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Neuromuscular Disorders : NMD|March 30, 2010
Progressive skeletal muscle weakness in transgenic mice expressing CTG expansions is associated with the activation of the ubiquitin-proteasome pathwayAlban Vignaud, Arnaud Ferry, Aline Huguet, et al.
Neuromuscular Disorders : NMD|May 11, 2010
Drosophila indirect flight muscle specific Act88F actin mutants as a model system for studying congenital myopathies of the human ACTA1 skeletal muscle actin geneSarah E Haigh, Sheetal S Salvi, Maria Sevdali, et al.
Neuromuscular Disorders : NMD|May 14, 2010
Nephrogenic systemic fibrosis presenting as myopathy: a case report with histopathologic correlationEric Edgar, Randy Woltjer, Ruth Whitham, et al.
Neuromuscular Disorders : NMD|June 2, 2009
Left ventricular dysfunction and cardiac arrhythmias are frequent in type 2 myotonic dystrophy: a case control studyKarim Wahbi, Christophe Meune, Henri Marc Bécane, et al.
Neuromuscular Disorders : NMD|June 9, 2009
Novel mutations in the GDAP1 gene in patients affected with early-onset axonal Charcot-Marie-Tooth type 4AIsabella Moroni, Michela Morbin, Micaela Milani, et al.
Neuromuscular Disorders : NMD|September 24, 2009
Isolated inflammatory myopathy with rimmed vacuoles presenting with dropped headHiroshi Kataoka, Kazuma Sugie, Mari Terashima, et al.
Neuromuscular Disorders : NMD|August 29, 2009
Scaled-down genetic analysis of myotonic dystrophy type 1 and type 2Masayuki Nakamori, Krzysztof Sobczak, Richard T Moxley, et al.
Neuromuscular Disorders : NMD|July 21, 2009
Muscle MRI in FHL1-linked reducing body myopathyG Astrea, J Schessl, E Clement, et al.
Neuromuscular Disorders : NMD|September 9, 2009
Progressive myofiber loss with extensive fibro-fatty replacement in a child with mitochondrial DNA depletion syndrome and novel thymidine kinase 2 gene mutationsJames Collins, Kevin E Bove, David Dimmock, et al.
Neuromuscular Disorders : NMD|August 15, 2009
An unusual presentation of muscle-eye-brain disease: severe eye abnormalities with mild muscle and brain involvementErcan Demir, Kivilcim Gucuyener, Aysima Akturk, et al.
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