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Neuromuscular Disorders : NMD|January 1, 1995
Rimmed basophilic vacuoles and filamentous inclusions in neuromuscular disordersP J Jongen, H J Ter Laak, A M StadhoudersNeuromuscular Disorders : NMD|March 1, 1995
The effect of glucocorticoids on the accumulation of utrophin by cultured normal and dystrophic human skeletal muscle satellite cellsF Pasquini, C Guerin, D Blake, et al.Neuromuscular Disorders : NMD|March 1, 1995
Neonatal carnitine palmitoyltransferase-2 deficiency: a case presenting with myopathyJ M Land, S Mistry, M Squier, et al.Neuromuscular Disorders : NMD|March 1, 1995
Coexistence of scleromyositis associated with PM-Scl antibody and myastheniaI Hausmanowa-Petrusewicz, M Blaszczyk, S JablońskaNeuromuscular Disorders : NMD|March 1, 1994
Continuous muscle fibre activity (Isaacs' syndrome) in infancy: a report of two casesN H Thomas, J Z Heckmatt, E Rodillo, et al.Neuromuscular Disorders : NMD|July 1, 1994
Some unanswered questions in Duchenne muscular dystrophyA E EmeryNeuromuscular Disorders : NMD|July 1, 1994
A possible missense mutation detected in the dystrophin gene by Double-Strand Conformation Analysis (DSCA)F A Saad, G Vita, L Toffolatti, et al.Neuromuscular Disorders : NMD|July 1, 1994
Prevalent cardiac involvement in dystrophin Becker type mutationG Siciliano, M Fanin, C Angelini, et al.Neuromuscular Disorders : NMD|July 1, 1994
Dystrophinopathy presenting as congenital muscular dystrophyT Kyriakides, G Gabriel, A Drousiotou, et al.Neuromuscular Disorders : NMD|September 1, 1994
Carrier detection in DMD families with point mutations, using PCR-SSCP and direct sequencingU Lenk, R Hanke, A SpeerPageof 340