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Translocase
Results: 51

#	Item
21	Microsoft Word - CPT2_update_2013 Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2013-12-01 02:35:36 Rare diseases Chemistry Fatty-acid metabolism disorder Fatty acids Carnitine Newborn screening Fatty acid metabolism Carnitine palmitoyltransferase II deficiency Carnitine-acylcarnitine translocase deficiency Health Medicine Hepatology
22	Disorders Detected By Mississippi Genetic Newborn Screening Secondary Conditions Methylmalonic acidemia with homocystinuria Malonic acidemia Isobutyrylglycinuria Add to Reading List Source URL: msdh.ms.gov Language: English - Date: 2012-03-28 12:35:21 Medical genetics Newborn screening Methylmalonic acidemia Glutaric aciduria type 1 Propionic acidemia Isovaleric acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency Glutaric acidemia type 2 Carnitine-acylcarnitine translocase deficiency Health Rare diseases Genetic genealogy
23	Microsoft Word - CPT2 update, 2011.doc Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2011-05-26 16:26:05 Rare diseases Chemistry Fatty-acid metabolism disorder Fatty acids Carnitine Newborn screening Fatty acid metabolism Carnitine palmitoyltransferase II deficiency Carnitine-acylcarnitine translocase deficiency Health Medicine Hepatology
24	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: www.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
25	Carnitine Palmitoyl Transferase 2 Deficiency (CPT2) / Carnitine Acylcarnitine Translocase Deficiency (CACT) What is a positive newborn screen? Newborn screening is done on tiny samples of blood taken from your baby’s h Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 21:09:48 Rare diseases Hepatology CPT2 Carnitine palmitoyltransferase II deficiency Solute carrier family Carnitine-acylcarnitine translocase deficiency Carnitine O-palmitoyltransferase Carnitine Newborn screening Health Medicine Biology
26	Microsoft Word[removed]Condition list.doc Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2014-09-16 08:12:01 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
27	Microsoft Word - RCPU Newborn Screening.doc Add to Reading List Source URL: www.peds.ufl.edu Language: English - Date: 2007-12-31 10:54:00 Rare diseases Newborn screening Inborn error of lipid metabolism Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Inborn error of metabolism Medical genetics Carnitine-acylcarnitine translocase deficiency Isovaleric acidemia Health Medicine Biology
28	Microsoft Word - mso31.doc Add to Reading List Source URL: www.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
29	Microsoft Word - FAOD.doc Add to Reading List Source URL: health.tn.gov 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
30	Medium chain acyl-CoA Dehydrogenase Deficiency (MCADD) Add to Reading List Source URL: health.tn.gov 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

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