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In a double-blind, placebo-controlled, multi-center clinical study in Italy, 2,330 patients with an acute front wall infarction received either an L-carnitine preparation (9 g/day intravenously for 5 days, 4 g/day orally for 6 months) or a placebo
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To achieve this goal, we randomly selected 2-3 samples from each group infected by a distinct pathogen and de-identified the species
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