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Missing data: discussion points from the PSI missing data expert group.
Burzykowski T, Carpenter J, Coens C, Evans D, France L, Kenward M, Lane P, Matcham J, Morgan D, Phillips A, Roger J, Sullivan B, White I, Yu LM; of the PSI Missing Data Expert Group. Burzykowski T, et al. Among authors: roger j. Pharm Stat. 2010 Oct-Dec;9(4):288-97. doi: 10.1002/pst.391. Pharm Stat. 2010. PMID: 19844946
Response to comments by Seaman et al. on "Analysis of longitudinal trials with protocol deviation: a framework for relevant, accessible assumptions, and inference via multiple imputation," Journal of Biopharmaceutical Statistics 23:1352-1371.
Carpenter JR, Roger JH, Cro S, Kenward MG. Carpenter JR, et al. Among authors: roger jh. J Biopharm Stat. 2014;24(6):1363-9. doi: 10.1080/10543406.2014.960085. J Biopharm Stat. 2014. PMID: 25215553 No abstract available.
The adaptive designs CONSORT extension (ACE) statement: a checklist with explanation and elaboration guideline for reporting randomised trials that use an adaptive design.
Dimairo M, Pallmann P, Wason J, Todd S, Jaki T, Julious SA, Mander AP, Weir CJ, Koenig F, Walton MK, Nicholl JP, Coates E, Biggs K, Hamasaki T, Proschan MA, Scott JA, Ando Y, Hind D, Altman DG; ACE Consensus Group. Dimairo M, et al. Trials. 2020 Jun 17;21(1):528. doi: 10.1186/s13063-020-04334-x. Trials. 2020. PMID: 32546273 Free PMC article.
635 results