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Hydroxyacyl-Coenzyme A dehydrogenase
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51	` 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
52	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
53	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
54	Microsoft Word - Rhode Island insert Khmer.doc Add to Reading List Source URL: nergg.org Language: English - Date: 2007-10-17 09:01:33 Medical genetics Newborn screening Isovaleric acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Mitochondrial trifunctional protein deficiency Methylcrotonyl-CoA 3-Methylcrotonyl-CoA carboxylase deficiency Health Rare diseases Genetic genealogy
55	Microsoft Word - TFP_update_2013 Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2013-12-01 02:48:50 Mitochondrial trifunctional protein deficiency Fatty-acid metabolism disorder Newborn screening Very long-chain acyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
56	Disease Name LONG-CHAIN HYDROXYACYL-CoA DEHYDROGENASE (LCHAD) (LCHAD; MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFECT; LONG-CHAIN HYDROXYACYL-CoA DEHYDROGENASE; LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY) Fatty aci Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:36:38 Fatty acids Metabolism Mitochondrial trifunctional protein Proteins Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Hepatology Hydroxyacyl-Coenzyme A dehydrogenase HADHA Biology Health Chemistry
57	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
58	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
59	Microsoft Word - Vermont Insert English FINAL.doc Add to Reading List Source URL: nergg.org Language: English - Date: 2008-04-01 13:39:57 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Maple syrup urine disease Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
60	Microsoft Word - Haitian_Rhode_Island_insert.doc Add to Reading List Source URL: nergg.org Language: English - Date: 2007-10-17 09:01:30 Medical genetics Isovaleric acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylcrotonyl-CoA Very long-chain acyl-coenzyme A dehydrogenase deficiency Acyl CoA dehydrogenase Acyl-CoA dehydrogenase Methylmalonic acidemia Health Rare diseases Genetic genealogy