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  1. The hippocampus: Relational processor or antiprocessor?Neil McNaughton - 1994 - Behavioral and Brain Sciences 17 (3):487-488.
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  • What exactly do amnesics fail to store normally?Andrew R. Mayes - 1994 - Behavioral and Brain Sciences 17 (3):486-487.
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  • Hippocampus and memory for time.Raymond P. Kesner - 1994 - Behavioral and Brain Sciences 17 (3):485-486.
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  • Sculpting the space of actions. Explaining human action by integrating intentions and mechanisms.Machiel Keestra - 2014 - Dissertation, University of Amsterdam
    How can we explain the intentional nature of an expert’s actions, performed without immediate and conscious control, relying instead on automatic cognitive processes? How can we account for the differences and similarities with a novice’s performance of the same actions? Can a naturalist explanation of intentional expert action be in line with a philosophical concept of intentional action? Answering these and related questions in a positive sense, this dissertation develops a three-step argument. Part I considers different methods of explanations in (...)
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  • How long do relational representations in the hippocampus last during classical eyelid conditioning?Donald B. Katz & Joseph E. Steinmetz - 1994 - Behavioral and Brain Sciences 17 (3):484-485.
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  • A call for greater concern regarding the underlying anatomy.Leonard E. Jarrard - 1994 - Behavioral and Brain Sciences 17 (3):483-484.
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  • Going from task descriptions to memory structures.Michael S. Humphreys & Simon Dennis - 1994 - Behavioral and Brain Sciences 17 (3):483-483.
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  • The localization of general memory functions.James A. Horel - 1994 - Behavioral and Brain Sciences 17 (3):482-482.
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  • Neocortical memory traces.Earl K. Miller - 1994 - Behavioral and Brain Sciences 17 (3):488-489.
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  • Hippocampal representations of DMS/DNMS in the rat.Robert E. Hampson & Sam A. Deadwyler - 1994 - Behavioral and Brain Sciences 17 (3):480-482.
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  • Hippocampal modulation of recognition, conditioning, timing, and space: Why so many functions?Stephen Grossberg - 1994 - Behavioral and Brain Sciences 17 (3):479-480.
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  • Psychoarithmetic or pick your own?Jeffrey A. Gray, John Sinden & Helen Hodges - 1994 - Behavioral and Brain Sciences 17 (3):478-479.
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  • A step linking memory to understanding?Mark A. Good & Richard G. M. Morris - 1994 - Behavioral and Brain Sciences 17 (3):477-478.
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  • A computational perspective on dissociating hippocampal and entorhinal function.Mark A. Gluck, Catherine E. Myers & James K. Goebel - 1994 - Behavioral and Brain Sciences 17 (3):476-477.
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  • In search of the engrammer.Joaquin M. Fuster - 1994 - Behavioral and Brain Sciences 17 (3):476-476.
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  • Multiple memory systems : a neurophilosophical analysis.Elizabeth Leigh Ennen - unknown
    Neuroscientific data may be usefully invoked in the arbitration of debates concerning the scope of representational theories of the mind. Contemporary cognitivists tend toward theoretical imperialism in that they argue that all types of intelligent behaviour, including perceptual-motor skills, can be explained within the framework of representationalism. Phenomenologists argue that the scope of cognitivism is not as vast as its proponents suppose. They claim that perceptual-motor skills are non-representational and thus fall beyond the purview of cognitivism. I argue that this (...)
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  • Two functional components of the hippocampal memory system.Howard Eichenbaum, Tim Otto & Neal J. Cohen - 1994 - Behavioral and Brain Sciences 17 (3):449-472.
    There is considerable evidence that the hippocampal system contributes both to (1) the temporary maintenance of memories and to (2) the processing of a particular type of memory representation. The findings on amnesia suggest that these two distinguishing features of hippocampal memory processing are orthogonal. Together with anatomical and physiological data, the neuropsychological findings support a model of cortico-hippocampal interactions in which the temporal and representational properties of hippocampal memory processing are mediated separately. We propose that neocortical association areas maintain (...)
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  • The hippocampal memory system and its functional comments: Further explication and clarification.Howard Eichenbaum, Tim Otto & Neal J. Cohen - 1994 - Behavioral and Brain Sciences 17 (3):500-517.
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  • Functional distinctions within the medical temporal lobe memory system: What is the evidence?Stuart Zola-Morgan & Pablo Alvarez - 1994 - Behavioral and Brain Sciences 17 (3):495-496.
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  • On the neural mechanisms of sequence learning.Tim Curran - 1995 - PSYCHE: An Interdisciplinary Journal of Research On Consciousness 2.
    Nissen and Bullemer's serial reaction time task has proven to be a useful model task for exploring implicit sequence learning. Neuropsychological research indicates that SRT learning may depend on the integrity of the basal ganglia, but not on medial temporal and diencephalic structures that are crucial for explicit learning. Recent neuroimaging research demonstrates that motor cortical areas , prefrontal, and parietal cortex also may be involved. This paper reviews this neuropsychological and neuroimaging research, but finds it lacking specific links between (...)
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  • Recording the recognition due to the parahippocampal region places hippocampal relational encoding in context.M. W. Brown - 1994 - Behavioral and Brain Sciences 17 (3):474-476.
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  • The hippocampal system, time, and memory representations.J. J. Bolhuis & I. C. Reid - 1994 - Behavioral and Brain Sciences 17 (3):474-474.
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  • Remembering spatial cognition as a hippocampal functional component.Verner P. Bingman - 1994 - Behavioral and Brain Sciences 17 (3):473-474.
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  • Is Eichenbaum et al.'s proposal testable and how extensive is the hippocampal memory system?John P. Aggleton - 1994 - Behavioral and Brain Sciences 17 (3):472-473.
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  • Does it still make sense to develop a declarative memory theory of hippocampal function?J. N. P. Rawlins, R. M. J. Deacon, B. K. Yee & H. J. Cassaday - 1994 - Behavioral and Brain Sciences 17 (3):492-493.
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  • What do animal models of memory model?Endel Tulving & Hans J. Markowitsch - 1994 - Behavioral and Brain Sciences 17 (3):498-499.
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  • A Conceptual and Computational Model of Moral Decision Making in Human and Artificial Agents.Wendell Wallach, Stan Franklin & Colin Allen - 2010 - Topics in Cognitive Science 2 (3):454-485.
    Recently, there has been a resurgence of interest in general, comprehensive models of human cognition. Such models aim to explain higher-order cognitive faculties, such as deliberation and planning. Given a computational representation, the validity of these models can be tested in computer simulations such as software agents or embodied robots. The push to implement computational models of this kind has created the field of artificial general intelligence (AGI). Moral decision making is arguably one of the most challenging tasks for computational (...)
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  • Hippocampus, space, and relations.Lynn Nadel - 1994 - Behavioral and Brain Sciences 17 (3):490-491.
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  • Relational but not spatial memory: The task at hand.Elisabeth A. Murray - 1994 - Behavioral and Brain Sciences 17 (3):489-490.
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  • What can neuroanatomy tell us about the functional components of the hippocampal memory system?Wendy A. Suzuki - 1994 - Behavioral and Brain Sciences 17 (3):496-498.
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  • Functional components of the hippocampal memory system: Implications for future learning and memory research in nonhuman primates.Peter R. Rapp - 1994 - Behavioral and Brain Sciences 17 (3):491-492.
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  • From Heisenberg's cat to Eichenbaum's rat: Uncertainty in predicting the neural requirements for animal behavior.Matthew L. Shapiro - 1994 - Behavioral and Brain Sciences 17 (3):493-494.
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  • What are the best strategies for understanding hippocampal function?Paul R. Solomon & Bo-Yi Yang - 1994 - Behavioral and Brain Sciences 17 (3):494-495.
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  • Hippocampal neuronal activity in rat and primate: Memory and movement.Frasar A. W. Wilson - 1994 - Behavioral and Brain Sciences 17 (3):499-500.
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