Organic acidemia - PDFSEARCH.IO - Document Search Engine

Organic acidemia
Results: 73

#	Item
21	Isovaleric acidemia (IVA) (metabolic condition: organic acid disorder) Also known as: • isovaleric acid-CoA dehydrogenase deficiency Add to Reading List Source URL: www.albertahealthservices.ca Language: English - Date: 2013-09-16 18:33:30 Isovaleric acidemia Organic acidemia Medical genetics Metabolism Isovaleryl-CoA Newborn screening Medicine Health Rare diseases
22	Isovaleric Acidemia A Guide for Parents Sponsored by the Pacific Northwest Add to Reading List Source URL: www.westernstatesgenetics.org Language: English - Date: 2010-03-11 16:13:19 Genetic genealogy Isovaleric acidemia Organic acidemia 3-Methylbutanoic acid Acidosis Protein Human nutrition Phenylketonuria Amino acid Health Rare diseases Medicine
23	Microsoft Word - Isoval update 2011.doc Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2011-06-22 18:01:20 Pediatrics Medical genetics Isovaleric acidemia Newborn screening 3-Methylbutanoic acid Organic acidemia Acidosis Inborn error of metabolism Genetic testing Health Medicine Rare diseases
24	Diagnosis: Argininosuccinic Aciduria or Arginosuccinic Lyase Deficiency (ASA) ASA is an inherited disorder that limits the body’s ability to convert ammonia to urea. During periods of illness, fasting or protein overlo Add to Reading List Source URL: www.wadsworth.org Language: English - Date: 2009-07-15 13:48:21 Argininosuccinic aciduria Hyperammonemia Organic acidemia Carnitine Medical genetics Medicine Health Rare diseases
25	Microsoft Word - GA-1_update_2013 Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2013-11-28 02:21:42 Pediatrics Glutaric aciduria type 1 Metabolism Newborn screening Glutaryl-CoA dehydrogenase Acidosis Inborn error of metabolism Organic acidemia Metabolic acidosis Health Medicine Rare diseases
26	NEWBORN SCREENING FACT SHEET GA-1 (Glutaric Acidemia, Type 1) What is it? GA-1 stands for glutaric acidemia, type 1. It is one type of organic acid disorder. People Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:31:55 Rare diseases Pediatrics Essential amino acids Ketogenic amino acids Proteinogenic amino acids Glutaric aciduria type 1 Newborn screening Phenylketonuria Glutaryl-CoA dehydrogenase Health Medicine Biology
27	MICHIGAN DEPARTMENT OF COMMUNITY HEALTH BUREAU OF LABORATORIES Newborn Screening – Organic Acid Oxidation Disorders Rev. Date[removed] Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2013-03-15 16:30:31 Methylmalonic acidemia Methylmalonic acid Organic acidemia Health Rare diseases Newborn screening
28	NEWBORN SCREENING FACT SHEET MMA (Methylmalonic Acidemia) What is it? MMA stands for methylmalonic academia. It is one type of organic acid disorder. People with Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-20 12:55:04 Nutrition Vitamin B12 Cofactors Methylmalonic acidemia Methylmalonic acid Newborn screening Hydroxocobalamin Methylmalonyl-CoA mutase Vitamin Health Medicine Rare diseases
29	Disease Name 2-METHYL-3-HYDROXYBUTYRYL-CoA DEHYDROGENASE DEFICIENCY (MHBD) (HYDROXYL-CoA DEHYDROGENASE DEFICIENCY; 3-HYDROXY-2METHYLBUTYRYL-COA DEHYDROGENASE DEFICIENCY) Organic aciduria Classification: Inheritance: Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:36:49 Medicine Epidemiology Newborn screening Pediatrics 3-hydroxybutyryl-CoA dehydrogenase Carnitine Organic acidemia Hyperammonemia Butyryl-CoA dehydrogenase Chemistry Health EC 1.1.1
30	Disease Name GLUTARIC ACIDEMIA TYPE II (GA II) (GLUTARIC ACIDURIA TYPE II; GA II; ETHYLMALONIC-ADIPIC ACIDURIA; ELECTRON TRANSFER FLAVOPROTEIN DEHYDROGENASE DEFICIENCY; ETF/ETF QO DEFICIENCY) Classification: Fatty acid o Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:36:18 Glutaric acidemia type 2 Pediatrics Newborn screening Hepatology Glutaric aciduria type 1 Organic acidemia Systemic primary carnitine deficiency Hypoglycemia Electron-transferring-flavoprotein dehydrogenase Health Medicine Rare diseases