Atypical form of Alzheimer's disease with prominent posterior cortical atrophy: A review of lesion distribution and circuit disconnection in cortical visual pathways
Open accessAbstract
In recent years, the existence of visual variants of Alzheimer's disease characterized by atypical clinical presentation at onset has been increasingly recognized. In many of these cases post-mortem neuropathological assessment revealed that correlations could be established between clinical symptoms and the distribution of neurodegenerative lesions. We have analyzed a series of Alzheimer's disease patients presenting with prominent visual symptomatology as a cardinal sign of the disease. In these cases, a shift in the distribution of pathological lesions was observed such that the primary visual areas and certain visual association areas within the occipito-parieto-temporal junction and posterior cingulate cortex had very high densities of lesions, whereas the prefrontal cortex had fewer lesions than usually observed in Alzheimer's disease. Previous quantitative analyses have demonstrated that in Alzheimer's disease, primary sensory and motor cortical areas are less damaged than the multimodal association areas of the frontal and temporal lobes, as indicated by the laminar and regional distribution patterns of neurofibrillary tangles and senile plaques. The distribution of pathological lesions in the cerebral cortex of Alzheimer's disease cases with visual symptomatology revealed that specific visual association pathways were disrupted, whereas these particular connections are likely to be affected to a less severe degree in the more common form of Alzheimer's disease. These data suggest that in some cases with visual variants of Alzheimer's disease, the neurological symptomatology may be related to the loss of certain components of the cortical visual pathways, as reflected by the particular distribution of the neuropathological markers of the disease.
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The molecular, anatomic, and clinical changes of AD may not progress in a uniform fashion.
“Another challenge of CPC studies is that the molecular, anatomic, and clinical changes of AD may not progress in a uniform fashion (7, 12-15).”
From Correlation of Alzheimer Disease Neuropathologic Changes With Cognitive Status: A Review of the Literature (2012) · cites this paper as [15]
Not all Alzheimer disease cases fall within the same spatial continuum with regard to brain neurofibrillary tangle distributions.
“and that not all AD cases fall within the same spatial continuum with regard to brain NFT distributions (12, 15, 151).”
From Correlation of Alzheimer Disease Neuropathologic Changes With Cognitive Status: A Review of the Literature (2012) · cites this paper as [15]
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Cites
Distributed hierarchical processing in the primate cerebral cortex
Felleman, D. J., & Van Essen, D. C. (1991) · Cerebral Cortex · doi:10.1093/cercor/1.1.1 · Cited by 7,783 · see citing works
Object vision and spatial vision: Two cortical pathways
Mishkin, M., Ungerleider, L. G., & Macko, K. A. (1983) · Trends in Neurosciences · doi:10.1016/0166-2236(83)90190-x · Cited by 2,947 · see citing works
Borders of Multiple Visual Areas in Humans Revealed by Functional Magnetic Resonance Imaging
Sereno, M. I., Dale, A. M., Reppas, J. B., Kwong, K. K., Belliveau, J. W., Brady, T. J., Rosen, B. R., & Tootell, R. B. H. (1995) · Science · doi:10.1126/science.7754376 · Cited by 2,623 · see citing works
(1909) · Cited by 2,575 · see citing works
Functional analysis of human MT and related visual cortical areas using magnetic resonance imaging
Tootell, R. B. H., Reppas, J. B., Kwong, K. K., Malach, R., Born, R. T., Brady, T., Rosen, B. R., & Belliveau, J. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-04-03215.1995 · Cited by 1,412 · see citing works
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
Dissociation of object and spatial processing domains in primate prefrontal cortex.
Wilson, F. A., Scalaidhe, S. P. Ó., & Goldman-Rakic, P. (1993) · Science · doi:10.1126/science.8316836 · Cited by 1,374 · see citing works
Reiman, E. M., Caselli, R. J., Yun, L. S., Chen, K., Bandy, D., Minoshima, S., Thibodeau, S. N., & Osborne, D. (1996) · New England Journal of Medicine · doi:10.1056/nejm199603213341202 · Cited by 1,366 · see citing works
Watson, J. D. G., Myers, R., Frackowiak, R. S. J., Hajnal, J. V., Woods, R. P., Mazziotta, J. C., Shipp, S. D., & Zeki, S. (1993) · Cerebral Cortex · doi:10.1093/cercor/3.2.79 · Cited by 1,235 · see citing works
Concurrent processing streams in monkey visual cortex
DeYoe, E. A., & Essen, D. C. V. (1988) · Trends in Neurosciences · doi:10.1016/0166-2236(88)90130-0 · Cited by 1,118 · see citing works
Laminar origins and terminations of cortical connections of the occipital lobe in the rhesus monkey
Rockland, K. S., & Pandya, D. Ν. (1979) · Brain Research · doi:10.1016/0006-8993(79)90485-2 · Cited by 1,076 · see citing works
The functional logic of cortical connections
Zeki, S., & Shipp, S. (1988) · Nature · doi:10.1038/335311a0 · Cited by 1,067 · see citing works
Mapping striate and extrastriate visual areas in human cerebral cortex.
DeYoe, E. A., Carman, G. J., Bandettini, P. A., Glickman, S., Wieser, J., Cox, R. W., Miller, D. A., & Jay Neitz, A. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.6.2382 · Cited by 1,047 · see citing works
Pearson, R. C., Esiri, M. M., Hiorns, R. W., Wilcock, G. K., & Powell, T. P. (1985) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.82.13.4531 · Cited by 987 · see citing works
Principles of behavioral neurology
Mesulam, M.-M. (1985) · Davis eBooks · Cited by 976 · see citing works
Cingulate cortex of the rhesus monkey: II. Cortical afferents
Vogt, B. A., & Pandya, D. N. (1987) · Journal of Comparative Neurology · doi:10.1002/cne.902620208 · Cited by 854 · see citing works
Self-citationSome morphometric aspects of the brain in senile dementia of the alzheimer type
Terry, R. D., Peck, A., DeTeresa, R., Schechter, R., & Horoupian, D. S. (1981) · Annals of Neurology · doi:10.1002/ana.410100209 · Cited by 801 · see citing works
Neurobiology of Cingulate Cortex and Limbic Thalamus
Vogt, B. A., & Gabriel, M. (1993) · Birkhäuser Boston eBooks · doi:10.1007/978-1-4899-6704-6 · Cited by 772 · see citing works
Benson, D. F., Davis, R. J., & Snyder, B. D. (1988) · Archives of Neurology · doi:10.1001/archneur.1988.00520310107024 · Cited by 754 · see citing works
Optic-Nerve Degeneration in Alzheimer's Disease
Hinton, D. R., Sadun, A. A., Blanks, J. C., & Miller, C. A. (1986) · New England Journal of Medicine · doi:10.1056/nejm198608213150804 · Cited by 700 · see citing works
Perforant pathway changes and the memory impairment of Alzheimer's disease
Hyman, B. T., Van Hoesen, G. W., Kromer, L. J., & Damasio, A. R. (1986) · Annals of Neurology · doi:10.1002/ana.410200406 · Cited by 672 · see citing works
Organization of visual inputs to the inferior temporal and posterior parietal cortex in macaques
Baizer, J. S., Ungerleider, L. G., & Desimone, R. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-01-00168.1991 · Cited by 626 · see citing works
Lewis, D., Campbell, M., Terry, R., & Morrison, J. (1987) · The Journal of Neuroscience · doi:10.1523/jneurosci.07-06-01799.1987 · Cited by 578 · see citing works
Self-citationRegional pattern of degeneration in Alzheimer's disease: neuronal loss and histopathological grading
Brun, A., & Englund, E. M. (1981) · Histopathology · doi:10.1111/j.1365-2559.1981.tb01818.x · Cited by 559 · see citing works
Cortical connections between rat cingulate cortex and visual, motor, and postsubicular cortices
Vogt, B. A., & Miller, M. W. (1983) · The Journal of Comparative Neurology · doi:10.1002/cne.902160207 · Cited by 528 · see citing works
Self-citationSeelenlähmung des “Schauens”, optische Ataxie, räumliche Störung der Aufmerksamkeit. pp. 51–66
Bálint, R. (2009) · Monatsschrift für Psychiatrie und Neurologie · doi:10.1159/000210464 · Cited by 481 · see citing works
Making the diagnosis of Alzheimer's disease. A primer for practicing pathologists.
Mirra, S. S., Hart, M. N., & Terry, R. D. (1993) · PubMed · Cited by 412 · see citing works
Rogers, J., & Morrison, J. (1985) · Journal of Neuroscience · doi:10.1523/jneurosci.05-10-02801.1985 · Cited by 410 · see citing works
Self-citationClarke, S., & Judith Miklossy, A. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902980205 · Cited by 399 · see citing works
Brodmann’s Localisation in the Cerebral Cortex
Brodmann, K. (2005) · Springer eBooks · doi:10.1007/b138298 · Cited by 396 · see citing works
Thalamic and Cortical Afferents Differentiate Anterior from Posterior Cingulate Cortex in the Monkey
Vogt, B. A., Rosene, D. L., & Pandya, D. Ν. (1979) · Science · doi:10.1126/science.107587 · Cited by 394 · see citing works
Self-citationHof, P. R., Morrison, J. H., & Cox, K. (1990) · Journal of Comparative Neurology · doi:10.1002/cne.903010105 · Cited by 365 · see citing works
Self-citationSeelenlahmung des "schauens" optische Ataxie, raumliche Storung der Aufmerksamkeit
Bálint, R. (1909) · Medical Entomology and Zoology · Cited by 360 · see citing works
Principles of Behavioral Neurology
Boller, F. (1986) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-198607000-00011 · Cited by 357 · see citing works
Retinal pathology in Alzheimer's disease. I. Ganglion cell loss in foveal/parafoveal retina.
Blanks, J., Torigoe, Y., Hinton, D., & Blanks, R. (1996) · Neurobiology of Aging · doi:10.1016/0197-4580(96)00010-3 · Cited by 351 · see citing works
Anatomie des menschlichen Gehirns und Rückenmarks : auf myelogenetischer Grundlage
Flechsig, P. (1920) · Medical Entomology and Zoology · Cited by 341 · see citing works
Complex visual disturbances in Alzheimer's disease
Mendez, M. F., Mendez, M. A., Martin, R. J., Smyth, K. A., & Whitehouse, P. J. (1990) · Neurology · doi:10.1212/wnl.40.3_part_1.439 · Cited by 335 · see citing works
Retinal ganglion cells in Alzheimer's disease and aging
Curcio, C., & Drucker, D. (1993) · Annals of Neurology · doi:10.1002/ana.410330305 · Cited by 323 · see citing works
Posterior cingulate cortex in Alzheimer's disease
MINOSHIMA, S. (1994) · The Lancet · doi:10.1016/s0140-6736(94)92871-1 · Cited by 316 · see citing works
Hof, P. R., & Morrison, J. H. (1990) · Journal of Comparative Neurology · doi:10.1002/cne.903010106 · Cited by 294 · see citing works
Self-citationRetinal pathology in Alzheimer's disease. II. Regional neuron loss and glial changes in GCL
Blanks, J. C., Schmidt, S. Y., Torigoe, Y., Porrello, K. V., Hinton, D. R., & Blanks, R. H. I. (1996) · Neurobiology of Aging · doi:10.1016/0197-4580(96)00009-7 · Cited by 287 · see citing works
The visual variant of Alzheimer's disease
Levine, D. N., Lee, J. M., & Fisher, C. M. (1993) · Neurology · doi:10.1212/wnl.43.2.305 · Cited by 282 · see citing works
Hof, P. R., & Morrison, J. H. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903520202 · Cited by 265 · see citing works
Self-citationAnatomical Evidence for MT and Additional Cortical Visual Areas in Humans
Tootell, R. B. H., & Taylor, J. B. (1995) · Cerebral Cortex · doi:10.1093/cercor/5.1.39 · Cited by 253 · see citing works
Kowall, N. W., & Beal, M. F. (1988) · Annals of Neurology · doi:10.1002/ana.410230202 · Cited by 236 · see citing works
Hof, P. R., Bouras, C., Constantinidis, J., & Morrison, J. H. (1990) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-199003000-00008 · Cited by 219 · see citing works
Self-citationThe modular organization of projections from areas V1 and V2 to areas V4 and TEO in macaques
Nakamura, H., Gattass, R., Desimone, R., & Ungerleider, L. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-09-03681.1993 · Cited by 211 · see citing works
Visual Disturbances With Focal Progressive Dementing Disease
Cogan, D. G. (1985) · American Journal of Ophthalmology · doi:10.1016/s0002-9394(14)74985-2 · Cited by 201 · see citing works
Effects of fornix transection and cingulate cortical ablation on spatial memory in rhesus monkeys
Murray, E. A., Davidson, M., Gaffan, D., Olton, D. S., & Suomi, S. (1989) · Experimental Brain Research · doi:10.1007/bf00248291 · Cited by 200 · see citing works
Hof, P. R., & Morrison, J. H. (1991) · Experimental Neurology · doi:10.1016/0014-4886(91)90096-u · Cited by 196 · see citing works
Self-citationOphthalmologic manifestations of Alzheimer's disease
Katz, B., & Rimmer, S. (1989) · Survey of Ophthalmology · doi:10.1016/0039-6257(89)90127-6 · Cited by 180 · see citing works
Balit's syndrome in Alzheimer's disease: specific disruption of the occipito-parietal visual pathway
Hof, P. R., Bouras, C., Constandinidis, J., & Morrison, J. H. (1989) · Brain Research · doi:10.1016/0006-8993(89)91173-6 · Cited by 177 · see citing works
Self-citationBiopsy‐proved Alzheimer disease presenting as a right parietal lobe syndrome
Crystal, H., Horoupian, D. S., Katzman, R., & Jotkowitz, S. (1982) · Annals of Neurology · doi:10.1002/ana.410120210 · Cited by 173 · see citing works
Vallet, P. G., Guntern, R., Hof, P. R., Golaz, J., Delacourte, A., Robakis, N. K. R. K., & Bouras, C. (1992) · Acta Neuropathologica · doi:10.1007/bf00308476 · Cited by 170 · see citing works
Self-citationPosterior Cortical Atrophy: Neuropathologic Correlations
Victoroff, J., Ross, G., Benson, D., Verity, M., & Vinters, H. (1994) · Archives of Neurology · doi:10.1001/archneur.1994.00540150063018 · Cited by 169 · see citing works
Diseases of the Nervous System: Clinical Neurobiology.
(1988) · Annals of Internal Medicine · doi:10.7326/0003-4819-108-3-505_14 · Cited by 162 · see citing works
Buée‐Scherrer, V., Condamines, O., Mourton-Gilles, C., Jakes, R., Goedert, M., Pau, B., & Delacourte, A. (1996) · Molecular Brain Research · doi:10.1016/0169-328x(96)00003-4 · Cited by 155 · see citing works
Albert, M. S. (1981) · Journal of Consulting and Clinical Psychology · doi:10.1037//0022-006x.49.6.835 · Cited by 151 · see citing works
Alzheimer's disease: areal and laminar pathology in the occipital isocortex
Braak, H., Braak, E., & Kalus, P. (1989) · Acta Neuropathologica · doi:10.1007/bf00687251 · Cited by 141 · see citing works
Spatial Vision in Alzheimer's Disease
Nissen, M. J. (1985) · Archives of Neurology · doi:10.1001/archneur.1985.04060070057015 · Cited by 135 · see citing works
A motion area in human visual cortex.
Orban, G. A., Dupont, P. J., Bruyn, B. D., Vogels, R., Vandenberghe, R. R., & Mortelmans, L. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.4.993 · Cited by 133 · see citing works
Neurobiology of Cingulate Cortex and Limbic Thalamus
Asanuma, C. (1994) · Trends in Neurosciences · doi:10.1016/0166-2236(94)90144-9 · Cited by 132 · see citing works
Alzheimer's Disease with Prominent Visual Symptoms
Kiyosawa, M., Bosley, T. M., Chawluk, J. B., Jamieson, D. G., Schatz, N. J., Savino, P. J., Sergott, R. C., Reivich, M., & Alavi, A. A. (1989) · Ophthalmology · doi:10.1016/s0161-6420(89)32769-2 · Cited by 132 · see citing works
Disorders of the visual system in Alzheimer's disease.
Mendez, M. F., Tomsak, R. L., & Remler, B. F. (1990) · PubMed · Cited by 129 · see citing works
Delacourte, A., Flament, S., Dibe, E. M., Hublau, P., Sablnni�re, P., H�mon, B., Sh�rrer, V., & D�fossez, A. (1990) · Acta Neuropathologica · doi:10.1007/bf00308912 · Cited by 127 · see citing works
Smooth pursuit dysfunction in Alzheimer's disease
Fletcher, W. A., & Sharpe, J. A. (1988) · Neurology · doi:10.1212/wnl.38.2.272 · Cited by 124 · see citing works
Beach, T. G., & McGeer, E. G. (1988) · Brain Research · doi:10.1016/0006-8993(88)90410-6 · Cited by 123 · see citing works
Diseases of the nervous system: Clinical neurobiology
STARK, G. D. (1992) · Neuromuscular Disorders · doi:10.1016/0960-8966(92)90013-v · Cited by 118 · see citing works
Incomplete achromatopsia in alzheimer's disease
Cronin‐Golomb, A., Sugiura, R., Corkin, S., & Growdon, J. H. (1993) · Neurobiology of Aging · doi:10.1016/0197-4580(93)90105-k · Cited by 112 · see citing works
Hof, P. R., Archin, N. M., Osmand, A. P., Dougherty, J. H., Wells, C. E., Bouras, C., & Morrison, J. H. (1993) · Acta Neuropathologica · doi:10.1007/bf00304135 · Cited by 106 · see citing works
Self-citationHof, P. R., & Bouras, C. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90191-u · Cited by 98 · see citing works
Self-citationMcCarthy, G., Spicer, M., Adrignolo, A., Luby, M. L., Gore, J. C., & Allison, T. (1994) · Human Brain Mapping · doi:10.1002/hbm.460020405 · Cited by 96 · see citing works
Pathology of subcortical visual centres in relation to cortical degeneration in Alzheimer's disease
Leuba, G., & Saini, K. (1995) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.1995.tb01078.x · Cited by 93 · see citing works
Baleydier, C., & Maugui�re, F. (1987) · Experimental Brain Research · doi:10.1007/bf00243312 · Cited by 92 · see citing works
Jagust, W. J., Davies, P., Borcich, J. K., & Reed, B. (1990) · Neurology · doi:10.1212/wnl.40.1.14 · Cited by 92 · see citing works
Vogt, B. A., Sikes, R. W., Swadlow, H. A., & Weyand, T. G. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902480106 · Cited by 90 · see citing works
Self-citationAlzheimer's disease in a patient with posterior cortical atrophy.
Berthier, M. L., Leiguarda, R. C., STARKSTEIN, S. E., Sevlever, G. E., & Taratuto, A. L. (1991) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.54.12.1110 · Cited by 89 · see citing works
Fries, W., Keizer, K., & Kuypers, H. G. J. M. (1985) · Experimental Brain Research · doi:10.1007/bf00235878 · Cited by 89 · see citing works
Vickers, J. C., Chin, D., Edwards, A.-M., Sampson, V., Harper, C. G., & Morrison, J. H. (1996) · Experimental Neurology · doi:10.1006/exnr.1996.0133 · Cited by 86 · see citing works
Self-citationOlson, C. R., & Musil, S. Y. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903240207 · Cited by 85 · see citing works
Alzheimer's Disease and Other Dementing Disorders
Raskind, M. A., & Peskind, E. R. (1992) · Elsevier eBooks · doi:10.1016/b978-0-12-101277-9.50022-x · Cited by 77 · see citing works
Laminar distribution of neuron degeneration in posterior cingulate cortex in Alzheimer's disease
Vogt, B. A., Hoesen, G. W. V., & Vogt, L. J. (1990) · Acta Neuropathologica · doi:10.1007/bf00307624 · Cited by 74 · see citing works
Self-citationClarke, S. (1994) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1994.tb00984.x · Cited by 73 · see citing works
Gaspar, P., Duyckaerts, C. J., Febvret, A., Benoit, R., Beck, B., & Berger, B. (1989) · Brain Research · doi:10.1016/0006-8993(89)90424-1 · Cited by 65 · see citing works
Broad-band visual capacities are not selectively impaired in Alzheimer's disease
Kurylo, D. D., Corkin, S., Dolan, R. P., Rizzo, J. F., Parker, S. W., & Growdon, J. H. (1994) · Neurobiology of Aging · doi:10.1016/0197-4580(94)90025-6 · Cited by 65 · see citing works
Functional Organisation of the Human Visual Cortex
Gulyás, B. Z., Ottoson, D., & Roland, P. E. (1993) · Cited by 64 · see citing works
Sorenson, E. M., & Chiappinelli, V. A. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903230102 · Cited by 62 · see citing works
Alien hand sign in association with Alzheimer's histopathology.
Ball, J. A., Lantos, P. L., Jackson, M., MARSDEN, C. D., Scadding, J. W., & Rossor, M. N. (1993) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.56.9.1020 · Cited by 57 · see citing works
Balint's Syndrome in Alzheimer's Disease: Visuospatial Functions
Mendez, M. F., Turner, J. E., Gilmore, G. C., Remler, B. F., & Tomsak, R. L. (1990) · International Journal of Neuroscience · doi:10.3109/00207459008986653 · Cited by 53 · see citing works
Simultanagnosia as the Initial Sign of Degenerative Dementia
Graff‐Radford, N. R., Bolling, J. P., Earnest, F., Shuster, E. A., Caselli, R. J., & Brazis, P. W. (1993) · Mayo Clinic Proceedings · doi:10.1016/s0025-6196(12)62267-8 · Cited by 52 · see citing works
Lesions in the Pulvinar in Patients with Alzheimerʼs Disease
Kuljiš, R. O. (1994) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-199403000-00012 · Cited by 51 · see citing works
Posterior Cingulate Cortex: Sensory and Oculomotor Properties of Single Neurons in Behaving Cat
Olson, C. R., & Musil, S. Y. (1992) · Cerebral Cortex · doi:10.1093/cercor/2.6.485 · Cited by 51 · see citing works
Beach, T. G., & McGeer, E. G. (1992) · Acta Neuropathologica · doi:10.1007/bf00296792 · Cited by 49 · see citing works
Dissociation between the detection and perception of motion in Alzheimer's disease
Silverman, S. E., Tran, D. B., Zimmerman, K. M., & Feldon, S. E. (1994) · Neurology · doi:10.1212/wnl.44.10.1814 · Cited by 45 · see citing works
Association and intrinsic connections of human extrastriate visual cortex
Clarke, S. (1994) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1994.0098 · Cited by 44 · see citing works
Vogt, B. A., Crino, P. B., & Vogt, L. J. (1992) · Cerebral Cortex · doi:10.1093/cercor/2.6.526 · Cited by 42 · see citing works
Self-citationOphthalmological aspects of Alzheimer??s disease
Fletcher, W. A. (1994) · Current Opinion in Ophthalmology · doi:10.1097/00055735-199412000-00007 · Cited by 39 · see citing works
Functional Organisation of the Human Visual Cortex
Engel, A. K. (1994) · Trends in Neurosciences · doi:10.1016/0166-2236(94)90036-1 · Cited by 36 · see citing works
Motor Cortex Involvement in Presenile Dementia: Report of a Case
Golaz, J., Bouras, C., & Hof, P. R. (1992) · Journal of Geriatric Psychiatry and Neurology · doi:10.1177/002383099200500205 · Cited by 34 · see citing works
Self-citationSmooth Pursuit Eye Movements in Dementia of the Alzheimer Type
Kuskowski, M. A., Malone, S. M., Mortimer, J. A., & Dysken, M. W. (1989) · Alzheimer Disease & Associated Disorders · doi:10.1097/00002093-198903030-00005 · Cited by 29 · see citing works
Permanne, B., Buée, L., David, J., Fallet-Bianco, C., Dimenza, C., & Delacourte, A. (1995) · Brain Research · doi:10.1016/0006-8993(95)00431-o · Cited by 25 · see citing works
Neuronal responses in rabbit cingulate cortex linked to quick-phase eye movements during nystagmus
Sikes, R. W., Vogt, B. A., & Swadlow, H. A. (1988) · Journal of Neurophysiology · doi:10.1152/jn.1988.59.3.922 · Cited by 25 · see citing works
Self-citationKunel, Willams, A. C., Forsythe, J., & Rutherford (1998) · Medical Entomology and Zoology · Cited by 22 · see citing works
Callosal Connections and Functional Subdivision of the Human Occipital Cortex
Clarke, S. (1993) · Elsevier eBooks · doi:10.1016/b978-0-08-042004-2.50014-9 · Cited by 20 · see citing works
[Progressive severity of left unilateral apraxia in 2 cases of Alzheimer disease].
Ceccaldi, M. P., Poncet, M., Gambarelli, D., Guinot, H., & Billé, J. (1995) · PubMed · Cited by 20 · see citing works
[Visuo-constructional disorders and alexia-agraphia associated with posterior cortical atrophy].
Croisile, B., Trillet, M., Hibert, O., Cinotti, L., Bars, D. L., Mauguı̀ere, F., & Aimard, G. (1991) · PubMed · Cited by 20 · see citing works
[Posterior cortical atrophy: anatomo-clinical variant of Alzheimer's disease].
Jacquet, M., Boucquey, D., Theaux, R. A., Smidts, M., Callewaert, A., Brucher, J., & Kevers, L. (1990) · PubMed · Cited by 13 · see citing works
Morel, F. (2007) · Stereotactic and Functional Neurosurgery · doi:10.1159/000105974 · Cited by 13 · see citing works
[Bioccipital atrophic lesions of uncertain nature at the source of visual agnosia].
Magnani, G., Bettoni, L., & Mazzucchi, A. (1982) · PubMed · Cited by 11 · see citing works
The incredible shrinking brain
Savino, P. J., Levy, M. H., Hart, W. M., Sonstein, F. M., & Ballinger, W. E. (1995) · Survey of Ophthalmology · doi:10.1016/s0039-6257(05)80109-2 · Cited by 7 · see citing works
Flagged first, then by citations
3 of the 113 references couldn’t be matched to a known paper.
Research works printed but not linked: 3
- Flechsig, P. (1920). Anatomie des menschlichen Gehirns und Ru'cken- marks. Leipzig: Thieme.
- Hof, P. R. & Morrison J. H. (1994). The cellular basis of cortical disconnection in Alzheimer disease and related dementing condi- tions. In Terry, R. D., Katzman, R. & Bick, K. L. (Eds), Alzheimer disease (pp. 197-229). New York: Raven Press.
- Vogt, B. A. & Pandya, D. N. (1987). Cingulate cortex of rhesus monkey: 1I. Cortical afferents. Journal of Comparative Neurology, 262, 271-289.
Cited by
Sorted by citations
Neurodegenerative Diseases Target Large-Scale Human Brain Networks
Seeley, W. W., Crawford, R. K., Zhou, J., Miller, B. L., & Greicius, M. D. (2009) · Neuron · doi:10.1016/j.neuron.2009.03.024 · Cited by 2,350 · see citing works
Nelson, P. T., Alafuzoff, I., Bigio, E. H., Bouras, C., Braak, H., Cairns, N. J., Castellani, R. J., Crain, B. J., Davies, P., Tredici, K. D., et al. (2012) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e31825018f7 · Cited by 2,050 · see citing works
“Nevertheless, Braak staging also masks the fact that marked variability in pathologic lesion density across cases exists within a given Braak stage (7, 12) and that not all AD cases fall within the same spatial continuum with regard to brain NFT distributions (12, 15, 151).”
BackgroundSelf-citationPrimary age-related tauopathy (PART): a common pathology associated with human aging
Crary, J. F., Trojanowski, J. Q., Schneider, J. A., Abisambra, J. F., Abner, E. L., Alafuzoff, I., Arnold, S. E., Attems, J., Beach, T. G., Bigio, E. H., et al. (2014) · Acta Neuropathologica · doi:10.1007/s00401-014-1349-0 · Cited by 1,467 · see citing works
Self-citationThe neuropathology of probable Alzheimer disease and mild cognitive impairment
Schneider, J. A., Arvanitakis, Z., Leurgans, S. E., & Bennett, D. A. (2009) · Annals of Neurology · doi:10.1002/ana.21706 · Cited by 935 · see citing works
Webster, S. J., Bachstetter, A. D., Nelson, P. T., Schmitt, F. A., & Van Eldik, L. J. (2014) · Frontiers in Genetics · doi:10.3389/fgene.2014.00088 · Cited by 755 · see citing works
“Not all AD cases fall within the standard NFT distribution described by the Braak staging (Hof et al., 1997; Abner et al., 2011; Murray et al., 2011).”
BackgroundWeıntraub, S., Besser, L. M., Dodge, H. H., Teylan, M., Ferris, S. H., Goldstein, F. C., Giordani, B., Kramer, J. H., Loewenstein, D., Marson, D., et al. (2017) · Alzheimer Disease & Associated Disorders · doi:10.1097/wad.0000000000000223 · Cited by 677 · see citing works
Alzheimer’s Disease: Past, Present, and Future
Bondi, M. W., Edmonds, E. C., & Salmon, D. P. (2017) · Journal of the International Neuropsychological Society · doi:10.1017/s135561771700100x · Cited by 649 · see citing works
Clinical, genetic, and neuropathologic characteristics of posterior cortical atrophy
Tang‐Wai, D. F., Graff‐Radford, N. R., Boeve, B. F., Dickson, D. W., Parisi, J. E., Crook, R., Caselli, R. J., Knopman, D. S., & Petersen, R. C. (2004) · Neurology · doi:10.1212/01.wnl.0000140289.18472.15 · Cited by 624 · see citing works
Galton, C. J. (2000) · Brain · doi:10.1093/brain/123.3.484 · Cited by 613 · see citing works
Crutch, S. J., Lehmann, M., Schott, J. M., Rabinovici, G. D., Rossor, M. N., & Fox, N. C. (2012) · The Lancet Neurology · doi:10.1016/s1474-4422(11)70289-7 · Cited by 580 · see citing works
Focal cortical presentations of Alzheimer's disease
Alladi, S., Xuereb, J., Bak, T., Nestor, P., Knibb, J., Patterson, K., & Hodges, J. R. (2007) · Brain · doi:10.1093/brain/awm213 · Cited by 581 · see citing works
The Neuropsychological Profile of Alzheimer DiseasePreprint
Weıntraub, S., Wicklund, A. H., & Salmon, D. P. (2012) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a006171 · Cited by 569 · see citing works
Alzheimer and frontotemporal pathology in subsets of primary progressive aphasia
Mesulam, M., Wicklund, A., Johnson, N., Rogalski, E., Léger, G. C., Rademaker, A., Weintraub, S., & Bigio, E. H. (2008) · Annals of Neurology · doi:10.1002/ana.21388 · Cited by 513 · see citing works
Early-Versus Late-Onset Alzheimer's Disease: More than Age Alone
Koedam, E. L. G. E., Lauffer, V., van der Vlies, A. E., van der Flier, W. M., Scheltens, P., & Pijnenburg, Y. A. L. (2010) · Journal of Alzheimer's Disease · doi:10.3233/jad-2010-1337 · Cited by 452 · see citing works
Aggleton, J. P., Pralus, A., Nelson, A. J. D., & Hornberger, M. (2016) · Brain · doi:10.1093/brain/aww083 · Cited by 378 · see citing works
Posterior Cortical Atrophy: Clinical Characteristics and Differences Compared to Alzheimer’s Disease
Mendez, M. F., Ghajarania, M., & Perryman, K. M. (2002) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000058331 · Cited by 364 · see citing works
Lithfous, S., Dufour, A., & Després, O. (2012) · Ageing Research Reviews · doi:10.1016/j.arr.2012.04.007 · Cited by 349 · see citing works
Lehmann, M., Ghosh, P. M., Madison, C., Laforce, R., Corbetta-Rastelli, C., Weiner, M. W., Greicius, M. D., Seeley, W. W., Gorno-Tempini, M. L., Rosen, H. J., et al. (2013) · Brain · doi:10.1093/brain/aws327 · Cited by 325 · see citing works
Mesulam, M.-M., Weintraub, S., Rogalski, E. J., Wieneke, C., Geula, C., & Bigio, E. H. (2014) · Brain · doi:10.1093/brain/awu024 · Cited by 334 · see citing works
Progressive posterior cortical dysfunction
Renner, J. A., Burns, J. M., Hou, C. E., McKeel, D. W., Storandt, M., & Morris, J. C. (2004) · Neurology · doi:10.1212/01.wnl.0000140290.80962.bf · Cited by 311 · see citing works
Connections of the retrosplenial granular b cortex in the rat
van Groen, T., & Wyss, J. M. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10757 · Cited by 297 · see citing works
Retinal thickness in patients with mild cognitive impairment and Alzheimer's disease
Kesler, A., Vakhapova, V., Korczyn, A. D., Naftaliev, E., & Neudorfer, M. (2011) · Clinical Neurology and Neurosurgery · doi:10.1016/j.clineuro.2011.02.014 · Cited by 298 · see citing works
A walk through tau therapeutic strategies
Jadhav, S., Ávila, J., Schöll, M., Kovács, G. G., Kövari, E., Škrabana, R., Evans, L., Kontseková, E., Malawska, B., de Silva, R., et al. (2019) · Acta Neuropathologica Communications · doi:10.1186/s40478-019-0664-z · Cited by 286 · see citing works
Nestor, P. J. (2003) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.74.11.1521 · Cited by 217 · see citing works
Marziani, E., Pomati, S., Ramolfo, P., Cigada, M., Giani, A., Mariani, C. B., & Staurenghi, G. (2013) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.13-12046 · Cited by 215 · see citing works
Lehmann, M., Crutch, S. J., Ridgway, G. R., Ridha, B. H., Barnes, J., Warrington, E. K., Rossor, M. N., & Fox, N. C. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2009.08.017 · Cited by 208 · see citing works
The paradox of syndromic diversity in Alzheimer disease
Warren, J. D., Fletcher, P. D., & Golden, H. L. (2012) · Nature Reviews Neurology · doi:10.1038/nrneurol.2012.135 · Cited by 197 · see citing works
Ascaso, F. J., Cruz, N., Modrego, P. J., López‐Antón, R., Santabárbara, J., Pascual, L. F., Lobo, A., & Cristóbal, J. Á. (2014) · Journal of Neurology · doi:10.1007/s00415-014-7374-z · Cited by 197 · see citing works
Saccade Reward Signals in Posterior Cingulate Cortex
McCoy, A. N., Crowley, J. C., Haghighian, G., Dean, H. L., & Platt, M. L. (2003) · Neuron · doi:10.1016/s0896-6273(03)00719-0 · Cited by 193 · see citing works
Neural correlates of cognitive impairment in posterior cortical atrophy
Kas, A., de Souza, L. C., Samri, D., Bartolomeo, P., Lacomblez, L., Kalafat, M., Migliaccio, R., de Schotten, M. T., Cohen, L., Dubois, B., et al. (2011) · Brain · doi:10.1093/brain/awr055 · Cited by 177 · 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
Giannakopoulos, P., Hof, P. R., Michel, J., Guimón, J., & Bouras, C. (1997) · Brain Research Reviews · doi:10.1016/s0165-0173(97)00023-4 · Cited by 173 · see citing works
Self-citationAlbert, M. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.09.010 · Cited by 149 · see citing works
Clinically concordant variations of Alzheimer pathology in aphasic versus amnestic dementia
Gefen, T. D., Gasho, K., RADEMAKER, A. W., Lalehzari, M., Weıntraub, S., Rogalski, E. J., Wieneke, C., Bigio, E. H., Geula, C., & Mesulam, M. M. (2012) · Brain · doi:10.1093/brain/aws076 · Cited by 131 · see citing works
Distinct clinical and metabolic deficits in PCA and AD are not related to amyloid distribution
Rosenbloom, M. H., Alkalay, A., Agarwal, N., Baker, S. L., O’Neil, J. P., Janabi, M., Yen, I. V., Growdon, M. E., Jang, J., Madison, C. M., et al. (2011) · Neurology · doi:10.1212/wnl.0b013e31821cccad · Cited by 121 · see citing works
The language profile of posterior cortical atrophy
Crutch, S. J., Lehmann, M., Warren, J. D., & Rohrer, J. D. (2012) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2012-303309 · Cited by 112 · see citing works
Mapping Neurodegenerative Disease Onset and ProgressionPreprint
Seeley, W. W. (2017) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a023622 · Cited by 104 · see citing works
Pierantozzi, M., Panella, M., Palmieri, M., Koch, G., Giordano, A., Marciani, M., Bernardi, G., Stanzione, P., & Stefani, A. (2004) · Clinical Neurophysiology · doi:10.1016/j.clinph.2004.04.022 · Cited by 90 · see citing works
Amyloid PET in clinical practice: Its place in the multidimensional space of Alzheimer's disease
Vandenberghe, R., Adamczuk, K., Dupont, P., Laere, K. V., & Chételat, G. (2013) · NeuroImage: Clinical · doi:10.1016/j.nicl.2013.03.014 · Cited by 99 · see citing works
“In atypical variants of AD, such as posterior cortical atrophy (Hof et al., 1993, 1997; von Gunten et al., 2006) or the logopenic variant of primary progressive aphasia (Gefen et al., 2012), the unusual clinical phenotype at initial presentation is mirrored by an unusual distribution of neuronal…”
BackgroundStaged decline of visual processing capacity in mild cognitive impairment and Alzheimer's disease
Bublak, P., Redel, P., Sorg, C., Kurz, A., Förstl, H., Müller, H. J., Schneider, W. X., & Finke, K. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2009.07.012 · Cited by 99 · see citing works
Vision function abnormalities in Alzheimer disease
Tzekov, R., & Mullan, M. (2014) · Survey of Ophthalmology · doi:10.1016/j.survophthal.2013.10.002 · Cited by 94 · see citing works
Shining a light on posterior cortical atrophy
Crutch, S. J., Schott, J. M., Rabinovici, G. D., Boeve, B. F., Cappa, S. F., Dickerson, B. C., Dubois, B., Graff‐Radford, N. R., Krolak‐Salmon, P., Lehmann, M., et al. (2012) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2012.11.004 · Cited by 92 · see citing works
Neuro-ophthalmic findings in the visual variant of Alzheimer's disease
Lee, A. G., & Martin, C. O. (2004) · Ophthalmology · doi:10.1016/s0161-6420(03)00732-2 · Cited by 90 · see citing works
van Groen, T., Kadish, I., & Wyss, J. M. (2004) · Behavioural Brain Research · doi:10.1016/j.bbr.2004.03.016 · Cited by 89 · see citing works
Primary progressive aphasia and the language network
Mesulam, M. M. (2013) · Neurology · doi:10.1212/wnl.0b013e31829d87df · Cited by 85 · see citing works
Neuroanatomic correlates of visual agnosia in Alzheimer’s disease
Giannakopoulos, P., Gold, G., Duc, M., Michel, J., Hof, P. R., & Bouras, C. (1999) · Neurology · doi:10.1212/wnl.52.1.71 · Cited by 84 · see citing works
Self-citationLongitudinal neuroanatomical and cognitive progression of posterior cortical atrophy
Firth, N. C., Primativo, S., Marinescu, R. V., Shakespeare, T. J., Gonzalez, A. S., Lehmann, M., Carton, A. M., Ocal, D., Pavisic, I. M., Paterson, R. W., et al. (2019) · Brain · doi:10.1093/brain/awz136 · Cited by 83 · see citing works
Object Orientation Agnosia: A Failure to Find the Axis?
Harris, I. M., Harris, J. A., & Caine, D. (2001) · Journal of Cognitive Neuroscience · doi:10.1162/08989290152541467 · Cited by 82 · see citing works
Neuropsychological Features of Mild Cognitive Impairment and Preclinical Alzheimer’s Disease
Salmon, D. P. (2011) · Current Topics in Behavioral Neurosciences · doi:10.1007/7854_2011_171 · Cited by 83 · see citing works
Aphasic variant of Alzheimer disease
Rogalski, E. J., Sridhar, J., Rader, B. M., Martersteck, A., Chen, K., Cobia, D. J., Thompson, C. K., Weıntraub, S., Bigio, E. H., & Mesulam, M. M. (2016) · Neurology · doi:10.1212/wnl.0000000000003165 · Cited by 82 · see citing works
Basic Visual Function and Cortical Thickness Patterns in Posterior Cortical Atrophy
Lehmann, M., Barnes, J., Ridgway, G. R., Wattam-Bell, J., Warrington, E. K., Fox, N. C., & Crutch, S. J. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq287 · Cited by 80 · see citing works
Sartucci, F., Borghetti, D., Bocci, T., Murri, L., Orsini, P., Porciatti, V., Origlia, N., & Domenici, L. (2010) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2010.04.001 · Cited by 79 · see citing works
Ventral and dorsal visual streams in posterior cortical atrophy: A DT MRI study
Migliaccio, R., Agosta, F., Scola, E., Magnani, G., Cappa, S. F., Pagani, E., Canu, E., Comı, G., Falini, A., Gorno‐Tempini, M. L., et al. (2012) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.12.025 · Cited by 76 · see citing works
Neural substrates of cognitive and behavioral deficits in atypical Alzheimer's disease
von Gunten, A., Bouras, C., Kövari, E., Giannakopoulos, P., & Hof, P. R. (2006) · Brain Research Reviews · doi:10.1016/j.brainresrev.2005.11.003 · Cited by 75 · see citing works
Self-citationKwon, J. Y., Yang, J. H., Han, J. S., & Kim, D. (2017) · Korean Journal of Ophthalmology · doi:10.3341/kjo.2016.0118 · Cited by 74 · see citing works
Visual Hallucinations in Posterior Cortical Atrophy
Josephs, K. A., Whitwell, J. L., Boeve, B. F., Knopman, D. S., Tang‐Wai, D. F., Drubach, D. A., Jack, C. R., & Petersen, R. C. (2006) · Archives of Neurology · doi:10.1001/archneur.63.10.1427 · Cited by 72 · see citing works
Formaglio, M., Costes, N., Seguin, J., Tholance, Y., Bars, D. L., Roullet‐Solignac, I., Mercier, B., Krolak‐Salmon, P., & Vighetto, A. (2011) · Journal of Neurology · doi:10.1007/s00415-011-6030-0 · Cited by 71 · see citing works
Hof, P. R., Nimchinsky, E. A., Young, W. G., & Morrison, J. H. (2000) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(20000424)420:1 · Cited by 71 · see citing works
Self-citationSensory cortical interactions in aging, mild cognitive impairment, and Alzheimer’s disease
Golob, E. J., Miranda, G. G., Johnson, J. K., & Starr, A. (2001) · Neurobiology of Aging · doi:10.1016/s0197-4580(01)00244-5 · Cited by 70 · see citing works
Neurophysiological and perceptual correlates of navigational impairment in Alzheimer's disease
Kavcic, V., Fernandez, R., Logan, D. J., & Duffy, C. J. (2006) · Brain · doi:10.1093/brain/awh727 · Cited by 69 · see citing works
Schott, J. M., & Crutch, S. J. (2019) · CONTINUUM Lifelong Learning in Neurology · doi:10.1212/con.0000000000000696 · Cited by 69 · see citing works
Tau PET imaging predicts cognition in atypical variants of Alzheimer's disease
Phillips, J. S., Das, S. R., McMillan, C. T., Irwin, D. J., Roll, E. E., Da Re, F., Nasrallah, I. M., Wolk, D. A., & Grossman, M. (2018) · Human Brain Mapping · doi:10.1002/hbm.23874 · Cited by 68 · see citing works
Motor cortex inhibitory circuits in dementia with Lewy bodies and in Alzheimer’s disease
Nardone, R., Bratti, A., & Tezzon, F. (2006) · Journal of neural transmission · doi:10.1007/s00702-006-0551-1 · Cited by 66 · see citing works
Vogt, B. A., Vogt, L. J., Vrana, K. E., Gioia, L., Meadows, R. S., Challa, V. R., Hof, P. R., & Van Hoesen, G. W. (1998) · Experimental Neurology · doi:10.1006/exnr.1998.6852 · Cited by 64 · see citing works
Self-citationFirth, N. C., Primativo, S., Brotherhood, E., Young, A. L., Yong, K. X. X., Crutch, S. J., Alexander, D. C., & Oxtoby, N. P. (2020) · Alzheimer s & Dementia · doi:10.1002/alz.12083 · Cited by 64 · see citing works
Posterior Cortical Atrophy: A Review of the Literature
Caine, D. (2004) · Neurocase · doi:10.1080/13554790490892239 · Cited by 63 · see citing works
Heterogeneity of semantic and visuospatial deficits in early Alzheimer's disease.
Caine, D., & Hodges, J. R. (2001) · Neuropsychology · doi:10.1037/0894-4105.15.2.155 · Cited by 61 · see citing works
Drawing Disorders in Alzheimer’s Disease and Other Forms of Dementia
Trojano, L., & Gainotti, G. (2016) · Journal of Alzheimer s Disease · doi:10.3233/jad-160009 · Cited by 59 · see citing works
Pathologic Correlates of Apraxia in Alzheimer Disease
Giannakopoulos, P., Duc, M., Gold, G., Hof, P. R., Michel, J., & Bouras, C. (1998) · Archives of Neurology · doi:10.1001/archneur.55.5.689 · Cited by 58 · see citing works
Self-citationVisual Dysfunction in Posterior Cortical Atrophy
da Silva, M. N. M., Millington, R. S., Bridge, H., James-Galton, M., & Plant, G. T. (2017) · Frontiers in Neurology · doi:10.3389/fneur.2017.00389 · Cited by 56 · see citing works
Neural substrates of spatial and temporal disorientation in Alzheimer's disease
Giannakopoulos, P., Gold, G., Duc, M., Michel, J., Hof, P. R., & Bouras, C. (2000) · Acta Neuropathologica · doi:10.1007/s004019900166 · Cited by 55 · see citing works
Self-citationCharles, R. F., & Hillis, A. E. (2005) · Behavioural Neurology · doi:10.1155/2005/762569 · Cited by 55 · see citing works
Zeller, J., Herrmann, M., Ehlis, A., Polak, T., & Fallgatter, A. (2010) · The American journal of geriatric psychiatry · doi:10.1097/jgp.0b013e3181c65821 · Cited by 50 · see citing works
Tsai, P., Teng, E., Liu, C., & Mendez, M. F. (2011) · American Journal of Alzheimer s Disease & Other Dementias® · doi:10.1177/1533317511418955 · Cited by 51 · 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
Diagnosis and Management of Posterior Cortical Atrophy
Yong, K. X. X., Graff-Radford, J., Ahmed, S., Chapleau, M., Ossenkoppele, R., Putcha, D., Rabinovici, G. D., Suarez-Gonzalez, A., Schott, J. M., Crutch, S., et al. (2023) · Current Treatment Options in Neurology · doi:10.1007/s11940-022-00745-0 · Cited by 51 · see citing works
Global gray matter changes in posterior cortical atrophy: A serial imaging study
Lehmann, M., Barnes, J., Ridgway, G. R., Ryan, N. S., Warrington, E. K., Crutch, S. J., & Fox, N. C. (2012) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2011.09.225 · Cited by 49 · see citing works
Neuroinflammation is increased in the parietal cortex of atypical Alzheimer’s disease
Boon, B. D. C., Hoozemans, J. J. M., Lopuhaä, B. V., Eigenhuis, K. N., Scheltens, P., Kamphorst, W., Rozemüller, A. J. M., & Bouwman, F. H. (2018) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1180-y · Cited by 47 · see citing works
Chapter 19 Visuospatial and visuoconstructive deficits
Trojano, L., & Conson, M. (2008) · Handbook of clinical neurology · doi:10.1016/s0072-9752(07)88019-5 · Cited by 48 · see citing works
Visuospatial dysfunction in the neurodegenerative diseases
Geldmacher, D. (2003) · Frontiers in bioscience · doi:10.2741/1143 · Cited by 47 · see citing works
Neurophysiologic analyses of low- and high-level visual processing in Alzheimer disease
Fernandez, R., Kavcic, V., & Duffy, C. J. (2007) · Neurology · doi:10.1212/01.wnl.0000264873.62313.81 · Cited by 46 · see citing works
Patterns of cognitive impairment in Alzheimer s disease assessment and differential diagnosis
Storey, E. (2002) · Frontiers in bioscience · doi:10.2741/a914 · Cited by 45 · see citing works
Computerized visual field defects in posterior cortical atrophy
Pelak, V. S., Smyth, S. F., Boyer, P. J., & Filley, C. M. (2011) · Neurology · doi:10.1212/wnl.0b013e31823e9f2a · Cited by 45 · see citing works
Category Specific Deficits in Alzheimer's Disease: Fact or Artefact?
Tippett, L. J., Meier, S. L., Blackwood, K., & Diaz-Asper, C. M. (2007) · Cortex · doi:10.1016/s0010-9452(08)70690-7 · Cited by 45 · see citing works
Tippett, L. J. (2003) · Neuropsychologia · doi:10.1016/s0028-3932(02)00140-9 · Cited by 45 · see citing works
Neuro-cognitive mechanisms of simultanagnosia in patients with posterior cortical atrophy
Neitzel, J., Ortner, M., Haupt, M., Redel, P., Grimmer, T., Yakushev, I. Y., Drzezga, A. E., Bublak, P., Preul, C., Sorg, C., et al. (2016) · Brain · doi:10.1093/brain/aww235 · Cited by 42 · see citing works
Visual Perceptual Organization Deficits in Alzheimer’s Dementia
Uhlhaas, P. J., Pantel, J., Lanfermann, H., Prvulovic, D., Haenschel, C., Maurer, K., & Linden, D. E. J. (2008) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000125671 · Cited by 42 · see citing works
Aβ1–42 stimulated T cells express P-PKC-δ and P-PKC-ζ in Alzheimer disease
Miscia, S., Ciccocioppo, F., Lanuti, P., Velluto, L., Bascelli, A., Pierdomenico, L., Genovesi, D., Di Siena, A., Santavenere, E., Gambi, F., et al. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.07.011 · Cited by 40 · see citing works
APOE is a correlate of phenotypic heterogeneity in Alzheimer disease in a national cohort
Weıntraub, S., Teylan, M., Rader, B. M., Chan, K. C. G., Bollenbeck, M., Kukull, W. A., Coventry, C., Rogalski, E. J., Bigio, E. H., & Mesulam, M. M. (2019) · Neurology · doi:10.1212/wnl.0000000000008666 · Cited by 40 · see citing works
Prominent effects and neural correlates of visual crowding in a neurodegenerative disease population
Yong, K. X. X., Shakespeare, T. J., Cash, D. M., Henley, S. M. D., Nicholas, J. M., Ridgway, G. R., Golden, H. L., Warrington, E. K., Carton, A. M., Kaski, D. N., et al. (2014) · Brain · doi:10.1093/brain/awu293 · Cited by 40 · see citing works
Visual impairments in dementia with Lewy bodies and posterior cortical atrophy.
Metzler‐Baddeley, C., Baddeley, R. J., Lovell, P. G., Laffan, A. J., & Jones, R. W. (2010) · Neuropsychology · doi:10.1037/a0016834 · Cited by 38 · see citing works
Abnormal visual phenomena in posterior cortical atrophy
Crutch, S. J., Lehmann, M., Gorgoraptis, N., Kaski, D. N., Ryan, N. S., Masud Husain, B., & Warrington, E. K. (2010) · Neurocase · doi:10.1080/13554794.2010.504729 · Cited by 39 · see citing works
Atypical Motor and Behavioral Presentations of Alzheimer Disease
Duker, A. P., Espay, A. J., Wszołek, Z. K., Rademakers, R., Dickson, D. W., & Kelley, B. J. (2012) · The Neurologist · doi:10.1097/nrl.0b013e3182675376 · Cited by 38 · see citing works
Pathology in Primary Progressive Aphasia Syndromes
Harris, J., & Jones, M. S. (2014) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-014-0466-4 · Cited by 38 · see citing works
Are Alzheimer's disease patients able to learn visual prototypes?
Kéri, S., Kálmán, J., Kelemen, O., Benedek, G., & Janka, Z. (2001) · Neuropsychologia · doi:10.1016/s0028-3932(01)00046-x · Cited by 38 · see citing works
Brain metabolic signatures across the Alzheimer’s disease spectrum
Sala, A., Caprioglio, C., Santangelo, R., Vanoli, E. G., Iannaccone, S., Magnani, G., & Perani, D. (2019) · European Journal of Nuclear Medicine and Molecular Imaging · doi:10.1007/s00259-019-04559-2 · Cited by 37 · see citing works
Crutch, S. J., & Warrington, E. K. (2009) · Cognitive Neuropsychology · doi:10.1080/02643290903465819 · Cited by 37 · see citing works
Yoshida, T., Shiga, K., Yoshikawa, K., Yamada, K., & Nakagawa, M. (2004) · European Neurology · doi:10.1159/000079750 · Cited by 36 · see citing works
“Apperceptive” Alexia in Posterior Cortical Atrophy
Mendez, M. F., Shapira, J. S., & Clark, D. G. (2007) · Cortex · doi:10.1016/s0010-9452(08)70481-7 · Cited by 35 · see citing works
Cortical Neuropathology in Aging and Dementing Disorders
Hof, P. R., Bouras, C., & Morrison, J. H. (1999) · Cerebral cortex · doi:10.1007/978-1-4615-4885-0_8 · Cited by 35 · see citing works
Self-citation
- Authors
- Hof, P. R., Vogt, B. A., Bouras, C., & Morrison, J. H.
- Affiliations
- Icahn School of Medicine at Mount Sinai (US)
- Atrium Health Wake Forest Baptist (US)
- University of Geneva (CH)
- Corresponding author
- Hof, Patrick R.
- Venue
- Vision Research
- Publisher
- Elsevier BV
- Published
- 1997-12
- Volume
- 37
- Issue
- 24
- Pages
- 3609-3625
- ISSN
- 0042-6989 (ISSN-L)
- OpenAlex
- W2064772069
- Cited by
- 246
- References
- 113
- Citations by year
- 2026: 11 · 2025: 4 · 2024: 1 · 2023: 2 · 2022: 4 · 2021: 3 · 2020: 5 · 2019: 10 · 2018: 7 · 2017: 12 · 2016: 9 · 2015: 11 · 2014: 15 · 2013: 12 · 2012: 18
- FWCI
- 4.90
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Vision Research (publishedVersion)
- PubMed (publishedVersion)
- Funders
- American Health Assistance Foundation (AG05138)
- Brookdale Foundation
- National Institutes of Health (5r01ag011480-03, AG06647, AG05138)
- National Institute on Aging (AG 05138, AG11480, P50AG005138, AG-06647)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Keywords
- Alzheimer's disease, posterior cortical atrophy, lesion distribution, circuit disconnection, posterior cingulate cortex, visual association areas, neurofibrillary tangles, amyloid plaques, visual disturbances
- MeSH terms
- Aged, Alzheimer Disease, Atrophy, Humans, Parietal Lobe, Vision Disorders, Visual Cortex, Plaque, Amyloid
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