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Orphanet Journal of Rare Diseases, ISSN 1750-1172, 02/2015, Volume 10, Issue 1, pp. 21 - 21
Journal Article
Acta Paediatrica, ISSN 0803-5253, 12/2016, Volume 105, Issue 12, pp. 1451 - 1460
Journal Article
Acta Paediatrica, ISSN 0803-5253, 05/2016, Volume 105, Issue 5, pp. 549 - 554
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 2002, Volume 110, Issue 2, pp. 259 - 269
The current dietary treatment of long-chain fatty acid oxidation defects (high carbohydrate with medium-even-chain triglycerides and reduced amounts of... 
Index Medicus | Abridged Index Medicus
Journal Article
European Journal of Paediatric Neurology, ISSN 1090-3798, 2015, Volume 20, Issue 1, pp. 38 - 44
Abstract Background The neonatal screening and early start of the dietary therapy have improved the outcome of long-chain 3-hydroxyacyl-CoA dehydrogenase... 
Pediatrics | Neurology | Fatty acid oxidation disorders | Inborn errors of metabolism | Mitochondrial fatty acid β-oxidation | Polyneuropathy | DEFECTS | MITOCHONDRIAL TRIFUNCTIONAL PROTEIN | FATTY-ACID OXIDATION | CLINICAL PRESENTATION | Mitochondrial fatty acid beta-oxidation | OPTIMAL DIETARY THERAPY | PIGMENTARY RETINOPATHY | PEDIATRICS | CLINICAL NEUROLOGY | Peripheral Nervous System Diseases - diagnosis | Lipid Metabolism, Inborn Errors - diet therapy | Lipid Metabolism, Inborn Errors - genetics | Age Factors | Follow-Up Studies | Humans | Middle Aged | Child, Preschool | Male | Peripheral Nervous System Diseases - physiopathology | Neonatal Screening | Nervous System Diseases - genetics | Young Adult | Cardiomyopathies - genetics | Electrodiagnosis | Rhabdomyolysis - diet therapy | Adult | Female | Electromyography | Diet Therapy | Child | Infant, Newborn | Mitochondrial Trifunctional Protein - genetics | Peripheral Nervous System Diseases - etiology | Cardiomyopathies - diet therapy | Nervous System Diseases - diet therapy | Mutation - genetics | Mitochondrial Myopathies - diet therapy | Disease Progression | Mitochondrial Myopathies - genetics | Rhabdomyolysis - genetics | Adolescent | Age of Onset | Patient Compliance | Mitochondrial Trifunctional Protein - deficiency | Medicine, Experimental | Medical research | Metabolites | Fatty acids | Medical imaging equipment | Neurophysiology | Index Medicus
Journal Article
Cardiology Journal, ISSN 1897-5593, 2017, Volume 24, Issue 1, pp. 101 - 104
FOLLOW-UP | DEFECTS | CARDIAC & CARDIOVASCULAR SYSTEMS | DILATED CARDIOMYOPATHY | Lipid Metabolism, Inborn Errors - mortality | Lipid Metabolism, Inborn Errors - genetics | Arrhythmias, Cardiac - mortality | Humans | Child, Preschool | Rhabdomyolysis - complications | Male | Rhabdomyolysis - mortality | Cardiomyopathy, Hypertrophic - therapy | Child | Cardiomyopathy, Dilated - mortality | Genetic Predisposition to Disease | Arrhythmias, Cardiac - therapy | Risk Factors | Nervous System Diseases - diet therapy | Nervous System Diseases - complications | Phenotype | Diet, Fat-Restricted | Adolescent | Arrhythmias, Cardiac - diagnosis | Lipid Metabolism, Inborn Errors - complications | Mutation | Cardiomyopathy, Dilated - therapy | Mitochondrial Trifunctional Protein - deficiency | Lipid Metabolism, Inborn Errors - diet therapy | Mitochondrial Trifunctional Protein, alpha Subunit - genetics | Infant | Nervous System Diseases - genetics | Cardiomyopathies - genetics | Rhabdomyolysis - diet therapy | Cardiomyopathies - mortality | Female | Mitochondrial Myopathies - mortality | Cardiomyopathy, Hypertrophic - diagnostic imaging | Cardiomyopathy, Hypertrophic - etiology | Mitochondrial Trifunctional Protein - genetics | Nervous System Diseases - mortality | Cardiomyopathies - diet therapy | Mitochondrial Myopathies - complications | Treatment Outcome | Arrhythmias, Cardiac - etiology | Mitochondrial Myopathies - diet therapy | Triglycerides - administration & dosage | Cardiomyopathy, Dilated - diagnostic imaging | Cardiomyopathy, Hypertrophic - mortality | Mitochondrial Myopathies - genetics | Cardiomyopathy, Dilated - etiology | Rhabdomyolysis - genetics | Cardiomyopathies - complications | Index Medicus
Journal Article
Journal of Inherited Metabolic Disease, ISSN 0141-8955, 3/2015, Volume 38, Issue 2, pp. 315 - 322
Children with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHAD) have a defect in the degradation of long-chain fatty acids and are at risk of... 
Human Genetics | Biochemistry, general | Pediatrics | Internal Medicine | Medicine & Public Health | Metabolic Diseases | COA DEHYDROGENASE | GROWTH-HORMONE | INSULIN-RESISTANCE | FATTY-ACID | ENDOCRINOLOGY & METABOLISM | GENETICS & HEREDITY | TRIFUNCTIONAL PROTEIN-DEFICIENCY | GLYCEMIC RESPONSE | INDUCED HYPOGLYCEMIA | ACID OXIDATION DISORDERS | ADIPOSE-TISSUE | GLUCOSE-PRODUCTION | Nervous System Diseases - enzymology | 3-Hydroxyacyl CoA Dehydrogenases - blood | Lipid Metabolism, Inborn Errors - diet therapy | Nervous System Diseases - blood | Rhabdomyolysis - enzymology | Age Factors | Humans | Child, Preschool | Male | Cardiomyopathies - enzymology | Lipid Metabolism, Inborn Errors - enzymology | Nervous System Diseases - diagnosis | Mitochondrial Myopathies - blood | Rhabdomyolysis - diagnosis | Rhabdomyolysis - diet therapy | Hyperglycemia - diagnosis | Time Factors | Fasting - blood | Cardiomyopathies - diagnosis | Postprandial Period | Isotope Labeling | Female | Carnitine - analogs & derivatives | Mitochondrial Myopathies - diagnosis | Child | Cardiomyopathies - blood | Cardiomyopathies - diet therapy | Lipid Metabolism, Inborn Errors - blood | Lipid Metabolism, Inborn Errors - diagnosis | Carnitine - blood | Calorimetry, Indirect | Biomarkers - blood | Nervous System Diseases - diet therapy | Mitochondrial Myopathies - diet therapy | Lipolysis | Microdialysis | Energy Metabolism | Hyperglycemia - blood | Mitochondrial Myopathies - enzymology | Hyperglycemia - enzymology | 3-Hydroxyacyl CoA Dehydrogenases - deficiency | Glycerol - blood | Rhabdomyolysis - blood | Blood Glucose - metabolism | Mitochondrial Trifunctional Protein - deficiency | Fatty acids | Dextrose | Glucose | Index Medicus | Clinical Medicine | Medical and Health Sciences | Endokrinologi och diabetes | Klinisk medicin | Medicin och hälsovetenskap | Endocrinology and Diabetes
Journal Article
Journal Article
Journal Article
Veterinary Clinics of North America - Equine Practice, ISSN 0749-0739, 04/2009, Volume 25, Issue 1, pp. 121 - 135
Journal Article
BMJ Case Reports, ISSN 1757-790X, 04/2014, Volume 2014, Issue apr01 1, pp. bcr2013202677 - bcr2013202677
Journal Article