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Mitochondrial diseases
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21	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
22	Romani research reveals cause for inherited condition Add to Reading List Source URL: medicalxpress.com Language: English - Date: 2014-12-04 03:10:25 Lactic acidosis Mitochondrial disease Mitochondrion Genetic disorder Acidosis Rare diseases Biology Medicine Health
23	Mitochondrial mechanisms of perinatal hypoxic brain injury Ferenc Bari ............................................................................. University of Szeged Faculty of Medicine Add to Reading List Source URL: www.fulbright.hu Language: English - Date: 2012-02-21 11:20:28 Neurotrauma Angiology Cerebrovascular diseases Brain ischemia Stroke Ischemia Glutamate receptor Astrocyte Neuroprotection Biology Medicine Neurology
24	HOPE. ENERGY. LIFE. HOPE. ENERGY. LIFE. HOPE. ENERGY. LIFE. HOPE. ENERGY. LIFE. HOPE. ENERGY. LIFE. HOPE. ENERGY. LIFE Add to Reading List Source URL: www.umdf.org Language: English - Date: 2008-08-29 10:47:09 Mitochondrial diseases Rare diseases Mitochondrion Carnitine Amyotrophic lateral sclerosis Fatigue Dysautonomia Mitochondrial DNA Human mitochondrial genetics Health Biology Medicine
25	Fetal Fatty Acid Oxidation Defects and Maternal Liver Disease in Pregnancy Marsha F. Browning, MD, MPH, Harvey L. Levy, Cecilia Larson, MD, and Vivian E. Shih, MD OBJECTIVE: The objective was to evaluate the relationship Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:40:41 Fatty acids Rare diseases Medical emergencies Metabolism Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Mitochondrial trifunctional protein Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Acute fatty liver of pregnancy Health Medicine Biology
26	Am J Physiol Endocrinol Metab 284: E1098–E1105, 2003. First published February 11, 2003; [removed]ajpendo[removed]Human placenta metabolizes fatty acids: implications for fetal fatty acid oxidation disorders and mat Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:14 Metabolism Fatty acids Developmental biology Fatty-acid metabolism disorder Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Mitochondrial trifunctional protein deficiency Mitochondrial trifunctional protein Rare diseases Medium-chain acyl-coenzyme A dehydrogenase deficiency Biology Health Medicine
27	Figure 2 † Morava et al., 2006 Criteria for Mitochondrial Disorder Section I: Clinical signs and symptoms (1-2 points per sign/symptom as indicated. 4 points max this section) (2 points max this category) Points Add to Reading List Source URL: www.arkansasautismalliance.org Language: English - Date: 2012-09-18 10:12:30 Mitochondrial diseases Cellular respiration Mitochondrion Organelles
28	• Name of therapy: Treatments for Mitochondrial Dysfunction • Add to Reading List Source URL: www.arkansasautismalliance.org Language: English - Date: 2012-09-14 17:11:55 Mitochondrial diseases Dietary supplements Cofactors Mitochondrion Carnitine Lipoic acid Autism spectrum Autism Mitochondrial decay Chemistry Biology Health
29	MS/MS-BASED NEWBORN AND FAMILY SCREENING DETECTS ASYMPTOMATIC PATIENTS WITH VERY-LONG-CHAIN ACYL-COA DEHYDROGENASE DEFICIENCY UTE SPIEKERKOETTER, MD, BIN SUN, MD, THOMAS ZYTKOVICZ, PHD, RONALD WANDERS, PHD, ARNOLD W. STR Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:14 Rare diseases Medium-chain acyl-coenzyme A dehydrogenase deficiency Newborn screening Very long-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Acyl CoA dehydrogenase Phenylketonuria Mitochondrial trifunctional protein Inborn error of lipid metabolism Health Genetic genealogy Medical genetics
30	Tri-Functional Protein (TFP) Deficiency (metabolic condition: fatty acid oxidation disorder) Also known as: • mitochondrial trifunctional protein deficiency • trifunctional enzyme deficiency Add to Reading List Source URL: www.albertahealthservices.ca Language: English - Date: 2013-09-16 18:36:24 Fatty acids Mitochondrial trifunctional protein deficiency Fatty-acid metabolism disorder Hepatology Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Mitochondrial trifunctional protein 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty acid metabolism Medical genetics Medicine Health Rare diseases