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Mitochondrial trifunctional protein
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1	Microsoft Word - pocket facts.docx Add to Reading List Source URL: ndhealth.gov Language: English - Date: 2011-12-12 15:42:57 Rare diseases Pediatrics Inborn errors of carbohydrate metabolism Hepatology Epidemiology Newborn screening Very long-chain acyl-coenzyme A dehydrogenase deficiency Systemic primary carnitine deficiency Mitochondrial trifunctional protein deficiency Health Medicine Genetic genealogy
2	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
3	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:51:53 Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty acids Fatty-acid metabolism disorder Acute fatty liver of pregnancy Hepatology Newborn screening Fatty acid metabolism Mitochondrial trifunctional protein Health Medicine Rare diseases
4	Microsoft Word - FAOD.doc Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 14:47:24 Fatty-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
5	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
6	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
7	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
8	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
9	MS/MS-BASED NEWBORN AND FAMILY SCREENING DETECTS ASYMPTOMATIC PATIENTS WITH VERY-LONG-CHAIN ACYL-COA DEHYDROGENASE DEFICIENCY UTE SPIEKERKOETTER, MD, BIN SUN, MD, THOMAS ZYTKOVICZ, PHD, RONALD WANDERS, PHD, ARNOLD W. STR Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:14 Rare diseases Medium-chain acyl-coenzyme A dehydrogenase deficiency Newborn screening Very long-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Acyl CoA dehydrogenase Phenylketonuria Mitochondrial trifunctional protein Inborn error of lipid metabolism Health Genetic genealogy Medical genetics
10	Tri-Functional Protein (TFP) Deficiency (metabolic condition: fatty acid oxidation disorder) Also known as: • mitochondrial trifunctional protein deficiency • trifunctional enzyme deficiency Add to Reading List Source URL: www.albertahealthservices.ca Language: English - Date: 2013-09-16 18:36:24 Fatty acids Mitochondrial trifunctional protein deficiency Fatty-acid metabolism disorder Hepatology Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Mitochondrial trifunctional protein 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty acid metabolism Medical genetics Medicine Health Rare diseases

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