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
Diagnosis and Discussion -- Case 944
Medium‐chain Acyl‐COA dehydrogenase deficiency: Pathogenesis, diagnosis, and treatment - Mason - 2023 - Endocrinology, Diabetes & Metabolism - Wiley Online Library
Management and diagnosis of mitochondrial fatty acid oxidation disorders: focus on very-long-chain acyl-CoA dehydrogenase deficiency | Journal of Human Genetics
Very Long Chain Acyl-CoA Dehydrogenase Deficiency (VLCADD) — New England Consortium of Metabolic Programs
Medium-chain acyl-CoA dehydrogenase - Wikipedia
The fate of medium-chain fatty acids in very long-chain acyl‑CoA dehydrogenase deficiency (VLCADD): A matter of sex? - ScienceDirect
Internet Scientific Publications
Personalised modelling of clinical heterogeneity between medium-chain acyl-CoA dehydrogenase patients | BMC Biology | Full Text
Sudden death in medium chain acyl-coenzyme a dehydrogenase deficiency (MCADD) despite newborn screening - ScienceDirect
Acyl-CoA dehydrogenase - Wikipedia
Oxidized phosphatidylcholines suggest oxidative stress in patients with medium-chain acyl-CoA dehydrogenase deficiency - ScienceDirect
Metabolites | Free Full-Text | Metabolic Outcomes of Anaplerotic Dodecanedioic Acid Supplementation in Very Long Chain Acyl-CoA Dehydrogenase (VLCAD) Deficient Fibroblasts
Child Neurology: Medium-chain acyl-coenzyme A dehydrogenase deficiency | Neurology
A Rare Case of Short-Chain Acyl-COA Dehydrogenase Deficiency: The Apparent Rarity of the Disorder Results in Under Diagnosis | Indian Journal of Clinical Biochemistry
Acyl-CoA dehydrogenase - Wikipedia
MCADD (medium chain acyl-CoA dehydrogenase deficiency) – newbornscreening.info
![PDF] Screening for medium-chain acyl CoA dehydrogenase deficiency: current perspectives | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/491bd7920e46f2b3f6648e1c1720e1c608c72149/2-Figure1-1.png "PDF] Screening for medium-chain acyl CoA dehydrogenase deficiency: current perspectives | Semantic Scholar")
PDF] Screening for medium-chain acyl CoA dehydrogenase deficiency: current perspectives | Semantic Scholar
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MCAD: Symptoms, Causes, Diagnosis, and Treatment
![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](https://d3i71xaburhd42.cloudfront.net/a96e4200059e68561417f0bc22d68c2459fcc7ec/3-Figure1-1.png "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")
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
Medium-chain acyl-Coenzyme A dehydrogenase deficiency (MCADD): a cause of severe hypoglycaemia in an apparently well child | BMJ Case Reports
Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency - ppt download
Medium-chain acyl-CoA dehydrogenase deficiency | MedLink Neurology
Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCADD) — New England Consortium of Metabolic Programs
Fatty Oxidation Disorders
Medium Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency - The Medical Biochemistry Page
Multiple acyl-CoA dehydrogenase deficiency: a rare cause of acidosis with an increased anion gap - British Journal of Anaesthesia
