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  1. The cerebellum and memory.Richard F. Thompson - 1992 - Behavioral and Brain Sciences 15 (4):801-802.
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  • Implicit Transfer of Reversed Temporal Structure in Visuomotor Sequence Learning.Kanji Tanaka & Katsumi Watanabe - 2014 - Cognitive Science 38 (3):565-579.
    Some spatio-temporal structures are easier to transfer implicitly in sequential learning. In this study, we investigated whether the consistent reversal of triads of learned components would support the implicit transfer of their temporal structure in visuomotor sequence learning. A triad comprised three sequential button presses ([1][2][3]) and seven consecutive triads comprised a sequence. Participants learned sequences by trial and error, until they could complete it 20 times without error. Then, they learned another sequence, in which each triad was reversed ([3][2][1]), (...)
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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.
  • 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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  • 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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  • Codes and their vicissitudes.Bernhard Hommel, Jochen Müsseler, Gisa Aschersleben & Wolfgang Prinz - 2001 - Behavioral and Brain Sciences 24 (5):910-926.
    First, we discuss issues raised with respect to the Theory of Event Coding (TEC)'s scope, that is, its limitations and possible extensions. Then, we address the issue of specificity, that is, the widespread concern that TEC is too unspecified and, therefore, too vague in a number of important respects. Finally, we elaborate on our views about TEC's relations to other important frameworks and approaches in the field like stages models, ecological approaches, and the two-visual-pathways model. Footnotes1 We acknowledge the precedence (...)
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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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  • 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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  • 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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  • 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.
  • 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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