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Medium-chain acyl-coenzyme A dehydrogenase deficiency
Results: 161

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31	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
32	Microsoft Word - Isobut update 2011.doc Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2011-06-21 21:44:19 Rare diseases Isobutyryl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Newborn screening Carnitine Biotinidase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Genetic genealogy Medical genetics
33	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
34	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
35	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
36	FOD FAMILY SUPPORT GROUP Deb Lee Gould, MEd, Director MISSION ♥ CREATE AWARENESS & EDUCATE the Public & Professionals about Fatty Oxidation Add to Reading List Source URL: fodsupport.org Language: English - Date: 2012-05-31 13:40:55 Fatty-acid metabolism disorder Newborn screening Carnitine Hypoglycemia Blood sugar Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases
37	MEDIUM CHAIN ACYL-COENZYME A DEHYDROGENASE DEFICIENCY (MCADD) Add to Reading List Source URL: www.cpsp.cps.ca Language: English - Date: 2012-10-22 14:28:34 Hematology Medical emergencies Transfusion reactions Blood products Transfusion related acute lung injury Transfusion medicine Acute lung injury Blood plasma Sepsis Medicine Anatomy Health
38	A rough guide to Acylcarnitines Roy Talbot & Nigel Manning [removed] Dept. of Clinical Chemistry, Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:07 Tandem mass spectrometry Medium-chain acyl-coenzyme A dehydrogenase deficiency Triple quadrupole mass spectrometer CH2 Quadrupole mass analyzer Gas chromatography–mass spectrometry Acyl-CoA Electrospray ionization Coenzyme A Chemistry Mass spectrometry Carnitine
39	Microsoft Word - May_13__05_Just_a_Simple_Blood_Test_-_Toronto_Star.doc Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:16 Rare diseases Epidemiology Newborn screening Medical tests Phenylketonuria Medium-chain acyl-coenzyme A dehydrogenase deficiency Medical genetics Screening Infant Medicine Health Pediatrics
40	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

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