Glutaric acid - PDFSEARCH.IO - Document Search Engine

Glutaric acid
Results: 52

#	Item
41	Disorders screened for by the CT Newborn Screening Program Add to Reading List Source URL: www.ct.gov Language: English - Date: 2007-07-09 15:51:44 Rare diseases Newborn screening Fatty-acid metabolism disorder Hyperammonemia Glutaric aciduria type 1 Glutaric acidemia type 2 Propionic acidemia Isovaleric acidemia Biotinidase deficiency Health Genetic genealogy Medical genetics
42	Microsoft Word - FINALDisordersDetectableTable42511 Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2014-08-13 12:31:27 Rare diseases Newborn screening Carnitine-acylcarnitine translocase deficiency Fatty-acid metabolism disorder Carnitine Phenylketonuria Glutaric aciduria type 1 Systemic primary carnitine deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Genetic genealogy
43	California Department of Public Health Genetic Disease Screening Program Newborn Screening Program i Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2014-08-13 12:31:27 Rare diseases Newborn screening Fatty-acid metabolism disorder Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Glutaric aciduria type 1 Hyperammonemia Thalassemia Health Genetic genealogy Medical genetics
44	Microsoft Word - refusal and disorders combination FINAL[removed]doc Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2013-01-31 08:10:27 Genetic genealogy Newborn screening Methylmalonic acidemia Fatty-acid metabolism disorder Propionic acidemia Isovaleric acidemia Carnitine palmitoyltransferase I Glutaric aciduria type 1 Malonyl-CoA Health Rare diseases Medicine
45	Appendix[removed]C 86 Inborn Errors of Metabolism Inborn errors of metabolism generally refer to gene mutations or gene deletions that alter metabolism in the body, including but not limited to: Amino Acid Disorders Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2013-02-08 13:02:17 Genetic genealogy Inborn errors of carbohydrate metabolism Hepatology Pediatrics Inborn error of metabolism Isovaleric acidemia Propionic acidemia Methylmalonic acidemia Glutaric aciduria type 1 Health Medicine Rare diseases
46	Microsoft Word[removed]Condition list.doc Add to Reading List Source URL: ndhealth.gov Language: English - Date: 2012-08-28 15:52:15 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
47	Parent Fact Sheet DISORDER Hydroxymethylglutaric Aciduria (3-OH 3 CH3 glutaric aciduria) (HMG) CAUSE Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 02:11:05 Medical genetics Coenzymes Thioesters HMG-CoA Organic acidemia 3-hydroxy-3-methylglutaryl-CoA lyase Fatty-acid metabolism disorder 3-hydroxy-3-methylglutaryl-CoA lyase deficiency Health Genetic genealogy
48	Parent Fact Sheet DISORDER Methylmalonic Acidemia Mutase Deficiency (MUT) CAUSE MMA stands for "methylmalonic acidemia". It is one type of organic acid disorder. People with MMA have Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-08 18:18:59 Genetic genealogy Methylmalonic acidemia Vitamin B12 Acidosis Methylmalonic acid Protein Propionic acidemia Glutaric aciduria type 1 Health Medicine Rare diseases
49	Microsoft Word[removed]Condition list.doc Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2012-08-28 15:52:15 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
50	SACHDNC Recommended Uniform Screening Panel1 Add to Reading List Source URL: www.hrsa.gov Language: English - Date: 2013-05-02 18:14:46 Newborn screening Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Fatty-acid metabolism disorder Glutaric aciduria type 1 Glutaric acidemia type 2 Carnitine-acylcarnitine translocase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine