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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.The Journal of the Acoustical Society of America|January 15, 2008
Spatial field shifts in ocean acoustic environmental sensitivity analysisStan E Dosso, Michael G Morley, Peter M Giles, et al.Neurology|February 1, 1986
Controlled trial of thyrotropin releasing hormone in amyotrophic lateral sclerosisM H Brooke, J M Florence, S L Heller, et al.Neurology|January 1, 1987
Use of serum creatine kinase, pyruvate kinase, and genetic linkage for carrier detection in Duchenne and Becker dystrophyC L Hyser, R C Griggs, J R Mendell, et al.Neurology|September 1, 1987
Carrier assessment for mothers and sisters of isolated Duchenne dystrophy cases: the importance of serum enzyme determinationsC L Hyser, R A Doherty, R C Griggs, et al.Pageof 7