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Acyl-CoA dehydrogenase
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41	NEWBORN SCREENING FACT SHEET SCADD (Short Chain Acyl-CoA Dehydrogenese Deficiency) What is it? SCADD stands for short chain acyl-CoA dehydrogenase deficiency. It is one type of Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-20 12:54:56 Rare diseases Epidemiology Newborn screening Pediatrics Fatty-acid metabolism disorder Inborn errors of carbohydrate metabolism Screening Biotinidase deficiency Phenylketonuria Health Medicine Genetic genealogy
42	NEWBORN SCREENING FACT SHEET MCADD (Medium Chain Acyl-CoA Dehydrogenese Deficiency) What is it? MCADD stands for medium chain acyl-CoA dehydrogenase deficiency. It is one type of Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:32:00 Hypoglycemia Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Inborn errors of carbohydrate metabolism Newborn screening Glycogen storage disease type I Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases
43	` NEWBORN SCREENING FACT SHEET VLCADD (Very Long Chain Acyl-CoA Dehydrogenese Deficiency) It is common for babies and children with the Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:32:01 Very long-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Hepatology Hypoglycemia Carnitine Newborn screening Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Glycogen storage disease type I Health Medicine Rare diseases
44	review April 2006 � Vol. 8 � No. 4 The epidemiology of medium chain acyl-CoA dehydrogenase deficiency: An update Add to Reading List Source URL: www.cdc.gov Language: English - Date: 2010-06-07 14:27:50 Epidemiology Newborn screening Pediatrics Medium-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder ACADM Acyl CoA dehydrogenase Medical genetics Screening Medicine Health Rare diseases
45	Microsoft Word - New Hampshire Insert English FINAL.doc Add to Reading List Source URL: nergg.org Language: English - Date: 2007-10-17 09:01:06 Medical genetics Newborn screening 3-Methylcrotonyl-CoA carboxylase deficiency Methylcrotonyl-CoA carboxylase Propionic acidemia Biotinidase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Thiolase Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
46	MICHIGAN DEPARTMENT OF COMMUNITY HEALTH BUREAU OF LABORATORIES Newborn Screening – Fatty Acid Oxidation Disorders Rev. Date[removed] Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2013-03-15 16:30:13 Fatty acids Fatty-acid metabolism disorder Newborn screening Thiolase 2 4 Dienoyl-CoA reductase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Fatty acid metabolism Carnitine Health Medicine Chemistry
47	Microsoft Word - mcad_ref Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:36:44 Fatty acids Biochemistry Coenzymes Pediatrics Inborn error of lipid metabolism Rare diseases Medium-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Acyl CoA dehydrogenase Biology Metabolism Chemistry
48	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
49	Disease Name VERY LONG-CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY (VLCADD) (VLCAD DEFICIENCY) Fatty acid oxidation disorder Classification: Inheritance: Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:38:00 Rare diseases Very long-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Metabolism ACADVL Newborn screening Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Hypoglycemia Carnitine Health Medicine Chemistry
50	Disease Name 2-METHYLBUTYRYL-CoA DEHYDROGENASE DEFICIENCY (2MBCD) (SHORT/BRANCHED CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY; 2METHYLBUTYRYLGLYCINURIA) Organic aciduria and fatty acid oxidation defect. Classification: Inher Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:35:43 2-Methylbutyryl-CoA dehydrogenase deficiency 2-Methylbutyryl-CoA Newborn screening Hypoglycemia Carnitine Health Medicine Rare diseases

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