| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Bayesian Approach for Dose-Escalation in a Phase I Clinical Trial Incorporating Pharmacodynamic Endpoints
|
Whitehead, John
|
|
2007
|
|
6 |
p. 1117-1129
|
artikel
|
| 2 |
A Bayesian Meta-Analysis on Published Sample Mean and Variance Pharmacokinetic Data with Application to Drug-Drug Interaction Prediction
|
Yu, Menggang
|
|
2008
|
|
6 |
p. 1063-1083
|
artikel
|
| 3 |
A Comparison of Doubly Hierarchical Discriminant Analyses for Multiple Class Longitudinal Data from EEG Experiments
|
Wouters, Kristien
|
|
2008
|
|
6 |
p. 1120-1135
|
artikel
|
| 4 |
Adaptive Allocation and Failure Saving in Randomised Clinical Trials
|
Bandyopadhyay, Uttam
|
|
2006
|
|
6 |
p. 817-829
|
artikel
|
| 5 |
Adaptive Designs for Dose-Finding Studies Based on Sigmoid Emax Model
|
Dragalin, Vladimir
|
|
2007
|
|
6 |
p. 1051-1070
|
artikel
|
| 6 |
Adaptive Designs in Clinical Drug Development: Opportunities, Challenges, and Scope Reflections Following PhRMA's November 2006 Workshop
|
Krams, Michael
|
|
2007
|
|
6 |
p. 957-964
|
artikel
|
| 7 |
Adaptive Group Sequential Test for Clinical Trials with Changing Patient Population
|
Feng, Huaibao
|
|
2007
|
|
6 |
p. 1227-1238
|
artikel
|
| 8 |
Adaptive Seamless Designs: Selection and Prospective Testing of Hypotheses
|
Jennison, Christopher
|
|
2007
|
|
6 |
p. 1135-1161
|
artikel
|
| 9 |
A Mixture Model Approach in Gene-Gene and Gene-Environmental Interactions for Binary Phenotypes
|
Li, Lang
|
|
2008
|
|
6 |
p. 1150-1177
|
artikel
|
| 10 |
A Modeling Approach to the Analysis of Nerve Regenerative Experiments
|
Van Sanden, Suzy
|
|
2006
|
|
6 |
p. 843-859
|
artikel
|
| 11 |
Analysis Strategies for Adaptive Designs with Multiple Endpoints
|
Chang, Mark
|
|
2007
|
|
6 |
p. 1189-1200
|
artikel
|
| 12 |
Analyzing Receiver Operating Characteristic Curves with SAS, by M. Gonen
|
Banerjee, Sibabrata
|
|
2008
|
|
6 |
p. 1228-1229
|
artikel
|
| 13 |
Application of Semiparametric Mixed Models and Simultaneous Confidence Bands in a Cardiovascular Safety Experiment with Longitudinal Data
|
Maringwa, John T.
|
|
2008
|
|
6 |
p. 1043-1062
|
artikel
|
| 14 |
A Review of: “Applied Survival Analysis: Regression Modeling of Time-to-Event Data, 2nd ed., by D. W. Hosmer, S. Lemeshow, and S. May”
|
Moore, Dirk F.
|
|
2008
|
|
6 |
p. 1234-1236
|
artikel
|
| 15 |
A Review of: “Data Monitoring in Clinical Trials: A Case Studies Approach, by D. L. DeMets, C. D. Furberg, and L. M. Friedman (Eds.)”
|
Ashby, Mark
|
|
2006
|
|
6 |
p. 895-898
|
artikel
|
| 16 |
A Review of: “Practical Guide to Clinical Data Management, Second Edition, by S. Prokscha”
|
Lim, Johann
|
|
2007
|
|
6 |
p. 1247-1250
|
artikel
|
| 17 |
A Review of: “Regression Methods in Biostatistics: Linear, Logistic, Survival and Repeated Measures Models”
|
Hudson, Suzanne
|
|
2005
|
|
6 |
p. 1013-1015
|
artikel
|
| 18 |
A Review of: “Statistical Analysis of Cost-Effectiveness Data, by A. R. Willan and A. H. Briggs”
|
Cook, John R.
|
|
2007
|
|
6 |
p. 1243-1245
|
artikel
|
| 19 |
A Review of: “Statistical Evaluation of Measurement Errors: Design and Analysis of Reliability Studies”
|
Klar, Neil
|
|
2005
|
|
6 |
p. 1009-1011
|
artikel
|
| 20 |
A Review of: “Statistical Monitoring of Clinical Trials: A Unified Approach, by M. A. Proschan, K. K. G. Lan, and J. T. Wittes”
|
Wassmer, Gernot
|
|
2007
|
|
6 |
p. 1239-1242
|
artikel
|
| 21 |
A Review of: “Statistics in the Pharmaceutical Industry, Third Edition, by C. R. Buncher and J.-Y. Tsay (Eds.)”
|
Mietlowski, William
|
|
2006
|
|
6 |
p. 899-903
|
artikel
|
| 22 |
A Threshold Regression Mixture Model for Assessing Treatment Efficacy in a Multiple Myeloma Clinical Trial
|
Lee, Mei-Ling Ting
|
|
2008
|
|
6 |
p. 1136-1149
|
artikel
|
| 23 |
Combined Models for Data from In Vitro-In Vivo Correlation Experiments
|
Jacobs, Tom
|
|
2008
|
|
6 |
p. 1197-1211
|
artikel
|
| 24 |
Comparison of Model-Based Tests and Selection Strategies to Detect Genetic Polymorphisms Influencing Pharmacokinetic Parameters
|
Bertrand, Julie
|
|
2008
|
|
6 |
p. 1084-1102
|
artikel
|
| 25 |
Detecting Outliers in Multivariate Laboratory Data
|
Southworth, Harry
|
|
2008
|
|
6 |
p. 1178-1183
|
artikel
|
| 26 |
Detecting Qualitative Interactions in Clinical Trials: An Extension of Range Test
|
Li, Jianjun
|
|
2006
|
|
6 |
p. 831-841
|
artikel
|
| 27 |
Discussion of “p-Value Calculation for Multistage Phase II Cancer Clinical Trials”
|
Cook, Thomas D.
|
|
2006
|
|
6 |
p. 777-780
|
artikel
|
| 28 |
Discussion of the Paper “Adaptive Dose-Ranging Designs”
|
Burman, Carl-Fredrik
|
|
2007
|
|
6 |
p. 1005-1011
|
artikel
|
| 29 |
Discussion of the “White Paper of the PhRMA PISC Working Group on Adaptive Dose-Ranging Designs”
|
Leonov, Sergei
|
|
2007
|
|
6 |
p. 1013-1014
|
artikel
|
| 30 |
Discussion of “The White Paper of the PhRMA Working Group on Adaptive Dose-Ranging Designs”
|
Hemmings, Robert
|
|
2007
|
|
6 |
p. 1021-1027
|
artikel
|
| 31 |
Discussion of the “White Paper of the PhRMA Working Group on Adaptive Dose-Ranging Designs”
|
Wang, Sue-Jane
|
|
2007
|
|
6 |
p. 1015-1020
|
artikel
|
| 32 |
Discussion of the “White Paper of the PhRMA Working Group on Adaptive Dose-Ranging Designs”
|
Grieve, A. P.
|
|
2007
|
|
6 |
p. 997-1004
|
artikel
|
| 33 |
Dose Finding Designs for Continuous Responses and Binary Utility
|
Fedorov, Valerii V.
|
|
2007
|
|
6 |
p. 1085-1096
|
artikel
|
| 34 |
Duffy-Santner Confidence Intervals for the Two-Stage Three-Outcome Design
|
Furth, Alfred F.
|
|
2006
|
|
6 |
p. 875-880
|
artikel
|
| 35 |
Flexible Design and Efficient Implementation of Adaptive Dose-Finding Studies
|
Weir, Christopher J.
|
|
2007
|
|
6 |
p. 1033-1050
|
artikel
|
| 36 |
Guest Editorial—Statistical Issues in Adaptive Design Methods in Clinical Trials
|
Dragalin, Vladimir
|
|
2007
|
|
6 |
p. 955-956
|
artikel
|
| 37 |
Guest-Editor's Note: “Statistical Issues in Adaptive Design Methods in Clinical Trials”
|
Pong, Annpey
|
|
2007
|
|
6 |
p. 1133-1134
|
artikel
|
| 38 |
Innovative Approaches for Designing and Analyzing Adaptive Dose-Ranging Trials
|
Bornkamp, Bjorn
|
|
2007
|
|
6 |
p. 965-995
|
artikel
|
| 39 |
Introduction to Statistical Methods for Clinical Trials, by T. D. Cook and D. L. DeMets
|
McDermott, Michael P.
|
|
2008
|
|
6 |
p. 1230-1233
|
artikel
|
| 40 |
Mixture of Normal Distributions in Multivariate Null Intercept Measurement Error Model
|
Aoki, Reiko
|
|
2006
|
|
6 |
p. 785-802
|
artikel
|
| 41 |
Optimal Crossover Designs for Logistic Regression Models in Pharmacodynamics
|
Waterhouse, T. H.
|
|
2006
|
|
6 |
p. 881-894
|
artikel
|
| 42 |
Optimal Designs for Estimating the Interesting Part of a Dose-Effect Curve
|
Miller, Frank
|
|
2007
|
|
6 |
p. 1097-1115
|
artikel
|
| 43 |
Power Approximation for the Van Elteren Test Based on Location-Scale Family of Distributions
|
Zhao, Yan D.
|
|
2006
|
|
6 |
p. 803-815
|
artikel
|
| 44 |
p-Value Calculation for Multistage Phase II Cancer Clinical Trials
|
Jung, Sin-Ho
|
|
2006
|
|
6 |
p. 765-775
|
artikel
|
| 45 |
Recent Developments in Adaptive Designs for Phase I/II Dose-Finding Studies
|
Zohar, Sarah
|
|
2007
|
|
6 |
p. 1071-1083
|
artikel
|
| 46 |
Rejoinder
|
Jung, Sin-Ho
|
|
2006
|
|
6 |
p. 781-783
|
artikel
|
| 47 |
Rejoinder
|
|
|
2007
|
|
6 |
p. 1029-1032
|
artikel
|
| 48 |
Sample Size Calculation for the van Elteren Test Adjusting for Ties
|
Zhao, Yan D.
|
|
2008
|
|
6 |
p. 1112-1119
|
artikel
|
| 49 |
Sample Size Calculations for Population Pharmacodynamic Experiments Involving Repeated Dichotomous Observations
|
Ogungbenro, Kayode
|
|
2008
|
|
6 |
p. 1212-1227
|
artikel
|
| 50 |
Sample Size Re-Estimation for Adaptive Sequential Design in Clinical Trials
|
Gao, Ping
|
|
2008
|
|
6 |
p. 1184-1196
|
artikel
|
| 51 |
Seamless Phase II/III Combination Study Through Response Adaptive Randomization
|
Wang, Lin
|
|
2007
|
|
6 |
p. 1177-1187
|
artikel
|
| 52 |
Statistical Analysis for Two-Stage Seamless Design with Different Study Endpoints
|
Chow, Shein-Chung
|
|
2007
|
|
6 |
p. 1163-1176
|
artikel
|
| 53 |
Statistical Considerations for Testing Multiple Endpoints in Group Sequential or Adaptive Clinical Trials
|
Hung, H. M. James
|
|
2007
|
|
6 |
p. 1201-1210
|
artikel
|
| 54 |
Statistical Quality Control Process for Traditional Chinese Medicine
|
Tse, Siu-Keung
|
|
2006
|
|
6 |
p. 861-874
|
artikel
|
| 55 |
Strategies for Including Patients Recruited During Interim Analysis of Clinical Trials
|
Faldum, Andreas
|
|
2007
|
|
6 |
p. 1211-1225
|
artikel
|
| 56 |
Wilcoxon-Mann-Whitney Test: Stratify or Not?
|
Qu, Yongming
|
|
2008
|
|
6 |
p. 1103-1111
|
artikel
|
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