Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCADD) — New England Consortium of Metabolic Programs
Very long-chain acyl-CoA dehydrogenase deficiency presenting as acute hypercapnic respiratory failure | European Respiratory Society
Multiple acyl-CoA dehydrogenase deficiency: a rare cause of acidosis with an increased anion gap - British Journal of Anaesthesia
SCADD (short chain acyl-CoA dehydrogenase deficiency) – newbornscreening.info
Short chain acyl CoA dehydrogenase deficiency bioquímica biochemistry deficiencia acil CoA deshidrog - YouTube
Very Long Chain Acyl-CoA Dehydrogenase Deficiency (VLCADD) — New England Consortium of Metabolic Programs
PDF] Screening for medium-chain acyl CoA dehydrogenase deficiency: current perspectives | Semantic Scholar
Sudden death in medium chain acyl-coenzyme a dehydrogenase deficiency (MCADD) despite newborn screening. | Semantic Scholar
Simplified pathway of medium chain acyl-CoA dehydrogenase (MCAD)... | Download Scientific Diagram
Long Chain Acyl Coenzyme A Dehydrogenase - an overview | ScienceDirect Topics
Medium-chain acyl-CoA dehydrogenase deficiency - ScienceDirect
Evidence in Colombia of 625G>A polymorphism in the short chain acyl-CoA dehydrogenase gene, a variation which could cause glutaric aciduria in our populations
Very Long Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency - The Medical Biochemistry Page
Fatty Oxidation Disorders
Medium-chain acyl-CoA dehydrogenase deficiency | MedLink Neurology
PDF] Exercise testing in patients with short- chain acyl-CoA dehydrogenase deficiency: biochemical responses and effects of riboflavin therapy | Semantic Scholar
Diagnosis and Discussion -- Case 944
Acyl-CoA dehydrogenase - Wikipedia
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
Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency - ppt download
Biochemical pathways for short-and long-chain fatty acyl-CoA... | Download Scientific Diagram
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
Child Neurology: medium-chain acyl-coenzyme A dehydrogenase deficiency. - Abstract - Europe PMC
Short-chain acyl-CoA dehydrogenase deficiency: from gene to cell pathology and possible disease mechanisms | SpringerLink
The fate of medium-chain fatty acids in very long-chain acyl‑CoA dehydrogenase deficiency (VLCADD): A matter of sex? - ScienceDirect
Outcome of neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency in Australia: a cohort study - The Lancet
First very long-chain acyl-CoA dehydrogenase deficiency (VLCADD) patient detected through newborn screening in Croatia
Multiple acyl-CoA dehydrogenase deficiency kills Mycobacterium tuberculosis in vitro and during infection | Nature Communications
Medium Chain ACYL-CoA Dehydrogenase Deficiency: MCAD
JCI - Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of β-oxidation in insulin secretion
Mitochondrial dysfunction due to long-chain Acyl-CoA dehydrogenase deficiency causes hepatic steatosis and hepatic insulin resistance | PNAS
Internet Scientific Publications
Management and diagnosis of mitochondrial fatty acid oxidation disorders: focus on very-long-chain acyl-CoA dehydrogenase deficiency | Journal of Human Genetics
Long Chain Hydroxy Acyl-CoA Dehydrogenase Deficiency ( LCHADD) — New England Consortium of Metabolic Programs
Medium-chain acyl-Coenzyme A dehydrogenase deficiency (MCADD): a cause of severe hypoglycaemia in an apparently well child | BMJ Case Reports
Very-long-chain acyl-CoA dehydrogenase - Wikipedia
MCADD - "Medium Chain Acyl-Coa Dehydrogenase Deficiency" by AcronymsAndSlang.com
Disruption of putative short-chain acyl-CoA dehydrogenases compromised free radical scavenging, conidiogenesis, and pathogenesis of Magnaporthe oryzae - ScienceDirect
Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase (LCHAD) Deficiency: Background, Pathophysiology, Epidemiology
Clinical manifestation and classification of very long-chain acyl-CoA... | Download Table
A Rare Case of Short-Chain Acyl-COA Dehydrogenase Deficiency: The Apparent Rarity of the Disorder Results in Under Diagnosis. - Abstract - Europe PMC
Medium Chain Acyl CoA Dehydrogenase (MCAD) Deficiency - YouTube
Short chain acyl-CoA dehydrogenase deficiency and short-term high-fat diet perturb mitochondrial energy metabolism and transcriptional control of lipid-handling in liver | Nutrition & Metabolism | Full Text
MCAD - "Medium chain acyl-CoA dehydrogenase deficiency" by AcronymsAndSlang.com
PDF] Characterization of mitochondrial dynamics in multiple acyl-CoA dehydrogenase deficiency | Semantic Scholar
2MBC (2-methylbutyryl-CoA dehydrogenase deficiency) – newbornscreening.info
Fulminant lipid storage myopathy due to multiple acyl‐coenzyme a dehydrogenase deficiency - Whitaker - 2015 - Muscle & Nerve - Wiley Online Library
Short-Chain Acyl-CoA Dehydrogenase - an overview | ScienceDirect Topics
Multiple acyl-CoA dehydrogenase deficiency kills Mycobacterium tuberculosis in vitro and during infection | Nature Communications
Clinical manifestation and classification of very long-chain acyl-CoA... | Download Table
JCM | Free Full-Text | Biochemical Markers for the Diagnosis of Mitochondrial Fatty Acid Oxidation Diseases
Fatty Acid Oxidation Disorders
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
Frontiers | Hepatic Presentation of Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency (MADD): Case Report and Systematic Review
Beta oxidation - Wikipedia
Surviving Inborn Errors of Metabolism with Diet: Multiple Acyl CoA Dehydrogenase Deficiency - Hormones Matter
Multiple acyl-CoA dehydrogenase deficiency kills Mycobacterium tuberculosis in vitro and during infection | bioRxiv
MCAD deficiency
Medium‐chain Acyl‐COA dehydrogenase deficiency: Pathogenesis, diagnosis, and treatment - Mason - Endocrinology, Diabetes & Metabolism - Wiley Online Library
1.3.8.8: long-chain acyl-CoA dehydrogenase - BRENDA Enzyme Database
Vulnerability to Oxidative Stress In Vitro in Pathophysiology of Mitochondrial Short-Chain Acyl-CoA Dehydrogenase Deficiency: Response to Antioxidants | PLOS ONE
D,L-3-hydroxybutyrate treatment of multiple acyl-CoA dehydrogenase deficiency (MADD) - The Lancet
MCAD Deficiency DNA – genebase
Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency Disorder
Development of a newborn screening follow-up algorithm for the diagnosis of isobutyryl-CoA dehydrogenase deficiency | Genetics in Medicine
Beta-oxidation of Fatty Acid
Pregnancy & Newborn Screening Developments Medium Chain Acyl CoA Dehydrogenase Deficiency (MCADD) - ppt download
MADD - "Multiple Acyl-Coa Dehydrogenase Deficiency" by AcronymsAndSlang.com
MCADD - medium-chain acyl-CoA dehydrogenase deficiency
Frontiers | New Ratios for Performance Improvement for Identifying Acyl-CoA Dehydrogenase Deficiencies in Expanded Newborn Screening: A Retrospective Study
Causes and Treatments of Seizures
Simplified pathway of medium chain acyl-CoA dehydrogenase (MCAD)... | Download Scientific Diagram
Medium-Chain Acyl-CoA Deficiency: Outlines from Newborn Screening, In Silico Predictions, and Molecular Studies
Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency (MCADD): Background, Pathophysiology, Epidemiology
Oxidized phosphatidylcholines suggest oxidative stress in patients with medium-chain acyl-CoA dehydrogenase deficiency - ScienceDirect
Multiple Acyl CoA dehydrogenase deficiency: Uncommon yet treatable disorder
Acyl-CoA dehydrogenase - Wikipedia
Medium-chain acyl-CoA dehydrogenase deficiency: prevalence of ACADM pathogenic variants c.985A>G and c.199T>C in a healthy population in Rio Grande do Sul, Brazil | Reproductive and Developmental Medicine
Medium‐chain Acyl‐COA dehydrogenase deficiency: Pathogenesis, diagnosis, and treatment - Mason - Endocrinology, Diabetes & Metabolism - Wiley Online Library
Medium-chain Acyl-CoA dehydrogenase deficiency: a characterization of the most common variant and current and future therapeutics
Genetic pathogenesis, diagnosis, and treatment of short-chain 3-hydroxyacyl- coenzyme A dehydrogenase hyperinsulinism | Orphanet Journal of Rare Diseases | Full Text
PPT – Acyl CoA Dehydrogenase Deficiency PowerPoint presentation | free to view - id: c464b-ZDc1Z
Molecular Heterogeneity in Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency Causing Pediatric Cardiomyopathy and Sudden Death | Circulation
▷ Is it advisable to do exercise when affected by Very Long Chain Acyl CoA Dehydrogenase Deficiency (LCAD)? Which activities would you suggest and how intense should they be?
JCM | Free Full-Text | Biochemical Markers for the Diagnosis of Mitochondrial Fatty Acid Oxidation Diseases
2-Methylbutyryl-Coenzyme A Dehydrogenase Deficiency: A New Inborn Error of L-Isoleucine Metabolism | Pediatric Research
Beta-oxidation of Fatty Acid
Acute fatty liver of pregnancy: An update on pathogenesis and clinical implications
Newborn screening for medium-chain acyl-CoA dehydrogenase deficiency: regional experience and high incidence of carnitine deficiency – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on
PDF] 2-ethylhydracrylic aciduria in short/branched-chain acyl-CoA dehydrogenase deficiency: application to diagnosis and implications for the R-pathway of isoleucine oxidation. | Semantic Scholar
Multiple Acyl-Coenzyme A dehydrogenase deficiency
Biochemical Correction of Very Long–chain Acyl-CoA Dehydrogenase Deficiency Following Adeno-associated Virus Gene Therapy: Molecular Therapy
1.3.8.7: medium-chain acyl-CoA dehydrogenase - BRENDA Enzyme Database
Medium-chain Acyl-CoA Dehydrogenase Deficiency by Sarah Louise Long
Retinal dystrophy in long chain 3-hydroxy-acyl-coA dehydrogenase deficiency | British Journal of Ophthalmology
Nature Communications on Twitter: "Multiple acyl-CoA dehydrogenase deficiency kills Mycobacterium tuberculosis in vitro and during infection @tiagobeites @saehrt @EhrtSchnapLab @WeillCornell https://t.co/Sy0WyDhLcy https://t.co/ru1a5VQVVV" / Twitter
The natural history of medium-chain acyl CoA dehydrogenase deficiency in the Netherlands: Clinical presentation and outcome - The Journal of Pediatrics
Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials