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Clinica Chimica Acta; International Journal of Clinical Chemistry|April 9, 1981
Assay of adenylate cyclase in homogenates of control and Duchenne human skeletal muscleC Cerri, J H Willner, L P RowlandMuscle & Nerve. Supplement|January 1, 1995
The molecular genetic basis of myophosphorylase deficiency (McArdle's disease)S Tsujino, S Shanske, I Nonaka, et al.Archives of Neurology|December 1, 1979
Adult polysaccharidosis. Clinicopathological, ultrastructural, and biochemical featuresN S Peress, S DiMauro, V A RoxburghMuscle & Nerve|December 1, 1988
Metabolic myopathy in canine muscle-type phosphofructokinase deficiencyU Giger, Z Argov, M Schnall, et al.Neurology|February 1, 1987
Bioenergetic heterogeneity of human mitochondrial myopathies: phosphorus magnetic resonance spectroscopy studyZ Argov, W J Bank, J Maris, et al.Medicine and Science in Sports and Exercise|May 1, 1992
The use of nuclear magnetic resonance to evaluate muscle injuryK McCully, F G Shellock, W J Bank, et al.Annals of Neurology|November 1, 1978
Tissue carnitine in Reye syndromeJ H Willner, A M Chutorian, S DiMauroNature Reviews. Genetics|May 2, 2001
The genetics and pathology of oxidative phosphorylationJ Smeitink, L van den Heuvel, S DiMauroAnnals of Neurology|February 1, 1990
Metabolic causes of myoglobinuriaP Tonin, P Lewis, S Servidei, et al.Pageof 44