3-hydroxyacyl-CoA dehydrogenase - PDFSEARCH.IO - Document Search Engine

3-hydroxyacyl-CoA dehydrogenase
Results: 57

#	Item
1	APPLIED AND ENVIRONMENTAL MICROBIOLOGY, Apr. 2001, p. 1728–/$04.00⫹0 DOI: AEM–Copyright © 2001, American Society for Microbiology. All Rights Reserved. Vol. 67, No. 4 Add to Reading List Source URL: microbiology.okstate.edu Language: English - Date: 2012-10-04 11:09:05 EC 1.1.1 4-Hydroxybenzoic acid Monomers Xenoestrogens 3-hydroxyacyl-CoA dehydrogenase Coenzyme A Benzoyl-CoA Beta oxidation Enoyl-CoA hydratase Benzoic acid BenzoateCoA ligase
2	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
3	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
4	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
5	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
6	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
7	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:51:53 Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty acids Fatty-acid metabolism disorder Acute fatty liver of pregnancy Hepatology Newborn screening Fatty acid metabolism Mitochondrial trifunctional protein Health Medicine Rare diseases
8	Microsoft Word - Canada NBS status Nov23.2006.doc Add to Reading List Source URL: www.raredisorders.ca Language: English - Date: 2009-06-26 12:21:32 Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Hyperammonemia Glutaric aciduria type 1 Thiolase Methylmalonyl-CoA mutase Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
9	Delaware Division of Public Health Newborn Screening Program Disorder Name & Abbreviation Analyte / Marker Endocrine Disorder Add to Reading List Source URL: www.dhss.delaware.gov Language: English - Date: 2012-07-26 14:33:28 Genetic genealogy Newborn screening Carnitine Fatty-acid metabolism disorder Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Glutaric aciduria type 1 Methylmalonic acidemia Glutaric acidemia type 2 Acyl CoA dehydrogenase Health Rare diseases Medicine
10	Maine Newborn Screening Program List of Conditions Each baby born in Maine is screened for the conditions listed below. This list is correct as of July 1, 2008 but may change as conditions are added to or removed from th Add to Reading List Source URL: www.maine.gov Language: English - Date: 2011-11-10 05:38:14 Medical genetics Newborn screening Hyperammonemia 3-Methylcrotonyl-CoA carboxylase deficiency Isovaleric acidemia Glutaric acidemia type 2 Glutaric aciduria type 1 Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy