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  1. Human and nonhuman systems are adaptive in a different sense.Tamás Zétényi - 1991 - Behavioral and Brain Sciences 14 (3):507-508.
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  • Systematic, idiosyncratic reaching errors.David Zipser - 1992 - Behavioral and Brain Sciences 15 (2):353-354.
  • Biological variability and control of movements via δλ.Charles E. Wright & Rebecca A. States - 1995 - Behavioral and Brain Sciences 18 (4):786-786.
    Three issues related to Feldman and Levin's treatment of biological variability are discussed. We question the usefulness of the indirect component of δλ. We suggest that trade-offs between speed and accuracy in aimed movements support identification of δλ, rather than λ, as a control variable. We take issue with the authors' proposal for resolving redundancy in multi-joint movements, given recent data.
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  • Towards functional movement: Implications for research and therapy.C. J. Worringham, G. K. Kerr & C. O'Brien - 1996 - Behavioral and Brain Sciences 19 (1):92-94.
  • Distance errors: Pointing to the range effect.Charles J. Worringham & Robert G. Dennis - 1992 - Behavioral and Brain Sciences 15 (2):352-353.
  • Strategies for goal-directed fast movements are byproducts of satisfying performance criteria.Jack M. Winters & Amir H. Seif-Naraghi - 1991 - Behavioral and Brain Sciences 14 (2):357-359.
  • Levers to generate movement.U. Windhorst - 1995 - Behavioral and Brain Sciences 18 (4):784-785.
    The following questions are discussed: (1) Who determines the nature of “control variables”? (2) Is the “positional monopoly” healthy? (3) Does a descending command alter reflex threshold alone without eoncomitantly altering stiffness? (4) How does the CNS deal with history-dependent effects? (5) Should we abandon the idea that the CNS controls classical Newtonian variables such as muscle length?
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  • How far should we extend the equilibrium point (lambda) hypothesis?Jack M. Winters - 1995 - Behavioral and Brain Sciences 18 (4):785-786.
    A key feature of the lambda model is the hypothesis of a local spring-like muscle-reflex system defined by a central control variable that has units of position. This is intriguing, especially for a study of postural stability in large-scale systems, but it has limited direct application to skilled everyday movements. If movement is considered as a goal-directed, neuro-optimization problem, however, theavailabilityof lambda-like peripheral models (vs. conventional musculoskeletal models) deserves exploration.
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  • Altered bilateral muscle synergies after stroke.Alan M. Wing, Stephen Kirker & John R. Jenner - 1996 - Behavioral and Brain Sciences 19 (1):92-92.
  • The mystery-mastery-imagery complex.H. T. A. Whiting & R. P. Ingvaldsen - 1994 - Behavioral and Brain Sciences 17 (2):228-229.
  • Reaching the point where you have to move a head.John Wann - 1992 - Behavioral and Brain Sciences 15 (2):351-352.
  • Potential disparities between imagining and preparing motor skills.Charles B. Walter & Stephan P. Swinnen - 1994 - Behavioral and Brain Sciences 17 (2):227-228.
  • Optimal search strategies for optimal motor solutions: Self-determination or informed guidance?C. B. Walter & K. Kamm - 1996 - Behavioral and Brain Sciences 19 (1):91-92.
  • Anthropomorphizing the CNS: Is it what or who you know?Michael G. Wade & Jinhua Guan - 1996 - Behavioral and Brain Sciences 19 (1):90-91.
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  • Imagery needs preparation too.Stefan Vogt - 1994 - Behavioral and Brain Sciences 17 (2):226-227.
  • On optimality and movement disorders: A dynamic systems perspective.R. E. A. van Emmerik & R. C. Wagenaar - 1996 - Behavioral and Brain Sciences 19 (1):90-90.
  • Equifinality and phase-resetting: The role of control parameter manipulations.R. E. A. van Emmerik & R. C. Wagenaar - 1995 - Behavioral and Brain Sciences 18 (4):783-784.
    It is argued that the equilibrium point model can lead to new insights regarding transition and stability processes in movement coordination. The role of movement control parameters on equifinality and phase-resetting is discussed; not only control but also external control parameters can affect the global dynamical regime.
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  • Action and attention.A. H. C. Van der Heijden & Bruce Bridgeman - 1994 - Behavioral and Brain Sciences 17 (2):225-226.
  • Computational resources do constrain behavior.John K. Tsotsos - 1991 - Behavioral and Brain Sciences 14 (3):506-507.
  • Generic mechanisms of coordination in special populations.Paul J. Treffner & J. A. Scott Kelso - 1996 - Behavioral and Brain Sciences 19 (1):89-89.
  • Approximations might lead to errors in brain science.James P. Trevelyan - 1992 - Behavioral and Brain Sciences 15 (2):350-351.
  • The cerebellum and memory.Richard F. Thompson - 1992 - Behavioral and Brain Sciences 15 (4):801-802.
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  • Origins of origins of motor control.Esther Thelen - 1995 - Behavioral and Brain Sciences 18 (4):780-783.
    Examination of infant spontaneous and goal-directed arm movements supports Feldman and Levin's hypothesis of a functional hierarchy. Early infant movements are dominated by biomechanical and dynamic factors without external frames of reference. Development involves not only learning to generate these frames of reference, but also protecting the higher-level goal of the movement from internal and external perturbations.
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  • Developmental “movement disorders” and problem solving.Esther Thelen - 1996 - Behavioral and Brain Sciences 19 (1):88-89.
  • Strategies for the control of voluntary movements in patients with Parkinson's disease.Normand Teasdale, George E. Stelmach & Friedemann Mueller - 1991 - Behavioral and Brain Sciences 14 (2):357-357.
  • Is motor pathology associated with setting new CNS priorities or with increased difficulty in overcoming or suppressing preexisting CNS priorities?Stephan P. Swinnen, Sabine M. P. Verschueren & Natalia Dounskaia - 1996 - Behavioral and Brain Sciences 19 (1):87-88.
  • When are adaptive motor patterns nonadaptive?Jeffery J. Summers & Julie Thomas - 1996 - Behavioral and Brain Sciences 19 (1):87-87.
  • Separability of reference frame distinctions from motor and visual images.Gary W. Strong - 1994 - Behavioral and Brain Sciences 17 (2):224-225.
  • The representation of egocentric space in the posterior parietal cortex.J. F. Stein - 1992 - Behavioral and Brain Sciences 15 (4):691-700.
  • Control parameters, equilibria, and coordination dynamics.Dagmar Sternad & M. T. Turvey - 1995 - Behavioral and Brain Sciences 18 (4):780-780.
    Important similarities exist between the dynamical concepts implicit in Feldman & Levin's extended λ model and those basic to a dynamical systems approach. We argue that careful application of the key concepts of control and order parameters, equilibria, and stability, can relate known facts of neuromuscular processes to the observables of functional, task-specific behavior.
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  • What is the appropriate criterion for therapeutic intervention in the motor domain?W. A. Sparrow - 1996 - Behavioral and Brain Sciences 19 (1):86-86.
  • 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.
  • Rationality and irrationality: Still fighting words.Paul Snow - 1991 - Behavioral and Brain Sciences 14 (3):505-506.
  • A Bayesian theory of thought.Howard Smokler - 1991 - Behavioral and Brain Sciences 14 (3):505-505.
  • Two joints are more than twice one joint.Jeroen B. J. Smeets - 1995 - Behavioral and Brain Sciences 18 (4):779-780.
    An alternative multi-joint extension to the lambda model is proposed. According to this extension, the activity of a muscle depends not only on the difference between lambda and length of that muscle, but also on the difference between lambda and length of other muscles. This 2-D extension can describe more neurophysiological experiments than the extension proposed in the target article.
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  • But how does the brain think?Steven L. Small - 1991 - Behavioral and Brain Sciences 14 (3):504-505.
  • How do we satisfy our goals?Paul G. Skokowski - 1994 - Behavioral and Brain Sciences 17 (2):224-224.
  • Canonical representations and constructive praxis: Some developmental and linguistic considerations.Chris Sinha - 1994 - Behavioral and Brain Sciences 17 (2):223-224.
  • The rationality of causal inference.Thomas R. Shultz - 1991 - Behavioral and Brain Sciences 14 (3):503-504.
  • On the nonapplicability of a rational analysis to human cognition.Eldar Shafir - 1991 - Behavioral and Brain Sciences 14 (3):502-503.
  • Can the λ model be used to interpret the activity of single neurons?Stephen H. Scott - 1995 - Behavioral and Brain Sciences 18 (4):778-779.
    Whereas the λ model provides a useful technique to describe complex movements, the focus on control variables in this model limits its potential for interpreting the activity and function of many cells in motor areas of the CNS.
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  • Rational analysis will not throw off the yoke of the precision-importance trade-off function.Wolfgang Schwarz - 1991 - Behavioral and Brain Sciences 14 (3):501-502.
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  • How functional are atypical motor patterns?John P. Scholz - 1996 - Behavioral and Brain Sciences 19 (1):85-86.
  • Neurophysiology of preparation, movement and imagery.Jerome N. Sanes - 1994 - Behavioral and Brain Sciences 17 (2):221-223.
  • Kinaesthetic illusions as tools in understanding motor imagery.J. P. Roll, J. C. Gilhodes & R. Roll - 1994 - Behavioral and Brain Sciences 17 (2):220-221.
  • 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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  • Nonconscious motor images.Giacomo Rizzolatti - 1994 - Behavioral and Brain Sciences 17 (2):220-220.
  • To dream is not to (intend to) do.Jean Requin - 1994 - Behavioral and Brain Sciences 17 (2):218-219.
  • The cognitive laboratory, the library and the Skinner box.Howard Rachlin - 1991 - Behavioral and Brain Sciences 14 (3):501-501.
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  • Position is everything?Karl H. Pribram - 1995 - Behavioral and Brain Sciences 18 (4):776-778.
    Neurophysiological evidence consonant with F&L's lambda model is reviewed and results of additional experiments are presented. The evidence shows that there are neurons in the motor cortex that respond to selective band widths of passive sinusoidal movements; the additional data show how, with movement, directionally sensitive population vectors can be shown to emerge from the data.
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