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Isobutyryl-coenzyme A dehydrogenase deficiency
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1	IMD Program List of Disorders, Covered Drugs, Supplements and Specialty Foods Add to Reading List Source URL: www.health.gov.on.ca Language: English - Date: 2016-03-07 08:48:57 Health Medicine Rare diseases Clinical medicine Malonyl-CoA decarboxylase deficiency Glutaric aciduria type 1 Isobutyryl-coenzyme A dehydrogenase deficiency Isovaleric acidemia Inborn error of metabolism Hyperammonemia 2-Methylbutyryl-CoA dehydrogenase deficiency Newborn screening
2	-0031 PEDIATRIC RESEARCH Copyright © 2011 International Pediatric Research Foundation, Inc. Vol. 70, No. 1, 2011 Printed in U.S.A. Add to Reading List Source URL: www.ibms.sinica.edu.tw Language: English - Date: 2015-08-05 05:36:02 Biology Metabolism Cellular respiration Biochemistry Fatty acids Carnitine palmitoyltransferase I Isobutyryl-coenzyme A dehydrogenase deficiency ACAD8 Mitochondrion Beta oxidation ACADL
3	Microsoft Word - Isobut update 2011.doc Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2011-06-21 21:44:19 Rare diseases Isobutyryl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Newborn screening Carnitine Biotinidase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Genetic genealogy Medical genetics
4	Overview of Newborn Screening for Amino Acid Disorders – 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 con Add to Reading List Source URL: www.in.gov Language: English - Date: 2014-10-22 10:08:32 Amino acid Maple syrup urine disease Phenylketonuria Newborn screening Urea cycle disorder Protein Metabolism Hypermethioninemia Isobutyryl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases
5	Overview of Newborn Screening for MCAD Deficiency (MCADD) – For Parents What is newborn screening? What are the symptoms of MCADD? Before babies go home from the nursery, they Add to Reading List Source URL: www.in.gov Language: English - Date: 2014-10-23 17:39:45 Medium-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Newborn screening Hypoglycemia Fatty acid metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Isobutyryl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases
6	Overview of Newborn Screening for 3-MCC Deficiency – For Parents What is newborn screening? What are the symptoms of 3-MCC deficiency? Before babies go home from the nursery, they Add to Reading List Source URL: www.in.gov Language: English - Date: 2014-10-23 17:39:41 Rare diseases 3-Methylcrotonyl-CoA carboxylase deficiency Newborn screening Biotinidase deficiency Isobutyryl-coenzyme A dehydrogenase deficiency Health Genetic genealogy Medical genetics