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  1. 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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  • Early stages in a sensorimotor transformation.Martha Flanders, Stephen I. Helms Tillery & John F. Soechting - 1992 - Behavioral and Brain Sciences 15 (2):309-320.
    We present a model for several early stages of the sensorimotor transformations involved in targeted arm movement. In psychophysical experiments, human subjects pointed to the remembered locations of randomly placed targets in three-dimensional space. They made consistent errors in distance, and from these errors stages in the sensorimotor transformation were deduced. When subjects attempted to move the right index finger to a virtual target they consistently undershot the distance of the more distal targets. Other experiments indicated that the error was (...)
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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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  • S-O-R: Wrong model for pointing.William T. Powers - 1992 - Behavioral and Brain Sciences 15 (2):349-350.
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  • Central spatial representations and mapping the sensorimotor interface: How early is early, how late is late, and what difference does it all make anyhow?Paul Grobstein - 1992 - Behavioral and Brain Sciences 15 (2):339-341.
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  • Are errors in final position destined before the movement begins?Z. Hasan - 1992 - Behavioral and Brain Sciences 15 (2):341-342.
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  • Physical modeling applies to physiology, too.Vincent Hayward - 1992 - Behavioral and Brain Sciences 15 (2):342-343.
    A physical model was utilized to show that the neural system can memorize a target position and is able to cause motor and sensory events that move the arm to a target with more accuracy. However, this cannot indicate in which coordinates the necessary computations are carried out. Turning off the lights causes the error to increase which is accomplished by cutting off one feedback path. The geometrical properties of arm kinematics and the properties of the kinesthetic and visual sensorial (...)
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  • The mapping of visual space is a function of the structure of the visual field.J. Blouin, N. Teasdale, C. Bard & M. Fleury - 1992 - Behavioral and Brain Sciences 15 (2):326-327.
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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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  • Sensorimotor transformations for saccades in the primate posterior parietal cortex.R. Martyn Bracewell - 1992 - Behavioral and Brain Sciences 15 (2):329-330.
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  • For effective sensorimotor processing must there be explicit representations and reconciliation of differing frames of reference?Garrett E. Alexander - 1992 - Behavioral and Brain Sciences 15 (2):321-322.
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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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  • Do reaches in the dark shed sufficient light on internal representations?Daniel Bullock, Douglas Greve & Frank Guenther - 1992 - Behavioral and Brain Sciences 15 (2):330-332.
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  • Approximations might lead to errors in brain science.James P. Trevelyan - 1992 - Behavioral and Brain Sciences 15 (2):350-351.
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  • Now you see it, now you don't: How delaying an action system can transform a theory.Melvyn A. Goodale & Philip Servos - 1992 - Behavioral and Brain Sciences 15 (2):335-336.
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  • The cerebellum and memory.Richard F. Thompson - 1992 - Behavioral and Brain Sciences 15 (4):801-802.
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  • Invariants of the second transformation expressed in activation ranges.Gin McCollum - 1992 - Behavioral and Brain Sciences 15 (2):346-348.
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  • Schemas, grasping, tensors and avoidance.Michael A. Arbib - 1992 - Behavioral and Brain Sciences 15 (2):322-323.
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  • Coordinate transformations in postural control.Francesco Lacquaniti - 1992 - Behavioral and Brain Sciences 15 (2):345-345.
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  • Error analysis, regression and coordinate systems.Fred L. Bookstein - 1992 - Behavioral and Brain Sciences 15 (2):327-329.
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  • In the dark about pointing: What's the point?John F. Soechting, Stephen I. Helms Tillery & Martha Flanders - 1992 - Behavioral and Brain Sciences 15 (2):354-362.
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  • Coordinate transformations or dynamic models?Peter D. Neilson - 1992 - Behavioral and Brain Sciences 15 (2):348-348.
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  • Cortical mechanisms of visuomotor transformations underlying arm movements to visual targets.Yves Burnod & Roberto Caminiti - 1992 - Behavioral and Brain Sciences 15 (2):332-333.
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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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  • Distance errors: Pointing to the range effect.Charles J. Worringham & Robert G. Dennis - 1992 - Behavioral and Brain Sciences 15 (2):352-353.
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  • In reaching, the task is to move the hand to a target.J. Gordon, M. F. Ghilardi & C. Ghez - 1992 - Behavioral and Brain Sciences 15 (2):337-339.
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  • Two paradoxes of pointing.Michail Berkinblit, Olga Fookson, Sergey Adamovich & Howard Poizner - 1992 - Behavioral and Brain Sciences 15 (2):324-325.
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  • Coordinate transformations in orofacial movements.D. J. Ostry, J. R. Flanagan & L. E. Sergio - 1992 - Behavioral and Brain Sciences 15 (2):348-349.
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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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  • 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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  • Coordinate transformations: Some basic questions.Lina L. E. Massone - 1992 - Behavioral and Brain Sciences 15 (2):345-346.
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  • What do pointing errors really tell us about internal coordinate transformations?H. Cruse & J. Dean - 1992 - Behavioral and Brain Sciences 15 (2):333-335.
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  • Systematic, idiosyncratic reaching errors.David Zipser - 1992 - Behavioral and Brain Sciences 15 (2):353-354.
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  • Reaching the point where you have to move a head.John Wann - 1992 - Behavioral and Brain Sciences 15 (2):351-352.
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  • Limitations on the what reaching can tell us about sensorimotor transformations.Michael Kalish - 1992 - Behavioral and Brain Sciences 15 (2):344-344.
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  • Information decay during response delay.Dennis H. Holding - 1992 - Behavioral and Brain Sciences 15 (2):343-344.
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  • Kinesthesia and unique solutions for control of multijoint movements.S. C. Gandevia - 1992 - Behavioral and Brain Sciences 15 (2):335-335.
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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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  • Coordinate transformation and limb movements: There may be more complexity than meets the eye.James R. Bloedel - 1992 - Behavioral and Brain Sciences 15 (2):326-326.
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  • Apparent approximations in sensorimotor transformations are due to errors in pointing.David J. Bennett & Eric P. Loeb - 1992 - Behavioral and Brain Sciences 15 (2):323-324.
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