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  1. On the stabilization of behavioral selection.Werner K. Honig - 1984 - Behavioral and Brain Sciences 7 (4):491-492.
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  • On doing research on consciousness without being aware of it.Daniel Holender - 1990 - Behavioral and Brain Sciences 13 (4):612-614.
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  • Effective procedures versus elementary units of behavior.John M. Hollerbach - 1981 - Behavioral and Brain Sciences 4 (4):625-627.
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  • Moving with control: Using control theory to understand motor behavior.Neville Hogan - 1982 - Behavioral and Brain Sciences 5 (4):550-551.
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  • Hierarchy and behavior.Jerry A. Hogan - 1981 - Behavioral and Brain Sciences 4 (4):625-625.
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  • Central control and reflex regulation of mechanical impedance: The basis for a unified motor-control scheme.J. A. Hoffer - 1982 - Behavioral and Brain Sciences 5 (4):548-549.
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  • The unobservability of central commands: Why testing hypotheses is so difficult.Antony Hodgson - 1995 - Behavioral and Brain Sciences 18 (4):763-764.
    The experiments Feldman and Levin suggest do not definitively test their proposed solution to the problem of selecting muscle activations. Their test of the movement directions that elicit EMG activity can be interpreted without regard to the form of the central commands, and their fast elbow flexion test is based on a forward computation that obscures the insensitivity of the predicted trajectory to the details of the putative commands.
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  • “Consciousness” is the name of a nonentity.Deborah Hodgkin & Alasdair I. Houston - 1990 - Behavioral and Brain Sciences 13 (4):611-612.
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  • Matter, levels, and consciousness.Jerry R. Hobbs - 1990 - Behavioral and Brain Sciences 13 (4):610-611.
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  • Ethology has progressed.Robert A. Hinde - 1984 - Behavioral and Brain Sciences 7 (3):391-391.
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  • Searle's vision of psychology.James Higginbotham - 1990 - Behavioral and Brain Sciences 13 (4):608-610.
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  • Positive cerebellar feedback loops.Germund Hesslow - 1996 - Behavioral and Brain Sciences 19 (3):455-456.
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  • The Default Mode Network and the Problem of Determining Intrinsic Mental Contents.Marek Havlík & Tomáš Marvan - 2015 - Studies in Logic, Grammar and Rhetoric 40 (1):145-160.
    We provide a brief overview of the shift toward the intrinsic view of brain activity, describing in particular the structural and functional connectivity patterns of the “Default mode network”. We then consider the Default mode network in a specifically cognitive setting and ask what changes the focus on the Default mode network and other sorts of intrinsic activity require from models put forward by cognitive neuroscientists.
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  • Neuronal communication: don't forget the glia!Glenn I. Hatton - 1979 - Behavioral and Brain Sciences 2 (3):426-427.
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  • Do control variables exist?Nicholas G. Hatsopoulos & William H. Warren - 1995 - Behavioral and Brain Sciences 18 (4):762-762.
    We argue that the concept of a control variable (CV) as described by Feldman and Levin needs to be revised because it does not account for the influence of sensory feedback from the periphery. We provide evidence from the realm of rhythmic movements that sensory feedback can permanently alter the frequency and phase of a centrally generated rhythm.
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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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  • Do subprograms for movement always seek equilibrium?Z. Hasan - 1986 - Behavioral and Brain Sciences 9 (4):609-610.
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  • “What's in a name?” A case for redefining the autonomic nervous system.John H. Haring - 1990 - Behavioral and Brain Sciences 13 (2):304-305.
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  • Two separate pathways for cerebellar LTD: NO-dependent and NO-independent.Nick A. Hartell - 1996 - Behavioral and Brain Sciences 19 (3):453-455.
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  • Tracking brain functions in space and time.Riitta Hari - 1995 - Behavioral and Brain Sciences 18 (2):359-360.
    The authors ofImages of mindhave been highly successful in unravelling the neural basis of complex brain functions. Their emphasis on top-down processingin experimental neuroscience is especially important and, it is hoped, influential. Tracking brain activation accurately botli in space and in time would benefit from studiesofindividual subjects without relying on grand average data.
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  • Intentionality: Some distinctions.Gilbert Harman - 1990 - Behavioral and Brain Sciences 13 (4):607-608.
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  • Force and stiffness: Further considerations.Nigel Harvey & Kerry Greer - 1982 - Behavioral and Brain Sciences 5 (4):547-548.
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  • Is λ an appropriate control variable for locomotion?Thomas M. Hamm & Zong-Sheng Han - 1995 - Behavioral and Brain Sciences 18 (4):761-762.
    The lambda model predicts that the command received by each motor nucleus during locomotion is specific for the joint at which its muscle acts and is independent of external conditions. However, investigation of the commands received by motor nuclei during fictive locomotion and of the sensitivity of these commands to feedback from the limb during locomotion indicates that neither condition is satisfied.
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  • The physiology of Descartes and its modern developments.J. S. Haldane - 1935 - Acta Biotheoretica 1 (1-2):5-16.
    Nach einer kurzen Übersicht überDescartes' mechanistiche Theorie der somatischen Funktionen und der Reproduktion, wird in der vorliegenden Arbeit die Entwicklung dieser Theorie bis zur neuesten Zeit beschrieben. Sodann wird eine Übersicht gegeben über die vitalistische Theorie, welche unter wissenschaftlichen Forschern bis zur Mitte des vorigen Jahrhunderts vorherrschte. Dann werden die Gründe dafür angegeben, dass diese Theorie des Vitalismus ungefähr um diese Zeit verlassen wurde, um durch die mechanistische Theorie ersetzt zu werden. Diese ihrerseits ist jedoch auf einer unbegründeten metaphysischen Auffassung (...)
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  • PET may image the gates of awareness, not its center.Eric Halgren - 1995 - Behavioral and Brain Sciences 18 (2):358-359.
    PET detects changes in metabolism between task periods and is thus insensitive to areas that are activated during all or most of cognition. Depth-recorded, evokedpotentials indicate that many multimodal and limbic cortical areas may be activated during most cognitive tasks. Thus, PET may be insensitive to some core processes of awareness that are difficult to eliminate from the control periods.
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  • Fitting culture into a Skinner box.C. R. Hallpike - 1984 - Behavioral and Brain Sciences 7 (4):489-490.
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  • Twisted pairs: Does the motor system really care about joint configurations?Patrick Haggard, Chris Miall & John Stein - 1995 - Behavioral and Brain Sciences 18 (4):758-761.
    Extrapersonal frames of reference for aimed movements are representationally convenient. They may, however, carry associated costs when the movement is executed in terms of the complex coordination of multiple joints they require. Studies that have measured both fingertip and joint paths suggest the motor systems may seek a compromise between simplicity of extrapersonal spatial representation and computational simplicity of multi-joint execution.
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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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  • B-afferents: The basis for autonomic reflexes?D. Grundy - 1990 - Behavioral and Brain Sciences 13 (2):304-304.
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  • Stable self-organization of sensory recognition codes: Is chaos necessary?Stephen Grossberg - 1987 - Behavioral and Brain Sciences 10 (2):179-180.
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  • Neuroethology and theoretical neurobiology.Stephen Grossberg - 1984 - Behavioral and Brain Sciences 7 (3):388-390.
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  • A new synthesis?Sten Grillner - 1981 - Behavioral and Brain Sciences 4 (4):624-625.
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  • Multiple roles of muscular afferents.Ragnar Granit - 1982 - Behavioral and Brain Sciences 5 (4):547-547.
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  • Fables of the prefrontal cortex.Jordan Grafman, Arnaud Partiot & Caroline Hollnagel - 1995 - Behavioral and Brain Sciences 18 (2):349-358.
    On the basis of neuroiinaging studies, Posner & Raichle summarily report that the prefrontal cortex is involved in executive functioning and attention. In contrast to that superficial view, we briefly describe a testable model of the kinds of representations that are stored in prefrontal cortex, which, when activated, are expressed via plans, actions, thematic knowledge, and schemas.
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  • Do force-measuring sense organs contribute to the reflex control of motor output in insects?D. Graham - 1982 - Behavioral and Brain Sciences 5 (4):547-547.
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  • The invariant characteristic isn't.Gerald L. Gottlieb & Gyan C. Agarwal - 1986 - Behavioral and Brain Sciences 9 (4):608-609.
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  • Shifting frames of reference but the same old point of view.Gerald L. Gottlieb - 1995 - Behavioral and Brain Sciences 18 (4):758-758.
    Models of central control variables (CVs) that are expressed in positional reference frames and rely on proprioception as the dominant specifier of muscle activation patterns have not yet been shown to be adequate for the description of fast, voluntary movement, even of single joints. An alternative model with illustrative data is proposed.
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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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  • Inverse kinematic problem: Solutions by pseudoinversion, inversion and no-inversion.Simon R. Goodman - 1995 - Behavioral and Brain Sciences 18 (4):756-758.
    Kinematic properties of reaching movements reflect constraints imposed on the joint angles. Contemporary models present solutions to the redundancy problem by a pseudoinverse procedure (Whitney 1969) or without any inversion (Berkenblit et al. 1986). Feldman & Levin suggest a procedure based on a regular inversion. These procedures are considered as an outcome of a more general approach.
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  • What are the building blocks of the frog's wiping reflex?Ilan Golani - 1986 - Behavioral and Brain Sciences 9 (4):607-608.
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  • The neurodynamics of heavy PETing, at/intention, learning, functional recovery, and rehabilitation.Gary Goldberg & Nathaniel H. Mayer - 1995 - Behavioral and Brain Sciences 18 (2):348-349.
    Research reported by Posner & Raichle may be usefully applied to the rehabilitation of persons with brain damage. Their findings are related to the “dual premotorsystems hypothesis” that reciprocally interactive medial and lateral brain systems are involved in attention and learning. Recent studies show that “brain healing” occurs through dynamic reorganization involving attentional networks postulated by Posner & Raichle.
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  • The James-Lange theory: A logical post-mortem.Cornelius L. Golightly - 1953 - Philosophy of Science 20 (4):286-299.
    The following statement from James’ 1884 essay in Mind is repeated in his later work and appears often in secondary sources as a summary of his celebrated theory of the emotions:Our natural way of thinking about these standard emotions is that the mental perception of some fact excites the mental affection called the emotion, and that this latter state of mind gives rise to the bodily expression. My thesis on the contrary is that the bodily changes follow directly the Perception (...)
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  • Images in search of a theory.Ben Goertzel - 1995 - Behavioral and Brain Sciences 18 (2):347-348.
    Images of mindis an exciting book, well-written and wellorganized, but many of the connections the authors draw between PET scan results and more general psychological issues are somewhat strained.
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  • Unconscious mental processes.Clark Glymour - 1990 - Behavioral and Brain Sciences 13 (4):606-607.
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  • The case of the missing CVs: Multi-joint primitives.Simon Giszter - 1995 - Behavioral and Brain Sciences 18 (4):755-756.
    The search for simplifying principles in motor control motivates the target article. One method that the CNS uses to simplify the task of controlling a limb's mechanical properties is absent from the article. Evidence from multi-joint, force-field measurements and from kinematics that points to the existence of multi-joint primitives as control variables is discussed.
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  • How and what does the cerebellum learn?Peter F. C. Gilbert - 1996 - Behavioral and Brain Sciences 19 (3):449-450.
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  • Simple changes in reflex threshold cannot explain all aspects of rapid voluntary movements.C. Gielen & J. C. Houk - 1986 - Behavioral and Brain Sciences 9 (4):605-607.
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  • Reciprocal and coactivation commands are not sufficient to describe muscle activation patterns.C. C. A. M. Gielen & B. van Bolhuis - 1995 - Behavioral and Brain Sciences 18 (4):754-755.
    Recent results have shown that the relative activation of muscles is different for isometric contractions and for movements. These results exclude an explanation of muscle activation patterns by a combination ofreciprocal and coactivation commands. These results also indicate that joint stiffness is not uniquely determined and that it may be different for isometric contractions and movements.
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  • Cerebellum does more than recalibration of movements after perturbations.C. Gielen - 1996 - Behavioral and Brain Sciences 19 (3):448-449.
    We argue that the function of the cerebellum is more than just an error-detecting mechanism. Rather, the cerebellum plays an important role in all movements. The bias in (re)calibration is an unfortunate restrictive result of a very successful and important experiment, [SMITH, THACH].
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  • Metaphor and monophony in the 20th-century psychology of emotions.Kenneth J. Gergen - 1995 - History of the Human Sciences 8 (2):1-23.
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