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Nederlands Tijdschrift Voor Geneeskunde
|
January 23, 2014
[Introduction of next-generation sequencing in health care: what are the implications for physicians and patients?]
Corrette Ploem, Wybo Dondorp, Guido de Wert, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
November 7, 2013
[Compare new therapies with old, not with a placebo: a plea for revision of the Declaration of Helsinki]
Dick L Willems, M Corrette Ploem, M Rien Vermeulen
European Journal of Medical Genetics
|
March 25, 2019
Experts reflecting on the duty to recontact patients and research participants; why professionals should take the lead in developing guidelines
Colin Mitchell, Corrette Ploem, Valesca Retèl, et al.
European Journal of Human Genetics : EJHG
|
April 16, 2015
Regulating biobanking with children's tissue: a legal analysis and the experts' view
Elcke J Kranendonk, M Corrette Ploem, Raoul C M Hennekam
European Journal of Pediatrics
|
October 23, 2015
Data research on child abuse and neglect without informed consent? Balancing interests under Dutch law
Eva M M Hoytema van Konijnenburg, Arianne H Teeuw, M Corrette Ploem
Health Policy (Amsterdam, Netherlands)
|
May 27, 2023
Towards a less voluntary vaccination policy in the Netherlands? Findings from an expert interview study
Rogier C Simons, Marieke A R Bak, Johan Legemaate, et al.
Health Research Policy and Systems
|
January 30, 2020
Exempting low-risk health and medical research from ethics reviews: comparing Australia, the United Kingdom, the United States and the Netherlands
Anna Mae Scott, Simon Kolstoe, M C Corrette Ploem, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
October 16, 2015
[The 'interesting case' and patient privacy: handling patient data in medical education]
Lieve G J Leijssen, Gabor E Linthorst, Vincent G Geukers, et al.
BMC Medical Ethics
|
November 24, 2021
A genetic researcher's devil's dilemma: Warn relatives about their genetic risk or respect confidentiality agreements with research participants?
Lieke M van den Heuvel, Els L M Maeckelberghe, M Corrette Ploem, et al.
Healthcare (Basel, Switzerland)
|
June 13, 2025
Bridging Barriers: Engaging Ethnic Minorities in Cardiovascular Research
Nora Bacour, Simran Grewal, M Corrette Ploem, et al.
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Search research articles
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Showing results (11-20 of 39) with videos related to
Sort By:
Page
of 4
Nederlands Tijdschrift Voor Geneeskunde
|
January 23, 2014
[Introduction of next-generation sequencing in health care: what are the implications for physicians and patients?]
Corrette Ploem, Wybo Dondorp, Guido de Wert, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
November 7, 2013
[Compare new therapies with old, not with a placebo: a plea for revision of the Declaration of Helsinki]
Dick L Willems, M Corrette Ploem, M Rien Vermeulen
European Journal of Medical Genetics
|
March 25, 2019
Experts reflecting on the duty to recontact patients and research participants; why professionals should take the lead in developing guidelines
Colin Mitchell, Corrette Ploem, Valesca Retèl, et al.
European Journal of Human Genetics : EJHG
|
April 16, 2015
Regulating biobanking with children's tissue: a legal analysis and the experts' view
Elcke J Kranendonk, M Corrette Ploem, Raoul C M Hennekam
European Journal of Pediatrics
|
October 23, 2015
Data research on child abuse and neglect without informed consent? Balancing interests under Dutch law
Eva M M Hoytema van Konijnenburg, Arianne H Teeuw, M Corrette Ploem
Health Policy (Amsterdam, Netherlands)
|
May 27, 2023
Towards a less voluntary vaccination policy in the Netherlands? Findings from an expert interview study
Rogier C Simons, Marieke A R Bak, Johan Legemaate, et al.
Health Research Policy and Systems
|
January 30, 2020
Exempting low-risk health and medical research from ethics reviews: comparing Australia, the United Kingdom, the United States and the Netherlands
Anna Mae Scott, Simon Kolstoe, M C Corrette Ploem, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
October 16, 2015
[The 'interesting case' and patient privacy: handling patient data in medical education]
Lieve G J Leijssen, Gabor E Linthorst, Vincent G Geukers, et al.
BMC Medical Ethics
|
November 24, 2021
A genetic researcher's devil's dilemma: Warn relatives about their genetic risk or respect confidentiality agreements with research participants?
Lieke M van den Heuvel, Els L M Maeckelberghe, M Corrette Ploem, et al.
Healthcare (Basel, Switzerland)
|
June 13, 2025
Bridging Barriers: Engaging Ethnic Minorities in Cardiovascular Research
Nora Bacour, Simran Grewal, M Corrette Ploem, et al.
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of 4