|
Nr. |
Eintrag |
|
1 |
Apold, Victoria Smith; Downie, Jocelyn:
Bad news about bad news: the disclosure of risks to insurability in research consent processes.
In: Accountability in research, 2011, Vol. 18 (1), 31-44 |
|
2 |
Markestad, Trond:
[Information about hereditary disposition in connection with health insurance application]. = Opplysninger om arvelig disposisjon ved søknad om helseforsikring.
In: Tidsskrift for den Norske lægeforening : tidsskrift for praktisk medicin, ny række, 2011, Vol. 131 (9-10), 975-7 |
|
3 |
Goldgar, Constance:
GINA: What PAs need to know to protect patients and their families.
In: JAAPA : official journal of the American Academy of Physician Assistants, 2010, Vol. 23 (7), 56-9 |
|
4 |
Kious, Brent M:
Genetic nondiscrimination and health care as an entitlement.
In: The Journal of medicine and philosophy 2010 Apr ; 35(2): 86-100 |
|
5 |
Kious, Brent M.:
Genetic nondiscrimination and health care as an entitlement.
In: Journal of Medicine and Philosophy, 2010, Vol. 35 (2), 86-100 |
|
6 |
Pauly, Mark V.:
Avoiding side effects in implementing health insurance reform.
In: New England Journal of Medicine, 2010, Vol. 362 (8), 671-673 |
|
7 |
Wilkinson, Ruth:
Unjustified discrimination: is the moratorium on the use of genetic test results by insurers a contradiction in terms?
In: Health care analysis : HCA : journal of health philosophy and policy, 2010, Vol. 18 (3), 279-93 |
|
8 |
Cut-price DNA tests [news]
In: New Scientist, 2010, Vol. 205 (2748), 4 |
|
9 |
Affleck, Paul:
Is it ethical to deny genetic research participants individualised results?
In: Journal of Medical Ethics, 2009, Vol. 35 (4), 209-213 |
|
10 |
Barlow-Stewart, Kristine et al.:
Verification of consumers' experiences and perceptions of genetic discrimination and its impact on utilization of genetic testing.
In: Genetics in Medicine, 2009, Vol. 11 (3), 193-201 |
|
11 |
Blumberg, Linda J.; Holahan, John:
The individual mandate -- an affordable and fair approach to achieving universal coverage [commentary]
In: New England Journal of Medicine, 2009, Vol. 361 (1), 6-7 |
|
12 |
Payne, Perry W. et al.:
Health insurance and the Genetic Information Nondiscrimination Act of 2008: implications for public health policy and practice.
In: Public Health Reports, 2009, Vol. 124 (2), 328-331 |
|
13 |
Health law - genetics - Congress restricts use of genetic information by insurers and employers. - Genetic Information Nondiscrimination Act of 2008, Pub. L. No. 110-233, 122 Stat. 881 (to be codified in scattered sections of 26, 29, and 42 U.S.C.).
In: Harvard Law Review, 2009, Vol. 122 (3), 1038-1045 |
|
14 |
Asmonga, Don:
Getting to know GINA. An overview of the Genetic Information Nondiscrimination Act.
In: Journal of the American Health Information Management Association, 2008, Vol. 79 (7), 18, 20, 22 |
|
15 |
Bombard, Yvonne et al.:
Engagement with genetic discrimination: concerns and experiences in the context of Huntington disease.
In: European Journal of Human Genetics, 2008, Vol. 16 (3), 279-289 |
|
16 |
Evans, James P.:
Health care in the age of genetic medicine
In: Genetics in Medicine, 2008, Vol. 10 (1), 1-3 |
|
17 |
Friedman, David D.:
The more you know ....
In: Friedman, David D. Future Imperfect: Technology and Freedom in an Uncertain World. New York: Cambridge University Press, 2008: 202-215 |
|
18 |
Homsma, Sietske J.M. et al.:
Molecular screening for familial hypercholesterolaemia: consequences for life and disability insurance
In: European Journal of Human Genetics, 2008, Vol. 16 (1), 14-17 |
|
19 |
Hudson, Kathy L.; Holohan, M.K.; Collins, Francis S.:
Keeping pace with the times -- the Genetic Information Nondiscrimination Act of 2008
In: New England Journal of Medicine, 2008, Vol. 358 (25), 2661-2663 |
|
20 |
Korobkin, Russell; Rajukumar, Rahul:
The Genetic Information Nondiscrimination Act -- a half-step toward risk sharing
In: New England Journal of Medicine, 2008, Vol. 359 (4), 335-337 |
