These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

356 related articles for article (PubMed ID: 11216659)

  • 1. Disclosure of Huntington's disease to family members: the dilemma of known but unknowing parties.
    Hakimian R
    Genet Test; 2000; 4(4):359-64. PubMed ID: 11216659
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The Double Helix: Applying an Ethic of Care to the Duty to Warn Genetic Relatives of Genetic Information.
    Weaver M
    Bioethics; 2016 Mar; 30(3):181-7. PubMed ID: 26194147
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic testing: do healthcare professionals have a duty to tell a patient's family members that they may be at risk?
    Marta MR
    J Healthc Risk Manag; 1999; 19(3):26-38. PubMed ID: 10538434
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Beyond the diagnosis of a genetic disease, the question of informing the relatives].
    Pellerin P
    Ann Pharm Fr; 2009 Jan; 67(1):20-4. PubMed ID: 19152847
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Case vignette: genetic secrets.
    McCormick RA; Korf BR; Wexler NS
    Ethics Behav; 1992; 2(2):129-39. PubMed ID: 11651254
    [TBL] [Abstract][Full Text] [Related]  

  • 6. It's been a privilege: advising patients of the Tarasoff duty and its legal consequences for the federal psychotherapist-patient privilege.
    Klinka E
    Fordham Law Rev; 2009 Nov; 78(2):863-931. PubMed ID: 19938380
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A physician's duty to warn family members of genetic risks: limiting the importance of Tarasoff.
    Russell S
    J Biolaw Bus; 2003; 6(1):28-38. PubMed ID: 15239180
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Psychological aspects of genetic counseling: a legal perspective.
    Sharpe NF
    Am J Med Genet; 1994 Apr; 50(3):234-8. PubMed ID: 8042666
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Legal and ethical issues in genetic testing and counseling for susceptibility to breast, ovarian and colon cancer.
    Dickens BM; Pei N; Taylor KM
    CMAJ; 1996 Mar; 154(6):813-8. PubMed ID: 8634959
    [TBL] [Abstract][Full Text] [Related]  

  • 10. What should the law say about disclosure of genetic information to relatives?
    Clayton EW
    J Health Care Law Policy; 1998; 1(2):373-90. PubMed ID: 16281334
    [No Abstract]   [Full Text] [Related]  

  • 11. Ethical and social issues in presymptomatic testing for Huntington's disease: a European Community collaborative study. European Community Huntington's Disease Collaborative Study Group.
    J Med Genet; 1993 Dec; 30(12):1028-35. PubMed ID: 8133502
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [The limits of the physician's secrecy duty in risk situations. Special reference to genetics].
    Gómez Rivero Mdel C
    Rev Derecho Genoma Hum; 2007; (26):43-89. PubMed ID: 18201038
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [The genetic diagnosis law: Who may know how much?].
    Hügler S
    Dtsch Med Wochenschr; 2009 Mar; 134(13):p12. PubMed ID: 19326337
    [No Abstract]   [Full Text] [Related]  

  • 14. The family covenant and genetic testing.
    Doukas DJ; Berg JW
    Am J Bioeth; 2001; 1(3):3-10. PubMed ID: 11954587
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Legal aspects of genetic information.
    Andrews LB
    Yale J Biol Med; 1991; 64(1):29-40. PubMed ID: 1897258
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The "duty to warn" a patient's family members about hereditary disease risks.
    Offit K; Groeger E; Turner S; Wadsworth EA; Weiser MA
    JAMA; 2004 Sep; 292(12):1469-73. PubMed ID: 15383518
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Whose genes are these anyway?: familial conflicts over access to genetic information.
    Suter SM
    Mich Law Rev; 1993 Jun; 91(7):1854-908. PubMed ID: 10129309
    [No Abstract]   [Full Text] [Related]  

  • 18. Patient autonomy and relatives' right to know genetic information.
    Gilbar R
    Med Law; 2007 Dec; 26(4):677-97. PubMed ID: 18284110
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Informed consent and Huntington disease: a model for communication.
    Sharpe NF
    Am J Med Genet; 1994 Apr; 50(3):239-46. PubMed ID: 8042667
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Privacy, confidentiality, and privilege in psychotherapeutic relationships.
    Smith-Bell M; Winslade WJ
    Am J Orthopsychiatry; 1994 Apr; 64(2):180-93. PubMed ID: 8037228
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.