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Journal Abstract Search

177 related items for PubMed ID: 8060609

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Molecular genetic predictive testing for Alzheimer's disease: deliberations and preliminary recommendations.
    Lennox A, Karlinsky H, Meschino W, Buchanan JA, Percy ME, Berg JM.
    Alzheimer Dis Assoc Disord; 1994; 8(2):126-47. PubMed ID: 8060605
    [Abstract] [Full Text] [Related]

  • 3. Ethical issues in Huntington disease presymptomatic testing.
    Turner DR, Willoughby JO.
    Aust N Z J Med; 1990 Aug; 20(4):545-7. PubMed ID: 2145829
    [No Abstract] [Full Text] [Related]

  • 4. Issues in genetic testing for susceptibility to alcoholism: lessons from Alzheimer's disease and Huntington's disease.
    Quaid KA, Dinwiddie H, Conneally PM, Nurnberger JI.
    Alcohol Clin Exp Res; 1996 Nov; 20(8):1430-7. PubMed ID: 8947321
    [Abstract] [Full Text] [Related]

  • 5. Attitudes toward direct predictive testing for the Huntington disease gene. Relevance for other adult-onset disorders. The Canadian Collaborative Group on Predictive Testing for Huntington Disease.
    Babul R, Adam S, Kremer B, Dufrasne S, Wiggins S, Huggins M, Theilmann J, Bloch M, Hayden MR.
    JAMA; 1993 Nov 17; 270(19):2321-5. PubMed ID: 8230594
    [Abstract] [Full Text] [Related]

  • 6. Presymptomatic testing for Huntington's disease.
    Bird SJ.
    JAMA; 1985 Jun 14; 253(22):3286-91. PubMed ID: 3158756
    [Abstract] [Full Text] [Related]

  • 7. Predictive testing for Huntington's disease: a challenge for persons at risk and for professionals.
    Evers-Kiebooms G, Decruyenaere M.
    Patient Educ Couns; 1998 Sep 14; 35(1):15-26. PubMed ID: 9832893
    [Abstract] [Full Text] [Related]

  • 8. To know or not to know: a review of behaviour and suicidal ideation in preclinical Huntington's disease.
    Robins Wahlin TB.
    Patient Educ Couns; 2007 Mar 14; 65(3):279-87. PubMed ID: 17000074
    [Abstract] [Full Text] [Related]

  • 9. [Analysis of 14 individuals who requested predictive genetic testing for hereditary neuromuscular diseases].
    Yoshida K, Tamai M, Kubota T, Kawame H, Amano N, Ikeda S, Fukushima Y.
    Rinsho Shinkeigaku; 2002 Feb 14; 42(2):113-7. PubMed ID: 12424959
    [Abstract] [Full Text] [Related]

  • 10. 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 14; 30(12):1028-35. PubMed ID: 8133502
    [Abstract] [Full Text] [Related]

  • 11. Predictive Genetic Counseling for Neurodegenerative Diseases: Past, Present, and Future.
    Goldman JS.
    Cold Spring Harb Perspect Med; 2020 Jul 01; 10(7):. PubMed ID: 31548223
    [Abstract] [Full Text] [Related]

  • 12. Ethical issues involved in establishing a registry for familial Alzheimer's disease.
    Godard B, Knoppers BM, Glass K, Grenon M, Bouchard R, Bouvier M, Goulet J, Gauvreau D.
    Alzheimer Dis Assoc Disord; 1994 Jul 01; 8(2):79-93. PubMed ID: 8060610
    [Abstract] [Full Text] [Related]

  • 13. Psychological costs and benefits of predictive testing for Huntington's disease.
    Codori AM, Brandt J.
    Am J Med Genet; 1994 Sep 15; 54(3):174-84. PubMed ID: 7810575
    [Abstract] [Full Text] [Related]

  • 14. Predictive genetic test decisions for Huntington's disease: context, appraisal and new moral imperatives.
    Taylor SD.
    Soc Sci Med; 2004 Jan 15; 58(1):137-49. PubMed ID: 14572927
    [Abstract] [Full Text] [Related]

  • 15. Psychological reactions to predictive genetic testing for Huntington's disease: A qualitative study.
    Tillerås KH, Kjoelaas SH, Dramstad E, Feragen KB, von der Lippe C.
    J Genet Couns; 2020 Dec 15; 29(6):1093-1105. PubMed ID: 32162754
    [Abstract] [Full Text] [Related]

  • 16. Analysis of the Reasons for Non-Uptake of Predictive Testing for Huntington's Disease in Spain: A Qualitative Study.
    Rivera-Navarro J, Cubo E, Mariscal N.
    J Genet Couns; 2015 Dec 15; 24(6):1011-21. PubMed ID: 25921556
    [Abstract] [Full Text] [Related]

  • 17. Genetic counseling and testing for Huntington's disease: A historical review.
    Nance MA.
    Am J Med Genet B Neuropsychiatr Genet; 2017 Jan 15; 174(1):75-92. PubMed ID: 27174011
    [Abstract] [Full Text] [Related]

  • 18. Disclosure of Huntington's disease to family members: the dilemma of known but unknowing parties.
    Hakimian R.
    Genet Test; 2000 Jan 15; 4(4):359-64. PubMed ID: 11216659
    [Abstract] [Full Text] [Related]

  • 19. To test or not to test: an ethical conflict with presymptomatic testing of individuals at 25% risk for Huntington's disorder.
    Lindblad AN.
    Clin Genet; 2001 Dec 15; 60(6):442-6. PubMed ID: 11846736
    [Abstract] [Full Text] [Related]

  • 20. Ethical principles and pitfalls of genetic testing for dementia.
    Hedera P.
    J Geriatr Psychiatry Neurol; 2001 Dec 15; 14(4):213-21. PubMed ID: 11794449
    [Abstract] [Full Text] [Related]

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