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Short-chain dehydrogenase
Results: 32

#	Item
1	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
2	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
3	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
4	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
5	Public Comment to the Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children Add to Reading List Source URL: www.hrsa.gov Language: English - Date: 2014-12-04 01:13:27 Pediatrics Epidemiology Newborn screening Medical tests Screening Short-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
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	WILDLIFE DAMAGE CONTROL PERMIT Add to Reading List Source URL: www.dnr.maryland.gov Language: English - Date: 2014-07-29 13:56:39 Short-chain dehydrogenase Retroviral aspartyl protease Protein domains Peptidase Seventh chords
10	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

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