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Neuromuscular Disorders : NMD|November 2, 1999
Genetic heterogeneity of congenital muscular dystrophy with rigid spine syndromeB Moghadaszadeh, H Topaloglu, L Merlini, et al.Neuromuscular Disorders : NMD|April 30, 1999
Autosomal dominant distal myopathy not linked to the known distal myopathy lociK J Felice, C Meredith, N Binz, et al.Neuromuscular Disorders : NMD|March 27, 1999
Cardiac transplantation in a Duchenne muscular dystrophy carrierP Melacini, M Fanin, A Angelini, et al.Neuromuscular Disorders : NMD|January 1, 1994
Experimental regeneration in canine muscular dystrophy--2. Expression of myosin heavy chain isoformsL A Wilson, L Dux, B J Cooper, et al.Neuromuscular Disorders : NMD|May 1, 1995
Motor activity patterns in rat soleus muscle after neonatal partial denervationU Slawińska, R Navarrete, S Kasicki, et al.Neuromuscular Disorders : NMD|May 1, 1995
Familial concordance of brain magnetic resonance imaging changes in congenital muscular dystrophyJ Philpot, H Topaloglu, J Pennock, et al.Neuromuscular Disorders : NMD|May 1, 1993
Ventricular arrhythmia in Duchenne muscular dystrophy: prevalence, significance and prognosisA A Chenard, H M Becane, F Tertrain, et al.Neuromuscular Disorders : NMD|March 1, 1995
Sarcolemmal indentation in cardiomyopathy with mental retardation and vacuolar myopathyN Murakami, Y Goto, M Itoh, et al.Neuromuscular Disorders : NMD|September 1, 1995
Possible strategies for treatment of SMA patients: a neurobiologist's viewL Greensmith, G VrbováNeuromuscular Disorders : NMD|September 1, 1995
A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding geneG Manfredi, E A Schon, C T Moraes, et al.Pageof 340