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Short-chain fatty acid
Results: 19

#	Item
1	Discovery of organic acids in deep marine environments from ODP pore waters Janet A. Haggerty, Department of Geosciences, University of Tulsa, and J. Berton Fisher, Gardere & Wynne, L.L.P. Pore waters collected from thr Add to Reading List Source URL: www.odplegacy.org Language: English - Date: 2014-09-04 08:44:56 Plate tectonics Forearc Guyot Sedimentary rock Organic acid Short-chain fatty acid
2	Medium chain acyl-CoA Dehydrogenase Deficiency (MCADD) Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 10:02:30 Hepatology Metabolism Fatty acids Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Short-chain acyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases
3	Microsoft Word - VLCAD.doc Add to Reading List Source URL: health.mo.gov Language: English - Date: 2007-09-14 09:09:50 Medical genetics Fatty-acid metabolism disorder Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Newborn screening Fatty acid metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Short-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
4	Microsoft Word - SCAD.doc Add to Reading List Source URL: health.mo.gov Language: English - Date: 2007-09-14 09:00:00 Fatty-acid metabolism disorder Newborn screening Fatty acid metabolism Short-chain acyl-coenzyme A dehydrogenase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
5	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
6	Microsoft Word - SCADD update 2011.doc Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2011-04-27 16:22:45 Chemistry Fatty-acid metabolism disorder Newborn screening Short-chain acyl-coenzyme A dehydrogenase deficiency Acyl CoA dehydrogenase ACADS Carnitine Very long-chain acyl-coenzyme A dehydrogenase deficiency Fatty acid metabolism Health Rare diseases Medicine
7	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
8	Eur J Pediatr DOI[removed]s00431[removed]SHORT REPORT Post-mortem MRI reveals CPT2 deficiency after sudden Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:06 Hepatology Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Sudden infant death syndrome Fatty-acid metabolism disorder Carnitine palmitoyltransferase I deficiency Carnitine-acylcarnitine translocase Fatty liver Carnitine Health Medicine Rare diseases
9	NEWBORN SCREENING FACT SHEET SCADD (Short Chain Acyl-CoA Dehydrogenese Deficiency) What is it? SCADD stands for short chain acyl-CoA dehydrogenase deficiency. It is one type of Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-20 12:54:56 Rare diseases Epidemiology Newborn screening Pediatrics Fatty-acid metabolism disorder Inborn errors of carbohydrate metabolism Screening Biotinidase deficiency Phenylketonuria Health Medicine Genetic genealogy
10	Disease Name 2-METHYLBUTYRYL-CoA DEHYDROGENASE DEFICIENCY (2MBCD) (SHORT/BRANCHED CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY; 2METHYLBUTYRYLGLYCINURIA) Organic aciduria and fatty acid oxidation defect. Classification: Inher Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:35:43 2-Methylbutyryl-CoA dehydrogenase deficiency 2-Methylbutyryl-CoA Newborn screening Hypoglycemia Carnitine Health Medicine Rare diseases