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Isovaleric acidemia
Results: 160

#	Item
51	Newborn Screening Annual Report SFY12 Newborn Screening in Arkansas SFY12 Report of Results from July 1, 2011 – June 30, 2012 Child and Adolescent Health Section Add to Reading List Source URL: www.healthy.arkansas.gov Language: English - Date: 2014-07-17 12:11:10 Rare diseases Newborn screening Galactosemia Screening Congenital adrenal hyperplasia Galactose-1-phosphate uridylyltransferase deficiency Biotinidase deficiency Isovaleric acidemia Phenylketonuria Health Medicine Pediatrics
52	Microsoft Word - Vermont Insert English FINAL.doc Add to Reading List Source URL: nergg.org Language: English - Date: 2008-04-01 13:39:57 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Maple syrup urine disease Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
53	Microsoft Word - Pilot Project Add to Reading List Source URL: health.hawaii.gov Language: English - Date: 2013-04-30 21:57:10 Epidemiology Newborn screening Isovaleric acidemia Health Rare diseases Pediatrics
54	Newborn Screening in Arkansas SFY11 Report of Results from July 1, 2010 – June 30, 2011 Child and Adolescent Health Section Family Health Branch Arkansas Department of Health Add to Reading List Source URL: www.healthy.arkansas.gov Language: English - Date: 2014-07-17 12:11:09 Pediatrics Inborn errors of carbohydrate metabolism Mental retardation Epidemiology Newborn screening Screening Galactose-1-phosphate uridylyltransferase deficiency Isovaleric acidemia Biotinidase deficiency Health Medicine Rare diseases
55	Microsoft Word - Haitian_Rhode_Island_insert.doc Add to Reading List Source URL: nergg.org Language: English - Date: 2007-10-17 09:01:30 Medical genetics Isovaleric acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylcrotonyl-CoA Very long-chain acyl-coenzyme A dehydrogenase deficiency Acyl CoA dehydrogenase Acyl-CoA dehydrogenase Methylmalonic acidemia Health Rare diseases Genetic genealogy
56	Microsoft Word - Haitian_Maine_Insert.doc Add to Reading List Source URL: nergg.org Language: English - Date: 2007-10-17 09:00:32 Rare diseases Isovaleric acidemia Glutaric acidemia type 2 Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Glutaric aciduria type 1 Acyl CoA dehydrogenase Very long-chain acyl-coenzyme A dehydrogenase deficiency Propionic acidemia Health Genetic genealogy Medical genetics
57	Microsoft Word - Vermont_Haitian_Insert.doc Add to Reading List Source URL: nergg.org Language: English - Date: 2008-04-01 13:43:08 Medical genetics Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Methylmalonic acid Maple syrup urine disease Acyl CoA dehydrogenase Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Acyl-CoA dehydrogenase Health Rare diseases Genetic genealogy
58	Microsoft Word - Vermont_Russian_Insert.doc Add to Reading List Source URL: nergg.org Language: English - Date: 2008-04-01 13:42:54 Medical genetics Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Maple syrup urine disease Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylmalonic acid Very long-chain acyl-coenzyme A dehydrogenase deficiency Newborn screening Health Rare diseases Genetic genealogy
59	Overview of Newborn Screening for Organic Acidemias – For Parents What is newborn screening? Before babies go home from the nursery, they have a small amount of blood taken from their heel to test for a group of condit Add to Reading List Source URL: www.in.gov Language: English - Date: 2014-10-22 10:08:32 Genetic genealogy Isovaleric acidemia Newborn screening Organic acidemia Glutaric aciduria type 1 Methylmalonic acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Metabolism Acidosis Health Rare diseases Medicine
60	Disorders Detected By Mississippi Genetic Newborn Screening Secondary Conditions Methylmalonic acidemia with homocystinuria Malonic acidemia Isobutyrylglycinuria Add to Reading List Source URL: msdh.ms.gov Language: English - Date: 2012-03-28 12:35:21 Medical genetics Newborn screening Methylmalonic acidemia Glutaric aciduria type 1 Propionic acidemia Isovaleric acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency Glutaric acidemia type 2 Carnitine-acylcarnitine translocase deficiency Health Rare diseases Genetic genealogy

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