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Carnitine palmitoyltransferase I
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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	Information taken from the article “Why Aging Humans Need More Carnitine” by Julius G. Goepp, MD published in Life Extension Magazine Sept 2006 The observation that carnitine makes cultured nerve cells much more sens Add to Reading List Source URL: members.upnaway.com Language: English - Date: 2013-08-06 00:11:17 Dietary supplements Quaternary ammonium compounds Carnitine Diabetic neuropathy Peripheral neuropathy Nerve growth factor Poliomyelitis Retina Carnitine palmitoyltransferase I Acetylcarnitine
4	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
5	ORIGINAL ARTICLE Perilipin 2 Improves Insulin Sensitivity in Skeletal Muscle Despite Elevated Intramuscular Lipid Levels Madeleen Bosma,1 Matthijs K.C. Hesselink,2 Lauren M. Sparks,1 Silvie Timmers,1 Maria João Ferraz, Add to Reading List Source URL: diabetes.diabetesjournals.org Language: English Diabetes Signal transduction Peptide hormones Insulin resistance Insulin Mammalian target of rapamycin FGF21 Carnitine palmitoyltransferase I Skeletal striated muscle Biology Biochemistry Metabolism
6	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
7	Newborn Screening in Canada Status Report – Page 1 of 3 – updated April 18, 2012 ¹Follows format used by the U.S. National Newborn Screening & Genetics Resource Center A dot "" indicates that universal screening Add to Reading List Source URL: raredisorders.ca Language: English - Date: 2012-04-20 11:01:56 Chemistry Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Glutaric aciduria type 1 Thiolase Malonyl-CoA Carnitine palmitoyltransferase I Health Rare diseases Medicine
8	Newborn Screening in Canada Status Report – Page 1 of 3 – updated May 5, 2012 ¹Follows format used by the U.S. National Newborn Screening & Genetics Resource Center A dot "" indicates that universal screening for Add to Reading List Source URL: raredisorders.ca Language: English - Date: 2012-05-07 10:53:44 Chemistry Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Glutaric aciduria type 1 Thiolase Malonyl-CoA Carnitine palmitoyltransferase I Health Rare diseases Medicine
9	PDF Document Add to Reading List Source URL: www.city.sapporo.jp Language: English - Date: 2014-03-10 22:00:22 Newborn screening Propionic acidemia Isovaleric acidemia Methylmalonic acidemia Carnitine palmitoyltransferase I Galactosemia Carnitine Organic acidemia Inborn error of metabolism Health Rare diseases Medicine
10	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