Secondary Symptoms Dementia: Huntington Disease Dementia
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Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-030-12852-4_5-1
Reference31 articles.
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2. Bombard, Y., Penziner, E., Decolongon, J., Klimek, M. L. N., Creighton, S., Suchowersky, O., … Hayden, M. R. (2007). Managing genetic discrimination: Strategies used by individuals found to have the Huntington disease mutation. Clinical Genetics, 71, 220–231.
3. Bombard, Y., Veenstra, G., Friedman, J. M., Creighton, S., Currie, L., Paulsen, J. S., … Hayden, M. R. (2009). Perceptions of genetic discrimination among people at risk for Huntington’s disease: A cross sectional survey. BMJ, 338, b2175.
4. Cox, S. M. (2003). Stories in decisions: How at-risk individuals decide to request predictive testing for Huntington disease. Qualitative Sociology, 26, 257–280.
5. Cox, S. M., & McKellin, W. (1999). ‘There’s this thing in our family’: Predictive testing and the construction of risk for Huntington disease. Sociology of Health & Illness, 21, 622–646.
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