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

204 related items for PubMed ID: 18327721

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

  • 2. 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]

  • 3. 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 20; 50(2):224-36. PubMed ID: 18264992
    [Abstract] [Full Text] [Related]

  • 4. Interval estimation of risk ratio in the simple compliance randomized trial.
    Lui KJ.
    Contemp Clin Trials; 2007 Feb 20; 28(2):120-9. PubMed ID: 16820329
    [Abstract] [Full Text] [Related]

  • 5. Five interval estimators for proportion ratio under a stratified randomized clinical trial with noncompliance.
    Lui KJ, Chang KC.
    Biom J; 2007 Aug 20; 49(4):613-26. PubMed ID: 17634977
    [Abstract] [Full Text] [Related]

  • 6. Five interval estimators of the risk difference under stratified randomized clinical trials with noncompliance and repeated measurements.
    Lui KJ, Chang KC.
    J Biopharm Stat; 2013 Aug 20; 23(4):756-73. PubMed ID: 23786643
    [Abstract] [Full Text] [Related]

  • 7. Interval estimation of the proportion ratio in repeated binary measurements under a stratified randomized clinical trial with noncompliance.
    Lui KJ, Chang KC.
    J Biopharm Stat; 2012 Aug 20; 22(1):109-32. PubMed ID: 22204530
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. 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]

  • 10. Interval estimation of the proportion ratio under multiple matching.
    Lui KJ.
    Stat Med; 2005 Apr 30; 24(8):1275-85. PubMed ID: 15565736
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Sample size determination for testing equality in a cluster randomized trial with noncompliance.
    Lui KJ, Chang KC.
    J Biopharm Stat; 2011 Jan 30; 21(1):1-17. PubMed ID: 21191850
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. Multiple imputation methods for treatment noncompliance and nonresponse in randomized clinical trials.
    Taylor L, Zhou XH.
    Biometrics; 2009 Mar 30; 65(1):88-95. PubMed ID: 18397338
    [Abstract] [Full Text] [Related]

  • 15. Testing homogeneity of the risk ratio in stratified noncompliance randomized trials.
    Lui KJ.
    Contemp Clin Trials; 2007 Sep 30; 28(5):614-25. PubMed ID: 17409026
    [Abstract] [Full Text] [Related]

  • 16. Interval estimation of the difference in proportions under m-to-one matching.
    Lui KJ.
    Stat Med; 2005 Jun 15; 24(11):1765-76. PubMed ID: 15736281
    [Abstract] [Full Text] [Related]

  • 17. Interval estimation of generalized odds ratio in data with repeated measurements.
    Lui KJ.
    Stat Med; 2002 Oct 30; 21(20):3107-17. PubMed ID: 12369085
    [Abstract] [Full Text] [Related]

  • 18. Covariate adjustment in clinical trials with non-ignorable missing data and non-compliance.
    Levy DE, O'Malley AJ, Normand SL.
    Stat Med; 2004 Aug 15; 23(15):2319-39. PubMed ID: 15273951
    [Abstract] [Full Text] [Related]

  • 19. Notes on interval estimation of the attributable risk in cross-sectional sampling.
    Lui KJ.
    Stat Med; 2001 Jun 30; 20(12):1797-809. PubMed ID: 11406842
    [Abstract] [Full Text] [Related]

  • 20. Performance of statistical methods for analysing survival data in the presence of non-random compliance.
    Odondi L, McNamee R.
    Stat Med; 2010 Dec 20; 29(29):2994-3003. PubMed ID: 20963732
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.