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Glutaric acidemia type 2
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1	IMD Program List of Disorders, Covered Drugs, Supplements and Specialty Foods Add to Reading List Source URL: www.health.gov.on.ca Language: English - Date: 2016-03-07 08:48:57 Health Medicine Rare diseases Clinical medicine Malonyl-CoA decarboxylase deficiency Glutaric aciduria type 1 Isobutyryl-coenzyme A dehydrogenase deficiency Isovaleric acidemia Inborn error of metabolism Hyperammonemia 2-Methylbutyryl-CoA dehydrogenase deficiency Newborn screening
2	Microsoft Word - mso8C.doc Add to Reading List Source URL: health.mo.gov Language: English - Date: 2007-11-28 16:03:24 Medical genetics Glutaric aciduria type 1 Newborn screening Organic acidemia Glutaric acidemia type 2 Propionic acidemia Health Rare diseases Genetic genealogy
3	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:51:42 Genetic genealogy Glutaric acidemia type 2 Fatty-acid metabolism disorder Glutaric aciduria type 1 Newborn screening Fatty acid metabolism Propionic acidemia Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
4	VI. Metabolic Formulas Formulas for WIC participants with metabolic conditions are available according to physician prescription. All metabolic formulas must be prescribed by a licensed health care provider prior to issu Add to Reading List Source URL: www.maine.gov Language: English - Date: 2014-10-02 08:03:50 Medical genetics Nutricia North America Glutaric aciduria type 1 Glutaric acidemia type 2 Maple syrup urine disease Isovaleric acidemia Phenylketonuria Inborn error of metabolism Numico Health Medicine Rare diseases
5	Microsoft Word - PROP.doc Add to Reading List Source URL: health.mo.gov Language: English - Date: 2007-09-14 08:57:50 Medical genetics Propionic acidemia Newborn screening Organic acidemia Methylmalonic acidemia Glutaric acidemia type 2 Health Rare diseases Genetic genealogy
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	Delaware Division of Public Health Newborn Screening Program Disorder Name & Abbreviation Analyte / Marker Endocrine Disorder Add to Reading List Source URL: www.dhss.delaware.gov Language: English - Date: 2012-07-26 14:33:28 Genetic genealogy Newborn screening Carnitine Fatty-acid metabolism disorder Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Glutaric aciduria type 1 Methylmalonic acidemia Glutaric acidemia type 2 Acyl CoA dehydrogenase Health Rare diseases Medicine
8	Microsoft PowerPoint - rinaldolab.ppt Add to Reading List Source URL: www.hrsa.gov Language: English - Date: 2014-12-04 01:13:27 Medical genetics Newborn screening Methylmalonic acidemia Glutaric acidemia type 2 Isovaleric acidemia Propionic acidemia Glutaric aciduria type 1 Maple syrup urine disease Methylmalonic acid Health Rare diseases Genetic genealogy
9	SERGG/Region 3 Long Term Follow-Up, An Overview Presented by: Rani Singh, PhD, RD The Health/Disease Continuum & Nutrition Intervention for NBS Add to Reading List Source URL: www.hrsa.gov Language: English - Date: 2014-12-04 01:13:24 Medical genetics Newborn screening Methylmalonic acidemia Glutaric acidemia type 2 Isovaleric acidemia Glutaric aciduria type 1 Propionic acidemia Fatty-acid metabolism disorder Maple syrup urine disease Health Rare diseases Genetic genealogy
10	Microsoft Word - GA-2_update_2013 Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2013-11-28 02:24:58 Rare diseases Metabolism Pediatrics Glutaric acidemia type 2 Glutaric aciduria type 1 Hepatology Newborn screening Fatty-acid metabolism disorder Inborn error of metabolism Health Medicine Genetic genealogy

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