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Biometrics|September 1, 1995
A two-stage procedure for survival studies with surrogate endpointsP Flandre, J O'QuigleyProceedings of the National Academy of Sciences of the United States of America|March 15, 1994
Predictive capability of proportional hazards regressionJ O'Quigley, P FlandreRevue D'Epidemiologie Et De Sante Publique|January 1, 1988
[Correlate non-Gaussian measurement]J O'QuigleyStatistics in Medicine|October 16, 1999
Another look at two phase I clinical trial designsJ O'QuigleyRevue D'Epidemiologie Et De Sante Publique|January 1, 1993
[Reduction in follow-up period of a study using criteria supplemental to death]P FlandreJournal of Clinical Epidemiology|August 1, 1996
On the use of auxiliary data to estimate the survival function and its variance: an application to acquired immunodeficiency syndromeP FlandreFundamental & Clinical Pharmacology|January 1, 1990
Sequential design and analysis of dose finding studies in patients with life threatening diseaseJ O'QuigleyBiometrics|September 1, 1992
Estimating the probability of toxicity at the recommended dose following a phase I clinical trial in cancerJ O'QuigleyBiostatistics (Oxford, England)|August 23, 2003
Estimating average regression effect under non-proportional hazardsR Xu, J O'QuigleyRevue D'Epidemiologie Et De Sante Publique|January 1, 1986
[Comparison of several percentages when the theoretical determinants are weak]J O'Quigley, D SchwartzPageof 7