Pathophysiology of fatty acid oxidation disorders

Journal of Inherited Metabolic Disease

Volumn 33, Issue 5, 2010, Pages 533-537

  Bennett, M J ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARNITINE PALMITOYLTRANSFERASE I; CARNITINE PALMITOYLTRANSFERASE IA; GLUTAMATE DEHYDROGENASE; UNCLASSIFIED DRUG;

CALORIC RESTRICTION; CARNITINE PALMITOYLTRANSFERASE IA DEFICIENCY; EXERCISE; FATTY ACID OXIDATION; FATTY ACID OXIDATION DISORDER; GENE MUTATION; HUMAN; HYPERAMMONEMIA; HYPOGLYCEMIA; INBORN ERROR OF METABOLISM; KETOGENESIS; LIVER FAILURE; LONG CHAIN 3 HYDROXYACYL COENZYME A DEHYDROGENASE DEFICIENCY; MEDIUM CHAIN 3 HYDROXYACYL COENZYME A DEHYDROGENASE DEFICIENCY; MEDIUM CHAIN ACYL COENZYME A DEHYDROGENASE DEFICIENCY; MITOCHONDRIAL MEMBRANE; MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; NEWBORN SCREENING; PATHOPHYSIOLOGY; PERIPHERAL NEUROPATHY; RETINA PIGMENT DEGENERATION; REVIEW; RHABDOMYOLYSIS; SHORT CHAIN 3 HYDROXYACYL COENZYME A DEHYDROGENASE DEFICIENCY; SHORT CHAIN ACYL COENZYME A DEHYDROGENASE DEFICIENCY;

ANIMALS; ENERGY METABOLISM; FATTY ACIDS; GENOTYPE; HUMANS; LIPID METABOLISM, INBORN ERRORS; MITOCHONDRIA; MITOCHONDRIAL DISEASES; OXIDATION-REDUCTION; PHENOTYPE;

EID: 77957554125     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-010-9170-y     Document Type: Review

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