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Neuromuscular Disorders : NMD|January 1, 1992
Gene therapy: present situation and future prospectsF GrosNeuromuscular Disorders : NMD|December 1, 2009
Coenzyme Q10 is frequently reduced in muscle of patients with mitochondrial myopathySabrina Sacconi, Eva Trevisson, Leonardo Salviati, et al.Neuromuscular Disorders : NMD|November 4, 2009
Autosomal recessive inheritance of classic Bethlem myopathyA Reghan Foley, Ying Hu, Yaqun Zou, et al.Neuromuscular Disorders : NMD|December 26, 2009
The contribution of human synovial stem cells to skeletal muscle regenerationJinhong Meng, Carl F Adkin, Virginia Arechavala-Gomeza, et al.Neuromuscular Disorders : NMD|December 26, 2009
Myositis in Griscelli syndrome type 2 treated with hematopoietic cell transplantationAlfred Peter Born, Klaus Müller, Hanne Vibeke Marquart, et al.Neuromuscular Disorders : NMD|January 1, 1994
The status of HMSN type IIIA A Gabreëls-Festen, F J Gabreëls, F G Jennekens, et al.Neuromuscular Disorders : NMD|November 17, 2009
Attenuation of adverse cardiac effects in prednisolone-treated delta-sarcoglycan-deficient mice by mineralocorticoid-receptor-antagonismRalf Bauer, Alison Blain, Elizabeth Greally, et al.Neuromuscular Disorders : NMD|December 17, 2009
Rigid spine syndrome revealing late-onset Pompe diseasePascal Laforêt, Valérie Doppler, Catherine Caillaud, et al.Neuromuscular Disorders : NMD|July 1, 1993
Monomelic muscle atrophyM Takemitsu, K Murayama, T Saga, et al.Neuromuscular Disorders : NMD|September 21, 2000
A novel myopathy-associated mitochondrial DNA mutation altering the conserved size of the tRNA(Gln) anticodon loopR Dey, C H Tengan, M P Morita, et al.Pageof 340