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


     


Clinical Chemistry 45: 315-316, 1999;
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
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 Web of Science (12)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Eliason, S. C.
Right arrow Articles by Creer, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Eliason, S. C.
Right arrow Articles by Creer, M.
Related Collections
Right arrow Drug Monitoring and Toxicology
(Clinical Chemistry. 1999;45:315-316.)
© 1999 American Association for Clinical Chemistry, Inc.


Letters

Interlaboratory Variability for Total Homocysteine Analysis in Plasma

Stephen C. Eliason1, Detlef Ritter1,2,a, Hyung D. Chung1,2 and Michael Creer1

1 Department of Pathology, Saint Louis University, School of Medicine, St. Louis, MO 63104,
2 Pathology and, Laboratory Medical Service, John Cochran Veterans Affairs, Medical Center, St. Louis, MO 63106
a Address correspondence to this author at: Clinical Laboratories, 3635 Vista at Grand, St. Louis, MO 63110-0250. Fax 314-289-7073; e-mail ritterdg@slu.edu.


To the Editor:

Total plasma homocysteine consists of free homocysteine and homocysteine that is complexed with itself or with other amino acids or proteins. Free homocysteine has been measured previously as part of a biochemical screen for inherited metabolic disorders. More recently, increased total plasma homocysteine has been suggested as an independent risk factor for atherosclerotic coronary artery disease [reviewed in Ref. (1)]. In addition, increased total homocysteine is associated with a poor prognosis in patients with angiographically demonstrated coronary artery disease(2). These studies have prompted clinicians to include total homocysteine analysis as part of the risk assessment profile of patients with premature coronary artery disease. . . . [Full Text of this Article]


References




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


Home page
Clin. Chem.Home page
N. L. Duarte, X. L. Wang, and D. E. L. Wilcken
Effects of Anticoagulant and Time of Plasma Separation on Measurement of Homocysteine
Clin. Chem., April 1, 2002; 48(4): 665 - 668.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1999 by the American Association for Clinical Chemistry.