Methylcrotonyl-CoA carboxylase - PDFSEARCH.IO - Document Search Engine

Methylcrotonyl-CoA carboxylase
Results: 68

#	Item
31	(ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY; IVA; IVD) Add to Reading List Source URL: health.tn.gov 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
32	Amino Acid Disorders Information for Parents  Overview Amino acid disorders are a group of rare, inherited conditions that affect infants from birth. They are caused by enzymes that do not work properly. Protein is ma Add to Reading List Source URL: www.kdheks.gov Language: English - Date: 2013-09-05 15:51:35 Genetic genealogy Newborn screening Phenylketonuria Maple syrup urine disease Amino acid Protein 3-Methylcrotonyl-CoA carboxylase deficiency Organic acidemia Health Medicine Rare diseases
33	Newborn Screening for Biotinidase Deficiency Add to Reading List Source URL: www.kdheks.gov Language: English - Date: 2012-02-06 15:23:10 Medicine Biotinidase Rare diseases Biotin Newborn screening Biotin deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Health Genetics Biotinidase deficiency
34	Baby is Home! KIDSNET All babies born in Rhode Island are enrolled in KIDSNET, the Rhode Island information system that helps families and doctors make sure that Add to Reading List Source URL: www.nergg.org Language: English - Date: 2012-04-06 15:58:29 Genetic genealogy Newborn screening Phenylketonuria Methylmalonic acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Biotinidase deficiency Propionic acidemia Isovaleric acidemia Health Rare diseases Medicine
35	STATE OF NEW HAMPSHIRE DEPARTMENT OF HEALTH AND HUMAN SERVICES Nicholas A. Toumpas Commissioner Add to Reading List Source URL: www.dhhs.state.nh.us Language: English - Date: 2014-08-08 09:16:27 Newborn screening Propionic acidemia Methylmalonic acidemia Acyl CoA dehydrogenase Medium-chain acyl-coenzyme A dehydrogenase deficiency Malonyl-CoA decarboxylase deficiency Isovaleric acidemia Carnitine palmitoyltransferase I 3-Methylcrotonyl-CoA carboxylase deficiency Health Rare diseases Medicine
36	Microsoft Word - mso20.doc Add to Reading List Source URL: www.health.mo.gov Language: English - Date: 2007-09-14 08:02:14 Rare diseases Hypermethioninemia Newborn screening Medical genetics 2-Methylbutyryl-CoA dehydrogenase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Medicine Health Genetic genealogy
37	Organic Acid Disorders Information for Parents  Overview Add to Reading List Source URL: www.kdheks.gov Language: English - Date: 2013-09-05 15:51:36 Medical genetics Newborn screening 3-Methylcrotonyl-CoA carboxylase deficiency Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Organic acidemia Beta-ketothiolase deficiency Multiple carboxylase deficiency Health Rare diseases Genetic genealogy
38	Disease Name 3-methylcrotonyl-CoA carboxylase deficiency Alternate name(s) Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-12 06:23:51 3-Methylcrotonyl-CoA carboxylase deficiency Rare diseases Coenzymes Newborn screening Methylcrotonyl-CoA carboxylase Hepatology Methylcrotonyl-CoA Carnitine Asymptomatic Health Medicine Pediatrics
39	Microsoft Word - 3MCC.doc Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-09 15:58:40 3-Methylcrotonyl-CoA carboxylase deficiency Carnitine Rare diseases Amino acid Protein Very long-chain acyl-coenzyme A dehydrogenase deficiency Biotinidase deficiency Health Chemistry Medicine
40	Rhode Island screens babies for 28 health conditions and hearing loss. The conditions are grouped in the categories explained below, and a list of all the conditions is on the other side of this card. Early detection and Add to Reading List Source URL: health.ri.gov Language: English - Date: 2014-06-27 15:48:15 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Glutaric aciduria type 1 Biotinidase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Biotin Health Rare diseases Genetic genealogy

UPDATE