Works matching IS 0140525X AND DT 2004 AND VI 27 AND IP 4
Results: 79
Autism and schizophrenia: Similar perceptual consequence, different neurobiological etiology?
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 952, doi. 10.1017/S0140525X04260137
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Let's not forget about sensory consciousness.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 601, doi. 10.1017/S0140525X04290136
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The comparative psychology of uncertainty monitoring and metacognition.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 601
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Unity and diversity in disorders of cognitive coordination.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 594, doi. 10.1017/S0140525X0428013X
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A common link between aging, schizophrenia, and autism?
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 593, doi. 10.1017/S0140525X04270133
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Convergence of biological and psychological perspectives on cognitive coordination in schizophrenia.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 592
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From reifying mental pictures to reifying spatial models.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 590, doi. 10.1017/S0140525X04250130
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Spatial inference: No difference between mental images and mental models.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 589, doi. 10.1017/S0140525X04240134
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Mental imagery? In search of a theory.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 589
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Does TEC explain the emergence of distal representations?
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 588, doi. 10.1017/S0140525X04230138
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The Theory of Event Coding (TEC): A framework for perception and action planning.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 588
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Chaotic itinerancy is a key to mental diversity.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 586, doi. 10.1017/S0140525X04220131
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Complexity is a cue to the mind.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 585, doi. 10.1017/S0140525X04210135
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Toward an interpretation of dynamic neural activity in terms of chaotic dynamical system.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 585
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Tolerated reciprocity, reciprocal scrounging, and unrelated kin: Making sense of multiple models.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 572, doi. 10.1017/S0140525X04350120
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Nonmarket cooperation in the indigenous food economy of Taimyr, Arctic Russia: Evidence for control and benefit.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 571, doi. 10.1017/S0140525X04340124
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The details of food-sharing interactions - their cost in social prestige.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 570, doi. 10.1017/S0140525X04330128
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Cognitive constraints on reciprocity and tolerated scrounging.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 569, doi. 10.1017/S0140525X04320121
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Insights from Ifaluk: Food sharing among cooperative fishers.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 568, doi. 10.1017/S0140525X04310125
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The complexity of human sharing.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 567, doi. 10.1017/S0140525X04300129
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The history of human food transfers: Tinbergen's other question.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 566, doi. 10.1017/S0140525X04290124
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On sharing a ple: Modeling costly prosocial behavior.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 565, doi. 10.1017/S0140525X04280128
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The purpose of exchange helps shape the mode of exchange.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 564, doi. 10.1017/S0140525X04270121
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A kind man benefits himself - but how? Evolutionary models of human food sharing.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 563, doi. 10.1017/S0140525X04260125
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Key variables in tests of food sharing.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 563, doi. 10.1017/S0140525X04250129
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Tolerated scrounging in nonhuman primates.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 562
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Where's the beef? It's less about cooperation, more about conflict.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 561, doi. 10.1017/S0140525X04230126
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Good hunters keep smaller shares of larger pies.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 560, doi. 10.1017/S0140525X0422012X
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To give and to give not: The behavioral ecology of human food transfers.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 543, doi. 10.1017/S0140525X04000123
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The "putting the baby down" hypothesis: Bipedalism, babbling, and baby slings.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 527, doi. 10.1017/S0140525X0448011X
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Language from gesture.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 525, doi. 10.1017/S0140525X04470113
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Putting infants in their place.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 524, doi. 10.1017/S0140525X04460117
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Is it always really mothers' fault?
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 523, doi. 10.1017/S0140525X04450110
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Cached, carried, or crèched.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 523
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Did australopithecines (or early Homo) sling?
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 522, doi. 10.1017/S0140525X04430118
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Prosody as an intermediary evolutionary stage between a manual communication system and a fully developed language faculty.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 521, doi. 10.1017/S0140525X04420111
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Walkie-talkie evolution: Bipedalism and vocal production.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 520, doi. 10.1017/S0140525X04410115
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Motherese by any other name: Mother-infant communication in non-hominin mammals.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 519, doi. 10.1017/S0140525X04400119
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Affective prosody: Whence motherese.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 518, doi. 10.1017/S0140525X04390114
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Baby talk and the emergence of first words.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 517, doi. 10.1017/S0140525X04380118
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In the beginning was the song: The complex multimodal timing of mother-infant musical interaction.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 516
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Trickle-up phonetics: A vocal role for the infant.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 516, doi. 10.1017/S0140525X04360115
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Beyond prosody and infant-directed speech: Affective, social construction of meaning in the origins of language.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 515, doi. 10.1017/S0140525X04350119
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Aspects of human language: Where motherese?
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 514, doi. 10.1017/S0140525X04340112
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Chimpanzees are not proto-hominins and early human mothers may not have foraged alone.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 513, doi. 10.1017/S0140525X04330116
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Motherese is but one part of a ritualized, multimodal, temporally organized, affiliative interaction.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 512, doi. 10.1017/S0140525X0432011X
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Syntax: An evolutionary stepchild.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 511, doi. 10.1017/S0140525X04310113
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Which came first: Infants learning language or motherese?
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 505, doi. 10.1017/S0140525X04240110
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Prelinguistic evolution in hominins: Whence motherese?
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 491, doi. 10.1017/S0140525X04000111
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Continuity, displaced reference, and deception.
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- Behavioral & Brain Sciences, 2004, v. 27, n. 4, p. 510, doi. 10.1017/S0140525X04300117
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