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Muscle & Nerve|March 1, 1978
Biochemical and physiologic consequences of carnitine palmityltransferase deficiencyJ E Carroll, M H Brooke, D C DeVivo, et al.Metabolism: Clinical and Experimental|June 1, 1979
Fasting as a provocative test in neuromuscular diseasesJ E Carroll, D C DeVivo, M H Brooke, et al.The American Journal of Physiology|January 1, 1980
Contractile, biochemical, and histochemical properties of thyrotoxic rat soleus muscleR H Fitts, W W Winder, M H Brooke, et al.Neurology|June 1, 1987
McArdle's disease with myoadenylate deaminase deficiency: observations in a combined enzyme deficiencyS L Heller, K K Kaiser, G J Planer, et al.The Journal of Pediatrics|August 1, 1976
Inflammatory myopathy, IgA deficiency, and intestinal malabsorptionJ E Carroll, A Silverman, Y Isobe, et al.Journal of Applied Physiology: Respiratory, Environmental and Exercise Physiology|April 1, 1982
Exercise hyperventilation in patients with McArdle's diseaseJ M Hagberg, E F Coyle, J E Carroll, et al.Archives of Neurology|April 1, 1991
Prednisone in Duchenne dystrophy. A randomized, controlled trial defining the time course and dose response. Clinical Investigation of Duchenne Dystrophy GroupR C Griggs, R T Moxley, J R Mendell, et al.Muscle & Nerve|February 1, 1983
Clinical investigation in Duchenne dystrophy: 2. Determination of the "power" of therapeutic trials based on the natural historyM H Brooke, G M Fenichel, R C Griggs, et al.Neurology|June 1, 1980
Carnitine "deficiency": lack of response to carnitine therapyJ E Carroll, M H Brooke, D C DeVivo, et al.Pageof 7