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Society of General Physiologists Series|January 1, 1995
In vivo sodium channel structure/function studies: consecutive Arg1448 changes to Cys, His, and Pro at the extracellular surface of IVS4J Wang, V Dubowitz, F Lehmann-Horn, et al.Neuromuscular Disorders : NMD|August 26, 1998
Fifty year follow-up of a patient with central core disease shows slow but definite progressionP J Lamont, V Dubowitz, D N Landon, et al.Journal of Medical Genetics|November 1, 1989
Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophyS Hodgson, K Hart, S Abbs, et al.Muscle & Nerve|November 1, 1980
Polymyositis--an immunofluorescence study on the distribution of collagen typesV C Duance, C M Black, V Dubowitz, et al.Journal of the Neurological Sciences|January 1, 1982
Collagen types in neuromuscular diseasesH R Stephens, V C Duance, M J Dunn, et al.Neuromuscular Disorders : NMD|April 30, 1999
Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imagingJ Philpot, F Cowan, J Pennock, et al.Journal of Medical Genetics|December 1, 1986
Linkage studies in Duchenne and Becker muscular dystrophiesA Walker, K Hart, C Cole, et al.Neuropediatrics|August 1, 1987
A syndrome with juvenile cataract, cerebellar atrophy, mental retardation and myopathyR Herva, L von Wendt, G von Wendt, et al.Archives of Disease in Childhood|September 1, 1986
Low serum thyroxine concentrations and neural maturation in preterm infantsL S De Vries, J Z Heckmatt, J M Burrin, et al.American Journal of Medical Genetics|March 1, 1986
A balanced de novo X/autosome translocation in a girl with manifestations of Lowe syndromeS V Hodgson, J Z Heckmatt, E Hughes, et al.Pageof 24