Physician-assisted suicide

Por van Delden, Johannes JM
Publicado em 1998

Terminal sedation: source of a restless ethical debate

Por van Delden, Johannes J M
Publicado em 2007

Filial obligations to elderly parents: a duty to care?

Por Stuifbergen, Maria C., Van Delden, Johannes J. M.
Publicado em 2010

Strengths and weaknesses of guideline approaches to safeguard voluntary informed consent of patients within a dependent relationship

Por Dekking, Sara AS, van der Graaf, Rieke, van Delden, Johannes JM
Publicado em 2014

The social value of clinical research

Por Habets, Michelle GJL, van Delden, Johannes JM, Bredenoord, Annelien L
Publicado no BMC Med Ethics (2014)

Consent procedures in pediatric biobanks

Por Giesbertz, Noor AA, Bredenoord, Annelien L, van Delden, Johannes JM
Publicado no Eur J Hum Genet (2015)

Inclusion of Residual Tissue in Biobanks: Opt-In or Opt-Out?

Por Giesbertz, Noor A. A., Bredenoord, Annelien L., van Delden, Johannes J. M.
Publicado em 2012

Clarifying assent in pediatric research

Por Giesbertz, Noor A A, Bredenoord, Annelien L, van Delden, Johannes J M
Publicado em 2014

Reply to Waligora

Por Giesbertz, Noor A A, Bredenoord, Annelien L, van Delden, Johannes J M
Publicado em 2014

When Children Become Adults: Should Biobanks Re-Contact?

Por Giesbertz, Noor A. A., Bredenoord, Annelien L., van Delden, Johannes J. M.
Publicado no PLoS Med (2016)

Organoid biobanking: identifying the ethics: Organoids revive old and raise new ethical challenges for basic research and therapeutic use

Por Boers, Sarah N, van Delden, Johannes JM, Clevers, Hans, Bredenoord, Annelien L
Publicado no EMBO Rep (2016)

Big Data in medical research and EU data protection law: challenges to the consent or anonymise approach

Por Mostert, Menno, Bredenoord, Annelien L, Biesaart, Monique CIH, van Delden, Johannes JM
Publicado no Eur J Hum Genet (2016)

The fiduciary obligation of the physician-researcher in phase IV trials

Por Bernabe, Rosemarie DLC, van Thiel, Ghislaine JMW, Raaijmakers, Jan AM, van Delden, Johannes JM
Publicado em 2014

Patient representatives' contributions to the benefit‐risk assessment tasks of the European Medicines Agency scientific committees

Por Bernabe, Rosemarie D L C, van Thiel, Ghislaine J M W, van Delden, Johannes
Publicado no Br J Clin Pharmacol (2014)

Patients' evaluation of informed consent to postponed information: cohort study

Por Boter, Han, van Delden, Johannes J M, de Haan, Rob J, Rinkel, Gabriël J E
Publicado em 2004

Modified informed consent procedure: consent to postponed information

Por Boter, Han, van Delden, Johannes J M, de Haan, Rob J, Rinkel, Gabriël J E
Publicado em 2003

Big Data in medical research and EU data protection law: challenges to the consent or anonymise approach

Por Mostert, Menno, Bredenoord, Annelien L, Biesaart, Monique C I H, van Delden, Johannes J M
Publicado no Eur J Hum Genet (2016)

What do international ethics guidelines say in terms of the scope of medical research ethics?

Por Bernabe, Rosemarie D. L. C., van Thiel, Ghislaine J. M. W., van Delden, Johannes J. M.
Publicado no BMC Med Ethics (2016)

Personalized assent for pediatric biobanks

Por Giesbertz, Noor A. A., Melham, Karen, Kaye, Jane, van Delden, Johannes J. M., Bredenoord, Annelien L.
Publicado no BMC Med Ethics (2016)

One Size Fits All?: Ethical Considerations for Examining Efficacy in First-in-Human Pluripotent Stem Cell Studies

Por Habets, Michelle GJL, van Delden, Johannes JM, Niemansburg, Sophie L, Atkins, Harold L, Bredenoord, Annelien L
Publicado no Mol Ther (2016)