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Neuromuscular Disorders : NMD|March 1, 1994
A Danish family with limb-girdle muscular dystrophy with autosomal dominant inheritanceJ F Nielsen, J JakobsenNeuromuscular Disorders : NMD|July 1, 1994
Cognitive impairment in Duchenne muscular dystrophyN Bresolin, E Castelli, G P Comi, et al.Neuromuscular Disorders : NMD|September 1, 1993
Prader-Willi syndrome: diagnostic strategy with a cytogenetic and molecular approachP Malzac, A Moncla, M A Voelckel, et al.Neuromuscular Disorders : NMD|September 1, 1994
Expression of dystrophin-associated glycoproteins and utrophin in carriers of Duchenne muscular dystrophyC A Sewry, K Matsumura, K P Campbell, et al.Neuromuscular Disorders : NMD|September 1, 1994
Evidence of two mechanisms of prostaglandin release in an in vitro model of muscle damage. Possible therapeutic implicationsR Majumdar, V A Cwik, M H BrookeNeuromuscular Disorders : NMD|September 1, 1994
The wasted leg syndrome, a single fibre electromyographic study of arms and legsR Kay, Y W Chan, M S SchwartzNeuromuscular Disorders : NMD|December 1, 2006
MRI in DNM2-related centronuclear myopathy: evidence for highly selective muscle involvementJoachim Schessl, Livija Medne, Ying Hu, et al.Neuromuscular Disorders : NMD|October 20, 2006
Multiplex ligation-dependent probe amplification improves diagnostics in spinal muscular atrophyEva L Arkblad, Niklas Darin, Kerstin Berg, et al.Neuromuscular Disorders : NMD|September 2, 2006
Fatal hypertrophic cardiomyopathy and nemaline myopathy associated with ACTA1 K336E mutationAdele D'Amico, Claudio Graziano, Giuseppe Pacileo, et al.Neuromuscular Disorders : NMD|October 24, 2006
Pompe disease (glycogen storage disease type II) in Argentineans: clinical manifestations and identification of 9 novel mutationsRachel E Palmer, Hernan M Amartino, Gabriela Niizawa, et al.Pageof 341