A study of urinary metabolites in patients with dicarboxylic aciduria for differential diagnosis
Author:
Publisher
Wiley
Subject
Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1442-200X.1994.tb03149.x/fullpdf
Reference25 articles.
1. The differential diagnosis of dicarboxylic aciduria;Duran;J. Inker. Metab. Dis.,1984
2. Defects of metabolism of fatty acids in the sudden infant death syndrome;Howat;Br. Med. J.,1985
3. Sudden infant death syndrome (SIDS) and multiple acyl-CoA dehydrogenase deficiency, ethylmalonic adipic aciduria, or systemic carnitine deficiency;Harpey;J. Pediatr.,1987
4. A case of glutaric aciduria type I with unique abnormalities in the cerebral CT findings;Yamaguchi;Tohoku J. Exp. Med.,1987
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