Thesis (M.S. in Computer Science)--Vanderbilt University, May 2005. / Title from title screen. Includes bibliographical references.

Project requirement (M.Ed.)--University of Toledo, 2005. / Typescript. "Submitted as partial fulfillment of the requirements of the Master of Education degree in Physical Education" Bibliography: leaves 43-46.

Thesis (Ph. D.)--University of California, San Diego, 2006. / Title from first page of PDF file (viewed July 11, 2006). Available via ProQuest Digital Dissertations. Vita. Includes bibliographical references.

Thesis (Ph. D.)--University of California, San Diego and San Diego State University, 2006. / Vita. Includes bibliographical references (leaves 139-148).

Thesis (Ph.D.) - University of Queensland, 2005. / Includes bibliography.

Thesis (Ph.D.)--York University, 2002. Graduate Programme in Psychology. / Typescript. Includes bibliographical references (leaves 63-76). Also available on the Internet. MODE OF ACCESS via web browser by entering the following URL: http://wwwlib.umi.com/cr/yorku/fullcit?pNQ99177

Ten people with multiple sclerosis (MS) who felt they had cognitive difficulties because of their MS were investigated. This study had multiple aims. Firstly, to explore the subjective experience of cognitive deficits. Secondly, to assess whether or not there was objective evidence of cognitive difficulties on neuropsychological testing, and whether this was commensurate with a pattern of subcortical dementia. Thirdly, to determine whether their magnetic resonance imaging (MRI) scans replicated the patterns of atrophy frequently reported in MS patients with cognitive difficulties. And finally, to investigate the psychological well-being of the subjects. In depth neuropsychiatric interviews, psychiatric and psychological inventories, a comprehensive neuropsychological battery, and MRI investigations were done. The mean Full Scale Intelligence Quotient (FSIQ) fell within the superior range, at the 89th percentile. On tests of general intelligence, mental state examinations, there was little or no indication of cognitive deterioration. However, on sophisticated neuropsychological testing, there was convincing evidence of cognitive problems. Magnetic resonance imaging lesions were atypical of the reported research on cognitively compromised MS patients.

No description available.

The brain activities are characterized by spontaneous and persistent irregular fluctuations in space and time. Criticality theory from statistical physics has been proposed as a principle to explain the variability in normal brain spontaneous activity and has suggested the functional benefits of variability, such as maximized dynamic range of response to stimuli and information capacity. In parallel, the brains show variability in other aspects, such as the structural heterogeneity across brain regions, the intra-individual variability across experimental trials, and the behavior difference across groups and individuals. The associations between the variability of spontaneous activities and these different types of structural, intra and inter-individual variabilities remain elusive. My doctoral study thus aimed to bridge the brain variability and the above-mentioned variations based on criticality theory and analysis of empirical data. As a preparatory analysis, we first collected evidence to prove criticality in human functional magnetic resonance imaging (fMRI) data. The advanced statistical criteria were used to exclude potential artefacts that can induce power-law scaling without the mechanism of criticality. In the first part of the study, we addressed methodological issue and tested whether several measures of either spatial or temporal complexity due to experimental limitations could be reliable proxy of spatiotemporal variability (related to criticality) in vivo. The high spatiotemporal resolutions of whole-cortex optical voltage imaging in mice brain during the waking up from anesthesia enabled simultaneous investigation of functional connectivity (FC), Multi-Scale Entropy (MSE, measure of temporal variability), Regional Entropy (RE, quantity of spatiotemporal variability) and the interdependency among them under different brain states. The results suggested that MSE and FC could be effective measures to capture spatiotemporal variability under limitation of imaging modalities applicable to human subjects. This study also lays methodological basis for the third study in this thesis. In the second study, we explored the interaction between spontaneous activity and evoked activity from mice brain imaging under whisker stimulus. The whisker stimulus will first evoke the local activation in sensory cortex and then trigger whole-cortex activity with variable patterns in different experimental trials. This trial-to-trial variability in the cortical evoked component was then attributed to the changes of ongoing activity state at stimulus onset. The study links ongoing activity variability and evoked activity variability, which further consolidates the association between ongoing activity and brain functions. In the third study, we measured the signal variability of the whole brain from resting state fMRI, and developed the multivariate pattern of cortical entropy, called entropy profile, as reliable and interpretable biomarker of individual difference in cognitive ability. We showed that the whole cortical entropy profile from resting- state fMRI is a robust personalized measure. We tested the predictive power for general and specific cognitive abilities based on cortical entropy profiles with out- of-sample prediction. Furthermore, we revealed the anatomical features underlying cross-region and cross-individual variations in cortical entropy profiles. This study provides new potential biomarker based on brain spontaneous variability which could benefit the applications in psychology and psychiatry studies. The whole study laid a foundation for brain criticality-/variability-based studies and applications and broadened our understanding of the associations between neural structures, functional dynamics and cognitive ability

The brain activities are characterized by spontaneous and persistent irregular fluctuations in space and time. Criticality theory from statistical physics has been proposed as a principle to explain the variability in normal brain spontaneous activity and has suggested the functional benefits of variability, such as maximized dynamic range of response to stimuli and information capacity. In parallel, the brains show variability in other aspects, such as the structural heterogeneity across brain regions, the intra-individual variability across experimental trials, and the behavior difference across groups and individuals. The associations between the variability of spontaneous activities and these different types of structural, intra and inter-individual variabilities remain elusive. My doctoral study thus aimed to bridge the brain variability and the above-mentioned variations based on criticality theory and analysis of empirical data. As a preparatory analysis, we first collected evidence to prove criticality in human functional magnetic resonance imaging (fMRI) data. The advanced statistical criteria were used to exclude potential artefacts that can induce power-law scaling without the mechanism of criticality. In the first part of the study, we addressed methodological issue and tested whether several measures of either spatial or temporal complexity due to experimental limitations could be reliable proxy of spatiotemporal variability (related to criticality) in vivo. The high spatiotemporal resolutions of whole-cortex optical voltage imaging in mice brain during the waking up from anesthesia enabled simultaneous investigation of functional connectivity (FC), Multi-Scale Entropy (MSE, measure of temporal variability), Regional Entropy (RE, quantity of spatiotemporal variability) and the interdependency among them under different brain states. The results suggested that MSE and FC could be effective measures to capture spatiotemporal variability under limitation of imaging modalities applicable to human subjects. This study also lays methodological basis for the third study in this thesis. In the second study, we explored the interaction between spontaneous activity and evoked activity from mice brain imaging under whisker stimulus. The whisker stimulus will first evoke the local activation in sensory cortex and then trigger whole-cortex activity with variable patterns in different experimental trials. This trial-to-trial variability in the cortical evoked component was then attributed to the changes of ongoing activity state at stimulus onset. The study links ongoing activity variability and evoked activity variability, which further consolidates the association between ongoing activity and brain functions. In the third study, we measured the signal variability of the whole brain from resting state fMRI, and developed the multivariate pattern of cortical entropy, called entropy profile, as reliable and interpretable biomarker of individual difference in cognitive ability. We showed that the whole cortical entropy profile from resting- state fMRI is a robust personalized measure. We tested the predictive power for general and specific cognitive abilities based on cortical entropy profiles with out- of-sample prediction. Furthermore, we revealed the anatomical features underlying cross-region and cross-individual variations in cortical entropy profiles. This study provides new potential biomarker based on brain spontaneous variability which could benefit the applications in psychology and psychiatry studies. The whole study laid a foundation for brain criticality-/variability-based studies and applications and broadened our understanding of the associations between neural structures, functional dynamics and cognitive ability