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Journal of Biopharmaceutical Statistics|March 1, 1995
Dose response studies. II. Analysis and interpretationS J RubergJournal of Biopharmaceutical Statistics|October 24, 2018
Interval estimators of relative potency in toxicology and radiation countermeasure studies: comparing methods and experimental designsReid D Landes, Shelly Y Lensing, Martin Hauer-JensenJournal of Biopharmaceutical Statistics|December 13, 2016
Statistical inference for response adaptive randomization procedures with adjusted optimal allocation proportionsHongjian ZhuJournal of Biopharmaceutical Statistics|December 15, 2016
Efficient estimation in two-stage randomized clinical trials using ranked setsSyed Shahadat Hossain, Nabil AwanJournal of Biopharmaceutical Statistics|March 11, 2008
Estimation of the risk difference under a noncompliance randomized clinical trial with missing outcomesKung-Jong LuiJournal of Biopharmaceutical Statistics|March 11, 2008
Joint one-sided and two-sided simultaneous confidence intervalsS Braat, D Gerhard, L A HothornJournal of Biopharmaceutical Statistics|March 11, 2008
What we want versus what we can get: a closer look at failure time endpoints for cardiovascular studiesRui Song, Thomas D Cook, Michael R KosorokJournal of Biopharmaceutical Statistics|March 11, 2014
A multiple-imputation-based approach to sensitivity analyses and effectiveness assessments in longitudinal clinical trialsBirhanu Teshome Ayele, Ilya Lipkovich, Geert Molenberghs, et al.Journal of Biopharmaceutical Statistics|March 11, 2014
A multiple imputation method for sensitivity analyses of time-to-event data with possibly informative censoringYue Zhao, Amy H Herring, Haibo Zhou, et al.Journal of Biopharmaceutical Statistics|March 11, 2014
Sample size estimation of multiregional clinical trials with heterogeneous variability across regionsYuh-Jenn Wu, Te-Sheng Tan, Shein-Chung Chow, et al.Pageof 216