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Propionic acidemia
Results: 173

#	Item
111	Agency of Human Services Division of Maternal and Child Health Children with Special Health Needs Vermont Newborn Screening Program REFUSAL TO CONSENT TO NEWBORN SCREENING Add to Reading List Source URL: healthvermont.gov Language: English - Date: 2011-07-21 16:18:35 Genetic genealogy Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Biotinidase deficiency Maple syrup urine disease Glutaric aciduria type 1 Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
112	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
113	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
114	Agency of Human Services Division of Maternal and Child Health Children with Special Health Needs Vermont Newborn Screening Program REFUSAL TO CONSENT TO NEWBORN SCREENING Add to Reading List Source URL: www.healthvermont.gov Language: English - Date: 2011-07-21 16:18:35 Genetic genealogy Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Biotinidase deficiency Maple syrup urine disease Glutaric aciduria type 1 Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
115	Arizona Administrative Register / Secretary of State Notices of Final Rulemaking NOTICES OF FINAL RULEMAKING The Administrative Procedure Act requires the publication of the final rules of the state’s agencies. Final r Add to Reading List Source URL: azdhs.gov Language: English - Date: 2014-05-29 18:43:12 Pediatrics Newborn screening Biotinidase deficiency Methylmalonic acidemia Congenital hypothyroidism Propionic acidemia Galactosemia Health care provider 3-Methylcrotonyl-CoA carboxylase deficiency Health Medicine Rare diseases
116	2011 Newborn Screening data as of August 2012.xlsx Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2012-09-04 18:41:39 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Glutaric aciduria type 1 Medium-chain acyl-coenzyme A dehydrogenase deficiency Biotinidase deficiency Maple syrup urine disease Health Rare diseases Genetic genealogy
117	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
118	2009 Summary including hearing.xlsx Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2012-04-12 12:46:56 Medical genetics Propionic acidemia Isovaleric acidemia Methylmalonic acidemia Biotinidase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Thiolase Multiple carboxylase deficiency Thalassemia Health Rare diseases Genetic genealogy
119	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
120	2012 NBS Data--Final.xlsx Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2014-02-19 10:12:57 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Glutaric aciduria type 1 Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Thiolase Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy

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