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Dehydrogenase
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#	Item
661	Alcohol Research and Health 31.4 Add to Reading List Source URL: pubs.niaaa.nih.gov Language: English - Date: 2009-04-17 17:36:44 Addiction Alcoholism Alcohol dependence Disease theory of alcoholism Alcohol dehydrogenase Substance dependence Alcoholic beverage Substance use disorder Substance abuse Alcohol abuse Addiction psychiatry Alcohol
662	Microsoft Word - Current News on Expanded Newborn Screening[removed]doc Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 12:19:04 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Inborn error of lipid metabolism Glutaric aciduria type 1 Medium-chain acyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
663	Alcohol Research: Current Reviews Add to Reading List Source URL: pubs.niaaa.nih.gov Language: English - Date: 2012-07-09 14:16:58 Molecular biology Genetic genealogy Alcohol dehydrogenase ADH1B Alcoholism Gene Genome-wide association study Single-nucleotide polymorphism Allele frequency Biology Genetics Population genetics
664	PARENT FACT SHEET DISORDER Isovaleric Acidemia (IVA) CAUSE IVA occurs when an enzyme called “isovaleryl-CoA dehydrogenase” is either missing or not working properly. Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 08:43:51 Rare diseases Isovaleric acidemia Carnitine Amino acid Leucine Protein Acidosis Health Chemistry Medicine
665	Effects of Pregnancy and Nutritional Status on Alcohol Metabolism Add to Reading List Source URL: pubs.niaaa.nih.gov Language: English - Date: 2007-07-12 10:55:32 Biology Teratogens Drinking culture Mental retardation Syndromes Fetal alcohol spectrum disorder Alcoholism Fetal alcohol syndrome Alcohol dehydrogenase Alcohol abuse Chemistry Health
666	Disease Name Glutaric acidemia, type 1 Alternate name(s) Acronym Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-08 18:36:55 Health Medicine Glutaryl-CoA dehydrogenase Glutaryl-CoA Carnitine Lysine Riboflavin Organic acidemia Cerebral palsy Chemistry Coenzymes Glutaric aciduria type 1
667	FOCUS ON SPECIAL POPULATIONS ALDH2, ADH1B, AND ADH1C GENOTYPES IN ASIANS: A LITERATURE REVIEW Add to Reading List Source URL: pubs.niaaa.nih.gov Language: English - Date: 2007-07-12 10:56:56 Population genetics Classical genetics Chemistry ALDH2 Acetaldehyde dehydrogenase Alcohol dehydrogenase ADH1B Aldehyde dehydrogenase Ethanol metabolism Biology Alcohol abuse Drinking culture
668	deCODE Genetics Navigenics New Hope Medical Add to Reading List Source URL: www.dnapolicy.org Language: English - Date: 2011-02-24 16:26:06 Medical genetics Navigenics 23andMe Glucose-6-phosphate dehydrogenase deficiency Knome DeCODE genetics Fragile X syndrome Nutrigenomics Genomics Biology Health Genetics
669	Microsoft Word[removed]Condition list.doc Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2012-08-28 15:52:15 Medical genetics Hyperammonemia Glutaric aciduria type 1 Isovaleric acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Propionic acidemia Fatty-acid metabolism disorder Carnitine-acylcarnitine translocase deficiency Health Rare diseases Genetic genealogy
670	SACHDNC Recommended Uniform Screening Panel1 Add to Reading List Source URL: www.hrsa.gov Language: English - Date: 2013-05-02 18:14:46 Newborn screening Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Fatty-acid metabolism disorder Glutaric aciduria type 1 Glutaric acidemia type 2 Carnitine-acylcarnitine translocase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine

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