Medium Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency - The Medical Biochemistry Page
1.3.8.7: medium-chain acyl-CoA dehydrogenase - BRENDA Enzyme Database
Medium Chain Acyl-CoA Dehydrogenase Deficiency: Check your genetic data
Diagnosis and Discussion -- Case 944
PDF] Déficit en acyl-CoA-déshydrogénase des acides gras à chaı̂ne moyenne (MCAD) : consensus français pour le dépistage, le diagnostic, et la prise en charge Medium-chain acyl-CoA-dehydrogenase (MCAD) deficiency: French consensus for neonatal
MCAD: Symptoms, Causes, Diagnosis, and Treatment
Inborn Errors of Fatty Acid Oxidation (Chapter 34) - Liver Disease in Children
Very long-chain acyl-CoA dehydrogenase deficiency presenting as acute hypercapnic respiratory failure | European Respiratory Society
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
Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency - ppt download
Very Long Chain Acyl-CoA Dehydrogenase Deficiency (VLCADD) — New England Consortium of Metabolic Programs
Management and diagnosis of mitochondrial fatty acid oxidation disorders: focus on very-long-chain acyl-CoA dehydrogenase deficiency | Journal of Human Genetics
Oxidized phosphatidylcholines suggest oxidative stress in patients with medium-chain acyl-CoA dehydrogenase deficiency - ScienceDirect
PDF] Screening for medium-chain acyl CoA dehydrogenase deficiency: current perspectives | Semantic Scholar