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Journal Abstract Search

107 related items for PubMed ID: 23438681

  • 1. Doing the right thing for one's children: deciding whether to take the genetic test for Huntington's disease as a moral dilemma.
    Smith JA, Stephenson M, Jacobs C, Quarrell O.
    Clin Genet; 2013 May; 83(5):417-21. PubMed ID: 23438681
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  • 2. Predictive genetic test decisions for Huntington's disease: elucidating the test/no-test dichotomy.
    Taylor SD.
    J Health Psychol; 2005 Jul; 10(4):597-612. PubMed ID: 16014395
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  • 3. 'You don't make genetic test decisions from one day to the next'--using time to preserve moral space.
    Scully JL, Porz R, Rehmann-Sutter C.
    Bioethics; 2007 May; 21(4):208-17. PubMed ID: 17845479
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  • 4. Risk Perception and Decision-making Processes in Candidates for Genetic Testing for Huntington's Disease: An Interpretative Phenomenological Analysis.
    Smith JA, Michie S, Stephenson M, Quarrell O.
    J Health Psychol; 2002 Mar; 7(2):131-44. PubMed ID: 22114233
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  • 5. The complexity of reproductive decision-making in asymptomatic carriers of the Huntington mutation.
    Decruyenaere M, Evers-Kiebooms G, Boogaerts A, Philippe K, Demyttenaere K, Dom R, Vandenberghe W, Fryns JP.
    Eur J Hum Genet; 2007 Apr; 15(4):453-62. PubMed ID: 17245406
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  • 6. Predictive genetic test decisions for Huntington's disease: context, appraisal and new moral imperatives.
    Taylor SD.
    Soc Sci Med; 2004 Jan; 58(1):137-49. PubMed ID: 14572927
    [Abstract] [Full Text] [Related]

  • 7. Genetic Counselling for Predictive Testing in Huntington's Disease in One Centre since 1993. Gender-Specific Aspects of Decision-Making.
    Arning L, Witt CN, Epplen JT, Stemmler S.
    J Huntingtons Dis; 2015 Jan; 4(1):87-98. PubMed ID: 26333260
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  • 15. Using the Best Interests Standard to decide whether to test children for untreatable, late-onset genetic diseases.
    Kopelman LM.
    J Med Philos; 2007 Jan; 32(4):375-94. PubMed ID: 17712709
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  • 16. Recommendations for the predictive genetic test in Huntington's disease.
    MacLeod R, Tibben A, Frontali M, Evers-Kiebooms G, Jones A, Martinez-Descales A, Roos RA, Editorial Committee and Working Group ‘Genetic Testing Counselling’ of the European Huntington Disease Network.
    Clin Genet; 2013 Mar; 83(3):221-31. PubMed ID: 22642570
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  • 18. [Psychosocial consequences of presymptomatic genetic testing. A retrospective study of testing for Huntington disease].
    Jakobsen LB, Malt U, Nilsson B, Rosenlund S, Heiberg A.
    Tidsskr Nor Laegeforen; 1999 May 20; 119(13):1913-6. PubMed ID: 10382341
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  • 19. Genetic discrimination in Huntington's disease.
    Tibben A.
    BMJ; 2009 Jun 09; 338():b1281. PubMed ID: 19509423
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