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MCAD: Symptoms, Causes, Diagnosis, and Treatment
MCAD: Symptoms, Causes, Diagnosis, and Treatment

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

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

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

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

Diagnosis and Discussion -- Case 944
Diagnosis and Discussion -- Case 944

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

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

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

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

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

Fatty Oxidation Disorders
Fatty Oxidation Disorders

Management and diagnosis of mitochondrial fatty acid oxidation disorders: focus on very-long-chain acyl-CoA dehydrogenase deficiency | Journal of Human Genetics
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
Very Long Chain Acyl-CoA Dehydrogenase Deficiency (VLCADD) — New England Consortium of Metabolic Programs

1.3.8.7: medium-chain acyl-CoA dehydrogenase - BRENDA Enzyme Database
1.3.8.7: medium-chain acyl-CoA dehydrogenase - BRENDA Enzyme Database

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

Medium-Chain Acyl-CoA Dehydrogenase Deficiency
Medium-Chain Acyl-CoA Dehydrogenase Deficiency

Outcome of neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency in Australia: a cohort study - The Lancet
Outcome of neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency in Australia: a cohort study - The Lancet

Diagram of the mitochondrial metabolic LC-FAOD and C7 pathways.... | Download Scientific Diagram
Diagram of the mitochondrial metabolic LC-FAOD and C7 pathways.... | Download Scientific Diagram

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 (MCAD) Deficiency - The Medical Biochemistry Page
Medium Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency - The Medical Biochemistry Page

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

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

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
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