Clinical Chemistry
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Clinical Chemistry 27: 223-227, 1981;
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Muskiet, F. A.
Right arrow Articles by Wolthers, B. G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Muskiet, F. A.
Right arrow Articles by Wolthers, B. G.

Clinical Chemistry, Vol 27, 223-227, Copyright © 1981 by American Association for Clinical Chemistry

Simultaneous determination of the four major catecholamine metabolites and estimation of a serotonin metabolite in urine by capillary gas chromatography of their tert-butyldimethylsilyl derivatives

FA Muskiet, MC Stratingh, GJ Stob and BG Wolthers

We have developed a routine capillary gas-chromatographic profiling method for simultaneous quantitative determination of the tert- butyldimethylsilyl derivatives of homovanillic acid, vanilmandelic acid, 3-methoxy-4-hydroxyphenylethylene glycol, and 3,4- dihydroxyphenylacetic acid and the estimation of 5-hydroxyindole-3- acetic acid in urine. The method is useful for diagnosis and followup of patients with functional tumors characterized by increased urinary excretion of metabolites originating from the metabolism of tyrosine and tryptophan--e.g., neuroblastoma, pheochromocytoma, carcinoid, and melanoma. It may also be applicable in pharmacokinetic studies of administered aromatic amino acids (parkinsonism, mental diseases, loading tests) and for diagnosis and followup of patients with inborn errors of metabolism that are characterized by organic aciduria (for instance, tyrosyluria and phenylketonuria).


The following articles in journals at HighWire Press have cited this article:


Home page
JNMHome page
P. L. Jager, W. G. Meijer, I. P. Kema, P. H.B. Willemse, D. A. Piers, and E. G.E. de Vries
L-3-[123I]Iodo-{alpha}-Methyltyrosine Scintigraphy in Carcinoid Tumors: Correlation with Biochemical Activity and Comparison with [111In-DTPA-D-Phe1]-Octreotide Imaging
J. Nucl. Med., November 1, 2000; 41(11): 1793 - 1800.
[Abstract] [Full Text] [PDF]


Home page
J Child NeurolHome page
R. D. Craver, S. E. Golladay, R. P. Warrier, A. J. Gates, and J. S. Nelson
Neurocutaneous Melanosis With Dandy-Walker Malformation Complicated by Primary Spinal Leptomeningeal Melanoma
J Child Neurol, September 1, 1996; 11(5): 410 - 414.
[PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1981 by the American Association for Clinical Chemistry.