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Coenzyme A
Results: 370

#	Item
51	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:51:42 Genetic genealogy Glutaric acidemia type 2 Fatty-acid metabolism disorder Glutaric aciduria type 1 Newborn screening Fatty acid metabolism Propionic acidemia Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
52	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
53	Microsoft Word - MCAD.doc Add to Reading List Source URL: health.mo.gov Language: English - Date: 2007-09-14 07:57:54 Medium-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Newborn screening Medical genetics Fatty acid metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Malonyl-CoA decarboxylase deficiency Medicine Health Rare diseases
54	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
55	CYP98A3 from Arabidopsis thaliana is a 3'-hydroxylase of phenolic esters, a missing link in the phenylpropanoid pathway Add to Reading List Source URL: eurekamag.com Language: English - Date: 2014-09-23 04:27:42 Coenzymes Metabolism Phenylpropanoid Coumaric acid Caffeic acid Coumaroyl-CoA Cytochrome P450 Caffeoyl-CoA O-methyltransferase Coenzyme A Chemistry Hydroxycinnamic acids Phenolic compounds in wine
56	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
57	Table of Contents Contents Page What is MCADD? ........................................ 1-5 Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2014-10-06 16:45:48 Hepatology Medium-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Hypoglycemia Blood sugar Very long-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Health Medicine Diabetes
58	Table of Contents Contents Page What is VLCADD? ....................................... 1-7 Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2014-10-06 16:45:49 Very long-chain acyl-coenzyme A dehydrogenase deficiency Diabetes Hepatology Fatty-acid metabolism disorder Blood sugar Hypoglycemia Cardiovascular disease Glycogen storage disease type I Adiposopathy Medicine Health Biology
59	Table of Contents Contents Page What is SCADD? ......................................... 1-5 Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2014-10-06 16:45:49 Epidemiology Newborn screening Pediatrics Weakness Fatty-acid metabolism disorder Inborn errors of carbohydrate metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Galactosemia Health Medicine Rare diseases
60	DRAFT[removed]ARTICLE 2. NEWBORN AND INFANT SCREENING Section R9[removed]. Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2013-08-21 11:09:22 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Biotinidase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Malonyl-CoA decarboxylase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Isovaleric acidemia Health Rare diseases Genetic genealogy

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