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Methylmalonyl-CoA mutase
Results: 18

#	Item
1	LIGAND Chemical Database for Enzymatic Reactions: A Link between enzyme structures and chemical reactions Takaaki Nishioka 1 Add to Reading List Source URL: www.jsbi.org Language: English - Date: 1998-01-09 02:50:19 Chemistry Metabolism Biology Biochemistry Enzymes Catalysis Chemical reaction Cofactor Methylmalonyl-CoA mutase Protein Metabolic pathway KEGG
2	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
3	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
4	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
5	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
6	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
7	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
8	METABOLIC/SICKLE CELL SCREENING GUIDELINES As mandated by KRS[removed], Newborn Screening tests include: Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-12-04 13:18:40 Medical genetics Newborn screening Methylmalonic acidemia Glutaric aciduria type 1 Galactosemia Methylmalonyl-CoA mutase deficiency Phenylketonuria Isovaleric acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
9	Microsoft Word - MMA update 2011.doc Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2011-07-11 21:19:31 Vitamin B12 Methylmalonic acidemia Methylmalonic acid Newborn screening Methylmalonyl-CoA mutase Hydroxocobalamin Acidosis Propionic acidemia Maple syrup urine disease Health Rare diseases Medicine
10	Methylmalonic Acidemia (MMA) (metabolic condition: organic acid disorder) Also known as: • methylmalonic aciduria • adenosylcobalamin deficiency Add to Reading List Source URL: www.albertahealthservices.ca Language: English - Date: 2013-09-16 18:34:05 Vitamin B12 Methylmalonic acidemia Methylmalonic acid Methylmalonyl-CoA mutase Megaloblastic anemia Medical genetics Organic acidemia Metabolism Newborn screening Medicine Health Rare diseases

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