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Propionic acid
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51	Vermont routinely screens newborns for 29 conditions. They are: • • • • Add to Reading List Source URL: healthvermont.gov Language: English - Date: 2011-07-21 16:18:35 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Methylmalonic acid Glutaric aciduria type 1 3-Methylcrotonyl-CoA carboxylase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
52	Vermont routinely screens newborns for 29 conditions. They are: • • • • Add to Reading List Source URL: www.healthvermont.gov Language: English - Date: 2011-07-21 16:18:35 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Methylmalonic acid Glutaric aciduria type 1 3-Methylcrotonyl-CoA carboxylase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
53	Disorders screened for by the CT Newborn Screening Program Add to Reading List Source URL: www.ct.gov Language: English - Date: 2007-07-09 15:51:44 Rare diseases Newborn screening Fatty-acid metabolism disorder Hyperammonemia Glutaric aciduria type 1 Glutaric acidemia type 2 Propionic acidemia Isovaleric acidemia Biotinidase deficiency Health Genetic genealogy Medical genetics
54	Microsoft Word - MoD Fact Sheet 2011 Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2012-04-12 12:46:55 Medical genetics Newborn screening Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylmalonic acid Maple syrup urine disease Acyl CoA dehydrogenase Health Rare diseases Genetic genealogy
55	Arizona Department of Health Services Newborn Screening Program MSMS Pilot Project – Secondary Markers Amino Acid Disorders Analytes Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2013-07-03 16:56:45 Methylmalonic acidemia Newborn screening Isovaleric acidemia Methylmalonic acid Acyl CoA dehydrogenase Maple syrup urine disease Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Rare diseases Propionic acidemia
56	NEWBORN SCREENING CONFIRMED CASE REPORT PRIMARY PANEL OF 29 DISORDERS DOB[removed] – [removed]Disorder Abbreviation Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2012-04-12 12:46:51 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Maple syrup urine disease Medium-chain acyl-coenzyme A dehydrogenase deficiency Methylmalonic acid Health Rare diseases Genetic genealogy
57	California Department of Public Health Genetic Disease Screening Program Newborn Screening Program i Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2014-08-13 12:31:27 Rare diseases Newborn screening Fatty-acid metabolism disorder Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Glutaric aciduria type 1 Hyperammonemia Thalassemia Health Genetic genealogy Medical genetics
58	HEEL STICK NEWS RAISING AWARENESS OF IOWA NEONATAL METABOLIC SCREENING PROGRAM (INMSP) OCTOBER 2003 “I like to think of Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:37:22 Rare diseases Pediatrics Newborn screening Galactosemia Fatty-acid metabolism disorder Inborn error of metabolism Biotinidase deficiency Propionic acidemia Hyperammonemia Health Medicine Genetic genealogy
59	Hygienic Laboratory The University of Iowa For Questions About Resubmission and Result Interpretation Contact Medical Consultants LABORATORY HOSPITAL Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:37:50 Rare diseases Fatty-acid metabolism disorder Propionic acidemia Carnitine palmitoyltransferase I Biotinidase deficiency Isovaleric acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency 2-Methylbutyryl-CoA dehydrogenase deficiency Health Genetic genealogy Medical genetics
60	Hygienic Laboratory The University of Iowa For Questions About Resubmission and Result Interpretation Contact Medical Consultants LABORATORY HOSPITAL Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:37:49 Rare diseases Fatty-acid metabolism disorder Propionic acidemia Carnitine palmitoyltransferase I Biotinidase deficiency Isovaleric acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency 2-Methylbutyryl-CoA dehydrogenase deficiency Health Genetic genealogy Medical genetics

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