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Neurology|May 1, 1978
Intracellular calcium accumulation in Duchenne dystrophy and other myopathies: a study of 567,000 muscle fibers in 114 biopsiesJ B Bodensteiner, A G EngelThe Journal of Biological Chemistry|September 25, 1980
Significance of renal gamma-butyrobetaine hydroxylase for carnitine biosynthesis in manC J Rebouche, A G EngelBrain Research|September 24, 1993
Ephedrine: effects on neuromuscular transmissionJ P Sieb, A G EngelNeurology|July 1, 1981
Primary systemic carnitine deficiency: I. Carnitine biosynthesisC J Rebouche, A G EngelAnnals of Neurology|April 18, 1998
Quinidine sulfate therapy for the slow-channel congenital myasthenic syndromeC M Harper, A G EngelIn Vitro|May 1, 1982
Carnitine transport in cultured muscle cells and skin fibroblasts from patients with primary systemic carnitine deficiencyC J Rebouche, A G EngelJournal of the Neurological Sciences|January 1, 1978
Experimental lipid storage myopathy. A quantitative ultrastructural and biochemical studyA K Brownell, A G EngelNeurology|September 1, 1987
Are hypercontracted muscle fibers artifacts and do they cause rupture of the plasma membrane?B P Lotz, A G EngelThe American Journal of Medicine|March 1, 1978
Acid maltase deficiency in adults presenting as respiratory failureE C Rosenow, A G EngelAnnals of Neurology|February 9, 2000
The spectrum of mutations causing end-plate acetylcholinesterase deficiencyK Ohno, A G Engel, J M Brengman, et al.Pageof 88