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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 [TBL] [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; 270(19):2321-5. PubMed ID: 8230594 [TBL] [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; 35(1):15-26. PubMed ID: 9832893 [TBL] [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; 65(3):279-87. PubMed ID: 17000074 [TBL] [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; 42(2):113-7. PubMed ID: 12424959 [TBL] [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; 30(12):1028-35. PubMed ID: 8133502 [TBL] [Abstract][Full Text] [Related]
11. Predictive Genetic Counseling for Neurodegenerative Diseases: Past, Present, and Future. Goldman JS Cold Spring Harb Perspect Med; 2020 Jul; 10(7):. PubMed ID: 31548223 [TBL] [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; 8(2):79-93. PubMed ID: 8060610 [TBL] [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; 54(3):174-84. PubMed ID: 7810575 [TBL] [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; 58(1):137-49. PubMed ID: 14572927 [TBL] [Abstract][Full Text] [Related]
15. Psychological reactions to predictive genetic testing for Huntington's disease: A qualitative study. TillerĂ¥s 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]
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; 24(6):1011-21. PubMed ID: 25921556 [TBL] [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; 174(1):75-92. PubMed ID: 27174011 [TBL] [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; 4(4):359-64. PubMed ID: 11216659 [TBL] [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; 60(6):442-6. PubMed ID: 11846736 [TBL] [Abstract][Full Text] [Related]
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