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3-Methylcrotonyl-CoA carboxylase deficiency
Results: 66

#	Item
51	Hygienic Laboratory The University of Iowa For Questions About Resubmission and Result Interpretation Contact Medical Consultants LABORATORY HOSPITAL Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:37:49 Rare diseases Fatty-acid metabolism disorder Propionic acidemia Carnitine palmitoyltransferase I Biotinidase deficiency Isovaleric acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency 2-Methylbutyryl-CoA dehydrogenase deficiency Health Genetic genealogy Medical genetics
52	Microsoft Word - Rhode Island Insert English FINAL.doc Add to Reading List Source URL: www.nergg.org Language: English - Date: 2007-10-17 09:01:25 Medical genetics Newborn screening Isovaleric acidemia Propionic acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Methylmalonic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Biotinidase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
53	State of Illinois Illinois Department of Public Health Newborn Screening Practitioner’s Manual January 2011 Add to Reading List Source URL: www.idph.state.il.us Language: English - Date: 2011-05-31 16:09:41 Medical tests Mental retardation Medical genetics Epidemiology Newborn screening Maternal and Child Health Bureau Screening Galactosemia 3-Methylcrotonyl-CoA carboxylase deficiency Health Medicine Pediatrics
54	Microsoft Word - Disorder list Jan 10 Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2012-04-12 12:47:40 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Fatty-acid metabolism disorder 3-Methylcrotonyl-CoA carboxylase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Maple syrup urine disease Health Rare diseases Genetic genealogy
55	Hygienic Laboratory The University of Iowa For Questions About Resubmission and Result Interpretation Contact Medical Consultants LABORATORY HOSPITAL Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:38:00 Rare diseases Newborn screening Fatty-acid metabolism disorder Biotinidase deficiency Propionic acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Carnitine palmitoyltransferase I 2-Methylbutyryl-CoA dehydrogenase deficiency Isovaleric acidemia Health Genetic genealogy Medical genetics
56	A Guide for Prenatal Educators This booklet is made possible by & Add to Reading List Source URL: www.babysfirsttest.org Language: English - Date: 2014-03-24 17:53:47 Pediatrics Rare diseases Inborn errors of carbohydrate metabolism B vitamins Epidemiology Newborn screening Phenylketonuria 3-Methylcrotonyl-CoA carboxylase deficiency Galactosemia Health Medicine Genetic genealogy
57	Disease Name 3-methylcrotonyl-CoA carboxylase deficiency Alternate name(s) Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 11:48:25 3-Methylcrotonyl-CoA carboxylase deficiency Rare diseases Coenzymes Newborn screening Methylcrotonyl-CoA carboxylase Hepatology Methylcrotonyl-CoA Carnitine Asymptomatic Health Medicine Pediatrics
58	Microsoft Word - 3MCC.doc Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 04:53:48 3-Methylcrotonyl-CoA carboxylase deficiency Carnitine Rare diseases Amino acid Protein Very long-chain acyl-coenzyme A dehydrogenase deficiency Biotinidase deficiency Health Chemistry Medicine
59	Rhode Island screens babies for 28 health conditions and hearing loss. The conditions are grouped in the categories explained below, and a list of all the conditions is on the other side of this card. Early detection and Add to Reading List Source URL: www.health.ri.gov Language: English - Date: 2014-06-27 15:48:15 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Glutaric aciduria type 1 Biotinidase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Biotin Health Rare diseases Genetic genealogy
60	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

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