nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A Bayesian adaptive Phase I–II clinical trial for evaluating efficacy and toxicity with delayed outcomes
|
Koopmeiners, Joseph S |
|
2014 |
11 |
1 |
p. 38-48 |
artikel |
2 |
A Bayesian adaptive Phase I–II clinical trial for evaluating efficacy and toxicity with delayed outcomes
|
Koopmeiners, Joseph S |
|
2014 |
11 |
1 |
p. 38-48 |
artikel |
3 |
A phase I/II seamless dose escalation/expansion with adaptive randomization scheme (SEARS)
|
Pan, Haitao |
|
2014 |
11 |
1 |
p. 49-59 |
artikel |
4 |
A phase I/II seamless dose escalation/expansion with adaptive randomization scheme (SEARS)
|
Pan, Haitao |
|
2014 |
11 |
1 |
p. 49-59 |
artikel |
5 |
A randomized trial of the clinical utility of genetic testing for obesity: Design and implementation considerations
|
Wang, Catharine |
|
2014 |
11 |
1 |
p. 102-113 |
artikel |
6 |
A randomized trial of the clinical utility of genetic testing for obesity: Design and implementation considerations
|
Wang, Catharine |
|
2014 |
11 |
1 |
p. 102-113 |
artikel |
7 |
Beyond intention to treat: What is the right question?
|
Shrier, Ian |
|
2014 |
11 |
1 |
p. 28-37 |
artikel |
8 |
Beyond intention to treat: What is the right question?
|
Shrier, Ian |
|
2014 |
11 |
1 |
p. 28-37 |
artikel |
9 |
Bumps and bridges on the road to responsible sharing of clinical trial data
|
Berlin, Jesse A |
|
2014 |
11 |
1 |
p. 7-12 |
artikel |
10 |
Bumps and bridges on the road to responsible sharing of clinical trial data
|
Berlin, Jesse A |
|
2014 |
11 |
1 |
p. 7-12 |
artikel |
11 |
Clinical and Health Outcomes Initiative in Comparative Effectiveness for Bipolar Disorder (Bipolar CHOICE): A pragmatic trial of complex treatment for a complex disorder
|
Nierenberg, Andrew A |
|
2014 |
11 |
1 |
p. 114-127 |
artikel |
12 |
Clinical and Health Outcomes Initiative in Comparative Effectiveness for Bipolar Disorder (Bipolar CHOICE): A pragmatic trial of complex treatment for a complex disorder
|
Nierenberg, Andrew A |
|
2014 |
11 |
1 |
p. 114-127 |
artikel |
13 |
Clinician-trialist rounds: 19. Faux pas or fraud? Identifying centers that have fabricated their data in your multi-center trial
|
Pogue, Janice |
|
2014 |
11 |
1 |
p. 128-130 |
artikel |
14 |
Clinician-trialist rounds: 19. Faux pas or fraud? Identifying centers that have fabricated their data in your multi-center trial
|
Pogue, Janice |
|
2014 |
11 |
1 |
p. 128-130 |
artikel |
15 |
Commentary on Berlin et al.
|
Fergusson, Dean A |
|
2014 |
11 |
1 |
p. 13-14 |
artikel |
16 |
Commentary on Berlin et al.
|
Goldacre, Ben |
|
2014 |
11 |
1 |
p. 15-18 |
artikel |
17 |
Commentary on Berlin et al.
|
Fergusson, Dean A |
|
2014 |
11 |
1 |
p. 13-14 |
artikel |
18 |
Commentary on Berlin et al.
|
Goldacre, Ben |
|
2014 |
11 |
1 |
p. 15-18 |
artikel |
19 |
Corrigendum
|
|
|
2014 |
11 |
1 |
p. 133 |
artikel |
20 |
Corrigendum
|
|
|
2014 |
11 |
1 |
p. 133-133 |
artikel |
21 |
Editorial transition
|
Begg, Colin B |
|
2014 |
11 |
1 |
p. 5-6 |
artikel |
22 |
Editorial transition
|
Begg, Colin B |
|
2014 |
11 |
1 |
p. 5-6 |
artikel |
23 |
Expectations and experiences of investigators and parents involved in a clinical trial for Duchenne/Becker muscular dystrophy
|
Peay, Holly L |
|
2014 |
11 |
1 |
p. 77-85 |
artikel |
24 |
Expectations and experiences of investigators and parents involved in a clinical trial for Duchenne/Becker muscular dystrophy
|
Peay, Holly L |
|
2014 |
11 |
1 |
p. 77-85 |
artikel |
25 |
Marker Sequential Test (MaST) design
|
Freidlin, Boris |
|
2014 |
11 |
1 |
p. 19-27 |
artikel |
26 |
Marker Sequential Test (MaST) design
|
Freidlin, Boris |
|
2014 |
11 |
1 |
p. 19-27 |
artikel |
27 |
2013 Peer Reviewers
|
|
|
2014 |
11 |
1 |
p. 131-132 |
artikel |
28 |
2013 Peer Reviewers
|
|
|
2014 |
11 |
1 |
p. 131-132 |
artikel |
29 |
Satisfying the needs of Japanese cancer patients: A comparative study of detailed and standard informed consent documents
|
Sato, Keiko |
|
2014 |
11 |
1 |
p. 86-95 |
artikel |
30 |
Satisfying the needs of Japanese cancer patients: A comparative study of detailed and standard informed consent documents
|
Sato, Keiko |
|
2014 |
11 |
1 |
p. 86-95 |
artikel |
31 |
Survey of consent practices in cluster randomized trials: Improvements are needed in ethical conduct and reporting
|
Taljaard, Monica |
|
2014 |
11 |
1 |
p. 60-69 |
artikel |
32 |
Survey of consent practices in cluster randomized trials: Improvements are needed in ethical conduct and reporting
|
Taljaard, Monica |
|
2014 |
11 |
1 |
p. 60-69 |
artikel |
33 |
Understanding and retention of trial-related information among participants in a clinical trial after completing the informed consent process
|
Mexas, Fernanda |
|
2014 |
11 |
1 |
p. 70-76 |
artikel |
34 |
Understanding and retention of trial-related information among participants in a clinical trial after completing the informed consent process
|
Mexas, Fernanda |
|
2014 |
11 |
1 |
p. 70-76 |
artikel |
35 |
Use of health plan combined with registry data to predict clinical trial recruitment
|
Curtis, Jeffrey R |
|
2014 |
11 |
1 |
p. 96-101 |
artikel |
36 |
Use of health plan combined with registry data to predict clinical trial recruitment
|
Curtis, Jeffrey R |
|
2014 |
11 |
1 |
p. 96-101 |
artikel |