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  1. Sensory events with variable central latencies provide inaccurate clocks.Gary B. Rollman - 1985 - Behavioral and Brain Sciences 8 (4):551-552.
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  • Unconscious cerebral initiative and the role of conscious will in voluntary action.Benjamin Libet - 1985 - Behavioral and Brain Sciences 8 (4):529-66.
    Voluntary acts are preceded by electrophysiological (RPs). With spontaneous acts involving no preplanning, the main negative RP shift begins at about200 ms. Control experiments, in which a skin stimulus was timed (S), helped evaluate each subject's error in reporting the clock times for awareness of any perceived event.
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  • Is stiffness the mainspring of posture and movement?Z. Hasan - 1992 - Behavioral and Brain Sciences 15 (4):756-758.
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  • Perceiving Intentions.Joelle Proust - 2003 - In Johannes Roessler & Naomi Eilan (eds.), Agency and Self-Awareness: Issues in Philosophy and Psychology. New York: Oxford University Press.
    This paper defends the view that knowledge about one's own intentions can be gained in part through perception, although not through introspection. The various kinds of misperception of one's intentions are discussed. The latter distinction is applied to the analysis of schizophrenic patients' delusion of control.
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  • A provisional sensory/motor “complementarity” model for adaptation effects.Ivo Kohler - 1979 - Behavioral and Brain Sciences 2 (1):73-74.
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  • Non-Visual Determinants of Perception.Arien Mack - 1979 - Behavioral and Brain Sciences 2 (1):75-76.
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  • Adaptation and the two-visual-systems hypothesis.Bruce Bridgeman - 1979 - Behavioral and Brain Sciences 2 (1):64-65.
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  • Are position-control systems active during leg movement of walking arthropods?H. Cruse - 1982 - Behavioral and Brain Sciences 5 (4):543-544.
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  • How modest is the gain of the stretch reflex?James A. Mortimer & Peter Eisenberg - 1982 - Behavioral and Brain Sciences 5 (4):557-558.
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  • Neural/mental chronometry and chronotheology.Gerald S. Wasserman - 1985 - Behavioral and Brain Sciences 8 (4):556-557.
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  • The uncertainty principle in psychology.John S. Stamm - 1985 - Behavioral and Brain Sciences 8 (4):553-554.
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  • Some further observations on the functional properties of neurons in the parietal lobe of the waking monkey.V. B. Mountcastle, B. C. Motter & R. A. Andersen - 1980 - Behavioral and Brain Sciences 3 (4):520-523.
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  • The influence of motivation on the responses of neurons in the posterior parietal association cortex.E. T. Rolls, D. Perrett & S. J. Thorpe - 1980 - Behavioral and Brain Sciences 3 (4):514-515.
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  • Are parietal saccade neurons sensory or motor? Is the question worth asking?John Schlag - 1980 - Behavioral and Brain Sciences 3 (4):515-516.
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  • A command or association funtion for the posterior parietal cortex?J. Stein - 1980 - Behavioral and Brain Sciences 3 (4):516-517.
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  • Parietal cortex: Columns, connectivity, ans convergence.E. G. Jones - 1980 - Behavioral and Brain Sciences 3 (4):507-508.
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  • The functional organization of posterior parietal association cortex.James C. Lynch - 1980 - Behavioral and Brain Sciences 3 (4):485-499.
    Posterior parietal cortex has traditionally been considered to be a sensory association area in which higher-order processing and intermodal integration of incoming sensory information occurs. In this paper, evidence from clinical reports and from lesion and behavioral-electrophysiological experiments using monkeys is reviewed and discussed in relation to the overall functional organization of posterior parietal association cortex, and particularly with respect to a proposed posterior parietal mechanism concerned with the initiation and control of certain classes of eye and limb movements. Preliminary (...)
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  • Do we “control” our brains?Donald M. MacKay - 1985 - Behavioral and Brain Sciences 8 (4):546-546.
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  • When is sensory-motor information necessary, when only useful, and when superfluous?Ralph Norman Haber - 1979 - Behavioral and Brain Sciences 2 (1):68-70.
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  • Motor control: Which themes do we orchestrate?J. A. S. Kelso & E. L. Saltzman - 1982 - Behavioral and Brain Sciences 5 (4):554-557.
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  • Successive approximation in targeted movement: An alternative hypothesis.Paul J. Cordo & Leslie Bevan - 1992 - Behavioral and Brain Sciences 15 (4):729-730.
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  • The cerebellum and memory.Richard F. Thompson - 1992 - Behavioral and Brain Sciences 15 (4):801-802.
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  • The problem of adaptation to prismatically-altered shape.Irvin Rock - 1979 - Behavioral and Brain Sciences 2 (1):78-79.
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  • Methodological considerations in replicating Held and Rekosh's perceptual adaptation study.Martin J. Steinbach - 1979 - Behavioral and Brain Sciences 2 (1):81-81.
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  • The thesis of the efference-mediation of vision cannot be rationalized.M. T. Turvey - 1979 - Behavioral and Brain Sciences 2 (1):81-83.
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  • Neurological ballistic movements: Sampled data or intermittent open-loop control.Lawrence Stark - 1982 - Behavioral and Brain Sciences 5 (4):564-566.
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  • Reductionism cannot answer questions of movement control.C. A. Terzuolo & J. F. Soechting - 1982 - Behavioral and Brain Sciences 5 (4):567-568.
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  • Conscious decisions.Chris Mortensen - 1985 - Behavioral and Brain Sciences 8 (4):548-549.
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  • Are the origins of any mental process available to introspection?Michael D. Rugg - 1985 - Behavioral and Brain Sciences 8 (4):552-552.
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  • The posterior parietal association cortex in man.P. E. Roland - 1980 - Behavioral and Brain Sciences 3 (4):513-514.
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  • Reappraisal of the corollary discharge hypothesis.Hideo Sakata - 1980 - Behavioral and Brain Sciences 3 (4):515-515.
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  • Posterior parietal cortex and visual control of the hand.Mitchell Glickstein - 1980 - Behavioral and Brain Sciences 3 (4):503-503.
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  • Neglect in man: Hemispheric asymmetries and hemispatial neglect.Kenneth M. Heilman, Robert T. Watson, Edward Valenstein & Dawn Bowers - 1980 - Behavioral and Brain Sciences 3 (4):505-506.
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  • How does the nervous system control the equilibrium trajectory?S. V. Adamovich - 1992 - Behavioral and Brain Sciences 15 (4):704-705.
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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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  • Movement control views: From diversity to unity.R. B. Stein - 1982 - Behavioral and Brain Sciences 5 (4):568-577.
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  • Libet's dualism.R. J. Nelson - 1985 - Behavioral and Brain Sciences 8 (4):550-550.
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  • Global and local processing in the primate brain.R. J. W. Mansfield - 1980 - Behavioral and Brain Sciences 3 (4):509-510.
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  • An anatomical basis for the functional specialization of the parietal lobe in directed attention.M.-Marsel Mesulam - 1980 - Behavioral and Brain Sciences 3 (4):510-511.
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  • Problems in comparing the behavioural effects of parietal contex lesions in man and monkey and of integrating these with electrophysiological data.Richard Latto - 1980 - Behavioral and Brain Sciences 3 (4):508-509.
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  • The compass of the parietal “command” system.Edoardo Bisiach - 1980 - Behavioral and Brain Sciences 3 (4):499-500.
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  • Implications of neural networks for how we think about brain function.David A. Robinson - 1992 - Behavioral and Brain Sciences 15 (4):644-655.
    Engineers use neural networks to control systems too complex for conventional engineering solutions. To examine the behavior of individual hidden units would defeat the purpose of this approach because it would be largely uninterpretable. Yet neurophysiologists spend their careers doing just that! Hidden units contain bits and scraps of signals that yield only arcane hints about network function and no information about how its individual units process signals. Most literature on single-unit recordings attests to this grim fact. On the other (...)
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  • The encoding of spatial position in the brain.Joseph S. Lappin - 1979 - Behavioral and Brain Sciences 2 (1):74-75.
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  • Control theoretic concepts and motor control.Gerald L. Gottlieb & Gyan C. Agarwal - 1982 - Behavioral and Brain Sciences 5 (4):546-547.
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  • 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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  • Three functions of motor-sensory feedback in object perception.Hans Wallach - 1979 - Behavioral and Brain Sciences 2 (1):84-85.
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  • Visual-motor conflict resolved by motor adaptation without perceptual change.Joel M. Miller - 1979 - Behavioral and Brain Sciences 2 (1):76-76.
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  • Voluntary movement and perception in intrapersonal and extrapersonal space.P. E. Roland - 1979 - Behavioral and Brain Sciences 2 (1):79-80.
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  • Motor system changes are not necessary for changes in perception.George Singer, Meredith Wallace & John K. Collins - 1979 - Behavioral and Brain Sciences 2 (1):80-81.
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  • Movement control: Signal or strategy?T. D. M. Roberts - 1982 - Behavioral and Brain Sciences 5 (4):563-564.
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