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Neuromuscular Disorders : NMD|June 19, 1998
Merosin-deficient congenital muscular dystrophy with severe mental retardation and normal cranial MRI: a report of two siblingsH Topaloğlu, B Talim, N Vignier, et al.
Neuromuscular Disorders : NMD|June 19, 1998
Hereditary motor and sensory neuropathy Lom type in an Italian Gypsy familyL Merlini, M Villanova, P Sabatelli, et al.
Neuromuscular Disorders : NMD|June 19, 1998
Critical illness myopathy unrelated to corticosteroids or neuromuscular blocking agentsN Deconinck, V Van Parijs, G Beckers-Bleukx, et al.
Neuromuscular Disorders : NMD|June 19, 1998
Commentary: extraocular muscle sparing in muscular dystrophy: a critical evaluation of potential protective mechanismsJ D Porter
Neuromuscular Disorders : NMD|June 19, 1998
Heterogeneity in chronic fatigue syndrome: evidence from magnetic resonance spectroscopy of muscleR J Lane, M C Barrett, D J Taylor, et al.
Neuromuscular Disorders : NMD|December 18, 2003
Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutationM Kefi, R Amouri, A Driss, et al.
Neuromuscular Disorders : NMD|December 18, 2003
A novel homozygous missense mutation in the GNE gene of a patient with quadriceps-sparing hereditary inclusion body myopathy associated with muscle inflammationSabine Krause, Beate Schlotter-Weigel, Maggie C Walter, et al.
Neuromuscular Disorders : NMD|October 16, 2004
Expression profiling in spinal muscular atrophy reveals an RNA binding protein deficitKirstie N Anderson, Dilair Baban, Peter L Oliver, et al.
Neuromuscular Disorders : NMD|October 16, 2004
Mutation screening in Korean hypokalemic periodic paralysis patients: a novel SCN4A Arg672Cys mutationMyeong-Kyu Kim, Seung-Han Lee, Man-Seok Park, et al.
Neuromuscular Disorders : NMD|November 27, 2004
Sleep disordered breathing in spinal muscular atrophyUwe Mellies, Christian Dohna-Schwake, Florian Stehling, et al.
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