev, Sophie Demeret, Francis Bolgert, et al.Pageof 340