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Acyl-CoA
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41	Treatment and Emergency Protocol Example For Medium-Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) For Teens and Adults Diagnosis: Medium-Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Clinical Presentation: Vomiting, le Add to Reading List Source URL: fodsupport.org Language: English - Date: 2012-05-31 13:41:17 Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine Medical emergencies Fatty-acid metabolism disorder Systemic primary carnitine deficiency Hypoglycemia Medicine Health Chemistry
42	Microsoft Word - 2MBCD_update_2013 Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2013-11-28 02:11:01 Epidemiology Newborn screening Pediatrics 2-Methylbutyryl-CoA dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Health Genetic genealogy Medical genetics
43	Very Long Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency (metabolic condition: fatty acid oxidation disorder) Also known as: • acyl-CoA dehydrogenase very long chain deficiency • very long-chain acyl coenzyme A de Add to Reading List Source URL: www.albertahealthservices.ca Language: English - Date: 2013-09-16 18:37:04 Fatty acids Fatty-acid metabolism disorder Rare diseases Fatty acid metabolism Carnitine Acyl CoA dehydrogenase Medical genetics Inborn error of lipid metabolism Medium-chain acyl-coenzyme A dehydrogenase deficiency Medicine Health Very long-chain acyl-coenzyme A dehydrogenase deficiency
44	Ginger Armbrust School of Oceanography University of Washington Sequencing Algal Genomes Add to Reading List Source URL: www.nrel.gov Language: English - Date: 2008-04-22 11:42:02 Biochemistry Coenzymes Thioesters Fatty acids Cellular respiration Coenzyme A Malonyl-CoA Acetyl-CoA Acyl-CoA Chemistry Biology Metabolism
45	Nutrition and Mitochondrial Fatty Acid Oxidation Defects Phyllis B. Acosta, DrPH, RD INTRODUCTION Three forms of energy (fuel) are used by the body: glucose, fatty acids and ketone bodies. Glucose, after eating and until Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:17 Medicine Fatty acids Hepatology Fatty acid metabolism Carnitine Lipid Glycogen Triglyceride Acyl-CoA Biology Chemistry Metabolism
46	Microsoft Word - MCADD_update_2013 Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2013-12-01 02:44:28 Rare diseases Metabolism Fatty acids Medium-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Newborn screening Carnitine ACADM Acyl CoA dehydrogenase Health Biology Medicine
47	Microsoft Word - VLCAD_update_ 2013 Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2013-12-01 02:58:04 Rare diseases Metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Fatty acids Fatty-acid metabolism disorder Carnitine Fatty acid metabolism Newborn screening Acyl CoA dehydrogenase Health Medicine Biology
48	NEWBORN SCREENING FACT SHEET SCADD (Short Chain Acyl-CoA Dehydrogenese Deficiency) What is it? SCADD stands for short chain acyl-CoA dehydrogenase deficiency. It is one type of Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-20 12:54:56 Rare diseases Epidemiology Newborn screening Pediatrics Fatty-acid metabolism disorder Inborn errors of carbohydrate metabolism Screening Biotinidase deficiency Phenylketonuria Health Medicine Genetic genealogy
49	NEWBORN SCREENING FACT SHEET MCADD (Medium Chain Acyl-CoA Dehydrogenese Deficiency) What is it? MCADD stands for medium chain acyl-CoA dehydrogenase deficiency. It is one type of Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:32:00 Hypoglycemia Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Inborn errors of carbohydrate metabolism Newborn screening Glycogen storage disease type I Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases
50	` NEWBORN SCREENING FACT SHEET VLCADD (Very Long Chain Acyl-CoA Dehydrogenese Deficiency) It is common for babies and children with the Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:32:01 Very long-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Hepatology Hypoglycemia Carnitine Newborn screening Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Glycogen storage disease type I Health Medicine Rare diseases