Results for ' cerebral dominance'

969 found
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  1.  22
    Imagery, cerebral dominance, and style of thinking: A unified field model.Robert Zenhausern - 1978 - Bulletin of the Psychonomic Society 12 (5):381-384.
  2.  89
    Cerebral dominance for consciousness.M. L. Albert, R. Silverberg, A. Reches & M. Berman - 1976 - Archives of Neurology 33:453-4.
  3.  23
    Atypical cerebral dominance in Down’s syndrome.Daniel J. Weeks & Digby Elliott - 1992 - Bulletin of the Psychonomic Society 30 (1):23-25.
  4.  26
    Human laterality: cerebral dominance and handedness.Gina Geffen - 1978 - Behavioral and Brain Sciences 1 (2):295-296.
  5.  22
    Is There a Cerebral Dominance for Consciousness?E. A. Serafetinides - 1993 - Perspectives in Biology and Medicine 36 (3):420-428.
  6.  31
    Patterns of cerebral dominance in wholistic and featural stages of facial processing.Alan J. Parkin & Pamela Williamson - 1986 - In H. Ellis, M. Jeeves, F. Newcombe & Andrew W. Young, Aspects of Face Processing. Martinus Nijhoff. pp. 223--227.
  7. Handedness and cerebral dominance.A. Subirana - 1969 - In P. J. Vinken & G. W. Bruyn, Handbook of Clinical Neurology. North Holland. pp. 4--248.
  8.  32
    Some observations on the relation of the principle of physiological polarity and symmetry and the doctrine of cerebral dominance to the perception of symbols.G. A. Kelly - 1935 - Journal of Experimental Psychology 18 (2):202.
  9.  26
    The inadequacy of the concept of unilateral cerebral dominance in learning.S. I. Franz - 1933 - Journal of Experimental Psychology 16 (6):873.
  10.  20
    The biology of cerebral dominance: implications for cognition.N. Geschwind - 1984 - Cognition 17 (3):193-208.
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  11. The relationship of cerebral dominance to hand, auditory and ophthalmic preference.L. Roberts - 1969 - In P. J. Vinken & G. W. Bruyn, Handbook of Clinical Neurology. North Holland. pp. 4--312.
  12.  26
    Possible anatomic basis for cerebral dominance in infrahuman vertebrate species.Roland Puccetti - 1981 - Behavioral and Brain Sciences 4 (1):33-33.
  13.  18
    Interhemispheric asymmetry of electrical activity of the brain in sleep and “cerebral dominance”.Michael S. Myslobodsky, Varda Ben-Mayor, Batia Yedid-Levy & Matti Minz - 1976 - Bulletin of the Psychonomic Society 7 (5):465-467.
  14. Developmental Disorders of Higher Nervous Activity and Cerebral Dominance.J. A. M. Frederiks - 1969 - In P. J. Vinken & G. W. Bruyn, Handbook of Clinical Neurology. North Holland. pp. 4.
     
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  15.  25
    Objections to a growth gradient theory of cerebral dominance.Harold Goodglass - 1978 - Behavioral and Brain Sciences 1 (2):296-297.
  16. Aphasia, apraxia and agnosia in abnormal states of cerebral dominance.L. Roberts - 1969 - In P. J. Vinken & G. W. Bruyn, Handbook of Clinical Neurology. North Holland. pp. 4--312.
     
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  17.  12
    Cerebral faith and faith in praxis in the churches of European origin: The Presbyterian Church of South(ern) Africa.Graham A. Duncan - 2023 - HTS Theological Studies 79 (1):11.
    This article investigated the paradox between church response to apartheid and resulting action at the local level in the South African churches of European origin from the perspective of the Presbyterian Church of South(ern) Africa (PCSA). It indicated that this discrepancy arose between the reflections (cerebral faith) at the highest levels of church councils, which operated in an intermittent manner and at a distance, compared with the responses (praxis as faith in action) of local church members who lived at (...)
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  18. Goltz against cerebral localization: Methodology and experimental practices.J. P. Gamboa - 2020 - Studies in History and Philosophy of Science Part C: Studies in History and Philosophy of Biological and Biomedical Sciences 84:101304.
    In the late 19th century, physiologists such as David Ferrier, Eduard Hitzig, and Hermann Munk argued that cerebral brain functions are localized in discrete structures. By the early 20th century, this became the dominant position. However, another prominent physiologist, Friedrich Goltz, rejected theories of cerebral localization and argued against these physiologists until his death in 1902. I argue in this paper that previous historical accounts have failed to comprehend why Goltz rejected cerebral localization. I show that Goltz (...)
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  19. From mouth to hand: Gesture, speech, and the evolution of right-handedness.Michael C. Corballis - 2003 - Behavioral and Brain Sciences 26 (2):199-208.
    The strong predominance of right-handedness appears to be a uniquely human characteristic, whereas the left-cerebral dominance for vocalization occurs in many species, including frogs, birds, and mammals. Right-handedness may have arisen because of an association between manual gestures and vocalization in the evolution of language. I argue that language evolved from manual gestures, gradually incorporating vocal elements. The transition may be traced through changes in the function of Broca's area. Its homologue in monkeys has nothing to do with (...)
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  20. Split-brain reveals separate but equal self-recognition in the two cerebral hemispheres.Lucina Q. Uddin, Jan Rayman & Eran Zaidel - 2005 - Consciousness and Cognition 14 (3):633-640.
    To assess the ability of the disconnected cerebral hemispheres to recognize images of the self, a split-brain patient was tested using morphed self-face images presented to one visual hemifield at a time while making “self/other” judgments. The performance of the right and left hemispheres of this patient as assessed by a signal detection method was not significantly different, though a measure of bias did reveal hemispheric differences. The right and left hemispheres of this patient independently and equally possessed the (...)
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  21.  25
    Individuals with cerebral palsy show altered responses to visual perturbations during walking.Ashwini Sansare, Maelyn Arcodia, Samuel C. K. Lee, John Jeka & Hendrik Reimann - 2022 - Frontiers in Human Neuroscience 16:977032.
    Individuals with cerebral palsy (CP) have deficits in processing of somatosensory and proprioceptive information. To compensate for these deficits, they tend to rely on vision over proprioception in single plane upper and lower limb movements and in standing. It is not known whether this also applies to walking, an activity where the threat to balance is higher. Through this study, we used visual perturbations to understand how individuals with and without CP integrate visual input for walking balance control. Additionally, (...)
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  22. How is consciousness expressed in the cerebral activation manifold?Marcel Kinsbourne - 2000 - Brain and Mind 1 (2):265-74.
    I dispute that consciousness is generated by core circuitry in the forebrain, with predominance of motor areas, as Cotterillproposes in Enchanted Looms and other theorists do also. Ipropose instead that conscious contents are the momentary modeof action of the integrated cortical field, expressed as a point vector ( dominant focus ), to which, in varying degree, allsectors of the network contribute. Consciousness is the brain''saccess to its own activity space, and is identical with the moment''sdominant mode of activity. The dominant (...)
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  23. Dominant and nondominant hemispherectomy.Flourens Haller - 1974 - In Marcel Kinsbourne & Wallace Lynn Smith, Hemispheric Disconnection and Cerebral Function. Charles C. pp. 5.
  24.  44
    Lack of hemispheric dominance for consciousness in acute ischaemic stroke.B. Cucchiara, S. E. Kasner, D. A. Wolk, P. D. Lyden, V. A. Knappertz, T. Ashwood, T. Odergren & A. Nordlund - 2003 - Journal of Neurology, Neurosurgery and Psychiatry 74 (7):889-892.
  25.  48
    On the biological basis of human laterality: II. The mechanisms of inheritance.Michael J. Morgan & Michael C. Corballis - 1978 - Behavioral and Brain Sciences 1 (2):270-277.
    This paper focuses on the inheritance of human handedness and cerebral lateralization within the more general context of structural biological asymmetries. The morphogenesis of asymmetrical structures, such as the heart in vertebrates, depends upon a complex interaction between information coded in the cytoplasm and in the genes, but the polarity of asymmetry seems to depend on the cytoplasmic rather than the genetic code. Indeed it is extremely difficult to find clear-cut examples in which thedirectionof an asymmetry is under genetic (...)
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  26. Dominance of the minor hemisphere in commissurotomized man for the perception of part-whole relationships.Robert D. Nebes - 1974 - In Marcel Kinsbourne & Wallace Lynn Smith, Hemispheric Disconnection and Cerebral Function. Charles C. pp. 155--164.
  27.  35
    Why homolaterality of language and hand dominance may not be the expression of a specific evolutionary link.Bencie Woll & Jechil S. Sieratzki - 2003 - Behavioral and Brain Sciences 26 (2):241-241.
    Although gestures have surface similarities with language, there are significant organisational and neurolinguistic differences that argue against the evolutionary connection proposed by Corballis. Dominance for language and handedness may be related to a basic specialisation of the left cerebral hemisphere for target-directed behaviour and sequential processing, with the right side specialised for holistic-environmental monitoring and spatial processing.
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  28.  17
    The correlations between kinematic profiles and cerebral hemodynamics suggest changes of motor coordination in single and bilateral finger movement.Guangquan Zhou, Yuzhao Chen, Xiaohan Wang, Hao Wei, Qinghua Huang & Le Li - 2022 - Frontiers in Human Neuroscience 16:957364.
    ObjectiveThe correlation between the performance of coordination movement and brain activity is still not fully understood. The current study aimed to identify activated brain regions and brain network connectivity changes for several coordinated finger movements with different difficulty levels and to correlate the brain hemodynamics and connectivity with kinematic performance.MethodsTwenty-one right-dominant-handed subjects were recruited and asked to complete circular motions of single and bilateral fingers in the same direction and in opposite directions on a plane. Kinematic data including radius and (...)
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  29. My right I: Deception detection and hemispheric differences in self-awareness.Sarah Malcolm & Julian Paul Keenan - 2003 - Social Behavior and Personality 31 (8):767-772.
  30.  38
    Hemispheric laterality in animals and the effects of early experience.Victor H. Denenberg - 1981 - Behavioral and Brain Sciences 4 (1):1-21.
    A review of research with chicks, songbirds, rodents, and nonhuman primates indicates that the brain is lateralized for a number of behavioral functions. These findings can be understood in terms of three hypothetical brain processes derived from a brain model based on general systems theory: hemispheric activation, interhemispheric inhibition, and interhemispheric coupling.Left-hemisphere activation occurs in songbirds and nonhuman primates in response to salient auditory or visual input, or when a communicative output is required. The right hemisphere is activated in rats (...)
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  31. Right hemispheric self-awareness: A critical assessment.Alain Morin - 2002 - Consciousness and Cognition 11 (3):396-401.
    In this commentaryI evaluate the claim made byKeenan, Nelson, OÕConnor, and Pascual-Leone (2001) that since self-recognition results from right hemispheric activity, self-awareness too is likely to be produced by the activity of the same hemisphere. This reasoning is based on the assumption that self-recognition represents a valid operationalization of self-awareness; I present two views that challenge this rationale. Keenan et al. also support their claim with published evidence relating brain activityand self-awareness; I closelyexamine their analysis of one specific review of (...)
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  32.  69
    Protosign and protospeech: An expanding spiral.Michael A. Arbib - 2003 - Behavioral and Brain Sciences 26 (2):209-210.
    The intriguing observation that left-cerebral dominance for vocalization is ancient, occurring in frogs, birds, and mammals, grounds Corballis's argument that the predominance of right-handedness may result from an association between manual gestures and vocalization in the evolution of language. This commentary supports the general thesis that language evolved “From hand to mouth” (Corballis 2002), while offering alternatives for some of Corballis's supporting arguments.
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  33.  20
    The secret of lateralisation is trust.Chris Knight - 2003 - Behavioral and Brain Sciences 26 (2):231-232.
    Human right-handedness does not originate in vocalisation as such but in selection pressures for structuring complex sequences of digital signals internally, as if in a vacuum. Cautious receivers cannot automatically accept signals in this way. Biological displays are subjected to contextual scrutiny on a signal-by-signal basis – a task requiring coordination of both hemispheres. In order to explain left cerebral dominance in human manual and vocal signalling, we must therefore ask why it became adaptive for receivers to abandon (...)
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  34.  56
    On the biological basis of human laterality: I. Evidence for a maturational left–right gradient.Michael C. Corballis & Michael J. Morgan - 1978 - Behavioral and Brain Sciences 1 (2):261-269.
  35.  39
    Honour subcultures and the reciprocal model.James Steele - 1998 - Behavioral and Brain Sciences 21 (3):385-386.
    Tests of models of reciprocal interactions of testosterone and behaviour patterns in honour subcultures, if based on adult samples measured at a single point in time, would be aided by measures of behaviour in such samples that indirectly index basal testosterone levels at earlier developmental ages, for example, hand preference and other measures of cerebral dominance. Such models raise questions about the social preconditions of honour subcultures, and their indirect effects on health.
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  36. Criteria for consciousness in humans and other mammals.Anil K. Seth, Bernard J. Baars & David B. Edelman - 2005 - Consciousness and Cognition 14 (1):119-39.
    The standard behavioral index for human consciousness is the ability to report events with accuracy. While this method is routinely used for scientific and medical applications in humans, it is not easy to generalize to other species. Brain evidence may lend itself more easily to comparative testing. Human consciousness involves widespread, relatively fast low-amplitude interactions in the thalamocortical core of the brain, driven by current tasks and conditions. These features have also been found in other mammals, which suggests that consciousness (...)
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  37.  31
    Dissociation of hemifield reaction time differences from verbal stimulus directionality.Ami Isseroff, Amiram Carmon & Israel Nachshon - 1974 - Journal of Experimental Psychology 103 (1):145.
  38.  30
    Bilateral electroencephalograms from normal speakers and stutterers.J. R. Knott & T. D. Tjossem - 1943 - Journal of Experimental Psychology 32 (4):357.
  39.  81
    Living in the borderland: the evolution of consciousness and the challenge of healing trauma.Jerome S. Bernstein - 2005 - New York: Routledge, Taylor & Francis Group.
    Living in the Borderland addresses the evolution of Western consciousness and describes the emergence of the "Borderland," a spectrum of reality that is beyond the rational yet is palpable to an increasing number of individuals. Building on Jungian theory, Jerome Bernstein argues that a greater openness to transrational reality experienced by Borderland personalities allows new possibilities for understanding and healing confounding clinical and developmental enigmas." "Living in the Borderland challenges the standard clinical model, which views normality as an absence of (...)
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  40.  91
    Convergence of biological and psychological perspectives on cognitive coordination in schizophrenia.William A. Phillips & Steven M. Silverstein - 2003 - Behavioral and Brain Sciences 26 (1):65-82.
    The concept of locally specialized functions dominates research on higher brain function and its disorders. Locally specialized functions must be complemented by processes that coordinate those functions, however, and impairment of coordinating processes may be central to some psychotic conditions. Evidence for processes that coordinate activity is provided by neurobiological and psychological studies of contextual disambiguation and dynamic grouping. Mechanisms by which this important class of cognitive functions could be achieved include those long-range connections within and between cortical regions that (...)
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  41.  47
    Nineteenth-century ideas on hemisphere differences and "duality of mind".Anne Harrington - 1985 - Behavioral and Brain Sciences 8 (4):617-660.
    It is widely felt that the sorts of ideas current in modern laterality and split-brain research are largely without precedent in the behavioral and brain sciences. This paper not only challenges that view, but makes a first attempt to define the relevance of older concepts and data to present research programs.
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  42.  27
    Editorial: Manual Skills, Handedness, and the Organization of Language in the Brain.Gregory Króliczak, Claudia L. R. Gonzalez & David P. Carey - 2019 - Frontiers in Psychology 10:460245.
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  43.  35
    We are far from understanding sex-related differences in spatial-mathematical abilities despite the theory of sexual selection.Üner Tan - 1996 - Behavioral and Brain Sciences 19 (2):264-264.
    I have provided evidence that Geary's model does not explain male dominance in spatial abilities by sexual selection. The current literature concerning the relations of nonverbal IQ to testosterone, hand preference, and right- and left-hand skill, as well as the organizing effects of testosterone on cerebral lateralization during the perinatal period, does not support Geary's arguments.
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  44.  16
    Inattentive Perception, Time, and the Incomprehensibility of Consciousness.Jürgen Krüger - 2022 - Frontiers in Psychology 12:804652.
    Cerebral energy supply is insufficient to support continuous neuronal processing of the plethora of time-constant objects that we are aware of. As a result, the brain is forced to limit processing resources to (the most relevant) cases ofchange. The neuronally generated world is thus temporally discontinuous. This parallels the fact that, in all relevant microscopic fundamental equations of nature, temporalchangeplays a dominant role. When a scientist calculates a “solution” to such an equation, integration over time is an essential step. (...)
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  45. Developmental Dynamic Dysphasia: Are Bilateral Brain Abnormalities a Signature of Inefficient Neural Plasticity?Marcelo L. Berthier, Guadalupe Dávila, María José Torres-Prioris, Ignacio Moreno-Torres, Jordi Clarimón, Oriol Dols-Icardo, María J. Postigo, Victoria Fernández, Lisa Edelkraut, Lorena Moreno-Campos, Diana Molina-Sánchez, Paloma Solo de Zaldivar & Diana López-Barroso - 2020 - Frontiers in Human Neuroscience 14:478142.
    The acquisition and evolution of speech production, discourse and communication can be negatively impacted by brain malformations. We describe, for the first time, a case of developmental dynamic dysphasia (DDD) in a right-handed adolescent boy (subject D) with cortical malformations involving language-eloquent regions (inferior frontal gyrus) in both the left and the right hemispheres. Language evaluation revealed a markedly reduced verbal output affecting phonemic and semantic fluency, phrase and sentence generation and verbal communication in everyday life. Auditory comprehension, repetition, naming, (...)
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  46.  86
    Body, brain, and culture.Victor Turner - 1983 - Zygon 18 (3):221-245.
    Recent work in cerebral neurology should be used to fashion a new synthesis with anthropological studies. Beginning with Paul D. Madean's model of the triune brain, we explore Ralph Wendell Burhoe's question whether creative processes result from a coadaptation, perhaps in ritual itself, of genetic and cultural information. Then we examine the division of labor between right and left cerebral hemispheres and its implications for the notions of play and “ludic recombination.” Intimately related to ritual, play may function (...)
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  47. Hemispheric specialization for the conscious and unconscious perception of emotional stimuli.Stephen D. Smith - 2005
  48.  58
    Women: A more balanced brain?Paul D. MucLeun - 1996 - Zygon 31 (3):421-439.
    On the basis of knowledge prior to 1988, Ashbrook pointed out that whereas most men are primarily dependent on the left cerebral hemisphere (“dominant hemisphere”) for verbally related functions, women show a greater hemispheric balance in this respect. For men, he argues, their possession of a “speaking” and a “non‐speaking hemisphere” results in a positive‐negative, bipolar way of thinking that may be characterized as dualistic and dialectically hierarchical. In contrast, the greater balance of hemispheric function in women appears to (...)
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  49.  7
    Consciousness and Commissurotomy: VI. Evidence for Normal Dual Consciousness?Thomas Natsoulas - 1995 - Journal of Mind and Behavior 16 (2):181-206.
    This article addresses the problem of evidence for Puccetti's hypothesis of normal dual consciousness, i.e., the hypothesis that a stream of consciousness flows in each cerebral hemisphere when both are functioning normally in intact, healthy people. Evidence counts as supportive only if it is not explainable by a certain close alternative hypothesis that holds consciousness to proceed in the nondominant hemisphere only when the dominant hemisphere is unable to inhibit it . From this perspective, I discuss two experiments involving (...)
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  50.  16
    The brain takes shape: an early history.Robert L. Martensen - 2004 - New York: Oxford University Press.
    This fine book tells an important story of how long-standing notions about the body as dominated by spirit-like humors were transformed into scientific descriptions of its solid tissues. Vesalius, Harvey, Descartes, Willis, and Locke all played roles in this transformation, as the cerebral hemispheres and cranial nerves began to take precedence over the role of spirit, passion, and the heart in human thought and behavior. Non of this occurred in a social vacuum, and the book describes the historical context (...)
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