Propionic acidemia - PDFSEARCH.IO - Document Search Engine

Propionic acidemia
Results: 173

#	Item
21	(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
22	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
23	Microsoft Word - PROP.doc Add to Reading List Source URL: health.mo.gov Language: English - Date: 2007-09-14 08:57:50 Medical genetics Propionic acidemia Newborn screening Organic acidemia Methylmalonic acidemia Glutaric acidemia type 2 Health Rare diseases Genetic genealogy
24	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:52:31 Medical genetics Methylmalonic acidemia Newborn screening Organic acidemia Malonyl-CoA decarboxylase deficiency Propionic acidemia Methylmalonyl-CoA mutase deficiency Health Rare diseases Genetic genealogy
25	Microsoft Word - Canada NBS status updated May[removed]doc Add to Reading List Source URL: www.raredisorders.ca Language: English - Date: 2009-06-26 12:21:46 Medicine Coenzymes Metabolism Epidemiology Newborn screening Pediatrics Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Health Rare diseases Chemistry
26	Newborn Screening in Canada Status Report – Page 1 of 3 – updated November 8, 2013 ¹Follows format used by the U.S. National Newborn Screening & Genetics Resource Center A dot "" indicates that universal screenin Add to Reading List Source URL: www.raredisorders.ca Language: English - Date: 2013-11-18 10:15:10 Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Glutaric aciduria type 1 Medical genetics Thiolase Carnitine Malonyl-CoA decarboxylase deficiency Health Rare diseases Medicine
27	Microsoft Word - Canada NBS status Nov23.2006.doc Add to Reading List Source URL: www.raredisorders.ca Language: English - Date: 2009-06-26 12:21:32 Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Hyperammonemia Glutaric aciduria type 1 Thiolase Methylmalonyl-CoA mutase Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
28	Newborn Screening in C anada Status Report ± Page 1 of 3 - updated Dec. 15, 2009 ¹Follows format used by the U.S. National Newborn Screening & Genetics Resource Center A dot "z" indicates that universal screening for t Add to Reading List Source URL: www.raredisorders.ca Language: English - Date: 2010-01-29 12:16:11 Coenzymes Metabolism Biology Newborn screening Propionic acidemia Carnitine Methylmalonic acidemia Glutaric aciduria type 1 Isovaleric acidemia Health Rare diseases Chemistry
29	Microsoft Word - Canada NBS status April[removed]JA.doc Add to Reading List Source URL: www.raredisorders.ca Language: English - Date: 2009-06-26 12:21:38 Chemistry Coenzymes Metabolism Epidemiology Newborn screening Pediatrics Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Health Rare diseases Medicine
30	Newborn Screening in Canada Status Report – Page 1 of 3 – updated June 21, 2013 ¹Follows format used by the U.S. National Newborn Screening & Genetics Resource Center A dot "" indicates that universal screening f Add to Reading List Source URL: www.raredisorders.ca Language: English - Date: 2013-06-27 10:49:23 Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Glutaric aciduria type 1 Medical genetics Thiolase Carnitine Malonyl-CoA decarboxylase deficiency Health Rare diseases Medicine

UPDATE