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Frontiers | Recent Advances in the Pathophysiology of Fatty Acid Oxidation Defects: Secondary Alterations of Bioenergetics and Mitochondrial Calcium Homeostasis Caused by the Accumulating Fatty Acids
Frontiers | Recent Advances in the Pathophysiology of Fatty Acid Oxidation Defects: Secondary Alterations of Bioenergetics and Mitochondrial Calcium Homeostasis Caused by the Accumulating Fatty Acids

IJMS | Free Full-Text | Mitochondrial Fatty Acid β-Oxidation Disorders: From Disease to Lipidomic Studies—A Critical Review
IJMS | Free Full-Text | Mitochondrial Fatty Acid β-Oxidation Disorders: From Disease to Lipidomic Studies—A Critical Review

Very Long Chain Acyl-CoA Dehydrogenase Deficiency (VLCADD) — New England Consortium of Metabolic Programs
Very Long Chain Acyl-CoA Dehydrogenase Deficiency (VLCADD) — New England Consortium of Metabolic Programs

Multiple acyl-CoA dehydrogenase deficiency: a rare cause of acidosis with an increased anion gap - British Journal of Anaesthesia
Multiple acyl-CoA dehydrogenase deficiency: a rare cause of acidosis with an increased anion gap - British Journal of Anaesthesia

Fatty Oxidation Disorders
Fatty Oxidation Disorders

Clinical, Biochemical, and Molecular Analyses of Medium-Chain Acyl-CoA Dehydrogenase Deficiency in Chinese Patients - Frontiers
Clinical, Biochemical, and Molecular Analyses of Medium-Chain Acyl-CoA Dehydrogenase Deficiency in Chinese Patients - Frontiers

Very long-chain acyl-CoA dehydrogenase deficiency presenting as acute hypercapnic respiratory failure | European Respiratory Society
Very long-chain acyl-CoA dehydrogenase deficiency presenting as acute hypercapnic respiratory failure | European Respiratory Society

Simplified pathway of medium chain acyl-CoA dehydrogenase (MCAD)... | Download Scientific Diagram
Simplified pathway of medium chain acyl-CoA dehydrogenase (MCAD)... | Download Scientific Diagram

Medium‐chain Acyl‐COA dehydrogenase deficiency: Pathogenesis, diagnosis, and treatment - Mason - 2023 - Endocrinology, Diabetes & Metabolism - Wiley Online Library
Medium‐chain Acyl‐COA dehydrogenase deficiency: Pathogenesis, diagnosis, and treatment - Mason - 2023 - Endocrinology, Diabetes & Metabolism - Wiley Online Library

Sudden death in medium chain acyl-coenzyme a dehydrogenase deficiency (MCADD) despite newborn screening - ScienceDirect
Sudden death in medium chain acyl-coenzyme a dehydrogenase deficiency (MCADD) despite newborn screening - ScienceDirect

Oxidized phosphatidylcholines suggest oxidative stress in patients with medium-chain acyl-CoA dehydrogenase deficiency - ScienceDirect
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
Metabolites | Free Full-Text | Metabolic Outcomes of Anaplerotic Dodecanedioic Acid Supplementation in Very Long Chain Acyl-CoA Dehydrogenase (VLCAD) Deficient Fibroblasts

Medium-chain acyl-CoA dehydrogenase - Wikipedia
Medium-chain acyl-CoA dehydrogenase - Wikipedia

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 (MCADD): a cause of severe hypoglycaemia in an apparently well child | BMJ Case Reports

The fate of medium-chain fatty acids in very long-chain acyl‑CoA dehydrogenase deficiency (VLCADD): A matter of sex? - ScienceDirect
The fate of medium-chain fatty acids in very long-chain acyl‑CoA dehydrogenase deficiency (VLCADD): A matter of sex? - ScienceDirect

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

Child Neurology: Medium-chain acyl-coenzyme A dehydrogenase deficiency | Neurology
Child Neurology: Medium-chain acyl-coenzyme A dehydrogenase deficiency | Neurology

Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCADD) — New England Consortium of Metabolic Programs
Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCADD) — New England Consortium of Metabolic Programs

Fatty Acid Oxidation Disorders
Fatty Acid Oxidation Disorders

Acyl-CoA dehydrogenase - Wikipedia
Acyl-CoA dehydrogenase - Wikipedia

MCADD: by Natalie Tran on Prezi Next
MCADD: by Natalie Tran on Prezi Next

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-CoA dehydrogenase deficiency – a review - ScienceDirect
Medium-chain acyl-CoA dehydrogenase deficiency – a review - ScienceDirect

Internet Scientific Publications
Internet Scientific Publications

Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency (MCADD): Background, Pathophysiology, Epidemiology
Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency (MCADD): Background, Pathophysiology, Epidemiology