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Neuromuscular Disorders : NMD|October 12, 2001
Selective changes in mitochondria respiratory properties in oxidative or glycolytic muscle fibers isolated from G93AhumanSOD1 transgenic miceN Leclerc, F Ribera, J Zoll, et al.
Neuromuscular Disorders : NMD|May 23, 2001
X-linked myopathy with excessive autophagy: a clinicopathological study of five new familiesB Chabrol, D Figarella-Branger, M Coquet, et al.
Neuromuscular Disorders : NMD|May 23, 2001
Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuriaR Cagliani, G P Comi, L Tancredi, et al.
Neuromuscular Disorders : NMD|May 23, 2001
A case of amyotrophic lateral sclerosis with a very slow progression over 44 yearsK Grohme, M V Maravic, T Gasser, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB lociB Talim, A Ferreiro, B Cormand, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Evaluation of heart involvement in gamma-sarcoglycanopathy (LGMD2C). A study of ten patientsF Calvo, S Teijeira, J M Fernandez, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Hereditary motor and sensory neuropathy-Lom (HMSNL) in a Spanish family: clinical, electrophysiological, pathological and genetic studiesJ Colomer, C Iturriaga, L Kalaydjieva, et al.
Neuromuscular Disorders : NMD|June 6, 2000
A homozygous nonsense mutation in delta-sarcoglycan exon 3 in a case of LGMD2FP Dinçer, C G Bönnemann, O Erdir Aker, et al.
Neuromuscular Disorders : NMD|June 19, 2001
A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagiaM Spagnolo, G Tomelleri, G Vattemi, et al.
Neuromuscular Disorders : NMD|June 19, 2001
Neonatal arthrogryposis and absent limb muscles: a muscle developmental gene defect?J Philpot, S Counsell, G Bydder, et al.
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