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Annals 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 EngelInternational Journal of Oncology|May 14, 2011
Increases of stromelysin messenger-RNA expression in ras-transformed ref cells in-vivoG Engel, P Popowicz, S LinderNeurology|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 EngelJournal of Palliative Medicine|October 20, 2023
Emergency Palliative Care: Acute Presentation of a Nonsurvivable ConditionKirsten G Engel, Tammie E QuestJournal of Neuropathology and Experimental Neurology|November 1, 1982
Ultrastructural aspects of acetylcholine receptor turnover at the normal end-plate and in autoimmune myasthenia gravisG Fumagalli, A G Engel, J LindstromNeurology|June 1, 1991
Necrotizing myopathy with pipestem capillaries, microvascular deposition of the complement membrane attack complex (MAC), and minimal cellular infiltrationA M Emslie-Smith, A G EngelBrain Research|September 23, 1985
beta-Adrenoceptor blocking agents recognize a subpopulation of serotonin receptors in brainA Pazos, G Engel, J M PalaciosPageof 1,551