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Dehydrogenase
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#	Item
671	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 fro Add to Reading List Source URL: www.maine.gov Language: English - Date: 2011-12-13 06:47:38 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
672	Inside: Continuing Medical Education for U.S. Physicians and Nurses April 13, [removed]Vol[removed]No. RR-3 Recommendations and Add to Reading List Source URL: www.cdc.gov Language: English - Date: 2001-08-06 09:59:11 Chemistry Newborn screening Phenylketonuria Tandem mass spectrometry Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Isovaleric acidemia Carnitine Biotinidase deficiency Health Rare diseases Medicine
673	PDF Document Add to Reading List Source URL: www.cdc.gov Language: English - Date: 2014-05-14 10:33:18 Pathology Infancy Sudden infant death syndrome Coroner Forensic pathology Death certificate Medium-chain acyl-coenzyme A dehydrogenase deficiency Autopsy Infant bed Human development Childhood Medicine
674	PDF Document Add to Reading List Source URL: www.dhhs.nh.gov Language: English - Date: 2010-10-25 15:14:39 Newborn screening Propionic acidemia Methylmalonic acidemia Acyl CoA dehydrogenase Medium-chain acyl-coenzyme A dehydrogenase deficiency Malonyl-CoA decarboxylase deficiency Isovaleric acidemia Carnitine palmitoyltransferase I 3-Methylcrotonyl-CoA carboxylase deficiency Health Rare diseases Medicine
675	[removed]–[removed]08:13 Uhr Seite 391 Add to Reading List Source URL: www.wiley-vch.de Language: English - Date: 2004-04-15 03:16:41 EC 1.1.1 Cellular respiration Enzymes Oxidoreductases Protein families Alcohol dehydrogenase Nicotinamide adenine dinucleotide Cofactor Electron transport chain Chemistry Biology Biochemistry
676	(ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY; IVA; IVD) Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 10:03:12 Medical genetics Organic acidemia Isovaleric acidemia Propionic acidemia Newborn screening Methylmalonic acidemia Glutaric aciduria type 1 Malonyl-CoA decarboxylase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Health Rare diseases Genetic genealogy
677	Alcohol Pharmacogenetics in Mexican Americans Overview: The aim of this research grant, now in its 9th year of funding, is to investigate genetic factors that may contribute to the risk for development of alcohol depend Add to Reading List Source URL: www.niaaa.nih.gov Language: English - Date: 2012-03-30 18:46:43 Alcohol Household chemicals Alcoholism Binge drinking Disease theory of alcoholism Alcoholic beverage Alcohol dehydrogenase Alcohol dependence Aldehyde dehydrogenase Alcohol abuse Medicine Drinking culture
678	Microsoft Word - FAOD.doc Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 14:47:24 Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Short-chain acyl-coenzyme A dehydrogenase deficiency Fatty acid metabolism Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Mitochondrial trifunctional protein deficiency Newborn screening Lipid Health Medicine Rare diseases
679	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
680	STATE OF TENNESSEE DEPARTMENT OF HEALTH DIVISION OF LABORATORY SERVICES NEWBORN SCREENING PROGRAM Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2011-02-25 12:37:37 Medical genetics Fatty-acid metabolism disorder Newborn screening Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Hyperammonemia Carnitine Isovaleric acidemia Health Rare diseases Genetic genealogy

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