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Blood Acylcarnitine Levels in Normal Newborns and Heterozygotes for Medium-Chain Acyl-CoA Dehydrogenase Deficiency: A Relationship between Genotype and Biochemical Phenotype? Journal of Inherited Metabolic Disease , vol

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AEF0117 (15 g kg 1 ) significantly reduced intravenous (i.v.) self-administration of the CB 1 agonist WIN55,212-2 in CD-1 Swiss male mice (Fig

For a discrete injury like rotator cuff tendinitis, this targeted approach makes pharmacological sense

coli by the conversion of As to methylated forms (Qin et al., 2006)