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Translocase
Results: 51

#	Item
31	Disease Name Carnitine uptake deficiency Alternate name(s) Acronym Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-11 04:12:31 Systemic primary carnitine deficiency Dietary supplements Quaternary ammonium compounds Carnitine Fatty-acid metabolism disorder Medical genetics Cardiomyopathy Carnitine-acylcarnitine translocase Medicine Health Hepatology
32	PARENT FACT SHEET DISORDER Carnitine uptake defect (CUD) CAUSE CUD occurs when an enzyme, called “carnitine transporter” (CT), is either missing or not working properly. Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-11 03:22:03 Chemistry Dietary supplements Quaternary ammonium compounds Carnitine Systemic primary carnitine deficiency Hypoglycemia Carnitine palmitoyltransferase I deficiency Carnitine-acylcarnitine translocase deficiency Medicine Health Hepatology
33	STATE OF TENNESSEE DEPARTMENT OF HEALTH DIVISION OF LABORATORY SERVICES NEWBORN SCREENING PROGRAM Add to Reading List Source URL: health.tn.gov Language: English - Date: 2011-02-25 12:37:37 Medical genetics Fatty-acid metabolism disorder Newborn screening Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Hyperammonemia Carnitine Isovaleric acidemia Health Rare diseases Genetic genealogy
34	Newborn Screening Program Disorders Add to Reading List Source URL: health.utah.gov Language: English - Date: 2013-07-08 12:47:26 Genetic genealogy Fatty-acid metabolism disorder Newborn screening Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Propionic acidemia Malonyl-CoA decarboxylase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
35	2008 Life Sciences Away Day Add to Reading List Source URL: workspace.imperial.ac.uk Language: English - Date: 2011-07-14 10:10:55 Translocase Membrane biology Membrane proteins Solute carrier family
36	Microsoft Word - FINALDisordersDetectableTable42511 Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2014-08-13 12:31:27 Rare diseases Newborn screening Carnitine-acylcarnitine translocase deficiency Fatty-acid metabolism disorder Carnitine Phenylketonuria Glutaric aciduria type 1 Systemic primary carnitine deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Genetic genealogy
37	STATE OF TENNESSEE DEPARTMENT OF HEALTH DIVISION OF LABORATORY SERVICES NEWBORN SCREENING PROGRAM Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2011-02-25 12:37:37 Medical genetics Fatty-acid metabolism disorder Newborn screening Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Hyperammonemia Carnitine Isovaleric acidemia Health Rare diseases Genetic genealogy
38	Microsoft Word[removed]Condition list.doc Add to Reading List Source URL: ndhealth.gov Language: English - Date: 2012-08-28 15:52:15 Medical genetics Hyperammonemia Glutaric aciduria type 1 Isovaleric acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Propionic acidemia Fatty-acid metabolism disorder Carnitine-acylcarnitine translocase deficiency Health Rare diseases Genetic genealogy
39	PARENT FACT SHEET DISORDER Carnitine uptake defect (CUD) CAUSE CUD occurs when an enzyme, called “carnitine transporter” (CT), is either missing or not working properly. Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-08 20:00:05 Chemistry Dietary supplements Quaternary ammonium compounds Carnitine Systemic primary carnitine deficiency Hypoglycemia Carnitine palmitoyltransferase I deficiency Carnitine-acylcarnitine translocase deficiency Medicine Health Hepatology
40	Disease Name Carnitine uptake deficiency Alternate name(s) Acronym Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-08 19:16:40 Systemic primary carnitine deficiency Dietary supplements Quaternary ammonium compounds Carnitine Fatty-acid metabolism disorder Medical genetics Cardiomyopathy Carnitine-acylcarnitine translocase Medicine Health Hepatology

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