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Neuromuscular Disorders : NMD|September 11, 2002
Targeted exon skipping as a potential gene correction therapy for Duchenne muscular dystrophyAnnemieke Aartsma-Rus, Mattie Bremmer-Bout, Anneke A M Janson, et al.
Neuromuscular Disorders : NMD|September 11, 2002
A web-accessible complete transcriptome of normal human and DMD muscleMarina Bakay, Po Zhao, Josephine Chen, et al.
Neuromuscular Disorders : NMD|February 5, 2003
Cardiac assessment in childhood carriers of Duchenne and Becker muscular dystrophiesM A Nolan, O D H Jones, R L Pedersen, et al.
Neuromuscular Disorders : NMD|February 5, 2003
Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegiaG Van Goethem, J J Martin, B Dermaut, et al.
Neuromuscular Disorders : NMD|February 5, 2003
Transcriptional activation of the utrophin promoter B by a constitutively active Ets-transcription factorAlexandre Briguet, Dorothee Bleckmann, Mickaël Bettan, et al.
Neuromuscular Disorders : NMD|February 5, 2003
Childhood chronic inflammatory demyelinating polyneuropathy with central nervous system demyelination resembling multiple sclerosisM Victoria Rodriguez-Casero, Lloyd K Shield, Lee T Coleman, et al.
Neuromuscular Disorders : NMD|January 22, 2002
Defects of mitochondrial beta-oxidation: a growing group of disordersJerry Vockley, David A H Whiteman
Neuromuscular Disorders : NMD|January 22, 2002
Primary gamma-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profileC G Bönnemann, J Wong, K J Jones, et al.
Neuromuscular Disorders : NMD|December 12, 2001
Deficiency of a 180-kDa extracellular matrix protein in Fukuyama type congenital muscular dystrophy skeletal muscleYoshihide Sunada, Fumiaki Saito, Itsuro Higuchi, et al.
Neuromuscular Disorders : NMD|December 12, 2001
Abnormalities in brain biochemistry associated with lack of dystrophin: studies of the mdx mouseCaroline Rae, Julian L Griffin, Duncan H Blair, et al.
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