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Neuromuscular Disorders : NMD|January 14, 2009
A novel homozygous RRM2B missense mutation in association with severe mtDNA depletionGittan Kollberg, Niklas Darin, Karin Benan, et al.Neuromuscular Disorders : NMD|June 27, 2009
Immunohistochemical analysis of calpain 3: advantages and limitations in diagnosing LGMD2ARichard Charlton, Matthew Henderson, Julie Richards, et al.Neuromuscular Disorders : NMD|August 22, 2009
Genetic variants in the promoter of TARDBP in sporadic amyotrophic lateral sclerosisNatasha Luquin, Bing Yu, Rebecca B Saunderson, et al.Neuromuscular Disorders : NMD|September 16, 2009
Myasthenia gravis precipitated by trauma: latent myasthenia and the concept of 'threshold'Russell Lane, John Wade, Dennis McGonagleNeuromuscular Disorders : NMD|September 29, 2009
Unusual presentation of phosphoglycerate mutase deficiency due to two different mutations in PGAM-M genePaola Tonin, Claudio Bruno, Denise Cassandrini, et al.Neuromuscular Disorders : NMD|October 2, 2009
Oestrogen receptor alpha gene intronic polymorphisms and autoimmune myasthenia gravis in Caucasian womenZsuzsanna Pal, Anikó Gal, Viktória Remenyi, et al.Neuromuscular Disorders : NMD|October 6, 2009
Gait analysis using accelerometry in dystrophin-deficient dogsInès Barthélémy, Eric Barrey, Jean-Laurent Thibaud, et al.Neuromuscular Disorders : NMD|February 24, 2009
Becker muscular dystrophy caused by an intronic mutation reducing the efficiency of the splice donor site of intron 26 of the dystrophin geneBerivan Baskin, Brenda Banwell, Reem Al Khater, et al.Neuromuscular Disorders : NMD|February 24, 2009
The exon 55 deletion in the nebulin gene--one single founder mutation with world-wide occurrenceVilma-Lotta Lehtokari, Rebecca S Greenleaf, Elizabeth T DeChene, et al.Neuromuscular Disorders : NMD|February 10, 2009
Glucocorticoids may trigger attacks in several types of periodic paralysisMarianne Arzel-Hézode, Suzanne McGoey, Damien Sternberg, et al.Pageof 340