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Neuromuscular Disorders : NMD|July 17, 1999
Cardiac involvement in carriers of Duchenne and Becker muscular dystrophyE M Hoogerwaard, P A van der Wouw, A A Wilde, et al.Neuromuscular Disorders : NMD|March 21, 2001
A new dysferlin gene mutation in two Japanese families with limb-girdle muscular dystrophy 2B and Miyoshi myopathyH Ueyama, T Kumamoto, S Nagao, et al.Neuromuscular Disorders : NMD|March 21, 2001
Longitudinal data analysis: an application to construction of a natural history profile of Duchenne muscular dystrophyS A Hyde, B F Steffensen, I Fløytrup, et al.Neuromuscular Disorders : NMD|March 11, 2000
Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entityM A Salih, T Maisonobe, M Kabiraj, et al.Neuromuscular Disorders : NMD|March 11, 2000
Two distal mutations in the gene encoding emerin have profoundly different effects on emerin protein expressionJ A Ellis, C A Brown, L D Tilley, et al.Neuromuscular Disorders : NMD|March 11, 2000
Identification of homozygous and heterozygous dy2J mice by PCRJ T Vilquin, N Vignier, J P Tremblay, et al.Neuromuscular Disorders : NMD|March 14, 2000
Fibrillation potential amplitude to quantitatively assess denervation muscle atrophyG L Jiang, L Y Zhang, L Y Shen, et al.Neuromuscular Disorders : NMD|March 14, 2000
Immunolabelling of mitochondrial superoxide dismutase and of Hsp60 in muscles harbouring a respiratory chain deficiencyH Carrier, F Flocard, V Tagliati, et al.Neuromuscular Disorders : NMD|October 29, 2000
Hereditary motor and sensory neuropathy--Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countriesD Chandler, D Angelicheva, L Heather, et al.Neuromuscular Disorders : NMD|January 5, 2000
Cardiac involvement in Becker's muscular dystrophy, necessitating heart transplantation, 6 years before apparent skeletal muscle involvementJ Finsterer, R E Bittner, M GrimmPageof 341