Coenzyme A

Results: 370



#Item
201Newborn screening / Pediatrics / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Medical genetics / Screening / Tandem mass spectrometry / Phenylketonuria / Fatty-acid metabolism disorder / March of Dimes / Medicine / Health / Epidemiology

Genomics and Population Health: United States 2003

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Source URL: www.cdc.gov

Language: English - Date: 2009-06-23 14:22:13
202Rare diseases / Epidemiology / Newborn screening / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Phenylketonuria / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Short-chain acyl-coenzyme A dehydrogenase deficiency / Inborn error of metabolism / Galactosemia / Health / Medicine / Pediatrics

CHAPTER 31 PDF p. 1 of 1 CHAPTER 31 (SB 31)

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Source URL: www.lrc.state.ky.us

Language: English - Date: 2001-05-18 14:22:18
203Epidemiology / Newborn screening / Pediatrics / Short-chain acyl-coenzyme A dehydrogenase deficiency / Infant / Screening / Health / Rare diseases / Medicine

Short-chain acyl-CoA Dehydrogenase Deficiency (SCAD) What is a positive newborn screen? Newborn screening is done on tiny samples of blood taken from your baby’s heel 24 to 36 hours after birth. The blood is tested for

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Source URL: www.michigan.gov

Language: English - Date: 2012-12-07 14:06:00
204Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Newborn screening / Mitochondrial trifunctional protein deficiency / Fatty-acid metabolism disorder / Mitochondrial trifunctional protein / Health / Medicine / Rare diseases

Long-chain L-3-hydroxy acyl-CoA Dehydrogenase Deficiency (LCHAD) Trifunctional Protein Deficiency (TFP) What is a positive newborn screen? Newborn screening is done on tiny samples of blood taken from your baby’s heel

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Source URL: www.michigan.gov

Language: English - Date: 2012-12-07 10:42:23
205Medical genetics / Hyperammonemia / Glutaric aciduria type 1 / Isovaleric acidemia / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Methylmalonic acidemia / Propionic acidemia / Fatty-acid metabolism disorder / Carnitine-acylcarnitine translocase deficiency / Health / Rare diseases / Genetic genealogy

Microsoft Word[removed]Condition list.doc

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Source URL: www.ndhealth.gov

Language: English - Date: 2014-09-16 08:12:01
206Medium-chain acyl-coenzyme A dehydrogenase deficiency / Newborn screening / Infancy / Screening / Infant / Health / Medicine / Pediatrics

Medium-Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) What is a positive newborn screen? Newborn screening is done on tiny samples of blood taken from your baby’s heel 24 to 36 hours after birth. The blood is tested fo

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Source URL: www.michigan.gov

Language: English - Date: 2012-12-07 14:13:24
207Rare diseases / Newborn screening / Inborn error of lipid metabolism / Fatty-acid metabolism disorder / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Inborn error of metabolism / Medical genetics / Carnitine-acylcarnitine translocase deficiency / Isovaleric acidemia / Health / Medicine / Biology

Microsoft Word - RCPU Newborn Screening.doc

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Source URL: www.peds.ufl.edu

Language: English - Date: 2007-12-31 10:54:00
208Newborn screening / Isovaleric acidemia / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Methylmalonic acidemia / Propionic acidemia / Short-chain acyl-coenzyme A dehydrogenase deficiency / 3-Methylcrotonyl-CoA carboxylase deficiency / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Glutaric aciduria type 1 / Health / Medicine / Rare diseases

CHAPTER 66 PDF p. 1 of 3 CHAPTER 66 (SB 24)

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Source URL: www.lrc.ky.gov

Language: English - Date: 2005-07-07 13:26:35
209Newborn screening / Infant / Screening / Health / Medicine / Very long-chain acyl-coenzyme A dehydrogenase deficiency

Very-Long Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD) What is a positive newborn screen? Newborn screening is done on tiny samples of blood taken from your baby’s heel 24 to 36 hours after birth. The blood is teste

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Source URL: www.michigan.gov

Language: English - Date: 2012-12-07 10:38:10
210Medicine / Carnitine / Newborn screening / Short-chain acyl-coenzyme A dehydrogenase deficiency / Acyl-CoA / Inborn error of lipid metabolism / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Chemistry

Minnesota Department of Health[removed]SCAD

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Source URL: www.health.state.mn.us

Language: English - Date: 2014-04-04 11:40:23
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