Short-chain dehydrogenase - PDFSEARCH.IO - Document Search Engine

Short-chain dehydrogenase
Results: 32

#	Item
11	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
12	Microsoft Word - scad_ref Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:37:49 Fatty acids Health Coenzymes Rare diseases Inborn error of lipid metabolism Fatty-acid metabolism disorder Acyl CoA dehydrogenase Short-chain acyl-coenzyme A dehydrogenase deficiency Fatty acid metabolism Chemistry Biology Metabolism
13	Disease Name SHORT-CHAIN ACYL-COA DEHYDROGENASE DEFICIENCY (SCADD) (ACADS DEFICIENCY; SCADH DEFICIENCY; SCAD DEFICIENCY) Fatty acid oxidation defect Classification: Inheritance: Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:37:49 Chemistry Metabolism Fatty acids Short-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Hepatology ACADS Malonyl-CoA decarboxylase deficiency Newborn screening Health Medicine Rare diseases
14	CHAPTER 31 PDF p. 1 of 1 CHAPTER 31 (SB 31) Add to Reading List Source URL: www.lrc.state.ky.us Language: English - Date: 2001-05-18 14:22:18 Rare diseases Epidemiology Newborn screening Medium-chain acyl-coenzyme A dehydrogenase deficiency Phenylketonuria Very long-chain acyl-coenzyme A dehydrogenase deficiency Short-chain acyl-coenzyme A dehydrogenase deficiency Inborn error of metabolism Galactosemia Health Medicine Pediatrics
15	Short-chain acyl-CoA Dehydrogenase Deficiency (SCAD) What is a positive newborn screen? Newborn screening is done on tiny samples of blood taken from your baby’s heel 24 to 36 hours after birth. The blood is tested for Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 14:06:00 Epidemiology Newborn screening Pediatrics Short-chain acyl-coenzyme A dehydrogenase deficiency Infant Screening Health Rare diseases Medicine
16	WILDLIFE DAMAGE CONTROL PERMIT Add to Reading List Source URL: dnr.maryland.gov Language: English - Date: 2014-07-29 13:56:39 Short-chain dehydrogenase Retroviral aspartyl protease Protein domains Peptidase Seventh chords
17	CHAPTER 66 PDF p. 1 of 3 CHAPTER 66 (SB 24) Add to Reading List Source URL: www.lrc.ky.gov Language: English - Date: 2005-07-07 13:26:35 Newborn screening Isovaleric acidemia Very long-chain acyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Propionic acidemia Short-chain acyl-coenzyme A dehydrogenase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Glutaric aciduria type 1 Health Medicine Rare diseases
18	Medium and short-chain L-3-hydroxy acyl-CoA Dehydrogenase Deficiency (M/SCHAD) What is a positive newborn screen? Newborn screening is done on tiny samples of blood taken from your baby’s heel 24 to 48 hours Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 20:47:08
19	Minnesota Department of Health[removed]SCAD Add to Reading List Source URL: www.health.state.mn.us Language: English - Date: 2014-04-04 11:40:23 Medicine Carnitine Newborn screening Short-chain acyl-coenzyme A dehydrogenase deficiency Acyl-CoA Inborn error of lipid metabolism Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Chemistry
20	Microsoft Word - VLCAD.doc Add to Reading List Source URL: www.health.mo.gov Language: English - Date: 2007-09-14 09:09:50 Medical genetics Fatty-acid metabolism disorder Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Newborn screening Fatty acid metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Short-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy

UPDATE