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Neuromuscular Disorders : NMD|June 14, 2002
Hypermyelinating neuropathy, mental retardation and epilepsy in a case of merosin deficiencyF Deodato, M Sabatelli, E Ricci, et al.
Neuromuscular Disorders : NMD|June 14, 2002
Charcot-Marie-Tooth disease type 2C: a distinct genetic entity. Clinical and molecular characterization of the first European familyL Santoro, F Manganelli, L Di Maio, et al.
Neuromuscular Disorders : NMD|September 11, 2002
Recombinant micro-genes and dystrophin viral vectorsG Dickson, M L Roberts, D J Wells, et al.
Neuromuscular Disorders : NMD|September 11, 2002
Current protocol of a research phase I clinical trial of full-length dystrophin plasmid DNA in Duchenne/Becker muscular dystrophies. Part III. Ethical considerationsMichel Fardeau
Neuromuscular Disorders : NMD|September 11, 2002
Multivariate evaluation of the functional recovery obtained by the overexpression of utrophin in skeletal muscles of the mdx mouseJean-Marie Gillis
Neuromuscular Disorders : NMD|September 11, 2002
Expression profiling in stably regenerating skeletal muscle of dystrophin-deficient mdx miceJudith M Boer, Emile J de Meijer, Eveline M Mank, et al.
Neuromuscular Disorders : NMD|September 11, 2002
Collaborative translational research leading to multicenter clinical trials in Duchenne muscular dystrophy: the Cooperative International Neuromuscular Research Group (CINRG)Diana M Escolar, Erik K Henricson, Livia Pasquali, et al.
Neuromuscular Disorders : NMD|September 11, 2002
Considerations to the policy of future clinical therapeutic trials in DMDBernd Reitter
Neuromuscular Disorders : NMD|April 12, 2001
Cryptic splicing involving the splice site mutation in the canine model of Duchenne muscular dystrophyS Fletcher, T Ly, R M Duff, et al.
Neuromuscular Disorders : NMD|April 12, 2001
The lacZ gene under the control of the 7 kb of human dystrophin muscle specific promoter is expressed in cardiac muscle but not in adult skeletal muscle in transgenic miceM Ogawa, T Kaname, S Kimura, et al.
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