Search Results - "Halliday, Glenda M."
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Glia: Initiators and progressors of pathology in Parkinson's disease
Published in Movement disorders (01-01-2011)“…Background: Glia are traditionally known as support cells for neurons, and their role in neurodegeneration has been largely considered secondary to neuronal…”
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Toll-like receptor 2 is increased in neurons in Parkinson’s disease brain and may contribute to alpha-synuclein pathology
Published in Acta neuropathologica (01-02-2017)“…Inflammation is likely a key contributor to the pathogenesis of Parkinson’s disease (PD), a progressively debilitating neurodegenerative disease that is…”
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3
The frontotemporal dementia-motor neuron disease continuum
Published in The Lancet (British edition) (27-08-2016)“…Summary Early reports of cognitive and behavioural deficits in motor neuron disease might have been overlooked initially, but the concept of a frontotemporal…”
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4
Structural heterogeneity of α-synuclein fibrils amplified from patient brain extracts
Published in Nature communications (04-12-2019)“…Parkinson’s disease (PD) and Multiple System Atrophy (MSA) are clinically distinctive diseases that feature a common neuropathological hallmark of aggregated…”
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5
Disease duration and the integrity of the nigrostriatal system in Parkinson's disease
Published in Brain (London, England : 1878) (01-08-2013)“…The pace of nigrostriatal degeneration, both with regards to striatal denervation and loss of melanin and tyrosine hydroxylase-positive neurons, is poorly…”
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Recent Developments in TSPO PET Imaging as A Biomarker of Neuroinflammation in Neurodegenerative Disorders
Published in International journal of molecular sciences (28-06-2019)“…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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Cognitive fluctuations in Lewy body dementia: towards a pathophysiological framework
Published in Brain (London, England : 1878) (01-01-2020)“…Fluctuating cognition is a complex and disabling symptom that is seen most frequently in the context of Lewy body dementias encompassing dementia with Lewy…”
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TDP-43 proteinopathies: a new wave of neurodegenerative diseases
Published in Journal of neurology, neurosurgery and psychiatry (01-01-2021)“…Inclusions of pathogenic deposits containing TAR DNA-binding protein 43 (TDP-43) are evident in the brain and spinal cord of patients that present across a…”
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Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonism
Published in Proceedings of the National Academy of Sciences - PNAS (22-09-2015)“…Prions are proteins that adopt alternative conformations that become self-propagating; the PrPScprion causes the rare human disorder Creutzfeldt–Jakob disease…”
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The neurobiological basis of cognitive impairment in Parkinson's disease
Published in Movement disorders (15-04-2014)“…ABSTRACT The recent formalization of clinical criteria for Parkinson's disease with dementia (PDD) codifies many studies on this topic, including those…”
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Neuropathological assessment of Parkinson's disease: refining the diagnostic criteria
Published in Lancet neurology (01-12-2009)“…Summary To date, there have been few systematic attempts to provide a standard operating procedure for the neuropathological diagnosis of Parkinson's disease…”
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Time to redefine PD? Introductory statement of the MDS Task Force on the definition of Parkinson's disease
Published in Movement disorders (01-04-2014)“…ABSTRACT With advances in knowledge disease, boundaries may change. Occasionally, these changes are of such a magnitude that they require redefinition of the…”
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Loss of the metabolism and sleep regulating neuronal populations expressing orexin and oxytocin in the hypothalamus in amyotrophic lateral sclerosis
Published in Neuropathology and applied neurobiology (01-12-2021)“…Aims To determine the underlying cellular changes and clinical correlates associated with pathology of the hypothalamus in amyotrophic lateral sclerosis (ALS),…”
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14
Lysosomal-associated membrane protein 2 isoforms are differentially affected in early Parkinson's disease
Published in Movement disorders (01-10-2015)“…ABSTRACT Lysosomes are the primary catabolic compartment for the degradation of intracellular proteins through autophagy. The presence of abnormal…”
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15
Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathies
Published in Brain (London, England : 1878) (01-02-2018)“…See Josephs (doi:10.1093/brain/awx367) for a scientific commentary on this article. Mutations in the MAPT gene on chromosome 17 are associated with…”
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Amyotrophic lateral sclerosis and frontotemporal dementia: distinct and overlapping changes in eating behaviour and metabolism
Published in Lancet neurology (01-03-2016)“…Summary Metabolic changes incorporating fluctuations in weight, insulin resistance, and cholesterol concentrations have been identified in several…”
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LRRK2‐mediated Rab10 phosphorylation in immune cells from Parkinson's disease patients
Published in Movement disorders (01-03-2019)“…Background Leucine‐rich repeat kinase 2 is a potential therapeutic target for the treatment of Parkinson's disease, and clinical trials of leucine‐rich repeat…”
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The Sydney multicenter study of Parkinson's disease: The inevitability of dementia at 20 years
Published in Movement disorders (30-04-2008)“…After 20 years follow‐up of newly diagnosed patients with Parkinson's disease (PD), 100 of 136 (74%) have died. The mortality rate fell in the first 3 years of…”
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Role of the Long Non-Coding RNA MAPT-AS1 in Regulation of Microtubule Associated Protein Tau (MAPT) Expression in Parkinson's Disease
Published in PloS one (23-06-2016)“…Studies investigating the pathogenic role of the microtubule associated protein tau (MAPT) gene in Parkinson's disease (PD) have indicated that DNA methylation…”
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Neuronal network disintegration: common pathways linking neurodegenerative diseases
Published in Journal of Neurology, Neurosurgery and Psychiatry (01-11-2016)“…Neurodegeneration refers to a heterogeneous group of brain disorders that progressively evolve. It has been increasingly appreciated that many…”
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