The DOI matches its Crossref record; 41 of the 41 references it cites were found in a registry or an index.
The human entorhinal cortex: A cytoarchitectonic analysis
Abstract
The entorhinal cortex of man is in the medial aspect of the temporal lobe. As in other mammalian species, it constitutes an essential component of the hippocampal formation and the route through which the neocortex interacts with the hippocampus. The importance of knowing its architecture in detail arises from the possibility of extrapolating it to experimental findings, notably in the nonhuman primate. We have investigated the cytoarchitectonic features of the human entorhinal cortex by using as a base our previous study (D. G. Amaral, R. Insausti, and W. M. Cowan [1987] J. Comp. Neurol. 264:326–355) of the nonhuman primate entorhinal cortex. We prepared serial sections of the temporal lobe from 35 normal brains. Thionin‐ and myelin‐stained series were made of all cases. Sections spaced 500 μm apart through the full rostrocaudal extent of the entorhinal cortex were analyzed. The human entorhinal cortex is made up of six layers, of which layer IV does not appear throughout all subfields of the entorhinal cortex. The overall appearance resembles that of the adjacent neocortex in lateral and caudal portions. In harmony with general structural principles in the nonhuman primate entorhinal cortex, our analysis supports the partitioning of the human entorhinal cortex into eight different subfields. (1) The olfactory subfield (EO), the rostralmost field, is little laminated. (2) The lateral rostral subfield (ELr), laterally located, merges with the laterally adjacent perirhinal cortex. (3) The rostral subfield (ER) is between EO and ELr, with better differentiation of layers II and III than EO. (4) The medial intermediate subfield (EMI) is located at the medial border. (5) The intermediate field (EI) is a lateral continuation of EMI; lamina dissecans (layer IV) can be best appreciated in this field. (6) The lateral caudal subfield (ELc) laterally borders on EI as a continuation of ELr. (7) The caudal subfield (EC) lies caudal to the beginning of the hippocampal fissure, with a distinctive, clear space (Vc) between layers V and VI. (8) The caudal limiting field (ECL) forms the caudal termination of the entorhinal cortex. Thus our parcellation of the entorhinal cortex in man is largely parallel to that arrived at in the monkey. This close homology provides a rational basis for the application to clinical problems of anatomical and functional information obtained in experimental work in nonhuman primates.
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Citations
Cites
Neuropathological stageing of Alzheimer-related changes.
Braak, H., & Braak, E. (1991) · Acta Neuropathologica · doi:10.1007/bf00308809 · Cited by 16,123
Alzheimer's disease: cell-specific pathology isolates the hippocampal formation.
Hyman, B. T., Van Hoesen, G. W., Damasio, A. R., & Barnes, C. L. (1984) · Science · doi:10.1126/science.6474172 · Cited by 2,268
Zola-Morgan, S., Squire, L., & Amaral, D. (1986) · The Journal of Neuroscience · doi:10.1523/jneurosci.06-10-02950.1986 · Cited by 1,997
Silver Staining of Myelin by Means of Physical Development
Gallyas, F. (1979) · Neurological Research · doi:10.1080/01616412.1979.11739553 · Cited by 935
Activation of the hippocampus in normal humans: a functional anatomical study of memory.
Squire, L. R., Ojemann, J. G., Miezin, F. M., Petersen, S. E., Videen, T. O., & Raichle, M. E. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.5.1837 · Cited by 843
The entorhinal cortex of the monkey: II. Cortical afferents
Insausti, R., Amaral, D. G., & Cowan, W. M. (1987) · Journal of Comparative Neurology · doi:10.1002/cne.902640306 · Cited by 833
Self-citationPerforant 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
Architecture and Connections of Cortical Association Areas
Pandya, D. N., & Yeterian, E. H. (1985) · Cerebral Cortex · doi:10.1007/978-1-4757-9619-3_1 · Cited by 584
Some Cytoarchitectural Abnormalities of the Entorhinal Cortex in Schizophrenia
Arnold, S. E. (1991) · Archives of General Psychiatry · doi:10.1001/archpsyc.1991.01810310043008 · Cited by 526
Architectonics of the Human Telencephalic Cortex
Braak, H. (1980) · Studies of Brain Function · doi:10.1007/978-3-642-81522-5 · Cited by 508
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Pini, L., Pievani, M., Bocchetta, M., Altomare, D., Bosco, P., Cavedo, E., Galluzzi, S., Marizzoni, M., & Frisoni, G. B. (2016) · Ageing Research Reviews · doi:10.1016/j.arr.2016.01.002 · Cited by 836
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Doeller, C. F., Barry, C., & Burgess, N. (2010) · Nature · doi:10.1038/nature08704 · Cited by 828
Rempel-Clower, N. L., Zola, S. M., Squire, L. R., & Amaral, D. G. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-16-05233.1996 · Cited by 818
Karege, F., Vaudan, G., Schwald, M., Perroud, N., & La Harpe, R. (2005) · Molecular Brain Research · doi:10.1016/j.molbrainres.2004.12.020 · Cited by 600
Metadata
- Authors
- Insausti, R., Tuñón, T., Sobreviela, T., Insausti, A. M., & Gonzalo, L. M.
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1995-05
- Volume
- 355
- Issue
- 2
- Pages
- 171-198
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W1976405656
- Cited by
- 275
- References
- 41
- FWCI
- 5.81
- Type
- journal article
- Language
- en
- Open access
- closed
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