These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

1113 related items for PubMed ID: 17708514

  • 1. Sample size determination for assessing equivalence based on proportion ratio under a randomized trial with non-compliance and missing outcomes.
    Lui KJ, Chang KC.
    Stat Med; 2008 Jan 15; 27(1):47-67. PubMed ID: 17708514
    [Abstract] [Full Text] [Related]

  • 2. Test equality and sample size calculation based on risk difference in a randomized clinical trial with noncompliance and missing outcomes.
    Lui KJ, Chang KC.
    Biom J; 2008 Apr 15; 50(2):224-36. PubMed ID: 18264992
    [Abstract] [Full Text] [Related]

  • 3. Sample size determination for testing equality in a cluster randomized trial with noncompliance.
    Lui KJ, Chang KC.
    J Biopharm Stat; 2011 Jan 15; 21(1):1-17. PubMed ID: 21191850
    [Abstract] [Full Text] [Related]

  • 4. Test non-inferiority and sample size determination based on the odds ratio under a cluster randomized trial with noncompliance.
    Lui KJ, Chang KC.
    J Biopharm Stat; 2011 Jan 15; 21(1):94-110. PubMed ID: 21191857
    [Abstract] [Full Text] [Related]

  • 5. Testing homogeneity of the risk ratio in stratified noncompliance randomized trials.
    Lui KJ.
    Contemp Clin Trials; 2007 Sep 15; 28(5):614-25. PubMed ID: 17409026
    [Abstract] [Full Text] [Related]

  • 6. Five interval estimators for proportion ratio under a stratified randomized clinical trial with noncompliance.
    Lui KJ, Chang KC.
    Biom J; 2007 Aug 15; 49(4):613-26. PubMed ID: 17634977
    [Abstract] [Full Text] [Related]

  • 7. Estimation of the risk difference under a noncompliance randomized clinical trial with missing outcomes.
    Lui KJ.
    J Biopharm Stat; 2008 Aug 15; 18(2):273-92. PubMed ID: 18327721
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Interval estimation of risk ratio in the simple compliance randomized trial.
    Lui KJ.
    Contemp Clin Trials; 2007 Feb 15; 28(2):120-9. PubMed ID: 16820329
    [Abstract] [Full Text] [Related]

  • 10. Eight interval estimators of a common rate ratio under stratified Poisson sampling.
    Lui KJ.
    Stat Med; 2004 Apr 30; 23(8):1283-96. PubMed ID: 15083483
    [Abstract] [Full Text] [Related]

  • 11. Exact sample-size determination in testing non-inferiority under a simple crossover trial.
    Lui KJ, Chang KC.
    Pharm Stat; 2012 Apr 30; 11(2):129-34. PubMed ID: 22232060
    [Abstract] [Full Text] [Related]

  • 12. Tests of equivalence and non-inferiority for diagnostic accuracy based on the paired areas under ROC curves.
    Liu JP, Ma MC, Wu CY, Tai JY.
    Stat Med; 2006 Apr 15; 25(7):1219-38. PubMed ID: 16158400
    [Abstract] [Full Text] [Related]

  • 13. Interval estimation of the risk difference in non-compliance randomized trials with repeated binary measurements.
    Lui KJ.
    Stat Med; 2007 Jul 20; 26(16):3140-56. PubMed ID: 17177272
    [Abstract] [Full Text] [Related]

  • 14. Blinded sample size reassessment in non-inferiority and equivalence trials.
    Friede T, Kieser M.
    Stat Med; 2003 Mar 30; 22(6):995-1007. PubMed ID: 12627414
    [Abstract] [Full Text] [Related]

  • 15. A Monte Carlo approach for change-point detection in the Cox proportional hazards model.
    Liu M, Lu W, Shao Y.
    Stat Med; 2008 Aug 30; 27(19):3894-909. PubMed ID: 18254131
    [Abstract] [Full Text] [Related]

  • 16. Test homogeneity of odds ratio in a randomized clinical trial with noncompliance.
    Lui KJ, Chang KC.
    J Biopharm Stat; 2009 Sep 30; 19(5):916-32. PubMed ID: 20183452
    [Abstract] [Full Text] [Related]

  • 17. Likelihood methods for treatment noncompliance and subsequent nonresponse in randomized trials.
    O'Malley AJ, Normand SL.
    Biometrics; 2005 Jun 30; 61(2):325-34. PubMed ID: 16011678
    [Abstract] [Full Text] [Related]

  • 18. Sample size and statistical power assessing the effect of interventions in the context of mixture distributions with detection limits.
    Chu H, Nie L, Cole SR.
    Stat Med; 2006 Aug 15; 25(15):2647-57. PubMed ID: 16456897
    [Abstract] [Full Text] [Related]

  • 19. Methodology of superiority vs. equivalence trials and non-inferiority trials.
    Christensen E.
    J Hepatol; 2007 May 15; 46(5):947-54. PubMed ID: 17412447
    [Abstract] [Full Text] [Related]

  • 20. Sample size determination for constrained longitudinal data analysis.
    Lu K, Mehrotra DV, Liu G.
    Stat Med; 2009 Feb 15; 28(4):679-99. PubMed ID: 19051207
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 56.