SCOPUS 정보 검색 플랫폼

Volumn 55, Issue 6, 2001, Pages 524-534

Diagnostic approach and treatment of inherited mitochondrial fatty acid oxidation disorders;Aproximación diagnóstica y tratamiento de los errores innatos de la oxidación mitocondrial de los ácidos grasos

(2) Pena Quintana L a Sanjurjo Crespo, P a

a HOSPITAL UNIVERSITARIO MATERNO INFANTIL DE CANARIAS (Spain)

Author keywords

Acylcarnitines; Carnitine; Fatty acid metabolism; Fatty acid oxidation disorders; Hypoglycemia; Inborn errors of metabolism; Mitochondria; Prenatal diagnosis; Screening

Indexed keywords

ACYLCARNITINE; CARBAMYLGLUTAMATE; CARNITINE; GLUTAMIC ACID DERIVATIVE; HYDROXY FATTY ACID; MEDIUM CHAIN FATTY ACID; RIBOFLAVIN; SHORT CHAIN FATTY ACID; UNCLASSIFIED DRUG;

CARBOHYDRATE INTAKE; DIET RESTRICTION; DIET THERAPY; FAT INTAKE; FATTY ACID OXIDATION; GENETIC DISORDER; HUMAN; HYPOGLYCEMIA; METABOLIC DISORDER; MITOCHONDRION; MORTALITY; PROGNOSIS; REVIEW;

3-HYDROXYACYL COA DEHYDROGENASES; ACETYL-COA C-ACYLTRANSFERASE; CARBON-CARBON DOUBLE BOND ISOMERASES; ENOYL-COA HYDRATASE; FATTY ACIDS; HUMANS; LIPID METABOLISM, INBORN ERRORS; MITOCHONDRIAL DISEASES; OXIDATION-REDUCTION; RACEMASES AND EPIMERASES;

EID: 0035745257 PISSN: 03024342 EISSN: None Source Type: Journal
DOI: None Document Type: Review

Times cited : (10)

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