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What a perception–production link does for language
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- 04 February 2010, p. 216
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Apparent motion and the icon
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- 04 February 2010, p. 20
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Adaptationist theorizing and intentional system theory
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- 04 February 2010, p. 365
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Stone's revised aminergic hypothesis and the functional significance of receptor binding sensitivity
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- Published online by Cambridge University Press:
- 04 February 2010, pp. 555-556
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A rose by any other name
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- 04 February 2010, pp. 216-217
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The output hypothesis: New peripheral indicators of brain function?
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- 04 February 2010, pp. 556-557
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Iconoclasm avoided: What the single neuron tells the psychologist about the icon
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- 04 February 2010, pp. 20-21
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Belief accripton, parsimony, and rationality
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- 04 February 2010, pp. 365-366
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The adaptiveness of mentalism?,
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- 04 February 2010, p. 366
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The dependence of perception on persisting images and “icons”
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- 04 February 2010, pp. 21-22
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Stress: Cause and cure of depression?
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- 04 February 2010, p. 557
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On models, mechanisms and the evolution of human language
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- 04 February 2010, pp. 217-218
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Dennett's “Panglossian paradigm”
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- 04 February 2010, pp. 366-367
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Mapping speech: More analysis, less synthesis, please
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- Published online by Cambridge University Press:
- 04 February 2010, pp. 218-219
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Epinephrine, the neglected catecholamine
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- Published online by Cambridge University Press:
- 04 February 2010, pp. 557-558
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Distinguishing supraspan from subspan iconic storage
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- 04 February 2010, pp. 22-23
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Mode of action of antidepressant agents: Increased output or increased efficiency?
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- Published online by Cambridge University Press:
- 04 February 2010, p. 558
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Elementary errors about evolution
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- Published online by Cambridge University Press:
- 04 February 2010, pp. 367-368
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Optic flow, icons, and memory
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- 04 February 2010, pp. 23-24
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A precise timing mechanism may underlie a common speech perception and production area in the peri-Sylvian cortex of the dominant hemisphere
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- 04 February 2010, pp. 219-220
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