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Coenzyme A
Results: 370

#	Item
321	Parent Fact Sheet Disorder Short Chain Acyl-CoA Dehydrogenase Deficiency (SCAD) Cause People with Short Chain Acyl-CoA Dehydrogenase deficiency have problems breaking down fat into energy for their body. Most babies with Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-08 19:55:22 Rare diseases Coenzymes Metabolism Carnitine Newborn screening Riboflavin Acyl CoA dehydrogenase Acyl-CoA Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Chemistry Biology
322	TCNP Protocol – Cole Lab p. 1 A Selective Chemical Probe for Coenzyme-A Requiring Enzymes Add to Reading List Source URL: www.hopkinsmedicine.org Language: English
323	PARENT FACT SHEET DISORDER Medium-chain acyl-CoA dehydrogenase deficiency (MCAD) CAUSE MCAD occurs when an enzyme called “medium chain acyl-CoA dehydrogenase” is either missing or not working Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 10:59:34 Chemistry Hypoglycemia Metabolism Carnitine Fatty-acid metabolism disorder Very long-chain acyl-coenzyme A dehydrogenase deficiency Medicine Health Medium-chain acyl-coenzyme A dehydrogenase deficiency
324	Microsoft Word[removed]Condition list.doc Add to Reading List Source URL: 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
325	Parent Fact Sheet DISORDER Methylmalonic Acidemia (Cbl A, B) CAUSE MMA stands for "methylmalonic acidemia". It is one type of organic acid disorder. People with MMA have problems Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 13:38:50 Genetic genealogy Vitamin B12 Methylmalonic acidemia Methylmalonic acid Acidosis Protein Propionic acidemia Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases
326	Microsoft Word - 3MCC.doc Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 04:53:48 3-Methylcrotonyl-CoA carboxylase deficiency Carnitine Rare diseases Amino acid Protein Very long-chain acyl-coenzyme A dehydrogenase deficiency Biotinidase deficiency Health Chemistry Medicine
327	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
328	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
329	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
330	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

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