nach oben

Neuropsychology Review

Erschienen in:

01.06.2010 | Review

Contribution of Callosal Connections to the Interhemispheric Integration of Visuomotor and Cognitive Processes

verfasst von: Tilman Schulte, Eva M. Müller-Oehring

Erschienen in: Neuropsychology Review | Ausgabe 2/2010

Einloggen, um Zugang zu erhalten

Abstract

In recent years, cognitive neuroscience has been concerned with the role of the corpus callosum and interhemispheric communication for lower-level processes and higher-order cognitive functions. There is empirical evidence that not only callosal disconnection but also subtle degradation of the corpus callosum can influence the transfer of information and integration between the hemispheres. The reviewed studies on patients with callosal degradation with and without disconnection indicate a dissociation of callosal functions: while anterior callosal regions were associated with interhemispheric inhibition in situations of semantic (Stroop) and visuospatial (hierarchical letters) competition, posterior callosal areas were associated with interhemispheric facilitation from redundant information at visuomotor and cognitive levels. Together, the reviewed research on selective cognitive functions provides evidence that the corpus callosum contributes to the integration of perception and action within a subcortico-cortical network promoting a unified experience of the way we perceive the visual world and prepare our actions.

Aboitiz, F., Scheibel, A. B., Fisher, R. S., & Zaidel, E. (1992). Individual differences in brain asymmetries and fiber composition in the human corpus callosum. Brain Research, 598, 154–161.PubMed

Aglioti, S., Smania, N., Manfredi, M., & Berlucchi, G. (1996). Disownership of left hand and objects related to it in a patient with right brain damage. Neuroreport, 20, 293–296.

Aralasmak, A., Ulmer, J. L., Kocak, M., Salvan, C. V., Hillis, A. E., & Yousem, D. M. (2006). Association, commissural, and projection pathways and their functional deficit reported in literature. Journal of Computer Assisted Tomography, 30, 695–715.PubMed

Aziz-Zadeh, L., Koski, L., Zaidel, E., Mazziotta, J., & Iacoboni, M. (2006). Lateralization of the human mirror neuron system. Journal of Neuroscience, 26, 2964–2970.PubMed

Baird, A. E., & Warach, S. (1998). Magnetic resonance imaging of acute stroke. Journal of Cerebral Blood Flow & Metabolism, 18, 583–609.

Banich, M. T. (1995). Interhemispheric processing: Theoretical and empirical considerations. In R. Davidson & K. Hugdahl (Eds.), Brain asymmetry (pp. 427–450). Cambridge: MIT.

Banich, M. T. (1998). The missing link: the role of interhemispheric interaction in attentional processing. Brain and Cognition, 36, 128–157.PubMed

Banich, M. T., & Belger, A. (1990). Interhemispheric interaction: how do the hemispheres divide and conquer a task? Cortex, 26, 77–94.PubMed

Banich, M. T., & Shenker, J. (1994). Investigations of interhemispheric processing: methodological considerations. Neuropsychology, 8, 263–277.

Banich, M. T., Milham, M. P., Atchley, R., Cohen, N. J., Webb, A., Wszalek, T., et al. (2000). fMRI studies of Stroop tasks reveal unique roles of anterior and posterior brain systems in attentional selection. Journal of Cognitive Neuroscience, 12, 988–1000.PubMed

Barnett, K. J., & Corballis, M. C. (2005). Speeded right-to-left information transfer: the result of speeded transmission in right-hemisphere axons? Neuroscience Letters, 380, 88–92.PubMed

Bartzokis, G., Sultzer, D., Lu, P. H., Nuechterlein, K. H., Mintz, J., & Cummings, J. L. (2004). Heterogeneous age-related breakdown of white matter structural integrity: implications for cortical “disconnection” in aging and Alzheimer’s disease. Neurobiology of Aging, 25, 843–851.PubMed

Bartzokis, G., Lu, P. H., Tingus, K., Mendez, M. F., Richard, A., Peters, D. G., et al. (2008). Lifespan trajectory of myelin integrity and maximum motor speed. Neurobiology of Aging. In press.

Bashore, T. R. (1981). Vocal and manual reaction time estimates of interhemispheric transmission time. Psychology Bulletin, 89, 352–368.

Battelli, L., Cavanagh, P., Martini, P., & Barton, J. J. (2003). Bilateral deficits of transient visual attention in right parietal patients. Brain, 126, 2164–2174.PubMed

Bauer, R. M. (1982). Visual hypoemotionality as a symptom of visual-limbic disconnection in man. Archives of Neurology, 39, 702–708.PubMed

Bayard, S., Gosselin, N., Robert, M., & Lassonde, M. (2004). Inter-and intra-hemispheric processing of visual event-related potentials in the absence of the corpus callosum. Journal of Cognitive Neuroscience, 16, 401–414.PubMed

Berlucchi, G., Heron, W., Hyman, R., Rizzolatti, G., & Umilta, C. (1971). Simple reaction times of ipsilateral and contralateral hand to lateralized visual stimuli. Brain, 94, 419–430.PubMed

Berlucchi, G., Aglioti, S., Marzi, C. A., & Tassinari, G. (1995). Corpus callosum and simple visuomotor integration. Neuropsychologia, 33, 923–936.PubMed

Blanca, M. J., Zalabardo, C., Garcia-Criado, F., & Siles, R. (1994). Hemispheric differences in global and local processing dependent on exposure duration. Neuropsychologia, 32, 1343–1351.PubMed

Bloom, J. S., & Hynd, G. W. (2005). The role of the corpus callosum in interhemispheric transfer of information: excitation or inhibition? Neuropsychology Review, 15, 59–71.PubMed

Blumstein, S., & Cooper, W. E. (1974). Hemispheric processing of intonation contours. Cortex, 10, 146–158.PubMed

Braun, C. M., Daigneault, S., Dufresne, A., Miljours, S., & Collin, I. (1995). Does so-called interhemispheric transfer time depend on attention? American Journal of Psychology, 108, 527–546.PubMed

Broadbent, D. E. (1977). The hidden preattentive process. American Psychologist, 32, 109–118.PubMed

Bucur, B., Madden, D. J., & Allen, P. A. (2005). Age-related differences in the processing of redundant visual dimensions. Psychology and Aging, 20, 435–446.PubMed

Caminiti, R., Ghaziri, H., Galuske, R., Hof, P. R., & Innocenti, G. M. (2009). Evolution amplified processing with temporally dispersed slow neuronal connectivity in primates. Proceedings of the National Academy of Sciences of the United States of America, 106, 19551–19556.PubMed

Carter, C. S., MacDonald, A. M., Botvinick, M., Ross, L. L., Stenger, V. A., Noll, D., et al. (2000). Parsing executive processes: strategic vs. evaluative functions of the anterior cingulate cortex. Proceedings of the National Academy of Sciences of the United States of America, 97, 1944–1948.PubMed

Catani, M., & ffytche, D. H. (2005). The rises and falls of disconnection syndromes. Brain, 128, 2224–2239.PubMed

Chiarello, C., & Maxfield, L. (1996). Varieties of interhemispheric inhibition, or how to keep a good hemisphere down. Brain and Cognition, 30, 81–108.PubMed

Christman, S. D. (2001). Individual differences in stroop and local-global processing: a possible role of interhemispheric interaction. Brain and Cognition, 45, 97–118.PubMed

Clarke, J. M., & Zaidel, E. (1989). Simple reaction times to lateralized light flashes. Varieties of interhemispheric communication routes. Brain, 112, 849–870.PubMed

Clarke, J. M., & Zaidel, E. (1994). Anatomical-behavioral relationships: corpus callosum morphometry and hemispheric specialization. Behavioural Brain Research, 64, 185–202.PubMed

Cook, N. D. (1984). Callosal inhibition: the key to the brain code. Behavioral Science, 29, 98–110.PubMed

Corballis, M. C. (1998). Interhemispheric neural summation in the absence of the corpus callosum. Brain, 121, 1795–1807.PubMed

Corballis, M. C. (2002). Hemispheric interactions in simple reaction time. Neuropsychologia, 40, 423–434.PubMed

Corballis, M. C., Hamm, J. P., Barnett, K. J., & Corballis, P. M. (2002). Paradoxical interhemispheric summation in the split brain. Journal of Cognitive Neuroscience, 14, 1151–1157.PubMed

Corballis, M. C., Corballis, P. M., & Fabri, M. (2003). Redundancy gain in simple reaction time following partial and complete callosotomy. Neuropsychologia, 42, 71–81.

Corbetta, M., Shulman, G. L., Miezin, F. M., & Petersen, S. E. (1995). Superior parietal cortex activation during spatial attention shifts and visual feature conjunction. Science, 270, 802–805.PubMed

Corbetta, M., Tansy, A. P., Stanley, C. M., Astafiev, S. V., Snyder, A. Z., & Shulman, G. L. (2005). A functional MRI study of preparatory signals for spatial location and objects. Neuropsychologia, 43, 2041–2056.PubMed

Creem-Regehr, S. H. (2009). Sensory-motor and cognitive functions of the human posterior parietal cortex involved in manual actions. Neurobiology of Learning and Memory, 91, 166–171.PubMed

Damasio, A. R., & Damasio, H. (1993). Brain and language, In “Mind and Brain”, a Scientific American Book. New York: Freeman.

Doricchi, F., Thiebaut de Schotten, M., Tomaiuolo, F., & Bartolomeo, P. (2008). White matter (dis)connections and gray matter (dys)functions in visual neglect: gaining insights into the brain networks of spatial awareness. Cortex, 44, 983–995.PubMed

Dean, P., Redgrave, P., & Westby, G. W. (1989). Event or emergency? Two response systems in the mammalian superior colliculus. Trends in Neurosciences, 12, 137–147.PubMed

Delis, D. C., Robertson, L. C., & Efron, R. (1986). Hemispheric specialization of memory for visual hierarchical stimuli. Neuropsychologia, 24, 205–214.PubMed

Delis, D. C., Kiefner, M., & Fridlund, A. J. (1988). Visuospatial dysfunction following unilateral brain damage: dissociations in hierarchical and hemispatial analysis. Journal of Clinical and Experimental Neuropsychology, 10, 421–431.PubMed

Diederich, A., & Colonius, H. (1987). Intersensory facilitation in the motor component? A reaction time analysis. Psychological Research, 49, 23–29.

Doricchi, F., & Tomaiuolo, F. (2003). The anatomy of neglect without hemianopia: a key role for parietal-frontal disconnection? Neuroreport, 14, 2239–2243.PubMed

Doron, K. W., & Gazzaniga, M. S. (2008). Neuroimaging techniques offer new perspectives on callosal transfer and interhemispheric communication. Cortex, 44, 1023–1029.PubMed

Duffau, H., Capelle, L., Sichez, N., Denvil, D., Lopes, M., Sichez, J. P., et al. (2002). Intraoperative mapping of the subcortical language pathways using direct stimulations. An anatomo-functional study. Brain, 125, 199–214.PubMed

Duara, R., Kushch, A., Gross-Glenn, K., Barker, W. W., Jallad, B., Pascal, S., et al. (1991). Neuroanatomic differences between dyslexic and normal readers on magnetic resonance imaging scans. Archives of Neurology, 48, 410–416.PubMed

Evans, M. A., Shedden, J. M., Hevenor, S. J., & Hahn, M. C. (2000). The effect of variability of unattended information on global and local processing: evidence for lateralization at early stages of processing. Neuropsychologia, 38, 225–239.PubMed

Evert, D. L., & Kmen, M. (2003). Hemispheric asymmetries for global and local processing as a function of stimulus exposure duration. Brain and Cognition, 51, 115–142.PubMed

Fabri, M., Polonara, G., Del Pesce, M., Quattrini, A., Salvolini, U., & Manzoni, T. (2001). Posterior corpus callosum and interhemispheric transfer of somatosensory information: an fMRI and neuropsychological study of a partially callosotomized patient. Journal of Cognitive Neuroscience, 13, 1071–1079.PubMed

Felleman, D. J., Burkhalter, A., & Van Essen, D. C. (1997). Cortical connections of areas V3 and VP of macaque monkey extrastriate visual cortex. The Journal of Comparative Neurology, 379, 21–47.PubMed

Fendrich, R., Hutsler, J. J., & Gazzaniga, M. S. (2004). Visual and tactile interhemispheric transfer compared with the method of Poffenberger. Experimental Brain Research, 158, 67–74.

Fink, G. R., Halligan, P. W., Marshall, J. C., Frith, C. D., Frackowiak, R. S. J., & Dolan, R. J. (1996). Where in the brain does visual attention select the forest and the trees? Nature, 382, 626–628.PubMed

Fink, G. R., Halligan, P. W., Marshall, J. C., Frith, C. D., Frackowiak, R. S., & Dolan, R. J. (1997). Neural mechanisms involved in the processing of global and local aspects of hierarchically organized visual stimuli. Brain, 120, 1779–1791.PubMed

Fink, G. R., Marshall, J. C., Halligan, P. W., & Dolan, R. J. (1999). Hemispheric asymmetries in global/local processing are modulated by perceptual salience. Neuropsychologia, 37, 31–40.PubMed

Forster, B., & Corballis, M. C. (1998). Interhemispheric transmission times in the presence and absence of the forebrain commissures: effects of luminance and equiluminance. Neuropsychologia, 36, 925–934.PubMed

Forster, B., & Corballis, M. C. (2000). Interhemispheric transfer of colour and shape information in the presence and absence of the corpus callosum. Neuropsychologia, 38, 32–45.PubMed

Galaburda, A. M., & Geschwind, N. (1980). The human language areas and cerebral asymmetries. Revue Medicale de la Suisse Romande, 100, 119–128.PubMed

Gazzaniga, M. S. (2000). Cerebral specialization and interhemispheric communication: does the corpus callosum enable the human condition? Brain, 123, 1293–1326.PubMed

Gazzaniga, M. S. (2005). Forty-five years of split-brain research and still going strong. Nature Reviews Neuroscience, 6, 653–659.PubMed

Geschwind, N. (1965). Disconnexion syndromes in animals and man. I. Brain, 88, 237–294.PubMed

Giray, M., & Ulrich, R. (1993). Motor coactivation revealed by response force in divided and focused attention. Journal of Experimental Psychology: Human Perception and Performance, 19, 1278–1291.PubMed

Gur, R. C., Packer, I. K., Hungerbuhler, J. P., Reivich, M., Obrist, W. D., Amarnek, W. S., et al. (1980). Differences in the distribution of gray and white matter in human cerebral hemispheres. Science, 207, 1226–1228.PubMed

Habib, M. (1986). Visual hypoemotionality and prosopagnosia associated with right temporal lobe isolation. Neuropsychologia, 24, 577–582.PubMed

Hagmann, P., Thiran, J. P., Jonasson, L., Vandergheynst, P., Clarke, S., Maeder, P., et al. (2003). DTI mapping of human brain connectivity: statistical fibre tracking and virtual dissection. Neuroimage, 19, 545–554.PubMed

Han, S., He, X., Yund, E. W., & Woods, D. L. (2001). Attentional selection in the processing of hierarchical patterns: an ERP study. Biological Psychology, 5, 31–48.

Han, S., Weaver, J. A., Murray, S. O., Kang, X., Yund, E. W., & Woods, D. L. (2002). Hemispheric asymmetry in global/local processing: effects of stimulus position and spatial frequency. Neuroimage, 17, 1290–1299.PubMed

Han, S., Yund, E. W., & Woods, D. L. (2003). An ERP study of the global precedence effect: the role of spatial frequency. Clinical Neurophysiology, 114, 1850–1865.PubMed

Hanajima, R., Ugawa, Y., Machii, K., Mochizuki, H., Terao, Y., Enomoto, H., et al. (2001). Interhemispheric facilitation of the hand motor area in humans. Journal of Physiology, 531, 849–859.PubMed

Harper, C. G., & Kril, J. J. (1988). Corpus callosal thickness in alcoholics. British Journal of Addiction, 83, 577–580.PubMed

Harper, C. G., & Kril, J. J. (1990). Neuropathology of alcoholism. Alcohol and Alcoholism, 25, 207–216.PubMed

Harper, C., & Matsumoto, I. (2005). Ethanol and brain damage. Current Opinion in Pharmacology, 5, 73–78.PubMed

Hartje, W., Willmes, K., & Weniger, D. (1985). Is there parallel and independent hemispheric processing of intonational and phonetic components of dichotic speech stimuli? Brain and Language, 24, 83–99.PubMed

Heinze, H. J., & Münte, T. F. (1993). Electrophysiological correlates of hierarchical stimulus processing: dissociation between onset and later stages of global and local target processing. Neuropsychologia, 31, 841–852.PubMed

Heinze, H. J., Hinrichs, H., Scholz, M., Burchert, W., & Mangun, G. R. (1998). Neural mechanisms of global and local processing. A combined PET and ERP study. Journal of Cognitive Neuroscience, 10, 485–498.PubMed

Hiatt, K. D., & Newman, J. P. (2007). Behavioral evidence of prolonged interhemispheric transfer time among psychopathic offenders. Neuropsychology, 21, 313–318.PubMed

Hofer, S., & Frahm, J. (2006). Topography of the human corpus callosum revisited-comprehensive fiber tractography using diffusion tensor magnetic resonance imaging. Neuroimage, 32, 989–994.PubMed

Hopkins, W. D., & Rilling, J. K. (2000). A comparative MRI study of the relationship between neuroanatomical asymmetry and interhemispheric connectivity in primates: implication for the evolution of functional asymmetries. Behavioral Neuroscience, 114, 739–748.PubMed

Hübner, R. (1997). The effect of spatial frequency on global precedence and hemispheric differences. Perception & Psychophysics, 59, 187–201.

Hugdahl, K., & Davidson, R. J. (2003). The asymmetrical brain (pp. 259–302). Cambridge: MIT.

Hutner, N., & Oscar-Berman, M. (1996). Visual laterality patterns for the perception of emotional words in alcoholic and aging individuals. Journal of Studies on Alcohol, 57, 144–154.PubMed

Iacoboni, M., & Zaidel, E. (1995). Channels of the corpus callosum. Evidence from simple reaction times to lateralized flashes in the normal and the split brain. Brain, 118, 779–788.PubMed

Iacoboni, M., & Zaidel, E. (2003). Interhemispheric visuo-motor integration in humans: the effect of redundant targets. European Journal of Neuroscience, 17, 1981–1986.PubMed

Iacoboni, M., & Zaidel, E. (2004). Interhemispheric visuo-motor integration in humans: the role of the superior parietal cortex. Neuropsychologia, 42, 419–425.PubMed

Iacoboni, M., Ptito, A., Weekes, N. Y., & Zaidel, E. (2000). Parallel visuomotor processing in the split brain: cortico-subcortical interactions. Brain, 123, 759–769.PubMed

Ignashchenkova, A., Dicke, P. W., Haarmeier, T., & Their, P. (2004). Neuron-specific contribution of the superior colliculus to overt and covert shifts of attention. Nature Neuroscience, 7, 56–64.PubMed

Innocenti, G. M. (1986). Postnatal development of corticocortical connections. Italian Journal of Neurological Sciences, Suppl, 5, 25–28.

Innocenti, G. M. (1995). Exuberant development of connections, and its possible permissive role in cortical evolution. Trends in Neurosciences, 18, 397–402.PubMed

Iwabuchi, S. J., & Kirk, I. J. (2009). Atypical interhemispheric communication in left-handed individuals. Neuroreport, 20, 166–169.PubMed

Jancke, L., & Steinmetz, H. (1994). Interhemispheric transfer time and corpus callosum size. Neuroreport, 5, 2385–2388.PubMedCrossRef

Jeeves, M. A., & Moes, P. (1996). Interhemispheric transfer time differences related to aging and gender. Neuropsychologia, 34, 627–636.PubMed

Keary, C. J., Minshew, N. J., Bansal, R., Goradia, D., Fedorov, S., Keshavan, M. S., et al. (2009). Corpus callosum volume and neurocognition in autism. Journal of Autism and Developmental Disorders, 39, 834–841.PubMed

Kennedy, K. M., & Raz, N. (2009). Aging white matter and cognition: differential effects of regional variations in diffusion properties on memory, executive functions, and speed. Neuropsychologia, 47, 916–927.PubMed

Kimchi, R. (1992). Primacy of wholistic processing and global/local paradigm: a critical review. Psychological Bulletin, 112, 24–38.PubMed

Kimchi, R., & Palmer, S. E. (1982). Form and texture in hierarchically constructed patterns. Journal of Experimental Psychology: Human Perception and Performance, 8, 521–535.PubMed

Kinchla, R. A., & Wolfe, J. M. (1979). The order of visual processing: “Top–down,” “bottom–up”, or “middle–out”. Perception & Psychophysics, 25, 225–231.

Kinsbourne, M. (1977). Hemi-neglect and hemisphere rivalry. Advances in Neurology, 18, 41–49.PubMed

Kinsbourne, M. (2003). The corpus callosum equilibrates hemispheric activation. In E. Zaidel & M. Iacoboni (Eds.), The parallel brain: The cognitive neuroscience of the corpus callosum (pp. 271–281). Cambridge: MIT.

Kinsbourne, M., & Hicks, R. B. (1978). Functional cerebral space: A model for overflow, transfer and interference effects in human performance: A tutorial review. In J. Requin (Ed.), Attention and performance VII. Hillsdale: Erlbaum.

Kinsbourne, M. (1993). Orientational bias model of unilateral neglect: Evidence from attentional gradients within hemispace. In I. H. Robertson & J. C. Marshall (Eds.), Unilateral neglect: Clinical and experimental studies (pp. 63–86). Hillsdale, NJ: Erlbaum.

Kinsbourne, M., & Bruce, R. (1987). Shift in visual laterality within blocks of trials. ACTA Psychologica (Amsterdam), 66, 139–155.

Klier, E. M., Wang, H., & Crawford, J. D. (2003). Three-dimensional eye-head coordination is implemented downstream from the superior colliculus. Journal of Neurophysiology, 89, 2839–2853.PubMed

Kraus, M. F., Susmaras, T., Caughlin, B. P., Walker, C. J., Sweeney, J. A., & Little, D. M. (2007). White matter integrity and cognition in chronic traumatic brain injury: a diffusion tensor imaging study. Brain, 130, 2508–2519.PubMed

Kubicki, M., Westin, C. F., Nestor, P. G., Wible, C. G., Frumin, M., Maier, S. E., et al. (2003). Cingulate fasciculus integrity disruption in schizophrenia: a magnetic resonance diffusion tensor imaging study. Biological Psychiatry, 54, 1171–1180.PubMed

Lamb, M. R., & Robertson, L. C. (1987). Do response time advantage and interference reflect the order of processing of global-and local-level information? Perception & Psychophysics, 46, 254–258.

Lamb, M. R., & Robertson, L. C. (1988). The processing of hierarchical stimuli: effects of retinal locus, locational uncertainty, and stimulus identity. Perception & Psychophysics, 44, 172–181.

Lamb, M. R., & Yund, E. W. (2000). The role of spatial frequency in cued shifts of attention between global and local forms. Perception & Psychophysics, 62, 753–761.

Lamb, M. R., Robertson, L. C., & Knight, R. T. (1989). Attention and interference in the processing of global and local information: effects of unilateral temporal–parietal junction lesions. Neuropsychologia, 27, 471–483.PubMed

Lansberg, M. G., Thijs, V. N., O’Brien, M. W., Ali, J. O., de Crespigny, A. J., Tong, D. C., et al. (2001). Evolution of apparent diffusion coefficient, diffusion-weighted, and T2-weighted signal intensity of acute stroke. American Journal of Neuroradiology, 22, 637–644.PubMed

Lassonde, M., & Ouimet, C. (2010). The split-brain. Wiley Interdisciplinary Reviews: Cognitive Science, 1, 191–202.

Le Bihan, D. (2003). Looking into the functional architecture of the brain with diffusion MRI. Nature Reviews Neuroscience, 4, 469–480.PubMed

Le Bihan, D., Mangin, J. F., Poupon, C., Clark, C. A., Pappata, S., Molko, N., et al. (2001). Diffusion tensor imaging: concepts and applications. Journal of Magnetic Resonance Imaging, 13, 534–546.PubMed

Liederman, J., & Meehan, P. (1986). When is between-hemisphere division of labor advantageous? Neuropsychologia, 24, 863–874.PubMed

Lim, K. O., & Helpern, J. A. (2002). Neuropsychiatric applications of DTI—a review. NMR in Biomedicine, 15, 587–593.PubMed

Livingstone, M. S., & Hubel, D. H. (1987). Psychophysical evidence for separate channels for the perception of form, color, movement, and depth. Journal of Neuroscience, 7, 3416–3468.PubMed

Luders, E., Rex, D. E., Narr, K. L., Woods, R. P., Jancke, L., Thompson, P. M., et al. (2003). Relationships between sulcal asymmetries and corpus callosum size: gender and handedness effects. Cerebral Cortex, 13, 1084–1093.PubMed

Luo, Y. J., Hu, S., Weng, X. C., & Wei, J. H. (1999). Effects of semantic discrimination of Chinese words on N400 component of event-related potentials. Perceptual and Motor Skills, 89, 185–193.PubMed

Lux, S., Thimm, M., Marshall, J. C., & Fink, G. R. (2006). Directed and divided attention during hierarchical processing in patients with visuo-spatial neglect and matched healthy volunteers. Neuropsychologia, 44, 436–444.PubMed

MacDonald, A. W., 3rd, Cohen, J. D., Stenger, V. A., & Carter, C. S. (2000). Dissociating the role of the dorsolateral prefrontal and anterior cingulate cortex in cognitive control. Science, 288, 1835–1838.PubMed

MacLeod, C. M. (1991). Half a century of research on the Stroop effect: an integrative review. Psychological Bulletin, 109, 163–203.PubMed

Madden, D. J., Spaniol, J., Costello, M. C., Bucur, B., White, L. E., Cabeza, R., et al. (2009). Cerebral white matter integrity mediates adult age differences in cognitive performance. Journal of Cognitive Neuroscience, 21, 289–302.PubMed

Magat, M., & Brown, C. (2009). Laterality enhances cognition in Australian parrots. Proceedings of the Royal Society. Biological sciences, 276, 4155–4162.PubMed

Malinowski, P., Hubner, R., Keil, A., & Gruber, T. (2002). The influence of response competition on cerebral asymmetries for processing hierarchical stimuli revealed by ERP recordings. Experimental Brain Research, 144, 136–139.

Marchant, L. F., & McGrew, W. C. (1996). Laterality of limb function in wild chimpanzees of Gombe National Park: comprehensive study of spontaneous activities. Journal of Human Evolution, 30, 427–443.

Marks, N. L., & Hellige, J. B. (2003). Interhemispheric interaction in bilateral redundancy gain: effects of stimulus format. Neuropsychology, 17, 578–593.PubMed

Marzi, C. A., Bisiacchi, P., & Nicoletti, R. (1991). Is interhemispheric transfer of visuomotor information asymmetric? Evidence from a meta-analysis. Neuropsychologia, 29, 1163–1177.PubMed

Marzi, C. A., Smania, N., Martini, M. C., Gambina, G., Tomelleri, G., Palamara, A., et al. (1996). Implicit redundant-targets effect in visual extinction. Neuropsychologia, 34, 9–22.PubMed

Marzi, C. A., Fanini, A., Girelli, M., Ipata, A. E., Miniussi, C., Smania, N., et al. (1997). Is extinction following parietal damage an interhemispheric disconnection phenomenon? In P. Their & H. O. Karnath (Eds.), Parietal lobe contribution to orientation in 3D space. Heidelberg: Springer.

McCulloch, W. S., & Garol, H. W. (1941). Cortical origin and distribution of corpus callosum and anterior commissure in the monkey (Macaca mulatta). Journal of Neurophysiology, 4, 555–563.

Meister, I. G., Wienemann, M., Buelte, D., Grunewald, C., Sparing, R., Dambeck, N., et al. (2006). Hemiextinction induced by transcranial magnetic stimulation over the right temporo-parietal junction. Neuroscience, 142, 119–123.PubMed

Miller, J. (1982). Divided attention: evidence for coactivation with redundant signals. Cognitive Psychology, 14, 247–279.PubMed

Miller, J. (1986). Timecourse of coactivation in bimodal divided attention. Perception & Psychophysics, 40, 331–343.

Miller, J. (1991). Channel interaction and the redundant-targets effect in bimodal divided attention. Journal of Experimental Psychology: Human Perception and Performance, 17, 160–169.PubMed

Miller, J. O. (2004). Exaggerated redundancy gain in the split brain: A hemispheric coactivation account. Cognitive Psychology, 49, 118–154.PubMed

Miller, J., & Ulrich, R. (2003). Simple reaction time and statistical facilitation: a parallel grains model. Cognitive Psychology, 46, 101–151.PubMed

Miniussi, C., Girelli, M., & Marzi, C. A. (1998). Neural site of the redundant target effect electrophysiological evidence. Journal of Cognitive Neuroscience, 10, 216–230.PubMed

Moes, P. E., Brown, W. S., & Minnema, M. T. (2007). Individual differences in interhemispheric transfer time (IHTT) as measured by event related potentials. Neuropsychologia, 45, 2626–2630.PubMed

Mooshagian, E., Kaplan, J., Zaidel, E., & Iacoboni, M. (2008). Fast visuomotor processing of redundant targets: the role of the right temporo-parietal junction. PLoS One, 3, e2348.PubMed

Mooshagian, E., Iacoboni, M., & Zaidel, E. (2009). Spatial attention and interhemispheric visuomotor integration in the absence of the corpus callosum. Neuropsychologia, 47, 933–937.PubMed

Mordkoff, J. T., & Yantis, S. (1991). An interactive race model of divided attention. Journal of Experimental Psychology: Human Perception and Performance, 17, 520–538.PubMed

Mordkoff, J. T., & Yantis, S. (1993). Dividing attention between color and shape: evidence of coactivation. Perception & Psychophysics, 53, 357–366.

Mori, S., Kaufmann, W. E., Davatzikos, C., Stieltjes, B., Amodei, L., Fredericksen, K., et al. (2002). Imaging cortical association tracts in the human brain using diffusion-tensor-based axonal tracking. Magnetic Resonance in Medicine, 47, 215–223.PubMed

Mort, D. J., Malhotra, P., Mannan, S. K., Rorden, C., Pambakian, A., Kennard, C., et al. (2003). The anatomy of visual neglect. Brain, 126, 1986–1997.

Moseley, M. E., Cohen, Y., Kucharczyk, J., Mintorovitch, J., Asgari, H. S., Wendland, M. F., et al. (1990). Diffusion-weighted MR imaging of anisotropic water diffusion in cat central nervous system. Radiology, 176, 439–445.PubMed

Muetzel, R. L., Collins, P. F., Mueller, B. A. M., Schissel, A., Lim, K. O., & Luciana, M. (2008). The development of corpus callosum microstructure and associations with bimanual task performance in healthy adolescents. Neuroimage, 39, 1918–1925.PubMed

Müller-Oehring, E. M., Schulte, T., Raassi, C., Pfefferbaum, A., & Sullivan, E. V. (2007). Local-global interference is modulated by age, sex and anterior corpus callosum size. Brain Research, 1142, 189–205.PubMed

Müller-Oehring, E. M., Schulte, T., Kasten, E., Poggel, D. A., Müller, I., Wüstenberg, T., et al. (2009a). Parallel interhemispheric processing in hemineglect: relation to visual field defects. Neuropsychologia, 47, 2397–2408.

Müller-Oehring, E. M., Schulte, T., Fama, R., Pfefferbaum, A., & Sullivan, E. V. (2009b). Global-local interference is related to callosal compromise in alcoholism: a behavior-DTI association study. Alcoholism: Clinical and Experimental Research, 33, 477–489.

Müller-Oehring, E. M., Schulte, T., Rosenbloom, M. J., Pfefferbaum, A., & Sullivan, E. V. (2010). Callosal degradation in HIV-1 infection predicts hierarchical perception: A DTI study. Neuropsychologia, 48, 1133–1143.

Murray, M. M., Foxe, J. J., Higgins, B. A., Javitt, D. C., & Schroeder, C. E. (2001). Visuo-spatial neural response interactions in early cortical processing during a simple reaction time task: a high-density electrical mapping study. Neuropsychologia, 39, 828–844.PubMed

Nassi, J. J., & Callaway, E. M. (2009). Parallel processing strategies of the primate visual system. Nature Reviews Neuroscience, 10, 360–372.PubMed

Navon, D. (1977). Forest before trees: the precedence of global features in visual perception. Cognitive Psychology, 9, 353–383.

Neumann-Haefelin, T., Moseley, M. E., & Albers, G. W. (2000). New magnetic resonance imaging methods for cerebrovascular disease: emerging clinical applications. Annals of Neurology, 47, 559–570.PubMed

Nowicka, A., Grabowska, A., & Fersten, E. (1996). Interhemispheric transmission of information and functional asymmetry of the human brain. Neuropsychologia, 34, 147–151.PubMed

Ouimet, C., Jolicoeur, P., Miller, J., Ptito, A., Paggi, A., Foschi, N., et al. (2009). Sensory and motor involvement in the enhanced redundant target effect: a study comparing anterior-and totally split-brain individuals. Neuropsychologia, 47, 684–692.PubMed

Pandya, D. N., & Sanides, F. (1973). Architectonic parcellation of the temporal operculum in rhesus monkey and its projection pattern. Zeitschrift fur Anatomie und Entwicklungsgeschichte, 139, 127–161.PubMed

Park, H. J., Kim, J. J., Lee, S. K., Seok, J. H., Chun, J., Kim, D. I., et al. (2008). Corpus callosal connection mapping using cortical gray matter parcellation and DT-MRI. Human Brain Mapping, 29, 503–516.PubMed

Paul, L. K., Brown, W. S., Adolphs, R., Tyszka, J. M., Richards, L. J., Mukherjee, P., et al. (2007). Agenesis of the corpus callosum: genetic, developmental and functional aspects of connectivity. Nature Reviews Neuroscience, 8, 287–299.PubMed

Pfefferbaum, A., & Sullivan, E. V. (2002). Microstructural but not macrostructural disruption of white matter in women with chronic alcoholism. Neuroimage, 15, 708–718.PubMed

Pfefferbaum, A., & Sullivan, E. V. (2003). Increased brain white matter diffusivity in normal adult aging: relationship to anisotropy and partial voluming. Magnetic Resonance in Medicine, 49, 953–961.PubMed

Pfefferbaum, A., & Sullivan, E. V. (2005). Disruption of brain white matter microstructure by excessive intracellular and extracellular fluid in alcoholism: evidence from diffusion tensor imaging. Neuropsychopharmacology, 30, 423–432.PubMed

Pfefferbaum, A., Adalsteinsson, E., & Sullivan, E. V. (2003). Replicability of diffusion tensor imaging measurements of fractional anisotropy and trace in brain. Journal of Magnetic Resonance Imaging, 18, 427–433.PubMed

Pfefferbaum, A., Adalsteinsson, E., & Sullivan, E. V. (2006). Dysmorphology and microstructural degradation of the corpus callosum: interaction of age and alcoholism. Neurobiology of Aging, 27, 994–1009.PubMed

Pierpaoli, C., & Basser, P. J. (1996). Toward a quantitative assessment of diffusion anisotropy. Magnetic Resonance in Medicine, 36, 893–906.PubMed

Poffenberger, A. T. (1912). Reaction time to retinal stimulation with special reference to time lost in conduction through nerves center. Archiv fur die gesamte Psychologie, 23, 1–173.

Pollmann, S., & Zaidel, E. (1998). The role of the corpus callosum in visual orienting: importance of interhemispheric visual transfer. Neuropsychologia, 36, 763–774.PubMed

Pomerantz, J. R. (1983). Global and local precedence: selective attention in form and motion perception. Journal of Experimental Psychology: General, 112, 516–540.

Posner, M. I. (1980). Orienting of attention. Quarterly Journal of Experimental Psychology, 32, 3–25.PubMed

Poupon, C., Mangin, J., Clark, C. A., Frouin, V., Régis, J., Le Bihan, D., et al. (2001). Towards inference of human brain connectivity from MR diffusion tensor data. Medical Image Analysis, 5, 1–15.PubMed

Pujol, J., López-Sala, A., Deus, J., Cardoner, N., Sebastián-Gallés, N., Conesa, G., et al. (2002). The lateral asymmetry of the human brain studied by volumetric magnetic resonance imaging. Neuroimage, 17, 670–679.PubMed

Putnam, M. C., Wig, G. S., Grafton, S. T., Kelley, W. M., & Gazzaniga, M. S. (2008). Structural organization of the corpus callosum predicts the extent and impact of cortical activity in the nondominant hemisphere. Journal of Neuroscience, 28, 2912–2918.PubMed

Putnam, M. C., Steven, M. S., Doron, K. W., Riggall, A. C., & Gazzaniga, M. S. (2009). Cortical projection topography of the human splenium: Hemispheric asymmetry and individual differences. Journal of Cognitive Neuroscience. In press.

Raab, D. H. (1962). Statistical facilitation of simple reaction times. Transactions of the New York Academy of Sciences, 24, 574–590.PubMed

Rakic, P., & Yakovlev, P. I. (1968). Development of the corpus callosum and cavum septi in man. Journal of Comparative Neurology, 132, 45–72.PubMed

Reinholz, J., & Pollmann, S. (2007). Neural basis of redundancy effects in visual object categorization. Neuroscience Letters, 412, 123–128.PubMed

Reuter-Lorenz, P. A., & Stanczak, L. (2000). Differential effects of aging on the functions of the corpus callosum. Developmental Neuropsychology, 18, 113–137.PubMed

Reuter-Lorenz, P. A., Kinsbourne, M., & Moscovitch, M. (1990). Hemispheric control of spatial attention. Brain and Cognition, 12, 240–266.PubMed

Reuter-Lorenz, P. A., Nozawa, G., Gazzaniga, M. S., & Hughes, H. C. (1995). Fate of neglected targets: a chronometric analysis of redundant target effects in the bisected brain. Journal of Experimental Psychology. Human Perception and Performance, 21, 211–230.PubMed

Ringo, J. L., Doty, R. W., Demeter, S., & Simard, P. Y. (1994). Time is of the essence: a conjecture that hemispheric specialization arises from interhemispheric conduction delay. Cerebral Cortex, 4, 331–343.PubMed

Rizzo, M., & Vecera, S. P. (2002). Psychoanatomical substrates of Bálint’s syndrome. Journal of Neurology, Neurosurgery, and Psychiatry, 72, 162–178.PubMed

Robertson, L. C., Lamb, M. R., & Knight, R. T. (1988). Effects of lesions of temporal–parietal junction on perceptual and attentional processing in humans. Journal of Neuroscience, 8, 3757–3769.PubMed

Robertson, L. C., Lamb, M. R., & Knight, R. T. (1991). Normal global-local analysis in patients with dorsolateral frontal lobe lesions. Neuropsychologia, 29, 959–967.PubMed

Robertson, L. C., Lamb, M. R., & Zaidel, E. (1993). Callosal transfer and hemisphere laterality in response to hierarchical patterns: evidence from normal and commissurotomized subjects. Neuropsychology, 7, 325–342.

Rohlfing, T., Zahr, N. M., Sullivan, E. V., & Pfefferbaum, A. (2010). The SRI24 multichannel atlas of normal adult human brain structure. Human Brain Mapping. In press.

Roser, M., & Corballis, M. C. (2002). Interhemispheric neural summation in the split brain with symmetrical and asymmetrical displays. Neuropsychologia, 40, 1300–1312.PubMed

Roser, M., & Corballis, M. C. (2003). Interhemispheric neural summation in the split brain: effects of stimulus colour and task. Neuropsychologia, 41, 830–846.PubMed

Rugg, M. D., & Beaumont, J. G. (1978). Interhemispheric asymmetries in the visual evoked response: effects of stimulus lateralisation and task. Biological Psychology, 6, 283–292.PubMed

Ryberg, C., Rostrup, E., Stegmann, M. B., Barkhof, F., Scheltens, P., van Straaten, E. C., et al. (2007). Clinical significance of corpus callosum atrophy in a mixed elderly population. Neurobiology of Aging, 28, 955–963.PubMed

Salvan, C. V., Ulmer, J. L., DeYoe, E. A., Wascher, T., Mathews, V. P., Lewis, J. W., et al. (2004). Visual object agnosia and pure word alexia: correlation of functional magnetic resonance imaging and lesion localization. Journal of Computer Assisted Tomography, 28, 63–67.PubMed

Saron, C. D., & Davidson, R. J. (1989). Visual evoked potential measures of interhemispheric transfer time in humans. Behavioral Neuroscience, 103, 1115–1138.PubMed

Savazzi, S., & Marzi, C. A. (2002). Speeding up reaction time with invisible stimuli. Current Biology, 12, 403–407.PubMed

Savazzi, S., & Marzi, C. A. (2004). The superior colliculus subserves interhemispheric neural summation in both normals and patients with a total section or agenesis of the corpus callosum. Neuropsychologia, 42, 1608–1618.PubMed

Schatz, J., & Erlandson, F. (2003). Level-repetition effects in hierarchical stimulus processing: timing and location of cortical activity. International Journal of Psychophysiology, 47, 255–269.

Schendel, K. L., & Robertson, L. C. (2002). Using reaction time to assess patients with unilateral neglect and extinction. Journal of Clinical and Experimental Neuropsychology, 24, 941–950.PubMed

Schiefer, U., Strasburger, H., Becker, S. T., Vonthein, R., Schiller, J., Dietrich, T. J., et al. (2001). Reaction time in automated kinetic perimetry: effects of stimulus luminance, eccentricity, and movement direction. Vision Research, 41, 2157–2164.PubMed

Schmahmann, J. D., & Pandya, D. N. (2006). Corpus callosum. In J. D. Schmahmann & D. N. Pandya (Eds.), Fiber pathways of the brain (pp. 485–496). New York: Oxford.

Schrift, M. J., Bandla, H., Shah, P., & Taylor, M. A. (1986). Interhemispheric transfer in major psychoses. Journal of Nervous and Mental Disease, 174, 203–207.PubMed

Schulte, T., Müller-Oehring, E. M., Strasburger, H., Warzel, H., & Sabel, B. A. (2001). Acute effects of alcohol on divided and covert attention in men. Psychopharmacology, 154, 61–69.PubMed

Schulte, T., Pfefferbaum, A., & Sullivan, E. V. (2004). Parallel interhemispheric processing in aging and alcoholism: relation to corpus callosum size. Neuropsychologia, 42, 257–271.PubMed

Schulte, T., Sullivan, E. V., Muller-Oehring, E. M., Adalsteinsson, E., & Pfefferbaum, A. (2005). Corpus callosal microstructural integrity influences interhemispheric processing: a diffusion tensor imaging study. Cerebral Cortex, 15, 1384–1392.PubMed

Schulte, T., Chen, S. H. A., Müller-Oehring, E. M., Adalsteinsson, E., Pfefferbaum, A., & Sullivan, E. V. (2006a). fMRI Evidence for frontal modulation of the extrastriate—dependent redundant targets effect. Neuroimage, 30, 973–982.

Schulte, T., Müller-Oehring, E. M., Pfefferbaum, A., & Sullivan, E. V. (2006b). Callosal involvement in a lateralized Stroop task in alcoholic and healthy subjects. Neuropsychology, 20, 727–736.

Schulte, T., Müller-Oehring, E. M., Pfefferbaum, A., & Sullivan, E. V. (2008). Callosal compromise differentially affects conflict processing and attentional allocation in alcoholism, HIV-infection, and their comorbidity. Brain Imaging and Behavior, 2, 27–38.PubMed

Schulte, T., Müller-Oehring, E. M., Vinco, S., Hoeft, F., Pfefferbaum, A., & Sullivan, E. V. (2009). Double dissociation between action-driven and perception-driven conflict resolution invoking anterior versus posterior brain systems. Neuroimage, 48, 381–390.PubMed

Silvanto, J., Walsh, V., & Cowey, A. (2009). Abnormal functional connectivity between ipsilesional V5/MT + and contralesional striate cortex (V1) in blindsight. Experimental Brain Research, 193, 645–650.

Shirani, P., Thorn, J., Davis, C., Heidler-Gary, J., Newhart, M., Gottesman, R. F., et al. (2009). Severity of hypoperfusion in distinct brain regions predicts severity of hemispatial neglect in different reference frames. Stroke, 40, 3563–3566.

Skiba, M., Diekamp, B., Prior, H., & Güntürkün, O. (2000). Lateralized interhemispheric transfer of color cues: evidence for dynamic coding principles of visual lateralization in pigeons. Brain and Language, 73, 254–273.PubMed

Stephan, K. E., Marshall, J. C., Friston, K. J., Rowe, J. B., Ritzl, A., Zilles, K., et al. (2003). Lateralized cognitive processes and lateralized task control in the human brain. Science, 301, 384–386.PubMed

Stroop, J. R. (1935). Studies of interference in serial verbal reactions. Journal of Experimental Psychology, 12, 643–662.

Sullivan, E. V., & Pfefferbaum, A. (2003). Diffusion tensor imaging in normal aging and neuropsychiatric disorders. European Journal of Radiology, 45, 244–255.PubMed

Sullivan, E. V., Adalsteinsson, E., Hedehus, M., Ju, C., Moseley, M., Lim, K. O., et al. (2001). Equivalent disruption of regional white matter microstructure in ageing healthy men and women. Neuroreport, 12, 99–104.PubMed

Sullivan, E. V., Pfefferbaum, A., Adalsteinsson, E., Swan, G. E., & Carmelli, D. (2002). Differential rates of regional brain change in callosal and ventricular size: a 4-year longitudinal MRI study of elderly men. Cerebral Cortex, 12, 438–445.PubMed

Sullivan, E. V., Adalsteinsson, E., & Pfefferbaum, A. (2006). Selective age-related degradation of anterior callosal fiber bundles quantified in vivo with fiber tracking. Cerebral Cortex, 16, 1030–1039.PubMed

Sullivan, E. V., Rohlfing, T., & Pfefferbaum, A. (2010). Quantitative fiber tracking of lateral and interhemispheric white matter systems in normal aging: relations to timed performance. Neurobiology of Aging, 31, 464–481.PubMed

Tanabe, H., Sawada, T., Inoue, N., Ogawa, M., Kuriyama, Y., & Shiraishi, J. (1987). Conduction aphasia and arcuate fasciculus. Acta Neurologica Scandinavica, 76, 422–427.PubMed

Tardif, E., & Clarke, S. (2002). Commissural connections of human superior colliculus. Neuroscience, 111, 363–372.PubMed

Tarnowska-Dziduszko, E., Bertrand, E., & Szpak, G. M. (1995). Morphological changes in the corpus callosum in chronic alcoholism. Folia Neuropathologica, 33, 25–29.PubMed

Tettamanti, M., Paulesu, E., Scifo, P., Maravita, A., Fazio, F., Perani, D., et al. (2002). Interhemispheric transmission of visuomotor information in humans: fMRI evidence. Journal of Neurophysiology, 88, 1051–1058.PubMed

Turatto, M., Mazza, V., Savazzi, S., & Marzi, C. A. (2004). The role of the magnocellular and parvocellular systems in the redundant target effect. Experimental Brain Research, 158, 141–150.

Virta, A., Barnett, A., & Pierpaoli, C. (1999). Visualizing and characterizing white matter fiber structure and architecture in the human pyramidal tract using diffusion tensor MRI. Magnetic Resonance Imaging, 17, 1121–1133.PubMed

Volberg, G., & Hübner, R. (2004). On the role of response conflicts and stimulus position for hemispheric differences in global/local processing: an ERP study. Neuropsychologia, 42, 1805–1813.PubMed

Wahl, M., Lauterbach-Soon, B., Hattingen, E., Jung, P., Singer, O., Volz, S., et al. (2007). Human motor corpus callosum: topography, somatotopy, and link between microstructure and function. Journal of Neuroscience, 27, 12132–12138.PubMed

Warlop, N. P., Achten, E., Debruyne, J., & Vingerhoets, G. (2008). Diffusion weighted callosal integrity reflects interhemispheric communication efficiency in multiple sclerosis. Neuropsychologia, 46, 2258–2264.PubMed

Weber, B., Schwarz, U., Kneifel, S., Treyer, V., & Buck, A. (2000). Hierarchical visual processing is dependent on the oculomotor system. NeuroReport, 11, 241–247.PubMed

Weber, B., Treyer, V., Oberholzer, N., Jaermann, T., Boesiger, P., Brugger, P., et al. (2005). Attention and interhemispheric transfer: a behavioral and fMRI study. Journal of Cognitive Neuroscience, 17, 113–123.PubMed

Weekes, N. Y., & Zaidel, E. (1996). The effects of procedural variations on lateralized Stroop effects. Brain and Cognition, 31, 308–330.PubMed

Weekes, N. Y., Carusi, D., & Zaidel, E. (1997). Interhemispheric relations in hierarchical perception: a second look. Neuropsychologia, 35, 37–44.PubMed

Weissman, D. H., Gopalakrishnan, A., Hazlett, C. J., & Woldorff, M. G. (2005). Dorsal anterior cingulate cortex resolves conflict from distracting stimuli by boosting attention toward relevant events. Cerebral Cortex, 15, 229–237.PubMed

Westerhausen, R., Kreuder, F., Woerner, W., Huster, R. J., Smit, C. M., Schweiger, E., et al. (2006). Interhemispheric transfer time and structural properties of the corpus callosum. Neuroscience Letters, 409, 140–145.PubMed

Westerhausen, R., Grüner, R., Specht, K., & Hugdahl, K. (2009). Functional relevance of interindividual differences in temporal lobe callosal pathways: a DTI tractography study. Cerebral Cortex, 19, 1322–1329.PubMed

Witelson, S. F. (1989). Hand and sex differences in the isthmus and genu of the human corpus callosum. A postmortem morphological study. Brain, 112, 799–835.PubMed

Woodruff, P. W., Phillips, M. L., Rushe, T., Wright, I. C., Murray, R. M., & David, A. S. (1997). Corpus callosum size and inter-hemispheric function in schizophrenia. Schizophrenia Research, 23, 189–196.PubMed

Yamaguchi, S., Yamagata, S., & Kobayashi, S. (2000). Cerebral asymmetry of the “top-down” allocation of attention to global and local features. Journal of Neuroscience, 20, RC72.PubMed

Yamauchi, H., Fukuyama, H., Nagahama, Y., Katsumi, Y., Dong, Y., Konishi, J., et al. (1997). Atrophy of the corpus callosum, cognitive impairment, and cortical hypometabolism in progressive supranuclear palsy. Annals of Neurology, 41, 606–614.PubMed

Yovel, G., Levy, J., & Yovel, I. (2001). Hemispheric asymmetries for global and local visual perception: effects of stimulus and task factors. Journal of Experimental Psychology: Human Perception and Performance, 27, 1369–1385.PubMed

Zahr, N. M., Rohlfing, T., Pfefferbaum, A., & Sullivan, E. V. (2009). Problem solving, working memory, and motor correlates of association and commissural fiber bundles in normal aging: a quantitative fiber tracking study. Neuroimage, 44, 1050–1062.PubMed

Zaidel, E., & Iacoboni, M. (2003). Poffenberger’s simple reaction time paradigm for measuring interhemispheric transfer time. In E. Zaidel & M. Iacoboni (Eds.), The parallel brain (pp. 1–8). Cambridge: MIT.

Titel: Contribution of Callosal Connections to the Interhemispheric Integration of Visuomotor and Cognitive Processes
verfasst von: Tilman Schulte
Eva M. Müller-Oehring
Publikationsdatum: 01.06.2010
Verlag: Springer US
Erschienen in: Neuropsychology Review / Ausgabe 2/2010
Print ISSN: 1040-7308
Elektronische ISSN: 1573-6660
DOI: https://doi.org/10.1007/s11065-010-9130-1

Leitlinien kompakt für die Neurologie

Mit medbee Pocketcards sicher entscheiden.

^{Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag}

Kostenlos registrieren

Neu im Fachgebiet Neurologie

25.04.2024 | Hypotonie | Nachrichten

Update Neurologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.

Newsletter bestellen

Springer Medizin

Contribution of Callosal Connections to the Interhemispheric Integration of Visuomotor and Cognitive Processes

Abstract

Leitlinien kompakt für die Neurologie

Neu im Fachgebiet Neurologie

Niedriger diastolischer Blutdruck erhöht Risiko für schwere kardiovaskuläre Komplikationen

Demenzkranke durch Antipsychotika vielfach gefährdet

Parkinson-Therapie im Wandel – aktuelle Leitlinie im Fokus

Auf diese Krankheiten bei Geflüchteten sollten Sie vorbereitet sein

Update Neurologie

Springer Medizin

Abstract

Bitte loggen Sie sich ein, um Zugang zu diesem Inhalt zu erhalten

Weitere Artikel der Ausgabe 2/2010

Disconnexion Syndromes in Animals and Man: Part I

Parkinson’s Disease as a Disconnection Syndrome

A Commentary on “Disconnexion Syndromes in Animals and Man”

MR Diffusion Tensor Imaging: A Window into White Matter Integrity of the Working Brain

White Matter: Organization and Functional Relevance

Are you Related to “the Geschwind?”

Leitlinien kompakt für die Neurologie

Neu im Fachgebiet Neurologie

Niedriger diastolischer Blutdruck erhöht Risiko für schwere kardiovaskuläre Komplikationen

Demenzkranke durch Antipsychotika vielfach gefährdet

Parkinson-Therapie im Wandel – aktuelle Leitlinie im Fokus

Auf diese Krankheiten bei Geflüchteten sollten Sie vorbereitet sein

Update Neurologie