Thiolase - PDFSEARCH.IO - Document Search Engine

Thiolase
Results: 55

#	Item
11	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:51:33 Newborn screening Thiolase Organic acidemia Beta-ketothiolase deficiency Propionic acidemia Health Rare diseases Medicine
12	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
13	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
14	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
15	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
16	Newborn Screening in Canada Status Report – Page 1 of 3 – updated April 18, 2012 ¹Follows format used by the U.S. National Newborn Screening & Genetics Resource Center A dot "" indicates that universal screening Add to Reading List Source URL: raredisorders.ca Language: English - Date: 2012-04-20 11:01:56 Chemistry Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Glutaric aciduria type 1 Thiolase Malonyl-CoA Carnitine palmitoyltransferase I Health Rare diseases Medicine
17	Newborn Screening in Canada Status Report – Page 1 of 3 - updated Nov. 11, 2010 ¹Follows format used by the U.S. National Newborn Screening & Genetics Resource Center A dot "" indicates that universal screening for Add to Reading List Source URL: www.raredisorders.ca Language: English - Date: 2010-11-11 13:21:56 Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Hyperammonemia Glutaric aciduria type 1 Thiolase Maple syrup urine disease Methylmalonyl-CoA mutase Health Rare diseases Medicine
18	Newborn Screening in Canada Status Report – Page 1 of 3 – updated May 5, 2012 ¹Follows format used by the U.S. National Newborn Screening & Genetics Resource Center A dot "" indicates that universal screening for Add to Reading List Source URL: raredisorders.ca Language: English - Date: 2012-05-07 10:53:44 Chemistry Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Glutaric aciduria type 1 Thiolase Malonyl-CoA Carnitine palmitoyltransferase I Health Rare diseases Medicine
19	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
20	doi:[removed]j.ymgme[removed] Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:40:39 Medicine ACADS Fatty-acid metabolism disorder Malonyl-CoA decarboxylase deficiency Newborn screening Acyl CoA dehydrogenase Acyl-CoA Carnitine Thiolase Health Rare diseases Chemistry

UPDATE