Morphological criteria for the recognition of Alzheimer's disease and the distribution pattern of cortical changes related to this disorder

Neuropathological stageing of Alzheimer-related changes.

Braak, H., & Braak, E. (1991) · Acta Neuropathologica · doi:10.1007/bf00308809 · Cited by 16,123 · see citing works

The Consortium to Establish a Registry for Alzheimer's Disease (CERAD): Part II. Standardization of the neuropathologic assessment of Alzheimer's disease

Mirra, S. S., Heyman, A., McKeel, D., Sumi, S. M., Crain, B. J., Brownlee, L. M., Vogel, F. S., Hughes, J. P., Belle, G. V., Berg, L., et al. (1991) · Neurology · doi:10.1212/wnl.41.4.479 · Cited by 4,961 · see citing works

Diagnosis of Alzheimer's Disease

Khachaturian, Z. S. (1985) · Archives of Neurology · doi:10.1001/archneur.1985.04060100083029 · Cited by 2,499 · see citing works

The human nervous system

Paxinos, G., & Jürgen, K. (2004) · Cited by 1,482 · see citing works

The topographical and neuroanatomical distribution of neurofibrillary tangles and neuritic plaques in the cerebral cortex of patients with Alzheimer's disease

Arnold, S. E., Hyman, B. T., Flory, J., Damasio, A. R., & Van Hoesen, G. W. (1991) · Cerebral Cortex · doi:10.1093/cercor/1.1.103 · Cited by 1,380 · see citing works

The distribution of tangles, plaques and related immunohistochemical markers in healthy aging and Alzheimer's disease

Price, J. L., Davis, P. B., Morris, J. C., & White, D. L. (1991) · Neurobiology of Aging · doi:10.1016/0197-4580(91)90006-6 · Cited by 818 · see citing works

The NINCDS‐ADRDA Work Group criteria for the clinical diagnosis of probable Alzheimer's disease: A clinicopathologic study of 57 cases

Tierney, M. C., Fisher, R. H., Lewis, A. J., Zorzitto, M. L., Snow, W. G., Reid, D. W., & Nieuwstraten, P. (1988) · Neurology · doi:10.1212/wnl.38.3.359 · Cited by 613 · see citing works

Architectonics of the Human Telencephalic Cortex

Braak, H. (1980) · Studies of brain function · doi:10.1007/978-3-642-81522-5 · Cited by 504 · see citing works

Entorhinal cortex pathology in Alzheimer's disease

van Hoesen, G. W., Hyman, B. T., & Damasio, A. R. (1991) · Hippocampus · doi:10.1002/hipo.450010102 · Cited by 475 · see citing works

The human entorhinal cortex: normal morphology and lamina-specific pathology in various diseases

Braak, H., & Braak, E. (1992) · Neuroscience Research · doi:10.1016/0168-0102(92)90014-4 · Cited by 334 · see citing works

The significance of morphometric procedures in the investigation of age changes in cytoarchitectonic structures of human brain.

Haug, H., Kühl, S., Mecke, E., Nl, S., & Wasner, K. (1984) · PubMed · Cited by 157 · see citing works

Alzheimer's disease: Mismatch between amyloid plaques and neuritic plaques

Braak, H., Braak, E., Ohm, T. G., & Böhl, J. (1989) · Neuroscience Letters · doi:10.1016/0304-3940(89)90479-5 · Cited by 90 · see citing works

Chapter 12 Ratio of pyramidal cells versus non-pyramidal cells in the human frontal isocortex and changes in ratio with ageing and Alzheimer's disease

Braak, H., & Braak, E. (1986) · Progress in brain research · doi:10.1016/s0079-6123(08)64305-8 · Cited by 63 · see citing works

Isocortical Pathology in Type C Niemann-Pick Disease

Braak, H., Braak, E., & Goebel, H. H. (1983) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-198311000-00007 · Cited by 23 · see citing works

Microglia-mediated neurotoxicity: uncovering the molecular mechanisms

Block, M. L., Zecca, L., & Hong, J.-S. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2038 · Cited by 4,110 · see citing works

The spectrum of disease in chronic traumatic encephalopathy

McKee, A. C., Stein, T. D., Nowinski, C. J., Stern, R. A., Daneshvar, D. H., Alvarez, V. E., Lee, H.-S., Hall, G., Wojtowicz, S. M., Baugh, C. M., et al. (2013) · Brain · doi:10.1093/brain/aws307 · Cited by 2,098 · see citing works

Microglia and inflammation-mediated neurodegeneration: Multiple triggers with a common mechanism

Block, M. L., & Hong, J.-S. (2005) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2005.06.004 · Cited by 1,557 · see citing works

Biomarker Modeling of Alzheimer’s Disease

Jack, C. R., & Holtzman, D. M. (2013) · Neuron · doi:10.1016/j.neuron.2013.12.003 · Cited by 1,002 · see citing works

Liquid–liquid phase separation of the microtubule-binding repeats of the Alzheimer-related protein Tau

Ambadipudi, S., Biernat, J., Riedel, D., Mandelkow, E., & Zweckstetter, M. (2017) · Nature Communications · doi:10.1038/s41467-017-00480-0 · Cited by 782 · see citing works

Comparison of different MRI brain atrophy rate measures with clinical disease progression in AD

Jack, C. R., Shiung, M. M., Gunter, J. L., O’Brien, P. C., Weigand, S. D., Knopman, D. S., Boeve, B. F., Ivnik, R. J., Smith, G. E., Cha, R. H., et al. (2004) · Neurology · doi:10.1212/01.wnl.0000110315.26026.ef · Cited by 827 · see citing works

Evolution of the neuropathology of Alzheimer's disease

Braak, H., & Braak, E. (1996) · Acta Neurologica Scandinavica · doi:10.1111/j.1600-0404.1996.tb05866.x · Cited by 710 · see citing works

At the interface of sensory and motor dysfunctions and Alzheimer’s disease.

Albers, M. W., Gilmore, G. C., Kaye, J., Murphy, C., Wingfield, A., Bennett, D. A., Boxer, A. L., Buchman, A. S., Cruickshanks, K. J., Devanand, D. P., et al. (2015) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2014.04.514 · Cited by 589 · see citing works

Amyloid cascade hypothesis: Pathogenesis and therapeutic strategies in Alzheimer's disease

Barage, S. H., & Sonawane, K. D. (2015) · Neuropeptides · doi:10.1016/j.npep.2015.06.008 · Cited by 579 · see citing works

Ventricular enlargement as a possible measure of Alzheimer’s disease progression validated using the Alzheimer’s disease neuroimaging initiative database

Nestor, S. M., Rupsingh, R., Borrie, M., Smith, M., Accomazzi, V., Wells, J. L., Fogarty, J., Bartha, R., & Initiative, T. A. D. N. (2008) · Brain · doi:10.1093/brain/awn146 · Cited by 543 · see citing works

Human wild-type tau interacts with wingless pathway components and produces neurofibrillary pathology in Drosophila

Jackson, G. R., Wiedau-Pazos, M., Sang, T.-K., Wagle, N., Brown, C. A., Massachi, S., & Geschwind, D. H. (2002) · Neuron · doi:10.1016/s0896-6273(02)00706-7 · Cited by 488 · see citing works

Cognitive reserve and the neurobiology of cognitive aging

Whalley, L. J., Deary, I. J., Appleton, C. L., & Starr, J. M. (2004) · Ageing Research Reviews · doi:10.1016/j.arr.2004.05.001 · Cited by 460 · see citing works

Alzheimer's disease diagnosis in individual subjects using structural MR images: Validation studies

Vemuri, P., Gunter, J. L., Senjem, M. L., Whitwell, J. L., Kantarci, K., Knopman, D. S., Boeve, B. F., Petersen, R. C., & Jack, C. R. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.09.073 · Cited by 455 · see citing works

Networks of anatomical covariance

Evans, A. C. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.054 · Cited by 429 · see citing works

Olfactory and other sensory impairments in Alzheimer disease

Murphy, C. (2019) · Nature Reviews Neurology · doi:10.1038/s41582-018-0097-5 · Cited by 425 · see citing works

Usefulness of MRI measures of entorhinal cortex versus hippocampus in AD

de Leon, M. J., Bobinski, M., Convit, A. J., Wolf, O. T., & Insausti, R. (2001) · Neurology · doi:10.1212/wnl.56.6.820 · Cited by 351 · see citing works

Usefulness of MRI measures of entorhinal cortex versus hippocampus in AD

Xu, Y., Jack, C. R., O’Brien, P. C., Kokmen, E., Smith, G. E., Ivnik, R. J., Boeve, B. F., Tangalos, R. G., & Petersen, R. C. (2000) · Neurology · doi:10.1212/wnl.54.9.1760 · Cited by 335 · see citing works

Targeting neuroinflammation in Alzheimer’s disease

Bronzuoli, M. R., Iacomino, A., Steardo, L., & Scuderi, C. (2016) · Journal of Inflammation Research · doi:10.2147/jir.s86958 · Cited by 255 · see citing works

Mild cognitive impairment

Luis, C. A., Loewenstein, D., Acevedo, A., Barker, W. W., & Duara, R. (2003) · Neurology · doi:10.1212/01.wnl.0000080366.90234.7f · Cited by 245 · see citing works

Alzheimer's disease: a comprehensive review of epidemiology, risk factors, symptoms diagnosis, management, caregiving, advanced treatments and associated challenges

Safiri, S., Jolfayi, A. G., Fazlollahi, A., Morsali, S., Sarkesh, A., Sorkhabi, A. D., Golabi, B., Aletaha, R., Asghari, K. M., Hamidi, S., et al. (2024) · Frontiers in Medicine · doi:10.3389/fmed.2024.1474043 · Cited by 242 · see citing works

Alzheimer disease: new concepts on its neurobiology and the clinical role imaging will play

Jack, C. R. (2012) · Radiology · doi:10.1148/radiol.12110433 · Cited by 211 · see citing works

Topography of Brain Atrophy During Normal Aging and Alzheimer's Disease

Double, K. L., Halliday, G. M., Kril, J. J., Harasty, J., Cullen, K. M., Brooks, W. S., Creasey, H. M., & Broe, G. A. (1996) · Neurobiology of Aging · doi:10.1016/0197-4580(96)00005-x · Cited by 196 · see citing works

Chronic intermittent hypoxia induces oxidative stress and inflammation in brain regions associated with early-stage neurodegeneration

Snyder, B., Shell, B., Cunningham, J. T., & Cunningham, R. L. (2017) · Physiological Reports · doi:10.14814/phy2.13258 · Cited by 189 · see citing works

Neprilysin: An Enzyme Candidate to Slow the Progression of Alzheimer's Disease

El‐Amouri, S. S., Zhu, H., Yu, J., Marr, R. A., Verma, I. M., & Kindy, M. S. (2008) · American Journal Of Pathology · doi:10.2353/ajpath.2008.070620 · Cited by 188 · see citing works

Calcium Dyshomeostasis in Alzheimer’s Disease Pathogenesis

Cascella, R., & Cecchi, C. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094914 · Cited by 189 · see citing works

Reduced hippocampal glutamate in Alzheimer disease

Rupsingh, R., Borrie, M., Smith, M., Wells, J. L., & Bartha, R. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2009.05.002 · Cited by 177 · see citing works

Antemortem MRI based STructural Abnormality iNDex (STAND)-scores correlate with postmortem Braak neurofibrillary tangle stage

Vemuri, P., Whitwell, J. L., Kantarci, K., Josephs, K. A., Parisi, J. E., Shiung, M. S., Knopman, D. S., Boeve, B. F., Petersen, R. C., Dickson, D. W., et al. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.05.012 · Cited by 172 · see citing works

The role of beta amyloid in Alzheimer?s disease: still a cause of everything or the only one who got caught?

Verdile, G. (2004) · Pharmacological Research · doi:10.1016/j.phrs.2003.12.028 · Cited by 177 · see citing works

Atrophy of presubiculum and subiculum is the earliest hippocampal anatomical marker of Alzheimer's disease

Carlesimo, G. A., Piras, F., Orfei, M. D., Iorio, M., Caltagirone, C., & Spalletta, G. (2015) · Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring · doi:10.1016/j.dadm.2014.12.001 · Cited by 159 · see citing works

Tauopathy with paired helical filaments in an aged chimpanzee

Rosen, R. F., Farberg, A. S., Gearing, M., Dooyema, J., M. Long, P., Anderson, D. C., Davis‐Turak, J., Coppola, G., Geschwind, D. H., Paré, J., et al. (2008) · Journal of Comparative Neurology · doi:10.1002/cne.21744 · Cited by 153 · see citing works

Loss of olfactory function in dementing disease.

Murphy, C. (1999) · Physiology and Behavior · doi:10.1016/s0031-9384(98)00262-5 · Cited by 163 · see citing works

Conformational changes specific for pseudophosphorylation at serine 262 selectively impair binding of tau to microtubules

Fischer, D., Mukrasch, M. D., Biernat, J., Bibow, S., Blackledge, M., Griesinger, C., Mandelkow, E., & Zweckstetter, M. (2009) · Biochemistry · doi:10.1021/bi901090m · Cited by 149 · see citing works

Multi-Target Directed Donepezil-Like Ligands for Alzheimer's Disease

Unzeta, M., Esteban, G., Bolea, I., Fogel, W. A., Ramsay, R. R., Youdim, M. B. H., Tipton, K. F., & Marco, J. L. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00205 · Cited by 151 · see citing works

Diffusion tensor imaging in normal aging and neuropsychiatric disorders

Sullivan, E. V., & Pfefferbaum, A. (2003) · European Journal of Radiology · doi:10.1016/s0720-048x(02)00313-3 · Cited by 148 · see citing works

Dysregulation of leptin signaling in Alzheimer disease: evidence for neuronal leptin resistance

Bonda, D., Stone, J. G., Torres, S. L., Siedlak, S. L., Perry, G. L., Kryscio, R. J., Jicha, G. A., Casadesús, G., Smith, M. A., Zhu, X., et al. (2013) · Journal of Neurochemistry · doi:10.1111/jnc.12380 · Cited by 145 · see citing works

Functional Magnetic Resonance Imaging Study of Human Olfaction and Normal Aging

Wang, J., Eslinger, P. J., Smith, M. B. H., & Yang, Q. X. (2005) · The Journals of Gerontology Series A · doi:10.1093/gerona/60.4.510 · Cited by 145 · see citing works

Left hippocampal volume loss in Alzheimer's disease is reflected in performance on odor identification: A structural MRI study

Murphy, C., Jernigan, T. L., & Fennema‐Notestine, C. (2003) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617703930116 · Cited by 142 · see citing works

In vivo brain concentrations of N-acetyl compounds, creatine, and choline in Alzheimer disease.

Pfefferbaum, A., Adalsteinsson, E., Spielman, D., Sullivan, E., & Lim, K. O. (1999) · Archives of General Psychiatry · doi:10.1001/archpsyc.56.2.185 · Cited by 141 · see citing works

Oxidative state in platelets and erythrocytes in aging and Alzheimer's disease

Kawamoto, E. M., Munhoz, C. D., Glezer, I., Bahia, V. S., Caramelli, P., Nitríni, R., Gorjão, R., Curi, R., Scavone, C., & Marcourakis, T. (2004) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2004.08.011 · Cited by 129 · see citing works

Multiple sclerosis and Alzheimer's disease

Dal Bianco, A., Bradl, M., Frischer, J., Kutzelnigg, A., Jellinger, K., & Lassmann, H. (2008) · Annals of Neurology · doi:10.1002/ana.21240 · Cited by 123 · see citing works

Hippocampal Aβ42 Levels Correlate with Spatial Memory Deficit in APP and PS1 Double Transgenic Mice

Puoliväli, J. T., Wang, J., Heikkinen, T., Heikkilä, M., Tapiola, T., van Groen, T., & Tanila, H. (2002) · Neurobiology of Disease · doi:10.1006/nbdi.2002.0481 · Cited by 118 · see citing works

Neurofibrillary Pathology in Transgenic Mice Overexpressing V717F β-Amyloid Precursor Protein

Masliah, E., Sisk, A., Mallory, M. E., & Games, D. (2001) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/60.4.357 · Cited by 117 · see citing works

Radial width of the temporal horn: a sensitive measure in Alzheimer disease.

Frisoni, G. B., Geroldi, C., Beltramello, A., Bianchetti, A., Binetti, G. G., Bordiga, G., DeCarli, C. S., Laakso, M. P., Soininen, H. S., Testa, C., et al. (2002) · PubMed Central · Cited by 103 · see citing works

EFAD transgenic mice as a human APOE relevant preclinical model of Alzheimerʼns disease

Tai, L. M., Balu, D., Avila-Munoz, E., Abdullah, L., Thomas, R., Collins, N., Valencia-Olvera, A. C., & LaDu, M. J. (2017) · Journal of Lipid Research · doi:10.1194/jlr.r076315 · Cited by 93 · see citing works

Physiological regulation of tau phosphorylation during hibernation

Su, B., Wang, X., Drew, K. L., Perry, G. L., Smith, M. A., & Zhu, X. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05294.x · Cited by 91 · see citing works

Structural networks in Alzheimer's disease

Reid, A., & Evans, A. C. (2013) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2012.11.010 · Cited by 90 · see citing works

Role of Synucleins in Alzheimer’s Disease

Crews, L. A., Tsigelny, I. F., Hashimoto, M., & Masliah, E. (2009) · Neurotoxicity Research · doi:10.1007/s12640-009-9073-6 · Cited by 84 · see citing works

Apolipoprotein E4 promotes the early deposition of Aβ42 and then Aβ40 in the elderly

Walker, L. C., Pahnke, J., Madauss, M., Vogelgesang, S., Pahnke, A., Herbst, E. W., Stausske, D., Walther, R., Kessler, C., & Warzok, R. (2000) · Acta Neuropathologica · doi:10.1007/s004010051190 · Cited by 81 · see citing works

Novel Method to Quantify Neuropil Threads in Brains from Elders With or Without Cognitive Impairment

Mitchell, T. W., Nissanov, J., Han, L.-Y., Mufson, E. J., Schneider, J. A., Cochran, E. J., Bennett, D. A., Lee, V. M.-Y., Trojanowski, J. Q., & Arnold, S. E. (2000) · Journal of Histochemistry & Cytochemistry · doi:10.1177/002215540004801206 · Cited by 78 · see citing works

Myths and truths about the cellular composition of the human brain: A review of influential concepts

von Bartheld, C. S. (2017) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2017.08.004 · Cited by 77 · see citing works

Assessing THK523 selectivity for tau deposits in Alzheimer’s disease and non–Alzheimer’s disease tauopathies

Fodero‐Tavoletti, M. T., Furumoto, S., Taylor, L. S., McLean, C., Mulligan, R. S., Birchall, I. E., Harada, R., Masters, C. L., Yanai, K., Kudo, Y., et al. (2014) · Alzheimer s Research & Therapy · doi:10.1186/alzrt240 · Cited by 73 · see citing works

Causes versus effects: the increasing complexities of Alzheimer’s disease pathogenesis

Mondragón‐Rodríguez, S., Basurto‐Islas, G., Lee, H., Perry, G. L., Zhu, X., Castellani, R. J., & Smith, M. A. (2010) · Expert Review of Neurotherapeutics · doi:10.1586/ern.10.27 · Cited by 72 · see citing works

Exploring the Therapeutic Potential of Phytochemicals in Alzheimer’s Disease: Focus on Polyphenols and Monoterpenes

Piccialli, I., Tedeschi, V., Caputo, L., D’Errico, S., Ciccone, R., De Feo, V., Secondo, A., & Pannaccione, A. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.876614 · Cited by 73 · see citing works

The Impact of APP on Alzheimer-like Pathogenesis and Gene Expression in Down Syndrome iPSC-Derived Neurons

Ovchinnikov, D. A., Korn, O., Virshup, I., Wells, C. A., & Wolvetang, E. J. (2018) · Stem Cell Reports · doi:10.1016/j.stemcr.2018.05.004 · Cited by 71 · see citing works

MAPK, β-amyloid and synaptic dysfunction: the role of RAGE

Origlia, N., Arancio, O., Domenici, L., & Yan, S. S. (2009) · Expert Review of Neurotherapeutics · doi:10.1586/ern.09.107 · Cited by 70 · see citing works

A Drosophila Model of Alzheimer's Disease

Crowther, D. C., Page, R., Chandraratna, D. S., & Lomas, D. A. (2006) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(06)12015-7 · Cited by 69 · see citing works

Functional Connectivity between the Resting-State Olfactory Network and the Hippocampus in Alzheimer’s Disease

Lu, J., Testa, N., Jordan, R., Elyan, R., Kanekar, S. G., Wang, J., Eslinger, P. J., Yang, Q. X., Zhang, B., & Karunanayaka, P. (2019) · Brain Sciences · doi:10.3390/brainsci9120338 · Cited by 66 · see citing works

Associations Between Diabetes Mellitus and Neurodegenerative Diseases

Szablewski, L. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26020542 · Cited by 74 · see citing works

The Chemical Senses and Nutrition in Older Adults

Murphy, C. (2008) · Journal of Nutrition for the Elderly · doi:10.1080/01639360802261862 · Cited by 67 · see citing works

Distribution of endogenous normal tau in the mouse brain

Kubo, A., Misonou, H., Matsuyama, M., Nomori, A., Wada‐Kakuda, S., Takashima, A., Kawata, M., Murayama, S., Ihara, Y., & Miyasaka, T. (2019) · Journal of Comparative Neurology · doi:10.1002/cne.24577 · Cited by 57 · see citing works

Mouse Genetic Models of Human Brain Disorders

Leung, C., & Jia, Z. (2016) · Frontiers in Genetics · doi:10.3389/fgene.2016.00040 · Cited by 59 · see citing works

Central and peripheral circadian clocks and their role in Alzheimer's disease

Chauhan, R., Chen, K.-F., Kent, B. A., & Crowther, D. C. (2017) · Disease Models & Mechanisms · doi:10.1242/dmm.030627 · Cited by 58 · see citing works

Type 2 diabetes mellitus in the pathophysiology of Alzheimer's disease

de Nazareth, A. M. (2017) · Dementia & Neuropsychologia · doi:10.1590/1980-57642016dn11-020002 · Cited by 60 · see citing works

Behavioural and cellular effects of exogenous amyloid-β peptides in rodents.

Chambon, C., Wegener, N., Gravius, A., & Danysz, W. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.08.024 · Cited by 64 · see citing works

Stress-induced microglial activation may facilitate the progression of neurodegenerative disorders

Sugama, S. (2009) · Medical Hypotheses · doi:10.1016/j.mehy.2009.02.047 · Cited by 52 · see citing works

The Na+/Ca2+exchanger in Alzheimer’s disease

Pannaccione, A., Piccialli, I., Secondo, A., Ciccone, R., Molinaro, P., Boscia, F., & Annunziato, L. (2020) · Cell Calcium · doi:10.1016/j.ceca.2020.102190 · Cited by 49 · see citing works

A randomized, two‐year study of the efficacy of cognitive intervention on elderly people: the Donostia Longitudinal Study

Buiza, C., Etxeberría, I., Galdona, N., Gonzalez, M. F., Arriola, E., de Munaín, A. L., Urdaneta, E., & Yanguas, J. J. (2007) · International Journal of Geriatric Psychiatry · doi:10.1002/gps.1846 · Cited by 49 · see citing works

Androgens modulate chronic intermittent hypoxia effects on brain and behavior

Snyder, B., Duong, P., Trieu, J., & Cunningham, R. L. (2018) · Hormones and Behavior · doi:10.1016/j.yhbeh.2018.09.005 · Cited by 48 · see citing works

Cascade of tau toxicity in inducible hippocampal brain slices and prevention by aggregation inhibitors

Messing, L., Decker, J. M., Joseph, M., Mandelkow�, E., & Mandelkow, E.-M. (2012) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2012.10.024 · Cited by 47 · see citing works

Olfactory impairment increases as a function of age in persons with Down syndrome

Nijjar, R. K., & Murphy, C. (2002) · Neurobiology of Aging · doi:10.1016/s0197-4580(01)00263-9 · Cited by 48 · see citing works

Disentangling the pathology of schizophrenia and paraphrenia

Casanova, M. F., Stevens, J. R., Brown, R., Royston, C., & Bruton, C. J. (2002) · Acta Neuropathologica · doi:10.1007/s00401-001-0468-6 · Cited by 47 · see citing works

Imaging in Alzheimer's disease

Scheltens, P. (2009) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2009.11.2/pscheltens · Cited by 46 · see citing works

Amyloid β‐peptide activates nuclear factor‐κB through an N‐methyl‐D‐aspartate signaling pathway in cultured cerebellar cells

Kawamoto, E. M., Lepsch, L. B., Cury‐Boaventura, M. F., Munhoz, C. D., Lima, L. S., Yshii, L., Avellar, M. C. W., Curi, R., Mattson, M. P., & Scavone, C. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21548 · Cited by 43 · see citing works

Neuroinflammation as a neurotoxic mechanism in alcoholism: Commentary on “Increased MCP-1 and microglia in various regions of human alcoholic brain”

Sullivan, E. V., & Zahr, N. M. (2008) · Experimental Neurology · doi:10.1016/j.expneurol.2008.05.016 · Cited by 40 · see citing works

Elevated phospholipase D isoform 1 in Alzheimer's disease patients' hippocampus: Relevance to synaptic dysfunction and memory deficits

Krishnan, B., Kayed, R., & Taglialatela, G. (2018) · Alzheimer s & Dementia Translational Research & Clinical Interventions · doi:10.1016/j.trci.2018.01.002 · Cited by 40 · see citing works

Amyloid imaging using fluorine-19 magnetic resonance imaging (19F-MRI)

Tooyama, I., Yanagisawa, D., Taguchi, H., Kato, T., Hirao, K., Shirai, N., Sogabe, T., Ibrahim, N. F., Inubushi, T., & Morikawa, S. (2016) · Ageing Research Reviews · doi:10.1016/j.arr.2015.12.008 · Cited by 40 · see citing works

Cortical degeneration associated with phonologic and semantic language impairments in AD

Harasty, J., Halliday, G. M., Xuereb, J. H., Croot, K., Bennett, H., & Hodges, J. R. (2001) · Neurology · doi:10.1212/wnl.56.7.944 · Cited by 40 · see citing works

Plasma metabolites related to cellular energy metabolism are altered in adults with Down syndrome and Alzheimer's disease

Gross, T. J., Doran, E. W., Cheema, A. K., Head, E., Lott, I. T., & Mapstone, M. E. (2019) · Developmental Neurobiology · doi:10.1002/dneu.22716 · Cited by 39 · see citing works

Aging-related changes in calcium-binding proteins in rat perirhinal cortex

Moyer, J. R., Furtak, S. C., McGann, J. P., & Brown, T. H. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2009.10.001 · Cited by 39 · see citing works

Comparison of odor identification among amnestic and non-amnestic mild cognitive impairment, subjective cognitive decline, and early Alzheimer’s dementia

Park, S. J., Lee, J., Lee, K., & Kim, J. (2018) · Neurological Sciences · doi:10.1007/s10072-018-3261-1 · Cited by 39 · see citing works

Large inter- and intra-case variability of first generation tau PET ligand binding in neurodegenerative dementias

Wren, M. C., Lashley, T., Årstad, E., & Sander, K. (2018) · Acta Neuropathologica Communications · doi:10.1186/s40478-018-0535-z · Cited by 37 · see citing works

Biomolecular condensation of the microtubule-associated protein tau

Ukmar, T., Wegmann, S., & Zweckstetter, M. (2019) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2019.06.007 · Cited by 39 · see citing works

Entorhinal cortex of aged subjects with Down's syndrome shows severe neuronal loss caused by neurofibrillary pathology

Sadowski, M. J., Wı́sniewski, H. M., Tarnawski, M. J., Kozlowski, P. B., Lach, B., & Węgiel, J. (1999) · Acta Neuropathologica · doi:10.1007/s004010050968 · Cited by 38 · see citing works

Differences in regional brain atrophy in genetic forms of Alzheimer's disease

Gregory, G. C., Macdonald, V., Schofield, P. R., Kril, J. J., & Halliday, G. M. (2005) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2005.03.011 · Cited by 36 · see citing works

The common dementias: a pictorial review

Bhogal, P., Mahoney, C., Graeme-Baker, S., Roy, A., Shah, S., Fraioli, F., Cowley, P., & Jäger, H. R. (2013) · European Radiology · doi:10.1007/s00330-013-3005-9 · Cited by 36 · see citing works

Multifaceted Alzheimer’s Disease: Building a Roadmap for Advancement of Novel Therapies

Kaur, D., Behl, T., Sehgal, A., Singh, S., Sharma, N., & BUNGAU, S. G. (2021) · Neurochemical Research · doi:10.1007/s11064-021-03415-w · Cited by 34 · see citing works

Patterns of cortical thinning in Alzheimer's disease and frontotemporal dementia

Richards, B. A., Chertkow, H. M., Singh, V., Robillard, A., Massoud, F., Evans, A. C., & Kabani, N. J. (2008) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.12.019 · Cited by 34 · see citing works

Biosensors toward behavior detection in diagnosis of alzheimer’s disease

Sun, X., Sun, X., Wang, Q., Wang, X., Feng, L., Yang, Y., Jing, Y., Yang, C., & Zhang, S. (2022) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2022.1031833 · Cited by 33 · see citing works

Polyphenols: Natural food grade biomolecules for treating neurodegenerative diseases from a multi-target perspective

Li, Z., Zhao, T., Shi, M., Wei, Y., Huang, X., Shen, J., Zhang, X., Xie, Z., Huang, P., Yuan, K., et al. (2023) · Frontiers in Nutrition · doi:10.3389/fnut.2023.1139558 · Cited by 33 · see citing works

Amyloid precursor protein expression is enhanced in human platelets from subjects with Alzheimer's disease and frontotemporal lobar degeneration: A Real-time PCR study

Vignini, A., Morganti, S., Salvolini, E., Sartini, D., Luzzi, S., Fiorini, R., Provinciali, L., Primio, R. D., Mazzanti, L., & Emanuelli, M. (2013) · Experimental Gerontology · doi:10.1016/j.exger.2013.10.008 · Cited by 29 · see citing works

The Distance between N and C Termini of Tau and of FTDP-17 Mutants Is Modulated by Microtubule Interactions in Living Cells

Primio, C. D., Quercioli, V., Siano, G., Rovere, M., Kováčech, B., Novák, M., & Cattaneo, A. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00210 · Cited by 27 · see citing works

Olfactory Dysfunction in ApoE ɛ4/4 Homozygotes with Alzheimer’s Disease

Oleson, S., & Murphy, C. A. (2015) · Journal of Alzheimer s Disease · doi:10.3233/jad-150089 · Cited by 27 · see citing works

Implication of matrix metalloproteinases in regulating neuronal disorder

Mukherjee, A., & Swarnakar, S. (2014) · Molecular Biology Reports · doi:10.1007/s11033-014-3752-y · Cited by 27 · see citing works

Ionizing radiation causes increased tau phosphorylation in primary neurons

Li, L., Wang, W., Welford, S. M., Zhang, T., Wang, X., & Zhu, X. (2014) · Journal of Neurochemistry · doi:10.1111/jnc.12769 · Cited by 26 · see citing works

Entorhinal cortex volume in older adults: Reliability and validity considerations for three published measurement protocols

Price, C. C., Wood, M. F., Leonard, C. M., Towler, S., Ward, J., Montijo, H., Kellison, I. L., Bowers, D., Monk, T. G., NEWCOMER, J. C., et al. (2010) · Journal of the International Neuropsychological Society · doi:10.1017/s135561771000072x · Cited by 27 · see citing works

Membrane lipid peroxidation in neurodegeneration: Role of thrombin and proteinase-activated receptor-1

Citron, B. A., Ameenuddin, S., Uchida, K., Suo, W. Z., SantaCruz, K. S., & Festoff, B. W. (2016) · Brain Research · doi:10.1016/j.brainres.2016.04.071 · Cited by 26 · see citing works

Sex differences in sleep apnea and comorbid neurodegenerative diseases

Snyder, B., & Cunningham, R. L. (2017) · Steroids · doi:10.1016/j.steroids.2017.12.006 · Cited by 25 · see citing works

Unraveling brain diseases: The promise of brain-on-a-chip models

Cerutti, L., & Brofiga, M. (2024) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2024.110105 · Cited by 24 · see citing works

Therapeutic targets from a Drosophila model of Alzheimer’s disease

Crowther, D. C., Kinghorn, K. J., Page, R., & Lomas, D. A. (2004) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2004.07.001 · Cited by 21 · see citing works

How Ionic Strength Affects the Conformational Behavior of Human and Rat Beta Amyloids – A Computational Study

Křı́ž, Z., Klusák, J., Krištofíková, Z., & Koča, J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062914 · Cited by 23 · see citing works

Common neurodegenerative disorders in the perioperative setting: Recommendations for screening from the Society for Perioperative Assessment and Quality Improvement (SPAQI)

Wiggins, M. E., Arias, F., Urman, R. D., Richman, D. C., Sweitzer, B. J., Edwards, A. F., Armstrong, M. J., Chopra, A., Libon, D. J., & Price, C. C. (2020) · Perioperative Care and Operating Room Management · doi:10.1016/j.pcorm.2020.100092 · Cited by 7 · see citing works

Symposium 06: Perioperative Neurocognitive Disorders With Considerations for Alzheimer’s Disease and Related Dementias

Price, C. C. (2023) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617723004162 · Cited by 1 · see citing works

Neurologic and Cognitive Changes in the Elderly

McCarten, J. R. (2011) · Springer eBooks · doi:10.1007/978-1-4419-0892-6_24 · Cited by 2 · see citing works

The New Frontier of Perioperative Cognitive Medicine for Alzheimer's Disease and Related Dementias

Price, C. C. (2022) · Neurotherapeutics · doi:10.1007/s13311-021-01180-w · Cited by 16 · see citing works

Dissecting the Possible Influences of Anesthesia and Surgery On Alzheimer’s Disease

Evered, L. A. (2013) · Neurodegenerative Disease Management · doi:10.2217/nmt.13.8 · Cited by 4 · see citing works