Selective Attention And The Processing Of Observed Actions.
Funder
National Health and Medical Research Council
Funding Amount
$343,812.00
Summary
Our ability to understand the hand and face gestures of others is a crucial part of social interaction. Deficits in the ability to perceive others' actions are associated with clinical disorders such as autism and apraxia. We will examine how specific regions of the brain operate to process and recognise actions that we observe. This is a crucial first-step toward understanding and redefining clinical disorders such as apraxia that involve deficits in the perception of actions and gestures.
The Impact Of Oxytocin On Social Cognition And Behaviour In Youth With Autism Spectrum Disorders.
Funder
National Health and Medical Research Council
Funding Amount
$261,117.00
Summary
Deficits in social functioning are one of the core features of Autism Spectrum Disorders and evidence suggests that the Oxytocin (OT) system may be dysregulated in these individuals. This proposal tests the effects of synthetic OT in a sample of youth with ASD on measures of social cognition and behaviour. This research may lead to more efficient and effective treatments for ASD and may enhance our understanding of the mechanisms underlying Autism and related disorders.
Long Term Outcome From Early Childhood Brain Injury: 10 Year Follow Up
Funder
National Health and Medical Research Council
Funding Amount
$338,900.00
Summary
The primary aim of this project is to further improve our understanding of the long-term consequences of childhood traumatic brain injury (TBI). Over the past decade our research team has ascertained a sample of children sustaining TBI, and systematically followed their progress over a 5-year period. The project has an international reputation, and is unique in terms of length of follow-up, prospective design and representative, well-maintained sample. Our findings challenge the traditionally he ....The primary aim of this project is to further improve our understanding of the long-term consequences of childhood traumatic brain injury (TBI). Over the past decade our research team has ascertained a sample of children sustaining TBI, and systematically followed their progress over a 5-year period. The project has an international reputation, and is unique in terms of length of follow-up, prospective design and representative, well-maintained sample. Our findings challenge the traditionally held view that children are resilient and recover fully from early brain insult. Rather, we have shown that, up to 5 years post-TBI, many children experience impairments in physical, cognitive and behavioural function. These impairments result in educational, vocational, social and emotional problems, limiting the child's capacity to meet developmental expectations and achieve adequate quality of life. The implication is that these problems will lead to life-long disability, resulting in high levels of individual, family and community burden. However, with follow-up data limited to 5 years, there remains a possibility that ongoing developmental processes may support an extended recovery period in childhood TBI, in comparison to the 2-year period cited in adult models. The review of this sample, 10 years post-injury, provides an unprecedented opportunity to address this possibility and to document recovery-outcome as children move into adolescence and adulthood. Not all children experience problems post-injury. However, predicting individual outcome remains a significant challenge, with particular clinical relevance to treatment and follow-up. Thus, the second aim of the proposed study is to examine factors that contribute to recovery and outcome.Read moreRead less
A Study Addressing Motor, Cognitive And Attentional Deficits In Presymptomatic Gene Carriers For Huntington's Disease
Funder
National Health and Medical Research Council
Funding Amount
$180,330.00
Summary
Since the discovery of the Huntington's disease (HD) gene mutation there has been much controversy in the literature relating to whether there are any preclinical deficits in individuals who are gene positive for HD but who have not yet been clinically diagnosed with the disease. Our aim is to examine, over a three year period, the cognitive, attentional and motor performance of presymptomatic gene-positive, and negative, individuals on a wide variety of computerized experimental procedures, whi ....Since the discovery of the Huntington's disease (HD) gene mutation there has been much controversy in the literature relating to whether there are any preclinical deficits in individuals who are gene positive for HD but who have not yet been clinically diagnosed with the disease. Our aim is to examine, over a three year period, the cognitive, attentional and motor performance of presymptomatic gene-positive, and negative, individuals on a wide variety of computerized experimental procedures, which we have previously shown to be sensitive to deficits in individuals who have already been diagnosed with HD. If progressive behavioural changes in gene-positive individuals can be reliably documented to occur before the clinical symptoms of HD are evident, this would be of profound significance as it would allow a set of criteria to be established to assist in early detection of clinical onset of symptoms, and possibly permit use of newly-emerging therapies.Read moreRead less
An Event Related Functional Magnetic Resonance Imaging (fMRI) Study Of Cognitive Deficits In Huntington's Disease
Funder
National Health and Medical Research Council
Funding Amount
$257,550.00
Summary
Huntington's disease (HD) is a progressive disorder clinically characterized by the onset of involuntary jerky movements, impaired voluntary movements, cognitive-attentional deterioration, and psychiatric symptoms. It is a consequence of progressive and selective brain degeneration. Over the last decade our research unit has made significant progress in describing the cognitive deficits in HD; however, we still don't know much about the parts of the brain that underlie these deficits. The aim of ....Huntington's disease (HD) is a progressive disorder clinically characterized by the onset of involuntary jerky movements, impaired voluntary movements, cognitive-attentional deterioration, and psychiatric symptoms. It is a consequence of progressive and selective brain degeneration. Over the last decade our research unit has made significant progress in describing the cognitive deficits in HD; however, we still don't know much about the parts of the brain that underlie these deficits. The aim of this project is to use event related functional magnetic resonance imaging (fMRI) to correlate structural and functional changes in the brain via the use of various cognitive behavioural measures. In this way we can elucidate what brain areas are responsible for various cognitive functions. In addition, we intend to ascertain how different brain areas decrement in function over time and to determine whether there is a relationship between rate of disease progression, age at onset and certain genetic characteristics. Understanding how the brain functions and how the disease progresses over time will be essential, from the point of view of patient management, when new drug treatments eventually permit prevention of the development, or slows further progress, of the disorder.Read moreRead less