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Isovaleric acidemia
Results: 160

#	Item
101	State AZ Person completing form Sondi Aponte, Quality Improvement Mgr. Add to Reading List Source URL: azdhs.gov Language: English - Date: 2012-04-12 12:46:53 Rare diseases Metabolism Coenzymes Hemoglobins Methylmalonic acidemia Isovaleric acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency Malonyl-CoA Carnitine Health Biology Medicine
102	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
103	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
104	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
105	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
106	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
107	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
108	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
109	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
110	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

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