Correlates of hippocampal neuron number in Alzheimer's disease and ischemic vascular dementia

A compendium of neuropsychological tests: administration, norms, and commentary

(1991) · Choice Reviews Online · doi:10.5860/choice.29-2400 · Cited by 6,117 · 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

Consensus guidelines for the clinical and pathologic diagnosis of dementia with Lewy bodies (DLB): Report of the consortium on DLB international workshop

McKeith, I. G., Galasko, D., Kosaka, K., Perry, E. K., Dickson, D. W., Hansen, L. A., Salmon, D. P., Lowe, J., Mirra, S. S., Byrne, E. J., et al. (1996) · Neurology · doi:10.1212/wnl.47.5.1113 · Cited by 3,960 · see citing works

Consortium to Establish a Registry for Alzheimer's Disease (CERAD)

Fillenbaum, G., & Heyman, A. (2002) · doi:10.1002/0470846410.ch42(iii · Cited by 2,859 · see citing works

Differences in the pattern of hippocampal neuronal loss in normal ageing and Alzheimer's disease

West, M. J., Coleman, P. D., Flood, D. G., & Troncoso, J. C. (1994) · The Lancet · doi:10.1016/s0140-6736(94)92338-8 · Cited by 1,267 · see citing works

Unbiased stereological estimation of the number of neurons in the human hippocampus

West, M. J., & Gundersen, H. J. G. (1990) · Journal of Comparative Neurology · doi:10.1002/cne.902960102 · Cited by 1,153 · cited 1× · see citing works

New stereological methods for counting neurons

West, M. J. (1993) · Neurobiology of Aging · doi:10.1016/0197-4580(93)90112-o · Cited by 940 · see citing works

Staging of Alzheimer-Related Cortical Destruction

Braak, H., Braak, E., & Bohl, J. (2008) · European Neurology · doi:10.1159/000116984 · Cited by 836 · see citing works

Cerebral amyloid angiopathy without and with cerebral hemorrhages: A comparative histological study

Vonsattel, J. P. G., Myers, R. H., Tessa Hedley‐Whyte, E., Ropper, A. H., Bird, E. D., & Richardson, E. P. (1991) · Annals of Neurology · doi:10.1002/ana.410300503 · Cited by 662 · see citing works

Memory and MRI-based hippocampal volumes in aging and AD

Petersen, R. C., Jack, C. R., Xu, Y.-C., Waring, S. C., O’Brien, P. C., Smith, G. E., Ivnik, R. J., Tangalos, E. G., Boeve, B. F., & Kokmen, E. (2000) · Neurology · doi:10.1212/wnl.54.3.581 · Cited by 426 · see citing works

Neuropathologic Substrates of Ischemic Vascular Dementia

Vinters, H. V., Ellis, W. G., Zarow, C., Zaias, B. W., Jagust, W. J., Mack, W. J., & Chui, H. C. (2000) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/59.11.931 · Cited by 304 · see citing works

Hippocampal sclerosis: a common pathological feature of dementia in very old (?80 years of age) humans

Dickson, D. W., Davies, P., Bevona, C., van Hoeven, K. H., Factor, S. M., Grober, E. H., Aronson, M. K., & Crystal, H. (1994) · Acta Neuropathologica · doi:10.1007/bf00293396 · Cited by 293 · see citing works

Comparison of automated and manual MRI volumetry of hippocampus in normal aging and dementia

Hsu, Y., Schuff, N. W., Du, A., Mark, K. E., Zhu, X., Hardin, D., & Weiner, M. W. (2002) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.10163 · Cited by 212 · see citing works

Pathological markers associated with normal aging and dementia in the elderly

Crystal, H. A., Dickson, D. W., Sliwinski, M. J., Lipton, R. B., Grober, E., Marks‐Nelson, H., & Antis, P. (1993) · Annals of Neurology · doi:10.1002/ana.410340410 · Cited by 161 · see citing works

Patients with vascular dementia due to microvascular pathology have significant hippocampal neuronal loss

Kril, J. J. (2002) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.72.6.747 · Cited by 144 · see citing works

Clinical and Neuropathological Characteristics of Hippocampal Sclerosis

Leverenz, J. B., Agustin, C. M., Tsuang, D. W., Peskind, E. R., Edland, S. D., Nochlin, D., DiGiacomo, L., Bowen, J. D., McCormick, W. C., Teri, L. L., et al. (2002) · Archives of Neurology · doi:10.1001/archneur.59.7.1099 · Cited by 144 · see citing works

Variation in hippocampal neuron number with age and brain volume

Harding, A. (1998) · Cerebral Cortex · doi:10.1093/cercor/8.8.710 · Cited by 120 · see citing works

Hippocampal Sclerosis Contributes to Dementia in the Elderly

Corey‐Bloom, J., Sabbagh, M. N., Bondi, M. W., Hansen, L., Alford, M. F., Masliah, E., & Thal, L. J. (1997) · Neurology · doi:10.1212/wnl.48.1.154 · Cited by 110 · see citing works

Psychometrically matched measures of global cognition, memory, and executive function for assesment of cognitive decline in older persons.

Mungas, D., Reed, B., & Kramer, J. H. (2003) · Neuropsychology · doi:10.1037/0894-4105.17.3.380 · Cited by 108 · see citing works

Structural Magnetic Resonance Imaging in Established and Prodromal Alzheimer Disease: A Review

Atiya, M., Hyman, B. T., Albert, M., & Killiany, R. (2003) · Alzheimer Disease & Associated Disorders · doi:10.1097/00002093-200307000-00010 · Cited by 96 · see citing works

Hippocampal size and memory function in the ninth and tenth decades of life: the Sydney Older Persons Study

Lye, T. C. (2004) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2003.010223 · Cited by 60 · see citing works

Different patterns of N-acetylaspartate loss in subcortical ischemic vascular dementia and AD

Schuff, N. W., Capizzano, A. A., Du, A., Amend, D. L., O’Neill, J., Norman, D. M., Jagust, W. J., Chui, H. C., Kramer, J. H., Reed, B. R., et al. (2003) · Neurology · doi:10.1212/01.wnl.0000078942.63360.22 · Cited by 60 · see citing works

No evidence for loss of hippocampal neurons in non-Alzheimer dementia patients

Korbo, L., Amrein, I., Lipp, H., Wolfer, D. P., Regeur, L., OSTER, S., & Pakkenberg, B. (2003) · Acta Neurologica Scandinavica · doi:10.1034/j.1600-0404.2003.00182.x · Cited by 41 · see citing works

A standardized method for brain-cutting suitable for both stereology and MRI-brain co-registration

Zarow, C., Kim, T.-S., Singh, M., & Chui, H. C. (2004) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2004.04.034 · Cited by 26 · see citing works

Volume and number of neurons of the human hippocampal formation in normal aging and Alzheimer’s disease

?imi?, G., Kostovi?, I., Winblad, B., & Bogdanovi?, N. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970324)379:4

NIA‐AA Research Framework: Toward a biological definition of Alzheimer's disease

Jack, C. R., Bennett, D. A., Blennow, K., Carrillo, M. C., Dunn, B., Haeberlein, S. B., Holtzman, D. M., Jagust, W., Jessen, F., Karlawish, J., et al. (2018) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2018.02.018 · Cited by 10,537 · see citing works

Tracking pathophysiological processes in Alzheimer's disease: an updated hypothetical model of dynamic biomarkers

Jack, C. R., Knopman, D. S., Jagust, W. J., Petersen, R. C., Weiner, M. W., Aisen, P. S., Shaw, L. M., Vemuri, P., Wiste, H. J., Weigand, S. D., et al. (2013) · The Lancet Neurology · doi:10.1016/s1474-4422(12)70291-0 · Cited by 4,396 · see citing works

Revised criteria for diagnosis and staging of Alzheimer's disease: Alzheimer's Association Workgroup

Jack, C. R., Andrews, J. S., Beach, T. G., Buracchio, T., Dunn, B., Graf, A., Hansson, O., Ho, C., Jagust, W., McDade, E., et al. (2024) · Alzheimer's & Dementia · doi:10.1002/alz.13859 · Cited by 2,803 · see citing works

National Institute of Neurological Disorders and Stroke–Canadian Stroke Network Vascular Cognitive Impairment Harmonization Standards

Hachinski, V., Iadecola, C., Petersen, R. C., Breteler, M. M., Nyenhuis, D. L., Black, S. E., Powers, W. J., DeCarli, C., Merino, J. G., Kalaria, R. N., et al. (2006) · Stroke · doi:10.1161/01.str.0000237236.88823.47 · Cited by 1,722 · see citing works

Limbic-predominant age-related TDP-43 encephalopathy (LATE): consensus working group report

Nelson, P. T., Dickson, D. W., Trojanowski, J. Q., Jack, C. R., Boyle, P. A., Arfanakis, K., Rademakers, R., Alafuzoff, I., Attems, J., Brayne, C., et al. (2019) · Brain · doi:10.1093/brain/awz099 · Cited by 1,547 · see citing works

Alzheimer’s Disease Neuroimaging Initiative

Mueller, S. G., Weiner, M. W., Thal, L. J., Petersen, R. C., Jack, C. R., Jagust, W. J., Trojanowski, J. Q., Toga, A. W., & Beckett, L. A. (2007) · Springer eBooks · doi:10.1007/978-0-387-72076-0_18 · Cited by 1,493 · see citing works

Serial PIB and MRI in normal, mild cognitive impairment and Alzheimer's disease: implications for sequence of pathological events in Alzheimer's disease

Jack, C. R., Lowe, V. J., Weigand, S. D., Wiste, H. J., Senjem, M. L., Knopman, D. S., Shiung, M. M., Gunter, J. L., Boeve, B. F., Kemp, B. J., et al. (2009) · Brain · doi:10.1093/brain/awp062 · Cited by 1,099 · 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

11C PiB and structural MRI provide complementary information in imaging of Alzheimer's disease and amnestic mild cognitive impairment

Jack, C. R., Lowe, V. J., Senjem, M. L., Weigand, S. D., Kemp, B. J., Shiung, M. M., Knopman, D. S., Boeve, B. F., Klunk, W. E., Mathis, C. A., et al. (2008) · Brain · doi:10.1093/brain/awm336 · Cited by 958 · see citing works

Hippocampal volume and asymmetry in mild cognitive impairment and Alzheimer's disease: meta-analyses of MRI studies

Shi, F., Liu, B., Zhou, Y., Yu, C., & Jiang, T. (2009) · Hippocampus · doi:10.1002/hipo.20573 · Cited by 470 · see citing works

Neuropathological diagnosis of vascular cognitive impairment and vascular dementia with implications for Alzheimer’s disease

Kalaria, R. N. (2016) · Acta Neuropathologica · doi:10.1007/s00401-016-1571-z · Cited by 441 · see citing works

Particulate air pollutants, APOE alleles and their contributions to cognitive impairment in older women and to amyloidogenesis in experimental models

Cacciottolo, M., Wang, X., Driscoll, I. F., Woodward, N., Saffari, A., Reyes, J. M., Serre, M. L., Vizuete, W., Sioutas, C., Morgan, T. E., et al. (2017) · Translational Psychiatry · doi:10.1038/tp.2016.280 · Cited by 433 · see citing works

MRI and CSF biomarkers in normal, MCI, and AD subjects

Vemuri, P., Wiste, H. J., Weigand, S. D., Shaw, L. M. J., Trojanowski, J. Q., Weiner, M. W., Knopman, D. S., Petersen, R. C., & Jack, C. R. (2009) · Neurology · doi:10.1212/wnl.0b013e3181af79fb · Cited by 398 · see citing works

Medial temporal lobe atrophy on MRI differentiates Alzheimer's disease from dementia with Lewy bodies and vascular cognitive impairment: a prospective study with pathological verification of diagnosis

Burton, E. J., Barber, R., Mukaetova‐Ladinska, E. B., Robson, J., Perry, R. H., Jaros, E., Kalaria, R. N., & O'Brien, J. T. (2008) · Brain · doi:10.1093/brain/awn298 · Cited by 373 · see citing works

Hippocampal atrophy patterns in mild cognitive impairment and Alzheimer's disease

Mueller, S. G., Schuff, N., Yaffe, K., Madison, C., Miller, B., & Weiner, M. W. (2010) · Human Brain Mapping · doi:10.1002/hbm.20934 · Cited by 361 · see citing works

Brain neural synchronization and functional coupling in Alzheimer's disease as revealed by resting state EEG rhythms

Babiloni, C., Lizio, R., Marzano, N., Capotosto, P., Soricelli, A., Triggiani, A. I., Cordone, S., Gesualdo, L., & Percio, C. D. (2015) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2015.02.008 · Cited by 365 · see citing works

Pathology and pathogenesis of vascular cognitive impairment—a critical update

Jellinger, K. A. (2013) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2013.00017 · Cited by 353 · see citing works

Modifiable factors that alter the size of the hippocampus with ageing

Fotuhi, M., Do, D., & Jack, C. R. (2012) · Nature Reviews Neurology · doi:10.1038/nrneurol.2012.27 · Cited by 350 · see citing works

Measuring cognitive reserve based on the decomposition of episodic memory variance

Reed, B. R., Mungas, D., Farias, S. T., Harvey, D., Beckett, L., Widaman, K., Hinton, L., & DeCarli, C. (2010) · Brain · doi:10.1093/brain/awq154 · Cited by 271 · see citing works

Neuropathological evaluation of mixed dementia

Jellinger, K. A., & Attems, J. (2007) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2007.01.045 · Cited by 273 · see citing works

Rates of hippocampal atrophy and presence of post-mortem TDP-43 in patients with Alzheimer’s disease: A longitudinal retrospective study

Josephs, K. A., Dickson, D. W., Tosakulwong, N., Weigand, S. D., Murray, M. E., Petrucelli, L., Liesinger, A. M., Senjem, M. L., Spychalla, A. J., Knopman, D. S., et al. (2017) · The Lancet Neurology · doi:10.1016/s1474-4422(17)30284-3 · Cited by 252 · see citing works

Selective effect of age, Apo e4, and Alzheimer's disease on hippocampal subfields

Mueller, S. G., & Weiner, M. W. (2009) · Hippocampus · doi:10.1002/hipo.20614 · Cited by 248 · see citing works

Pyroptosis in Alzheimer’s disease: cell type-specific activation in microglia, astrocytes and neurons

Moonen, S., Koper, M. J., Schoor, E. V., Schaeverbeke, J. M., Vandenberghe, R. R., Arnim, C. A. F. V., Tousseyn, T., Strooper, B. D., & Thal, D. R. (2022) · Acta Neuropathologica · doi:10.1007/s00401-022-02528-y · Cited by 257 · see citing works

MRI and CSF biomarkers in normal, MCI, and AD subjects

Vemuri, P., Wiste, H. J., Weigand, S. D., Shaw, L. M. J., Trojanowski, J. Q., Weiner, M. W., Knopman, D. S., Petersen, R. C., & Jack, C. R. (2009) · Neurology · doi:10.1212/wnl.0b013e3181af79e5 · Cited by 246 · see citing works

Emerging Concepts in Alzheimer's Disease

Vinters, H. V. (2014) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathol-020712-163927 · Cited by 232 · see citing works

Cerebrovascular Disease and Mechanisms of Cognitive Impairment

Kalaria, R. N. (2012) · Stroke · doi:10.1161/strokeaha.112.655803 · Cited by 225 · see citing works

The enigma of vascular cognitive disorder and vascular dementia

Jellinger, K. A. (2007) · Acta Neuropathologica · doi:10.1007/s00401-006-0185-2 · Cited by 221 · see citing works

Steps to standardization and validation of hippocampal volumetry as a biomarker in clinical trials and diagnostic criterion for Alzheimer's disease

Jack, C. R., Barkhof, F., Bernstein, M. A., Cantillon, M., Cole, P. E., DeCarli, C. S., Dubois, B., Duchesne, S., Fox, N. C., Frisoni, G. B., et al. (2011) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2011.04.007 · Cited by 219 · see citing works

Diagnostic and Prognostic Utility of the Synaptic Marker Neurogranin in Alzheimer Disease

Tarawneh, R. M., D’Angelo, G., Crimmins, D. L., Herries, E. M., Griest, T. A., Fagan, A. M., Zipfel, G. J., Ladenson, J. H., Morris, J. C., & Holtzman, D. M. (2016) · JAMA Neurology · doi:10.1001/jamaneurol.2016.0086 · Cited by 219 · see citing works

Effect of apolipoprotein E on biomarkers of amyloid load and neuronal pathology in Alzheimer disease

Vemuri, P., Wiste, H. J., Weigand, S. D., Knopman, D. S., Shaw, L. M., Trojanowski, J. Q., Aisen, P. S., Weiner, M., Petersen, R. C., Jack, C. R., et al. (2010) · Annals of Neurology · doi:10.1002/ana.21953 · Cited by 195 · see citing works

Hippocampal sclerosis of aging, a prevalent and high-morbidity brain disease

Nelson, P. T., Smith, C. D., Abner, E. L., Wilfred, B. R., Wang, W., Neltner, J. H., Baker, M., Fardo, D. W., Kryscio, R. J., Scheff, S. W., et al. (2013) · Acta Neuropathologica · doi:10.1007/s00401-013-1154-1 · Cited by 196 · see citing works

Relevance of Magnetic Resonance Imaging for Early Detection and Diagnosis of Alzheimer Disease

Teipel, S. J., Grothe, M. J., Lista, S., Toschi, N., Garaci, F., & Hampel, H. J. (2013) · Medical Clinics of North America · doi:10.1016/j.mcna.2012.12.013 · Cited by 192 · see citing works

The Amnestic Syndrome of Hippocampal type in Alzheimer's Disease: An MRI Study

Sarazin, M., Chauviré, V., Gérardin, E., Colliot, O., Kinkingnéhun, S., de Souza, L. C., Hugonot-Diener, L., Garnero, L., Lehéricy, S., Marie Chupin, A., et al. (2010) · Journal of Alzheimer s Disease · doi:10.3233/jad-2010-091150 · Cited by 184 · see citing works

Upregulation of neuronal PGC-1α ameliorates cognitive impairment induced by chronic cerebral hypoperfusion

Han, B., Jiang, W., Liu, H., Wang, J., Zheng, K., Cui, P., Feng, Y., Dang, C., Bu, Y., Wang, Q. M., et al. (2020) · Theranostics · doi:10.7150/thno.37119 · Cited by 178 · see citing works

Multimodality imaging characteristics of dementia with Lewy bodies

Kantarci, K., Lowe, V. J., Boeve, B. F., Weigand, S. D., Senjem, M. L., Przybelski, S. A., Dickson, D. W., Parisi, J. E., Knopman, D. S., Smith, G. E., et al. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.09.024 · Cited by 175 · see citing works

LATE-NC staging in routine neuropathologic diagnosis: an update

Nelson, P. T., Lee, E. B., Cykowski, M. D., Alafuzoff, I. I., Arfanakis, K., Attems, J., Brayne, C., Corrada, M. M., Dugger, B. N., Flanagan, M. E., et al. (2022) · Acta Neuropathologica · doi:10.1007/s00401-022-02524-2 · Cited by 175 · 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

Necrosome complex detected in granulovacuolar degeneration is associated with neuronal loss in Alzheimer’s disease

Koper, M. J., Schoor, E. V., Ospitalieri, S., Vandenberghe, R. R., Vandenbulcke, M., Arnim, C. A. F. V., Tousseyn, T., Balusu, S., Strooper, B. D., & Thal, D. R. (2019) · Acta Neuropathologica · doi:10.1007/s00401-019-02103-y · Cited by 164 · see citing works

Hippocampal Neuronal Atrophy and Cognitive Function in Delayed Poststroke and Aging-Related Dementias

Gemmell, E., Bosomworth, H. J., Allan, L. M., Hall, R., Khundakar, A. A., Oakley, A. E., Deramecourt, V., Polvikoski, T. M., O'Brien, J. T., & Kalaria, R. N. (2011) · Stroke · doi:10.1161/strokeaha.111.636498 · Cited by 165 · see citing works

TDP-43 in aging and Alzheimer's disease - a review.

Wilson, A. C., Dugger, B. N., Dickson, D. W., & Wang, D.-S. (2011) · PubMed Central · Cited by 165 · see citing works

Subcortical vascular dementia

Tomimoto, H. (2011) · Neuroscience Research · doi:10.1016/j.neures.2011.07.1820 · Cited by 161 · see citing works

Morphologic diagnosis of “vascular dementia” — A critical update

Jellinger, K. A. (2008) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2008.03.006 · Cited by 150 · see citing works

Independent contribution of temporal β-amyloid deposition to memory decline in the pre-dementia phase of Alzheimer’s disease

Chételat, G., Villemagne, V. L., Pike, K. E., Ellis, K. A., Bourgeat, P., Jones, G. R., O'Keefe, G. J., Salvado, O., Szoeke, C. E. I., Martins, R. N., et al. (2011) · Brain · doi:10.1093/brain/awq383 · Cited by 153 · see citing works

Age-related changes in the central auditory system

Ouda, L., Profant, O., & Syka, J. (2015) · Cell and Tissue Research · doi:10.1007/s00441-014-2107-2 · Cited by 146 · see citing works

The dynamics of Alzheimer's disease biomarkers in the Alzheimer's Disease Neuroimaging Initiative cohort

Caroli, A., & Frisoni, G. B. (2010) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2010.04.024 · Cited by 146 · see citing works

Three-dimensional surface mapping of hippocampal atrophy progression from MCI to AD and over normal aging as assessed using voxel-based morphometry

Chételat, G., Fouquet, M., Kalpouzos, G., Denghien, I., De la Sayette, V., Viader, F., Mézenge, F., Landeau, B., Baron, J. C., Eustache, F., et al. (2008) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2007.11.037 · Cited by 143 · see citing works

Why looking at the whole hippocampus is not enough—a critical role for anteroposterior axis, subfield and activation analyses to enhance predictive value of hippocampal changes for Alzheimer’s disease diagnosis

Maruszak, A., & Thuret, S. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00095 · Cited by 140 · see citing works

Perspective on future role of biological markers in clinical therapy trials of Alzheimer's disease: A long-range point of view beyond 2020

Hampel, H. J., Lista, S., Teipel, S. J., Garaci, F., Nisticò, R., Blennow, K., Zetterberg, H., Bertram, L., Duyckaerts, C. J., Bakardjian, H., et al. (2013) · Biochemical Pharmacology · doi:10.1016/j.bcp.2013.11.009 · Cited by 141 · see citing works

The enigma of mixed dementia

Jellinger, K. A. (2007) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2006.09.002 · Cited by 139 · see citing works

3D PIB and CSF biomarker associations with hippocampal atrophy in ADNI subjects

Apostolova, L. G., Hwang, K., Andrawis, J. P., Green, A. E., Babakchanian, S., Morra, J. H., Cummings, J. L., Toga, A. W., Trojanowski, J. Q., Shaw, L. M. J., et al. (2010) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2010.05.003 · Cited by 137 · see citing works

Ligustrazine suppresses neuron apoptosis via the Bax/Bcl‐2 and caspase‐3 pathway in PC12 cells and in rats with vascular dementia

Zhao, T., Fu, Y., Sun, H., & Liu, X. (2017) · IUBMB Life · doi:10.1002/iub.1704 · Cited by 131 · see citing works

Update on Vascular Dementia

Khan, A., Kalaria, R. N., Corbett, A., & Ballard, C. G. (2016) · Journal of Geriatric Psychiatry and Neurology · doi:10.1177/0891988716654987 · Cited by 125 · see citing works

Blockage of GSK3β-mediated Drp1 phosphorylation provides neuroprotection in neuronal and mouse models of Alzheimer's disease

Yan, J., Liu, X.-H., Han, M., Wang, Y., Sun, X., Yu, N., Li, T., Su, B., & Chen, Z.-Y. (2014) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2014.08.005 · Cited by 123 · see citing works

A blueberry-enriched diet provides cellular protection against oxidative stress and reduces a kainate-induced learning impairment in rats

Duffy, K. B., Spangler, E. L., Devan, B. D., Guo, Z., Bowker, J. L., Janas, A. M., Hagepanos, A., Minor, R. K., de Cabo, R., Mouton, P. R., et al. (2007) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.04.002 · Cited by 124 · see citing works

The Seed Extract of Cassia obtusifolia Ameliorates Learning and Memory Impairments Induced by Scopolamine or Transient Cerebral Hypoperfusion in Mice

Kim, D. H., Yoon, B. H., Kim, Y.-W., Lee, S.-J., Shin, B. Y., Jung, J. W., Kim, H. J., Lee, Y. S., Choi, J. S., Kim, S. Y., et al. (2007) · Journal of Pharmacological Sciences · doi:10.1254/jphs.fp0061565 · Cited by 120 · see citing works

Serial MRI and CSF biomarkers in normal aging, MCI, and AD

Vemuri, P., Wiste, H. J., Weigand, S. D., Knopman, D. S., Trojanowski, J. Q., Shaw, L. M., Bernstein, M. A., Aisen, P. S., Weiner, M., Petersen, R. C., et al. (2010) · Neurology · doi:10.1212/wnl.0b013e3181e7ca82 · Cited by 154 · see citing works

Hippocampal shape analysis in Alzheimer’s disease: A population-based study

Scher, I., Xu, Y., Korf, E. S. C., White, L. R., Scheltens, P., Toga, A. W., Thompson, P. M., Hartley, S. W., Witter, M. P., Valentino, D. J., et al. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2006.12.036 · Cited by 116 · see citing works

Antemortem differential diagnosis of dementia pathology using structural MRI: Differential-STAND

Vemuri, P., Simon, G., Kantarci, K., Whitwell, J. L., Senjem, M. L., Przybelski, S. A., Gunter, J. L., Josephs, K. A., Knopman, D. S., Boeve, B. F., et al. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.12.073 · Cited by 108 · see citing works

Relationship of medial temporal lobe atrophy, APOE genotype, and cognitive reserve in preclinical A lzheimer's disease

Soldan, A., Pettigrew, C. A., Lu, Y., Wang, M., Selnes, O. A., Albert, M., Brown, T., Ratnanather, J. T., Laurent Younes, B., & Miller, M. I. (2015) · Human Brain Mapping · doi:10.1002/hbm.22810 · Cited by 110 · see citing works

Modeling the Role of the Glymphatic Pathway and Cerebral Blood Vessel Properties in Alzheimer’s Disease Pathogenesis

Kyrtsos, C. R., & Baras, J. S. (2015) · PLoS ONE · doi:10.1371/journal.pone.0139574 · Cited by 106 · see citing works

Understanding hippocampal sclerosis in the elderly: Epidemiology, characterization, and diagnostic issues

Zarow, C., Sitzer, T. E., & Chui, H. C. (2008) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-008-0057-3 · Cited by 104 · see citing works

GABA and glutamate deficits from frontotemporal lobar degeneration are associated with disinhibition

Murley, A. G., Rouse, M. A., Jones, P. S., Ye, R., Hezemans, F. H., O’Callaghan, C., Frangou, P., Kourtzi, Z., Rua, C., Carpenter, T. A., et al. (2020) · Brain · doi:10.1093/brain/awaa305 · Cited by 101 · see citing works

Hippocampal sclerosis dementia differs from hippocampal sclerosis in frontal lobe degeneration

Amador, C., Ahmed, Z., Zehr, C., & Dickson, D. W. (2006) · Acta Neuropathologica · doi:10.1007/s00401-006-0183-4 · Cited by 100 · see citing works

Effects of acetylcholinesterase inhibitors and memantine on resting-state electroencephalographic rhythms in Alzheimer’s disease patients

Babiloni, C., Percio, C. D., Bordet, R., Bourriez, J., Bentivoglio, M., Payoux, P., Derambure, P., Dix, S. L., Infarinato, F., Lizio, R., et al. (2012) · Clinical Neurophysiology · doi:10.1016/j.clinph.2012.09.017 · Cited by 97 · see citing works

Cortical Sources of Resting State EEG Rhythms are Sensitive to the Progression of Early Stage Alzheimer's Disease

Babiloni, C., Lizio, R., Percio, C. D., Marzano, N., Soricelli, A., Salvatore, E., Ferri, R., Cosentino, F., Tedeschi, G., Montella, P., et al. (2013) · Journal of Alzheimer s Disease · doi:10.3233/jad-121750 · Cited by 99 · see citing works

Activated forms of astrocytes with higher GLT-1 expression are associated with cognitive normal subjects with Alzheimer pathology in human brain

Kobayashi, E., Nakano, M., Kubota, K., Himuro, N., Mizoguchi, S., Chikenji, T., Otani, M., Mizue, Y., Nagaishi, K., & Fujimiya, M. (2018) · Scientific Reports · doi:10.1038/s41598-018-19442-7 · Cited by 98 · see citing works

Cerebrospinal Fluid Markers of Neurodegeneration and Rates of Brain Atrophy in Early Alzheimer Disease

Tarawneh, R. M., Head, D. M., Allison, S. L., Buckles, V., Fagan, A. M., Ladenson, J. H., Morris, J. C., & Holtzman, D. M. (2015) · JAMA Neurology · doi:10.1001/jamaneurol.2015.0202 · Cited by 96 · see citing works

Tau and TDP-43 proteinopathies: kindred pathologic cascades and genetic pleiotropy

Chornenkyy, Y., Fardo, D. W., & Nelson, P. T. (2019) · Laboratory Investigation · doi:10.1038/s41374-019-0196-y · Cited by 93 · see citing works

Caspase-8 in inflammatory diseases: a potential therapeutic target

Zhang, W., Zhu, C., Liao, Y., Zhou, M., Xu, W., & Zou, Z. (2024) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-024-00646-x · Cited by 97 · see citing works

Review: Vascular dementia: clinicopathologic and genetic considerations

Vinters, H. V., Zarow, C., Borys, E., Whitman, J. D., Tung, S., Ellis, W. G., Zheng, L., & Chui, H. C. (2018) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12472 · Cited by 89 · see citing works

Hydrogen Sulfide Attenuates Neuronal Injury Induced by Vascular Dementia Via Inhibiting Apoptosis in Rats

Zhang, L., Jiang, C.-X., & Liu, D. (2009) · Neurochemical Research · doi:10.1007/s11064-009-0006-9 · Cited by 89 · see citing works

Hippocampal volume is an independent predictor of cognitive performance in CADASIL

O'Sullivan, M., Ngo, E., Viswanathan, A., Jouvent, E., Gschwendtner, A., Saemann, P. G., Duering, M., Pachai, C., Bousser, M.-G., Chabriat, H., et al. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.09.002 · Cited by 85 · see citing works

PART and SNAP

Jack, C. R. (2014) · Acta Neuropathologica · doi:10.1007/s00401-014-1362-3 · Cited by 88 · see citing works

Potential Therapeutics for Vascular Cognitive Impairment and Dementia

Sun, M. (2017) · Current Neuropharmacology · doi:10.2174/1570159x15666171016164734 · Cited by 87 · see citing works

Automated 3D mapping of baseline and 12-month associations between three verbal memory measures and hippocampal atrophy in 490 ADNI subjects

Apostolova, L. G., Morra, J. H., Green, A. E., Hwang, K., Avedissian, C., Woo, E., Cummings, J. L., Toga, A. W., Jack, C. R., Weiner, M. W., et al. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.12.125 · Cited by 85 · see citing works

Hippocampal Volumes, Proton Magnetic Resonance Spectroscopy Metabolites, and Cerebrovascular Disease in Mild Cognitive Impairment Subtypes

Kantarci, K., Petersen, R. C., Przybelski, S. A., Weigand, S. D., Shiung, M. M., Whitwell, J. L., Negash, S., Ivnik, R. J., Boeve, B. F., Knopman, D. S., et al. (2008) · Archives of Neurology · doi:10.1001/archneur.65.12.1621 · Cited by 85 · see citing works

Dementia and Cerebrovascular Disease

Knopman, D. S. (2006) · Mayo Clinic Proceedings · doi:10.4065/81.2.223 · Cited by 82 · see citing works

Relationship between hippocampal atrophy and neuropathology markers: A 7T MRI validation study of the EADC‐ADNI Harmonized Hippocampal Segmentation Protocol

Apostolova, L. G., Zarow, C., Biado, K., Hurtz, S., Boccardi, M., Somme, J. H., Honarpisheh, H., Blanken, A. E., Brook, J. K., Tung, S., et al. (2015) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2015.01.001 · Cited by 77 · see citing works

Epigenetic studies in Alzheimer's disease: Current findings, caveats, and considerations for future studies

Lunnon, K., & Mill, J. (2013) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics · doi:10.1002/ajmg.b.32201 · Cited by 78 · see citing works

Protein contributions to brain atrophy acceleration in Alzheimer’s disease and primary age-related tauopathy

Josephs, K. A., Martin, P. R., Weigand, S. D., Tosakulwong, N., Buciuc, M., Murray, M. E., Petrucelli, L., Senjem, M. L., Spychalla, A. J., Knopman, D. S., et al. (2020) · Brain · doi:10.1093/brain/awaa299 · Cited by 77 · see citing works

Blood pressure decrease correlates with tau pathology and memory decline in hypertensive elderly

Glodzik, L., Rusinek, H., Pirraglia, E., McHugh, P. F., Tsui, W., Williams, S., Cummings, M., Li, Y., Rich, K. E., Randall, C., et al. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2013.06.011 · Cited by 76 · see citing works

Volumetry of the human amygdala — An anatomical study

Brabec, J., Rulseh, A. M., Hoyt, B. S., Vízek, M., Hořínek, D., Hort, J., & Petrovický, P. (2010) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2009.11.005 · Cited by 77 · see citing works

Mild Cognitive Impairment after Lacunar Infarction: Voxel-Based Morphometry and Neuropsychological Assessment

Grau-Olivares, M., David Bartrés-faz, A., Arboix, A., Soliva, J.-C., Rovira, M., Targa, C., & Junqué, C. (2007) · Cerebrovascular Diseases · doi:10.1159/000099134 · Cited by 77 · see citing works

Comparing 3T and 1.5T MRI for Mapping Hippocampal Atrophy in the Alzheimer's Disease Neuroimaging Initiative

Chow, N., Hwang, K. S., Hurtz, S., Green, A. E., Somme, J. H., Thompson, P. M., Elashoff, D. A., Jack, C. R., Weiner, M. W., & Apostolova, L. G. (2015) · American Journal of Neuroradiology · doi:10.3174/ajnr.a4228 · Cited by 76 · see citing works

Incremental value of biomarker combinations to predict progression of mild cognitive impairment to Alzheimer’s dementia

Frölich, L., Peters, O., Lewczuk, P., Gruber, O., Teipel, S. J., Gertz, H., Jahn, H., Jessen, F., Kurz, A., Luckhaus, C., et al. (2017) · Alzheimer s Research & Therapy · doi:10.1186/s13195-017-0301-7 · Cited by 77 · see citing works

Insights into the neuropathology of cerebral ischemia and its mechanisms

Ahad, M. A., Kumaran, K. R., Tiang, N., Mansor, N. I., Effendy, M. A., Damodaran, T. K., Lingam, K., Wahab, H. A., Nordin, N., Liao, P. H., et al. (2020) · Reviews in the Neurosciences · doi:10.1515/revneuro-2019-0099 · Cited by 75 · see citing works

Proton MRS in mild cognitive impairment

Kantarci, K. (2013) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.23800 · Cited by 74 · see citing works

Region-Specific Genetic Alterations in the Aging Hippocampus: Implications For Cognitive Aging

Bürger, C. (2010) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2010.00140 · Cited by 73 · see citing works

Systematic review: fluid biomarkers and machine learning methods to improve the diagnosis from mild cognitive impairment to Alzheimer’s disease

Blanco, K., Salcidua, S., Orellana, P., Sauma-Pérez, T., León, T., Steinmetz, L. C. L., Ibañez, A., Duran-Aniotz, C., & de la Cruz, R. (2023) · Alzheimer's Research & Therapy · doi:10.1186/s13195-023-01304-8 · Cited by 73 · see citing works

Framingham Cardiovascular Risk Profile Correlates with Impaired Hippocampal and Cortical Vasoreactivity to Hypercapnia

Glodzik, L., Rusinek, H., Bryś, M., Tsui, W. H., Switalski, R., Mosconi, L., Mistur, R. L., Pirraglia, E., Santi, S. D., Li, Y., et al. (2010) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2010.145 · Cited by 73 · see citing works

Frequency and longitudinal clinical outcomes of Alzheimer's AT(N) biomarker profiles: A longitudinal study

Yu, J., Li, J., John Suckling, A., Feng, L., Pan, A., Wang, Y., Song, B., Zhu, S., Li, D., Wang, H.-F., et al. (2019) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2019.05.006 · Cited by 73 · see citing works

Radiological-Pathological Correlation in Alzheimer’s Disease: Systematic Review of Antemortem Magnetic Resonance Imaging Findings

Dallaire‐Théroux, C., Callahan, B. L., Potvin, O., Saïkali, S., & Duchesne, S. (2017) · Journal of Alzheimer s Disease · doi:10.3233/jad-161028 · Cited by 68 · see citing works

Is apolipoprotein E4 an important risk factor for vascular dementia?

Rohn, T. T. (2014) · PubMed Central · Cited by 68 · see citing works

Biomarkers in translational research of Alzheimer’s Disease

Tarawneh, R., & Holtzman, D. M. (2010) · Neuropharmacology · doi:10.1016/j.neuropharm.2010.04.006 · Cited by 67 · see citing works

Hippocampal subfield volumetry in patients with subcortical vascular mild cognitive impairment

Li, X., Li, D., Li, Q., Li, Y., Li, K., Li, S., & Han, Y. (2016) · Scientific Reports · doi:10.1038/srep20873 · Cited by 68 · see citing works

Toward an interpretable Alzheimer’s disease diagnostic model with regional abnormality representation via deep learning

Lee, E., Choi, J.-S., Kim, M., & Suk, H.-I. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.116113 · Cited by 61 · see citing works

Alliance for aging research AD biomarkers work group: structural MRI

Jack, C. R. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.09.011 · Cited by 64 · see citing works

Hippocampal Atrophy in Subcortical Vascular Dementia

van de Pol, L. A., Gertz, H., Scheltens, P., & Wolf, H. (2011) · Neurodegenerative Diseases · doi:10.1159/000326695 · Cited by 63 · see citing works

GABA‐containing compound gammapyrone protects against brain impairments in Alzheimer’s disease model male rats and prevents mitochondrial dysfunction in cell culture

Piļipenko, V., Narbute, K., Amara, I., Salinaro, A. T., Scuto, M. C., Pupure, J., Jansone, B., Poikāns, J., Bisenieks, E., Klusa, V. Z., et al. (2019) · Journal of Neuroscience Research · doi:10.1002/jnr.24396 · Cited by 57 · see citing works

Associations between hippocampal morphometry and neuropathologic markers of Alzheimer's disease using 7 T MRI

Blanken, A. E., Hurtz, S., Zarow, C., Biado, K., Honarpisheh, H., Somme, J. H., Brook, J. K., Tung, S., Kraft, E., Lo, D. C. W., et al. (2017) · NeuroImage Clinical · doi:10.1016/j.nicl.2017.04.020 · Cited by 57 · see citing works

Correlates of Hippocampal Neuron Number in Alzheimer’s Disease and Ischemic

Dementia, V., & Chui, H. C. (2013)

Relationship between hippocampal volume and CA1 neuron loss in brains of humans with and without Alzheimer's disease

Kril, J. J., Hodges, J. R., & Halliday, G. M. (2004) · Neuroscience Letters · doi:10.1016/j.neulet.2004.02.001 · Cited by 72 · see citing works

Relationship between hippocampal volume and CA1 neuron loss in brains of humans with and without Alzheimer's disease*1

Kril, J. J. (2004) · Neuroscience Letters · doi:10.1016/s0304-3940(04)00134-x · Cited by 12 · see citing works

Volume and number of neurons of the human hippocampal formation in normal aging and Alzheimer’s disease

?imi?, G., Kostovi?, I., Winblad, B., & Bogdanovi?, N. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970324)379:4

The CA1 Region of the Human Hippocampus Is a Hot Spot in Alzheimer's Disease

West, M. J., Kawas, C. H., Martin, L. J., & Troncoso, J. C. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06652.x · Cited by 137 · see citing works