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Coenzyme A
Results: 370

#	Item
291	NEWBORN SCREENING CONFIRMED CASE REPORT PRIMARY PANEL OF 29 DISORDERS DOB[removed] – [removed]Disorder Abbreviation Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2012-04-12 12:46:51 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Maple syrup urine disease Medium-chain acyl-coenzyme A dehydrogenase deficiency Methylmalonic acid Health Rare diseases Genetic genealogy
292	OFFICE OF NEWBORN SCREENING 2008 CONFIRMED CASE REPORT PRIMARY PANEL OF 28 BLOODSPOT DISORDERS DISORDER ANALYTE Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2012-04-12 12:46:54 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Biotinidase deficiency Glutaric aciduria type 1 Medium-chain acyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
293	PDF Document Add to Reading List Source URL: www.ok.gov Language: English - Date: 2012-11-29 10:48:21 Newborn screening Phenylketonuria Biotinidase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Biotin Galactosemia Congenital hypothyroidism Guthrie test Congenital adrenal hyperplasia Health Medicine Pediatrics
294	C O R P O R AT E PA RT N E R Become a Communities of Quality Corporate Partner Add to Reading List Source URL: www.nahma.org Language: English Benzoquinones Cellular respiration Coenzyme Q10 Coenzymes Glycolysis Affordable housing Biology Coq A. Le Coq Chemistry Biochemistry Antioxidants
295	Health Cadham Provincial Laboratory Provincial Programs and Services P.O. Box 8450 Add to Reading List Source URL: www.gov.mb.ca Language: English - Date: 2012-05-08 12:28:03 Pediatrics Epidemiology Newborn screening Mental retardation Metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Isovaleric acidemia Methylmalonic acidemia Biotinidase deficiency Health Medicine Rare diseases
296	STATE OF TENNESSEE DEPARTMENT OF HEALTH DIVISION OF LABORATORY SERVICES NEWBORN SCREENING PROGRAM Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2011-02-25 12:37:37 Medical genetics Fatty-acid metabolism disorder Newborn screening Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Hyperammonemia Carnitine Isovaleric acidemia Health Rare diseases Genetic genealogy
297	NEWBORN SCREENING IN NEBRASKA Newborn Screening for Metabolic and Inherited Disorders AND Early Hearing Detection & Intervention Add to Reading List Source URL: dhhs.ne.gov Language: English - Date: 2014-08-22 13:53:14 Rare diseases Epidemiology Newborn screening Inborn errors of carbohydrate metabolism Association of Public Health Laboratories Screening Galactosemia Very long-chain acyl-coenzyme A dehydrogenase deficiency Phenylketonuria Health Medicine Pediatrics
298	3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase and Mevalonate Kinase Activity in Turkey Liver and Kidney Add to Reading List Source URL: digital.library.okstate.edu Language: English - Date: 2009-01-09 17:06:08 HMG-CoA reductase Sterols Metabolic pathways Cholesterol Mevalonic acid Lipid Low-density lipoprotein HMG-CoA Mevalonate kinase Chemistry Biology EC 1.1.1
299	Hygienic Laboratory The University of Iowa For Questions About Resubmission and Result Interpretation Contact Medical Consultants LABORATORY HOSPITAL Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:37:50 Rare diseases Fatty-acid metabolism disorder Propionic acidemia Carnitine palmitoyltransferase I Biotinidase deficiency Isovaleric acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency 2-Methylbutyryl-CoA dehydrogenase deficiency Health Genetic genealogy Medical genetics
300	Microsoft Word - New Hampshire Insert English FINAL.doc Add to Reading List Source URL: www.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

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