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Clinical Trials (London, England)|March 17, 2006
Estimation of the average causal effect among subgroups defined by post-treatment variablesYutaka Matsuyama, Satoshi MoritaStatistics in Medicine|March 1, 2002
Correcting for non-compliance of repeated binary outcomes in randomized clinical trials: randomized analysis approachYutaka MatsuyamaStatistics in Medicine|June 17, 2010
A comparison of the results of intent-to-treat, per-protocol, and g-estimation in the presence of non-random treatment changes in a time-to-event non-inferiority trialYutaka MatsuyamaStatistics in Medicine|February 15, 2003
Sensitivity analysis for the estimation of rates of change with non-ignorable drop-out: an application to a randomized clinical trial of the vitamin D3Yutaka MatsuyamaPharmaceutical Statistics|September 1, 2018
Reasonable two-stage adaptive designs for single-arm phase II clinical trialsKosuke Kashiwabara, Yutaka MatsuyamaEpidemiology (Cambridge, Mass.)|October 22, 2003
Marginal structural models as a tool for standardizationTosiya Sato, Yutaka MatsuyamaBMC Medical Research Methodology|February 16, 2019
Dynamic prediction of repeated events data based on landmarking model: application to colorectal liver metastases dataIsao Yokota, Yutaka MatsuyamaJournal of Biopharmaceutical Statistics|September 23, 2015
Interim analysis based on the weighted log-rank test for delayed treatment effects under staggered patient entryMizuki Yoshida, Yutaka MatsuyamaPharmaceutical Statistics|June 8, 2007
Estimation of the marginal survival time in the presence of dependent competing risks using inverse probability of censoring weighted (IPCW) methodsYutaka Matsuyama, Takuhiro YamaguchiEpidemiology (Cambridge, Mass.)|August 15, 2015
Brief Report: Doubly Robust Estimation of Standardized Risk Difference and Ratio in the Exposed PopulationTomohiro Shinozaki, Yutaka MatsuyamaPageof 97