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  1. How and what does the cerebellum learn?Peter F. C. Gilbert - 1996 - Behavioral and Brain Sciences 19 (3):449-450.
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  • Cerebellar rhythms: Exploring another metaphor.Patrick D. Roberts, Gin McCollum & Jan E. Holly - 1996 - Behavioral and Brain Sciences 19 (3):471-472.
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  • Further evidence for the involvement of nitric oxide in trans-ACPD-induced suppression of AMPA responses in cultured chick Purkinje neurons.Junko Mori-Okamoto & Koichi Okamoto - 1996 - Behavioral and Brain Sciences 19 (3):467-468.
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  • Positive cerebellar feedback loops.Germund Hesslow - 1996 - Behavioral and Brain Sciences 19 (3):455-456.
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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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  • A bridge between cerebellar long-term depression and discrete motor learning: Studies on gene knockout mice.Masanobu Kano - 1996 - Behavioral and Brain Sciences 19 (3):488-490.
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  • A cerebellar long-term depression update.David J. Linden - 1996 - Behavioral and Brain Sciences 19 (3):482-487.
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  • Dysmetria of thought: Correlations and conundrums in the relationship between the cerebellum, learning, and cognitive processing.Jeremy D. Schmahmann - 1996 - Behavioral and Brain Sciences 19 (3):472-473.
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  • How to link the specificity of cerebellar anatomy to motor learning?Fahad Sultan, Detlef Heck & Harold Bekkering - 1996 - Behavioral and Brain Sciences 19 (3):474.
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  • Sensorimotor learning in structures “upstream” from the cerebellum.Paul van Donkelaar - 1996 - Behavioral and Brain Sciences 19 (3):477-478.
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  • What behavioral benefit does stiffness control have? An elaboration of Smith's proposal.Gerard P. Van Galen, Angelique W. Hendriks & Willem P. DeJong - 1996 - Behavioral and Brain Sciences 19 (3):478-479.
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  • Q: Is the cerebellum an adaptive combiner of motor and mental/motor activities? A: Yes, maybe, certainly not, who can say?W. Thomas Thach - 1996 - Behavioral and Brain Sciences 19 (3):501-528.
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  • World graphs: A partial model of spatial behavior.Israel Lieblich & Michael A. Arbib - 1982 - Behavioral and Brain Sciences 5 (4):651-659.
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  • Maps, space, and places.Roger M. Downs - 1982 - Behavioral and Brain Sciences 5 (4):641-642.
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  • What spaces? What subjects?Jean Pailhous & Patrick Peruch - 1982 - Behavioral and Brain Sciences 5 (4):646-647.
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  • Cognition is not computation, for the reasons that computers don't solve the mind-body problems.Walter B. Weimer - 1980 - Behavioral and Brain Sciences 3 (1):152-153.
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  • Criteria of cognitive impenetrability.Robert C. Moore - 1980 - Behavioral and Brain Sciences 3 (1):146-147.
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  • Pylyshyn and perception.William T. Powers - 1980 - Behavioral and Brain Sciences 3 (1):148-149.
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  • Computation, consciousness and cognition.George A. Miller - 1980 - Behavioral and Brain Sciences 3 (1):146-146.
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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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  • The borders of cognition.Earl Hunt - 1980 - Behavioral and Brain Sciences 3 (1):140-141.
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  • Reductionism and cognitive flexibility.Frank Keil - 1980 - Behavioral and Brain Sciences 3 (1):141-142.
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  • Computation, cognition, and representation.John Hell - 1980 - Behavioral and Brain Sciences 3 (1):139-139.
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  • Plasticity: conceptual and neuronal.Paul M. Churchland - 1980 - Behavioral and Brain Sciences 3 (1):133-134.
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  • A remark on the completeness of the computational model of mind.William Demopoulos - 1980 - Behavioral and Brain Sciences 3 (1):135-135.
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  • On the evolution of representational capacities.Merlin Donald - 1993 - Behavioral and Brain Sciences 16 (4):775-791.
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  • Stages versus continuity.Christopher Wills - 1993 - Behavioral and Brain Sciences 16 (4):773-773.
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  • Archaeological evidence for mimetic mind and culture.Thomas Wynn - 1993 - Behavioral and Brain Sciences 16 (4):774-774.
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  • External representation: An issue for cognition.Jiajie Zhang - 1993 - Behavioral and Brain Sciences 16 (4):774-775.
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  • Apes have mimetic culture.Robert W. Mitchell & H. Lyn Miles - 1993 - Behavioral and Brain Sciences 16 (4):768-768.
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  • Language equals mimesis plus speech.Aarre Laakso - 1993 - Behavioral and Brain Sciences 16 (4):765-766.
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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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  • The gradual evolution of enhanced control by plans: A view from below.Leonard D. Katz - 1993 - Behavioral and Brain Sciences 16 (4):764-765.
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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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  • Negation in Skinner's system.N. E. Wetherick - 1984 - Behavioral and Brain Sciences 7 (4):606-607.
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  • Is there such a thing as a problem situation?Kjell Raaheim - 1984 - Behavioral and Brain Sciences 7 (4):600-601.
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  • New wine in old glasses?Joseph M. Scandura - 1984 - Behavioral and Brain Sciences 7 (4):602-603.
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  • Can Skinner define a problem?Geir Kaufmann - 1984 - Behavioral and Brain Sciences 7 (4):599-599.
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  • An operant analysis of problem solving.B. F. Skinner - 1984 - Behavioral and Brain Sciences 7 (4):583-591.
    Behavior that solves a problem is distinguished by the fact that it changes another part of the solver's behavior and is strengthened when it does so. Problem solving typically involves the construction of discriminative stimuli. Verbal responses produce especially useful stimuli, because they affect other people. As a culture formulates maxims, laws, grammar, and science, its members behave more effectively without direct or prolonged contact with the contingencies thus formulated. The culture solves problems for its members, and does so by (...)
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  • The computing frog.G. Székely - 1987 - Behavioral and Brain Sciences 10 (3):446-446.
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  • Schema theory: A new approach?W. von Seelen - 1987 - Behavioral and Brain Sciences 10 (3):448-449.
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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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  • Eye of toad, and toe of frog?John C. Marshall - 1987 - Behavioral and Brain Sciences 10 (3):444-445.
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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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  • 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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  • The cerebellum and cerebral cortex: Contrasting and converging contributions to spatial navigation and memory.Shane M. O'Mara - 1996 - Behavioral and Brain Sciences 19 (3):469-470.
    Thach's target article presents a remarkable overview and integration of animal and human studies on the functions of the cerebellum and makes clear theoretical predictions for both the normal operation of the cerebellum and for the effects of cerebellar lesions in the mature human. Commentary is provided on three areas, namely, spatial navigation, implicit learning, and cerebellar agenesis to elicit further development of the themes already present in Thach's paper, [THACH].
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  • More on climbing fiber signals and their consequence(s).J. I. Simpson, D. R. W. Wylie & C. I. De Zeeuw - 1996 - Behavioral and Brain Sciences 19 (3):496-498.
    Several themes can be identified in the commentaries. The first is that the climbing fibers may have more than one function; the second is that the climbing fibers provide sensory rather than motor signals. We accept the possibility that climbing fibers may have more than one function consequence(s)’ in the title. Until we know more about the function of the inhibitory input to the inferior olive from the cerebellar nuclei, which are motor structures, we have to keep open the possibility (...)
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  • Eyeblink conditioning, motor control, and the analysis of limbic-cerebellar interactions.Craig Weiss & John F. Disterhoft - 1996 - Behavioral and Brain Sciences 19 (3):479-481.
    Several target articles in this BBS special issue address the topic of cerebellar and olivary functions, especially as they pertain to motor earning. Another important topic is the neural interaction between the limbic system and the cerebellum during associative learning. In this commentary we present some of our data on olivo-cerebellar and limbic-cerebellar interactions during eyeblink conditioning. [HOUK et al.; SIMPSON et al.; THACH].
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  • Spanning the levels in cerebellar function.Michael A. Arbib - 1996 - Behavioral and Brain Sciences 19 (3):434-435.
    We ask what cerebellum and basal ganglia arguing that cerebellum tunes motor schemas and their coordination. We argue for a synthesis of models addressing the real-time role and error signaling roles of climbing fibers. bridges between regional and neuro-physiological studies, while relates the neurochemis-try of learning to neural and behavioral levels. [CRÉPEL et al.; HOUK et al.; KANO; LINDEN; SIMPSON et al.; SMITH; THACH; VINCENT].
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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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