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Glutaric aciduria type 1
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41	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
42	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
43	Ketone Utilization Disorder (Beta-ketothiolase Deficiency) A Guide for Parents Add to Reading List Source URL: www.westernstatesgenetics.org Language: English - Date: 2010-03-11 16:13:17 Rare diseases Applied sciences Food science Health sciences Beta-ketothiolase deficiency Protein Glutaric aciduria type 1 Phenylketonuria Thiolase Health Medicine Genetic genealogy
44	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
45	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
46	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
47	Overview of Newborn Screening for Organic Acidemias – For Parents What is newborn screening? Before babies go home from the nursery, they have a small amount of blood taken from their heel to test for a group of condit Add to Reading List Source URL: www.in.gov Language: English - Date: 2014-10-22 10:08:32 Genetic genealogy Isovaleric acidemia Newborn screening Organic acidemia Glutaric aciduria type 1 Methylmalonic acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Metabolism Acidosis Health Rare diseases Medicine
48	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
49	Glutaric Acidemia, Type 1 (GA1) 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 rare, hidden disorde Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 21:12:30 Chemistry GA1 Newborn screening Screening Lysine Glutaric acid Health Medicine Glutaric aciduria type 1
50	Microsoft Word[removed]Condition list.doc Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2014-09-16 08:12:01 Medical genetics Hyperammonemia Glutaric aciduria type 1 Isovaleric acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Propionic acidemia Fatty-acid metabolism disorder Carnitine-acylcarnitine translocase deficiency Health Rare diseases Genetic genealogy

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