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Acyl-CoA
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#	Item
91	PARENT FACT SHEET Very long-chain acyl-CoA dehydrogenase deficiency (VLCAD) CAUSE VLCAD occurs when the very long chain acyl-CoA dehydrogenase enzyme is missing or not working properly. This enzyme’s job is to break do Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-09 02:37:56 Very long-chain acyl-coenzyme A dehydrogenase deficiency Rare diseases Newborn screening Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Carnitine Metabolism Acyl CoA dehydrogenase Acyl-CoA ACADVL Health Chemistry Medicine
92	Newborn Screening Brochure Add to Reading List Source URL: www.wadsworth.org Language: English - Date: 2011-10-11 08:14:49 Genetic genealogy Newborn screening Methylmalonic acidemia Propionic acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency 2-Methylbutyryl-CoA dehydrogenase deficiency Isovaleric acidemia Very long-chain acyl-coenzyme A dehydrogenase deficiency Glutaric aciduria type 1 Health Rare diseases Medicine
93	Baby is Home! KIDSNET All babies born in Rhode Island are enrolled in KIDSNET, the Rhode Island information system that helps families and doctors make sure that Add to Reading List Source URL: www.nergg.org Language: English - Date: 2012-04-06 15:58:29 Genetic genealogy Newborn screening Phenylketonuria Methylmalonic acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Biotinidase deficiency Propionic acidemia Isovaleric acidemia Health Rare diseases Medicine
94	STATE OF NEW HAMPSHIRE DEPARTMENT OF HEALTH AND HUMAN SERVICES Nicholas A. Toumpas Commissioner Add to Reading List Source URL: www.dhhs.state.nh.us Language: English - Date: 2014-08-08 09:16:27 Newborn screening Propionic acidemia Methylmalonic acidemia Acyl CoA dehydrogenase Medium-chain acyl-coenzyme A dehydrogenase deficiency Malonyl-CoA decarboxylase deficiency Isovaleric acidemia Carnitine palmitoyltransferase I 3-Methylcrotonyl-CoA carboxylase deficiency Health Rare diseases Medicine
95	State of Illinois Rod R. Blagojevich, Governor Department of Public Health Eric E. Whitaker, M.D., M.P.H., Director Newborn Metabolic Add to Reading List Source URL: www.idph.state.il.us Language: English - Date: 2007-07-24 10:41:11 Medical genetics Newborn screening Propionic acidemia Fatty-acid metabolism disorder 2-Methylbutyryl-CoA dehydrogenase deficiency Biotinidase deficiency Isovaleric acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Health Rare diseases Genetic genealogy
96	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: www.health.mo.gov Language: English - Date: 2009-02-03 16:51:23 Medical genetics Argininosuccinic aciduria Urea cycle disorder Newborn screening Argininosuccinate lyase Carbamoyl phosphate synthetase I deficiency Glutaric acidemia type 2 Health Rare diseases Genetic genealogy
97	Microsoft Word - 3MCC.doc Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-09 15:58:40 3-Methylcrotonyl-CoA carboxylase deficiency Carnitine Rare diseases Amino acid Protein Very long-chain acyl-coenzyme A dehydrogenase deficiency Biotinidase deficiency Health Chemistry Medicine
98	MCAD - Carson and Brynn: A Family’s Story We live in Phoenix, AZ and have two kids with Medium-chain acyl-CoA dehydrogenase deficiency (MCAD), Carson (age 9) and Brynn (age 4). Carson was born in 2004 and at that time Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2013-08-16 18:53:50 Newborn screening Medium-chain acyl-coenzyme A dehydrogenase deficiency Medicine Health Pediatrics Epidemiology
99	Microsoft Word - MoD Fact Sheet 2011 Add to Reading List Source URL: azdhs.gov Language: English - Date: 2012-04-12 12:46:55 Medical genetics Newborn screening Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylmalonic acid Maple syrup urine disease Acyl CoA dehydrogenase Health Rare diseases Genetic genealogy
100	Arizona Department of Health Services Newborn Screening Program MSMS Pilot Project – Secondary Markers Amino Acid Disorders Analytes Add to Reading List Source URL: azdhs.gov Language: English - Date: 2013-07-03 16:56:45 Methylmalonic acidemia Newborn screening Isovaleric acidemia Methylmalonic acid Acyl CoA dehydrogenase Maple syrup urine disease Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Rare diseases Propionic acidemia

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