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Acyl CoA dehydrogenase
Results: 122

#	Item
1	Newborn Screening Year in Review 86,586 For Babies Born in 2013 Bloodspot Samples Received Initial Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2015-01-29 18:14:10 Newborn screening Isovaleric acidemia Methylmalonic acidemia Acyl CoA dehydrogenase Biotinidase deficiency Galactosemia Methylmalonic acid Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Guthrie test Health Rare diseases Medicine
2	Timeliness of Newborn Screening – DACHDNC’s laboratory standards and procedures subcommittee draft findings Add to Reading List Source URL: www.hrsa.gov Language: English Medical genetics Newborn screening Isovaleric acidemia Propionic acidemia Methylmalonic acidemia Fatty-acid metabolism disorder Very long-chain acyl-coenzyme A dehydrogenase deficiency Galactosemia Malonyl-CoA decarboxylase deficiency Health Rare diseases Genetic genealogy
3	Newborn Screening Year in Review 86,586 For Babies Born in 2013 Bloodspot Samples Received Initial Add to Reading List Source URL: azdhs.gov Language: English - Date: 2015-01-29 18:14:10 Newborn screening Isovaleric acidemia Methylmalonic acidemia Acyl CoA dehydrogenase Biotinidase deficiency Galactosemia Methylmalonic acid Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Guthrie test Health Rare diseases Medicine
4	Disorders and Reference Ranges Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2014-12-15 13:01:02 Medical genetics Newborn screening Isovaleric acidemia Methylmalonic acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Acyl CoA dehydrogenase Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
5	Disorders and Reference Ranges Add to Reading List Source URL: azdhs.gov Language: English - Date: 2014-12-15 13:01:02 Medical genetics Newborn screening Isovaleric acidemia Methylmalonic acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Acyl CoA dehydrogenase Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
6	Missouri Newborn Screening Disorders Tested Biotinidase deficiency (BIOT) Classical galactosemia (GALT) Congenital adrenal hyperplasia (CAH) Congenital primary hypothyroidism (CH) Cystic fibrosis (CF) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2013-07-10 12:04:01 Rare diseases Newborn screening Methylmalonic acidemia Thiolase Propionic acidemia Isovaleric acidemia Malonyl-CoA Glutaric aciduria type 1 Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Genetic genealogy Medical genetics
7	Medium chain acyl-CoA Dehydrogenase Deficiency (MCADD) Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 10:02:30 Hepatology Metabolism Fatty acids Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Short-chain acyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases
8	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:52:41 Fatty-acid metabolism disorder Mitochondrial trifunctional protein deficiency Newborn screening Fatty acid metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Malonyl-CoA decarboxylase deficiency Health Medicine Rare diseases
9	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:52:02 Rare diseases 3-Methylcrotonyl-CoA carboxylase deficiency Newborn screening Methylcrotonyl-CoA carboxylase Biotinidase deficiency Propionic acidemia Health Genetic genealogy Medical genetics
10	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:51:33 Newborn screening Thiolase Organic acidemia Beta-ketothiolase deficiency Propionic acidemia Health Rare diseases Medicine

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