A study of urinary metabolites in patients with dicarboxylic aciduria for differential diagnosis

Pediatrics International

Volumn 36, Issue 2, 1994, Pages 139-145

  SHIMIZU, NOBUO ^a   YAMAGUCHI, SEIJI ^b   ORII, TADAO ^a  

^a GIFU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b SHIMANE UNIVERSITY   (Japan)

Author keywords

congenital organic acidemia; dicarboxylic aciduria; mass spectrometry

Indexed keywords

DICARBOXYLIC ACID;

ACIDEMIA; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DIFFERENTIAL DIAGNOSIS; HUMAN; INFANT; KETOACIDOSIS; MASS SPECTROMETRY; PRIORITY JOURNAL; REYE SYNDROME; URINALYSIS; ZELLWEGER SYNDROME;

AMINO ACID METABOLISM, INBORN ERRORS; CARNITINE; CHILD, PRESCHOOL; DIAGNOSIS, DIFFERENTIAL; DICARBOXYLIC ACIDS; FEMALE; HUMAN; INFANT; MALE; MASS FRAGMENTOGRAPHY; REYE SYNDROME; ZELLWEGER SYNDROME;

EID: 0028326692     PISSN: 13288067     EISSN: 1442200X     Source Type: Journal    
DOI: 10.1111/j.1442-200X.1994.tb03149.x     Document Type: Article

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