Very long chain fatty acid - PDFSEARCH.IO - Document Search Engine

Very long chain fatty acid
Results: 63

#	Item
31	The design of a diet restricted in saturated very long-chain fatty acids: therapeutic application in adrenoleukodystrophy1 4 MaryAnn Ned Add to Reading List Source URL: ajcn.nutrition.org Language: English Rare diseases Fatty acids Leukodystrophies Adrenoleukodystrophy Very long chain fatty acid Adrenomyeloneuropathy Carnitine BRAT diet Nutrition Health Medicine Peroxisomal disorders
32	Microsoft Word - VLCAD_update_ 2013 Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2013-12-01 02:58:04 Rare diseases Metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Fatty acids Fatty-acid metabolism disorder Carnitine Fatty acid metabolism Newborn screening Acyl CoA dehydrogenase Health Medicine Biology
33	Volume 16, Issue 2 July 2006 fatty oxidation disorder communication network Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:01 Epidemiology Newborn screening Pediatrics Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Fatty acid metabolism Carnitine Mitochondrial trifunctional protein deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Fatty acids
34	Volume 18, Issue 1 Jan 2008 fatty oxidation disorder communication network Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:01 Nutrition Fatty-acid metabolism disorder Diets Newborn screening Inborn error of lipid metabolism Fatty acid metabolism Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Dieting Health Medicine Fatty acids
35	Volume 16, Issue 1 January 2006 fatty oxidation disorder communication network FOD Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:40:38 Hepatology Rare diseases Fatty acids Fatty-acid metabolism disorder Metabolism Carnitine Newborn screening Fatty acid metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Anatomy
36	Volume 15, Issue 1 January 2005 fatty oxidation disorder communication network Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:15 Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Newborn screening Nutrition 9 Very long-chain acyl-coenzyme A dehydrogenase deficiency Insulin Health Medicine Fatty-acid metabolism disorder
37	Microsoft Word - Chart_of_Table_of_Metabolic_Disorders_rev.doc Add to Reading List Source URL: health.hawaii.gov Language: English - Date: 2013-05-30 20:03:03 Rare diseases Fatty-acid metabolism disorder Glutaric aciduria type 1 Very long-chain acyl-coenzyme A dehydrogenase deficiency Carnitine Biotinidase deficiency Biotin Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Genetic genealogy
38	Overview of Newborn Screening for Fatty Acid Oxidation Disorders – For Parents What is newborn screening? Before babies go home from the nursery, they have a small amount of blood taken from their heel to test for a gr Add to Reading List Source URL: www.in.gov Language: English - Date: 2014-10-23 17:39:47 Hepatology Fatty acids Fatty-acid metabolism disorder Fatty acid metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Carnitine palmitoyltransferase I deficiency Carnitine Newborn screening Health Medicine Rare diseases
39	NEWBORN SCREENING FACT SHEET CPT-2 Deficiency (Carnitine Palmitoyl Transferase Deficiency, CACT, Type 2) in infancy. Most people do not have symptoms until their teen years or early adulthood. This is called classic form Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:31:59 Fatty-acid metabolism disorder Hepatology Carnitine Newborn screening Carnitine-acylcarnitine translocase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases
40	NEWBORN SCREENING FACT SHEET MCADD (Medium Chain Acyl-CoA Dehydrogenese Deficiency) What is it? MCADD stands for medium chain acyl-CoA dehydrogenase deficiency. It is one type of Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:32:00 Hypoglycemia Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Inborn errors of carbohydrate metabolism Newborn screening Glycogen storage disease type I Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases