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Propionic acid
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#	Item
11	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:51:42 Genetic genealogy Glutaric acidemia type 2 Fatty-acid metabolism disorder Glutaric aciduria type 1 Newborn screening Fatty acid metabolism Propionic acidemia Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
12	Isovaleric Acidemia (IVA) An organic acid disorder What is it? Isovaleric Acidemia (also known as IVA) is an inherited organic acid disorder. People with organic acid disorders, like IVA, cannot properly break down certa Add to Reading List Source URL: health.mo.gov Language: English - Date: 2007-09-13 16:17:12 Medical genetics Isovaleric acidemia Newborn screening Organic acidemia Propionic acidemia Methylmalonic acidemia Health Rare diseases Genetic genealogy
13	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:51:01 Medical genetics Methylmalonic acidemia Propionic acidemia Organic acidemia Newborn screening Methylmalonic acid Malonyl-CoA decarboxylase deficiency Vitamin B12 Isovaleric acidemia Health Rare diseases Genetic genealogy
14	(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
15	Microsoft Word - Amino_Acidemias.doc Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 14:35:52 Medical genetics Maple syrup urine disease Glycine encephalopathy Newborn screening Phenylketonuria Amino acid Phenylalanine Organic acidemia Propionic acidemia Health Rare diseases Genetic genealogy
16	Microsoft Word - CA_nbsdisorders[removed]doc Add to Reading List Source URL: www.raredisorders.ca Language: English - Date: 2009-06-26 12:21:18 Medicine Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Glutaric aciduria type 1 Methylmalonyl-CoA mutase Methylmalonic acid Thiolase Health Rare diseases Chemistry
17	National Newborn Screening and Genetics Resource Center Page 1 of 3 - updated October 2, 2006 For consistency this report follows the format used by the U.S. National Newborn Screening & Genetics Resource Center Dot "z" Add to Reading List Source URL: www.raredisorders.ca Language: English - Date: 2009-06-26 12:21:25 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Glutaric aciduria type 1 Methylmalonyl-CoA mutase Methylmalonic acid Thiolase Health Rare diseases Genetic genealogy
18	Long-term Rescue of a Lethal Murine Model of Methylmalonic Acidemia Using Adeno associated Viral Gene Therapy Add to Reading List Source URL: www.oaanews.org Language: English - Date: 2011-08-22 15:08:14 Methylmalonyl-CoA mutase deficiency Methylmalonyl-CoA mutase Vitamin B12 Methylmalonic acid Newborn screening Propionic acidemia Health Rare diseases Methylmalonic acidemia
19	Table of Contents Contents Page What is PA?................................................. 1-6 Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2014-10-06 16:45:49 Rare diseases Propionic acidemia Amino acid Protein Metabolism Acidosis Maple syrup urine disease Glutaric aciduria type 1 Health Medicine Genetic genealogy
20	Microsoft PowerPoint - rinaldolab.ppt Add to Reading List Source URL: www.hrsa.gov Language: English - Date: 2014-12-04 01:13:27 Medical genetics Newborn screening Methylmalonic acidemia Glutaric acidemia type 2 Isovaleric acidemia Propionic acidemia Glutaric aciduria type 1 Maple syrup urine disease Methylmalonic acid Health Rare diseases Genetic genealogy

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