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  1. Multiple representations of space underlying behavior.Israel Lieblich & Michael A. Arbib - 1982 - Behavioral and Brain Sciences 5 (4):627-640.
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  • The notions of joint stiffness and synaptic plasticity in motor memory.Lev P. Latash & Mark L. Latash - 1996 - Behavioral and Brain Sciences 19 (3):465-466.
    We criticize the synaptic theory of long-term memory and the inappropriate usage of physical notions such as in motor control theories. Motor control and motor memory hypotheses should be based on explicitly specified hypothetical control variables that are sound from both physiological and physical perspectives. [HOUK et al.; SMITH; THACH].
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  • Structure and process in schema-based architectures.Pat Langley - 1987 - Behavioral and Brain Sciences 10 (3):442-442.
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  • Language equals mimesis plus speech.Aarre Laakso - 1993 - Behavioral and Brain Sciences 16 (4):765-766.
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  • Functional architecture and free will.Henry E. Kyburg - 1980 - Behavioral and Brain Sciences 3 (1):143-146.
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  • Problem solving as a cognitive process.Manfred Kochen - 1984 - Behavioral and Brain Sciences 7 (4):599-600.
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  • The elusive visual processing mode: Implications of the architecture/algorithm distinction.Roberta L. Klatzky - 1980 - Behavioral and Brain Sciences 3 (1):142-143.
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  • Can Skinner define a problem?Geir Kaufmann - 1984 - Behavioral and Brain Sciences 7 (4):599-599.
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  • Exploratory behavior without novelty drive?Arthur I. Karshmer, Derek Partridge & Victor Johnson - 1982 - Behavioral and Brain Sciences 5 (4):644-645.
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  • Contingencies, rules, and the “problem” of novel behavior.Pere Julià - 1984 - Behavioral and Brain Sciences 7 (4):598-599.
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  • The biotope of Rana computatrix.P. I. M. Johannesma - 1987 - Behavioral and Brain Sciences 10 (3):440-441.
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  • The evolved mind.Harry J. Jerison - 1993 - Behavioral and Brain Sciences 16 (4):763-764.
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  • The borders of cognition.Earl Hunt - 1980 - Behavioral and Brain Sciences 3 (1):140-141.
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  • A case study of how a paper containing good ideas, presented by a distinguished scientist, to an appropriate audience, had almost no influence at all.Earl Hunt - 1984 - Behavioral and Brain Sciences 7 (4):597-598.
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  • The reification of the mind-body problem?Stewart H. Hulse - 1980 - Behavioral and Brain Sciences 3 (1):139-140.
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  • More models of the cerebellum.James C. Houk & Andrew G. Barto - 1996 - Behavioral and Brain Sciences 19 (3):492-496.
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  • Cerebellar arm ataxia: Theories still have a lot to explain.J. Hore - 1996 - Behavioral and Brain Sciences 19 (3):457.
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  • On choosing the “right” stimulus and rule.Robin M. Hogarth - 1984 - Behavioral and Brain Sciences 7 (4):596-596.
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  • Positive cerebellar feedback loops.Germund Hesslow - 1996 - Behavioral and Brain Sciences 19 (3):455-456.
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  • Computation, cognition, and representation.John Hell - 1980 - Behavioral and Brain Sciences 3 (1):139-139.
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  • Two separate pathways for cerebellar LTD: NO-dependent and NO-independent.Nick A. Hartell - 1996 - Behavioral and Brain Sciences 19 (3):453-455.
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  • From mimetic to mythic culture: Stimulus equivalence effects and prelinguistic cognition.P. J. Hampson - 1993 - Behavioral and Brain Sciences 16 (4):763-763.
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  • Mythos and logos.John Halverson - 1993 - Behavioral and Brain Sciences 16 (4):762-762.
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  • A computer model of the temporal course of agrammatic sentence understanding: The effects of variation in severity and sentence complexity.Henk J. Haarmann & Herman H. J. Kolk - 1991 - Cognitive Science 15 (1):49-87.
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  • Semantic Interference and Facilitation: Understanding the Integration of Spatial Distance and Conceptual Similarity During Sentence Reading.Ernesto Guerra & Pia Knoeferle - 2018 - Frontiers in Psychology 9.
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  • The microscopic analysis of behavior: Toward a synthesis of instrumental, perceptual, and cognitive ideas.Stephen Grossberg - 1984 - Behavioral and Brain Sciences 7 (4):594-595.
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  • Human and computer rules and representations are not equivalent.Stephen Grossberg - 1980 - Behavioral and Brain Sciences 3 (1):136-138.
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  • Working memory and its extensions.K. J. Gilhooly - 1993 - Behavioral and Brain Sciences 16 (4):761-762.
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  • Cerebellum does more than recalibration of movements after perturbations.C. Gielen - 1996 - Behavioral and Brain Sciences 19 (3):448-449.
    We argue that the function of the cerebellum is more than just an error-detecting mechanism. Rather, the cerebellum plays an important role in all movements. The bias in (re)calibration is an unfortunate restrictive result of a very successful and important experiment, [SMITH, THACH].
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  • Cultural transitions occur when mind parasites learn new tricks.Liane M. Gabora - 1993 - Behavioral and Brain Sciences 16 (4):760-761.
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  • In defence of the armchair.Michael Fortescue - 1980 - Behavioral and Brain Sciences 3 (1):135-136.
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  • Evolution needs a modern theory of the mind.James H. Fetzer - 1993 - Behavioral and Brain Sciences 16 (4):759-760.
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  • Standards for neural modeling.Jerome A. Feldman & David Zipser - 1982 - Behavioral and Brain Sciences 5 (4):642-642.
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  • Grasping cerebellar function depends on our understanding the principles of sensorimotor integration: The frame of reference hypothesis.Anatol G. Feldman & Mindy F. Levin - 1996 - Behavioral and Brain Sciences 19 (3):442-445.
    The cerebellum probably obeys the rules of sensorimotor integration common in the nervous system. One such a rule is formulated: the nervous system organizes spatial frames of reference for the sensorimotor apparatus and produces voluntary movements by shifting their origin points. We give examples of spatial frames of reference for different single- and multi-joint movements including locomotion and also illustrate that the process of motor development and learning may depend critically on the formation of appropriate frames of reference and the (...)
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  • From mimesis to synthesis.Jerome A. Feldman - 1993 - Behavioral and Brain Sciences 16 (4):759-759.
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  • Advantage of modeling in neuroscience.J. -P. Ewert - 1987 - Behavioral and Brain Sciences 10 (3):438-439.
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  • Précis of Origins of the modern mind: Three stages in the evolution of culture and cognition.Merlin Donald - 1993 - Behavioral and Brain Sciences 16 (4):737-748.
    This book proposes a theory of human cognitive evolution, drawing from paleontology, linguistics, anthropology, cognitive science, and especially neuropsychology. The properties of humankind's brain, culture, and cognition have coevolved in a tight iterative loop; the main event in human evolution has occurred at the cognitive level, however, mediating change at the anatomical and cultural levels. During the past two million years humans have passed through three major cognitive transitions, each of which has left the human mind with a new way (...)
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  • On the depth and fit of behaviorist explanation.L. Jonathan Cohen - 1984 - Behavioral and Brain Sciences 7 (4):591-592.
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  • How can the cerebellum match “error signal” and “error correction”?Michel Dufossé - 1996 - Behavioral and Brain Sciences 19 (3):442-442.
    This study examines how a Purkinje cell receives its appropriate olivary error signal during the learning of compound movements. We suggest that the Purkinje cell only reinforces those target pyramidal cells which already participate in the movement, subsequently reducing any repeated error signal, such as its own climbing fiber input, [simpson et al.; smith].
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  • Maps, space, and places.Roger M. Downs - 1982 - Behavioral and Brain Sciences 5 (4):641-642.
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  • Can we analyze Skinner's problem-solving behavior in operant terms?P. C. Dodwell - 1984 - Behavioral and Brain Sciences 7 (4):592-593.
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  • What about pictures?J. B. Deregowski - 1993 - Behavioral and Brain Sciences 16 (4):757-758.
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  • Saccades and the adjustable pattern generator.Paul Dean - 1996 - Behavioral and Brain Sciences 19 (3):441-442.
    The adjustable pattern generator (APG) model addresses physiological detail in a manner that renders it eminently testable. However, the problem for which the APG was developed, namely, limb control, may be computationally too complex for this purpose. Instead, it is proposed that recent empirical and theoretical advances in understanding the role of the cerebellum in low-level saccadic control could be used to refine and extend the APG. [HOUK et al.].
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  • Ethological foxes and cognitive hedgehogs.Jeffrey Cynx & Stephen J. Clark - 1993 - Behavioral and Brain Sciences 16 (4):756-757.
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  • From computational metaphor to consensual algorithms.Kenneth Mark Colby - 1980 - Behavioral and Brain Sciences 3 (1):134-135.
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  • A natural history of the mind: A guide for cognitive science.Thomas L. Clarke - 1993 - Behavioral and Brain Sciences 16 (4):754-755.
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  • Neuroscience and psychology: should the labor be divided?Patricia Smith Churchland - 1980 - Behavioral and Brain Sciences 3 (1):133-133.
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  • Archaeology and the cognitive sciences in the study of human evolution.Philip G. Chase - 1993 - Behavioral and Brain Sciences 16 (4):752-753.
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  • Mimetic culture and modern sports: A synthesis.Bruce Bridgeman & Margarita Azmitia - 1993 - Behavioral and Brain Sciences 16 (4):751-752.
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  • Perhaps it's time to completely rethink cerebellar function.James M. Bower - 1996 - Behavioral and Brain Sciences 19 (3):438-439.
    The primary assumption made in this series of target articles is that the cerebellum is directly involved in motor control. However, in my opinion, there is ample and growing experimental evidence to question this classical view, whether or not learning is involved. I propose, instead, that the cerebellum is involved in the control of data acquisition for many different sensory systems, [CRÉPEL et al., HOUK et al., SMITH, THACH].
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