Hydroxyacyl-Coenzyme A Dehydrogenase - an overview | ScienceDirect Topics
Child Neurology: medium-chain acyl-coenzyme A dehydrogenase deficiency. - Abstract - Europe PMC
SCADD (short chain acyl-CoA dehydrogenase deficiency) – newbornscreening.info
Engineered Production of Short-Chain Acyl-Coenzyme A Esters in Saccharomyces cerevisiae | ACS Synthetic Biology
Medium-chain acyl-CoA dehydrogenase deficiency | MedLink Neurology
SCAD - "Short-chain acyl-CoA dehydrogenase deficiency" by AcronymsAndSlang.com
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
Screening for medium-chain acyl CoA dehydrogenase deficiency: current | RRN
Management and diagnosis of mitochondrial fatty acid oxidation disorders: focus on very-long-chain acyl-CoA dehydrogenase deficiency | Journal of Human Genetics
Simplified pathway of medium chain acyl-CoA dehydrogenase (MCAD)... | Download Scientific Diagram
1.3.8.1: short-chain acyl-CoA dehydrogenase - BRENDA Enzyme Database
Medium-chain acyl-CoA dehydrogenase deficiency – a review - ScienceDirect
Metabolic pathway of the branched-chain amino acids, isoleucine and... | Download Scientific Diagram
A Rare Case of Short-Chain Acyl-COA Dehydrogenase Deficiency: The Apparent Rarity of the Disorder Results in Under Diagnosis. - Abstract - Europe PMC
![PDF] 2-ethylhydracrylic aciduria in short/branched-chain acyl-CoA dehydrogenase deficiency: application to diagnosis and implications for the R-pathway of isoleucine oxidation. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/a82cc0c2d7c1cca4098d93fcc66a49313bc2ec79/2-Figure1-1.png "PDF] 2-ethylhydracrylic aciduria in short/branched-chain acyl-CoA dehydrogenase deficiency: application to diagnosis and implications for the R-pathway of isoleucine oxidation. | Semantic Scholar")
PDF] 2-ethylhydracrylic aciduria in short/branched-chain acyl-CoA dehydrogenase deficiency: application to diagnosis and implications for the R-pathway of isoleucine oxidation. | Semantic Scholar
Fetal Fatty Acid Oxidation Disorders, Their Effect on Maternal Health and Neonatal Outcome: Impact of Expanded Newborn Screening on Their Diagnosis and Management | Pediatric Research
Very long-chain acyl-CoA dehydrogenase deficiency presenting as acute hypercapnic respiratory failure | European Respiratory Society
Fatty acid metabolism and acyl-CoA synthetases in the liver-gut axis
Structural Mechanism of Regioselectivity in an Unusual Bacterial Acyl-CoA Dehydrogenase | Journal of the American Chemical Society
Sudden death in medium chain acyl-coenzyme a dehydrogenase deficiency (MCADD) despite newborn screening. | Semantic Scholar
Short-chain acyl-CoA dehydrogenase deficiency: from gene to cell pathology and possible disease mechanisms | SpringerLink
Vulnerability to Oxidative Stress In Vitro in Pathophysiology of Mitochondrial Short-Chain Acyl-CoA Dehydrogenase Deficiency: Response to Antioxidants | PLOS ONE
