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3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Results: 111

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11	Delaware Division of Public Health Newborn Screening Program Disorder Name & Abbreviation Analyte / Marker Endocrine Disorder Add to Reading List Source URL: www.dhss.delaware.gov Language: English - Date: 2012-07-26 14:33:28 Genetic 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
12	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 Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:40:41 Fatty 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
13	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 Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:14 Metabolism 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
14	To Request More Information: Please answer the following questions and mail to Deb at the address below. I am a: Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:40:36 Hepatology 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
15	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 Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:14 Mitochondrial 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
16	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 Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:07 Coenzymes 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
17	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 Add to Reading List Source URL: fodsupport.org Language: English - Date: 2012-05-31 13:41:16 Diabetes 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
18	HUMAN MUTATION 21:598^[removed]RESEARCH ARTICLE Molecular and Phenotypic Heterogeneity in Mitochondrial Trifunctional Protein Deficiency Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:14 Medicine 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
19	Microsoft Word - FS_039.2_HELLP AFLP and FAOs_ED.doc Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:07 HELLP syndrome Acute fatty liver of pregnancy Pre-eclampsia Fatty-acid metabolism disorder Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Complications of pregnancy Pregnancy Eclampsia Medicine Health Medical emergencies
20	PRENATAL DIAGNOSIS Prenat Diagn 2001; 21: 52±54. INVITED COMMENTARY: CURRENT ISSUES IN OBSTETRICS AND GENETICS Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:15 Medicine Coenzymes Fatty acids Inborn error of lipid metabolism Fatty-acid metabolism disorder Fatty acid metabolism Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Carnitine Very long-chain acyl-coenzyme A dehydrogenase deficiency Biology Chemistry Metabolism