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Sudden death in medium chain acyl-coenzyme a dehydrogenase deficiency (MCADD) despite newborn screening. | Semantic Scholar
Short-Chain Acyl-CoA Dehydrogenase - an overview | ScienceDirect Topics
Medium-chain acyl-CoA dehydrogenase deficiency – a review - ScienceDirect
Multiple acyl-CoA dehydrogenase deficiency: a rare cause of acidosis with an increased anion gap - British Journal of Anaesthesia
Disruption of putative short-chain acyl-CoA dehydrogenases compromised free radical scavenging, conidiogenesis, and pathogenesis of Magnaporthe oryzae - ScienceDirect
Child Neurology: medium-chain acyl-coenzyme A dehydrogenase deficiency. - Abstract - Europe PMC
Vulnerability to Oxidative Stress In Vitro in Pathophysiology of Mitochondrial Short-Chain Acyl-CoA Dehydrogenase Deficiency: Response to Antioxidants | PLOS ONE
Very long-chain acyl-CoA dehydrogenase deficiency presenting as acute hypercapnic respiratory failure | European Respiratory Society
1.3.8.1: short-chain acyl-CoA dehydrogenase - BRENDA Enzyme Database
Structural Mechanism of Regioselectivity in an Unusual Bacterial Acyl-CoA Dehydrogenase | Journal of the American Chemical Society
Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCADD) — New England Consortium of Metabolic Programs
Fatty Oxidation Disorders
Management and diagnosis of mitochondrial fatty acid oxidation disorders: focus on very-long-chain acyl-CoA dehydrogenase deficiency | Journal of Human Genetics
Evidence in Colombia of 625G>A polymorphism in the short chain acyl-CoA dehydrogenase gene, a variation which could cause glutaric aciduria in our populations
Mechanistic Bases of Neurotoxicity Provoked by Fatty Acids Accumulating in MCAD and LCHAD Deficiencies - Alexandre U. Amaral, Cristiane Cecatto, Janaína C. da Silva, Alessandro Wajner, Moacir Wajner, 2017
Metabolic pathway of the branched-chain amino acids, isoleucine and... | Download Scientific Diagram