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The New England Journal of Medicine|May 26, 1988
Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophyE P Hoffman, K H Fischbeck, R H Brown, et al.Journal of Applied Physiology (Bethesda, Md. : 1985)|July 23, 2002
Regenerated mdx mouse skeletal muscle shows differential mRNA expressionB S Tseng, P Zhao, J S Pattison, et al.Science (New York, N.Y.)|November 16, 1990
Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit geneB Fontaine, T S Khurana, E P Hoffman, et al.The Journal of Experimental Medicine|August 1, 1996
Selective loss of sarcolemmal nitric oxide synthase in Becker muscular dystrophyD S Chao, J R Gorospe, J E Brenman, et al.American Journal of Human Genetics|April 1, 1990
Skewed X inactivation in a female MZ twin results in Duchenne muscular dystrophyC S Richards, S C Watkins, E P Hoffman, et al.The Journal of Biological Chemistry|March 4, 1994
Molecular cloning, structure, and chromosomal localization of the human inducible nitric oxide synthase geneN A Chartrain, D A Geller, P P Koty, et al.Neurology|June 4, 2008
Sensitivity and specificity of decreased CSF asialotransferrin for eIF2B-related disorderA Vanderver, Y Hathout, J Maletkovic, et al.Human Gene Therapy|March 1, 1997
Viral gene delivery to skeletal muscle: insights on maturation-dependent loss of fiber infectivity for adenovirus and herpes simplex type 1 viral vectorsW G Feero, J D Rosenblatt, J Huard, et al.Nature|July 14, 1988
The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogsB J Cooper, N J Winand, H Stedman, et al.The American Journal of Pathology|November 1, 1989
Feline muscular dystrophy with dystrophin deficiencyJ L Carpenter, E P Hoffman, F C Romanul, et al.Pageof 19