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Propionic acidemia
Results: 173

#	Item
101	2012 NBS Data--Final.xlsx Add to Reading List Source URL: 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
102	2011 Newborn Screening data as of August 2012.xlsx Add to Reading List Source URL: 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
103	Arizona Department of Health Services Newborn Screening Program MSMS Pilot Project – Secondary Markers Amino Acid Disorders Analytes Add to Reading List Source URL: 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
104	2009 Summary including hearing.xlsx Add to Reading List Source URL: 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
105	Agency of Human Services Division of Maternal and Child Health Children with Special Health Needs Vermont Newborn Screening Program REFUSAL TO CONSENT to REPEAT 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 Maple syrup urine disease Glutaric aciduria type 1 Biotinidase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
106	Agency of Human Services Division of Maternal and Child Health Children with Special Health Needs Vermont Newborn Screening Program REFUSAL TO CONSENT to REPEAT 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 Maple syrup urine disease Glutaric aciduria type 1 Biotinidase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
107	National Newborn Screening Status Report Updated[removed]The U.S. National Screening Status Report lists the status of newborn screening in the United States. Add to Reading List Source URL: genes-r-us.uthscsa.edu Language: English - Date: 2012-07-09 12:55:31 Newborn screening Methylmalonic acidemia Propionic acidemia Glutaric aciduria type 1 Isovaleric acidemia Hyperammonemia Methylmalonyl-CoA mutase Thiolase Carnitine Health Rare diseases Medicine
108	Newborn Screening Program Disorders Add to Reading List Source URL: health.utah.gov Language: English - Date: 2013-07-08 12:47:26 Genetic genealogy Fatty-acid metabolism disorder Newborn screening Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Propionic acidemia Malonyl-CoA decarboxylase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
109	Microsoft Word - ND_Disorder List[removed]doc Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2013-07-08 13:17:03 Medical genetics Newborn screening Methylmalonic acidemia Isovaleric acidemia Glutaric aciduria type 1 Fatty-acid metabolism disorder Propionic acidemia Glutaric acidemia type 2 Carnitine Health Rare diseases Genetic genealogy
110	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

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