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Acyl-CoA
Results: 139

#	Item
1	Fat Metabolism and the Athlete Can the Ingestion of Medium Chain Triglycerides Enhance Performance by Producing A Glycogen Sparing Effect in Endurance Athletes? Paul Wilsher 2003 Add to Reading List Source URL: firefitsteeringgroup.co.uk Language: English - Date: 2011-06-17 09:29:58 Biochemistry Fatty acid metabolism Fatty acid degradation Lipolysis Glycolysis Acyl-CoA Lipid Citric acid cycle Triglyceride Biology Metabolism Chemistry
2	RZ_Flyer_NEFA_UK_290611:55 Uhr Seite 1 C M Y Add to Reading List Source URL: www.metabolic-syndrome.de Language: English - Date: 2014-05-02 11:03:34 Metabolism Diabetes Acyl-CoA Coenzymes Insulin resistance Insulin Lipid Endocrine system Biology Biochemistry
3	The four polychaete eaters, T.bernacchii (n=12 individuals), T.centronotus (n= 8), T.hansoni (n=2), and T.loennbergi (n=5), in all trials responded to pelvic fin and anal fin stimulation by the "worm" by repositioning th Add to Reading List Source URL: s3.amazonaws.com Language: English - Date: 2011-05-06 19:41:23 Coenzymes Biochemistry Coenzyme A Thiols Lipid Acyl-CoA Fatty acids Hepatology Thiolase Biology Metabolism Chemistry
4	Newborn Screening Year in Review 86,586 For Babies Born in 2013 Bloodspot Samples Received Initial Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2015-01-29 18:14:10 Newborn screening Isovaleric acidemia Methylmalonic acidemia Acyl CoA dehydrogenase Biotinidase deficiency Galactosemia Methylmalonic acid Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Guthrie test Health Rare diseases Medicine
5	Timeliness of Newborn Screening – DACHDNC’s laboratory standards and procedures subcommittee draft findings Add to Reading List Source URL: www.hrsa.gov Language: English Medical genetics Newborn screening Isovaleric acidemia Propionic acidemia Methylmalonic acidemia Fatty-acid metabolism disorder Very long-chain acyl-coenzyme A dehydrogenase deficiency Galactosemia Malonyl-CoA decarboxylase deficiency Health Rare diseases Genetic genealogy
6	Newborn Screening Year in Review 86,586 For Babies Born in 2013 Bloodspot Samples Received Initial Add to Reading List Source URL: azdhs.gov Language: English - Date: 2015-01-29 18:14:10 Newborn screening Isovaleric acidemia Methylmalonic acidemia Acyl CoA dehydrogenase Biotinidase deficiency Galactosemia Methylmalonic acid Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Guthrie test Health Rare diseases Medicine
7	Disorders and Reference Ranges Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2014-12-15 13:01:02 Medical genetics Newborn screening Isovaleric acidemia Methylmalonic acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Acyl CoA dehydrogenase Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
8	Disorders and Reference Ranges Add to Reading List Source URL: azdhs.gov Language: English - Date: 2014-12-15 13:01:02 Medical genetics Newborn screening Isovaleric acidemia Methylmalonic acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Acyl CoA dehydrogenase Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
9	Missouri Newborn Screening Disorders Tested Biotinidase deficiency (BIOT) Classical galactosemia (GALT) Congenital adrenal hyperplasia (CAH) Congenital primary hypothyroidism (CH) Cystic fibrosis (CF) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2013-07-10 12:04:01 Rare diseases Newborn screening Methylmalonic acidemia Thiolase Propionic acidemia Isovaleric acidemia Malonyl-CoA Glutaric aciduria type 1 Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Genetic genealogy Medical genetics
10	Medium chain acyl-CoA Dehydrogenase Deficiency (MCADD) Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 10:02:30 Hepatology Metabolism Fatty acids Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Short-chain acyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases