Search Results - "Loy, Clement"

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  1. 1

    Circular RNAs: The Brain Transcriptome Comes Full Circle by Gokool, Akira, Loy, Clement T., Halliday, Glenda M., Voineagu, Irina

    Published in Trends in neurosciences (Regular ed.) (01-10-2020)
    “…Circular RNAs (circRNAs) are a class of RNA molecules with a covalently closed loop structure formed by back-splicing of exon–exon junctions. The detection of…”
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    Genetics of dementia by Loy, Clement T, FRACP, Schofield, Peter R, Prof, Turner, Anne M, FRACP, Kwok, John BJ, Dr

    Published in The Lancet (British edition) (01-03-2014)
    “…Summary 25% of all people aged 55 years and older have a family history of dementia. For most, the family history is due to genetically complex disease, where…”
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    Recent Developments in TSPO PET Imaging as A Biomarker of Neuroinflammation in Neurodegenerative Disorders by Werry, Eryn L, Bright, Fiona M, Piguet, Olivier, Ittner, Lars M, Halliday, Glenda M, Hodges, John R, Kiernan, Matthew C, Loy, Clement T, Kril, Jillian J, Kassiou, Michael

    “…Neuroinflammation is an inflammatory response in the brain and spinal cord, which can involve the activation of microglia and astrocytes. It is a common…”
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    Neuroinflammation in frontotemporal dementia by Bright, Fiona, Werry, Eryn L., Dobson-Stone, Carol, Piguet, Olivier, Ittner, Lars M., Halliday, Glenda M., Hodges, John R., Kiernan, Matthew C., Loy, Clement T., Kassiou, Michael, Kril, Jillian J.

    Published in Nature reviews. Neurology (01-09-2019)
    “…Frontotemporal dementia (FTD) refers to a group of progressive neurodegenerative disorders with different pathological signatures, genetic variability and…”
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    Apathy and Depression in Huntington’s Disease: Distinct Longitudinal Trajectories and Clinical Correlates by Connors, Michael H., Teixeira-Pinto, Armando, Loy, Clement T.

    “…Objective:Huntington’s disease (HD) is an autosomal-dominant neurodegenerative disease resulting in motor disturbances, dementia, and psychiatric symptoms…”
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    Psychosis and longitudinal outcomes in Huntington disease: the COHORT Study by Connors, Michael H, Teixeira-Pinto, Armando, Loy, Clement T

    “…ObjectiveHuntington disease (HD) is an autosomal dominant neurodegenerative disease involving motor disturbances, cognitive decline and psychiatric symptoms…”
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    Causal Relationship Between Kidney Function and Cancer Risk: A Mendelian Randomization Study by Dobrijevic, Ellen, van Zwieten, Anita, Grant, Andrew J., Loy, Clement T., Craig, Jonathan C., Teixeira-Pinto, Armando, Wong, Germaine

    Published in American journal of kidney diseases (30-07-2024)
    “…Patients treated with kidney replacement therapy experience a 1.5- to 2-fold increased risk of cancer and cancer mortality compared with the general…”
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    The complex relationship between genotype, pathology and phenotype in familial dementia by Kwok, John B., Loy, Clement T., Dobson-Stone, Carol, Halliday, Glenda M.

    Published in Neurobiology of disease (01-11-2020)
    “…Causative genes involved in familial forms of dementias, including Alzheimer's disease (AD), frontotemporal lobar degeneration (FTLD) and dementia with Lewy…”
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    A meta-analysis of hippocampal atrophy rates in Alzheimer's disease by Barnes, Josephine, Bartlett, Jonathan W, van de Pol, Laura A, Loy, Clement T, Scahill, Rachael I, Frost, Chris, Thompson, Paul, Fox, Nick C

    Published in Neurobiology of aging (01-11-2009)
    “…Abstract Hippocampal atrophy rates are useful in both diagnosing and tracking Alzheimer's disease (AD). However, cohorts and methods used to determine such…”
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    Why aren't people with young onset dementia and their supporters using formal services? Results from the INSPIRED study by Cations, Monica, Withall, Adrienne, Horsfall, Ruth, Denham, Nicole, White, Fiona, Trollor, Julian, Loy, Clement, Brodaty, Henry, Sachdev, Perminder, Gonski, Peter, Demirkol, Apo, Cumming, Robert G, Draper, Brian

    Published in PloS one (19-07-2017)
    “…Despite reporting high levels of burden, supporters of people with young onset dementia (YOD) underuse formal community services. Previous quantitative studies…”
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    Robust Optimization and Data Classification for Characterization of Huntington Disease Onset via Duality Methods by Woolnough, Daniel, Jeyakumar, Niroshan, Li, Guoyin, Loy, Clement T, Jeyakumar, Vaithilingam

    “…The features that characterize the onset of Huntington disease (HD) are poorly understood yet have significant implications for research and clinical practice…”
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    Making Decisions About Long-Term Institutional Care Placement Among People With Dementia and Their Caregivers: Systematic Review of Qualitative Studies by Teng, Claris, Loy, Clement T, Sellars, Marcus, Pond, Dimity, Latt, Mark D, Waite, Louise M, Sinka, Victoria, Logeman, Charlotte, Tong, Allison

    Published in The Gerontologist (15-05-2020)
    “…Abstract Background and Objectives People with dementia become increasingly dependent on others for care as cognition declines. Decision making about placement…”
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    What do we know about Late Onset Huntington's Disease? by Chaganti, Sai S, McCusker, Elizabeth A, Loy, Clement T

    Published in Journal of Huntington's disease (01-01-2017)
    “…Although the typical age of onset for Huntington's disease (HD) is in the fourth decade, between 4.4-11.5% of individuals with HD have a late onset (over 60…”
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    The many facets of unawareness in huntington disease by McCusker, Elizabeth, Loy, Clement T

    “…BACKGROUNDUnawareness or diminished awareness is present when a patient's perception of obvious disease manifestations and impact differ from that of observers…”
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