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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

MCADD (medium chain acyl-CoA dehydrogenase deficiency) – newbornscreening.info
MCADD (medium chain acyl-CoA dehydrogenase deficiency) – newbornscreening.info

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

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

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

Acyl-CoA dehydrogenase - Wikipedia
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

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
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

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

Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials

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

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

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

Personalised modelling of clinical heterogeneity between medium-chain acyl-CoA dehydrogenase patients | BMC Biology | Full Text
Personalised modelling of clinical heterogeneity between medium-chain acyl-CoA dehydrogenase patients | BMC Biology | Full Text

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-Coenzyme A Dehydrogenase Deficiency - ppt download
Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency - ppt download

NCC Knowledge Nugget Series- Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency ACT Sheet - YouTube
NCC Knowledge Nugget Series- Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency ACT Sheet - YouTube

Medium-chain acyl-CoA dehydrogenase deficiency | MedLink Neurology
Medium-chain acyl-CoA dehydrogenase deficiency | MedLink Neurology

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

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

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

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

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

Frontiers | Physiological Perspectives on the Use of Triheptanoin as Anaplerotic Therapy for Long Chain Fatty Acid Oxidation Disorders
Frontiers | Physiological Perspectives on the Use of Triheptanoin as Anaplerotic Therapy for Long Chain Fatty Acid Oxidation Disorders