Carnitine - PDFSEARCH.IO - Document Search Engine

Carnitine
Results: 331

#	Item
111	Glutaric Acidemia Type 1 (GA1) (metabolic condition: organic acid disorder) Also known as: • glutaryl-CoA dehydrogenase deficiency • glutaric aciduria type 1 Add to Reading List Source URL: www.albertahealthservices.ca Language: English - Date: 2013-09-16 18:32:33 Pediatrics GA1 Organic acidemia Glutaryl-CoA dehydrogenase Medical genetics Carnitine Inborn error of metabolism Metabolism Medicine Health Glutaric aciduria type 1
112	Medium Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency (metabolic condition: fatty acid oxidation disorder) Also known as: • medium-chain acyl-coenzyme A dehydrogenase deficiency • ACADM deficiency Add to Reading List Source URL: www.albertahealthservices.ca Language: English - Date: 2013-09-16 18:33:57 Fatty acids Fatty-acid metabolism disorder Rare diseases ACADM Medical genetics Hypoglycemia Fatty acid metabolism Carnitine Inborn error of lipid metabolism Medicine Health Medium-chain acyl-coenzyme A dehydrogenase deficiency
113	Newborn_Screening_C8.indd Add to Reading List Source URL: www.mayomedicallaboratories.com Language: English - Date: 2013-09-19 17:08:41 Medium-chain acyl-coenzyme A dehydrogenase deficiency Newborn screening Dicarboxylic acid Carnitine Acyl CoA dehydrogenase Acyl-CoA Inborn error of lipid metabolism Chemistry Health Medicine
114	Nutrition and Mitochondrial Fatty Acid Oxidation Defects Phyllis B. Acosta, DrPH, RD INTRODUCTION Three forms of energy (fuel) are used by the body: glucose, fatty acids and ketone bodies. Glucose, after eating and until Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:17 Medicine Fatty acids Hepatology Fatty acid metabolism Carnitine Lipid Glycogen Triglyceride Acyl-CoA Biology Chemistry Metabolism
115	Newborn_Screening_C5.indd Add to Reading List Source URL: www.mayomedicallaboratories.com Language: English - Date: 2014-10-28 14:23:46 Rare diseases Coenzymes Epidemiology Newborn screening Pediatrics Isovaleryl-CoA Carnitine Urine Health Biology Chemistry
116	Treatment and Emergency Protocol Example For Medium-Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) For Teens and Adults Diagnosis: Medium-Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Clinical Presentation: Vomiting, le Add to Reading List Source URL: fodsupport.org Language: English - Date: 2012-05-31 13:41:17 Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine Medical emergencies Fatty-acid metabolism disorder Systemic primary carnitine deficiency Hypoglycemia Medicine Health Chemistry
117	MEDIUM CHAIN ACYL-COENZYME A DEHYDROGENASE DEFICIENCY (MCADD) Add to Reading List Source URL: www.cpsp.cps.ca Language: English - Date: 2012-10-22 14:28:32 Medium-chain acyl-coenzyme A dehydrogenase deficiency Chemistry Newborn screening Carnitine Health Rare diseases Medicine
118	Treatment of cardiomyopathy and rhabdomyolysis in long-chain fat oxidation disorders using an anaplerotic odd-chain triglyceride Charles R. Roe,1 Lawrence Sweetman,1 Diane S. Roe,1 France David,2 and Henri Brunengraber2 Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:17 Metabolism Fatty acids Rare diseases Coenzymes Cellular respiration Fatty-acid metabolism disorder Carnitine Fatty acid metabolism Beta oxidation Biology Chemistry Health
119	Carnitine Supplementation and VLCAD Deficiency There has been considerable controversy regarding the role of Lcarnitine (Carnitor®, Sigma-Tau Pharmaceuticals, Inc.) and its value as a supplemental therapy in fat oxidati Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:07 Dietary supplements Quaternary ammonium compounds Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine Very long-chain acyl-coenzyme A dehydrogenase deficiency Rare diseases Fatty-acid metabolism disorder Inborn error of lipid metabolism Health Chemistry Medicine
120	doi:[removed]j.ymgme[removed] Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:02 Nutrition Fatty-acid metabolism disorder Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Lipid Beta oxidation Fatty acid metabolism Palmitic acid Essential fatty acid Carnitine Fatty acids Chemistry Biology

UPDATE