| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A comparison of methods and results in recruiting white and black women into reproductive studies: The MMC–PSU cooperative center on reproduction experience
|
Sweet, Stephanie
|
|
2008
|
29 |
4 |
p. 478-481
4 p.
|
artikel
|
| 2 |
Analysis of a crossover clinical trial by permutation methods
|
Good, Phillip
|
|
2008
|
29 |
4 |
p. 565-568
4 p.
|
artikel
|
| 3 |
Analysis of duration of response in oncology trials
|
Ellis, Stuart
|
|
2008
|
29 |
4 |
p. 456-465
10 p.
|
artikel
|
| 4 |
Bayesian design and conduct of phase II single-arm clinical trials with binary outcomes: A tutorial
|
Zohar, Sarah
|
|
2008
|
29 |
4 |
p. 608-616
9 p.
|
artikel
|
| 5 |
Bayesian sample size calculations for a non-inferiority test of two proportions in clinical trials
|
Daimon, Takashi
|
|
2008
|
29 |
4 |
p. 507-516
10 p.
|
artikel
|
| 6 |
Can regional analgesia reduce the risk of recurrence after breast cancer?
|
Sessler, Daniel I
|
|
2008
|
29 |
4 |
p. 517-526
10 p.
|
artikel
|
| 7 |
Clinical trials attitudes and practices of Latino physicians
|
Ramirez, Amelie G.
|
|
2008
|
29 |
4 |
p. 482-492
11 p.
|
artikel
|
| 8 |
CTN-194 (PICCO): Design of a trial of citalopram for the prevention of depression and its consequences in HIV-Hepatitis C co-infected individuals initiating pegylated interferon/ribavirin therapy
|
Klein, Marina B.
|
|
2008
|
29 |
4 |
p. 617-630
14 p.
|
artikel
|
| 9 |
Determination of required content of the informed consent process for human participants in biomedical research conducted in the U.S.: A practical tool to assist clinical investigators
|
Chanaud, Cheryl M.
|
|
2008
|
29 |
4 |
p. 501-506
6 p.
|
artikel
|
| 10 |
Do “placebo responders” exist?
|
Kaptchuk, Ted J.
|
|
2008
|
29 |
4 |
p. 587-595
9 p.
|
artikel
|
| 11 |
Editorial Board
|
|
|
2008
|
29 |
4 |
p. iii-
1 p.
|
artikel
|
| 12 |
Estimating sample size for a randomized clinical trial of lung cancer screening
|
Obuchowski, Nancy A.
|
|
2008
|
29 |
4 |
p. 466-477
12 p.
|
artikel
|
| 13 |
Evaluating a two-step approach to sexual risk reduction in a publicly-funded STI clinic: Rationale, design, and baseline data from the Health Improvement Project-Rochester (HIP-R)
|
Carey, Michael P.
|
|
2008
|
29 |
4 |
p. 569-586
18 p.
|
artikel
|
| 14 |
Modelling overdispersion in longitudinal count data in clinical trials with application to epileptic data
|
Fotouhi, Ali Reza
|
|
2008
|
29 |
4 |
p. 547-554
8 p.
|
artikel
|
| 15 |
[No title]
|
Collins, Joseph F.
|
|
2008
|
29 |
4 |
p. 455-
1 p.
|
artikel
|
| 16 |
The process of nutrient analysis for controlled feeding trials: A comparative study of two South African nutrient databases with chemical analysis
|
van der Watt, Izette
|
|
2008
|
29 |
4 |
p. 493-500
8 p.
|
artikel
|
| 17 |
The Self-Management of OsteoArthritis in Veterans (SeMOA) Study: Design and methodology
|
Allen, Kelli D.
|
|
2008
|
29 |
4 |
p. 596-607
12 p.
|
artikel
|
| 18 |
Timing is everything: Methodologic issues locating and recruiting medically underserved women for abnormal mammography follow-up research
|
Fair, Alecia Malin
|
|
2008
|
29 |
4 |
p. 537-546
10 p.
|
artikel
|
| 19 |
Using the Internet to search for cancer clinical trials: A comparative audit of clinical trial search tools
|
Atkinson, Nancy L.
|
|
2008
|
29 |
4 |
p. 555-564
10 p.
|
artikel
|
| 20 |
Validation of treatment induced specific adverse effect as a predictor of treatment benefit: A case study of NCIC CTG BR21
|
Ding, K.
|
|
2008
|
29 |
4 |
p. 527-536
10 p.
|
artikel
|
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