Continuing Commentary
The behavioral role of the Mauthner neuron impulse
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- 04 February 2010, pp. 729-730
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Do K & W criteria define only command neurons?
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- 04 February 2010, pp. 730-732
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From command fibers to command systems to consensus. Are these labels really useful anymore?
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- 04 February 2010, pp. 732-733
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The crayfish position on command neurons
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- 04 February 2010, pp. 733-734
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Simple or complex systems?
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- 04 February 2010, p. 734
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What commands egg laying in Aplysia?
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- 04 February 2010, pp. 734-735
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The command neuron concept: Good in theory, difficult to justify in practice
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- 04 February 2010, pp. 735-736
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Authors' Response
Command performance
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- 04 February 2010, pp. 736-739
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Continuing Commentary
A theory of stories?
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- 04 February 2010, pp. 739-740
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Game theoretic models and respect for ownership
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- 04 February 2010, pp. 740-741
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Reliability in signalling motivation
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- 04 February 2010, pp. 741-742
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Author's Response
Ownership and honesty in competitive interaction
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- 04 February 2010, pp. 742-744
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Continuing Commentary
Kinesthetic aftereffects and evoked potentials constitute parallel measures of augmenting-reducing
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- 04 February 2010, pp. 744-746
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Evoked potential augmenting-reducing: A weak link in the biology-personality chain
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- 04 February 2010, pp. 746-747
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The myth of kinesthetic aftereffect's nonreliability
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- 04 February 2010, pp. 747-748
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Augmentation/reduction update
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- 04 February 2010, pp. 748-749
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Author's Response
Sensation seeking and augmenting-reducing: Evoked potentials and/or kinesthetic figural aftereffects?
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- 04 February 2010, pp. 749-754
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Continuing Commentary
Pain behaviour is not unitary
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- 04 February 2010, pp. 754-755
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Author's Response
Is it possible that pain is one thing?
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- 04 February 2010, p. 755
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Continuing Commentary
Sensitive periods, social interaction, and song acquisition: The dialectics of dialects?
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- 04 February 2010, pp. 756-757
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