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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 Brooke
Neuromuscular Disorders : NMD|September 1, 1994
The wasted leg syndrome, a single fibre electromyographic study of arms and legsR Kay, Y W Chan, M S Schwartz
Neuromuscular 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.
Neuromuscular Disorders : NMD|October 24, 2006
AbetaPP-overexpression and proteasome inhibition increase alphaB-crystallin in cultured human muscle: relevance to inclusion-body myositisSlawomir Wojcik, W King Engel, Janis McFerrin, et al.
Neuromuscular Disorders : NMD|October 24, 2006
A novel sporadic mutation G14739A of the mitochondrial tRNA(Glu) in a girl with exercise intoleranceJohannes A Mayr, Ali-Reza Moslemi, Holger Förster, et al.
Neuromuscular Disorders : NMD|October 24, 2006
Myotilin: a prominent marker of myofibrillar remodellingLena Carlsson, Ji-Guo Yu, Monica Moza, et al.
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