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Hydroxyacyl-Coenzyme A dehydrogenase
Results: 114

#	Item
21	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
22	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
23	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
24	MISSION FOD FAMILY SUPPORT GROUP Deb Lee Gould, MEd, Director ♥ CREATE AWARENESS & EDUCATE the Public & Professionals about Fatty Oxidation Add to Reading List Source URL: fodsupport.org Language: English - Date: 2012-05-31 13:40:54 Biology Fatty-acid metabolism disorder Newborn screening Carnitine-acylcarnitine translocase deficiency Carnitine-acylcarnitine translocase Very long-chain acyl-coenzyme A dehydrogenase deficiency Carnitine Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Systemic primary carnitine deficiency Health Medicine Rare diseases
25	Maine Newborn Screening Program List of Conditions Each baby born in Maine is screened for the conditions listed below. This list is correct as of July 1, 2008 but may change as conditions are added to or removed from th Add to Reading List Source URL: www.maine.gov Language: English - Date: 2011-11-10 05:38:14 Medical genetics Newborn screening Hyperammonemia 3-Methylcrotonyl-CoA carboxylase deficiency Isovaleric acidemia Glutaric acidemia type 2 Glutaric aciduria type 1 Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
26	doi:[removed]j.ymgme[removed] Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:40:41 Diets Nutrition Diabetes Proteins Obesity Leptin Insulin resistance Fatty-acid metabolism disorder Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Medicine Biology
27	Long Chain 3-Hydroxyacyl-CoA Dehydrogenase (LCHAD) Deficiency (metabolic condition: fatty acid oxidation disorder) Also known as: • long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency • long-chain 3-OH acy Add to Reading List Source URL: www.albertahealthservices.ca Language: English - Date: 2013-09-16 18:33:43 Fatty acids Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Mitochondrial trifunctional protein deficiency 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Hydroxyacyl-Coenzyme A dehydrogenase Fatty acid metabolism Mitochondrial trifunctional protein ACADL Health Chemistry Medicine
28	ABSTRACT: Mitochondrial trifunctional protein (TFP) deﬁciency is a rare disorder of the fatty acid ␤-oxidation cycle with heterogeneous phenotypes and occurs secondary to either ␣- or ␤-subunit mutations. We char Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:17 Rare diseases Hepatology Mitochondrial trifunctional protein Proteins Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty acids HADHB Hydroxyacyl-Coenzyme A dehydrogenase Mitochondrial trifunctional protein deficiency Health Medicine Genetic genealogy
29	doi:[removed]j.ymgme[removed] Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:40:41 Exercise physiology Amino acids Dietary supplements Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Mitochondrial trifunctional protein Fatty-acid metabolism disorder Carnitine Anaerobic exercise Physical exercise Chemistry Medicine Health
30	LCHAD…or is it… TFP? : An Update Jamal A. Ibdah, MD, PhD Associate Professor in Internal Medicine/Gastroenterology, Pediatrics and Biochemistry Wake Forest University School of Medicine Winston-Salem, NC Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:18 Mitochondrial trifunctional protein deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Health Medicine Acute fatty liver of pregnancy