nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A Bayesian Approach to the ICH Q8 Definition of Design Space
|
Peterson, John J. |
|
2008 |
|
5 |
p. 959-975 |
artikel |
2 |
A Bayesian Design and Analysis for Dose-Response Using Informative Prior Information
|
Smith, Michael K. |
|
2006 |
|
5 |
p. 695-709 |
artikel |
3 |
A Comparison of False Positive Rates of Peto and Poly-3 Methods for Long-Term Carcinogenicity Data Analysis Using Multiple Comparison Adjustment Method Suggested by Lin and Rahman
|
Rahman, Mohammad A. |
|
2008 |
|
5 |
p. 949-958 |
artikel |
4 |
Adaptive Dose Selection Using Efficacy-Toxicity Trade-Offs: Illustrations and Practical Considerations
|
Thall, Peter F. |
|
2006 |
|
5 |
p. 623-638 |
artikel |
5 |
Analysis of Treatment Effectiveness in Longitudinal Observational Data
|
Faries, Douglas |
|
2007 |
|
5 |
p. 809-826 |
artikel |
6 |
An Estimation Method of the Half-Life for a One-Compartment Model of a Single Bolus Intravenous Injection by a Single Sampling
|
Funatogawa, Takashi |
|
2007 |
|
5 |
p. 827-837 |
artikel |
7 |
A Permutation Two One-Sided Tests Procedure to Detect Minimal Fold Changes of Gene Expression Levels
|
Liu, Jen-pei |
|
2008 |
|
5 |
p. 808-826 |
artikel |
8 |
A Predictive Risk Probability Approach for Microarray Data with Survival as an Endpoint
|
Chen, Dung-Tsa |
|
2008 |
|
5 |
p. 841-852 |
artikel |
9 |
A Procedure for Group Sequential Comparative Poisson Trials
|
Xia, Qi |
|
2007 |
|
5 |
p. 869-881 |
artikel |
10 |
A Review of: “Assessing Quality of Life in Clinical Trials: Theory and Methods, Second Edition, by P. Fayers and R. Hays (eds.)”
|
Rodenberg, Cynthia A. |
|
2006 |
|
5 |
p. 761-763 |
artikel |
11 |
A Review of: “Flowgraph Models for Multistate Time-to-Event Data”
|
Commenges, Daniel |
|
2005 |
|
5 |
p. 883-884 |
artikel |
12 |
A Review of: “Introduction to Randomized Controlled Clinical Trials, Second Edition, by J. N. S. Matthews”
|
Kesler, Karen |
|
2007 |
|
5 |
p. 951-953 |
artikel |
13 |
A Review of: “Medical Statistics: A Textbook for the Health Sciences, Fourth Edition, by D. Machin, M. J. Campbell, and S. J. Walters”
|
Dhar, Sunil K. |
|
2008 |
|
5 |
p. 1036-1038 |
artikel |
14 |
A Review of: “Sample Size Calculations in Clinical Research, Second Edition, by S.-C. Chow, J. Shao, and H. Wang”
|
Filloon, Thomas G. |
|
2008 |
|
5 |
p. 1034-1035 |
artikel |
15 |
A Review of: “Selection Bias and Covariate Imbalances in Randomized Clinical Trials, by V. W. Berger”
|
Friede, Tim |
|
2006 |
|
5 |
p. 757-759 |
artikel |
16 |
A Review of: “Statistical Analysis of Epidemiologic Data”
|
Hudson, Suzanne |
|
2005 |
|
5 |
p. 885-887 |
artikel |
17 |
A Review of: “Statistical Evidence in Medical Trials: What Do the Data Really Tell Us?, by S. D. Simon”
|
Dhar, Sunil K. |
|
2007 |
|
5 |
p. 949-950 |
artikel |
18 |
A Review of: “Statistical Methods for Dose-Finding Experiments, by S. Chevret (Ed.)”
|
Bretz, Frank |
|
2007 |
|
5 |
p. 947-948 |
artikel |
19 |
A Review of: “The Statistical Analysis of Recurrent Events, by R. J. Cook and J. F. Lawless”
|
Noursalehi, Mojtaba |
|
2008 |
|
5 |
p. 1039-1041 |
artikel |
20 |
Assessing the Consistency of Traditional Chinese Medicine with Multiple Correlative Active Components
|
Lu, Qingshu |
|
2007 |
|
5 |
p. 791-808 |
artikel |
21 |
A Two-Stage Binomial Test Approach of Gene Identification in Oligonucleotide Arrays
|
Chen, Dung-Tsa |
|
2007 |
|
5 |
p. 903-918 |
artikel |
22 |
Bayesian Optimal Designs for a Quantal Dose-Response Study with Potentially Missing Observations
|
Baek, InYoung |
|
2006 |
|
5 |
p. 679-693 |
artikel |
23 |
Bayesian Optimal Designs for Pharmacokinetic Models: Sensitivity to Uncertainty
|
Dokoumetzidis, Aristides |
|
2007 |
|
5 |
p. 851-867 |
artikel |
24 |
Block Designs in Method Transfer Experiments
|
Altan, Stan |
|
2008 |
|
5 |
p. 996-1004 |
artikel |
25 |
Design and Analysis of Analytical Method Transfer Studies
|
Schwenke, James R. |
|
2008 |
|
5 |
p. 1013-1033 |
artikel |
26 |
Design and Analysis of Dose-Finding Studies Combining Multiple Comparisons and Modeling Procedures
|
Pinheiro, Jose |
|
2006 |
|
5 |
p. 639-656 |
artikel |
27 |
Equivalence Tests for Shelf Life and Average Drug Content in Stability Studies
|
Djira, Gemechis D. |
|
2008 |
|
5 |
p. 985-995 |
artikel |
28 |
Estimating a Positive False Discovery Rate for Variable Selection in Pharmacogenetic Studies
|
Li, Lang |
|
2007 |
|
5 |
p. 883-902 |
artikel |
29 |
Estimation of Lag Time Between Onset of and Death from an Occult Tumor
|
Ahn, Hongshik |
|
2008 |
|
5 |
p. 901-914 |
artikel |
30 |
Fallback Tests in Dose-Response Clinical Trials
|
Dmitrienko, Alex |
|
2006 |
|
5 |
p. 745-755 |
artikel |
31 |
Guest Editors' Note for the Special Issue on “Design and Analysis of Dose-Response Clinical Trials”
|
Ting, Naitee |
|
2006 |
|
5 |
p. 1-2 |
artikel |
32 |
Hypothesis Testing and Bayesian Estimation using a Sigmoid Emax Model Applied to Sparse Dose-Response Designs
|
Thomas, Neal |
|
2006 |
|
5 |
p. 657-677 |
artikel |
33 |
Identifying High-Dimensional Biomarkers for Personalized Medicine via Variable Importance Ranking
|
Baek, Songjoon |
|
2008 |
|
5 |
p. 853-868 |
artikel |
34 |
Incremental Forward Feature Selection with Application to Microarray Gene Expression Data
|
Lee, Yuh-Jye |
|
2008 |
|
5 |
p. 827-840 |
artikel |
35 |
Innovative Approaches in Drug Development
|
Chang, Mark |
|
2007 |
|
5 |
p. 775-789 |
artikel |
36 |
Mixture Model Framework Facilitates Understanding of Zero-Inflated and Hurdle Models for Count Data
|
Baughman, A. L. |
|
2007 |
|
5 |
p. 943-946 |
artikel |
37 |
Multiple Comparisons and Multiple Contrasts in Randomized Dose-Response Trials—Confidence Interval Oriented Approaches
|
Hothorn, Ludwig A. |
|
2006 |
|
5 |
p. 711-731 |
artikel |
38 |
Multispectra CWT-Based Algorithm (MCWT) in Mass Spectra for Peak Extraction
|
Hsueh, Huey-Miin |
|
2008 |
|
5 |
p. 869-882 |
artikel |
39 |
Overall Type I Error Rate and Power of Multiple Dunnett's Tests on Rodent Body Weights in Toxicology Studies
|
Hoffman, Wherly P. |
|
2008 |
|
5 |
p. 883-900 |
artikel |
40 |
Parametric Two-Tier Sequential Quality Assurance Test of Delivery Dose Uniformity of Multiple-Dose Inhaler and Dry Powder Inhaler Drug Products
|
Tsong, Yi |
|
2008 |
|
5 |
p. 976-984 |
artikel |
41 |
Phase I Studies of Chemotherapeutic Agents in Cancer Patients: A Review of the Designs
|
Potter, Douglas M. |
|
2006 |
|
5 |
p. 579-604 |
artikel |
42 |
Poly-k-Trend Tests for Survival Adjusted Analysis of Tumor Rates Formulated as Approximate Multiple Contrast Test
|
Schaarschmidt, Frank |
|
2008 |
|
5 |
p. 934-948 |
artikel |
43 |
Population Pharmacokinetic Measures, Their Estimation and Selection of Sampling Times
|
Fedorov, Valerii |
|
2007 |
|
5 |
p. 919-941 |
artikel |
44 |
Proof of Hazard and Proof of Safety in Toxicological Studies Using Simultaneous Confidence Intervals for Differences and Ratios to Control
|
Hothorn, Ludwig A. |
|
2008 |
|
5 |
p. 915-933 |
artikel |
45 |
Sample Size Calculation for Weighted Rank Tests Comparing Survival Distributions Under Cluster Randomization: A Simulation Method
|
Jung, Sin-Ho |
|
2007 |
|
5 |
p. 839-849 |
artikel |
46 |
Sequential Designs for Logistic Phase I Clinical Trials
|
Liu, Guohui |
|
2006 |
|
5 |
p. 605-621 |
artikel |
47 |
Special Issue on Non-Clinical Statistics Guest Editors' Notes
|
Chen, James J. |
|
2008 |
|
5 |
p. 805-807 |
artikel |
48 |
Statistical Assessment of Analytical Method Transfer
|
Zhong, Jinglin |
|
2008 |
|
5 |
p. 1005-1012 |
artikel |
49 |
Subgroup Analyses in Randomized Clinical Trials: Statistical and Regulatory Issues
|
Grouin, Jean-Marie |
|
2005 |
|
5 |
p. 869-882 |
artikel |
50 |
Using the Partitioning Principle to Adaptively Design Dose-Response Studies
|
Ling, Xiang |
|
2006 |
|
5 |
p. 733-743 |
artikel |