Fatty Oxidation Disorders
:max_bytes(150000):strip_icc()/mcad-overview-4175022_color1-5c454bfd46e0fb0001a4442d.png "MCAD: Symptoms, Causes, Diagnosis, and Treatment")
MCAD: Symptoms, Causes, Diagnosis, and Treatment
Medium Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency - The Medical Biochemistry Page
The fate of medium-chain fatty acids in very long-chain acyl‑CoA dehydrogenase deficiency (VLCADD): A matter of sex? - ScienceDirect
Acyl-CoA dehydrogenase - Wikipedia
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
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
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
Simplified pathway of medium chain acyl-CoA dehydrogenase (MCAD)... | Download Scientific Diagram
Acyl-CoA dehydrogenase - Wikipedia
Personalised modelling of clinical heterogeneity between medium-chain acyl-CoA dehydrogenase patients | BMC Biology | Full Text
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](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
Medium‐chain Acyl‐COA dehydrogenase deficiency: Pathogenesis, diagnosis, and treatment - Mason - 2023 - Endocrinology, Diabetes & Metabolism - Wiley Online Library
Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency (MCADD): Background, Pathophysiology, Epidemiology
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
Medium‐chain Acyl‐COA dehydrogenase deficiency: Pathogenesis, diagnosis, and treatment - Mason - 2023 - Endocrinology, Diabetes & Metabolism - Wiley Online Library
Clinical, Biochemical, and Molecular Analyses of Medium-Chain Acyl-CoA Dehydrogenase Deficiency in Chinese Patients - Frontiers
Very Long Chain Acyl-CoA Dehydrogenase Deficiency (VLCADD) — New England Consortium of Metabolic Programs
Medium-chain acyl-CoA dehydrogenase - Wikipedia
Management and diagnosis of mitochondrial fatty acid oxidation disorders: focus on very-long-chain acyl-CoA dehydrogenase deficiency | Journal of Human Genetics
Medium-chain acyl-CoA dehydrogenase deficiency – a review - ScienceDirect
Internet Scientific Publications
Multiple acyl-CoA dehydrogenase deficiency: a rare cause of acidosis with an increased anion gap - British Journal of Anaesthesia
