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Herman Nys

Showing results (71-80 of 84) with videos related to

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Journal of Medical Ethics|November 10, 2010
The return of individual research findings in paediatric genetic researchKristien Hens, Herman Nys, Jean-Jacques Cassiman, et al.
European Journal of Medical Genetics|July 14, 2010
The use of diagnostic collections of DNA for research: interviews at the eight Belgian centers for human geneticsKristien Hens, Herman Nys, Jean-Jacques Cassiman, et al.
Health Care Analysis : HCA : Journal of Health Philosophy and Policy|January 22, 2005
Patient capacity in mental health care: legal overviewHerman Nys, Sander Welie, Tina Garanis-Papadatos, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Genetic research on stored tissue samples from minors: a systematic review of the ethical literatureKristien Hens, Herman Nys, Jean-Jacques Cassiman, et al.
European Journal of Human Genetics : EJHG|March 10, 2011
Children, biobanks and the scope of parental consentKristien Hens, Jean-Jacques Cassiman, Herman Nys, et al.
Health Policy (Amsterdam, Netherlands)|March 24, 2007
Patient rights in EU Member States after the ratification of the Convention on Human Rights and BiomedicineHerman Nys, Loes Stultiëns, Pascal Borry, et al.
European Journal of Health Law|June 15, 2007
Minors and informed consent: a comparative approachLoes Stultiëns, Tom Goffin, Pascal Borry, et al.
European Journal of Health Law|September 25, 2004
CIOMS' placebo rule and the promotion of negligent medical practiceTrudo Lemmens, Dominique Sprumont, Herman Nys, et al.
Health Policy (Amsterdam, Netherlands)|May 25, 2005
Patient incompetence and substitute decision-making: an analysis of the role of the health care professional in Dutch lawSander P K Welie, Joseph Dute, Herman Nys, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
The use of cells from cystic fibrosis patients in research. A model consent formCaroline Trouet, Ingrid Dreezen, Kris Dierickx, et al.
Pageof 9

Showing results (71-80 of 84) with videos related to

Sort By:
Pageof 9
Journal of Medical Ethics|November 10, 2010
The return of individual research findings in paediatric genetic researchKristien Hens, Herman Nys, Jean-Jacques Cassiman, et al.
European Journal of Medical Genetics|July 14, 2010
The use of diagnostic collections of DNA for research: interviews at the eight Belgian centers for human geneticsKristien Hens, Herman Nys, Jean-Jacques Cassiman, et al.
Health Care Analysis : HCA : Journal of Health Philosophy and Policy|January 22, 2005
Patient capacity in mental health care: legal overviewHerman Nys, Sander Welie, Tina Garanis-Papadatos, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Genetic research on stored tissue samples from minors: a systematic review of the ethical literatureKristien Hens, Herman Nys, Jean-Jacques Cassiman, et al.
European Journal of Human Genetics : EJHG|March 10, 2011
Children, biobanks and the scope of parental consentKristien Hens, Jean-Jacques Cassiman, Herman Nys, et al.
Health Policy (Amsterdam, Netherlands)|March 24, 2007
Patient rights in EU Member States after the ratification of the Convention on Human Rights and BiomedicineHerman Nys, Loes Stultiëns, Pascal Borry, et al.
European Journal of Health Law|June 15, 2007
Minors and informed consent: a comparative approachLoes Stultiëns, Tom Goffin, Pascal Borry, et al.
European Journal of Health Law|September 25, 2004
CIOMS' placebo rule and the promotion of negligent medical practiceTrudo Lemmens, Dominique Sprumont, Herman Nys, et al.
Health Policy (Amsterdam, Netherlands)|May 25, 2005
Patient incompetence and substitute decision-making: an analysis of the role of the health care professional in Dutch lawSander P K Welie, Joseph Dute, Herman Nys, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
The use of cells from cystic fibrosis patients in research. A model consent formCaroline Trouet, Ingrid Dreezen, Kris Dierickx, et al.
Pageof 9