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Carnitine
Results: 331

#	Item
61	An Interpretive Analysis of Hospice Underutilization by Mexican-Americans in Lansing, Michigan: En Sus Propias Palabras (In Their Own Words) by Lisa M. Topoleski Add to Reading List Source URL: www.jsri.msu.edu Language: English - Date: 2013-06-20 09:56:32 Autism Autism spectrum Developmental neuroscience Developmental psychology Neurological disorders Pervasive developmental disorders Carnitine Leaky gut syndrome Medicine Health Psychiatry
62	doi:[removed]mehd.v23i0.19260 Add to Reading List Source URL: psychology.uwo.ca Language: English - Date: 2012-08-28 08:55:08 Autism Autism spectrum Developmental neuroscience Developmental psychology Neurological disorders Pervasive developmental disorders Carnitine Leaky gut syndrome Medicine Health Psychiatry
63	Medium chain acyl-CoA Dehydrogenase Deficiency (MCADD) Add to Reading List Source URL: health.state.tn.us 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
64	Volume 6, Issue 3 October 2011 State of Tennessee Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2011-10-04 10:57:09 Health sciences Pediatrics Epidemiology Newborn screening Medical specialties Amino acid Organic acidemia Maple syrup urine disease Carnitine Health Medicine Rare diseases
65	Microsoft Word - Parent MCAD.doc Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2008-05-30 09:44:30 Biology Medium-chain acyl-coenzyme A dehydrogenase deficiency Fatty acids Fatty-acid metabolism disorder Hepatology ACADM Newborn screening Fatty acid metabolism Carnitine Health Medicine Rare diseases
66	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: 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
67	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
68	Disorder Marker Abnormal Range “ > ” means “is greater than” “ < ” means “is less than” CUD Free Carnitine (C0) < 12 umol/L Add to Reading List Source URL: health.mo.gov - Date: 2011-12-05 18:05:33
69	Microsoft Word - CPT-11.doc Add to Reading List Source URL: health.mo.gov Language: English - Date: 2007-09-13 15:39:40 Hepatology Chemistry Fatty-acid metabolism disorder Fatty acids Fatty acid metabolism Carnitine O-palmitoyltransferase Carnitine Newborn screening Carnitine palmitoyltransferase II deficiency Health Medicine Rare diseases
70	Microsoft Word - FAOD.doc Add to Reading List Source URL: health.state.tn.us 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

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