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 101–200 of 246
Severe degenerative cortical and cerebellar atrophy and progressive dementia in a young adult
Markowitsch, H. J., Kessler, J., Schramm, U., & Frölich, L. (2000) · Neurocase · doi:10.1080/13554790008402783 · Cited by 35
Cue integration for the perception and control of self-movement in ageing and Alzheimer's disease
Mapstone, M. E., Logan, D., & Duffy, C. J. (2006) · Brain · doi:10.1093/brain/awl201 · Cited by 34
Agosta, F., Mandić‐Stojmenović, G., Canu, E., Stojković, T., Imperiale, F., Caso, F., Stefanova, E. D., Copetti, M., Kostić, V., & Filippi, M. (2018) · NeuroImage Clinical · doi:10.1016/j.nicl.2018.06.013 · Cited by 35
A Patient with Posterior Cortical Atrophy Possesses a Novel Mutation in the Presenilin 1 Gene
Sitek, E. J., Narożańska, E., Pepłońska, B., Filipek, S., Barczak, A. K., Styczyńska, M., Młynarczyk, K., Brockhuis, B., Portelius, E., Religa, D., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0061074 · Cited by 33
The Neuropsychiatric Profile of Posterior Cortical Atrophy
Isella, V., Villa, G., Mapelli, C., Ferri, F., Appollonio, I. M., & Ferrarese, C. (2014) · Journal of Geriatric Psychiatry and Neurology · doi:10.1177/0891988714554713 · Cited by 32
Kito, H., Ryokawa, A., Kinoshita, Y., Sasayama, D., Sugiyama, N., Ogihara, T., Yasaki, T., Hagiwara, T., Inuzuka, S., Takahashi, T., et al. (2014) · Behavioral and Brain Functions · doi:10.1186/1744-9081-10-8 · Cited by 32
Classification learning in Alzheimer's disease.
Kéri, S., Kálmán, J., Rapcsak, S., Antal, A., Benedek, G., & Janka, Z. (1999) · Brain : a journal of neurology · doi:10.1093/brain/122.6.1063 · Cited by 36
Hémianopsie latérale homonyme et atrophie corticale postérieure
Formaglio, M., Krolak‐Salmon, P., Tilikete, C., Bernard, M., Croisile, B., & Vighetto, A. (2009) · Revue Neurologique · doi:10.1016/j.neurol.2008.10.010 · Cited by 31
(Con)text-specific effects of visual dysfunction on reading in posterior cortical atrophy
Yong, K. X. X., Shakespeare, T. J., Cash, D. M., Henley, S. M. D., Warren, J. D., & Crutch, S. J. (2014) · Cortex · doi:10.1016/j.cortex.2014.03.010 · Cited by 31
Neurochemical organization of the primate visual cortex
Morrison, J. H., Hof, P. R., & Huntley, G. W. (1998) · Handbook of chemical neuroanatomy · doi:10.1016/s0924-8196(98)80004-3 · Cited by 31
Self-citationHayashi, R., Yamaguchi, S., Narimatsu, T., Miyata, H., Katsumata, Y., & Mimura, M. (2017) · Case Reports in Neurology · doi:10.1159/000481304 · Cited by 30
Neuronal Representations of Value
Platt, M. L., & Padoa‐Schioppa, C. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-374176-9.00029-4 · Cited by 31
Chapter VIII Primate cingulate cortex chemoarchitecture and its disruption in Alzheimer's disease
Vogt, B. A., Vogt, L. J., Nimchinsky, E. A., & Hof, P. R. (1997) · Handbook of chemical neuroanatomy · doi:10.1016/s0924-8196(97)80010-3 · Cited by 32
Self-citation3D Shape Perception in Posterior Cortical Atrophy: A Visual Neuroscience Perspective
Gillebert, C. R., Schaeverbeke, J. M., Bastin, C., Neyens, V., Bruffaerts, R., Weer, A. D., Seghers, A., Sunaert, S. G., Laere, K. V., Versijpt, J. J., et al. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3651-14.2015 · Cited by 29
Yamashita, A., Fuchs, E., Taira, M., Yamamoto, T., & Hayashi, M. (2012) · Journal of Medical Primatology · doi:10.1111/j.1600-0684.2012.00540.x · Cited by 28
Visuospatial Deficits with Preserved Reading Ability in a Patient with Posterior Cortical Atrophy
Mendez, M. F. (2001) · Cortex · doi:10.1016/s0010-9452(08)70592-6 · Cited by 29
Ocular Motility of Aging and Dementia
Pelak, V. S. (2010) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-010-0137-z · Cited by 29
Morgan, B. E., Gross, R. G., Clark, R., Dreyfuss, M., Boller, A., Camp, E., Liang, T., Avants, B., McMillan, C. T., & Grossman, M. (2011) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2011.09.005 · Cited by 29
Visualizing the emergence of posterior cortical atrophy
Kennedy, J., Lehmann, M., Sokolska, M., Archer, H. A., Warrington, E. K., Fox, N. C., & Crutch, S. J. (2011) · Neurocase · doi:10.1080/13554794.2011.588180 · Cited by 28
Disturbed visual processing contributes to impaired reading in Alzheimer's disease
Glosser, G. (2002) · Neuropsychologia · doi:10.1016/s0028-3932(01)00165-8 · Cited by 27
The temporal lobe in typical and atypical Alzheimer disease
Migliaccio, R., & Cacciamani, F. (2022) · Handbook of clinical neurology · doi:10.1016/b978-0-12-823493-8.00004-3 · Cited by 26
Newberg, A. B., Cotter, A. W., Udeshi, M., BRINKMAN, F., Glosser, G., Alavi, A. A., & Clark, C. (2003) · Nuclear Medicine Communications · doi:10.1097/01.mnm.0000080249.50447.99 · Cited by 26
Semantic word category processing in semantic dementia and posterior cortical atrophy
Shebani, Z., Patterson, K. E., Nestor, P. J., Diaz-de-Grenu, L. Z., Dawson, K. E., & Friedemann Pulvermüller, A. (2017) · Cortex · doi:10.1016/j.cortex.2017.04.016 · Cited by 28
Kéri, S., Antal, A., Kálmán, J., Janka, Z., & Benedek, G. (1999) · Vision Research · doi:10.1016/s0042-6989(98)00310-1 · Cited by 25
Imaging of the optic chiasm and retrochiasmal visual pathways
de Champfleur, N. M., de Champfleur, S. M., Damien Galanaud, E., Leboucq, N., & Bonafé, A. (2013) · Diagnostic and Interventional Imaging · doi:10.1016/j.diii.2013.06.012 · Cited by 22
Hyperphosphorylated Tau in the Occipital Cortex in Aged Nondemented Subjects
Pikkarainen, M., Kauppinen, T., & Alafuzoff, I. (2009) · Journal of Neuropathology and Experimental Neurology · doi:10.1097/nen.0b013e3181a6ee45 · Cited by 21
Wang, X., Lü, H., Shi, Z., Cai, L., Liu, S., Liu, S., Han, T., Wang, Y., Zhou, Y., Wang, X., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0134956 · Cited by 20
Everyday executive functioning influences adaptive skills in autism spectrum disorders
Peterson, R. K., Noggle, C. A., Thompson, J. C., & Davis, J. J. (2015) · Neuropsychological Trends · doi:10.7358/neur-2015-018-pete · Cited by 20
BACE1 Is Necessary for Experience-Dependent Homeostatic Synaptic Plasticity in Visual Cortex
Petrus, E., & Lee, H.-K. (2014) · Neural Plasticity · doi:10.1155/2014/128631 · Cited by 19
The Visual Agnosias and Related Disorders
Haque, S., Vaphiades, M. S., & Lueck, C. J. (2017) · Journal of Neuro-Ophthalmology · doi:10.1097/wno.0000000000000556 · Cited by 20
Glick-Shames, H., Backner, Y., Bick, A. S., Raz, N., & Levin, N. (2018) · Brain Imaging and Behavior · doi:10.1007/s11682-018-9952-7 · Cited by 19
Nawrot, M. (2003) · Neurologic Clinics · doi:10.1016/s0733-8619(02)00126-3 · Cited by 18
Dysfunctional visual word form processing in progressive alexia
Wilson, S. M., Rising, K., Stib, M. T., Rapcsak, S. Z., & Beeson, P. M. (2013) · Brain · doi:10.1093/brain/awt034 · Cited by 18
Noroozıan, M. (2015) · Neurologic Clinics · doi:10.1016/j.ncl.2015.08.005 · Cited by 18
Disentangling Heterogeneity in Alzheimer’s Disease: Two Empirically-Derived Subtypes
Blanken, A. E., Dutt, S., Li, Y., Nation, D. A., & Initiative, A. D. N. (2019) · Journal of Alzheimer s Disease · doi:10.3233/jad-190230 · Cited by 16
The neuropsychological and neuroradiological correlates of slowly progressive visual agnosia
Gıovagnolı, A. R., Aresi, A., Reati, F., Riva, A., Gobbo, C. L., & Bizzi, A. (2009) · Neurological Sciences · doi:10.1007/s10072-009-0019-9 · Cited by 16
Color Vision, Object Recognition, and Spatial Localization in Aging and Alzheimer's Disease
Cronin‐Golomb, A. (2001) · Elsevier eBooks · doi:10.1016/b978-012351830-9/50038-x · Cited by 16
Glial reaction in aging and Alzheimer's disease
Unger, J. W. (1998) · Microscopy Research and Technique · doi:10.1002/(sici)1097-0029(19981001)43:1 · Cited by 103
Prodromal posterior cortical atrophy: clinical, neuropsychological, and radiological correlation
Chan, L., Lynch, W., May, M. G. D., Horton, J. C., Miller, B. L., & Rabinovici, G. D. (2013) · Neurocase · doi:10.1080/13554794.2013.860176 · Cited by 16
Modeling Neurodegeneration in silico With Deep Learning
Tuladhar, A., Moore, J. A., Ismail, Z., & Forkert, N. D. (2021) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2021.748370 · Cited by 17
Complex visual hallucination and mirror sign in posterior cortical atrophy
Yoshida, T., Yuki, N., & Nakagawa, M. (2006) · Acta Psychiatrica Scandinavica · doi:10.1111/j.1600-0447.2006.00778.x · Cited by 15
Corticostriatal circuitry mediates fast-track visual categorization
Antal, A., Kéri, S., Kincses, Z. T., Kálmán, J., Dibó, G., Benedek, G., Janka, Z., & Vécsei, L. (2002) · Cognitive Brain Research · doi:10.1016/s0926-6410(01)00089-1 · Cited by 15
RE-PERG in early-onset Alzheimer’s disease: A double-blind, electrophysiological pilot study
Mavilio, A., Sisto, D., Prete, F., Guadalupi, V., Dammacco, R., & Alessio, G. (2020) · PLoS ONE · doi:10.1371/journal.pone.0236568 · Cited by 13
Magnocellular Deficit Hypothesis in Alzheimer's Disease
Gilmore, G. C., Morrison, S. R., & Groth, K. E. (2004) · KARGER eBooks · doi:10.1159/000080005 · Cited by 14
Posterior cortical atrophy: an exemplar for renovating diagnostic formulation in neuropsychiatry
Goldstein, M. A., Ivanov, I., & Silverman, M. E. (2010) · Comprehensive Psychiatry · doi:10.1016/j.comppsych.2010.06.013 · Cited by 14
How the cognitive reserve interacts with β-amyloid deposition in mitigating FDG metabolism
Carapelle, E., Serra, L., Modoni, S., Falcone, M., Caltagirone, C., Bozzali, M., Specchio, L. M., & Avolio, C. (2017) · Medicine · doi:10.1097/md.0000000000005876 · Cited by 13
Environmental reduplicative paramnesia in a case of atypical Alzheimer’s disease
von Gunten, A., Miklossy, J., Suvà, M.-L., Hof, P. R., & Glannakopoulos, P. (2005) · Neurocase · doi:10.1080/13554790590944825 · Cited by 13
Self-citationEarly Alzheimer's disease blocks responses to accelerating self-movement
Fernandez, R., & Duffy, C. J. (2012) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.12.031 · Cited by 13
Beaufils, É., Ribeiro, M. J., Vierron, E., Vercouillie, J., Dufour‐Rainfray, D., Cottier, J., Camus, V., Mondon, K., Guilloteau, D., & Hommet, C. (2014) · Dementia and Geriatric Cognitive Disorders Extra · doi:10.1159/000363761 · Cited by 12
Bilateral parietal dysfunctions and disconnections in simultanagnosia and Bálint syndrome
Chechlacz, M. (2018) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63622-5.00012-7 · Cited by 12
Kincses, Z. T., Chadaide, Z., Varga, E. T., Antal, A., & Paulus, W. (2006) · Brain Research · doi:10.1016/j.brainres.2006.07.044 · Cited by 12
Tang‐Wai, D. F., Josephs, K. A., & Petersen, R. C. (2005) · Cambridge University Press eBooks · doi:10.1017/cbo9780511544873.029 · Cited by 11
The Anterior Visual System and Circadian Function with Reference to Alzheimer's Disease
Valenti, D. A. (2004) · KARGER eBooks · doi:10.1159/000079995 · Cited by 11
Salmon, D. P., Smirnov, D. S., Coughlin, D. G., Hamilton, J. M., Landy, K. M., Filoteo, J. V., Hiniker, A. O., Hansen, L. A., & Galasko, D. R. (2022) · Neurology · doi:10.1212/wnl.0000000000201068 · Cited by 10
New Learning and Remote Memory in Atypical Alzheimer's Disease
Thompson, J. C., BESWICK, T., Foster, J. K., & Snowden, J. S. (2003) · Cortex · doi:10.1016/s0010-9452(08)70862-1 · Cited by 10
Effect of age at onset on cortical thickness and cognition in posterior cortical atrophy
Gonzalez, A. S., Lehmann, M., Shakespeare, T. J., Yong, K. X. X., Paterson, R. W., Slattery, C. F., Foulkes, A., Rabinovici, G. D., Gil-Neciga, E., Lora, F. R., et al. (2016) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.04.012 · Cited by 10
The syndrome of progressive posterior cortical dysfunction: A multiple case study and review
Areza‐Fegyveres, R., Caramelli, P., Porto, C. S., Ono, C. R., Buchpiguel, C. A., & Nitríni, R. (2007) · Dementia & Neuropsychologia · doi:10.1590/s1980-57642008dn10300014 · Cited by 9
Looking into posterior cortical atrophy
Tang‐Wai, D. F., & Graff‐Radford, N. R. (2011) · Neurology · doi:10.1212/wnl.0b013e31821ccd4f · Cited by 9
Posterior Cortical Atrophy: A Visual Variant of Alzheimer's Disease
Mendez, M. F. (2004) · KARGER eBooks · doi:10.1159/000080001 · Cited by 8
Kim, E.-J., Vatsavayai, S., & Seeley, W. W. (2016) · The Behavioral Neurology of Dementia · doi:10.1017/9781139924771.008 · Cited by 7
Hemispheric Asymmetry and Atypical Lobar Progression of Alzheimer-Type Tauopathy
Tremblay, C., Serrano, G. E., Intorcia, A. J., Curry, J. R., Sue, L. I., Nelson, C. M., Walker, J. E., Glass, M. J., Arce, R. A., Fleisher, A., et al. (2022) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlac008 · Cited by 8
Visual field defect as an uncommon presentation of posterior cortical atrophy
Shea, Y. F., & Chu, L. (2014) · Geriatrics and gerontology international/Geriatrics & gerontology international · doi:10.1111/ggi.12203 · Cited by 7
Convergence Along the Visual Hierarchy Is Altered in Posterior Cortical Atrophy
de Best, P. B., Abulafia, R., McKyton, A., & Levin, N. (2020) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.61.11.8 · Cited by 7
Visual impairment and posterior cortical atrophy preceding rapid progressive dementia
Müller, K. I., & Bekkelund, S. I. (2013) · BMJ Case Reports · doi:10.1136/bcr-2012-007624 · Cited by 6
Chapter 27 Neuropsychology of Alzheimer's disease
Albert, M. (2008) · Handbook of clinical neurology · doi:10.1016/s0072-9752(07)88027-4 · Cited by 6
Vogt, B. A., Vogt, L. J., & Hof, P. R. (2001) · Elsevier eBooks · doi:10.1016/b978-012351830-9/50012-3 · Cited by 6
Self-citationOrtner, M., & Kurz, A. (2015) · Der Nervenarzt · doi:10.1007/s00115-015-4265-1 · Cited by 5
Amyloid Deposition in the Central Nervous System
Rodríguez, F. J., Picken, M. M., & Lee, J. M. (2015) · Current clinical pathology · doi:10.1007/978-3-319-19294-9_8 · Cited by 5
Das, G. C., Dubey, S., Sinharoy, U., Mukherjee, A., Banerjee, S., Lahiri, D., & Biswas, A. (2020) · Acta Neurologica Belgica · doi:10.1007/s13760-020-01547-4 · Cited by 5
Posterior cortical atrophy with unilateral occipito-temporal degeneration
Koch, G., Stefani, A., Panella, M., Giordano, A., Schillaci, O., & Marfia, G. A. (2004) · Journal of Neurology · doi:10.1007/s00415-004-0573-2 · Cited by 5
Multifocal Cortical Neurodegeneration in Alzheimer’s Disease
Vogt, B. A., Martin, A. D., Vrana, K. E., Absher, J. R., Vogt, L. J., & Hof, P. R. (1999) · Cerebral cortex · doi:10.1007/978-1-4615-4885-0_16 · Cited by 5
Self-citationAtrophie corticale postérieure
Sarazin, M., Kas, A., Habert, M., Samri, D., Dubois, B., & de Souza, L. C. (2013) · Encyclopédie médico-chirurgicale. Neurologie · doi:10.1016/s0246-0378(13)59694-1 · Cited by 4
Fung, E. Y. S., & Herring, M. O. (2019) · Springer eBooks · doi:10.1007/978-1-4939-8722-1_13 · Cited by 4
What’s “up”? Impaired Spatial Preposition Processing in Posterior Cortical Atrophy
Shebani, Z., Nestor, P. J., & Friedemann Pulvermüller, A. (2021) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2021.731104 · Cited by 5
Visual disturbances in cortical degenerative disorders
Pelak, V. S. (2009) · Expert Review of Ophthalmology · doi:10.1586/eop.09.18 · Cited by 4
Ahmed, M., & Phillips, M. (2011) · Elsevier eBooks · doi:10.1016/b978-0-323-05929-9.10008-5 · Cited by 4
Locomotion and eye behaviour under controlled environment in individuals with Alzheimer's disease
Suzuki, T., Yong, K. X. X., Yang, B., Carton, A. M., McCarthy, I., Papadosifos, N. N., Boampong, D. K., Holloway, C., Tyler, N., & Crutch, S. J. (2015) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/embc.2015.7319904 · Cited by 3
Abdi, Z., Yong, K. X. X., Schott, J. M., Gatt, A. P., Révész, T., Crutch, S. J., & Lashley, T. (2025) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.70007 · Cited by 5
Posterior Cortical Atrophy: Advice for Diagnosis and Implications for Management
Shakespeare, T. J., Crutch, S. J., & Fox, N. C. (2012) · Neurodegenerative Disease Management · doi:10.2217/nmt.12.61 · Cited by 3
Camsari, G. B., Murray, M. E., & Graff‐Radford, N. R. (2016) · Neurologic Clinics · doi:10.1016/j.ncl.2016.04.008 · Cited by 3
Neuropathological Changes in Visuospatial Systems in Alzheimer's Disease
von Gunten, A., Giannakopoulos, P., Bouras, C., & Hof, P. R. (2004) · KARGER eBooks · doi:10.1159/000079968 · Cited by 3
Self-citationRoytman, M., & Ivanidze, J. (2021) · Springer eBooks · doi:10.1007/978-3-030-82367-2_24 · Cited by 3
Presenile dementia diagnosed as posterior cortical atrophy
TSUNODA, A., Iritani, S., & Ozaki, N. (2011) · Psychogeriatrics · doi:10.1111/j.1479-8301.2011.00366.x · Cited by 2
Salman, Y., Huyghe, L., Quenon, L., Ghysens, O., Malotaux, V., Tomé, S. O., Thal, D. R., & Hanseeuw, B. J. (2025) · Journal of Alzheimer s Disease · doi:10.1177/13872877251314199 · Cited by 2
Tippett, L. J. (2004) · KARGER eBooks · doi:10.1159/000080007 · Cited by 2
Reading and Visual Processing in Alzheimer's Disease
Glosser, G., & Grossman, M. (2004) · KARGER eBooks · doi:10.1159/000080011 · Cited by 2
Closing the Window of Spatial Attention: Effects on Navigational Cue Use In Alzheimer's Disease
Mapstone, M. E., & Weıntraub, S. (2004) · KARGER eBooks · doi:10.1159/000080014 · Cited by 2
Caravaglios, G., Castro, G., Muscoso, E. G., & Balconi, M. (2015) · Neuropsychological Trends · doi:10.7358/neur-2015-018-cara · Cited by 2
Posterior cortical atrophy: a single case cognitive and radiological follow-up
Esteves, S., Romero, D. A. R., Torralva, T., Cuitiño, M. M., Herndon, S., Couto, B., Ibáñez, A. M., Manes, F. F., & Roca, M. (2018) · Neurocase · doi:10.1080/13554794.2017.1421667 · Cited by 2
Non-Parametric Mixture Modelling and its Application to Disease Progression ModellingPreprint
Firth, N. C., Oxtoby, N. P., Primativo, S., Brotherhood, E., Young, A. L., Yong, K. X. X., Crutch, S. J., & Alexander, D. C. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/297978 · Cited by 2
Richards, L., & Woods, A. J. (2018) · Springer eBooks · doi:10.1007/978-3-319-57111-9_9108 · Cited by 2
Pietrini, P., Furey, M. L., Guazzelli, M., & Alexander, G. E. (2001) · Elsevier eBooks · doi:10.1016/b978-012351830-9/50020-2 · Cited by 2
Posterior cortical atrophy – clinical manifestation, differential diagnosis and management
Oddział Alzheimerowski, K. N., Barczak, A. K., Sitek, E. J., & Oddział Neurologiczny i Oddział Udarowy, S. S. W. (2014) · Aktualności Neurologiczne · doi:10.15557/an.2014.0021 · Cited by 1
Chapter 14 Cognitive Neuropsychology of Dementia Syndromes
Warren, J. D., & Warrington, E. K. (2007) · Blue books of neurology · doi:10.1016/s1877-184x(09)70065-6 · Cited by 1
Posteriore kortikale Atrophie: Pathologie, Diagnostik und Behandlung einer seltenen Form der Demenz
Ortner, M., & Kurz, A. (2015) · Der Nervenarzt · Cited by 1
Troubles visuels au cours de la maladie d'Alzheimer
Leruez, S., Annweiler, C., Etcharry‐Bouyx, F., Verny, C., Beauchet, O., & Miléa, D. (2011) · Encyclopédie médico-chirurgicale. Ophtalmologie · doi:10.1016/s0246-0343(11)45091-7 · Cited by 1
Lee, A. G. (2009) · Springer eBooks · doi:10.1007/978-1-4419-0014-2_9 · Cited by 1
TANTI, A. D., & Saviola, D. (2015) · Neuropsychological Trends · doi:10.7358/neur-2015-018-deta · Cited by 1
Architecture of the motor and premotor cortex of the capuchin monkey
Magalhães-Junior, E. G., Mayer, A., Nascimento‐Silva, M. L., Bonfim, V., Lima, B., Gattass, R., & Soares, J. G. M. (2023) · Frontiers in Mammal Science · doi:10.3389/fmamm.2023.1215424 · Cited by 1
Posterior cortical atrophy of a suspected non-Alzheimer type: a case report
Wagner, M. T., Szeles, D. M., Mulder, B., Sohn, M., & Walker, A. (2017) · The Clinical Neuropsychologist · doi:10.1080/13854046.2017.1391331 · Cited by 1
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
