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Cognitive, motor, and behavioral correlates of functional decline in Huntington's disease /Hamilton, Joanne M. January 2000 (has links)
Thesis (Ph. D.)--University of California, San Diego, 2000. / Vita. Includes bibliographical references (leaves 165-180).
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Molecular mechanisms of Huntington's Disease pathogenesis /Ryan, Amy Beth. January 2006 (has links)
Thesis (Ph. D.)--University of Virginia, 2006. / Includes bibliographical references. Also available online through Digital Dissertations.
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Unawareness of deficits in Huntington's diseaseMcGlynn, Susan Mary, 1960- January 1989 (has links)
Several new techniques were developed to assess quantitatively the degree to which patients with Huntington's disease (HD) are aware of their deficits, to evaluate the relation between cognitive impairment and unawareness of deficits, and to determine whether patients exhibit differential awareness of their motor disturbance and cognitive deficits. Results of a questionnaire measure indicated that HD patients rated their own difficulties with motor and cognitive activities of daily life significantly lower than relatives rated patients' problems, and this discrepancy was related to patients' level of cognitive impairment. In contrast, patients were reasonably accurate when predicting their performance on specific motor and cognitive tasks when compared to both their actual performance and relatives' predictions. Several interpretations of these findings are discussed, and the role of frontal lobe dysfunction in the awareness problems characterizing dementia is considered.
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Genetic testing in the age of anxiety. From rhetoric to narrative.Leontini, Rose, School of Sociology, UNSW January 2005 (has links)
The debate on genetic testing for Huntington???s disease has been dominated heavily by the bioethical and biomedical discourses. Yet upon analysis, both discourses are highly inadequate for understanding the complexity of the difficult choices people are faced with, and the inter-personal relations that are central to decisions regarding the uptake of genetic tests. The purpose of this thesis is two-fold. Firstly, to conduct a theoretically-informed critical analysis of the existing bioethical discourse on genetic testing for Huntington???s disease, that draws primarily on the work of contemporary feminist thinkers. Secondly, to explore how people with a genetic risk for Huntington???s disease negotiate the available choices between certainty and uncertainty; how they experience the liminality of ???being at risk??? in everyday life; how they manage their social environments; and how they interpret their own situation. The matter of ???choice??? is heightened because of the ready availability of genetic testing for Huntington???s disease, and the moral rhetoric that accompanies the provision of genetic services. Empirically, the research draws on the narratives by eleven people with a family history of Huntington???s disease, through which they discuss their fears of living in the shadow of the fatal disease, and consider their choices on reproduction and genetic testing. Their narratives will be analysed through the work of Foucault and Goffman, as well as a wide range of contemporary sociologists.The thesis being proposed is that decisions on genetic testing cannot be said to be ???individual???, but are instead dispersed among the social relations between the self and others, reflecting and transforming the values, competing desires, and the discourses that are prevalent in their social worlds. This is achieved through the discursive production of a web of narratives through which both individuals and institutions attempt to govern, with varying degrees of success, the implications of this relatively new field of knowledge.
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Genetic modifiers and therapeutic strategies in Huntington's diseaseUnderwood, Benjamin Russell January 2011 (has links)
No description available.
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Altered Adult Hippocampal Structural and Functional Plasticity in the YAC128 Transgenic Mouse Model of Huntington DiseaseSimpson, Jessica M. 30 September 2013 (has links)
Alterations in both structural and synaptic plasticity in the adult brain have been
implicated in impaired learning and memory. In the present study, we investigated if
hippocampal plasticity is affected in the transgenic YAC128 mouse model of Huntington
disease (HD). Reductions in adult hippocampal neurogenesis were observed in the
dentate gyrus (DG) of early symptomatic to end-stage mice compared with wild-type
(WT) controls, however there were no changes in cell proliferation and differentiation in
the subventricular zone. Early symptomatic mice also displayed attenuated paired-pulse
plasticity and long-term depression in the DG, while long-term potentiation was found to
be normal in YAC128 mice. The changes in hippocampal plasticity may contribute to the
cognitive abnormalities observed in these animals. / Graduate / 0306
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Genetic testing in the age of anxiety. From rhetoric to narrative.Leontini, Rose, School of Sociology, UNSW January 2005 (has links)
The debate on genetic testing for Huntington???s disease has been dominated heavily by the bioethical and biomedical discourses. Yet upon analysis, both discourses are highly inadequate for understanding the complexity of the difficult choices people are faced with, and the inter-personal relations that are central to decisions regarding the uptake of genetic tests. The purpose of this thesis is two-fold. Firstly, to conduct a theoretically-informed critical analysis of the existing bioethical discourse on genetic testing for Huntington???s disease, that draws primarily on the work of contemporary feminist thinkers. Secondly, to explore how people with a genetic risk for Huntington???s disease negotiate the available choices between certainty and uncertainty; how they experience the liminality of ???being at risk??? in everyday life; how they manage their social environments; and how they interpret their own situation. The matter of ???choice??? is heightened because of the ready availability of genetic testing for Huntington???s disease, and the moral rhetoric that accompanies the provision of genetic services. Empirically, the research draws on the narratives by eleven people with a family history of Huntington???s disease, through which they discuss their fears of living in the shadow of the fatal disease, and consider their choices on reproduction and genetic testing. Their narratives will be analysed through the work of Foucault and Goffman, as well as a wide range of contemporary sociologists.The thesis being proposed is that decisions on genetic testing cannot be said to be ???individual???, but are instead dispersed among the social relations between the self and others, reflecting and transforming the values, competing desires, and the discourses that are prevalent in their social worlds. This is achieved through the discursive production of a web of narratives through which both individuals and institutions attempt to govern, with varying degrees of success, the implications of this relatively new field of knowledge.
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A study of depression in Huntington's disease /Pang, Terence Yeow-Chwen. January 2008 (has links)
Thesis (Ph.D.)--University of Melbourne, Howard Florey Institute, Dept. of Anatomy & Cell Biology, 2009. / Typescript. Includes bibliographical references (leaves 223-261)
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Anatomical and experimental studies on the neuropeptide γ-immunoreactive neuronal system in the rat brainAllen, Yvonne Susan January 1985 (has links)
No description available.
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Reduction of huntingtin aggregation and transcript levels by utilization of guanine rich oligonucleotidesSkogen, Michael John. January 2007 (has links)
Thesis (M.S.)--University of Delaware, 2007. / Principal faculty advisor: Eric B. Kmiec, Dept. of Biological Sciences. Includes bibliographical references.
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