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Carnitine-acylcarnitine translocase
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1	Int. J. BiosciInternational Journal of Biosciences (IJB) ISSN: PrintOnline) Vol. 1, No. 6, p, 2011 Add to Reading List Source URL: www.innspub.net Language: English - Date: 2012-07-12 12:21:47 Nutrition Medicine Hepatology Carnitine Acetylcarnitine Systemic primary carnitine deficiency B vitamins Carnitine-acylcarnitine translocase Carnitine palmitoyltransferase I Chemistry Dietary supplements Quaternary ammonium compounds
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	Carnitine/Acylcarnitine Translocase Deficiency (CACT) A fatty acid oxidation disorder What is it? Carnitine/Acylcarnitine Translocase Deficiency (also known as CACT) is an inherited fatty acid oxidation disorder. Patient Add to Reading List Source URL: health.mo.gov Language: English - Date: 2007-09-13 15:09:34 Fatty-acid metabolism disorder Carnitine-acylcarnitine translocase deficiency Carnitine Newborn screening Health Rare diseases Medicine
4	Microsoft Word - mso31.doc Add to Reading List Source URL: health.mo.gov Language: English - Date: 2006-09-11 10:19:50 Rare diseases Systemic primary carnitine deficiency Fatty-acid metabolism disorder Carnitine Newborn screening Fatty acid metabolism Cud Carnitine palmitoyltransferase I deficiency Carnitine-acylcarnitine translocase deficiency Health Medicine Hepatology
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	Table of Contents Contents Page What is MCADD? ........................................ 1-5 Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2014-10-06 16:45:48 Hepatology Medium-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Hypoglycemia Blood sugar Very long-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Health Medicine Diabetes
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	Carnitine Uptake Defect (CUD) (metabolic condition: fatty acid oxidation disorder) Also known as: • carnitine transport defect • renal carnitine transport defect Add to Reading List Source URL: www.albertahealthservices.ca Language: English - Date: 2013-09-16 18:32:15 Systemic primary carnitine deficiency Carnitine Fatty-acid metabolism disorder Fatty acid metabolism Medical genetics Cud Carnitine palmitoyltransferase I deficiency Carnitine-acylcarnitine translocase deficiency Medicine Health Hepatology
9	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
10	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