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Volumn 37, Issue 1, 2014, Pages 137-139
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Clinical and biological features at diagnosis in mitochondrial fatty acid beta-oxidation defects: A French pediatric study from 187 patients. Complementary data
a
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Author keywords
[No Author keywords available]
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Indexed keywords
AMINOTRANSFERASE BLOOD LEVEL;
ATRIOVENTRICULAR BLOCK;
CHILD;
CHOLESTASIS;
CLINICAL FEATURE;
CONGESTIVE CARDIOMYOPATHY;
DISORDERS OF MITOCHONDRIAL FUNCTIONS;
FATTY ACID BETA OXIDATION DEFECT;
FATTY ACID OXIDATION;
FEMALE;
FRANCE;
HEART VENTRICLE FIBRILLATION;
HEART VENTRICLE TACHYCARDIA;
HEPATOMEGALY;
HUMAN;
HYPERAMMONEMIA;
HYPERLACTATEMIA;
HYPERTROPHIC CARDIOMYOPATHY;
HYPOGLYCEMIA;
INFANT;
LETTER;
LIVER FAILURE;
MAJOR CLINICAL STUDY;
MALE;
METABOLIC ACIDOSIS;
NEUROLOGIC DISEASE;
NEWBORN;
PRESCHOOL CHILD;
REYE SYNDROME;
RHABDOMYOLYSIS;
SHOCK;
STEATOSIS;
SUDDEN DEATH;
SUPRAVENTRICULAR TACHYCARDIA;
TORSADE DES POINTES;
ACYL-COA DEHYDROGENASE;
ACYL-COA DEHYDROGENASE, LONG-CHAIN;
FATTY ACIDS;
FEMALE;
HUMANS;
LIPID METABOLISM, INBORN ERRORS;
MALE;
MITOCHONDRIA;
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EID: 84891825018
PISSN: 01418955
EISSN: 15732665
Source Type: Journal
DOI: 10.1007/s10545-013-9628-9 Document Type: Letter |
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Times cited : (42)
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References (2)
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