Microglial activation in healthy aging

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Comparison and Evaluation of Retrospective Intermodality Brain Image Registration Techniques

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Microglial activation and dopamine terminal loss in early Parkinson's disease

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The peripheral benzodiazepine binding site in the brain in multiple sclerosis

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A comparison between voxel-based cortical thickness and voxel-based morphometry in normal aging

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MR-based automatic delineation of volumes of interest in human brain PET images using probability maps

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Relationship between atrophy and β‐amyloid deposition in Alzheimer disease

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Microglia in the Aging Brain

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Reference and target region modeling of [11C]-(R)-PK11195 brain studies.

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A voxel-based morphometric study to determine individual differences in gray matter density associated with age and cognitive change over time

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[ 11 C]( R )-PK11195 PET imaging of microglial activation in multiple system atrophy

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Immune reactive cells in senile plaques and cognitive decline in Alzheimer’s disease

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Enlarged and phagocytic, but not primed, interleukin-1α-immunoreactive microglia increase with age in normal human brain

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PET visualization of microglia in multiple sclerosis patients using [ 11 C]PK11195

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Synthesis of the enantiomers of [N-methyl-11C]PK 11195 and comparison of their behaviours as radioligands for PK binding sites in rats

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Activation of microglia in the brains of humans with heart disease and hypercholesterolemic rabbits

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Microglial Cell Activation in Aging and Alzheimer Disease: Partial Linkage with Neurofibrillary Tangle Burden in the Hippocampus

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Age-related networks of regional covariance in MRI gray matter: Reproducible multivariate patterns in healthy aging

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Physiological imaging of the brain with PET

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Evaluation of Methods for Generating Parametric ( R )-[ 11 C]PK11195 Binding Images

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In vivo Validation of Reconstruction-Based Resolution Recovery for Human Brain Studies

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Imaging Activated Microglia in the Aging Human Brain

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Imaging activated microglia in the ageing human brain

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Neuroinflammation: The Devil Is in the Details

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Overview of General and Discriminating Markers of Differential Microglia Phenotypes

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Microglia across the lifespan: from origin to function in brain development, plasticity and cognition

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Microglial cell dysregulation in brain aging and neurodegeneration

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Microglia during development and aging

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Microglial Activity in People at Ultra High Risk of Psychosis and in Schizophrenia: An [11C]PBR28 PET Brain Imaging Study

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Microglial priming and enhanced reactivity to secondary insult in aging, and traumatic CNS injury, and neurodegenerative disease

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Microglia Priming with Aging and Stress

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Microglia Phenotypes in Aging and Neurodegenerative Diseases

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CCL2 Is Associated with a Faster Rate of Cognitive Decline during Early Stages of Alzheimer's Disease

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Role of Microglia in Neurological Disorders and Their Potentials as a Therapeutic Target

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Aging Microglia—Phenotypes, Functions and Implications for Age-Related Neurodegenerative Diseases

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Microglial aging in the healthy CNS: phenotypes, drivers, and rejuvenation

Wong, W. T. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00022 · Cited by 227 · see citing works

Microglia

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In vivo microglia activation in very early dementia with Lewy bodies, comparison with Parkinson's disease

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Alzheimer's Disease: Redox Dysregulation As a Common Denominator for Diverse Pathogenic Mechanisms

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Microglial activation in Alzheimer's disease: an (R)-[11C]PK11195 positron emission tomography study

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Neuropathological correlates and genetic architecture of microglial activation in elderly human brain

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Antiageing strategy for neurodegenerative diseases: from mechanisms to clinical advances

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The endocannabinoid system in normal and pathological brain ageing

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Optimization of Supervised Cluster Analysis for Extracting Reference Tissue Input Curves in ( R )-[ 11 C]PK11195 Brain PET Studies

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Brain Microglia and Microglial Markers

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Brain excitability and connectivity of neuronal assemblies in Alzheimer's disease: From animal models to human findings

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Postoperative cognitive dysfunction in the aged: the collision of neuroinflammaging with perioperative neuroinflammation

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Forced turnover of aged microglia induces an intermediate phenotype but does not rebalance CNS environmental cues driving priming to immune challenge

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Regional changes in thalamic shape and volume with increasing age

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Cholinergic Modulation of Glial Function During Aging and Chronic Neuroinflammation

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Quantification of [ 18 F]DPA-714 Binding in the Human Brain: Initial Studies in Healthy Controls and Alzheimer'S Disease Patients

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Microglia in Aging and Alzheimer’s Disease: A Comparative Species Review

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Neuroimaging studies of the aging HIV-1-infected brain

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A Review and Hypothesized Model of the Mechanisms That Underpin the Relationship Between Inflammation and Cognition in the Elderly

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The role of innate immunity in Alzheimer's disease

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Diagnostic function of the neuroinflammatory biomarker YKL-40 in Alzheimer’s disease and other neurodegenerative diseases

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Effects of age, BMI and sex on the glial cell marker TSPO — a multicentre [11C]PBR28 HRRT PET study

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Neuroinflammation in Alzheimer’s disease wanes with age

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Fate of microglia during HIV‐1 infection: From activation to senescence?

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Interventions for age-related diseases: Shifting the paradigm

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Mapping of Thalamic Magnetic Susceptibility in Multiple Sclerosis Indicates Decreasing Iron with Disease Duration: A Proposed Mechanistic Relationship between Inflammation and Oligodendrocyte Vitality

Schweser, F., Martins, A. L. R. D., Hagemeier, J., Lin, F., Hanspach, J., Weinstock-Guttman, B., Hametner, S., Bergsland, N., Dwyer, M., & Zivadinov, R. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.10.063 · Cited by 86 · see citing works

Kinetic analysis of the translocator protein positron emission tomography ligand [18F]GE-180 in the human brain

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CHF5074 Reduces Biomarkers of Neuroinflammation in Patients with Mild Cognitive Impairment: A 12-Week, Double-Blind, Placebo- Controlled Study

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The P2X7 receptor tracer [11C]SMW139 as an in vivo marker of neuroinflammation in multiple sclerosis: a first-in man study

Hagens, M., Golla, S. S. V., Janssen, B., Vugts, D., Beaino, W., Windhorst, A., O'Brien-Brown, J., Kassiou, M., Schuit, R., Schwarte, L., et al. (2019) · European Journal of Nuclear Medicine and Molecular Imaging · doi:10.1007/s00259-019-04550-x · Cited by 66 · see citing works

Imaging Neuroinflammation in Neurodegenerative Disorders

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Imaging of neuroinflammation in Alzheimer's disease, multiple sclerosis and stroke: Recent developments in positron emission tomography.

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Neuroinflammation in healthy aging: A PET study using a novel Translocator Protein 18kDa (TSPO) radioligand, [18F]-FEPPA

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Gestational Exposure to Particulate Matter 2.5 (PM2.5) Leads to Spatial Memory Dysfunction and Neurodevelopmental Impairment in Hippocampus of Mice Offspring

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Diagnostic and Therapeutic Potential of TSPO Studies Regarding Neurodegenerative Diseases, Psychiatric Disorders, Alcohol Use Disorders, Traumatic Brain Injury, and Stroke: An Update

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In vivo PET imaging of neuroinflammation in Alzheimer’s disease

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In vivo (R)-[11C]PK11195 PET imaging of 18kDa translocator protein in recent onset psychosis

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Understanding Risk Factors for Alzheimer's Disease: Interplay of Neuroinflammation, Connexin-based Communication and Oxidative Stress

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Quantification of the Biological Age of the Brain Using Neuroimaging

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Microglia recapitulate a hematopoietic master regulator network in the aging human frontal cortex

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Brain and Systemic Inflammation in De Novo Parkinson's Disease

Yacoubian, T. A., Fang, Y.-H. D., Gerstenecker, A. T., Amara, A. W., Stover, N. P., Ruffrage, L., Collette, C., Kennedy, R., Zhang, Y., Hong, H., et al. (2023) · Movement Disorders · doi:10.1002/mds.29363 · Cited by 63 · see citing works

Microglial Activation and Connectivity in Alzheimer Disease and Aging

Rauchmann, B., Brendel, M., Franzmeier, N., Trappmann, L., Zaganjori, M., Ersoezlue, E., Morenas‐Rodriguez, E., Guersel, S., Burow, L., Kurz, C., et al. (2022) · Annals of Neurology · doi:10.1002/ana.26465 · Cited by 61 · see citing works

Age-Dependent Changes in the Activation and Regulation of Microglia

Cornejo, F., & Rommy von Bernhardi, M. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-40764-7_10 · Cited by 59 · see citing works

Aging, depression and dementia: The inflammatory process

Carrera-González, M. P., Cantón-Habas, V., & Rich‐Ruiz, M. (2022) · Advances in Clinical and Experimental Medicine · doi:10.17219/acem/149897 · Cited by 61 · see citing works

[11C]-(R)PK11195 tracer kinetics in the brain of glioma patients and a comparison of two referencing approaches

Su, Z., Herholz, K., Gerhard, A., Roncaroli, F., du Plessis, D., Jackson, A., Turkheimer, F., & Hinz, R. (2013) · European Journal of Nuclear Medicine and Molecular Imaging · doi:10.1007/s00259-013-2447-2 · Cited by 58 · see citing works

Sirtuins as Potential Therapeutic Targets for Mitigating Neuroinflammation Associated With Alzheimer’s Disease

Fernando, K., & Wijayasinghe, Y. S. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.746631 · Cited by 57 · see citing works

Brain TSPO Imaging and Gray Matter Volume in Schizophrenia Patients and in People at Ultra High Risk of Psychosis: An [11C]PBR28 Study

Selvaraj, S., Bloomfield, P. S., Bo, C., Veronese, M., Turkheimer, F., & Howes, O. (2017) · Schizophrenia Research · doi:10.1016/j.schres.2017.08.063 · Cited by 50 · see citing works

Acute exposure to diesel exhaust impairs adult neurogenesis in mice: prominence in males and protective effect of pioglitazone

Coburn, J. L., Cole, T. B., Dao, K., & Costa, L. G. (2018) · Archives of Toxicology · doi:10.1007/s00204-018-2180-5 · Cited by 55 · see citing works

Neuroinflammation and Tau Interact with Amyloid in Predicting Sleep Problems in Aging Independently of Atrophy

Fjell, A. M., Idland, A., Sala‐Llonch, R., Watne, L. O., Borza, T., Brækhus, A., Lona, T., Zetterberg, H., Blennow, K., Wyller, T. B., et al. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx157 · Cited by 52 · see citing works

Microglial Adenosine Receptors: From Preconditioning to Modulating the M1/M2 Balance in Activated Cells

Franco, R., Lillo, A., Rivas‐Santisteban, R., Reyes‐Resina, I., & Navarro, G. (2021) · Cells · doi:10.3390/cells10051124 · Cited by 49 · see citing works

Kinetic modeling and parameter estimation of TSPO PET imaging in the human brain

Wimberley, C., Lavisse, S., Hillmer, A. T., Hinz, R., Turkheimer, F., & Zanotti‐Fregonara, P. (2021) · European Journal of Nuclear Medicine and Molecular Imaging · doi:10.1007/s00259-021-05248-9 · Cited by 49 · see citing works

Aging, Senescence, and Dementia

Behfar, Q., Zuniga, A. R., & Adami, P. V. M. (2022) · The Journal of Prevention of Alzheimer s Disease · doi:10.14283/jpad.2022.42 · Cited by 49 · see citing works

Neuron loss associated with age but not Alzheimer's disease pathology in the chimpanzee brain

Edler, M. K., Munger, E. L., Meindl, R. S., Hopkins, W. D., Ely, J. J., ERWIN, J. M., Mufson, E. J., Hof, P. R., Sherwood, C. C., & Raghanti, M. A. (2020) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2019.0619 · Cited by 44 · see citing works

State-associated changes in longitudinal [18F]-PBR111 TSPO PET imaging of psychosis patients: Evidence for the accelerated ageing hypothesis?

Picker, L. D., Ottoy, J., Verhaeghe, J. A. J., Deleye, S., Wyffels, L., Fransén, E., Kosten, L., Sabbe, B., Coppens, V., Timmers, M., et al. (2018) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2018.11.318 · Cited by 43 · see citing works

Age-dependent differences in microglial responses to systemic inflammation are evident as early as middle age

Nikodémová, M., Small, A. L., Kimyon, R. S., & Watters, J. J. (2016) · Physiological Genomics · doi:10.1152/physiolgenomics.00129.2015 · Cited by 42 · see citing works

Supervised clustering for TSPO PET imaging

Schubert, J., Tonietto, M., Turkheimer, F., Zanotti-Fregonara, P., & Veronese, M. (2021) · European Journal of Nuclear Medicine and Molecular Imaging · doi:10.1007/s00259-021-05309-z · Cited by 40 · see citing works

Evidence for Cortical Neuronal Loss in Male Type 2 Diabetic Goto-Kakizaki Rats

Hussain, S., Mansouri, S., Sjöholm, Å., Patrone, C., & Darsalia, V. (2014) · Journal of Alzheimer s Disease · doi:10.3233/jad-131958 · Cited by 41 · see citing works

Age Influences Microglial Activation After Cuprizone-Induced Demyelination

Klein, B., Mrowetz, H., Barker, C. M., Lange, S., Rivera, F. J., & Aigner, L. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00278 · Cited by 42 · see citing works

Increased Inflammation and Unchanged Density of Synaptic Vesicle Glycoprotein 2A (SV2A) in the Postmortem Frontal Cortex of Alzheimer’s Disease Patients

Metaxas, A., Thygesen, C., Briting, S. R. R., Landau, A. M., Darvesh, S., & Finsen, B. R. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00538 · Cited by 41 · see citing works

Cannabinoid 1 Receptor Signaling on Hippocampal GABAergic Neurons Influences Microglial Activity

Ativie, F., Komorowska‐Müller, J. A., Beins, E. C., Albayram, Ö., Zimmer, T. S., Zimmer, A., Tejera, D., Heneka, M. T., & Bilkei‐Gorzó, A. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00295 · Cited by 39 · see citing works

Pharmacokinetics and Pharmacodynamics of CHF5074 After Short-term Administration in Healthy Subjects

Imbimbo, B. P., Frigerio, E., Breda, M., Fiorentini, F., Fernández, M., Sivilia, S., Giardino, L., Calzà, L., Norris, D., Casula, D., et al. (2012) · Alzheimer Disease & Associated Disorders · doi:10.1097/wad.0b013e3182622ace · Cited by 37 · see citing works

Biomarkers for Microglial Activation in Alzheimer′s Disease

Lautner, R., Mattsson, N., Schöll, M., Augutis, K., Blennow, K., Olsson, B., & Zetterberg, H. (2011) · International Journal of Alzheimer s Disease · doi:10.4061/2011/939426 · Cited by 36 · see citing works

In vivo evidence for pre‐symptomatic neuroinflammation in a <scp>MAPT</scp> mutation carrier

Bevan‐Jones, W. R., Cope, T. E., Jones, P. S., Passamonti, L., Hong, Y. T., Fryer, T., Arnold, R., Coles, J. P., Aigbirhio, F. I., O'Brien, J. T., et al. (2019) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.683 · Cited by 36 · see citing works

The Hallmarks of Ageing in Microglia

Carr, L. M., Mustafa, S., & Collins‐Praino, L. E. (2025) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-025-01564-y · Cited by 37 · see citing works

High BMI levels associate with reduced mRNA expression of IL10 and increased mRNA expression of iNOS (NOS2) in human frontal cortex

Lauridsen, J. K., Olesen, R. H., Vendelbo, J. H., Hyde, T. M., Kleinman, J. E., Bibby, B. M., Brock, B., Rungby, J., & Larsen, A. (2017) · Translational Psychiatry · doi:10.1038/tp.2016.259 · Cited by 32 · see citing works

Neuroinflammation and β Amyloid Deposition in Alzheimer's Disease: In vivo Quantification with Molecular Imaging

Hommet, C., Mondon, K., Camus, V., Ribeiro, M. J., Beaufils, É., Arlicot, N., Corcia, P., Paccalin, M., Minier, F., Gosselin, T., et al. (2013) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000354363 · Cited by 30 · see citing works

Induction of a Senescence-Like Phenotype in Cultured Human Fetal Microglia During HIV-1 Infection

Chen, N. C., Partridge, A. T., Tüzer, F., Cohen, J., Nacarelli, T., Navas, S., Sell, C., Torres, C. A., & Martín‐García, J. (2018) · The Journals of Gerontology Series A · doi:10.1093/gerona/gly022 · Cited by 30 · see citing works

Sirtuins promote brain homeostasis, preventing Alzheimer’s disease through targeting neuroinflammation

Wątroba, M., & Szukiewicz, D. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.962769 · Cited by 29 · see citing works

Aging of enteric neuromuscular systems in gastrointestinal tract

Nguyen, V. T. T., Taheri, N., Chandra, A., & Hayashi, Y. (2022) · Neurogastroenterology & Motility · doi:10.1111/nmo.14352 · Cited by 28 · see citing works

Parametric Binding Images of the TSPO Ligand 18F-DPA-714

Golla, S. S. V., Boellaard, R., Oikonen, V., Hoffmann, A., van Berckel, B. N. M., Windhorst, A. D., Virta, J. R., Beek, E. T. T., Groeneveld, G. J., Haaparanta‐Solin, M., et al. (2016) · Journal of Nuclear Medicine · doi:10.2967/jnumed.116.173013 · Cited by 27 · see citing works

Building a database for brain 18 kDa translocator protein imaged using [ 11 C]PBR28 in healthy subjects

Paul, S., Gallagher, E. P., Liow, J., Mabins, S. N., Henry, K. A., Zoghbi, S. S., Gunn, R. N., Kreisl, W. C., Richards, E. M., Zanotti‐Fregonara, P., et al. (2018) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x18771250 · Cited by 27 · see citing works

Test-retest reliability and convergent validity of (R)-[11C]PK11195 outcome measures without arterial input function

Plavén-Sigray, P., Matheson, G., Cselényi, Z., Jucaite, A., Farde, L., & Cervenka, S. (2018) · bioRxiv · doi:10.1186/s13550-018-0455-8 · Cited by 25 · see citing works

Annexin A3 as a Marker Protein for Microglia in the Central Nervous System of Rats

Zhang, Z., Li, Z., Ma, Z., Deng, M., Xing, M., Wu, J., Jiang, S., Wang, Q., Guo, Q., & Zou, W. (2021) · Neural Plasticity · doi:10.1155/2021/5575090 · Cited by 26 · see citing works

Aging reduces glial uptake and promotes extracellular accumulation of Aβ from a lentiviral vector

Zhao, W., Zhang, J., Davis, E. G., & Rebeck, G. W. (2014) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2014.00210 · Cited by 25 · see citing works

Do glia provide the link between low‐grade systemic inflammation and normal cognitive ageing? A 1H magnetic resonance spectroscopy study at 7 tesla

Lind, A., Boraxbekk, C., Petersen, E. T., Paulson, O. B., Andersen, O., Siebner, H. R., & Marsman, A. (2021) · Journal of Neurochemistry · doi:10.1111/jnc.15456 · Cited by 25 · see citing works

Preventive immunization of aged and juvenile non-human primates to beta-amyloid

Kofler, J., Lopresti, B. J., Janssen, C., Trichel, A. M., Masliah, E., Finn, O. J., Salter, R. D., MURDOCH, G. H., Mathis, C. A., & Wiley, C. A. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-84 · Cited by 25 · see citing works

Assessing brain immune activation in psychiatric disorders: clinical and preclinical PET imaging studies of the 18-kDa translocator protein

van der Doef, T. F., Doorduin, J., van Berckel, B. N. M., & Červenka, S. (2015) · Clinical and Translational Imaging · doi:10.1007/s40336-015-0140-0 · Cited by 25 · see citing works

Repeated social defeat induces transient glial activation and brain hypometabolism: A positron emission tomography imaging study

Feltes, P. K., de Vries, E. D., Juárez-Orozco, L., Kurtys, E., Dierckx, R., Moriguchi-Jeckel, C., & Doorduin, J. (2017) · Journal of Cerebral Blood Flow and Metabolism · doi:10.1177/0271678x17747189 · Cited by 23 · see citing works

The Aging Brain With HIV Infection: Effects of Alcoholism or Hepatitis C Comorbidity

Zahr, N. M. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00056 · Cited by 23 · see citing works

Gap Junctions and Connexins in Microglia-Related Oxidative Stress and Neuroinflammation: Perspectives for Drug Discovery

Caruso, G., Pietro, L. D., & Caraci, F. (2023) · Biomolecules · doi:10.3390/biom13030505 · Cited by 23 · see citing works

Single Inflammatory Trigger Leads to Neuroinflammation in LRRK2 Rodent Model without Degeneration of Dopaminergic Neurons

Schildt, A., Walker, M. D., Dinelle, K., Miao, Q., Schulzer, M., OʼKusky, J. R., Farrer, M. J., Doudet, D. J., & Sossi, V. (2018) · Journal of Parkinson s Disease · doi:10.3233/jpd-181446 · Cited by 23 · see citing works

Patterns of Mitochondrial TSPO Binding in Cerebral Small Vessel Disease: An in vivo PET Study With Neuropathological Comparison

Wright, P. K., Veronese, M., Mazibuko, N., Turkheimer, F., Rabiner, E. A., Ballard, C. G., Williams, S., Narayanan, A. K. H., Osrah, B., Williams, R., et al. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.541377 · Cited by 22 · see citing works

Loss of NF-κB p50 function synergistically augments microglial priming in the middle-aged brain

Taetzsch, T., Benusa, S. D., Levesque, S., Mumaw, C. L., & Block, M. L. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1446-z · Cited by 21 · see citing works

The Effects of Modified Curcumin Preparations on Glial Morphology in Aging and Neuroinflammation

Ullah, F., Gamage, R. V., Sen, M. K., & Gyengési, E. (2022) · Neurochemical Research · doi:10.1007/s11064-021-03499-4 · Cited by 21 · see citing works

Characterizing the Molecular Architecture of Cortical Regions Associated with High Educational Attainment in Older Individuals

Bartrés‐Faz, D., González‐Escamilla, G., Vaqué‐Alcázar, L., Abellaneda‐Pérez, K., Valls‐Pedret, C., Ros, E., & Grothe, M. J. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2370-18.2019 · Cited by 21 · see citing works

Quantitative imaging of neuroinflammation in human white matter: A positron emission tomography study with translocator protein 18 kDa radioligand, [18F]‐FEPPA

Suridjan, I., Rusjan, P., Kenk, M., Verhoeff, N. P. L. G., Voineskos, A. N., Rotenberg, D. J., Wilson, A. A., Meyer, J. H., Houle, S., & Mizrahi, R. (2014) · Synapse · doi:10.1002/syn.21765 · Cited by 20 · see citing works

Bioenergetic Impairment in the Neuro-Glia-Vascular Unit: An Emerging Physiopathology during Aging

Yuan, M., Wang, Y., Wang, S., Huang, Z., Jin, F., Zou, Q., Li, J., Pu, Y., & Cai, Z. (2021) · Aging and Disease · doi:10.14336/ad.2021.04017 · Cited by 19 · see citing works

Challenges of quantification of TSPO in the human brain

Hinz, R., & Boellaard, R. (2015) · Clinical and Translational Imaging · doi:10.1007/s40336-015-0138-7 · Cited by 19 · see citing works

Interaction of Cannabis Use and Aging: From Molecule to Mind

Yoo, H. B., DiMuzio, J. M., & Filbey, F. M. (2019) · Journal of Dual Diagnosis · doi:10.1080/15504263.2019.1665218 · Cited by 19 · see citing works

In-vivo measurement of activated microglia in dementia

Cagnin, A., Brooks, D. J., Kennedy, A. M., Gunn, R. N., Myers, R., Turkheimer, F. E., Jones, T., & Banati, R. B. (2001) · The Lancet · doi:10.1016/s0140-6736(01)05625-2 · Cited by 1,054 · see citing works

Microglial activation in Alzheimer's disease: an (R)-[11C]PK11195 positron emission tomography study

Schuitemaker, A., Kropholler, M. A., Boellaard, R., van der Flier, W. M., Kloet, R. W., van der Doef, T. F., Knol, D. L., Windhorst, A. D., Luurtsema, G., Barkhof, F., et al. (2012) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2012.04.021 · Cited by 167 · see citing works

PK11195 labels activated microglia in Alzheimer's disease and in vivo in a mouse model using PET

Venneti, S., Lopresti, B. J., Wang, G., Hamilton, R. L., Mathis, C. A., Klunk, W. E., Apte, U. M., & Wiley, C. A. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.11.005 · Cited by 138 · see citing works

Visualising microglial activation in vivo

Banati, R. B. (2002) · Glia · doi:10.1002/glia.10144 · Cited by 428 · see citing works

O1–03–01: Microglial activation in patients with mild cognitive impairment and Alzheimer's disease: A study using [11C](R)–PK11195 and PET

Schuitemaker, A., van Berckel, B. N. M., Boellaard, R., Kropholler, M. A., Lubberink, M., Jonker, C., Lammertsma, A. A., & Scheltens, P. (2006) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2006.05.044