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Translocase
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#	Item
11	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
12	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
13	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
14	Microsoft Word - CAT_update_2013 Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2013-12-01 02:16:23 Chemistry Carnitine-acylcarnitine translocase deficiency Fatty-acid metabolism disorder Carnitine Translocase Newborn screening Inborn error of lipid metabolism Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
15	NEWBORN SCREENING FACT SHEET CPT-2 Deficiency (Carnitine Palmitoyl Transferase Deficiency, CACT, Type 2) in infancy. Most people do not have symptoms until their teen years or early adulthood. This is called classic form Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:31:59 Fatty-acid metabolism disorder Hepatology Carnitine Newborn screening Carnitine-acylcarnitine translocase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases
16	NEWBORN SCREENING FACT SHEET LCHADD (Long Chain 3-Hydroxyacyl-CoA Dehydrogenese Deficiency) What is it? LCHADD stands for long chain 3-hydroxyacylCoA dehydrogenase deficiency. It is one type of fatty acid oxidation disor Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:31:59 Fatty-acid metabolism disorder Hepatology Hypoglycemia Mitochondrial trifunctional protein deficiency Carnitine Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Newborn screening Adipose tissue Carnitine-acylcarnitine translocase deficiency Health Medicine Rare diseases
17	` NEWBORN SCREENING FACT SHEET VLCADD (Very Long Chain Acyl-CoA Dehydrogenese Deficiency) It is common for babies and children with the Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:32:01 Very long-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Hepatology Hypoglycemia Carnitine Newborn screening Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Glycogen storage disease type I Health Medicine Rare diseases
18	Disease Name CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY (CACT) (SOLUTE CARRIER FAMILY 25 (CARNITINE/ACYLCARNITINE TRANSLOCASE), MEMBER 20; CARNITINE-ACYLCARNITINE CARRIER; CACT DEFICIENCY) Fatty acid oxidation defect Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:35:55 Chemistry Rare diseases Carnitine-acylcarnitine translocase deficiency Translocase Carnitine Hyperammonemia Ketotic hypoglycemia Hypoglycemia Carnitine palmitoyltransferase II deficiency Health Medicine Solute carrier family
19	Microsoft Word - cpt2_ref Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:36:03 Biology Carnitine palmitoyltransferase I Carnitine CPT2 Fatty-acid metabolism disorder Myoglobinuria Fatty acid metabolism Carnitine-acylcarnitine translocase deficiency Inborn error of lipid metabolism Medicine Hepatology Health
20	Microsoft Word - cact_ref Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:35:55 Chemistry Rare diseases Fatty acids Hepatology Carnitine Translocase Fatty-acid metabolism disorder Fatty acid metabolism Newborn screening Biology Solute carrier family Health

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