Carnitine palmitoyltransferase I deficiency - PDFSEARCH.IO - Document Search Engine

Carnitine palmitoyltransferase I deficiency
Results: 23

#	Item
1	-0031 PEDIATRIC RESEARCH Copyright © 2011 International Pediatric Research Foundation, Inc. Vol. 70, No. 1, 2011 Printed in U.S.A. Add to Reading List Source URL: www.ibms.sinica.edu.tw Language: English - Date: 2015-08-05 05:36:02 Biology Metabolism Cellular respiration Biochemistry Fatty acids Carnitine palmitoyltransferase I Isobutyryl-coenzyme A dehydrogenase deficiency ACAD8 Mitochondrion Beta oxidation ACADL
2	There is a lot of research information available now on carnitine, that wasn’t around when we first started looking at carnitine supplementation for polios in 1994 and recording carnitine blood levels via PMH. Answers Add to Reading List Source URL: members.upnaway.com Language: English - Date: 2013-08-06 00:11:00 Medicine Chemistry Health Hepatology Dietary supplements Quaternary ammonium compounds Fatty acids Carnitine Systemic primary carnitine deficiency Beta oxidation Triglyceride Carnitine palmitoyltransferase I
3	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
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	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
6	Fatty acid oxidation is important for immune cell function: The NIH MINI Study receives additional funding to study immune function Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2014-07-23 04:41:27 Immunology Fatty acids Very long-chain acyl-coenzyme A dehydrogenase deficiency Lipid Metabolism Carnitine palmitoyltransferase I T cells Immune system Fatty-acid metabolism disorder Medicine Health Biology
7	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
8	Overview of Newborn Screening for Fatty Acid Oxidation Disorders – For Parents What is newborn screening? Before babies go home from the nursery, they have a small amount of blood taken from their heel to test for a gr Add to Reading List Source URL: www.in.gov Language: English - Date: 2014-10-23 17:39:47 Hepatology Fatty acids Fatty-acid metabolism disorder Fatty acid metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Carnitine palmitoyltransferase I deficiency Carnitine Newborn screening Health Medicine Rare diseases
9	Disease Name CARNITINE PALMITOYL TRANSFERASE I DEFICIENCY (CPT1) (CARNITINE PALMITOYLTRANSFERASE IA DEFICIENCY; CPT I DEFICIENCY; CPT DEFICIENCY, HEPATIC, TYPE I) Fatty acid oxidation defect Classification: Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:36:02 Rare diseases Fatty acids Carnitine palmitoyltransferase I Carnitine Hypoglycemia Ketotic hypoglycemia Acute fatty liver of pregnancy Newborn screening Fatty acid metabolism Medicine Health Hepatology
10	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