A triple dissociation of memory systems: Hippocampus, amygdala, and dorsal striatum.

Memory for Space, Time, and Episodes ☆

Asem, J. S. A., & Fortin, N. J. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21015-8 · Cited by 5

Visual statistical learning deficits in memory-impaired individuals

Cerreta, A., Vickery, T. J., & Berryhill, M. E. (2018) · Neurocase · doi:10.1080/13554794.2019.1579843 · Cited by 3

Hippocampal Damage Causes Retrograde Amnesia and Slower Acquisition of a Cue-Place Discrimination in a Concurrent Cue-Place Water Task in Rats

Lee, J. Q., McDonald, R. J., & Sutherland, R. J. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.05.061 · Cited by 3

The spatial cerebral damage caused by larger infarct and β‐amyloid toxicity is driven by the anatomical/functional connectivity

Amtul, Z., Frías, C., Randhawa, J., Hill, D. J., & Arany, E. J. (2019) · The Journal of Comparative Neurology · doi:10.1002/cne.24738 · Cited by 3

The Role of Hp-NCL Network in Goal-Directed Routing Information Encoding of Bird: A Review

Li, M., Shang, Z., Zhao, K., Cheng, S., & Wan, H. (2020) · Brain Sciences · doi:10.3390/brainsci10090617 · Cited by 3

Cognitive Neuroscience

Wagels, L., Habel, U., & Nickl‐Jockschat, T. (2024) · Springer eBooks · doi:10.1007/978-3-030-51366-5_31 · Cited by 3

Combined hippocampal and amygdala lesions block learning of a response-independent form of occasion-setting.

Clarke, H. A., Skinner, D. M., & van der Kooy, D. (2001) · Behavioral Neuroscience · doi:10.1037/0735-7044.115.2.341 · Cited by 5

Mechanisms of Contextual Conditioning

McDonald, R. J., & Hong, N. S. (2016) · Wiley eBooks · doi:10.1002/9781118650813.ch12 · Cited by 3

Memory Systems

Eichenbaum, H. (2003) · Handbook of Psychology · doi:10.1002/0471264385.wei0319 · Cited by 3

Serial reversal learning in an olfactory discrimination task in 3xTg-AD micePreprint

Roddick, K. M., Schellinck, H. M., & Brown, R. E. (2023) · Learning & Memory · doi:10.1101/lm.053840.123 · Cited by 4

Attribute Memory Model and Behavioral Neurophysiology of Memory

Lee, I., & Lee, C. (2015) · Springer eBooks · doi:10.1007/978-3-319-15759-7_10 · Cited by 2

Aprendizaje motor y neuroplasticidad en el dolor crónico: narrativa

Palma, A. I., Araya‐Quintanilla, F., Aguilera-Eguía, R. A., & Muñoz-Yánez, M. J. (2018) · Rehabilitación · doi:10.1016/j.rh.2018.06.002 · Cited by 2

Memory Modulation

McGaugh, J. L., & Roozendaal, B. (2008) · Elsevier eBooks · doi:10.1016/b978-012370509-9.00113-3 · Cited by 11

Effect of electrolytic lesion of the dorsomedial striatum on sexual behaviour and locomotor activity in rats

Ortiz-Pulido, R., Hernández-Briones, Z. S., Tamariz-Rodríguez, A., Hernández‐Aguilar, M. E., Aranda-Abreu, G. E., Coria‐Ávila, G. A., Manzo, J. G., & García, L. I. (2017) · Neurología (English Edition) · doi:10.1016/j.nrleng.2015.11.008 · Cited by 2

Introduction

Sweatt, J. D. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-374951-2.00001-9 · Cited by 3

How independent are parallel memory systems? A theoretical comment on Gibson and Shettleworth (2005).

White, N. M. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.4.1158 · Cited by 2

Behavioral Correlates of Neuronal Activity Recorded as Single-Units: Promises and Pitfalls as Illustrated by the Rodent Head Direction Cell Signal

Stackman, R. W. (2010) · Neuromethods · doi:10.1007/978-1-60327-202-5_6 · Cited by 3

Cognitive and Stimulus–Response Habit Functions of the Neo-(Dorsal) Striatum

Devan, B. D., Chaban, N., Piscopello, J., Deibel, S. H., & McDonald, R. J. (2016) · Innovations in cognitive neuroscience · doi:10.1007/978-3-319-42743-0_18 · Cited by 2

Long-term value memory in primates

Vanduffel, W. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1800247115 · Cited by 2

NF-κB in Neurons

Levenson, J. M., Pizzi, M., & Sweatt, J. D. (2007) · Springer eBooks · doi:10.1007/0-387-33573-0_11 · Cited by 2

Capturing Context Is Not Enough

Lemelson, R., & Tucker, A. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108695374.023 · Cited by 2

Effects of bilateral microinjections of ibotenic acid into neostriatal region and forced exercise on spatial learning and memory and anthropometric characteristics of male rats

Modaberi, S., Shahbazi, M., Naghdi, N., & Bagherzadeh, F. (2021) · کومش · doi:10.52547/koomesh.23.5.654 · Cited by 2

Internet Sociality

Stendel, M. S., Ramstead, M. J. D., & Veissière, S. P. L. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108695374.026 · Cited by 2

Organizational effects of testosterone on learning strategy preference and muscarinic receptor binding in prepubertal rats

Grissom, E. M., Hawley, W. R., & Dohanich, G. P. (2019) · Hormones and Behavior · doi:10.1016/j.yhbeh.2019.02.005 · Cited by 2

Neural Mediation of Memory for Time

Kesner, R. P. (2002) · Springer eBooks · doi:10.1007/978-1-4615-0821-2_9 · Cited by 2

The meninges contribute to the conditioned taste avoidance induced by neural cooling in male rats

Wang, Y., & Chambers, K. C. (2002) · Behavioural Brain Research · doi:10.1016/s0166-4328(01)00453-3 · Cited by 2

Gonadal hormones modulate the potency of the disruptive effects of donepezil in male rats responding under a nonspatial operant learning and performance task

Leonard, S. T., Hearn, J. K., Catling, A. D., & Winsauer, P. J. (2010) · Behavioural Pharmacology · doi:10.1097/fbp.0b013e328337be3a · Cited by 2

A Brain System for Declarative Memory

Eichenbaum, H. (2002) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195141740.003.0009 · Cited by 3

Restoring striatal WAVE-1 improves maze exploration performance of GluN1 knockdown micePreprint

Chen, Y., Milenkovic, M., Salahpour, A., Soderling, S. H., & Ramsey, A. J. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/341479 · Cited by 2

Memory Systems

Eichenbaum, H. (2012) · Wiley eBooks · doi:10.1002/9781118133880.hop203020 · Cited by 2

Implication du système cholinergique dans l'altération de la mémoire de travail au cours du vieillissement chez la souris : approche comportementale, pharmacologique et neurofonctionnelle

Vandesquille, M. (2011) · theses.fr (ABES) · doi:10.70675/ad96bd3dz8a44z499czbeacz7a1e24572e30 · Cited by 2

The Neural Mechanisms Underlying Social Norms

Mu, Y., & Gelfand, M. J. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108695374.015 · Cited by 2

Exploring the potential impact of GPC-enriched egg yolk derivatives on cognitive vitality in aging brains: A preliminary study

Yu, W., Gao, Q. H., Yang, Y., Chang, C., Hu, W., Su, Y., Gu, L., & Li, J. (2025) · Food Bioscience · doi:10.1016/j.fbio.2025.107881 · Cited by 1

Chapter 3.3 Toward a neurobiology of episodic memory

Eichenbaum, H., Fortin, N. J., Ergorul, C., & Robitsek, R. J. (2008) · Handbook of behavioral neuroscience · doi:10.1016/s1569-7339(08)00216-6 · Cited by 2

A Brain System for Emotional Memory

Eichenbaum, H. (2002) · doi:10.1093/acprof:oso/9780195141740.003.0011 · Cited by 1

Exploring Declarative Memory Using Animal Models

Eichenbaum, H. (2002) · doi:10.1093/acprof:oso/9780195141740.003.0005 · Cited by 1

Multiple Memory Systems in Humans and Rodents ☆

White, N. M., & Bohbot, V. D. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.02801-7 · Cited by 1

Neurobiology of Procedural Learning in Animals ☆

Packard, M. G., & Goodman, J. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21086-9 · Cited by 1

Cognitive Function

Driscoll, L. L. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.02206-6 · Cited by 1

Memory Modulation ☆

McGaugh, J. L., & Roozendaal, B. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21092-4 · Cited by 1

Peripherally-administered amphetamine induces plasticity in medial prefrontal cortex and nucleus accumbens in rats with amygdala lesions: implications for neural models of memory modulation

McDonald, R., Hong, N. S., Germaine, C., & Kolb, B. (2023) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2023.1187976 · Cited by 1

Hippocampal Cortactin Levels are Reduced Following Spatial Working Memory Formation, an Effect Blocked by Chronic Calpain Inhibition

Olson, M. L., Ingebretson, A. E., & Harmelink, K. (2015) · Brain Sciences · doi:10.3390/brainsci5020241 · Cited by 1

Les méthodes de la neuropsychologie

Jaffard, R., Guillou, J., Desmedt, A., Etchamendy, N., & Marighetto, A. (2001) · Questions de personne · doi:10.3917/dbu.eusta.2001.01.0289 · Cited by 1

MODELING HUMAN INTELLIGENCE WITH SLOW INTELLIGENCE SYSTEMS

Dong, T. (2012) · International Journal of Software Engineering and Knowledge Engineering · doi:10.1142/s0218194012400141 · Cited by 1

Culture, Mind, and Brain in Human Evolution

Stout, D. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108695374.005 · Cited by 1

Liminal Brains in Uncertain Futures

Choudhury, S., & Berson, J. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108695374.020 · Cited by 1

Long-term potentiation at the lateral perforant path-nucleus accumbens synapse in the rat in vivo

Quiñones-Hinojosa, A., Derrick, B. E., Barea-Rodriguez, E. J., Janak, P., & Martinez, J. L. (1998) · Psychobiology · doi:10.3758/bf03330605 · Cited by 1

Tonically Active Neurons in the Striatum of the Monkey Rapidly Signal a Switch in Behavioral Set

Thomas, T. M., & Crutcher, M. D. (2002) · Advances in behavioral biology · doi:10.1007/978-1-4615-0179-4_34 · Cited by 1

The 70kDa Heat Shock Protein Family and Learning

Ammassari‐Teule, M., Mariucci, G., & Ambrosini, M. V. (2009) · Heat shock proteins · doi:10.1007/978-90-481-3381-9_13

Embryonic or Neural Stem Cells in Neurodegenerative Disease of the Central Nervous System (with Relevance to PD, HD, AD, MS, SCI, and Stroke)

Dunnett, S. B., Borlongan, C. V., & Sanberg, P. R. (2012) · doi:10.1002/9781118498453.ch17

Consolidación de la memoria, sustrato nervioso del refuerzo y adicción

Redolar-Ripoll, E. (2008) · Psiquiatría Biológica · doi:10.1016/s1134-5934(08)76481-9 · Cited by 1

Protective Effect of the Gastrodiae Rhizoma-gamibang on the Scopolamine-induced Hippocampal Damage in Sprague-Dawley Rats

Park, E.-H., Lee, S.-I., Jeong, J.-K., Kim, K.-O., & Kim, J.-S. (2015) · The Korea Journal of Herbology · doi:10.6116/kjh.2015.30.3.49

Windows into the Workings of Memory

Eichenbaum, H. (2002) · doi:10.1093/acprof:oso/9780195141740.003.0006

Cellular Mechanisms of Memory: Complex Circuits

Eichenbaum, H. (2002) · doi:10.1093/acprof:oso/9780195141740.003.0003

Two Distinct Stages of Memory Consolidation

Eichenbaum, H. (2002) · doi:10.1093/acprof:oso/9780195141740.003.0012

Multiple Memory Systems in the Brain

Eichenbaum, H. (2002) · doi:10.1093/acprof:oso/9780195141740.003.0008

Introduction: Four Themes in Research on the Neurobiology of Memory

Eichenbaum, H. (2002) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195141740.003.0001

The Cerebral Cortex and Memory

Eichenbaum, H. (2002) · doi:10.1093/acprof:oso/9780195141740.003.0007

Neurons and Simple Memory Circuits

Eichenbaum, H. (2002) · doi:10.1093/acprof:oso/9780195141740.003.0002

Memory Systems and Neural Dynamics

McKenzie, S., & Buzsáki, G. (2016) · Springer eBooks · doi:10.1007/978-1-4939-3474-4_142

Amnesia—Learning about Memory from Memory Loss

Eichenbaum, H. (2002) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195141740.003.0004

5-HT2C Receptors in Learning

Ángel, L.-V. M., Gutiérrez-Guzmán, B. E., Cervantes, M., & Olvera‐Cortés, M. E. (2010) · Humana Press eBooks · doi:10.1007/978-1-60761-941-3_24

The dorsolateral striatum regulates habits by way of performance vigor when actions are initiatedPreprint

Crego, A. C. G., Štoček, F., Marchuk, A. G., Carmichael, J. E., van der Meer, M. A. A., & Smith, K. S. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/426031

Repeated multi-domain, but not single-domain, cognitive training prevents cognitive decline and amyloid pathology found in the APP NL-G-F mouse model of Alzheimer diseasePreprint

Mehla, J., Deibel, S. H., Karem, H., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.24.264978

Social Neuroscience in Global Mental Health

Kohrt, B. A. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108695374.024 · Cited by 1

Literary Analysis and Weak Theories

Moses, O. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108695374.022

Cities, Psychosis, and Social Defeat

Sayanvala, F., Bornstein, L., Choudhury, S., Shah, J. L., Weinstock, D., & Gold, I. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108695374.025 · Cited by 1

Experience-Dependent Plasticity in the Hippocampus

West, G. L., & Bohbot, V. D. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108695374.019

Differential stress response to psychological and physical stressors in children using spatial versus response-dependent navigation strategies

West, G. L., Kurdi, V., Fouquet, C., Schachar, R. J., Boivin, M., Hastings, P. D., Robaey, P., & Bohbot, V. D. (2021) · Comprehensive Psychoneuroendocrinology · doi:10.1016/j.cpnec.2021.100043 · Cited by 2

Neural circuit dynamics of drug-context associative learning in the hippocampusPreprint

Sun, Y., & Giocomo, L. M. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.09.02.458796

How Social Coordination and Cooperation are Achieved

Kirmayer, L. J., Worthman, C. M., Kitayama, S., Lemelson, R., & Cummings, C. A. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108695374.013

Preface

Kirmayer, L. J., Worthman, C. M., Kitayama, S., Lemelson, R., & Cummings, C. A. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108695374.001

The Co-emergence of Culture, Mind, and Brain

Kirmayer, L. J., Worthman, C. M., Kitayama, S., Lemelson, R., & Cummings, C. A. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108695374.004

The Situated Brain

Kirmayer, L. J., Worthman, C. M., Kitayama, S., Lemelson, R., & Cummings, C. A. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108695374.008

Applications

(2020) · Cambridge University Press eBooks · doi:10.1017/9781108695374.017

Chronic FRAs

Hiroi, N., Chen, J., Nye, H. E., et al. (1996) · Advances in behavioral biology · doi:10.1007/978-1-4899-0194-1_48

Index

Kirmayer, L. J., Worthman, C. M., Kitayama, S., Lemelson, R., & Cummings, C. A. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108695374.029

Declarative and Procedural Memory as Individual Differences in Second Language AptitudePreprint

Buffington, J., & Morgan‐Short, K. (2018) · doi:10.31219/osf.io/p7bnt

Multiple Memory Systems

Gadberry, T. M., & Packard, M. G. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.23953-9

Copyright Page

(2002) · doi:10.1093/acprof:oso/9780195141740.002.0003

Preface

(2002) · doi:10.1093/acprof:oso/9780195141740.002.0004

Memory Systems and Neural Dynamics

McKenzie, S., & Buzsáki, G. (2016) · Springer eBooks · doi:10.1007/978-1-4614-6434-1_142-1

Memory Systems and Neural Dynamics

McKenzie, S., & Buzsáki, G. (2022) · Springer eBooks · doi:10.1007/978-3-030-88832-9_142

Are there disciplinary boundaries in the comparative study of primate cognition?

Manrique, H. M., & Canales, J. J. (2023) · Current Research in Neurobiology · doi:10.1016/j.crneur.2023.100088

Structural alterations in the amygdala and impaired social incentive learning in a mouse model of a genetic variant associated with neurodevelopmental disordersPreprint

Hiramoto, T., Sumiyoshi, A., Kato, R., Yamauchi, T., Kang, G., Matsumura, B., Stevens, L. J., Ryoke, R., Nonaka, H., Machida, A., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.06.14.545013

Cognitive Neuroscience

Wagels, L., Habel, U., & Nickl‐Jockschat, T. (2023) · Springer eBooks · doi:10.1007/978-3-030-42825-9_31-1

Cognitive Function

Driscoll, L. L. (2025) · Elsevier eBooks · doi:10.1016/b978-0-323-95488-4.00230-8

Réorganisation des systèmes anatomo-fonctionnels et de la topologie cérébrale entre les formes à début précoce et tardif de maladie d'Alzheimer. : approche comportementale et en IRMf de repos

Gour, N. (2013) · theses.fr (ABES) · doi:10.70675/ae7413f4z289fz49bez93c4zc085fb1b9c34

Rôle du cortex entorhinal médian dans le traitement des informations spatiales : études comportementales et électrophysiologiques

Jacob, P.-Y. (2014) · theses.fr (ABES) · doi:10.70675/ffe6a25az7899z4afcz8be8za1d283fb01c1

Bases neuronales de l’apprentissage associatif multisensoriel : implication différentielle du cortex entorhinal et de l’hippocampe chez le rat

Boisselier, L. (2016) · theses.fr (ABES) · doi:10.70675/ca67629fz2635z4501z95e1z49cf0b9b0be1

Conséquences de l'inhibition des interneurones cholinergiques du striatum sur la transmission corticostriée en conditions normale et parkinsonienne

Laverne, G. (2020) · theses.fr (ABES) · doi:10.70675/d58a850bz5ba6z4b96z946fza210d8730737

Neural and cognitive bases of confirmation bias-induced interference in declarative memory performance

Stevens, C. (2022) · theses.fr (ABES) · doi:10.70675/0227abb4z1b53z41c7zacd6z1982b681205d

Adjusting Behavior to Context: Striatal Network Functions in Learning and Memory

Graybiel, A. M., & Blázquez, P. M. (2002) · Advances in behavioral biology · doi:10.1007/978-1-4757-3538-3_86 · Cited by 1

Intrinsic circuits of the striatum

Benarroch, E. E. (2016) · Neurology · doi:10.1212/wnl.0000000000002599 · Cited by 24

Behavioural Effects of Manipulation of Basal Ganglia Neurotransmitters

Iversen, S. D. (1984) · Novartis Foundation symposium · doi:10.1002/9780470720882.ch10 · Cited by 31

Amygdaloid projections to ventromedial striatal subterritories in the primate

Fudge, J. L., Kunishio, K., Walsh, P., Richard, C., & Haber, S. N. (2002) · Neuroscience · doi:10.1016/s0306-4522(01)00546-2 · Cited by 226

A Telencephalic Nucleus Essential for Song Learning Contains Neurons with Physiological Characteristics of Both Striatum and Globus Pallidus

Farries, M. A., & Perkel, D. J. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-09-03776.2002 · Cited by 187