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Journal of Biopharmaceutical Statistics|September 3, 1999
Extending Goodman-Kruskal's gamma to the comparison of ordered treatments in multicenter clinical trialsF Kianifard, M ChenJournal of Biopharmaceutical Statistics|August 26, 2000
A two-stage dose selection strategy in phase I trials with wide dose rangesO Wang, D E FariesJournal of Biopharmaceutical Statistics|August 26, 2000
Equivalence in test assay method comparisons for the repeated-measure, matched-pair design in medical device studies: statistical considerationsC S LaoJournal of Biopharmaceutical Statistics|November 27, 1999
Resampling and multiplicity in cost-effectiveness inferenceR L ObenchainJournal of Biopharmaceutical Statistics|November 27, 1999
Statistical methods for monitoring clinical trialsM A ProschanJournal of Biopharmaceutical Statistics|December 5, 2000
On testing for drug/chemical interactions: definitions and inferenceC GenningsJournal of Biopharmaceutical Statistics|May 10, 2000
Center-weighting issues in multicenter clinical trialsP P GalloJournal of Biopharmaceutical Statistics|May 10, 2000
Multiple imputation compared with some informative dropout procedures in the estimation and comparison of rates of change in longitudinal clinical trials with dropoutsM W Ali, O SiddiquiJournal of Biopharmaceutical Statistics|May 10, 2000
Design and estimation in the limiting dilution assay when concentrations vary widely among samplesR S Parrish, L J HazlettJournal of Biopharmaceutical Statistics|July 19, 2001
Carry-over effects in bioequivalence studiesG Dangelo, D Potvin, J TurgeonPageof 216