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Neuromuscular Disorders : NMD|January 17, 2009
Facioscapulohumeral muscular dystrophy presenting with hypertrophic cardiomyopathy: a case studyMasahiro Tsuji, Makoto Kinoshita, Yukihiro Imai, et al.
Neuromuscular Disorders : NMD|October 4, 2005
Cytochrome c oxidase deficient muscle fibres: substantial variation in their proportions within skeletal muscles from patients with mitochondrial myopathyM J Barron, P F Chinnery, D Howel, et al.
Neuromuscular Disorders : NMD|October 4, 2005
Marked phenotypic variation in a family with a new myelin protein zero mutationA Szabo, S Züchner, E Siska, et al.
Neuromuscular Disorders : NMD|October 4, 2005
Novel EGR2 mutation R359Q is associated with CMT type 1 and progressive scoliosisE Mikesová, K Hühne, B Rautenstrauss, et al.
Neuromuscular Disorders : NMD|August 9, 2005
Terminal antisense oligonucleotide modifications can enhance induced exon skippingBijanka L Gebski, Stephen J Errington, Russell D Johnsen, et al.
Neuromuscular Disorders : NMD|August 9, 2005
Peripheral nerve lesions associated with a dominant missense mutation, E33D, of the lamin A/C geneAnne Vital, Xavier Ferrer, Cyril Goizet, et al.
Neuromuscular Disorders : NMD|August 9, 2005
Ryanodine receptor 1 mutations, dysregulation of calcium homeostasis and neuromuscular disordersSusan Treves, Ayuk A Anderson, Sylvie Ducreux, et al.
Neuromuscular Disorders : NMD|February 17, 2007
Dystrophinopathy carrier determination and detection of protein deficiencies in muscular dystrophy using lentiviral MyoD-forced myogenesisSandra T Cooper, Eddy Kizana, Jonathon D Yates, et al.
Neuromuscular Disorders : NMD|February 17, 2007
Ascorbic acid inhibits PMP22 expression by reducing cAMP levelsFerdinand Kaya, Sophie Belin, Patrice Bourgeois, et al.
Neuromuscular Disorders : NMD|February 28, 2007
Molecular characterization of myophosphorylase deficiency (McArdle disease) in 34 patients from Southern France: identification of 10 new mutations. Absence of genotype-phenotype correlationRobert Aquaron, Jean-Louis Bergé-Lefranc, Jean-Francois Pellissier, et al.
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