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  1. Neuronal models of cognitive functions.Jean-Pierre Changeux & Stanislas Dehaene - 1989 - Cognition 33 (1-2):63-109.
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  • The significance of the basal ganglia for schizophrenia.Reuven Sandyk & Stanley R. Kay - 1991 - Behavioral and Brain Sciences 14 (1):45-46.
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  • What is schizophrenia?Janice R. Stevens & James M. Gold - 1991 - Behavioral and Brain Sciences 14 (1):50-51.
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  • The neuropsychology of schizophrenia: In step but not in time.Jonathan H. Williams - 1991 - Behavioral and Brain Sciences 14 (1):55-56.
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  • The role of a behavior in evolution.Geoffrey P. Bingham - 1990 - Behavioral and Brain Sciences 13 (2):346-347.
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  • Brain evolution in Homo: The “radiator” theory.Dean Falk - 1990 - Behavioral and Brain Sciences 13 (2):333-344.
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  • Relating brains, blood, and bipedalism.Grover S. Krantz - 1990 - Behavioral and Brain Sciences 13 (2):362-363.
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  • Are rhythms of human cerebral development “traveling waves”?Robert W. Thatcher - 1991 - Behavioral and Brain Sciences 14 (4):575-575.
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  • Nesting cups and metatools in chimpanzees.Tetsuro Matsuzawa - 1991 - Behavioral and Brain Sciences 14 (4):570-571.
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  • Continuity versus discontinuity theories of the evolution of human and animal minds.Kathleen R. Gibson - 1991 - Behavioral and Brain Sciences 14 (4):560-560.
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  • Language, tools and brain: The ontogeny and phylogeny of hierarchically organized sequential behavior.Patricia M. Greenfield - 1991 - Behavioral and Brain Sciences 14 (4):531-551.
    During the first two years of human life a common neural substrate underlies the hierarchical organization of elements in the development of speech as well as the capacity to combine objects manually, including tool use. Subsequent cortical differentiation, beginning at age two, creates distinct, relatively modularized capacities for linguistic grammar and more complex combination of objects. An evolutionary homologue of the neural substrate for language production and manual action is hypothesized to have provided a foundation for the evolution of language (...)
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  • A case for auditory temporal processing as an evolutionary precursor to speech processing and language function.Roslyn Holly Fitch & Paula Tallal - 1995 - Behavioral and Brain Sciences 18 (1):189-189.
    Wilkins & Wakefield suggest that changes in the hominid brain made it uniquely “preadaptive” for language, yet no precursor functions served as adaptive substrates to the emergence of language. We present contrary evidence that the ability to discriminate and process rapid and complex auditory information is a cross-species function subserving communication processes including, but not limited to, human speech perception. We suggest that auditory temporal processing served as an evolutionary precursor to speech processing and consequent language development in humans.
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  • Manual versus speech motor control and the evolution of language.Philip Lieberman - 1995 - Behavioral and Brain Sciences 18 (1):197-198.
    Inferences made from endocasts of fossil skulls cannot provide information on the function of particular neocortical areas or the subcortical pathways to prefrontal cortex that form part of the neural substrate for speech, syntax, and certain aspects of cognition. The neural bases of syntax cannot be disassociated from “communication.” Manual motor control was probably a preadaptive factor in the evolution of humansyntactic ability, but neurophysiological data on living humans show that speech motor control and syntax are more closely linked. The (...)
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  • Complex behaviors: Evolution and the brain.William O. Dingwall - 1995 - Behavioral and Brain Sciences 18 (1):186-188.
    Three issues are addressed in this commentary. (1) Wilkins & Wakefield are commended for placing the complex behavior they discuss within an evolutionary matrix. (2) They err on a number of points in regard to their treatment of this complex behavior. These involve (a) their emphasis on the evolution of conceptual structure rather than language, (b) their equation of meaning with reference, (c) their minimalist view of learning theory, and (d) their separation of the evolution of speech from that of (...)
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  • Solving the language origins puzzle: Collecting and assembling all pertinent pieces.Kathleen R. Gibson - 1995 - Behavioral and Brain Sciences 18 (1):189-190.
    Wilkins & Wakefield fall short of solving the language origin puzzle because they underestimate the cognitive and linguistic capacities of great apes. A focus on ape capacities leads to the recognition of varied levels of cognition and language and to a gradualistic model of language emergence in which early hominid language skills exceed those of the apes but fall far short of those of modern humans or later fossil hominid groups.
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  • Brains evolution and neurolinguistic preconditions.Wendy K. Wilkins & Jennie Wakefield - 1995 - Behavioral and Brain Sciences 18 (1):161-182.
    This target article presents a plausible evolutionary scenario for the emergence of the neural preconditions for language in the hominid lineage. In pleistocene primate lineages there was a paired evolutionary expansion of frontal and parietal neocortex (through certain well-documented adaptive changes associated with manipulative behaviors) resulting, in ancestral hominids, in an incipient Broca's region and in a configurationally unique junction of the parietal, occipital, and temporal lobes of the brain (the POT). On our view, the development of the POT in (...)
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  • Integrating neuroscience, psychology, and evolutionary biology through a teleological conception of function.Jennifer Mundale & William Bechtel - 1996 - Minds and Machines 6 (4):481-505.
    The idea of integrating evolutionary biology and psychology has great promise, but one that will be compromised if psychological functions are conceived too abstractly and neuroscience is not allowed to play a contructive role. We argue that the proper integration of neuroscience, psychology, and evolutionary biology requires a telelogical as opposed to a merely componential analysis of function. A teleological analysis is required in neuroscience itself; we point to traditional and curent research methods in neuroscience, which make critical use of (...)
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  • Language Mapping Using Stereo Electroencephalography: A Review and Expert Opinion.Olivier Aron, Jacques Jonas, Sophie Colnat-Coulbois & Louis Maillard - 2021 - Frontiers in Human Neuroscience 15.
    Stereo-electroencephalography is a method that uses stereotactically implanted depth electrodes for extra-operative mapping of epileptogenic and functional networks. sEEG derived functional mapping is achieved using electrical cortical stimulations that are currently the gold standard for delineating eloquent cortex. As this stands true especially for primary cortices, ECS applied to higher order brain areas determine more subtle behavioral responses. While anterior and posterior language areas in the dorsal language stream seem to share characteristics with primary cortices, basal temporal language area in (...)
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  • Artificial syntactic violations activate Broca's region.K. Petersson - 2004 - Cognitive Science 28 (3):383-407.
    In the present study, using event-related functional magnetic resonance imaging, we investigated a group of participants on a grammaticality classification task after they had been exposed to well-formed consonant strings generated from an artificial regular grammar. We used an implicit acquisition paradigm in which the participants were exposed to positive examples. The objective of this studywas to investigate whether brain regions related to language processing overlap with the brain regions activated by the grammaticality classification task used in the present study. (...)
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  • Human language: Are nonhuman precursors lacking?Marc D. Hauser & Nathan D. Wolfea - 1995 - Behavioral and Brain Sciences 18 (1):190-191.
    Contra Wilkins & Wakefield, we argue that an evolutionarily inspired approach to language must consider different facets of language (i.e., more than syntax and semantics), and must explore the possibility of nonhuman precursors. Several examples are discussed, illustrating the power of the comparative approach in illuminating our understanding of language evolution.
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  • The thalamic dynamic core theory of conscious experience.Lawrence M. Ward - 2011 - Consciousness and Cognition 20 (2):464-486.
    I propose that primary conscious awareness arises from synchronized activity in dendrites of neurons in dorsal thalamic nuclei, mediated particularly by inhibitory interactions with thalamic reticular neurons. In support, I offer four evidential pillars: consciousness is restricted to the results of cortical computations; thalamus is the common locus of action of brain injury in vegetative state and of general anesthetics; the anatomy and physiology of the thalamus imply a central role in consciousness; neural synchronization is a neural correlate of consciousness.
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  • Cortical bases of speech perception:evidence from functional lesion studies.Dana Boatman - 2004 - Cognition 92 (1-2):47-65.
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  • Seeking the neurobiological bases of speech perception.Joanne L. Miller & Peter W. Jusczyk - 1989 - Cognition 33 (1-2):111-137.
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  • What should a theory of schizophrenia be able to do?Kurt Salzinger - 1991 - Behavioral and Brain Sciences 14 (1):44-45.
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  • Dopamine-GABA-cholinergic interactions and negative schizophrenic symptomatology.Martin Sarter - 1991 - Behavioral and Brain Sciences 14 (1):46-47.
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  • A hippocampal theory of schizophrenia.Nestor A. Schmajuk & James J. DiCarlo - 1991 - Behavioral and Brain Sciences 14 (1):47-49.
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  • A plausible theory marred by certain inconsistencies.Herbert E. Spohn - 1991 - Behavioral and Brain Sciences 14 (1):49-50.
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  • Neuropsychology of schizophrenia: The “hole” thing is wrong.Neal R. Swerdlow - 1991 - Behavioral and Brain Sciences 14 (1):51-53.
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  • A focalized deficit within an elegant system.Irene J. Elkins & Rue L. Cromwell - 1991 - Behavioral and Brain Sciences 14 (1):27-28.
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  • In what context is latent inhibition relevant to the symptoms of schizophrenia?Chris Frith - 1991 - Behavioral and Brain Sciences 14 (1):28-29.
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  • Novelty value in associative learning.Jonathan C. Gewirtz - 1991 - Behavioral and Brain Sciences 14 (1):29-29.
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  • Schizophrenia and stored memories: Left hemisphere dysfunction after all?Elkhonon Goldberg - 1991 - Behavioral and Brain Sciences 14 (1):30-30.
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  • The role of long-term memory and monitoring in schizophrenia: Multiple functions.Martin Harrow & Marshall Silverstein - 1991 - Behavioral and Brain Sciences 14 (1):30-31.
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  • A cardinal principle for neuropsychology, with implications for schizophrenia and mania.David Hestenes - 1991 - Behavioral and Brain Sciences 14 (1):31-32.
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  • The mechanism of positive symptoms in schizophrenia.Ralph E. Hoffman - 1991 - Behavioral and Brain Sciences 14 (1):33-34.
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  • A neuropsychology of psychosis.Loring J. Ingraham - 1991 - Behavioral and Brain Sciences 14 (1):34-34.
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  • Excitatory amino acids, NMDA and sigma receptors: A role in schizophrenia?Karl L. R. Jansen & Richard L. M. Faull - 1991 - Behavioral and Brain Sciences 14 (1):34-35.
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  • Schizophrenia and attention: In and out of context.R. E. Lubow - 1991 - Behavioral and Brain Sciences 14 (1):35-36.
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  • Approximations to a neuropsychological model of schizophrenia.Theo C. Manschreck & Brendan A. Maher - 1991 - Behavioral and Brain Sciences 14 (1):36-37.
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  • Neuropsychological vulnerability or episode factors in schizophrenia?Keith H. Nuechterlein & Michael Foster Green - 1991 - Behavioral and Brain Sciences 14 (1):37-38.
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  • Bases for irrelevant information processing in schizophrenia: Room for manoeuvre.R. D. Oades - 1991 - Behavioral and Brain Sciences 14 (1):38-39.
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  • Is another loop needed to explain schizophrenia?Arvin F. Oke & Ralph N. Adams - 1991 - Behavioral and Brain Sciences 14 (1):39-40.
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  • A realistic model will be much more complex and will consider longitudinal neuropsychodevelopment.Terry Patterson - 1991 - Behavioral and Brain Sciences 14 (1):40-41.
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  • Why don't preschizophrenic children have delusions and hallucinations?Lyn Pilowsky & Robin M. Murray - 1991 - Behavioral and Brain Sciences 14 (1):41-42.
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  • A heuristically useful but empirically weak neuropsychological model of schizophrenia.M. Pisa & J. M. Cleghorn - 1991 - Behavioral and Brain Sciences 14 (1):42-43.
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  • Neuro-developmental, brain imaging and psychophysiological perspectives on the neuropsychology of schizophrenia.Adrian Raine & Tyrone D. Cannon - 1991 - Behavioral and Brain Sciences 14 (1):43-44.
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  • A faulty negative feedback control underlies the schizophrenic syndrome?Arvid Carlsson & Maria Carlsson - 1991 - Behavioral and Brain Sciences 14 (1):20-21.
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  • Don't leave the “psyche” out of neuropsychology.Gordon Claridge & Tony Beech - 1991 - Behavioral and Brain Sciences 14 (1):21-21.
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  • The limbic-striatal interaction: A seesaw rather than a tandem.A. R. Cools & B. Ellenbroek - 1991 - Behavioral and Brain Sciences 14 (1):22-22.
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  • Motor disturbances in schizophrenia.Andrew Crider - 1991 - Behavioral and Brain Sciences 14 (1):22-23.
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