The Statistical Basis of Laboratory Data Normalization
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Public Health, Environmental and Occupational Health,Drug Guides,Pharmacology (nursing)
Link
http://link.springer.com/content/pdf/10.1177/009286150303700112.pdf
Reference5 articles.
1. European Agency for the Evaluation of Medical Products. ICH Topic E9, Statistical Principles for Clinical Trials. London, United Kingdom: European Agency for the Evaluation of Medical Products; 1998.
2. Chuang-Stein C. Summarizing laboratory data with different reference ranges in multi-center clinical trials. Drug Inf J. 1992;26(1):77–84.
3. Chuang-Stein C. Some issues concerning the normalization of laboratory data based on reference ranges. Drug Inf J. 2001;35(1):153–156.
4. Huang J, Brunelle R. A nonparametric method for combining multilaboratory data. Drug Inf J. 2002;36(2): 395–406.
5. Sogliero-Gilbert G, Mosher K, Zubkoff L. A procedure for the simplification and assesment of lab parameters in clinical trials. Drug Inf J. 1986; 20:279–296.
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