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Title: [Serum enzymatic activity in neuromuscular diseases]. Author: Strumień M. Journal: Neurol Neurochir Pol; 1975; 9(1):1-5. PubMed ID: 1121344. Abstract: In 200 patients with neuromuscular diseases the author studied malonic dehydrogenase and lactic dehydrogenase activity comparing it with the activity of serum creatine kinase and aldolase. A significant rise in the values of all these enzymes was found only in the Duchenne type of muscular dystrophy, in polymyositis, and less frequently in the limb-girdle type of muscular dystrophy. Raised activity of creatine kinase and sidolase was observed in mothers and sisters of patients with Duchenne type of dystrophy, in patients with non-progressive myopathy, periodic paralysis, amyotrophic lateral sclerosis and polyneuropathy. With progression of dystrophy the activity of these enzymes decreases.[Abstract] [Full Text] [Related] [New Search]