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Methylcrotonyl-CoA carboxylase
Results: 68

#	Item
61	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 fro Add to Reading List Source URL: www.maine.gov Language: English - Date: 2011-12-13 06:47:38 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
62	PDF Document Add to Reading List Source URL: www.dhhs.nh.gov Language: English - Date: 2010-10-25 15:14:39 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
63	(ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY; IVA; IVD) Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 10:03:12 Medical genetics Organic acidemia Isovaleric acidemia Propionic acidemia Newborn screening Methylmalonic acidemia Glutaric aciduria type 1 Malonyl-CoA decarboxylase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Health Rare diseases Genetic genealogy
64	Microsoft Word - Organic_Acidemias.doc Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 15:47:00 Genetic genealogy Isovaleric acidemia Propionic acidemia Organic acidemia Newborn screening Methylmalonic acidemia Malonyl-CoA decarboxylase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Medical genetics Health Rare diseases Medicine
65	American College of Medical Genetics ACT SHEET Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Genes Pediatrics Multiple carboxylase deficiency Newborn screening Biotinidase deficiency Holocarboxylase synthetase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Medical genetics Biotin Medicine Health Genetics
66	Visio-C5-OH[removed]edits.vsd Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Genes Rare diseases Epidemiology Newborn screening Pediatrics Biotin deficiency Biotinidase deficiency Cofactors 3-Methylcrotonyl-CoA carboxylase deficiency Health Genetics Medicine
67	NUTRITION ISSUES IN GASTROENTEROLOGY, SERIES #41 Carol Rees Parrish, R.D., M.S., Series Editor Add to Reading List Source URL: www.medicine.virginia.edu Language: English - Date: 2011-06-13 10:42:42 Rare diseases Newborn screening Guthrie test Galactose-1-phosphate uridylyltransferase deficiency Medical genetics Galactosemia Biotinidase deficiency Phenylketonuria 3-Methylcrotonyl-CoA carboxylase deficiency Health Medicine Genetic genealogy
68	- 138 - 1927 Add to Reading List Source URL: www.shc.usp.ac.jp Language: English - Date: 2005-08-09 00:27:49 Organic chemistry Thioesters Methylcrotonyl-CoA carboxylase Propionyl-CoA Methylcrotonyl-CoA Biotin Coenzyme A Acetyl-CoA Methylmalonyl-CoA Coenzymes Chemistry Metabolism

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