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Glutaric acidemia type 2
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11	Maine Newborn Screening Program List of Conditions Each baby born in Maine is screened for the conditions listed below. This list is correct as of July 1, 2008 but may change as conditions are added to or removed from th Add to Reading List Source URL: www.maine.gov Language: English - Date: 2011-11-10 05:38:14 Medical genetics Newborn screening Hyperammonemia 3-Methylcrotonyl-CoA carboxylase deficiency Isovaleric acidemia Glutaric acidemia type 2 Glutaric aciduria type 1 Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
12	Microsoft Word - HEALTH CARE Did she miss a chance Globe Dec[removed]doc Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:40:42 Pediatrics Epidemiology Newborn screening Medical genetics Medical specialties Phenylketonuria Glutaric acidemia type 2 Glutaric aciduria type 1 Genetic disorder Health Medicine Rare diseases
13	Glutaric Acidemia Type II A Guide for Parents Sponsored by the Pacific Northwest Add to Reading List Source URL: www.westernstatesgenetics.org Language: English - Date: 2010-03-11 16:13:21 Glutaric acidemia type 2 Applied sciences Food science Health sciences Self-care Glutaric aciduria type 1 Human nutrition Inborn error of metabolism Acidosis Health Medicine Genetic genealogy
14	FOD Communication Network (Fatty Oxidation Disorders) ‘All In This Together’ June 1997 Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:16 Food science Health sciences Self-care Glutaric aciduria type 1 Fatty-acid metabolism disorder Glutaric acidemia type 2 Newborn screening Carnitine The Organ Health Medicine Applied sciences
15	NEWBORN SCREENING FACT SHEET GA-2 (Glutaric Acidemia, Type 2) If GA-2 is not treated, what problems occur? GA-2 can cause bouts of illness called metabolic crises. Some of the first symptoms of Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:31:56 Diabetes Rare diseases Glutaric aciduria type 1 Hypoglycemia Newborn screening Fatty-acid metabolism disorder Acidosis Blood sugar Glutaric acidemia type 2 Health Medicine Genetic genealogy
16	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
17	Microsoft Word - Haitian_Maine_Insert.doc Add to Reading List Source URL: nergg.org Language: English - Date: 2007-10-17 09:00:32 Rare diseases Isovaleric acidemia Glutaric acidemia type 2 Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Glutaric aciduria type 1 Acyl CoA dehydrogenase Very long-chain acyl-coenzyme A dehydrogenase deficiency Propionic acidemia Health Genetic genealogy Medical genetics
18	GLUTARIC ACIDEMIA TYPE II (GAII) REFERENCES (GLUTARIC ACIDURIA TYPE II; GA II; ETHYLMALONIC-ADIPIC ACIDURIA; ELECTRON TRANSFER FLAVOPROTEIN DEHYDROGENASE DEFICIENCY; ETF/ETF QO DEFICIENCY[removed]. Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:36:18 Biochemistry Coenzymes Cellular respiration Fatty acids Pediatrics ETFA Electron-transferring-flavoprotein dehydrogenase Glutaric acidemia type 2 Glutaric aciduria type 1 Biology Metabolism Chemistry
19	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
20	Disorders Detected By Mississippi Genetic Newborn Screening Secondary Conditions Methylmalonic acidemia with homocystinuria Malonic acidemia Isobutyrylglycinuria Add to Reading List Source URL: msdh.ms.gov Language: English - Date: 2012-03-28 12:35:21 Medical genetics Newborn screening Methylmalonic acidemia Glutaric aciduria type 1 Propionic acidemia Isovaleric acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency Glutaric acidemia type 2 Carnitine-acylcarnitine translocase deficiency Health Rare diseases Genetic genealogy

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