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Journal of Biopharmaceutical Statistics|March 1, 1993
Multivariate nonparametric analysis for the two-period crossover design with application in clinical trialsW D Johnson, J M GrenderJournal of Biopharmaceutical Statistics|March 1, 1993
Some general estimation methods for nonlinear mixed-effects modelsM Davidian, D M GiltinanJournal of Biopharmaceutical Statistics|March 1, 1997
The multivariate assessment of bioequivalenceV M Chinchilli, R K ElswickJournal of Biopharmaceutical Statistics|March 1, 1997
Choice of student's t- or Wilcoxon-based confidence intervals for assessment of average bioequivalenceW W Hauck, D Hauschke, E Diletti, et al.Journal of Biopharmaceutical Statistics|May 1, 1997
Using aspects of study design in sample size estimationA Phillips, M CampbellJournal of Biopharmaceutical Statistics|May 1, 1997
Multiple-time-point dissolution specifications for a sampling acceptance planJ J Chen, Y TsongJournal of Biopharmaceutical Statistics|March 1, 1996
The assessment of individual and population bioequivalenceV M ChinchilliJournal of Biopharmaceutical Statistics|March 1, 1996
Mixed-model analysis of incomplete longitudinal data from a high-dose trial of tacrine (Cognex) in Alzheimer's patientsF SmithJournal of Biopharmaceutical Statistics|March 1, 1996
Generalized ridge analysis with application to population pharmacokinetics/dynamicsJ M Minor, H Namini, G A WatsonJournal of Biopharmaceutical Statistics|July 1, 1996
Factorial dose-response studies using frequency and magnitude of doseK B Hafner, S J RubergPageof 217