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Systemic primary carnitine deficiency
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1	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
2	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
3	What is Carnitine ? Nelson LS Tang, MBChB, FRCPA Associate Professor Department of Chemical Pathology The Chinese University of Hong Kong Add to Reading List Source URL: www.cpy.cuhk.edu.hk Language: English - Date: 2014-07-15 07:47:36 Chemistry Systemic primary carnitine deficiency Carnitine Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Fatty acid metabolism B vitamins Dicarboxylic acid Carnitine palmitoyltransferase II deficiency Medicine Hepatology Health
4	Possible causes of an elevated CK Cardiac muscle Infarction Myopathy Myocarditis Add to Reading List Source URL: protocols.sonichealthcare.com Language: English - Date: 2014-04-08 19:21:47 Myopathy Dermatomyositis Myositis Polymyositis Myoglobinuria Systemic primary carnitine deficiency Health Anatomy Hepatology
5	physician fact sheet Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency (MCAD) Dr Janice Fletcher, MD, FRACP, BSc, Clinical Geneticist (HGSA), FRCPA Add to Reading List Source URL: www.wch.sa.gov.au Language: English - Date: 2009-03-30 00:40:37 Rare diseases Medium-chain acyl-coenzyme A dehydrogenase deficiency Hypoglycemia Systemic primary carnitine deficiency Newborn screening Carnitine ACADM Ketotic hypoglycemia Hyperammonemia Health Medicine Hepatology
6	fact sheet for parents Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency (MCAD) D r J a n i c e F l e t c h e r , MD, FRACP, BSC, Clinical Geneticist (HGSA), FRCPA Add to Reading List Source URL: www.wch.sa.gov.au Language: English - Date: 2009-03-30 00:40:37 Hepatology Rare diseases Medium-chain acyl-coenzyme A dehydrogenase deficiency Fatty acids ACADM Carnitine Newborn screening Systemic primary carnitine deficiency Hypoglycemia Health Medicine Biology
7	Microsoft Word - pocket facts.docx Add to Reading List Source URL: ndhealth.gov Language: English - Date: 2011-12-12 15:42:57 Rare diseases Pediatrics Inborn errors of carbohydrate metabolism Hepatology Epidemiology Newborn screening Very long-chain acyl-coenzyme A dehydrogenase deficiency Systemic primary carnitine deficiency Mitochondrial trifunctional protein deficiency Health Medicine Genetic genealogy
8	RESEARCH NOTE The importance of molecular diagnosis in the accurate diagnosis of systemic carnitine deficiency TOSHIAKI HITOMI1,a, NORIO MATSUURA1,a, YOSUKE SHIGEMATSU2, YOSHIYUKI OKANO3, ERI SHINOZAKI4, MASAHIKO KAWAI5, Add to Reading List Source URL: www.ias.ac.in Language: English - Date: 2014-10-27 08:11:23 Chemistry Rare diseases Dietary supplements Quaternary ammonium compounds Systemic primary carnitine deficiency Carnitine SLC22A5 Newborn screening Health Medicine Hepatology
9	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
10	Facts About Metabolic Diseases of Muscle Add to Reading List Source URL: mdausa.org Language: English - Date: 2011-09-19 18:46:04 Hepatology Genetic genealogy Rare diseases Glycogen storage disease type V Phosphofructokinase deficiency Glycogen storage disease Systemic primary carnitine deficiency Myopathy Myalgia Health Medicine Inborn errors of carbohydrate metabolism