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Neuromuscular Disorders : NMD|September 1, 2004
Genotype-phenotype correlations in nemaline myopathy caused by mutations in the genes for nebulin and skeletal muscle alpha-actinCarina Wallgren-Pettersson, Katarina Pelin, Kristen J Nowak, et al.
Neuromuscular Disorders : NMD|September 1, 2004
Deflazacort in Duchenne muscular dystrophy: a comparison of two different protocolsW D Biggar, L Politano, V A Harris, et al.
Neuromuscular Disorders : NMD|September 1, 2004
In situ hybridization analysis of Dmpk mRNA in adult mouse tissuesPartha S Sarkar, Jennifer Han, Sita Reddy
Neuromuscular Disorders : NMD|September 1, 2004
Large-scale gene expression analysis of human skeletal myoblast differentiationEllen Sterrenburg, Rolf Turk, Peter A C 't Hoen, et al.
Neuromuscular Disorders : NMD|August 9, 2005
Subclinical semitendinosus and obturator externus involvement defines an autosomal dominant myopathy with early respiratory failureDaniel Birchall, Maja von der Hagen, David Bates, et al.
Neuromuscular Disorders : NMD|August 9, 2005
Prenatal diagnosis in laminin alpha2 chain (merosin)-deficient congenital muscular dystrophy: a collective experience of five international centersMariz Vainzof, Pascale Richard, Ralf Herrmann, et al.
Neuromuscular Disorders : NMD|April 19, 2005
A rapid PCR method for genotyping the Large(myd) mouse, a model of glycosylation-deficient congenital muscular dystrophyClaudia A Browning, Prabhjit K Grewal, Christopher J Moore, et al.
Neuromuscular Disorders : NMD|April 19, 2005
Dilated cardiomyopathy may be an early sign of the C826A Fukutin-related protein mutationT Müller, M Krasnianski, R Witthaut, et al.
Neuromuscular Disorders : NMD|July 15, 2005
Localization of coxsackie virus and adenovirus receptor (CAR) in normal and regenerating human muscleM Sinnreich, C A Shaw, G Pari, et al.
Neuromuscular Disorders : NMD|July 13, 2005
A novel desmin R355P mutation causes cardiac and skeletal myopathyAnna Fidziańska, Jerzy Kotowicz, Marta Sadowska, et al.
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