Medium‐chain Acyl‐COA dehydrogenase deficiency: Pathogenesis, diagnosis, and treatment - Mason - 2023 - Endocrinology, Diabetes & Metabolism - Wiley Online Library
Acyl-CoA dehydrogenase - Wikipedia
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
Medium-chain acyl-CoA dehydrogenase deficiency – a review - ScienceDirect
IJMS | Free Full-Text | Mitochondrial Fatty Acid β-Oxidation Disorders: From Disease to Lipidomic Studies—A Critical Review
Diagnosis and Discussion -- Case 944
MCADD (medium chain acyl-CoA dehydrogenase deficiency) – newbornscreening.info
Medium-chain acyl-CoA dehydrogenase deficiency | MedLink Neurology
Simplified pathway of medium chain acyl-CoA dehydrogenase (MCAD)... | Download Scientific Diagram
Very Long Chain Acyl-CoA Dehydrogenase Deficiency (VLCADD) — New England Consortium of Metabolic Programs
Internet Scientific Publications
Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCADD) — New England Consortium of Metabolic Programs
Clinical, Biochemical, and Molecular Analyses of Medium-Chain Acyl-CoA Dehydrogenase Deficiency in Chinese Patients - Frontiers
Management and diagnosis of mitochondrial fatty acid oxidation disorders: focus on very-long-chain acyl-CoA dehydrogenase deficiency | Journal of Human Genetics
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
Frontiers | Physiological Perspectives on the Use of Triheptanoin as Anaplerotic Therapy for Long Chain Fatty Acid Oxidation Disorders
Acyl-CoA dehydrogenase - Wikipedia
Child Neurology: Medium-chain acyl-coenzyme A dehydrogenase deficiency | Neurology
Outcome of neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency in Australia: a cohort study - The Lancet
Medium Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency - The Medical Biochemistry Page
![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
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
