Hydroxyacyl-Coenzyme A dehydrogenase

Results: 114



#Item
11Fatty-acid metabolism disorder / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Carnitine-acylcarnitine translocase deficiency / Short-chain acyl-coenzyme A dehydrogenase deficiency / Fatty acid metabolism / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Mitochondrial trifunctional protein deficiency / Newborn screening / Lipid / Health / Medicine / Rare diseases

Microsoft Word - FAOD.doc

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Source URL: health.state.tn.us

Language: English - Date: 2007-05-01 14:47:24
12Newborn screening / Methylmalonic acidemia / Propionic acidemia / Isovaleric acidemia / Hyperammonemia / Glutaric aciduria type 1 / Thiolase / Methylmalonyl-CoA mutase / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Medicine

Microsoft Word - Canada NBS status Nov23.2006.doc

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Source URL: www.raredisorders.ca

Language: English - Date: 2009-06-26 12:21:32
13Genetic genealogy / Newborn screening / Carnitine / Fatty-acid metabolism disorder / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Glutaric aciduria type 1 / Methylmalonic acidemia / Glutaric acidemia type 2 / Acyl CoA dehydrogenase / Health / Rare diseases / Medicine

Delaware Division of Public Health Newborn Screening Program Disorder Name & Abbreviation Analyte / Marker Endocrine Disorder

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Source URL: www.dhss.delaware.gov

Language: English - Date: 2012-07-26 14:33:28
14Fatty acids / Rare diseases / Medical emergencies / Metabolism / Fatty-acid metabolism disorder / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Mitochondrial trifunctional protein / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Acute fatty liver of pregnancy / Health / Medicine / Biology

Fetal Fatty Acid Oxidation Defects and Maternal Liver Disease in Pregnancy Marsha F. Browning, MD, MPH, Harvey L. Levy, Cecilia Larson, MD, and Vivian E. Shih, MD OBJECTIVE: The objective was to evaluate the relationship

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Source URL: www.fodsupport.org

Language: English - Date: 2012-05-31 13:40:41
15Metabolism / Fatty acids / Developmental biology / Fatty-acid metabolism disorder / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Mitochondrial trifunctional protein deficiency / Mitochondrial trifunctional protein / Rare diseases / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Biology / Health / Medicine

Am J Physiol Endocrinol Metab 284: E1098–E1105, 2003. First published February 11, 2003; [removed]ajpendo[removed]Human placenta metabolizes fatty acids: implications for fetal fatty acid oxidation disorders and mat

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Source URL: www.fodsupport.org

Language: English - Date: 2012-05-31 13:41:14
16Hepatology / Fatty-acid metabolism disorder / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Carnitine-acylcarnitine translocase deficiency / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Carnitine / Short-chain acyl-coenzyme A dehydrogenase deficiency / Newborn screening / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Health / Medicine / Rare diseases

To Request More Information: Please answer the following questions and mail to Deb at the address below. I am a:

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Source URL: www.fodsupport.org

Language: English - Date: 2012-05-31 13:40:36
17Mitochondrial trifunctional protein / Proteins / Thiolase / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Medium-chain acyl-coenzyme A dehydrogenase deficiency / NADH dehydrogenase / Newborn screening / HADHB / D-bifunctional protein deficiency / Biology / Health / Genetics

Articles in Press, Published on November 19, 2003 as[removed]PDR[removed][removed][removed]PEDIATRIC RESEARCH Copyright © 2003 International Pediatric Research Foundation, Inc. Vol. 55, No. 2, 2003

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Source URL: www.fodsupport.org

Language: English - Date: 2012-05-31 13:41:14
18Coenzymes / Fatty acids / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Carnitine / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Coenzyme A / Lipid / Inborn error of lipid metabolism / Fatty-acid metabolism disorder / Chemistry / Metabolism / Biology

My Experiences and Understanding of VLCAD Deficiency and its Treatment Charles R. Roe, MD June 26, 2011 (Now retired) This  disorder  is  characterized  by  the  deficiency  of  the  VLCAD  

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Source URL: www.fodsupport.org

Language: English - Date: 2012-05-31 13:41:07
19Diabetes / Hypoglycemia / Blood sugar / Carnitine / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Insulin / Hyperglycemia / Glycogen storage disease type I / Fatty-acid metabolism disorder / Medicine / Endocrine system / Health

LCHAD EMERGENCY CARE PROTOCOL NOTE OF CAUTION: Please check with your healthcare professionals regarding this protocol sheet. To Whom It May Concern: Page 1 of 2

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Source URL: fodsupport.org

Language: English - Date: 2012-05-31 13:41:16
20Medicine / Mitochondrial trifunctional protein deficiency / Mitochondrial trifunctional protein / Thiolase / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Hydroxyacyl-Coenzyme A dehydrogenase / Cytochrome P450 reductase / Fatty-acid metabolism disorder / Mutation / Biology / Health / HADHB

HUMAN MUTATION 21:598^[removed]RESEARCH ARTICLE Molecular and Phenotypic Heterogeneity in Mitochondrial Trifunctional Protein Deficiency

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Source URL: www.fodsupport.org

Language: English - Date: 2012-05-31 13:41:14
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