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Neuromuscular Disorders : NMD|September 5, 2002
Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p (RSMD1)Eugenio Mercuri, Beril Talim, Behzad Moghadaszadeh, et al.
Neuromuscular Disorders : NMD|September 5, 2002
Quantitative assessment of calf circumference in Duchenne muscular dystrophy patientsE A C Beenakker, J de Vries, J M Fock, et al.
Neuromuscular Disorders : NMD|September 5, 2002
Charcot-Marie-Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genesV A Street, G Meekins, H P Lipe, et al.
Neuromuscular Disorders : NMD|September 5, 2002
Mutations in the nebulin gene can cause severe congenital nemaline myopathyCarina Wallgren-Pettersson, Kati Donner, Caroline Sewry, et al.
Neuromuscular Disorders : NMD|September 11, 2002
Gene transfer studies in animals: what do they really tell us about the prospects for gene therapy in DMD?Dominic J Wells, Kim E Wells
Neuromuscular Disorders : NMD|September 11, 2002
Viral vectors for gene transfer of micro-, mini-, or full-length dystrophinJeannine M Scott, Sheng Li, Scott Q Harper, et al.
Neuromuscular Disorders : NMD|September 11, 2002
Strategies for muscle-specific targeting of adenoviral gene transfer vectorsChristian Thirion, Nancy Larochelle, Christoph Volpers, 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 I: rationaleChristine Thioudellet, Stéphane Blot, Patrick Squiban, et al.
Neuromuscular Disorders : NMD|September 11, 2002
CD45 fraction bone marrow cells as potential delivery vehicles for genetically corrected dystrophin lociR M I Kapsa, S H A Wong, I Bertoncello, et al.
Neuromuscular Disorders : NMD|September 11, 2002
Glucocorticoid-mediated regulation of utrophin levels in human muscle fibersIsabelle Courdier-Fruh, Lee Barman, Alexandre Briguet, et al.
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