Calcium-binding protein (calbindin-D28K) and parvalbumin immunocytochemistry in the normal and epileptic human hippocampus.

Studies on the structure of the cerebral cortex. II. Continuation of the study of the ammonic system.

de Nó, R. L. (1934) · Cited by 1,974

EPILEPSY AND THE TEMPORAL LOBES

Margerison, J. H., & Corsellis, J. (1966) · Brain · doi:10.1093/brain/89.3.499 · Cited by 1,260

Greenfield's Neuropathology

Lantos, P. L. (1985) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.48.5.496 · Cited by 1,156

Decreased Hippocampal Inhibition and a Selective Loss of Interneurons in Experimental Epilepsy

Sloviter, R. S. (1987) · Science · doi:10.1126/science.2879352 · Cited by 1,082

Permanently altered hippocampal structure, excitability, and inhibition after experimental status epilepticus in the rat: The “dormant basket cell” hypothesis and its possible relevance to temporal lobe epilepsy

Sloviter, R. S. (1991) · Hippocampus · doi:10.1002/hipo.450010106 · Cited by 707

Calcium‐binding protein (calbindin‐D 28k ) and parvalbumin immunocytochemistry: Localization in the rat hippocampus with specific reference to the selective vulnerability of hippocampal neurons to seizure activity

Sloviter, R. S. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902800203 · Cited by 686

Granule cell dispersion in the dentate gyrus of humans with temporal lobe epilepsy

Houser, C. R. (1990) · Brain Research · doi:10.1016/0006-8993(90)91601-c · Cited by 604

GABAergic neurons containing the Ca2+-binding protein parvalbumin in the rat hippocampus and dentate gyrus

Kosaka, T., Katsumaru, H., Hama, K., Wu, J.-Y., & Heizmann, C. W. (1987) · Brain Research · doi:10.1016/0006-8993(87)90575-0 · Cited by 536

Immunohistochemical localization of calcium-binding protein in the cerebellum, hippocampal formation and olfactory bulb of the rat

Baimbridge, K. G., & Miller, J. J. (1982) · Brain Research · doi:10.1016/0006-8993(82)90804-6 · Cited by 487

The Neuropathology of Temporal Lobe Epilepsy

Bruton, C. J. (1988) · Medical Entomology and Zoology · Cited by 398

Degree and pattern of calbindin immunoreactivity in granule cells of the dentate gyrus differ in mesial temporal sclerosis, cortical malformation- and tumor-related epilepsies

Ábrahám, H., Richter, Z., Gyimesi, C., Horváth, Z., Janszky, J., Doczi, T. P., & Seress, L. (2011) · Brain Research · doi:10.1016/j.brainres.2011.05.010 · Cited by 28

The hippocampus of the eastern rock sengi: cytoarchitecture, markers of neuronal function, principal cell numbers, and adult neurogenesis

Slomianka, L., Drenth, T., Cavegn, N., Menges, D., Lazic, S., Phalanndwa, M., Chimimba, C., & Amrein, I. (2013) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2013.00034 · Cited by 24

Morphologic and Neurochemical Abnormalities in the Auditory Brainstem of the Genetically Epilepsy‐prone Hamster (GPG/Vall)

Fuentes‐Santamaría, V., Cantos, R., Alvarado, J. C., García‐Atarés, N., & López, D. E. (2005) · Epilepsia · doi:10.1111/j.1528-1167.2005.68104.x · Cited by 28

Expression of heat shock protein 70 induced by 4-aminopyridine through glutamate-mediated excitotoxic stress in rat hippocampus in vivo

Ayala, G. X., & Tapia, R. (2003) · Neuropharmacology · doi:10.1016/s0028-3908(03)00230-2 · Cited by 26

Selective Loss and Axonal Sprouting of GABAergic Interneurons in the Sclerotic Hippocampus Induced by LiCl–Pilocarpine

Long, L., Xiao, B., Feng, L., Yi, F., Li, G., Li, S., Abuhamed, M. M., Chen, S., Bi, F., & Li, Y. (2010) · International Journal of Neuroscience · doi:10.3109/00207454.2010.530007 · Cited by 25

GABA bouton subpopulations in the human dentate gyrus are differentially altered in mesial temporal lobe epilepsy

Alhourani, A., Fish, K. N., Wozny, T. A., Sudhakar, V. R., Hamilton, R. L., & Richardson, R. M. (2019) · Journal of Neurophysiology · doi:10.1152/jn.00523.2018 · Cited by 26

Age-related morphological and morphometrical changes in parvalbumin- and calbindin-immunoreactive neurons in the rat hippocampal formation

Lolova, I. S., & Davidoff, M. S. (1992) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(92)90136-2 · Cited by 25

Radiosurgery of the Rat Hippocampus: Magnetic Resonance Imaging, Neurophysiological, Histological, and Behavioral Studies

Brisman, J. L., Cole, A. J., Cosgrove, G. R., Thornton, A. F., Rabinov, J., Bussière, M. R., Bradley-Moore, M., Hedley-Whyte, T. E., & Chapman, P. H. (2003) · Neurosurgery · doi:10.1227/01.neu.0000083629.92550.a5 · Cited by 25

Effects of chronic monocular enucleation on calcium binding proteins calbindin-D28k and parvalbumin in the lateral geniculate nucleus of adult rhesus monkeys

Gutiérrez, C., & Cusick, C. G. (1994) · Brain Research · doi:10.1016/0006-8993(94)90710-2 · Cited by 25

Morphology and synaptic input of substance P receptor-immunoreactive interneurons in control and epileptic human hippocampus

Tóth, K., Wittner, L., Urbán, Z., Doyle, W., Buzsáki, G., Shigemoto, R., Freund, T. F., & Maglóczky, Z. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.09.039 · Cited by 24

The relationship of calbindin-containing neurons with substance P, Leu-enkephalin and cholecystokinin fibres: An immunohistochemical study in the rat thalamus

Battaglia, G. S., Colacitti, C., & Bentivoglio, M. (1992) · Journal of Chemical Neuroanatomy · doi:10.1016/0891-0618(92)90002-8 · Cited by 24

Calbindin D28K expression in relation to granule cell dispersion, mossy fibre sprouting and memory impairment in hippocampal sclerosis: A surgical and post mortem series

Martinian, L., Catarino, C. B., Thompson, P. J., Sisodiya, S. M., & Thom, M. (2011) · Epilepsy Research · doi:10.1016/j.eplepsyres.2011.08.011 · Cited by 23

Preservation of nucleus basalis neurons containing choline acetyltransferase and the vesicular acetylcholine transporter in the elderly with mild cognitive impairment and early Alzheimer's disease

Gilmor, M. L., Erickson, J. D., Varoqui, H., Hersh, L. B., Bennett, D. A., Cochran, E. J., Mufson, E. J., & Levey, A. I. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990906)411:4 · Cited by 243

Alterations of Interneurons of the Gerbil Hippocampus after Transient Cerebral Ischemia: Effect of Pitavastatin

Himeda, T., Hayakawa, N., Tounai, H., Sakuma, M., Kato, H., & Araki, T. (2005) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300798 · Cited by 23

Ca2+-Dependent Inactivation of High-Threshold Ca2+ Currents in Hippocampal Granule Cells of Patients With Chronic Temporal Lobe Epilepsy

Beck, H., Steffens, R., Heinemann, U., & Elger, C. E. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.82.2.946 · Cited by 23

Age‐dependent increase of perineuronal nets in the human hippocampus and precocious aging in epilepsy

Lehner, A., Hoffmann, L., Rampp, S., Coras, R., Paulsen, F. P., Frischknecht, R., Hamer, H. M., Walther, K., Brandner, S., Hofer, W., et al. (2024) · Epilepsia Open · doi:10.1002/epi4.12963 · Cited by 23

Emerging Functions of the “Ca2+ Buffers” Parvalbumin, Calbindin D-28k and Calretinin in the Brain

Schwaller, B. (2007) · Springer eBooks · doi:10.1007/978-0-387-30379-6_5 · Cited by 21

Neuropathology of the limbic system and brainstem in West syndrome

Hayashi, M. (2001) · Brain and Development · doi:10.1016/s0387-7604(01)00310-2 · Cited by 21

Do Febrile Seizures Promote Temporal Lobe Epilepsy? Retrospective Studies

Cendes, F., & Andermann, F. (2002) · Elsevier eBooks · doi:10.1016/b978-012078141-6/50008-1 · Cited by 21

Alfentanil-induced activation: a promising tool in the presurgical evaluation of temporal lobe epilepsy patients

Ragazzo, P. C., & Galanopoulou, A. S. (2000) · Brain Research Reviews · doi:10.1016/s0165-0173(99)00098-3 · Cited by 21

Anticonvulsant and Neuroprotective Effects of Cannabidiol During the Juvenile Period

Friedman, L. K., & Wongvravit, J. P. (2018) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nly069 · Cited by 20

Role of A1 receptor-activated GIRK channels in the suppression of hippocampal seizure activity

Hill, E., Hickman, C., Diez, R., & Wall, M. J. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.107904 · Cited by 20

Retrosplenial/presubicular continuum in primates: a developmental approach in fetal macaques using neurotensin and parvalbumin as markers

Berger, B., Alvarez, C., & Pélaprat, D. (1997) · Developmental Brain Research · doi:10.1016/s0165-3806(97)00067-9 · Cited by 20

Hippocampal synaptic pathology in patients with temporal lobe epilepsy

Honer, W. G., Beach, T. G., Hu, L. J., Berry, K. J., Dorovini‐Zis, K., Moore, G. R. W., & Woodhurst, W. B. (1994) · Acta Neuropathologica · doi:10.1007/bf00296191 · Cited by 20

Interaction between electrical modulation of the brain and pharmacotherapy to control pharmacoresistant epilepsy

Rocha, L. (2013) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2013.01.009 · Cited by 21

Postnatal development of parvalbumin and calbindin D-28k immunoreactivities in the canine hippocampus

Yoon, S. P., Chung, Y. Y., Chang, I. Y., Kim, J. J., Moon, J. S., & Kim, H. S. (2000) · Journal of Chemical Neuroanatomy · doi:10.1016/s0891-0618(00)00059-4 · Cited by 19

On the altered expression of tyrosine hydroxylase and calbindin-D 28kD immunoreactivities and viability of neurons in the ventral tegmental area of Tsai following injections of 6-hydroxydopamine in the medial forebrain bundle in the rat

Tan, Y., Williams, E. A., Lancia, A. J., & Zahm, D. S. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02348-9 · Cited by 18

Distribution of parvalbumin-containing interneurons in the hippocampus of the gerbil — a qualitative and quantitative statistical analysis

Nitsch, C., Scotti, A. L., & Nitsch, F. M. (1995) · Journal of Chemical Neuroanatomy · doi:10.1016/0891-0618(95)00076-j · Cited by 18

Species-specific expression of parvalbumin in the entorhinal cortex of the Mongolian gerbil: dependence on local activity but not extrinsic afferents

Bender, R. A., Hoffmann, M.-C., Frotscher, M., & Nitsch, C. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00208-6 · Cited by 18

Altered functional efficacy of hippocampal interneuron during epileptogenesis following febrile seizures

Yu, Y. H., Lee, K., Sin, D. S., Park, K., Park, D., & Kim, D. (2017) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2017.02.009 · Cited by 18

Nucleus accumbens in the lizardPsammodromus algirus: chemoarchitecture and cortical afferent connections

Guirado, S., D�vila, J. C., Real, M. A., & Medina, L. M. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990301)405:1 · Cited by 33

The hippocampal region of rats and mice after a single i.p. dose of clioquinol: Loss of synaptic zinc, cell death and c-Fos induction

Ismail, T., Mauerhofer, E., & Slomianka, L. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.09.011 · Cited by 16

Precocious development of parvalbumin-like immunoreactive interneurons in the hippocampal formation and entorhinal cortex of the fetal cynomolgus monkey

Berger, B., Grissac, N. D., & Alvarez, C. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990118)403:3 · Cited by 16

Proportional loss of parvalbumin‐immunoreactive synaptic boutons and granule cells from the hippocampus of sea lions with temporal lobe epilepsy

Cameron, S., Lopez, A., Glabman, R. A., Abrams, E., Johnson, S., Field, C. L., Gulland, F. M. D., & Buckmaster, P. S. (2019) · The Journal of Comparative Neurology · doi:10.1002/cne.24680 · Cited by 15

Calbindin immunostaining in the CA1 hippocampal pyramidal cell layer of the human and mouse: A comparative study

Merino‐Serrais, P., Tapia‐González, S., & DeFelipe, J. (2020) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2020.101745 · Cited by 15

Neuropeptides in the developing human hippocampus under hypoxic–ischemic conditions

González-Fuentes, J., Serrano, R. I., Sánchez, S. C., Lagartos-Donate, M. J., Rivas, E., Jiménez, M. D. M. A., & Marcos, P. (2021) · Journal of Anatomy · doi:10.1111/joa.13458 · Cited by 15

Voltage Imaging Reveals the CA1 Region at the CA2 Border as a Focus for Epileptiform Discharges and Long-Term Potentiation in Hippocampal Slices

Chang, P. Y., Taylor, P. E., & Jackson, M. B. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00532.2007 · Cited by 15

Inherited Epilepsy in Mongolian Gerbils

Buckmaster, P. S. (2006) · Elsevier eBooks · doi:10.1016/b978-012088554-1/50023-2 · Cited by 15

Calcium-binding proteins in the inner ear ofXenopus laevis (Daudin)

Kerschbaum, H., & Hermann, A. (1993) · Brain Research · doi:10.1016/0006-8993(93)90610-y · Cited by 15

Nonprincipal neurons and CA2 pyramidal cells, but not mossy cells are immunoreactive for calcitonin gene-related peptide in the mouse hippocampus

Sakurai, O., & Kosaka, T. (2007) · Brain Research · doi:10.1016/j.brainres.2007.10.032 · Cited by 15

Calcium‐binding Proteins

Schwaller, B. (2005) · Encyclopedia of Life Sciences · doi:10.1038/npg.els.0003905 · Cited by 15

Reorganization of the Brain Extracellular Matrix in Hippocampal Sclerosis

Sitaš, B., Bobić‐Rasonja, M., Mrak, G., Trnski, S., Skorić, M. K., Orešković, D., Knezović, V., Gadže, Ž. P., Petanjek, Z., Šimić, G., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23158197 · Cited by 16

Chemical neuroanatomy of the hippocampal formation and the perirhinal and parahippocampal cortices

Kobayashi, Y., & Amaral, D. G. (1999) · Handbook of chemical neuroanatomy · doi:10.1016/s0924-8196(99)80026-8 · Cited by 14

Postnatal development of parvalbumin and calbindin D‐28k immunoreactivities in the canine anterior cingulate cortex: transient expression in layer V pyramidal cells

Moon, J. S., Kim, J. J., Chang, I. Y., Chung, Y. Y., Jun, J. Y., You, H. J., & Yoon, S. P. (2002) · International Journal of Developmental Neuroscience · doi:10.1016/s0736-5748(02)00056-4 · Cited by 13

Neuropathological analysis of the brainstem and cerebral cortex lesions on epileptogenesis in hereditary dentatorubral-pallidoluysian atrophy

Hayashi, M., Kumada, S., Shioda, K., & Fukatsu, R. (2007) · Brain and Development · doi:10.1016/j.braindev.2006.12.008 · Cited by 13

Decreased hippocampal expression of calbindin D28K and cognitive impairment in MELAS

Emmanuele, V., García‐Cazorla, À., Huang, H.-B., Çoku, J., Dorado, B., Cortes, E. P., Engelstad, K., Vivo, D. C. D., DiMauro, S., Bonilla, E., et al. (2012) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2012.03.005 · Cited by 13

Hippocampal fields in the hedgehog tenrec

Künzle, H., & Radtke‐Schuller, S. (2001) · Neuroscience Research · doi:10.1016/s0168-0102(01)00288-7 · Cited by 13

Evidence for the Colocalization of Parvalbumin and Glutamate, but Not GABA, in the Perforant Path of the Gerbil Hippocampal Formation: A Combined Immunocytochemical and Microquantitative Analysis

Nitsch, C., Maly, I. P., Mori, D., & Scotti, A. L. (1994) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1994.62041276.x · Cited by 13

Differential vulnerability of neuronal subpopulations of the subiculum in a mouse model for mesial temporal lobe epilepsy

Franz, J., Barheier, N., Wilms, H., Tulke, S., Haas, C. A., & Häussler, U. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1142507 · Cited by 12

Etiology-related Degree of Sprouting of Parvalbumin-immunoreactive Axons in the Human Dentate Gyrus in Temporal Lobe Epilepsy

Ábrahám, H., Molnár, J. E., Sóki, N., Gyimesi, C., Horváth, Z., Janszky, J., Doczi, T. P., & Seress, L. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.09.018 · Cited by 12

Regional variations in the localization of insoluble kinase A regulatory isoforms during rodent brain development

Mucignat‐Caretta, C., & Caretta, A. (2004) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2004.03.006 · Cited by 12

Effects of early environment on field CA2 pyramidal neurons in the guinea-pig

Bartesaghi, R., & Severi, S. (2003) · Neuroscience · doi:10.1016/j.neuroscience.2003.10.018 · Cited by 11

Distribution of glutamate receptor subunit GluR1 and GABA in human cerebral neocortex: a double immunolabelling and electron microscopic study

He, Y., Ong, W., Leong, S. K., & Garey, L. J. (1996) · Experimental Brain Research · doi:10.1007/bf00227188 · Cited by 11

Effect of seizures on hippocampal peptidergic neurons

Mitchell, J., Cook, I. S., & Hervey, V. (1997) · Neuropathology and Applied Neurobiology · doi:10.1046/j.1365-2990.1997.4298042.x · Cited by 11

Development of parvalbumin-immunoreactive neurons in the postnatal human hippocampal formation

Ábrahám, H., Kojima, H., Götzer, K., Molnár, A., Tornóczky, T., & Seress, L. (2023) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2023.1058370 · Cited by 10

Functional Implications of the Anatomical Localization of Neurotrophic Factors

Fallon, J. H., & Loughlin, S. E. (1993) · Elsevier eBooks · doi:10.1016/b978-0-08-057132-4.50005-8 · Cited by 10

Drosophila Cbp53E Regulates Axon Growth at the Neuromuscular Junction

Hagel, K. R., Beriont, J., & Tessier, C. R. (2015) · PLoS ONE · doi:10.1371/journal.pone.0132636 · Cited by 9

Neuronal localization in the rat brain of the messenger RNA encoding calcyphosine, a new calcium-binding protein

Mailleux, P., Halleux, P., Verslijpe, M., Segers, V., & Vanderhaeghen, J.-J. (1993) · Neuroscience Letters · doi:10.1016/0304-3940(93)90304-4 · Cited by 9

The Nonhuman Primate Hippocampus: Neuroanatomy and Patterns of Cortical Connectivity

Insausti, R., Marcos, M., Mohedano-Moriano, A., Arroyo-Jiménez, M. M., Córcoles-Parada, M., Artacho-Pérula, E., Ubero-Martínez, M., & Muñoz-López, M. (2017) · Springer eBooks · doi:10.1007/978-3-319-50406-3_1 · Cited by 14

Structural reorganization of hippocampal networks caused by seizure activity

Lowenstein, D. H. (2001) · International review of neurobiology · doi:10.1016/s0074-7742(01)45012-4 · Cited by 8

Distribution of nitric oxide synthase and neuropeptide Y neurones during the development of the hippocampal formation in the rat.

Moryś, J. M., Kowiański, P., & Moryś, J. (2002) · PubMed · Cited by 8

Localization of mRNAs for synaptojanin isoforms in the brain of developing and mature rats

Kudo, M., Saito, S., Sakagami, H., Suzaki, H., & Kondo, H. (1999) · Molecular Brain Research · doi:10.1016/s0169-328x(98)00322-2 · Cited by 7

Unilateral optogenetic kindling of hippocampus leads to more severe impairments of the inhibitory signaling in the contralateral hippocampus

Tescarollo, F. C., Valdivia, D. J., Chen, S. C., & Sun, H. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1268311 · Cited by 6

From Stumbling Blocks to Stepping Stones: Progress in Treating Temporal Lobe Epilepsy With Stem Cell Transplantation

Naegele, J. R. (2025) · Epiliepsy currents/Epilepsy currents · doi:10.1177/15357597251318571 · Cited by 7

Somatostatin interneurons exhibit enhanced functional output and resilience to axotomy after mild traumatic brain injury

Harris, A. C., Jin, X., Greer, J. E., Povlishock, J. T., & Jacobs, K. M. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105801 · Cited by 8

Analysis of pThr286-CaMKII and CaMKII immunohistochemistry in the hippocampus of patients with temporal lobe epilepsy

Lie, A. A., Sommersberg, B., & Elger, C. E. (2005) · Epilepsy Research · doi:10.1016/j.eplepsyres.2005.06.009 · Cited by 6

Modifications de l’activité épileptique spontanée par déconnexion sélective intrahippocampique dans un modèle chronique d’épilepsie mésiotemporale

Pallud, J., Devaux, B. C., & Depaulis, A. (2008) · Neurochirurgie · doi:10.1016/j.neuchi.2008.02.002 · Cited by 6

Activation of somatostatin‐synthesizing neurons in the hippocampal formation through kindling‐induced seizures

Pretel, S., Applegate, C. D., & Piekut, D. T. (1995) · Hippocampus · doi:10.1002/hipo.450050106 · Cited by 6

Nitric oxide synthase induction in astroglial cell cultures: Effect on heat shock protein 70 synthesis and oxidant/antioxidant balance

Calabrese, V., Copani, A., Testa, D., Ravagna, A., Spadaro, F., Tendi, E. A., Nicoletti, V. G., & Stella, A. M. G. (2000) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(20000601)60:5 · Cited by 104

Topical Review: Pathologic Basis of the Symptomatic Epilepsies in Childhood

Armstrong, D. D., & Mizrahi, E. M. (1998) · Journal of Child Neurology · doi:10.1177/088307389801300801 · Cited by 6

Absolute Number of Three Populations of Interneurons and All GABAergic Synapses in the Human Hippocampus

Takács, V. T., Papp, P., Orosz, Á., Bardóczi, Z., Zsoldos, T., Zichó, K., Watanabe, M., Maglóczky, Z., Gombás, P., Freund, T. F., et al. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.0372-24.2024 · Cited by 6

Parvalbumin expression during developmental differentiation of the rat ovary

Pohl, V., Pattyn, G., & Berchtold, M. W. (1995) · Differentiation · doi:10.1046/j.1432-0436.1995.5940235.x · Cited by 5

Localization of EF-Hand Ca2+-Binding Proteins in the CNS

Heizmann, C. W., & Braun, K. (1995) · Neuroscience intelligence unit · doi:10.1007/978-3-662-21689-7_4 · Cited by 5

Introduction to the special issue on: A new view of hippocampal area CA2

Dudek, S. M., Alexander, G. M., & Farris, S. (2023) · Hippocampus · doi:10.1002/hipo.23514 · Cited by 5

A companion to the preclinical common data elements and case report forms for neuropathology studies in epilepsy research. A report of the TASK3 WG2 Neuropathology Working Group of the ILAE / AES Joint Translational Task Force

Aronica, E., Binder, D. K., Drexel, M., Ikonomidou, C., Kadam, S. D., Sperk, G., & Steinhäuser, C. (2022) · Epilepsia Open · doi:10.1002/epi4.12638 · Cited by 4

Hippocampal Sclerosis in Temporal Lobe Epilepsy

Houser, C. R. (2024) · Oxford University Press eBooks · doi:10.1093/med/9780197549469.003.0002 · Cited by 3

NECAB1-3, parvalbumin, calbindin, and calretinin in the hippocampus of the European mole

Maliković, J., Amrein, I., Vinciguerra, L., Wolfer, D. P., & Slomianka, L. (2024) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2024.1452722 · Cited by 4

occ1 mRNA expression reveals a characteristic feature in the hippocampal CA2 field of adult macaques

Tochitani, S., Hashikawa, T., & Yamamori, T. (2003) · Neuroscience Letters · doi:10.1016/s0304-3940(03)00595-0 · Cited by 4

Changes in the numbers and distribution of calretinin in the epileptic rat hippocampus

Abuhamed, M. M., Xiao, B., Alsharafi, W. A., Li, J., Long, L., Zhiguo, W., & Zhi, S. (2010) · Neurosciences · doi:10.17712/1658-3183.1790 · Cited by 3

The Economic Impact of Medication-Resistant Epilepsy

Begley, C. E., & Jeong, S. (2020) · Cambridge University Press eBooks · doi:10.1017/9781316492376.004 · Cited by 3

Embryology and neuropathological examination of central nervous system malformations

Sarnat, H. B. (2007) · Handbook of clinical neurology · doi:10.1016/s0072-9752(07)87029-1 · Cited by 3

Epilepsy Treatment through Genetic Intervention of GABAergic Interneurons: Promises and Challenges

Podgorny, O. V., Petukhova, E. O., & Belousov, V. V. (2025) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.5c00747 · Cited by 2

Defining hippocampal area CA2 in the fox ( Vulpes vulpes ) brain

Dudek, S. M., Phoenix, A., Scappini, E., Shepeleva, D. V., Herbeck, Y. E., Trut, L. N., Farris, S., & Kukekova, A. V. (2023) · Hippocampus · doi:10.1002/hipo.23546 · Cited by 2

Medication-Resistant Epilepsy in Adults

Holtkamp, M., & Benninger, F. (2020) · Cambridge University Press eBooks · doi:10.1017/9781316492376.014 · Cited by 2

Parvalbumin immunoreactivity and protein content alter in the hippocampus after adrenalectomy in seizure sensitive gerbils

Hwang, I., Kim, D., Yoo, K., Kang, T., Kim, Y., Kwon, D., Moon, W., & Won, M. (2007) · Neurological Research · doi:10.1179/016164107x159270 · Cited by 2

Pharmacotherapy for Medication-Resistant Epilepsy

Powell, G. A., & Marson, A. G. (2020) · Cambridge University Press eBooks · doi:10.1017/9781316492376.016 · Cited by 2

GABAA receptors in human temporal lobe epilepsy

Hill, R. A. (2000) · ResearchSpace (University of Auckland) · Cited by 2

Colocalization of androgen receptors and mating-induced FOS immunoreactivity in neurons that project to the central tegmental field in male rats

Gr�co, B., Edwards, D. A., Michael, R. P., Zumpe, D., & Clancy, A. N. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990531)408:2 · Cited by 36

Psychiatric Comorbidities in Medication-Resistant Epilepsy

Kanner, A. M. (2020) · Cambridge University Press eBooks · doi:10.1017/9781316492376.023 · Cited by 1

Medication-Resistant Epilepsy Syndromes in Children

Pestana‐Knight, E., & Wyllie, E. (2020) · Cambridge University Press eBooks · doi:10.1017/9781316492376.013 · Cited by 1

Atrophy patterns of gray matter volume and the correlation with the disease duration in the cerebellum and hippocampal subregions in mesial temporal lobe epilepsy

Li, S., Chen, Y., Wang, Y., Xu, J., Qin, X., & Xu, G. (2025) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2025.110742 · Cited by 1

Chemogenetic activation of hippocampal area CA2 promotes acute and chronic seizures in a mouse model of epilepsy

LaFrancois, J. J., Kennedy, M., Rathod, M., Santoro, B., Lisgaras, C. P., Siegelbaum, S. A., & Scharfman, H. E. (2026) · Neurobiology of Disease · doi:10.1016/j.nbd.2025.107256 · Cited by 1

Hippocampal lesions in epilepsy: A historical review

Naquet, R. (2001) · International review of neurobiology · doi:10.1016/s0074-7742(01)45023-9 · Cited by 1

GABA A Receptors in Human Temporal Lobe Epilepsy

Loup, F. (2006) · Cited by 1

Social Consequences of Medication-Resistant Epilepsy

Crepeau, A. Z., & Sirven, J. I. (2020) · Cambridge University Press eBooks · doi:10.1017/9781316492376.005 · Cited by 1

Medication-Resistant Epilepsy

(2020) · Cambridge University Press eBooks · doi:10.1017/9781316492376 · Cited by 1

Ketogenic Diet and Epigenetic Mechanisms of Epileptogenesis

Murugan, M., Tescarollo, F. C., & Boison, D. (2022) · Oxford University Press eBooks · doi:10.1093/med/9780197501207.003.0025 · Cited by 1

Distribution of calretinin-immunoreactive interneurons in dorsal part of hippocampus in animal model of depression

Nowak, B., Braniewska, A., & Zadrożna, M. (2012) · Medicina internacia revuo · Cited by 1

Epilepsia y actividad física: conceptos desde la perspectiva de las ciencias básicas

de Antioquia, U., & Carrizosa-Moog, J. (2017) · IATREIA · doi:10.17533/udea.iatreia.v30n3a04 · Cited by 1

Positive effect of moderate-intensity aerobic activity on pentylenetetrazol-induced epileptic behaviors in pregnant mice and cognitive performance in adult male offspring

Sabaghi, A., Heyrani, A., Kiani, A., & Yousofvand, N. (2018) · Sport Sciences for Health · doi:10.1007/s11332-018-0485-7 · Cited by 1

Calcium‐binding protein (calbindin‐D 28k ) and parvalbumin immunocytochemistry: Localization in the rat hippocampus with specific reference to the selective vulnerability of hippocampal neurons to seizure activity

Sloviter, R. S. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902800203 · Cited by 686

Calcium-binding proteins are concentrated in the CA2 field of the monkey hippocampus: a possible key to this region's resistance to epileptic damage

Léránth, C., & Ribak, C. E. (1991) · Experimental Brain Research · doi:10.1007/bf00229993 · Cited by 132

Distribution, morphological features, and synaptic connections of parvalbumin‐ and calbindin D28k‐immunoreactive neurons in the human hippocampal formation

Seress, L., Gulyás, A. I., Ferrer, I., Tuñón, T., Soriano, E., & Freund, T. F. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903370204 · Cited by 130

Chapter 7 Chapter Immunocytochemical demonstration of the calcium-binding proteins calbindin-D 28k and parvalbumin in the subiculum, hippocampus and dentate area of the domestic pig

Holm, I. E., Geneser, F. A., Zimmer, J., & Baimbridge, K. G. (1990) · Progress in brain research · doi:10.1016/s0079-6123(08)61243-1 · Cited by 29

Pyramidal neurons are immunoreactive for calbindin D28k in the CA1 subfield of the human hippocampus

Seress, L., Gulyás, A. I., & Freund, T. F. (1992) · Neuroscience Letters · doi:10.1016/0304-3940(92)90928-z · Cited by 32