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 *

159 related articles for article (PubMed ID: 32568103)

  • 1. Family Communication Patterns and Challenges of Huntington's Disease Risk, the Decision to Pursue Presymptomatic Testing, and Test Results.
    Stuttgen K; Bollinger J; McCague A; Dvoskin R; Mathews D
    J Huntingtons Dis; 2020; 9(3):265-274. PubMed ID: 32568103
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Perspectives towards predictive testing in Huntington disease.
    Nagaraja SM; Jain S; Muthane UB
    Neurol India; 2006 Dec; 54(4):359-62. PubMed ID: 17114842
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 24(6):1011-21. PubMed ID: 25921556
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 29(6):1093-1105. PubMed ID: 32162754
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Communication and Huntington's disease: qualitative interviews and focus groups with persons with Huntington's disease, family members, and carers.
    Hartelius L; Jonsson M; Rickeberg A; Laakso K
    Int J Lang Commun Disord; 2010; 45(3):381-93. PubMed ID: 20144006
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Adults seeking presymptomatic gene testing for Huntington disease.
    Williams JK; Schutte DL; Evers CA; Forcucci C
    Image J Nurs Sch; 1999; 31(2):109-14. PubMed ID: 10380384
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Perspectives on Genetic Testing and Return of Results from the First Cohort of Presymptomatically Tested Individuals At Risk of Huntington Disease.
    Stuttgen KM; Bollinger JM; Dvoskin RL; McCague A; Shpritz B; Brandt J; Mathews DJH
    J Genet Couns; 2018 Dec; 27(6):1428-1437. PubMed ID: 29967967
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Perceptions of discrimination among persons who have undergone predictive testing for Huntington's disease.
    Penziner E; Williams JK; Erwin C; Bombard Y; Wallis A; Beglinger LJ; Hayden MR; Paulsen JS
    Am J Med Genet B Neuropsychiatr Genet; 2008 Apr; 147(3):320-5. PubMed ID: 17948904
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Disclosures of Huntington disease risk within families: patterns of decision-making and implications.
    Klitzman R; Thorne D; Williamson J; Chung W; Marder K
    Am J Med Genet A; 2007 Aug; 143A(16):1835-49. PubMed ID: 17632780
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 22 Years of predictive testing for Huntington's disease: the experience of the UK Huntington's Prediction Consortium.
    Baig SS; Strong M; Rosser E; Taverner NV; Glew R; Miedzybrodzka Z; Clarke A; Craufurd D; ; Quarrell OW
    Eur J Hum Genet; 2016 Oct; 24(10):1396-402. PubMed ID: 27165004
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The Changing Age of Individuals Seeking Presymptomatic Genetic Testing for Huntington Disease.
    Holman MA; Quillin J; York TP; Testa CM; Rosen AR; Norris VW
    J Genet Couns; 2018 Sep; 27(5):1157-1166. PubMed ID: 29460111
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 60(6):442-6. PubMed ID: 11846736
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Young People Living at Risk of Huntington's Disease: The Lived Experience.
    Lewit-Mendes MF; Lowe GC; Lewis S; Corben LA; Delatycki MB
    J Huntingtons Dis; 2018; 7(4):391-402. PubMed ID: 30372686
    [TBL] [Abstract][Full Text] [Related]  

  • 15. What to Do with a Second Chance in Life? Long-Term Experiences of Non-carriers of Huntington's Disease.
    Winnberg E; Winnberg U; Pohlkamp L; Hagberg A
    J Genet Couns; 2018 Dec; 27(6):1438-1446. PubMed ID: 29626325
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Impact of genetic testing for Huntington disease on the family system.
    Sobel SK; Cowan DB
    Am J Med Genet; 2000 Jan; 90(1):49-59. PubMed ID: 10602118
    [TBL] [Abstract][Full Text] [Related]  

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

  • 18. Presymptomatic testing for Huntington's disease. Emotional aspects.
    Zak JP; Zaglul JT; Mueller OT; Diamond T
    J Fla Med Assoc; 1994 Feb; 81(2):109-12. PubMed ID: 8169585
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Predictive testing for Huntington's disease: after the gene. The United Kingdom Huntington's Disease Prediction Consortium.
    Simpson SA; Harding AE
    J Med Genet; 1993 Dec; 30(12):1036-8. PubMed ID: 8133503
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.