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Neuromuscular Disorders : NMD|March 27, 2007
Impact on oxidative phosphorylation of immortalization with the telomerase geneK Auré, K Mamchaoui, P Frachon, et al.
Neuromuscular Disorders : NMD|March 16, 2007
Relationship between cardiac arrhythmias and sleep apnoea in permanently paced patients with type I myotonic dystrophyArnaud Lazarus, Jean Varin, Gael Jauvert, et al.
Neuromuscular Disorders : NMD|March 3, 2007
Expression of MBNL and CELF mRNA transcripts in muscles with myotonic dystrophyYuriko Nezu, Yoshihiro Kino, Noboru Sasagawa, et al.
Neuromuscular Disorders : NMD|February 16, 2007
Postnatal overexpression of the CT GalNAc transferase inhibits muscular dystrophy in mdx mice without altering muscle growth or neuromuscular development: evidence for a utrophin-independent mechanismRui Xu, Marybeth Camboni, Paul T Martin
Neuromuscular Disorders : NMD|February 16, 2007
Novel COLQ mutation 950delC in synaptic congenital myasthenic syndrome and symptomatic heterozygous relativesFelix Schreiner, Marc Hoppenz, Ruth Klaeren, et al.
Neuromuscular Disorders : NMD|March 23, 2007
Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) geneHeinz Jungbluth, Haiyan Zhou, Caroline A Sewry, et al.
Neuromuscular Disorders : NMD|March 23, 2007
A second pedigree with autosomal dominant nemaline myopathy caused by TPM3 mutation: a clinical and pathological studyIsabelle Pénisson-Besnier, Nicole Monnier, Annick Toutain, et al.
Neuromuscular Disorders : NMD|March 6, 2007
A novel FKRP mutation in congenital muscular dystrophy disrupts the dystrophin glycoprotein complexHeather MacLeod, Peter Pytel, Robert Wollmann, et al.
Neuromuscular Disorders : NMD|March 6, 2007
Paraneoplastic myopathy: response to intravenous immunoglobulinJ B Sampson, S M Smith, A G Smith, et al.
Neuromuscular Disorders : NMD|March 6, 2007
MYH7 gene mutation in myosin storage myopathy and scapulo-peroneal myopathyElena Pegoraro, Bruno F Gavassini, Carlo Borsato, et al.
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