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  1. Does the nervous system depend on kinesthetic information to control natural limb movements?S. C. Gandevia & David Burke - 1992 - Behavioral and Brain Sciences 15 (4):614-632.
    This target article draws together two groups of experimental studies on the control of human movement through peripheral feedback and centrally generated signals of motor commands. First, during natural movement, feedback from muscle, joint, and cutaneous afferents changes; in human subjects these changes have reflex and kinesthetic consequences. Recent psychophysical and microneurographic evidence suggests that joint and even cutaneous afferents may have a proprioceptive role. Second, the role of centrally generated motor commands in the control of normal movements and movements (...)
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  • The representation of egocentric space in the posterior parietal cortex.J. F. Stein - 1992 - Behavioral and Brain Sciences 15 (4):691-700.
    The posterior parietal cortex (PPC) is the most likely site where egocentric spatial relationships are represented in the brain. PPC cells receive visual, auditory, somaesthetic, and vestibular sensory inputs; oculomotor, head, limb, and body motor signals; and strong motivational projections from the limbic system. Their discharge increases not only when an animal moves towards a sensory target, but also when it directs its attention to it. PPC lesions have the opposite effect: sensory inattention and neglect. The PPC does not seem (...)
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  • Does the nervous system use equilibrium-point control to guide single and multiple joint movements?E. Bizzi, N. Hogan, F. A. Mussa-Ivaldi & S. Giszter - 1992 - Behavioral and Brain Sciences 15 (4):603-613.
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  • Why the computations must not be ignored.Chad J. Marsolek - 1990 - Behavioral and Brain Sciences 13 (3):554-555.
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  • The ups and downs of visual fields.David P. Crewther - 1990 - Behavioral and Brain Sciences 13 (3):550-551.
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  • Ecology and functional specialization: The whole is less than the sum of the parts.John M. Findlay - 1990 - Behavioral and Brain Sciences 13 (3):551-551.
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  • Does visual-field specialization really have implications for coordinated visual-motor behavior?Richard A. Abrams - 1990 - Behavioral and Brain Sciences 13 (3):542-543.
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  • The cognitive map must be a separate module.Benjamin Kuipers - 1982 - Behavioral and Brain Sciences 5 (4):645-646.
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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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  • The special nature of spatial information.Michael Potegal - 1982 - Behavioral and Brain Sciences 5 (4):647-648.
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  • Ecologizing world graphs.Robert E. Shaw & Ennio Mingolla - 1982 - Behavioral and Brain Sciences 5 (4):648-650.
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  • Looking for nodes and edges.Arnold Trehub - 1982 - Behavioral and Brain Sciences 5 (4):650-651.
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  • Is neuroethology wise?J. Z. Young - 1984 - Behavioral and Brain Sciences 7 (3):403-403.
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  • Neuroethology or motorethology?Joachim Erber - 1984 - Behavioral and Brain Sciences 7 (3):386-386.
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  • Can the aims of neuroethology be selective, while avoiding exclusivity?D. M. Guthrie - 1984 - Behavioral and Brain Sciences 7 (3):390-391.
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  • They are really complex when you get to know them.Irving Kupfermann - 1984 - Behavioral and Brain Sciences 7 (3):393-394.
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  • We are making good progress in the neural analysis of behaviour.David L. Macmillan - 1984 - Behavioral and Brain Sciences 7 (3):395-395.
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  • Resurrecting Lorenz's hydraulic model: Phlogiston explained by quantum mechanics.C. H. F. Rowell - 1984 - Behavioral and Brain Sciences 7 (3):397-398.
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  • Disregarding vertebrates is neither useful nor necessary.Günter Ehret - 1984 - Behavioral and Brain Sciences 7 (3):385-386.
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  • Connectionist computing and neural machinery: Examining the test of “timing”.John K. Tsotsos - 1986 - Behavioral and Brain Sciences 9 (1):106-107.
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  • Connectionist value units: Some concerns.John A. Barnden - 1986 - Behavioral and Brain Sciences 9 (1):92-93.
    This paper is a commentary on the target article by Dana H. Ballard, “Cortical connections and parallel processing: Structure and function”, in the same issue of the journal, pp. 67–120. -/- I raise some issues about the connectionist or neural-network implementation of information and information processing. Issues include the sharing of information by different parts of a connectionist/neural network, the copying of complex information from one place to another in a network, the possibility of connection weights not being synaptic weights, (...)
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  • Hippocampal–collicular interactions: An example of input linkages to the hippocampus.Thomas L. Bennett - 1987 - Behavioral and Brain Sciences 10 (1):119-119.
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  • Some limited neural and behavioral comparisons of the superior colliculus and the hippocampus.Walter Isaac - 1987 - Behavioral and Brain Sciences 10 (1):125-125.
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  • The assumptions of an interactive-modular model of the brain.Roger L. Mellgren - 1987 - Behavioral and Brain Sciences 10 (1):127-128.
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  • Different spatial frameworks.A. David Milner - 1987 - Behavioral and Brain Sciences 10 (1):128-129.
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  • Real-time attention theories of hippocampal function.Nestor A. Schmajuk - 1987 - Behavioral and Brain Sciences 10 (1):130-131.
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  • Hippocampus and superior colliculus: Interdependence or independence?Barry E. Stein - 1987 - Behavioral and Brain Sciences 10 (1):131-131.
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  • Does connectionism suffice?Steven W. Zucker - 1985 - Behavioral and Brain Sciences 8 (2):301-302.
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  • Four frames do not suffice.Stephen Grossberg - 1985 - Behavioral and Brain Sciences 8 (2):294-295.
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  • Identity and the Brain: The Biological Basis of Our Self.Andrew B. Newberg - 2023 - Zygon 58 (1):132-155.
    This article reviews the neuroscientific understanding of the self and personal identity, focusing on various elements of inclusivity and exclusivity as well as engaging religious and spiritual perspectives. We will also consider how the identity is comprised of biological, social, and ideological or spiritual aspects, and how they are interconnected. We will consider how the brain helps us to construct and maintain our representation of the self and what happens when we have self-transcendent experiences. Such an evaluation will have implications (...)
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  • The cerebellum and memory.Richard F. Thompson - 1992 - Behavioral and Brain Sciences 15 (4):801-802.
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  • Equilibrium-point hypothesis, minimum effort control strategy and the triphasic muscle activation pattern.Ning Lan & Patrick E. Crago - 1992 - Behavioral and Brain Sciences 15 (4):769-771.
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  • Scene-based and viewer-centered representations for comparing shapes.G. Hinton - 1988 - Cognition 30 (1):1-35.
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  • Properties of neurons in the dorsal visual pathway of the monkey.Ralph M. Siegel - 1990 - Behavioral and Brain Sciences 13 (3):555-556.
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  • Response field biases in parietal, temporal, and frontal lobe visual areas.Charles J. Bruce & Martha G. MacAvoy - 1990 - Behavioral and Brain Sciences 13 (3):546-547.
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  • Twisting the world by 90°.M. P. Bryden & Geoffrey Underwood - 1990 - Behavioral and Brain Sciences 13 (3):547-548.
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  • Pigeons, primates, and division of labor in the vertebrate visual system.M. A. Goodale & J. A. Graves - 1990 - Behavioral and Brain Sciences 13 (3):551-552.
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  • Seeing double: Dichotomizing the visual system.R. Martyn Bracewell - 1990 - Behavioral and Brain Sciences 13 (3):543-544.
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  • The benefits and constraints of visual processing dichotomies.Julie R. Brannan - 1990 - Behavioral and Brain Sciences 13 (3):544-545.
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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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  • A maze in graphs.Christopher K. Riesbeck - 1982 - Behavioral and Brain Sciences 5 (4):648-648.
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  • The ethology of neuroethology.Hubert Markl - 1984 - Behavioral and Brain Sciences 7 (3):396-397.
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  • Points of congruence between ethology and neuroscience.Wolfgang M. Schleidt - 1984 - Behavioral and Brain Sciences 7 (3):398-399.
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  • Ethology has progressed.Robert A. Hinde - 1984 - Behavioral and Brain Sciences 7 (3):391-391.
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  • Value, variable, and coarse coding by posterior parietal neurons.Richard A. Andersen - 1986 - Behavioral and Brain Sciences 9 (1):90-91.
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  • What's the connection?Leif H. Finkel & George N. Reeke - 1986 - Behavioral and Brain Sciences 9 (1):94-95.
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  • Invariant and programmable neuropsychological systems are fibrations.William C. Hoffman - 1986 - Behavioral and Brain Sciences 9 (1):99-100.
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  • What's in the term connectionist?.Christof Koch - 1986 - Behavioral and Brain Sciences 9 (1):100-101.
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  • The heterogeneity and plasticity of cerebral structures.Bruno E. Will, John C. Dalrymple-Alford & Georges Di Scala - 1987 - Behavioral and Brain Sciences 10 (1):131-132.
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  • Could three frames suffice?Roger A. Browse & Brian E. Butler - 1985 - Behavioral and Brain Sciences 8 (2):290-291.
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