The DOI matches its Crossref record; 110 of the 113 references it cites were found in a registry or an index.
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.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“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]
In the citing paper
“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]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
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
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
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 2,663
(1909) · Cited by 2,575
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 1,434
Dissociation of Object and Spatial Processing Domains in Primate Prefrontal Cortex
Wilson, F. A. W., Scalaidhe, S. P., & Goldman, P. S. (1993) · Science · doi:10.1126/science.8316836 · Cited by 1,408
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
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
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
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
Research works printed but not linked: 7
- Ceccaldi, 1995, Apraxie unilatérale gauche d'aggravation progressive dans deux cas de maladie d'Alzheimer, Revue Neurologique (Paris), 151, 240
- Croisile, 1991, Désordres visuo-constructifs et alexieagraphie associés à une atrophie corticale postérieure, Revue Neurologique (Paris), 147, 138
- Grünthal, 1928, Zur Himpathologischen Analyse der Alzheimerschen Krankheit, Psychiatrisch-Neurologische Wochenschrift, 36, 401
- Jacquet, 1990, L'atrophie corticale postérieure: variante anatomo-clinique de la maladie d'Alzheimer, Acta Neurologica Belgica, 90, 265
- Magnani, 1982, Lesioni atrofiche bioccipitali di incerta natura all'origine di una agnosia visiva, Rivista di Neurologia, 52, 137
- Mirra, 1993, Making the diagnosis of Alzheimer's disease, Archives of Pathology and Laboratory Medicine, 117, 132
- Young, 1995, NeuroZoom: computer software for quantitative neuroanatomic mapping and stereology, Society for Neuroscience Abstracts, 21, 1078
Cited by
Sorted by citations
Items 201–246 of 246
Spoken discourse in Alzheimer' disease: a review
Ahmed, S., & Garrard, P. (2012) · Linguistica · doi:10.4312/linguistica.52.1.9-25 · Cited by 3
Neuroanatomy of Apraxia and Visual Agnosia in Alzheimer�s Disease
Bouras, C., Gold, G., K�vari, E., Vallet, P. G., Duc, M., Michel, J., Hof, P. R., & Giannakopoulos, P. (1999) · KARGER eBooks · doi:10.1159/000061432 · Cited by 1
Self-citationYeast as a Model for Studying Aβ Aggregation, Toxicity and Clearance
Bharadwaj, P. (2011) · Australasian Journal of Paramedicine · Cited by 1
Perception and cognition in aging and Alzheimer‘s disease : visual psychophysics and neurophysiology
Monacelli, A., & Duffy, C. J. (n.d.) · UR Research (University of Rochester) · Cited by 1
Modelling the Neuroanatomical Progression of Alzheimer's Disease and Posterior Cortical AtrophyPreprint
Marinescu, R. V. (2020) · arXiv (Cornell University) · doi:10.48550/arxiv.2003.04805 · Cited by 1
Kurrle, S. E., Brodaty, H., & Hogarth, R. (2012) · Cambridge University Press eBooks · doi:10.1017/cbo9780511894534.010
Similarities of Visual Deficits in Alzheimer's Disease and Down Syndrome
Rocco, F. J. (2004) · KARGER eBooks · doi:10.1159/000080003
(1999) · Techniques in the behavioral and neural sciences · doi:10.1016/s0921-0709(99)80005-4
Neurobiologic Basis of Age-Related Dementing Disorders
Hof, P. R., Bussière, T., Buxbaum, J. D., & Morrison, J. H. (2006) · Springer eBooks · doi:10.1007/0-387-22621-4_76
Self-citation18F-FDG-PET and Neuropsychological Testing in Different Types of Neurodegenerative Dementias
Sydykova, D. (2007) · Elektronische Hochschulschriften der LMU München (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.6568
P4‐238: The syndrome of progressive posterior cortical dysfunction: A multiple case study
Areza‐Fegyveres, R., Caramelli, P., Porto, C. S., Ono, C. R., Buchpiguel, C. A., & Nitríni, R. (2009) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2009.04.704
A komplex vizuális környezet kategorizációjának neurofiziológiai mechanizmusai
Kéri, S., & Antal, A. (2001) · Magyar Pszichológiai Szemle · doi:10.1556/mpszle.55.2000.4.7
Imagerie du chiasma optique et des voies optiques rétro-chiasmatiques
de Champfleur, N. M., de Champfleur, S. M., Leboucq, N., Damien Galanaud, E., & Bonafé, A. (2013) · Journal de radiologie diagnostique et interventionnelle · doi:10.1016/j.jradio.2013.04.011
Atypical posterior cortical atrophy: a diagnostic and treatment dilemma
Williamson, P. (2006) · Acta Psychiatrica Scandinavica · doi:10.1111/j.1600-0447.2006.00779.x
Rodríguez, A. C. (2015) · UVaDOC UVaDOC University of Valladolid Documentary Repository (University of Valladolid) · doi:10.35376/10324/16526
Recipes no longer a piece of cake
Ryan, N. S., & Rossor, M. N. (2016) · doi:10.1093/med/9780199664771.003.0003
Posterior Cortical Atrophy and Dementia
Alagiakrishnan, K., Khan, K. A., & Saqqur, M. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-407824-6.00013-6
Cognitive impairment in Alzheimer's disease: An investigation using colour tasks.
Pringle, H. (2002) · Surrey Research Insight Open Access (The University of Surrey)
Visual Impairments in Dementia With Lewy Bodies and Posterior
Atrophy, C., Metzler‐Baddeley, C., Baddeley, R. J., Lovell, P. G., Laffan, A. J., & Jones, R. W. (2010)
Richards, L., & Woods, A. J. (2017) · Springer eBooks · doi:10.1007/978-3-319-56782-2_9108-1
Fonseca, L. M. (2019) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2019.tde-11022019-162727
The postsynaptic protein neurogranin: a new item in the Alzheimer’s disease biomarker toolbox
Kvartsberg, H. (2019) · Gothenburg University Publications Electronic Archive (Gothenburg University)
Experience Dependent Cross-modal Regulation of Cortical Circuitry
Petrus, E. (2014)
Lee, J. M., & Picken, M. M. (2012) · Humana Press eBooks · doi:10.1007/978-1-60761-389-3_7
Hillis, A. E. (2008) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1108393.564437
Chen, A., & Lee, A. G. (2019) · Springer eBooks · doi:10.1007/978-3-030-04019-2_9
Posterior cortical atrophy in logopenic progressive aphasia: A case report
Kumar, D. J., Goyal, S., Arshad, F., Vandana, V. P., Ramakrishnan, S., & Alladi, S. (2022) · Frontiers in Communication · doi:10.3389/fcomm.2022.979475
Gerhand, S. (2024) · Cambridge University Press eBooks · doi:10.1017/9781009025911.006
Abdi, Z., Harding, E., Pelak, V. S., Yong, K. X. X., & Crutch, S. J. (2025) · Cambridge University Press eBooks · doi:10.1017/9781108985055.016
Kim, E., Vatsavayai, S. C., & Seeley, W. W. (2025) · Cambridge University Press eBooks · doi:10.1017/9781108985055.004
da Silva, M.-N. M., James-Galton, M., Green, C. K., & Plant, G. T. (2026) · Frontiers in Neurology · doi:10.3389/fneur.2026.1759440
Posterior Cortical Atrophy in the Asia‐Pacific: A Report From the PCA Asian Workgroup
Likitjaroen, Y., Chang, Y., Lim, L., Chiu, P., Hsu, J., Kim, S., Narita, W., Ryoo, N. Y., Suzuki, K., Kandiah, N., et al. (2026) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.70347
Napolitano, L. (2026) · Firenze University Press eBooks · doi:10.36253/979-12-215-0993-9.05
Napolitano, L. (2026) · Firenze University Press eBooks · doi:10.36253/979-12-215-0993-9.references
Napolitano, L. (2026) · Firenze University Press eBooks · doi:10.36253/979-12-215-0993-9.07
Third Section: Design of a dimeric-nanobody specific for Aβ42 oligomers: the Dimeric-DesAb-O
Napolitano, L. (2026) · Firenze University Press eBooks · doi:10.36253/979-12-215-0993-9.06
Napolitano, L. (2026) · Firenze University Press eBooks · doi:10.36253/979-12-215-0993-9
Napolitano, L. (2026) · Firenze University Press eBooks · doi:10.36253/979-12-215-0993-9.03
Napolitano, L. (2026) · Firenze University Press eBooks · doi:10.36253/979-12-215-0993-9.04
Napolitano, L. (2026) · Firenze University Press eBooks · doi:10.36253/979-12-215-0993-9.02
Conclusion and Future Perspectives
Napolitano, L. (2026) · Firenze University Press eBooks · doi:10.36253/979-12-215-0993-9.08
Ritter, E. (2007) · OpenGrey (Institut de l'Information Scientifique et Technique)
Metadata
- 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
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › 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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review