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Neuromuscular Disorders : NMD|April 25, 2006
The gross motor function measure is a valid and sensitive outcome measure for spinal muscular atrophyLeslie Nelson, Hollis Owens, Linda S Hynan, et al.Neuromuscular Disorders : NMD|April 20, 2006
Long-term improvement of slow-channel congenital myasthenic syndrome with fluoxetineJ Colomer, J S Müller, A Vernet, et al.Neuromuscular Disorders : NMD|May 13, 2006
Demyelinating polyneuropathy in Leber hereditary optic neuropathyH J Gilhuis, H J Schelhaas, J R M Cruysberg, et al.Neuromuscular Disorders : NMD|April 18, 2006
Genetic heterogeneity within a consanguineous family involving the LGMD 2D and the LGMD 2C genesK Fendri, M Kefi, F Hentati, et al.Neuromuscular Disorders : NMD|August 28, 2007
False negative histochemical reaction for myophosphorylase activity in fulminant sepsis due to methicillin resistant Staphylococcus aureusM Cristina Pacheco, Lili Miles, Kevin E BoveNeuromuscular Disorders : NMD|July 17, 2007
From dog to man: the broad spectrum of inflammatory myopathiesG Diane SheltonNeuromuscular Disorders : NMD|July 14, 2007
Low bone mineral density and decreased bone turnover in Duchenne muscular dystrophyAnn-Charlott Söderpalm, Per Magnusson, Anne-Christine Ahlander, et al.Neuromuscular Disorders : NMD|July 1, 2008
Phenotype of combined Duchenne and facioscapulohumeral muscular dystrophyLawrence Korngut, Victoria M Siu, Shannon L Venance, et al.Neuromuscular Disorders : NMD|June 27, 2008
Autosomal dominant congenital spinal muscular atrophy--a possible developmental deficiency of motor neurones?S Reddel, R A Ouvrier, G Nicholson, et al.Neuromuscular Disorders : NMD|December 5, 2006
Inherited neuromyotonia: a clinical and genetic study of a familyAntonio Falace, Pasquale Striano, Fiore Manganelli, et al.Pageof 340