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Epilepsy and Cognitive Impairments in Alzheimer Disease
Open accessAbstract
Alzheimer disease (AD) is associated with cognitive decline and increased incidence of seizures. Seizure activity in AD has been widely interpreted as a secondary process resulting from advanced stages of neurodegeneration, perhaps in combination with other age-related factors. However, recent findings in animal models of AD have challenged this notion, raising the possibility that aberrant excitatory neuronal activity represents a primary upstream mechanism that may contribute to cognitive deficits in these models. The following observations suggest that such activity may play a similar role in humans with AD: (1) patients with sporadic AD have an increased incidence of seizures that appears to be independent of disease stage and highest in cases with early onset; (2) seizures are part of the natural history of many pedigrees with autosomal dominant early-onset AD, including those with mutations in presenilin-1, presenilin-2, or the amyloid precursor protein, or with duplications of wild-type amyloid precursor protein; (3) inheritance of the major known genetic risk factor for AD, apolipoprotein E4, is associated with subclinical epileptiform activity in carriers without dementia; and (4) some cases of episodic amnestic wandering and disorientation in AD are associated with epileptiform activity and can be prevented with antiepileptic drugs. Here we review recent experimental data demonstrating that high levels of beta-amyloid in the brain can cause epileptiform activity and cognitive deficits in transgenic mouse models of AD. We conclude that beta-amyloid peptides may contribute to cognitive decline in AD by eliciting similar aberrant neuronal activity in humans and discuss potential clinical and therapeutic implications of this hypothesis.
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“Patients with EOFAD have an 87-fold increased incidence of seizures relative to the age-matched population compared to a threefold increase in seizure incidence in LOAD individuals [6].”
From Microglia specific deletion of miR-155 in Alzheimer’s disease mouse models reduces amyloid-β pathology but causes hyperexcitability and seizures (2023) · cites this paper as [6]
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“Hyperexcitability is present in AD brain [142] and epilepsy was shown to promote plaque pathology [110].”
From Intraneuronal β-amyloid accumulation and synapse pathology in Alzheimer’s disease (2010) · cites this paper as [142]
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Walsh, D. M., Klyubin, I., Fadeeva, J. V., Cullen, W. K., Anwyl, R., Wolfe, M. S., Rowan, M. J., & Selkoe, D. J. (2002) · Nature · doi:10.1038/416535a · Cited by 4,291
Reducing Endogenous Tau Ameliorates Amyloid ß-Induced Deficits in an Alzheimer's Disease Mouse Model
Roberson, E. D., Scearce-Levie, K., Palop, J. J., Yan, F., Cheng, I. H., Wu, T., Gerstein, H., Yu, G.-Q., & Mucke, L. (2007) · Science · doi:10.1126/science.1141736 · Cited by 1,892
Self-citationPalop, J. J., Chin, J., Roberson, E. D., Wang, J., Thwin, M. T., Bien-Ly, N., Yoo, J., Ho, K. O., Yu, G.-Q., Kreitzer, A., et al. (2007) · Neuron · doi:10.1016/j.neuron.2007.07.025 · Cited by 1,653
Self-citationAPP Processing and Synaptic Function
Kamenetz, F., Tomita, T., Hsieh, H., Seabrook, G., Borchelt, D., Iwatsubo, T., Sisodia, S., & Malinow, R. (2003) · Neuron · doi:10.1016/s0896-6273(03)00124-7 · Cited by 1,644
Enhanced neurofibrillary degeneration in transgenic mice expressing mutant tau and APP
Lewis, J., Dickson, D. W., Lin, W.-L., Chisholm, L., Corral, A., Jones, G., Yen, S.-H., Sahara, N., Skipper, L., Yager, D., et al. (2001) · Science · doi:10.1126/science.1058189 · Cited by 1,611
Shankar, G. M., Bloodgood, B. L., Townsend, M., Walsh, D. M., Selkoe, D. J., & Sabatini, B. L. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.4970-06.2007 · Cited by 1,592
Plaque-independent disruption of neural circuits in Alzheimer’s disease mouse models
Hsia, A. Y., Masliah, E., McConlogue, L., Yu, G.-Q., Tatsuno, G., Hu, K., Kholodenko, D., Malenka, R. C., Nicoll, R. A., & Mucke, L. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.6.3228 · Cited by 1,123
AMPAR Removal Underlies Aβ-Induced Synaptic Depression and Dendritic Spine Loss
Hsieh, H., Boehm, J., Sato, C., Iwatsubo, T., Tomita, T., Sisodia, S., & Malinow, R. (2006) · Neuron · doi:10.1016/j.neuron.2006.10.035 · Cited by 1,042
Impaired synaptic plasticity and learning in aged amyloid precursor protein transgenic mice
Chapman, P. F., White, G. L., Jones, M. W., Cooper-Blacketer, D., Marshall, V. J., Irizarry, M., Younkin, L., Good, M. A., Bliss, T. V. P., Hyman, B. T., et al. (1999) · Nature Neuroscience · doi:10.1038/6374 · Cited by 946
Mahley, R. W., Weisgraber, K. H., & Huang, Y. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600549103 · Cited by 912
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Mandell, A. M., & Green, R. C. (2011) · Wiley eBooks · doi:10.1002/9781444344110.ch1 · Cited by 22
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Fu, Y.-H., Lv, R., Jin, L., Lü, Q., Shao, X., He, J., Wu, L., Zhang, L.-S., & Hu, H. (2010) · Epilepsy Research · doi:10.1016/j.eplepsyres.2010.07.020 · Cited by 20
Vadakkan, K. I. (2016) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2016.06.042 · Cited by 21
Coelho, D. S., & Moreno, E. (2020) · iScience · doi:10.1016/j.isci.2020.101468 · Cited by 22
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AMPA receptors in Alzheimer disease: Pathological changes and potential therapeutic targets
Ning, L., Shen, R., Xie, B., Jiang, Y., Geng, X., & Dong, W. (2024) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlae093 · Cited by 19
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Pasquini, L., Scherr, M., Tahmasian, M., Myers, N. E., Ortner, M., Kurz, A., Förstl, H., Zimmer, C., Grimmer, T., Akhrif, A., et al. (2016) · Journal of Alzheimer s Disease · doi:10.3233/jad-150823 · Cited by 20
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Song, Z., McDonough, I. M., Liu, P., Lu, H., & Park, D. C. (2016) · NeuroImage Clinical · doi:10.1016/j.nicl.2016.05.013 · Cited by 19
Koukouli, F., Rooy, M., & Maskos, U. (2016) · Aging · doi:10.18632/aging.101136 · Cited by 21
Blankenship, H. E., Carter, K. A., Pham, K. D., Cassidy, N. T., Markiewicz, A. N., Thellmann, M. I., Sharpe, A. L., Freeman, W. M., & Beckstead, M. J. (2024) · Nature Communications · doi:10.1038/s41467-024-53891-1 · Cited by 18
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Johnson, S. A., Turner, S. M., Lubke, K. N., Cooper, T. L., Fertal, K. E., Bizon, J. L., Maurer, A. P., & Burke, S. N. (2019) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2018.00072 · Cited by 18
Fu, Y., Li, L., Wang, Y., Chu, G., Kong, X., & Wang, J. (2019) · Neurochemistry International · doi:10.1016/j.neuint.2019.104542 · Cited by 18
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Larner, A. J., & Marson, A. G. (2011) · Journal of Alzheimer s Disease · doi:10.3233/jad-2011-102148 · Cited by 18
Giorgi, F. S., Baldacci, F., Dini, E., Tognoni, G., & Bonuccelli, U. (2015) · Neurological Sciences · doi:10.1007/s10072-015-2442-4 · Cited by 17
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Kreuzer, M., Keating, G. L., Fenzl, T., Härtner, L., Sinon, C. G., Hajjar, I. M., Ciavatta, V. T., Rye, D. B., & García, P. S. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21239290 · Cited by 17
Joseph, S., Patterson, R., Wang, W., Blumberger, D. M., Rajji, T. K., & Kumar, S. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-210311 · Cited by 17
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Lam, P., Vinnakota, C., Guzmán, B. C., Newland, J., Peppercorn, K., Tate, W. P., Waldvogel, H. J., Faull, R. L. M., & Kwakowsky, A. (2022) · Molecules · doi:10.3390/molecules27082440 · Cited by 17
Romero-García, R., Atienza, M., & Cantero, J. L. (2015) · International Journal of Neural Systems · doi:10.1142/s0129065716500039 · Cited by 17
Granzotto, A., Bomba, M., Castelli, V., Navarra, R., Massetti, N., D’Aurora, M., ONOFRJ, M. C., Cicalini, I., Boccio, P. D., Gatta, V., et al. (2019) · Aging · doi:10.18632/aging.102191 · Cited by 16
Epileptic seizure detection via logarithmic normalized functional values of singular values
Zhou, X., Ling, B. W., Li, C., & Zhao, K. (2020) · Biomedical Signal Processing and Control · doi:10.1016/j.bspc.2020.102086 · Cited by 16
Liguori, C., Spanetta, M., Romoli, M., Placidi, F., Cesarini, E. N., Mercuri, N. B., & Costa, C. (2021) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2021.111434 · Cited by 17
Russo, M. L., Molina-Campos, E., Ybarra, N., Rogalsky, A. E., Musial, T. F., Jiménez, V., Haddad, L. G., Voskobiynyk, Y., D’Souza, G. X., Carballo, G., et al. (2021) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2021.06.018 · Cited by 16
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Zhang, G., Gong, W.-X., Xu, Z.-Y.-R., & Guo, Y. C. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.926982 · Cited by 16
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Almeida, V. N., & Radanovic, M. (2022) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2022.108337 · Cited by 17
Bazan, N. G. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8897-0 · Cited by 15
Falcicchia, C., Tozzi, F., Gabrielli, M., Amoretti, S., Masini, G., Nardi, G., Guglielmo, S., Ratto, G. M., Arancio, O., Verderio, C., et al. (2023) · Brain Communications · doi:10.1093/braincomms/fcad170 · Cited by 15
Stephens, G. S., Park, J. K., Eagle, A. L., You, J. C., Silva‐Pérez, M., Fu, C.-H., Choi, S., Romain, C. P. S., Sugimoto, C., Buffington, S. A., et al. (2024) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2024.102612 · Cited by 16
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Pototskiy, E., Dellinger, J. R., Bumgarner, S., Patel, J. D., Sherrerd-Smith, W., & Musto, A. E. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.08.003 · Cited by 15
Zhang, X., Xu, L., Yang, S., Hu, L., Dong, F.-Y., Sun, B., & Shen, H. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-210585 · Cited by 15
Zhou, X., Ling, B. W., Zhou, Y., & Law, N. F. (2023) · Expert Systems with Applications · doi:10.1016/j.eswa.2023.119613 · Cited by 15
Localized proteomic differences in the choroid plexus of Alzheimer's disease and epilepsy patients
Leitner, D., Kanshin, E., Faustin, A., Thierry, M., Friedman, D. J., Devore, S., Ueberheide, B. M., Devinsky, O., & Wısnıewskı, T. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.1221775 · Cited by 17
Multitarget Anti-Alzheimer Hybrid Compounds
Muñoz‐Torrero, D. (2017) · Elsevier eBooks · doi:10.1016/b978-0-08-101011-2.00006-4 · Cited by 15
Genetic effect of Type 2 diabetes to the progression of neurological diseasesPreprint
Rahman, M. H., Peng, S., Chen, C., Lió, P., & Moni, M. A. (2018) · doi:10.7287/peerj.preprints.27323v1 · Cited by 15
Пономарева, Н. В., Андреева, Т. В., Protasova, M., Коновалов, Р. Н., Кротенкова, М. В., Kolesnikova, E. P., Malina, D. D., Kanavets, E. V., Алексеевич, М. А., Fokin, V. F., et al. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.931173 · Cited by 14
Reyes, A., Schneider, A. L. C., Kucharska‐Newton, A., Gottesman, R. F., Johnson, E. L., & McDonald, C. R. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.1230368 · Cited by 14
Tzavellas, N. P., Tsamis, K. I., Katsenos, A. P., Davri, A. S., Simos, Y. V., Nikas, I. P., Bellos, S., Lekkas, P., Kanellos, F. S., Konitsiotis, S., et al. (2024) · Cells · doi:10.3390/cells13050434 · Cited by 16
Benítez, M. J., Retana, D., Ordóñez‐Gutiérrez, L., Colmena, I., Goméz, M. J., Álvarez, R., Ciorraga, M., Dopazo, A., Wandosell, F. G., & Garrido, J. J. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-024-05485-9 · Cited by 17
Tabuena, D. R., Jang, S.-S., Grone, B. P., Yip, O., Jones, E. A. A., Blumenfeld, J. R., Liang, Z., Mann, R. S., Li, Y., Necula, D., et al. (2026) · Nature Aging · doi:10.1038/s43587-026-01096-0 · Cited by 17
Shohayeb, B., Ho, U. Y., Hassan, H., Piper, M., & Ng, D. C. H. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.549353 · Cited by 14
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Cretin, B. (2020) · Drugs & Aging · doi:10.1007/s40266-020-00826-2 · Cited by 14
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Wu, S., Zhou, J., Zhang, H., & Barger, S. W. (2022) · Current Alzheimer Research · doi:10.2174/1567205019666220805105106 · Cited by 14
A systematic approach for identifying shared mechanisms in epilepsy and its comorbidities
Hoyt, C. T., Domingo‐Fernándéz, D., Balzer, N. R., Güldenpfennig, A., & Hofmann‐Apitius, M. (2018) · Database · doi:10.1093/database/bay050 · Cited by 14
Wu, Y.-Y., Cheng, I. H.-J., Lee, C.-C., Chiu, M., Lee, M., Chen, T., & Hsu, J. (2011) · Journal of Alzheimer s Disease · doi:10.3233/jad-2011-102031 · Cited by 14
Exploring biomarkers of neurodegeneration in epilepsy: Critical insights
Farhan, R., Hashmi, S. A., Kapur, J., D’Abreu, A., Punia, V., Manning, C. A., Smith, V. L., & Zawar, I. (2025) · Epileptic Disorders · doi:10.1002/epd2.70023 · Cited by 14
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Huang, C., Boonyapisit, K., Gunadharma, S., Casanova-Gutierrez, J., Jin, L., Nayak, D., & Akamatsu, N. (2022) · Therapeutics and Clinical Risk Management · doi:10.2147/tcrm.s371396 · Cited by 13
Arab, H. H., Eid, A. H., Yahia, R., Alsufyani, S. E., Ashour, A. M., El‐Sheikh, A. A. K., Darwish, H. W., Saad, M. A., Al‐Shorbagy, M. Y., & Masoud, M. A. (2023) · Pharmaceuticals · doi:10.3390/ph16091214 · Cited by 13
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DiNuzzo, M., Walls, A. B., Öz, G., Seaquist, E. R., Waagepetersen, H. S., Bak, L. K., Nedergaard, M., & Schousboe, A. (2019) · Advances in neurobiology · doi:10.1007/978-3-030-27480-1_9 · Cited by 13
Cretin, B., Bousiges, O., Hautecloque, G., Philippi, N., Blanc, F., Bitonto, L. D., Martin‐Hunyadi, C., & Sellal, F. (2021) · Frontiers in Neurology · doi:10.3389/fneur.2021.623777 · Cited by 13
Alfaro‐Ruiz, R., Aguado, C., Martín‐Belmonte, A., Moreno‐Martínez, A. E., Merchán‐Rubira, J., Hernández, F., Ávila, J., Fukazawa, Y., & Luján, R. (2022) · Brain Pathology · doi:10.1111/bpa.13115 · Cited by 14
Chronic seizures induce sex-specific cognitive deficits with loss of presenilin 2 function
Knox, K. M., Beckman, M., Smith, C., Jayadev, S., & Barker‐Haliski, M. L. (2023) · Experimental Neurology · doi:10.1016/j.expneurol.2023.114321 · Cited by 13
Cavanagh, C., Colby-Milley, J., Farso, M. C., Krantic, S. M., & Quirion, R. (2011) · Future Neurology · doi:10.2217/fnl.11.50 · Cited by 15
Pitkänen, A., & Bolkvadze, T. (2012) · Oxford University Press eBooks · doi:10.1093/med/9780199746545.003.0025 · Cited by 13
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Campana, C., Assenza, G., Pellegrino, G., Benvenga, A., Assenza, F., Ursini, F., Vernieri, F., & Mario, T. (2011) · International Journal of Alzheimer s Disease · doi:10.4061/2011/690305 · Cited by 13
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Liang, Y., Liu, X., Qiu, L., & Zhang, S. (2018) · Computational Intelligence and Neuroscience · doi:10.1155/2018/1943565 · Cited by 13
Seizures and Epileptiform Activity in Early Alzheimer Disease: How Hard Should We be Looking?
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Cretin, B., Bitonto, L. D., Blanc, F., & Magnin, É. (2015) · Journal of Alzheimer s Disease · doi:10.3233/jad-141953 · Cited by 12
Degeneration of cholinergic basal forebrain nuclei after focally evoked status epilepticus
Biagioni, F., Gaglione, A., Giorgi, F. S., Bucci, D., Moyanova, S. G., Fusco, A. D., Madonna, M., & Fornai, F. (2018) · Neurobiology of Disease · doi:10.1016/j.nbd.2018.09.019 · Cited by 12
Turón, M., Abraira, L., Cazorla, S., Fonseca, E., Quintana, M., Toledo, M., Salas‐Puig, X., & Santamarina, E. (2019) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2019.106443 · Cited by 12
Citraro, R., Leo, A., Tallarico, M., Sciaccaluga, M., & Costa, C. (2022) · Current Neuropharmacology · doi:10.2174/1570159x20666220507020635 · Cited by 12
Babiloni, C., Noce, G., Bonaventura, C. D., Lizio, R., Pascarelli, M. T., Tucci, F., Soricelli, A., Ferri, R., Nobili, F. M., Famà, F., et al. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.514136 · Cited by 12
Joseph, D. J., Liu, C., Peng, J., Liang, G., & Wei, H. (2019) · PLoS ONE · doi:10.1371/journal.pone.0223509 · Cited by 11
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von Rüden, E., Zellinger, C., Gedon, J., Walker, A., Bierling, V., Deeg, C. A., Hauck, S. M., & Potschka, H. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.08.037 · Cited by 11
Eglen, R. M., & Reisine, T. (2018) · SLAS TECHNOLOGY · doi:10.1177/2472630318803277 · Cited by 11
Liu, S., He, Z., Shi, W., & Li, J. (2024) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2024.110070 · Cited by 10
Sohrabpour, A., Sarovic, D., Zetterberg, H., Hämäläinen, M., Baillet, S., & Khan, S. (2025) · Alzheimer s & Dementia · doi:10.1002/alz.70835 · Cited by 12
Irmen, R. E., Turner, S. M., Snipes, J. A., Schloss, K. H., Wang, X., Williams, H. C., Velmurugan, G. V., Hunt, J. B., Li, J., Sullivan, P. G., et al. (2026) · npj Dementia · doi:10.1038/s44400-025-00054-8 · Cited by 11
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Ismael, S., Sindi, G., Colvin, R. A., & Lee, D. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.101108 · Cited by 12
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Metadata
- Authors
- Palop, J. J.
- Affiliations
- University of California, San Francisco (US)
- Corresponding author
- Palop, Jorge J.
- ORCID
- Palop, Jorge J.
- Venue
- Archives of Neurology
- Publisher
- American Medical Association (AMA)
- Published
- 2009-04-01
- Volume
- 66
- Issue
- 4
- Pages
- 435
- ISSN
- 0003-9942 (ISSN-L)
- PMC
- PMC2812914
- OpenAlex
- W2098676436
- Cited by
- 684
- References
- 47
- Citations by year
- 2026: 16 · 2025: 31 · 2024: 47 · 2023: 50 · 2022: 38 · 2021: 46 · 2020: 34 · 2019: 47 · 2018: 33 · 2017: 40 · 2016: 47 · 2015: 42 · 2014: 43 · 2013: 41 · 2012: 39
- FWCI
- 28.49
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Archives of Neurology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute on Aging (AG023501, P50AG023501)
- National Institute of Neurological Disorders and Stroke (R01NS041787, NS041787)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Health Sciences › Medicine › Clinical Neurology › Epilepsy research and treatment
- Keywords
- Alzheimer's disease, epilepsy, cognitive impairment, amyloid-beta, epileptiform activity, presenilin mutations, amyloid precursor protein, APOE ε4, early-onset Alzheimer's disease, transgenic mouse model, antiepileptic drugs
- MeSH terms
- Alzheimer Disease, Amnesia, Animals, Brain, Cognition Disorders, Disease Models, Animal, Electroencephalography, Epilepsy, Genetic Carrier Screening, Hippocampus, Humans, Mice, Transgenic, Nerve Net, Neural Inhibition, Synaptic Transmission, Picrotoxin, Amyloid beta-Peptides, tau Proteins, GABA Antagonists, Dentate Gyrus, Mice, Apolipoprotein E4
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