The absolute configuration of urinary 5-hydroxyhexanoic acid — a product of fatty acid (ω-1)-oxidation — in patients with non-ketotic dicarboxylic aciduria
Author:
Publisher
Elsevier BV
Subject
Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine
Reference22 articles.
1. Suberylglycine excretion in the urine from a patient with dicarboxylic aciduria;Gregersen;Clin Chim Acta,1976
2. Nonketotic C6−C10 dicarboxylic aciduria: biochemical investigations of two cases;Gregersen;Clin Chim Acta,1980
3. Dicarboxylic aciduria: the response to fasting;Truscott;Clin Chim Acta,1979
4. Twin siblings with a Reye's-like syndrome associated with an abnormal organic aciduria, hypoglycemia, diarrhea, and vomiting with close similarities to Jamaican vomiting sickness;Chalmers;Pediatr Res,1980
5. Profiles in altered metabolism III. (Ω-1)-hydroxyacid excretion in a case of episodic hypoglycemia;Mamer;Biomed Mass Spectrom,1980
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