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Mayo Clinic Proceedings|August 1, 1983
Carnitine metabolism and deficiency syndromesC J Rebouche, A G EngelNeurology|March 17, 2000
AlphaB-crystallin immunolocalization yields new insights into inclusion body myositisB L Banwell, A G EngelJournal of Neurology, Neurosurgery, and Psychiatry|December 1, 1970
Acid maltase levels in muscle in heterozygous acid maltase deficiency and in non-weak and neuromuscular disease controlsA G Engel, M R GomezNeurology|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 EngelPageof 22