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Neuromuscular Disorders : NMD|April 30, 1999
A novel mutation (8342G-->A) in the mitochondrial tRNA(Lys) gene associated with progressive external ophthalmoplegia and myoclonusV Tiranti, F Carrara, P Confalonieri, et al.
Neuromuscular Disorders : NMD|April 30, 1999
Is there a future for gene therapy?J M Howell
Neuromuscular Disorders : NMD|April 30, 1999
Emerin and cardiomyopathy in Emery-Dreifuss muscular dystrophyM Funakoshi, Y Tsuchiya, K Arahata
Neuromuscular Disorders : NMD|July 17, 1999
Myopathy in very-long-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical differences with the fatal cardiac phenotypeH R Scholte, R N Van Coster, P C de Jonge, et al.
Neuromuscular Disorders : NMD|July 17, 1999
Prenatal diagnosis in a family affected with beta-sarcoglycan muscular dystrophyE Pegoraro, M Fanin, C Angelini, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Gene for hereditary motor and sensory neuropathy (proximal dominant form) mapped to 3q13.1H Takashima, M Nakagawa, M Suehara, et al.
Neuromuscular Disorders : NMD|November 2, 1999
No evidence of association between apolipoprotein E genotype and phenotypic severity in childhood onset proximal spinal muscular atrophyK E Morrison, G Steers, V Dubowitz
Neuromuscular Disorders : NMD|November 2, 1999
Fukuyama-type congenital muscular dystrophy: close relation between changes in the muscle basal lamina and plasma membraneS Matsubara, Y Mizuno, T Kitaguchi, et al.
Neuromuscular Disorders : NMD|July 10, 1999
Myopathy with trabecular muscle fibersB Weller, S Carpenter, H Lochmüller, et al.
Neuromuscular Disorders : NMD|July 10, 1999
Dysfunction of sensory nerves during attacks of hypokalemic periodic paralysisJ S Inshasi, V P Jose, C A van der Merwe, et al.
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