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Clinical Chemistry, Vol 18, 800-809, Copyright © 1972 by the American Association for Clinical Chemistry
1 Institute of Clinical Biochemistry, University of
Oslo, Rikshospitalet, Oslo, Norway.
We describe a system for multicomponent analyses of biological materials. The methods include
gas liquid chromatography (GLC) for separation
purpose, mass spectrometry for identification and
structure studies, and use of a computer for data
handling. Urine and serum samples as well as
biopsies and other biological materials can be
analyzed. The peaks from the eight different GLC-systems used are identified by computer matching
of the corresponding mass spectra against a
library file of 17,000 reference spectra. The system
is well suited for the diagnosis and study of inherited as well as other metabolic disturbances.
About 40 of the known inborn errors can be detected. The application of the methods to the
analysis of more than 700 patients has led to the
discovery of three new inborn errors: methylmalonic aciduria,
-methylcrotonyl-CoA carboxylase deficiency, and pyroglutamic aciduria. The
methods also represent a valuable tool in the
study of drug metabolism.
The following articles in journals at HighWire Press have cited this article:
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R. Rej Clinical Chemistry through Clinical Chemistry: A Journal Timeline Clin. Chem., December 1, 2004; 50(12): 2415 - 2458. [Abstract] [Full Text] [PDF] |
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C. D. Scott Health Care Delivery and Advanced Technology Science, June 29, 1973; 180(4093): 1339 - 1342. [Abstract] [PDF] |
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