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Neuromuscular Disorders : NMD|June 24, 2006
Muscle slowness in a family with nemaline myopathyInge M P Pauw-Gommans, Karin H L Gerrits, Arnold de Haan, et al.Neuromuscular Disorders : NMD|June 24, 2006
Myotilinopathy in a family with late onset myopathyIsabelle Pénisson-Besnier, Kati Talvinen, Catherine Dumez, et al.Neuromuscular Disorders : NMD|August 29, 2006
Refsum's disease may mimic familial Guillain Barre syndromeChristophe Verny, Adriana Prundean, Guillaume Nicolas, et al.Neuromuscular Disorders : NMD|August 29, 2006
Sleep disorders in childhood-onset myotonic dystrophy type 1Maria-Antonia Quera Salva, Marc Blumen, Aurelia Jacquette, et al.Neuromuscular Disorders : NMD|August 29, 2006
Familial inclusion body myositis in a mother and son with different ancestral MHC haplotypesFrank Mastaglia, Patricia Price, Susan Walters, et al.Neuromuscular Disorders : NMD|January 24, 2007
Skeletal dysplasia presenting as a neuromuscular disorder - report of three childrenJonas Bondestam, Helena Pihko, Sanna-Leena Vanhanen, et al.Neuromuscular Disorders : NMD|January 26, 2007
Diagnosis of myotubular myopathy in the oldest known manifesting female carrier: a clinical and genetic studyIsabelle Pénisson-Besnier, Valérie Biancalana, Pascal Reynier, et al.Neuromuscular Disorders : NMD|December 1, 2006
Dystrophin-dependent muscle degeneration requires a fully functional contractile machinery to occur in C. elegansMarie-Christine Mariol, Edwige Martin, Lucie Chambonnier, et al.Neuromuscular Disorders : NMD|December 1, 2006
Low dose formoterol administration improves muscle function in dystrophic mdx mice without increasing fatigueLeah J Harcourt, Jonathan D Schertzer, James G Ryall, et al.Neuromuscular Disorders : NMD|October 21, 2006
Deficiency of mitochondrial ATP synthase of nuclear genetic originW Sperl, P Jesina, J Zeman, et al.Pageof 340