Diffuse, Lake-like Amyloid-β Deposits in the Parvopyramidal Layer of the Presubiculum in Alzheimer Disease

Classification and basic pathology of Alzheimer disease

Duyckaerts, C., Delatour, B., & Potier, M.-C. (2009) · Acta Neuropathologica · doi:10.1007/s00401-009-0532-1 · Cited by 1,031 · see citing works

Sequence of Aβ-protein deposition in the human medial temporal lobe

Thal, D. R., Rüb, U., Schultz, C., Sassin, I., Ghebremedhin, E., Del Tredici, K., Braak, E., & Braak, H. (2000) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/59.8.733 · Cited by 370 · see citing works

Intraneuronal Aβ-Amyloid Precedes Development of Amyloid Plaques in Down Syndrome

Gyure, K. A., Durham, R., Stewart, W. F., Smialek, J. E., & Troncoso, J. C. (2001) · Archives of Pathology & Laboratory Medicine · doi:10.5858/2001-125-0489-iaapdo · Cited by 248 · see citing works

The role of activated astrocytes and of the neurotrophic cytokine S100B in the pathogenesis of Alzheimer's disease

Mrak, R. E. (2001) · Neurobiology of Aging · doi:10.1016/s0197-4580(01)00293-7 · Cited by 248 · see citing works

The Development of Amyloid β Protein Deposits in the Aged Brain

Thal, D. R., Capetillo-Zarate, E., Del Tredici, K., & Braak, H. (2006) · Science of Aging Knowledge Environment · doi:10.1126/sageke.2006.6.re1 · Cited by 234 · see citing works

The Parahippocampal Gyrus in Alzheimer's Disease: Clinical and Preclinical Neuroanatomical Correlates

VAN HOESEN, G. W., AUGUSTINACK, J. C., DIERKING, J., REDMAN, S. J., & THANGAVEL, R. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06731.x · Cited by 211 · see citing works

Memory loss in Alzheimer’s disease: implications for development of therapeutics

Gold, C. A., & Budson, A. E. (2008) · Expert Review of Neurotherapeutics · doi:10.1586/14737175.8.12.1879 · Cited by 170 · see citing works

Blocking the apolipoprotein E/amyloid-β interaction as a potential therapeutic approach for Alzheimer's disease

Sadowski, M. J., Pankiewicz, J., Scholtzova, H., Mehta, P. D., Prelli, F., Quartermain, D., & Wisniewski, T. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604011103 · Cited by 167 · see citing works

Beneficial effect of human anti-amyloid-β active immunization on neurite morphology and tau pathology

Serrano-Pozo, A., William, C. M., Ferrer, I., Uro-Coste, E., Delisle, M.-B., Maurage, C.-A., Hock, C., Nitsch, R. M., Masliah, E., Growdon, J. H., et al. (2010) · Brain · doi:10.1093/brain/awq056 · Cited by 159 · see citing works

The role of microglial cells and astrocytes in fibrillar plaque evolution in transgenic APPSW mice

Wegiel, J. (2001) · Neurobiology of Aging · doi:10.1016/s0197-4580(00)00181-0 · Cited by 159 · see citing works

Amyloid-β immunisation for Alzheimer's disease

Wisniewski, T., & Konietzko, U. (2008) · The Lancet Neurology · doi:10.1016/s1474-4422(08)70170-4 · Cited by 155 · see citing works

A Synthetic Peptide Blocking the Apolipoprotein E/β-Amyloid Binding Mitigates β-Amyloid Toxicity and Fibril Formation in Vitro and Reduces β-Amyloid Plaques in Transgenic Mice

Sadowski, M., Pankiewicz, J., Scholtzova, H., Ripellino, J. A., Li, Y., Schmidt, S. D., Mathews, P. M., Fryer, J. D., Holtzman, D. M., Sigurdsson, E. M., et al. (2004) · The American Journal of Pathology · doi:10.1016/s0002-9440(10)63355-x · Cited by 154 · see citing works

Regional Distribution of Amyloid-Bri Deposition and Its Association with Neurofibrillary Degeneration in Familial British Dementia

Holton, J. L., Ghiso, J. A., Lashley, T., Rostagno, A. A., Guérin, C. J., Gibb, G., Houlden, H., Ayling, H., Martinian, L., Anderton, B. H., et al. (2001) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)63993-4 · Cited by 131 · see citing works

Microglial cells are the driving force in fibrillar plaque formation, whereas astrocytes are a leading factor in plaque degradation

Wegiel, J., Wang, K. C., Tarnawski, M., & Lach, B. (2000) · Acta Neuropathologica · doi:10.1007/s004010000199 · Cited by 124 · see citing works

Amyloid-β Deposition Is Associated with Decreased Hippocampal Glucose Metabolism and Spatial Memory Impairment in APP/PS1 Mice

Sadowski, M., Pankiewicz, J. E., Scholtzova, H., Ji, Y., Quartermain, D., Jensen, C. H., Duff, K., Nixon, R. A., Gruen, R. J., & Wısnıewskı, T. (2004) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/63.5.418 · Cited by 108 · see citing works

Thal Amyloid Stages Do Not Significantly Impact the Correlation Between Neuropathological Change and Cognition in the Alzheimer Disease Continuum

Serrano‐Pozo, A., Qian, J., Muzikansky, A., Monsell, S. E., Montine, T. J., Frosch, M. P., Betensky, R. A., & Hyman, B. T. (2016) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlw026 · Cited by 105 · see citing works

Spreading of amyloid, tau, and microvascular pathology in Alzheimer’s disease: Findings from neuropathological and neuroimaging studies.

Thal, D. R., Attems, J., & Ewers, M. (2014) · Journal of Alzheimer s Disease · doi:10.3233/jad-141461 · Cited by 100 · see citing works

Links Between the Pathology of Alzheimer's Disease and Vascular Dementia

Sadowski, M., Pankiewicz, J., Scholtzova, H., Li, Y.-S., Quartermain, D., Duff, K., & Wisniewski, T. (2004) · Neurochemical Research · doi:10.1023/b:nere.0000023612.66691.e6 · Cited by 109 · see citing works

Blocking the Interaction between Apolipoprotein E and Aβ Reduces Intraneuronal Accumulation of Aβ and Inhibits Synaptic Degeneration

Kuszczyk, M. A., Sanchez, S., Pankiewicz, J., Kim, J., Duszczyk, M., Guridi, M., Asuni, A. A., Sullivan, P. M., Holtzman, D. M., & Sadowski, M. J. (2013) · The American Journal of Pathology · doi:10.1016/j.ajpath.2013.01.034 · Cited by 89 · see citing works

Dense‐core and diffuse Aβ plaques in TgCRND8 mice studied with synchrotron FTIR microspectroscopy

Rak, M., Bigio, M. R. D., Mai, S., Westaway, D. A., & Gough, K. M. (2007) · Biopolymers · doi:10.1002/bip.20820 · Cited by 85 · see citing works

Aβ plaques

Walker, L. C. (2020) · Free Neuropathology · doi:10.17879/freeneuropathology-2020-3025 · Cited by 95 · see citing works

Evidence of intraneuronal Aβ accumulation preceding tau pathology in the entorhinal cortex

Welikovitch, L. A., Carmo, S. D., Maglóczky, Z., Szocsics, P., Lőke, J., Freund, T. F., & Cuello, A. C. (2018) · Acta Neuropathologica · doi:10.1007/s00401-018-1922-z · Cited by 80 · see citing works

Ageing and dementia

Lowe, J. S., Mirra, S. S., Hyman, B. T., & Dickson, D. W. (2008) · CRC Press eBooks · doi:10.1201/b13319-15 · Cited by 68 · see citing works

Abnormal Intracellular Accumulation and Extracellular Aβ Deposition in Idiopathic and Dup15q11.2-q13 Autism Spectrum Disorders

Węgiel, J., Frackowiak, J., Mazur‐Kolecka, B., Schanen, N. C., Cook, E. H., Sigman, M., Brown, W. T., Kuchna, I., Wegiel, J., Nowicki, K., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0035414 · Cited by 64 · see citing works

Neuritic Plaques — Gateways to Understanding Alzheimer’s Disease

Tsering, W., & Prokop, S. (2024) · Molecular Neurobiology · doi:10.1007/s12035-023-03736-7 · Cited by 59 · see citing works

Chronic 5-HT4 receptor activation decreases Aβ production and deposition in hAPP/PS1 mice.

Tesseur, I., Pimenova, A. A., Lo, A. C., Ciesielska, M., Lichtenthaler, S., Maeyer, J. D. D., Schuurkes, J., D'Hooge, R., & de Strooper, B. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2013.01.020 · Cited by 53 · see citing works

Blocking the apoE/Aβ interaction ameliorates Aβ-related pathology in APOE ε2 and ε4 targeted replacement Alzheimer model mice

Pankiewicz, J. E., Guridi, M., Kim, J., Asuni, A. A., Sanchez, S., Sullivan, P. M., Holtzman, D. M., & Sadowski, M. J. (2014) · Acta Neuropathologica Communications · doi:10.1186/s40478-014-0075-0 · Cited by 57 · see citing works

Immunological and Anti-Chaperone Therapeutic Approaches for Alzheimer Disease

Wısnıewskı, T., & Frangione, B. (2006) · Brain Pathology · doi:10.1111/j.1750-3639.2005.tb00102.x · Cited by 54 · see citing works

Automated Segmentation of Hippocampal Subfields in Drug-Naïve Patients with Alzheimer Disease

Lim, H. K., Hong, S. C., Jung, W. S., Ahn, K. J., Won, W. Y., Hahn, C., Kim, I. S., & Lee, C. U. (2013) · American Journal of Neuroradiology · doi:10.3174/ajnr.a3293 · Cited by 52 · see citing works

Clinico-Pathological Correlations of the Most Common Neurodegenerative Dementias

Taipa, R. J. F., Pinho, J., & Pires, M. M. (2012) · Frontiers in Neurology · doi:10.3389/fneur.2012.00068 · Cited by 50 · see citing works

Apolipoprotein E co-localizes with newly formed amyloid β-protein (Aβ) deposits lacking immunoreactivity against N-terminal epitopes of Aβ in a genotype-dependent manner

Thal, D. R., Capetillo-Zarate, E., Schultz, C., Rüb, U., Saido, T. C., Yamaguchi, H., Haass, C., Griffin, W. S. T., Del Tredici, K., Braak, H., et al. (2005) · Acta Neuropathologica · doi:10.1007/s00401-005-1053-1 · Cited by 50 · see citing works

Peroxiredoxin 6 mediates protective function of astrocytes in Aβ proteostasis

Pankiewicz, J. E., Diaz, J. R., Martá-Ariza, M., Lizińczyk, A. M., Franco, L. A., & Sadowski, M. J. (2020) · Molecular Neurodegeneration · doi:10.1186/s13024-020-00401-8 · Cited by 45 · see citing works

Alzheimer's disease neuropathology and its estimation with fluid and imaging biomarkers

Thal, D. R., Poesen, K., Vandenberghe, R. R., & Meyer, S. D. (2025) · Molecular Neurodegeneration · doi:10.1186/s13024-025-00819-y · Cited by 47 · see citing works

Preventing β-amyloid fibrillization and deposition: β-sheet breakers and pathological chaperone inhibitors

Wısnıewskı, T., & Sadowski, M. J. (2008) · BMC Neuroscience · doi:10.1186/1471-2202-9-s2-s5 · Cited by 42 · see citing works

Therapeutic approaches for prion and Alzheimer's diseases

Wısnıewskı, T., & Sigurdsson, E. M. (2007) · FEBS Journal · doi:10.1111/j.1742-4658.2007.05919.x · Cited by 41 · see citing works

Synapses, Microglia, and Lipids in Alzheimer’s Disease

Paasila, P. J., Aramideh, J. A., Sutherland, G. T., & Graeber, M. B. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.778822 · Cited by 38 · see citing works

Hippocampal subfield volumes and pre-clinical Alzheimer’s disease in 408 cognitively normal adults born in 1946

Parker, T. D., Cash, D. M., Lane, C., Lu, K., Malone, I. B., Nicholas, J. M., James, S., Keshavan, A., Murray‐Smith, H., Wong, A., et al. (2019) · PLoS ONE · doi:10.1371/journal.pone.0224030 · Cited by 35 · see citing works

Developmental deficits and staging of dynamics of age associated Alzheimer’s disease neurodegeneration and neuronal loss in subjects with Down syndrome

Wegiel, J., Flory, M., Kuchna, I., Nowicki, K., Wegiel, J., Ma, S. Y., Zhong, N., Bobrowicz, T., de Leon, M. D., Lai, F., et al. (2022) · Acta Neuropathologica Communications · doi:10.1186/s40478-021-01300-9 · Cited by 27 · see citing works

Diffuse amyloid deposition, but not plaque number, is reduced in amyloid precursor protein/presenilin 1 double-transgenic mice by pathway lesions

Groen, T. V., Liu, L., Ikonen, S., & Kadish, I. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00215-x · Cited by 35 · see citing works

APOE Genotype Differentially Modulates Effects of Anti-Aβ, Passive Immunization in APP Transgenic Mice

Pankiewicz, J. E., Baquero-Buitrago, J., Sanchez, S., Lopez-Contreras, J., Kim, J., Sullivan, P. M., Holtzman, D. M., & Sadowski, M. J. (2017) · Molecular Neurodegeneration · doi:10.1186/s13024-017-0156-1 · Cited by 34 · see citing works

Neuropathology of Alzheimer's Disease and its Variants

Duyckaerts, C. J., & Dickson, D. W. (2011) · Wiley eBooks · doi:10.1002/9781444341256.ch10 · Cited by 34 · see citing works

Postmortale Diagnosestellung bei Morbus Alzheimer

Thal, D. R., & Braak, H. (2004) · Der Pathologe · doi:10.1007/s00292-004-0695-4 · Cited by 32 · see citing works

Modulation of amyloid precursor protein expression reduces β‐amyloid deposition in a mouse model

Asuni, A. A., Guridi, M., Pankiewicz, J. E., Sanchez, S., & Sadowski, M. J. (2014) · Annals of Neurology · doi:10.1002/ana.24149 · Cited by 28 · see citing works

Region-Specific Expression of Tau, Amyloid-β Protein Precursor, and Synaptic Proteins at Physiological Condition or Under Endoplasmic Reticulum Stress in Rats

Li, L., Yang, S., Chu, J., Wang, L., Ning, L., Zhang, T., Jiang, Q., Tian, Q., & Wang, J. (2014) · Journal of Alzheimer s Disease · doi:10.3233/jad-140207 · Cited by 27 · see citing works

The presubiculum links incipient amyloid and tau pathology to memory function in older persons

Jacobs, H. I. L., Augustinack, J. C., Schultz, A. P., Hanseeuw, B. J., Locascio, J. J., Amariglio, R. E., Papp, K. V., Rentz, D. M., Sperling, R. A., & Johnson, K. A. (2020) · Neurology · doi:10.1212/wnl.0000000000009362 · Cited by 24 · see citing works

High-Affinity Rabbit Monoclonal Antibodies Specific for Amyloid Peptides Amyloid-β40 and Amyloid-β42

Miller, D. L., Potempska, A., Węgiel, J., & Mehta, P. D. (2011) · Journal of Alzheimer s Disease · doi:10.3233/jad-2010-101341 · Cited by 24 · see citing works

Neuronal loss and β-amyloid removal in the amygdala of people with Down syndrome☆

Węgiel, J., Wı́sniewski, H. M., Moryś, J., Tarnawski, M. J., Kuchna, I., Dziewíatkowski, J., Pirttilä, T., Krivimäki, T., Lehtimäki, T. J., & Lach, B. (1999) · Neurobiology of Aging · doi:10.1016/s0197-4580(99)00060-3 · Cited by 23 · see citing works

Presubiculum principal cells are preserved from degeneration in knock-in APP/TAU mouse models of Alzheimer’s disease

Islam, A., Saito, T., Saido, T., & Ali, A. B. (2023) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2022.03.001 · Cited by 17 · see citing works

Distinct binding of amyloid imaging ligands to unique amyloid‐β deposited in the presubiculum of Alzheimer's disease

Ji, B., Chen, C.-J., Bando, K., Ashino, H., Shiraishi, H., Sano, H., Kasahara, H., Minamizawa, T., YAMADA, K., Ono, M., et al. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13293 · Cited by 17 · see citing works

Differential Vulnerability of Hippocampal Subfields to Amyloid and Tau Deposition in the Lewy Body Diseases

Ye, R., Goodheart, A. E., Locascio, J. J., Peterec, E., Properzi, M. J., Thibault, E. G., Chuba, E., Johnson, K. A., Brickhouse, M. J., Touroutoglou, A., et al. (2024) · Neurology · doi:10.1212/wnl.0000000000209460 · Cited by 17 · see citing works

Anti-prion Protein Antibody 6D11 Restores Cellular Proteostasis of Prion Protein Through Disrupting Recycling Propagation of PrPSc and Targeting PrPSc for Lysosomal Degradation

Pankiewicz, J. E., Sanchez, S., Kirshenbaum, K., Kascsak, R. B., Kascsak, R. J., & Sadowski, M. J. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1208-4 · Cited by 15 · see citing works

Neuropathology and cholinesterase expression in the brains of octogenarians and older

Maxwell, S. P., Cash, M. K., & Darvesh, S. (2022) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2022.110065 · Cited by 15 · see citing works

The presubiculum is preserved from neurodegenerative changes in Alzheimer’s disease

Murray, C. E., Gami‐Patel, P., Gkanatsiou, E., Brinkmalm, G., Portelius, E., Wirths, O., Heywood, W., Blennow, K., Ghiso, J. A., Holton, J. L., et al. (2018) · Acta Neuropathologica Communications · doi:10.1186/s40478-018-0563-8 · Cited by 15 · see citing works

Unveiling the hippocampal subfield changes across the Alzheimer’s disease continuum: a systematic review of neuroimaging studies

Zilioli, A., Pancaldi, B., Baumeister, H., Busi, G., Misirocchi, F., Mutti, C., Florindo, I., Morelli, N., Mohanty, R., Berron, D., et al. (2024) · Brain Imaging and Behavior · doi:10.1007/s11682-024-00952-0 · Cited by 14 · see citing works

Vaccines for conformational disorders

Sadowski, M. J., & Wısnıewskı, T. (2004) · Expert Review of Vaccines · doi:10.1586/14760584.3.3.279 · Cited by 14 · see citing works

Hippocampal Subfields in Mild Cognitive Impairment: Associations with Objective and Informant-Report of Memory Function

O’Shea, D. M., Wit, L. D., Tanner, J. J., Kurasz, A. M., Amofa, P., Perez-Lao, A. R., Levy, S.-A. T., Chandler, M. J., & Smith, G. E. (2022) · Archives of Clinical Neuropsychology · doi:10.1093/arclin/acac018 · Cited by 10 · see citing works

The relevance of hippocampal subfield integrity and clock drawing test performance for the diagnosis of Alzheimer’s disease and mild cognitive impairment

Hirjak, D., Sambataro, F., Remmele, B., Kubera, K. M., Schröder, J., Seidl, U., Thomann, A., Maier-Hein, K. H., Wolf, R. C., & Thomann, P. A. (2017) · The World Journal of Biological Psychiatry · doi:10.1080/15622975.2017.1355474 · Cited by 10 · see citing works

Neuropathology of the temporal lobe

Boluda, S., Seilhean, D., & Bielle, F. (2022) · Handbook of clinical neurology · doi:10.1016/b978-0-12-823493-8.00027-4 · Cited by 8 · see citing works

Henryk M. Wisniewski and the amyloid theory of Alzheimer's disease

Masters, C. L., & Beyreuther, K. T. (2001) · Journal of Alzheimer s Disease · doi:10.3233/jad-2001-3112 · Cited by 5 · see citing works

Apolipoproteins in Different Amyloidoses

Sadowski, M., & Wısnıewskı, T. (2007) · Springer eBooks · doi:10.1007/0-387-25919-8_6 · Cited by 3 · see citing works

S14 TRANSGENIC MICE MODELS FOR ALZHEIMER??S DISEASE

LEUVEN, F. V. (2006) · Behavioural Pharmacology · doi:10.1097/00008877-200609000-00033 · Cited by 2 · see citing works

Clinicopathological Stratification of Idiopathic Autism and Autism with 15q11.2–q13 Duplications

Węgiel, J., Schanen, N. C., Cook, E. H., Brown, W. T., Kuchna, I., Nowicki, K., Wegiel, J., Imaki, H., Ma, S. Y., London, E., et al. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-391924-3.00025-9

Protein Folding: From Normal Cellular Function to Pathophysiology

Rasool, M., Malik, A., Manan, A., Sultana, M., Qazi, M. H., & Pushparaj, P. N. (2015) · Springer eBooks · doi:10.1007/978-81-322-2467-9_5

Postmortale Diagnosestellung bei Morbus Alzheimer: Stadiengliederungen der kennzeichnenden Hirnveränderungen

Thal, D. R., & Braak, H. (2005) · Der Pathologe

Machine Learning Classification of Alzheimer’s Disease Pathology Reveals Diffuse Amyloid as a Major Predictor of Cognitive Impairment in Human Hippocampal SubregionsPreprint

Stephen, T., Korobkova, L., Breningstall, B. M., Nguyen, K., Mehta, S., Pachicano, M., Jones, K. T., Hawes, D., Cabeen, R. P., & Bienkowski, M. S. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.31.543117

Novel Monoclonal Antibody Specific toward Amyloid-β Binds to a Unique Epitope within the N-Terminal Region

Paterno, G., Moore, B. D., Bell, B. M., Gorion, K.-M. M., Ran, Y., Prokop, S., Golde, T. E., & Giasson, B. I. (2024) · Antibodies · doi:10.3390/antib13030068

Additional file 1 of Developmental deficits and staging of dynamics of age associated Alzheimer’s disease neurodegeneration and neuronal loss in subjects with Down syndrome

Węgiel, J., Flory, M. J., Kuchna, I., Nowicki, K., Wegiel, J., Ma, S. Y., Zhong, N., Wierzba‐Bobrowicz, T., de Leon, M., Lai, F., et al. (2022) · Figshare · doi:10.6084/m9.figshare.17870374

Développement et évaluation d'agents de contraste pour détecter la maladie d'Alzheimer par IRM : coloration par le Gadolinium et nanocorps ciblant les protéines Aβ et Tau

Dudeffant, C. (2018) · theses.fr (ABES) · doi:10.70675/57ec64bez172dz4174za587z371d74f16bc6

Propagation axonale des pathologies Tau et Aβ dans la maladie d'Alzheimer : à la recherche de propagons dans le circuit subiculo-fornico-mamillaire

Thierry, M. (2020) · theses.fr (ABES) · doi:10.70675/d2f36d94zaa16z4617z94c6zabb1ad26f3fb

Occurrence of diffuse amyloid deposits in the presubicular parvopyramidal layer in Alzheimer's disease

Akiyama, H., Tago, H., Itagaki, S., & McGeer, P. L. (1990) · Acta Neuropathologica · doi:10.1007/bf00296114 · Cited by 31 · see citing works

The presubicular region in Alzheimer's disease: topography of amyloid deposits and neurofibrillary changes

Kalus, P., Braak, H., Braak, E., & Böhl, J. (1989) · Brain Research · doi:10.1016/0006-8993(89)90164-9 · Cited by 56 · see citing works

[P2–158]: IS THE PRESUBICULUM PROTECTED FROM NEURODEGENERATIVE CHANGES? A PATHOLOGICAL AND BIOCHEMICAL INVESTIGATION

Murray, C. E., Gami‐Patel, P., Gkanatsiou, E., Brinkmalm, G., Portelius, E., Blennow, K., Ghiso, J. A., Holton, J. L., Zetterberg, H., Révész, T., et al. (2017) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2017.06.809

The presubiculum is preserved from neurodegenerative changes in Alzheimer’s disease

Murray, C. E., Gami‐Patel, P., Gkanatsiou, E., Brinkmalm, G., Portelius, E., Wirths, O., Heywood, W., Blennow, K., Ghiso, J. A., Holton, J. L., et al. (2018) · Acta Neuropathologica Communications · doi:10.1186/s40478-018-0563-8 · Cited by 15 · see citing works

Distinct binding of amyloid imaging ligands to unique amyloid‐β deposited in the presubiculum of Alzheimer's disease

Ji, B., Chen, C.-J., Bando, K., Ashino, H., Shiraishi, H., Sano, H., Kasahara, H., Minamizawa, T., YAMADA, K., Ono, M., et al. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13293 · Cited by 17 · see citing works