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Neuromuscular Disorders : NMD|January 24, 2006
Reliability of the Hammersmith functional motor scale for spinal muscular atrophy in a multicentric studyE Mercuri, S Messina, R Battini, et al.Neuromuscular Disorders : NMD|January 24, 2006
Eosinophilic fasciitis in a child mimicking a myopathySigrid Pillen, Baziel van Engelen, Frank van den Hoogen, et al.Neuromuscular Disorders : NMD|November 1, 1995
A gene for autosomal recessive nemaline myopathy assigned to chromosome 2q by linkage analysisC Wallgren-Pettersson, K Avela, S Marchand, et al.Neuromuscular Disorders : NMD|November 1, 1995
Morphological and functional study of extensor digitorum longus muscle regeneration after iterative crush lesions in mdx mouseJ P Louboutin, V Fichter-Gagnepain, C Pastoret, et al.Neuromuscular Disorders : NMD|November 26, 1998
PROMM: the expanding phenotype. A family with proximal myopathy, myotonia and deafnessM F Phillips, M T Rogers, R Barnetson, et al.Neuromuscular Disorders : NMD|November 26, 1998
Dystrophinopathy in a boy with Chediak-Higashi syndromeA von Moers, F K van Landeghem, R D Cohn, et al.Neuromuscular Disorders : NMD|November 26, 1998
Laminin alpha 2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophyI Naom, M D'Alessandro, C A Sewry, et al.Neuromuscular Disorders : NMD|November 26, 1998
Presence of emerinopathy in cases of rigid spine syndromeS Kubo, T Tsukahara, M Takemitsu, et al.Neuromuscular Disorders : NMD|August 1, 1996
Peripheral lymphoid tissue-like adhesion molecule expression in nodular infiltrates in inflammatory myopathiesJ L De Bleecker, A G Engel, E C ButcherNeuromuscular Disorders : NMD|August 1, 1996
Discordant clinical outcome in type III spinal muscular atrophy sibships showing the same deletion patternF Capon, C Levato, L Merlini, et al.Pageof 340