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Neural Plasticity
Volume 2013 (2013), Article ID 864920, 14 pages
http://dx.doi.org/10.1155/2013/864920
Review Article

Neural Pathways Conveying Novisual Information to the Visual Cortex

1Department of Radiology and Tianjin Key Laboratory of Functional Imaging, Tianjin Medical University General Hospital, Tianjin 300052, China
2School of Medical Imaging, Tianjin Medical University General Hospital, Tianjin 300052, China

Received 31 March 2013; Accepted 22 May 2013

Academic Editor: Małgorzata Kossut

Copyright © 2013 Wen Qin and Chunshui Yu. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. K. Grill-Spector and R. Malach, “The human visual cortex,” Annual Review of Neuroscience, vol. 27, pp. 649–677, 2004. View at Publisher · View at Google Scholar · View at Scopus
  2. B. A. Wandell, S. O. Dumoulin, and A. A. Brewer, “Visual field maps in human cortex,” Neuron, vol. 56, no. 2, pp. 366–383, 2007. View at Google Scholar · View at Scopus
  3. D. J. Felleman and D. C. Van Essen, “Distributed hierarchical processing in the primate cerebral cortex,” Cerebral Cortex, vol. 1, no. 1, pp. 1–47, 1991. View at Google Scholar · View at Scopus
  4. G. Golarai, D. G. Ghahremani, S. Whitfield-Gabrieli et al., “Differential development of high-level visual cortex correlates with category-specific recognition memory,” Nature Neuroscience, vol. 10, no. 4, pp. 512–522, 2007. View at Publisher · View at Google Scholar · View at Scopus
  5. K. Seymour, C. W. G. Clifford, N. K. Logothetis, and A. Bartels, “Coding and binding of color and form in visual cortex,” Cerebral Cortex, vol. 20, no. 8, pp. 1946–1954, 2010. View at Publisher · View at Google Scholar · View at Scopus
  6. J. V. Haxby, C. L. Grady, B. Horwitz et al., “Dissociation of object and spatial visual processing pathways in human extrastriate cortex,” Proceedings of the National Academy of Sciences of the United States of America, vol. 88, no. 5, pp. 1621–1625, 1991. View at Google Scholar · View at Scopus
  7. M. A. Goodale and A. David Milner, “Separate visual pathways for perception and action,” Trends in Neurosciences, vol. 15, no. 1, pp. 20–25, 1992. View at Google Scholar · View at Scopus
  8. C. S. Konen and S. Kastner, “Two hierarchically organized neural systems for object information in human visual cortex,” Nature Neuroscience, vol. 11, no. 2, pp. 224–231, 2008. View at Publisher · View at Google Scholar · View at Scopus
  9. A. W. McGee, Y. Yang, Q. S. Fischer, N. W. Daw, and S. H. Strittmatter, “Neuroscience: experience-driven plasticity of visual cortex limited by myelin and nogo receptor,” Science, vol. 309, no. 5744, pp. 2222–2226, 2005. View at Publisher · View at Google Scholar · View at Scopus
  10. E. Putignano, G. Lonetti, L. Cancedda et al., “Developmental downregulation of histone posttranslational modifications regulates visual cortical plasticity,” Neuron, vol. 53, no. 5, pp. 747–759, 2007. View at Publisher · View at Google Scholar · View at Scopus
  11. J. W. Triplett, M. T. Owens, J. Yamada et al., “Retinal input instructs alignment of visual topographic maps,” Cell, vol. 139, no. 1, pp. 175–185, 2009. View at Publisher · View at Google Scholar · View at Scopus
  12. Y. Li, S. D. Van Hooser, M. Mazurek, L. E. White, and D. Fitzpatrick, “Experience with moving visual stimuli drives the early development of cortical direction selectivity,” Nature, vol. 456, no. 7224, pp. 952–956, 2008. View at Publisher · View at Google Scholar · View at Scopus
  13. Y. Yazaki-Sugiyama, S. Kang, H. Cteau, T. Fukai, and T. K. Hensch, “Bidirectional plasticity in fast-spiking GABA circuits by visual experience,” Nature, vol. 462, no. 7270, pp. 218–221, 2009. View at Publisher · View at Google Scholar · View at Scopus
  14. J. Jiang, W. Zhu, F. Shi et al., “Thick visual cortex in the early blind,” Journal of Neuroscience, vol. 29, no. 7, pp. 2205–2211, 2009. View at Publisher · View at Google Scholar · View at Scopus
  15. H. Park, J. D. Lee, E. Y. Kim et al., “Morphological alterations in the congenital blind based on the analysis of cortical thickness and surface area,” NeuroImage, vol. 47, no. 1, pp. 98–106, 2009. View at Publisher · View at Google Scholar · View at Scopus
  16. H. Bridge, A. Cowey, N. Ragge, and K. Watkins, “Imaging studies in congenital anophthalmia reveal preservation of brain architecture in “visual“ cortex,” Brain, vol. 132, no. 12, pp. 3467–3480, 2009. View at Publisher · View at Google Scholar · View at Scopus
  17. W. Qin, Y. Liu, T. Jiang, and C. Yu, “The development of visual areas depends differently on visual experience,” PLoS ONE, vol. 8, no. 1, Article ID e53784, 2013. View at Google Scholar
  18. C. Liu, Y. Liu, W. Li et al., “Increased regional homogeneity of blood oxygen level-dependent signals in occipital cortex of early blind individuals,” NeuroReport, vol. 22, no. 4, pp. 190–194, 2011. View at Publisher · View at Google Scholar · View at Scopus
  19. A. G. De Volder, A. Bol, J. Blin et al., “Brain energy metabolism in early blind subjects: neural activity in the visual cortex,” Brain Research, vol. 750, no. 1-2, pp. 235–244, 1997. View at Publisher · View at Google Scholar · View at Scopus
  20. M. Mishina, M. Senda, M. Kiyosawa et al., “Increased regional cerebral blood flow but normal distribution of GABAA receptor in the visual cortex of subjects with early-onset blindness,” NeuroImage, vol. 19, no. 1, pp. 125–131, 2003. View at Publisher · View at Google Scholar · View at Scopus
  21. C. Veraart, A. G. De Volder, M. C. Wanet-Defalque, A. Bol, C. Michel, and A. M. Goffinet, “Glucose utilization in human visual cortex is abnormally elevated in blindness of early onset but decreased in blindness of late onset,” Brain Research, vol. 510, no. 1, pp. 115–121, 1990. View at Publisher · View at Google Scholar · View at Scopus
  22. F. Uhl, P. Franzen, I. Podreka, M. Steiner, and L. Deecke, “Increased regional cerebral blood flow in inferior occipital cortex and cerebellum of early blind humans,” Neuroscience Letters, vol. 150, no. 2, pp. 162–164, 1993. View at Publisher · View at Google Scholar · View at Scopus
  23. M. Ptito, F. C. G. Schneider, O. B. Paulson, and R. Kupers, “Alterations of the visual pathways in congenital blindness,” Experimental Brain Research, vol. 187, no. 1, pp. 41–49, 2008. View at Publisher · View at Google Scholar · View at Scopus
  24. U. Noppeney, K. J. Friston, J. Ashburner, R. Frackowiak, and C. J. Price, “Early visual deprivation induces structural plasticity in gray and white matter,” Current Biology, vol. 15, no. 13, pp. R488–R490, 2005. View at Publisher · View at Google Scholar · View at Scopus
  25. W. Pan, G. Wu, C. Li, F. Lin, J. Sun, and H. Lei, “Progressive atrophy in the optic pathway and visual cortex of early blind Chinese adults: a voxel-based morphometry magnetic resonance imaging study,” NeuroImage, vol. 37, no. 1, pp. 212–220, 2007. View at Publisher · View at Google Scholar · View at Scopus
  26. J. S. Shimony, H. Burton, A. A. Epstein, D. G. McLaren, S. W. Sun, and A. Z. Snyder, “Diffusion tensor imaging reveals white matter reorganization in early blind humans,” Cerebral Cortex, vol. 16, no. 11, pp. 1653–1661, 2006. View at Publisher · View at Google Scholar · View at Scopus
  27. N. Shu, J. Li, K. Li, C. Yu, and T. Jiang, “Abnormal diffusion of cerebral white matter in early blindness,” Human Brain Mapping, vol. 30, no. 1, pp. 220–227, 2009. View at Publisher · View at Google Scholar · View at Scopus
  28. N. Shu, Y. Liu, J. Li, Y. Li, C. Yu, and T. Jiang, “Altered anatomical network in early blindness revealed by diffusion tensor tractography,” PLoS ONE, vol. 4, no. 9, Article ID e7228, 2009. View at Publisher · View at Google Scholar · View at Scopus
  29. J. Li, Y. Liu, W. Qin et al., “Age of onset of blindness affects brain anatomical networks constructed using diffusion tensor tractography,” Cereb Cortex, vol. 23, no. 3, pp. 542–551, 2013. View at Google Scholar
  30. C. Yu, Y. Liu, J. Li et al., “Altered functional connectivity of primary visual cortex in early blindness,” Human Brain Mapping, vol. 29, no. 5, pp. 533–543, 2008. View at Publisher · View at Google Scholar · View at Scopus
  31. Y. Liu, C. Yu, M. Liang et al., “Whole brain functional connectivity in the early blind,” Brain, vol. 130, no. 8, pp. 2085–2096, 2007. View at Publisher · View at Google Scholar · View at Scopus
  32. D. Bavelier and H. J. Neville, “Cross-modal plasticity: where and how?” Nature Reviews Neuroscience, vol. 3, no. 6, pp. 443–452, 2002. View at Google Scholar · View at Scopus
  33. K. Fiehler and F. Rösler, “Plasticity of multisensory dorsal stream functions: evidence from congenitally blind and sighted adults,” Restorative Neurology and Neuroscience, vol. 28, no. 2, pp. 193–205, 2010. View at Publisher · View at Google Scholar · View at Scopus
  34. N. Sadato, “Chapter 11 Cross-modal plasticity in the blind revealed by functional neuroimaging,” Supplements to Clinical Neurophysiology, vol. 59, pp. 75–79, 2006. View at Publisher · View at Google Scholar · View at Scopus
  35. K. Sathian and R. Stilla, “Cross-modal plasticity of tactile perception in blindness,” Restorative Neurology and Neuroscience, vol. 28, no. 2, pp. 271–281, 2010. View at Publisher · View at Google Scholar · View at Scopus
  36. O. Collignon, P. Voss, M. Lassonde, and F. Lepore, “Cross-modal plasticity for the spatial processing of sounds in visually deprived subjects,” Experimental Brain Research, vol. 192, no. 3, pp. 343–358, 2009. View at Publisher · View at Google Scholar · View at Scopus
  37. E. Ricciardi, N. Vanello, L. Sani et al., “The effect of visual experience on the development of functional architecture in hMT+,” Cerebral Cortex, vol. 17, no. 12, pp. 2933–2939, 2007. View at Publisher · View at Google Scholar · View at Scopus
  38. P. Pietrini, M. L. Furey, E. Ricciardi et al., “Beyond sensory images: object-based representation in the human ventral pathway,” Proceedings of the National Academy of Sciences of the United States of America, vol. 101, no. 15, pp. 5658–5663, 2004. View at Publisher · View at Google Scholar · View at Scopus
  39. K. Sathian, A. Zangaladze, J. M. Hoffman, and S. T. Grafton, “Feeling with the mind's eye,” NeuroReport, vol. 8, no. 18, pp. 3877–3881, 1997. View at Google Scholar · View at Scopus
  40. A. Zangaladze, C. M. Epstein, S. T. Grafton, and K. Sathian, “Involvement of visual cortex in tactile discrimination orientation,” Nature, vol. 401, no. 6753, pp. 587–590, 1999. View at Publisher · View at Google Scholar · View at Scopus
  41. E. Ricciardi, D. Basso, L. Sani et al., “Functional inhibition of the human middle temporal cortex affects non-visual motion perception: a repetitive transcranial magnetic stimulation study during tactile speed discrimination,” Experimental Biology and Medicine, vol. 236, no. 2, pp. 138–144, 2011. View at Publisher · View at Google Scholar · View at Scopus
  42. M. Ptito, I. Matteau, A. Zhi Wang, O. B. Paulson, H. R. Siebner, and R. Kupers, “Crossmodal recruitment of the ventral visual stream in congenital blindness,” Neural Plasticity, vol. 2012, Article ID 304045, 9 pages, 2012. View at Publisher · View at Google Scholar
  43. T. W. James, G. K. Humphrey, J. S. Gati, R. S. Menon, and M. A. Goodale, “Differential effects of viewpoint on object-driven activation in dorsal and ventral streams,” Neuron, vol. 35, no. 4, pp. 793–801, 2002. View at Publisher · View at Google Scholar · View at Scopus
  44. T. W. James, G. K. Humphrey, J. S. Gati, P. Servos, R. S. Menon, and M. A. Goodale, “Haptic study of three-dimensional objects activates extrastriate visual areas,” Neuropsychologia, vol. 40, no. 10, pp. 1706–1714, 2002. View at Publisher · View at Google Scholar · View at Scopus
  45. A. Amedi, G. Jacobson, T. Hendler, R. Malach, and E. Zohary, “Convergence of visual and tactile shape processing in the human lateral occipital complex zohary,” Cerebral Cortex, vol. 12, no. 11, pp. 1202–1212, 2002. View at Google Scholar · View at Scopus
  46. A. Amedi, R. Malach, T. Hendler, S. Peled, and E. Zohary, “Visuo-haptic object-related activation in the ventral visual pathway,” Nature Neuroscience, vol. 4, no. 3, pp. 324–330, 2001. View at Publisher · View at Google Scholar · View at Scopus
  47. M. Zhang, V. D. Weisser, R. Stilla, S. C. Prather, and K. Sathian, “Multisensory cortical processing of object shape and its relation to mental imagery,” Cognitive, Affective and Behavioral Neuroscience, vol. 4, no. 2, pp. 251–259, 2004. View at Google Scholar · View at Scopus
  48. M. R. Stoesz, M. Zhang, V. D. Weisser, S. C. Prather, H. Mao, and K. Sathian, “Neural networks active during tactile form perception: common and differential activity during macrospatial and microspatial tasks,” International Journal of Psychophysiology, vol. 50, no. 1-2, pp. 41–49, 2003. View at Publisher · View at Google Scholar · View at Scopus
  49. S. C. Prather, J. R. Votaw, and K. Sathian, “Task-specific recruitment of dorsal and ventral visual areas during tactile perception,” Neuropsychologia, vol. 42, no. 8, pp. 1079–1087, 2004. View at Publisher · View at Google Scholar · View at Scopus
  50. I. Matteau, R. Kupers, E. Ricciardi, P. Pietrini, and M. Ptito, “Beyond visual, aural and haptic movement perception: hMT+ is activated by electrotactile motion stimulation of the tongue in sighted and in congenitally blind individuals,” Brain Research Bulletin, vol. 82, no. 5-6, pp. 264–270, 2010. View at Publisher · View at Google Scholar · View at Scopus
  51. F. Morrell, “Visual system's view of acoustic space,” Nature, vol. 238, no. 5358, pp. 44–46, 1972. View at Publisher · View at Google Scholar · View at Scopus
  52. C. Poirier, O. Collignon, A. G. DeVolder et al., “Specific activation of the V5 brain area by auditory motion processing: an fMRI study,” Cognitive Brain Research, vol. 25, no. 3, pp. 650–658, 2005. View at Publisher · View at Google Scholar · View at Scopus
  53. U. Zimmer, J. Lewald, M. Erb, W. Grodd, and H. Karnath, “Is there a role of visual cortex in spatial hearing?” European Journal of Neuroscience, vol. 20, no. 11, pp. 3148–3156, 2004. View at Publisher · View at Google Scholar · View at Scopus
  54. C. Poirier, O. Collignon, C. Scheiber et al., “Auditory motion perception activates visual motion areas in early blind subjects,” NeuroImage, vol. 31, no. 1, pp. 279–285, 2006. View at Publisher · View at Google Scholar · View at Scopus
  55. E. Ricciardi, “Brain response to visual, tactile and auditory flow in sighted and blind individuals supports a supramodal functional organization in hMT+ complex,” Neuroimage, vol. 31, no. 1, supplement, p. 512, 2006. View at Google Scholar
  56. J. Lewald, I. G. Meister, J. Weidemann, and R. Töpper, “Involvement of the superior temporal cortex and the occipital cortex in spatial hearing: evidence from repetitive transcranial magnetic stimulation,” Journal of Cognitive Neuroscience, vol. 16, no. 5, pp. 828–838, 2004. View at Publisher · View at Google Scholar · View at Scopus
  57. O. Collignon, M. Davare, E. Olivier, and A. G. De Volder, “Reorganisation of the right occipito-parietal stream for auditory spatial processing in early blind humans. a transcranial magnetic stimulation study,” Brain Topography, vol. 21, no. 3-4, pp. 232–240, 2009. View at Publisher · View at Google Scholar · View at Scopus
  58. O. Collignon, M. Davare, A. G. De Volder, C. Poirier, E. Olivier, and C. Veraart, “Time-course of posterior parietal and occipital cortex contribution to sound localization,” Journal of Cognitive Neuroscience, vol. 20, no. 8, pp. 1454–1463, 2008. View at Publisher · View at Google Scholar · View at Scopus
  59. E. Ricciardi, D. Bonino, L. Sani et al., “Do we really need vision? How blind people “see” the actions of others,” Journal of Neuroscience, vol. 29, no. 31, pp. 9719–9724, 2009. View at Publisher · View at Google Scholar · View at Scopus
  60. H. Burton, R. J. Sinclair, and D. G. McLaren, “Cortical activity to vibrotactile stimulation: an fMRI study in blind and sighted individuals,” Human Brain Mapping, vol. 23, no. 4, pp. 210–228, 2004. View at Publisher · View at Google Scholar · View at Scopus
  61. M. Ptito, I. Matteau, A. Gjedde, and R. Kupers, “Recruitment of the middle temporal area by tactile motion in congenital blindness,” NeuroReport, vol. 20, no. 6, pp. 543–547, 2009. View at Publisher · View at Google Scholar · View at Scopus
  62. R. Kupers, D. R. Chebat, K. H. Madsen, O. B. Paulson, and M. Ptito, “Neural correlates of virtual route recognition in congenital blindness,” Proceedings of the National Academy of Sciences of the United States of America, vol. 107, no. 28, pp. 12716–12721, 2010. View at Publisher · View at Google Scholar · View at Scopus
  63. M. Ptito, S. M. Moesgaard, A. Gjedde, and R. Kupers, “Cross-modal plasticity revealed by electrotactile stimulation of the tongue in the congenitally blind,” Brain, vol. 128, no. 3, pp. 606–614, 2005. View at Publisher · View at Google Scholar · View at Scopus
  64. R. Kupers, A. Fumal, A. M. De Noordhout, A. Gjedde, J. Schoenen, and M. Ptito, “Transcranial magnetic stimulation of the visual cortex induces somatotopically organized qualia in blind subjects,” Proceedings of the National Academy of Sciences of the United States of America, vol. 103, no. 35, pp. 13256–13260, 2006. View at Publisher · View at Google Scholar · View at Scopus
  65. P. Arno, A. G. De Volder, A. Vanlierde et al., “Occipital activation by pattern recognition in the early blind using auditory substitution for vision,” NeuroImage, vol. 13, no. 4, pp. 632–645, 2001. View at Publisher · View at Google Scholar · View at Scopus
  66. L. A. Renier, I. Anurova, A. G. De Volder, S. Carlson, J. VanMeter, and J. P. Rauschecker, “Preserved functional specialization for spatial processing in the middle occipital gyrus of the early blind,” Neuron, vol. 68, no. 1, pp. 138–148, 2010. View at Publisher · View at Google Scholar · View at Scopus
  67. R. Weeks, B. Horwitz, A. Aziz-Sultan et al., “A positron emission tomographic study of auditory localization in the congenitally blind,” Journal of Neuroscience, vol. 20, no. 7, pp. 2664–2672, 2000. View at Google Scholar · View at Scopus
  68. G. Dormal, F. Lepore, and O. Collignon, “Plasticity of the dorsal “spatial” stream in visually deprived individuals,” Neural Plasticity, vol. 2012, Article ID 687659, 12 pages, 2012. View at Publisher · View at Google Scholar
  69. O. Collignon, G. Vandewalle, P. Voss et al., “Functional specialization for auditory-spatial processing in the occipital cortex of congenitally blind humans,” Proceedings of the National Academy of Sciences of the United States of America, vol. 108, no. 11, pp. 4435–4440, 2011. View at Publisher · View at Google Scholar · View at Scopus
  70. T. Wolbers, P. Zahorik, and N. A. Giudice, “Decoding the direction of auditory motion in blind humans,” NeuroImage, vol. 56, no. 2, pp. 681–687, 2011. View at Publisher · View at Google Scholar · View at Scopus
  71. M. Bedny, T. Konkle, K. Pelphrey, R. Saxe, and A. Pascual-Leone, “Sensitive period for a multimodal response in human visual motion area MT/MST,” Current Biology, vol. 20, no. 21, pp. 1900–1906, 2010. View at Publisher · View at Google Scholar · View at Scopus
  72. A. Amedi, W. M. Stern, J. A. Camprodon et al., “Shape conveyed by visual-to-auditory sensory substitution activates the lateral occipital complex,” Nature Neuroscience, vol. 10, no. 6, pp. 687–689, 2007. View at Publisher · View at Google Scholar · View at Scopus
  73. J. Kim and R. J. Zatorre, “Tactile-auditory shape learning engages the lateral occipital complex,” Journal of Neuroscience, vol. 31, no. 21, pp. 7848–7856, 2011. View at Publisher · View at Google Scholar · View at Scopus
  74. E. Striem-Amit, O. Dakwar, L. Reich, and A. Amedi, “The large-scale organization of “visual” streams emerges without visual experience,” Cereb Cortex, vol. 22, no. 7, pp. 1698–1709, 2012. View at Google Scholar
  75. B. Röder, W. Teder-Sälejärvi, A. Sterr, F. Rösler, S. A. Hillyard, and H. J. Neville, “Improved auditory spatial tuning in blind humans,” Nature, vol. 400, no. 6740, pp. 162–166, 1999. View at Publisher · View at Google Scholar · View at Scopus
  76. C. Leclerc, S. J. Segalowitz, J. Desjardins, M. Lassonde, and F. Lepore, “EEG coherence in early-blind humans during sound localization,” Neuroscience Letters, vol. 376, no. 3, pp. 154–159, 2005. View at Publisher · View at Google Scholar · View at Scopus
  77. C. Leclerc, D. Saint-Amour, M. E. Lavoie, M. Lassonde, and F. Lepore, “Brain functional reorganization in early blind humans revealed by auditory event-related potentials,” NeuroReport, vol. 11, no. 3, pp. 545–550, 2000. View at Google Scholar · View at Scopus
  78. O. Collignon, M. Lassonde, F. Lepore, D. Bastien, and C. Veraart, “Functional cerebral reorganization for auditory spatial processing and auditory substitution of vision in early blind subjects,” Cerebral Cortex, vol. 17, no. 2, pp. 457–465, 2007. View at Publisher · View at Google Scholar · View at Scopus
  79. L. B. Merabet, L. Battelli, S. Obretenova, S. Maguire, P. Meijer, and A. Pascual-Leone, “Functional recruitment of visual cortex for sound encoded object identification in the blind,” NeuroReport, vol. 20, no. 2, pp. 132–138, 2009. View at Publisher · View at Google Scholar · View at Scopus
  80. R. Kupers, M. Beaulieu-Lefebvre, F. C. Schneider et al., “Neural correlates of olfactory processing in congenital blindness,” Neuropsychologia, vol. 49, no. 7, pp. 2037–2044, 2011. View at Publisher · View at Google Scholar · View at Scopus
  81. M. Beaulieu-Lefebvre, F. C. Schneider, R. Kupers, and M. Ptito, “Odor perception and odor awareness in congenital blindness,” Brain Research Bulletin, vol. 84, no. 3, pp. 206–209, 2011. View at Publisher · View at Google Scholar · View at Scopus
  82. I. Cuevas, P. Plaza, P. Rombaux, A. G. De Volder, and L. Renier, “Odour discrimination and identification are improved in early blindness,” Neuropsychologia, vol. 47, no. 14, pp. 3079–3083, 2009. View at Publisher · View at Google Scholar · View at Scopus
  83. N. Sadato, A. Pascual-Leone, J. Grafman et al., “Activation of the primary visual cortex by Braille reading in blind subjects,” Nature, vol. 380, no. 6574, pp. 526–528, 1996. View at Publisher · View at Google Scholar · View at Scopus
  84. L. G. Cohen, R. A. Weeks, N. Sadato, P. Celnik, K. Ishii, and M. Hallett, “Period of susceptibility for cross-modal plasticity in the blind,” Annals of Neurology, vol. 45, no. 4, pp. 451–460, 1999. View at Google Scholar
  85. N. Sadato, T. Okada, M. Honda, and Y. Yonekura, “Critical period for cross-modal plasticity in blind humans: a functional MRI study,” NeuroImage, vol. 16, no. 2, pp. 389–400, 2002. View at Publisher · View at Google Scholar · View at Scopus
  86. H. Burton, A. Z. Snyder, T. E. Conturo, E. Akbudak, J. M. Ollinger, and M. E. Raichle, “Adaptive changes in early and late blind: a fMRI study of Braille reading,” Journal of Neurophysiology, vol. 87, no. 1, pp. 589–607, 2002. View at Google Scholar · View at Scopus
  87. H. Burton, A. Z. Snyder, J. B. Diamond, and M. E. Raichle, “Adaptive changes in early and late blind: a fMRI study of verb generation to heard nouns,” Journal of Neurophysiology, vol. 88, no. 6, pp. 3359–3371, 2002. View at Google Scholar · View at Scopus
  88. H. Burton, J. B. Diamond, and K. B. McDermott, “Dissociating cortical regions activated by semantic and phonological tasks: a fMRI study in blind and sighted people,” Journal of Neurophysiology, vol. 90, no. 3, pp. 1965–1982, 2003. View at Publisher · View at Google Scholar · View at Scopus
  89. B. Röder, O. Stock, S. Bien, H. Neville, and F. Rösler, “Speech processing activates visual cortex in congenitally blind humans,” European Journal of Neuroscience, vol. 16, no. 5, pp. 930–936, 2002. View at Publisher · View at Google Scholar · View at Scopus
  90. L. Reich, M. Szwed, L. Cohen, and A. Amedi, “A ventral visual stream reading center independent of visual experience,” Current Biology, vol. 21, no. 5, pp. 363–368, 2011. View at Publisher · View at Google Scholar · View at Scopus
  91. M. Bedny, A. Pascual-Leone, D. Dodell-Feder, E. Fedorenko, and R. Saxe, “Language processing in the occipital cortex of congenitally blind adults,” Proceedings of the National Academy of Sciences of the United States of America, vol. 108, no. 11, pp. 4429–4434, 2011. View at Publisher · View at Google Scholar · View at Scopus
  92. L. G. Cohen, P. Celnik, A. Pascual-Leone et al., “Functional relevance of cross-modal plasticity in blind humans,” Nature, vol. 389, no. 6647, pp. 180–183, 1997. View at Publisher · View at Google Scholar · View at Scopus
  93. A. Amedi, A. Floel, S. Knecht, E. Zohary, and L. G. Cohen, “Transcranial magnetic stimulation of the occipital pole interferes with verbal processing in blind subjects,” Nature Neuroscience, vol. 7, no. 11, pp. 1266–1270, 2004. View at Publisher · View at Google Scholar · View at Scopus
  94. R. Hamilton, J. P. Keenan, M. Catala, and A. Pascual-Leone, “Alexia for Braille following bilateral occipital stroke in an early blind woman,” NeuroReport, vol. 11, no. 2, pp. 237–240, 2000. View at Google Scholar · View at Scopus
  95. K. Maeda, H. Yasuda, M. Haneda, and A. Kashiwagi, “Braille alexia during visual hallucination in a blind man with selective calcarine atrophy,” Psychiatry and Clinical Neurosciences, vol. 57, no. 2, pp. 227–229, 2003. View at Publisher · View at Google Scholar · View at Scopus
  96. A. A. Stevens, M. Snodgrass, D. Schwartz, and K. Weaver, “Preparatory activity in occipital cortex in early blind humans predicts auditory perceptual performance,” Journal of Neuroscience, vol. 27, no. 40, pp. 10734–10741, 2007. View at Publisher · View at Google Scholar · View at Scopus
  97. F. Gougoux, R. J. Zatorre, M. Lassonde, P. Voss, and F. Lepore, “A functional neuroimaging study of sound localization: visual cortex activity predicts performance in early-blind individuals,” PLoS Biology, vol. 3, no. 2, article e27, 2005. View at Google Scholar · View at Scopus
  98. H. Burton, R. J. Sinclair, and A. Agato, “Recognition memory for Braille or spoken words: an fMRI study in early blind,” Brain Research, vol. 1438, pp. 22–34, 2012. View at Publisher · View at Google Scholar · View at Scopus
  99. H. J. Park, “Activation of the occipital cortex and deactivation of the default mode network during working memory in the early blind,” Journal of the International Neuropsychological Society, vol. 17, pp. 407–422, 2011. View at Google Scholar
  100. D. Bonino, E. Ricciardi, L. Sani et al., “Tactile spatial working memory activates the dorsal extrastriate cortical pathway in congenitally blind individuals,” Archives Italiennes de Biologie, vol. 146, no. 3-4, pp. 133–146, 2008. View at Google Scholar · View at Scopus
  101. A. Amedi, N. Raz, P. Pianka, R. Malach, and E. Zohary, “Early “visual” cortex activation correlates with superior verbal memory performance in the blind,” Nature Neuroscience, vol. 6, no. 7, pp. 758–766, 2003. View at Publisher · View at Google Scholar · View at Scopus
  102. K. Sathian and A. Zangaladze, “Feeling with the mind's eye: the role of visual imagery in tactile perception,” Optometry and Vision Science, vol. 78, no. 5, pp. 276–281, 2001. View at Google Scholar · View at Scopus
  103. S. M. Kosslyn, W. L. Thompson, I. J. Kim, and N. M. Alpert, “Topographical representations of mental images in primary visual cortex,” Nature, vol. 378, no. 6556, pp. 496–498, 1995. View at Google Scholar · View at Scopus
  104. S. M. Kosslyn, A. Pascual-Leone, O. Felician et al., “The role of area 17 in visual imagery: convergent evidence from PET and rTMS,” Science, vol. 284, no. 5411, pp. 167–170, 1999. View at Publisher · View at Google Scholar · View at Scopus
  105. S. Lee, D. J. Kravitz, and C. I. Baker, “Disentangling visual imagery and perception of real-world objects,” NeuroImage, vol. 59, no. 4, pp. 4064–4073, 2012. View at Publisher · View at Google Scholar · View at Scopus
  106. Z. Cattaneo, S. Bona, and J. Silvanto, “Cross-adaptation combined with TMS reveals a functional overlap between vision and imagery in the early visual cortex,” NeuroImage, vol. 59, no. 3, pp. 3015–3020, 2012. View at Publisher · View at Google Scholar · View at Scopus
  107. R. Seurinck, F. P. de Lange, E. Achten, and G. Vingerhoets, “Mental rotation meets the motion aftereffect: the role of hV5/MT+ in visual mental imagery,” Journal of Cognitive Neuroscience, vol. 23, no. 6, pp. 1395–1404, 2011. View at Publisher · View at Google Scholar · View at Scopus
  108. A. Kaas, S. Weigelt, A. Roebroeck, A. Kohler, and L. Muckli, “Imagery of a moving object: the role of occipital cortex and human MT/V5+,” NeuroImage, vol. 49, no. 1, pp. 794–804, 2010. View at Publisher · View at Google Scholar · View at Scopus
  109. B. Z. Mahon, J. Schwarzbach, and A. Caramazza, “The representation of tools in left parietal cortex is independent of visual experience,” Psychological Science, vol. 21, no. 6, pp. 764–771, 2010. View at Google Scholar · View at Scopus
  110. B. Z. Mahon, S. Anzellotti, J. Schwarzbach, M. Zampini, and A. Caramazza, “Category-specific organization in the human brain does not require visual experience,” Neuron, vol. 63, no. 3, pp. 397–405, 2009. View at Publisher · View at Google Scholar · View at Scopus
  111. O. Collignon and A. G. De Voider, “Further evidence that congenitally blind participants react faster to auditory and tactile spatial targets,” Canadian Journal of Experimental Psychology, vol. 63, no. 4, pp. 287–293, 2009. View at Publisher · View at Google Scholar · View at Scopus
  112. O. Collignon, L. Renier, R. Bruyer, D. Tranduy, and C. Veraart, “Improved selective and divided spatial attention in early blind subjects,” Brain Research, vol. 1075, no. 1, pp. 175–182, 2006. View at Publisher · View at Google Scholar · View at Scopus
  113. N. Lessard, M. Paré, F. Lepore, and M. Lassonde, “Early-blind human subjects localize sound sources better than sighted subjects,” Nature, vol. 395, no. 6699, pp. 278–280, 1998. View at Publisher · View at Google Scholar · View at Scopus
  114. D. Goldreich and I. M. Kanics, “Tactile acuity is enhanced in blindness,” Journal of Neuroscience, vol. 23, no. 8, pp. 3439–3445, 2003. View at Google Scholar · View at Scopus
  115. R. W. Van Boven, R. H. Hamilton, T. Kauffman, J. P. Keenan, and A. Pascual-Leone, “Tactile spatial resolution in blind Braille readers,” Neurology, vol. 54, no. 12, pp. 2230–2236, 2000. View at Google Scholar · View at Scopus
  116. L. Sani, E. Ricciardi, C. Gentili, N. Vanello, J. V. Haxby, and P. Pietrini, “Effects of visual experience on the human MT+ functional connectivity networks: an fMRI study of motion perception in sighted and congenitally blind individuals,” Frontiers in Systems Neuroscience, vol. 4, article 159, 2010. View at Publisher · View at Google Scholar · View at Scopus
  117. J. P. Rauschecker, B. Tian, M. Korte, and U. Egert, “Crossmodal changes in the somatosensory vibrissa/barrel system of visually deprived animals,” Proceedings of the National Academy of Sciences of the United States of America, vol. 89, no. 11, pp. 5063–5067, 1992. View at Publisher · View at Google Scholar · View at Scopus
  118. J. P. Rauschecker and M. Korte, “Auditory compensation for early blindness in cat cerebral cortex,” Journal of Neuroscience, vol. 13, no. 10, pp. 4538–4548, 1993. View at Google Scholar · View at Scopus
  119. J. P. Rauschecker, “Compensatory plasticity and sensory substitution in the cerebral cortex,” Trends in Neurosciences, vol. 18, no. 1, pp. 36–43, 1995. View at Publisher · View at Google Scholar · View at Scopus
  120. A. Morel, M. Magnin, and D. Jeanmonod, “Multiarchitectonic and stereotactic atlas of the human thalamus,” Journal of Comparative Neurology, vol. 387, no. 4, pp. 588–630, 1997. View at Google Scholar
  121. G. Percheron, C. François, B. Talbi, J. Yelnik, and G. Fénelon, “The primate motor thalamus,” Brain Research Reviews, vol. 22, no. 2, pp. 93–181, 1996. View at Publisher · View at Google Scholar · View at Scopus
  122. A. M. Sillito, J. Cudeiro, and H. E. Jones, “Always returning: feedback and sensory processing in visual cortex and thalamus,” Trends in Neurosciences, vol. 29, no. 6, pp. 307–316, 2006. View at Publisher · View at Google Scholar · View at Scopus
  123. J. A. Winer, M. L. Chernock, D. T. Larue, and S. W. Cheung, “Descending projections to the inferior colliculus from the posterior thalamus and the auditory cortex in rat, cat, and monkey,” Hearing Research, vol. 168, no. 1-2, pp. 181–195, 2002. View at Publisher · View at Google Scholar · View at Scopus
  124. L. Li and F. F. Ebner, “Cortical modulation of spatial and angular tuning maps in the rat thalamus,” Journal of Neuroscience, vol. 27, no. 1, pp. 167–179, 2007. View at Publisher · View at Google Scholar · View at Scopus
  125. Y. Lam and S. M. Sherman, “Functional organization of the somatosensory cortical layer 6 feedback to the thalamus,” Cerebral Cortex, vol. 20, no. 1, pp. 13–24, 2010. View at Publisher · View at Google Scholar · View at Scopus
  126. M. Iacoboni, “Adjusting reaches: feedback in the posterior parietal cortex,” Nature Neuroscience, vol. 2, no. 6, pp. 492–494, 1999. View at Publisher · View at Google Scholar · View at Scopus
  127. M. A. Sommer and R. H. Wurtz, “What the brain stem tells the frontal cortex—I. Oculomotor signals sent from superior colliculus to frontal eye field via mediodorsal thalamus,” Journal of Neurophysiology, vol. 91, no. 3, pp. 1381–1402, 2004. View at Publisher · View at Google Scholar · View at Scopus
  128. L. M. Romanski, M. Giguere, J. F. Bates, and P. S. Goldman-Rakic, “Topographic organization of medial pulvinar connections with the prefrontal cortex in the rhesus monkey,” Journal of Comparative Neurology, vol. 379, no. 3, pp. 313–332, 1997. View at Google Scholar
  129. E. Salzmann, “Attention and memory trials during neuronal recording from the primate pulvinar and posterior parietal cortex (area PG),” Behavioural Brain Research, vol. 67, no. 2, pp. 241–253, 1995. View at Publisher · View at Google Scholar · View at Scopus
  130. C.-S. Lin and J. H. Kaas, “Projections from the medial nucleus of the inferior pulvinar complex to the middle temporal area of the visual cortex,” Neuroscience, vol. 5, no. 12, pp. 2219–2228, 1980. View at Publisher · View at Google Scholar · View at Scopus
  131. D. A. Simpson, “The projection of the pulvinar to the temporal lobe,” Journal of Anatomy, vol. 86, no. 1, pp. 20–28, 1952. View at Google Scholar · View at Scopus
  132. S. Shipp, “The functional logic of cortico-pulvinar connections,” Philosophical Transactions of the Royal Society B, vol. 358, no. 1438, pp. 1605–1624, 2003. View at Publisher · View at Google Scholar · View at Scopus
  133. N. Chabot, V. Charbonneau, M. Laramée, R. Tremblay, D. Boire, and G. Bronchti, “Subcortical auditory input to the primary visual cortex in anophthalmic mice,” Neuroscience Letters, vol. 433, no. 2, pp. 129–134, 2008. View at Publisher · View at Google Scholar · View at Scopus
  134. R. Izraeli, G. Koay, M. Lamish et al., “Cross-modal neuroplasticity in neonatally enucleated hamsters: structure, electrophysiology and behaviour,” European Journal of Neuroscience, vol. 15, no. 4, pp. 693–712, 2002. View at Publisher · View at Google Scholar · View at Scopus
  135. N. Doron and Z. Wollberg, “Cross-modal neuroplasticity in the blind mole rat Spalax Ehrenbergi: a WGA-HRP tracing study,” NeuroReport, vol. 5, no. 18, pp. 2697–2701, 1994. View at Google Scholar · View at Scopus
  136. M. Piché, N. Chabot, G. Bronchti, D. Miceli, F. Lepore, and J.-P. Guillemot, “Auditory responses in the visual cortex of neonatally enucleated rats,” Neuroscience, vol. 145, no. 3, pp. 1144–1156, 2007. View at Publisher · View at Google Scholar · View at Scopus
  137. M. Piché, S. Robert, D. Miceli, and G. Bronchti, “Environmental enrichment enhances auditory takeover of the occipital cortex in anophthalmic mice,” European Journal of Neuroscience, vol. 20, no. 12, pp. 3463–3472, 2004. View at Publisher · View at Google Scholar · View at Scopus
  138. G. Bronchti, P. Heil, R. Sadka, A. Hess, H. Scheich, and Z. Wollberg, “Auditory activation of “visual” cortical areas in the blind mole rat (Spalax ehrenbergi),” European Journal of Neuroscience, vol. 16, no. 2, pp. 311–329, 2002. View at Publisher · View at Google Scholar · View at Scopus
  139. N. Chabot, S. Robert, R. Tremblay, D. Miceli, D. Boire, and G. Bronchti, “Audition differently activates the visual system in neonatally enucleated mice compared with anophthalmic mutants,” European Journal of Neuroscience, vol. 26, no. 8, pp. 2334–2348, 2007. View at Publisher · View at Google Scholar · View at Scopus
  140. S. J. Karlen, D. M. Kahn, and L. Krubitzer, “Early blindness results in abnormal corticocortical and thalamocortical connections,” Neuroscience, vol. 142, no. 3, pp. 843–858, 2006. View at Publisher · View at Google Scholar · View at Scopus
  141. G. Rehkamper, R. Necker, and E. Nevo, “Functional anatomy of the thalamus in the blind mole rat Spalax ehrenbergi: an architectonic and electrophysiologically controlled tracing study,” Journal of Comparative Neurology, vol. 347, no. 4, pp. 570–584, 1994. View at Google Scholar · View at Scopus
  142. G. Bronchti, R. Rado, J. Terkel, and Z. Wollberg, “Retinal projections in the blind mole rat: a WGA-HRP tracing study of a natural degenertion,” Developmental Brain Research, vol. 58, no. 2, pp. 159–170, 1991. View at Publisher · View at Google Scholar · View at Scopus
  143. Y. B. Saalmann, M. A. Pinsk, L. Wang, X. Li, and S. Kastner, “The pulvinar regulates information transmission between cortical areas based on attention demands,” Science, vol. 337, no. 6095, pp. 753–756, 2012. View at Google Scholar
  144. J. H. Kaas and D. C. Lyon, “Pulvinar contributions to the dorsal and ventral streams of visual processing in primates,” Brain Research Reviews, vol. 55, no. 2, pp. 285–296, 2007. View at Publisher · View at Google Scholar · View at Scopus
  145. C. Casanova, L. Merabet, A. Desautels, and K. Minville, “Higher-order motion processing in the pulvinar,” Progress in Brain Research, vol. 134, pp. 71–82, 2001. View at Publisher · View at Google Scholar · View at Scopus
  146. K. L. Grieve, C. Acuña, and J. Cudeiro, “The primate pulvinar nuclei: vision and action,” Trends in Neurosciences, vol. 23, no. 1, pp. 35–39, 2000. View at Publisher · View at Google Scholar · View at Scopus
  147. A. Gaglianese, M. Costagli, G. Bernardi, E. Ricciardi, and P. Pietrini, “Evidence of a direct influence between the thalamus and hMT+ independent of V1 in the human brain as measured by fMRI,” NeuroImage, vol. 60, no. 2, pp. 1440–1447, 2012. View at Publisher · View at Google Scholar · View at Scopus
  148. M. A. Schoenfeld, H.-J. Heinze, and M. G. Woldorff, “Unmasking motion-processing activity in human brain area V5/MT+ mediated by pathways that bypass primary visual cortex,” NeuroImage, vol. 17, no. 2, pp. 769–779, 2002. View at Publisher · View at Google Scholar · View at Scopus
  149. L. G. Ungerleider, R. Desimone, T. W. Galkin, and M. Mishkin, “Subcortical projections of area MT in the Macaque,” Journal of Comparative Neurology, vol. 223, no. 3, pp. 368–386, 1984. View at Google Scholar · View at Scopus
  150. A. Lysakowski, G. P. Standage, and L. A. Benevento, “An investigation of collateral projections of the dorsal lateral geniculate nucleus and other subcortical structures to cortical areas V1 and V4 in the macaque monkey: a double label retrograde tracer study,” Experimental Brain Research, vol. 69, no. 3, pp. 651–661, 1988. View at Google Scholar · View at Scopus
  151. M. C. Schmid, S. W. Mrowka, J. Turchi et al., “Blindsight depends on the lateral geniculate nucleus,” Nature, vol. 466, no. 7304, pp. 373–377, 2010. View at Publisher · View at Google Scholar · View at Scopus
  152. A. S. Bock, C. D. Kroenke, E. N. Taber, and J. F. Olavarria, “Retinal input influences the size and corticocortical connectivity of visual cortex during postnatal development in the ferret,” Journal of Comparative Neurology, vol. 520, no. 5, pp. 914–932, 2012. View at Publisher · View at Google Scholar · View at Scopus
  153. A. Falchier, S. Clavagnier, P. Barone, and H. Kennedy, “Anatomical evidence of multimodal integration in primate striate cortex,” Journal of Neuroscience, vol. 22, no. 13, pp. 5749–5759, 2002. View at Google Scholar · View at Scopus
  154. E. Budinger, P. Heil, A. Hess, and H. Scheich, “Multisensory processing via early cortical stages: connections of the primary auditory cortical field with other sensory systems,” Neuroscience, vol. 143, no. 4, pp. 1065–1083, 2006. View at Publisher · View at Google Scholar · View at Scopus
  155. H. Ruth Clemo, G. K. Sharma, B. L. Allman, and M. Alex Meredith, “Auditory projections to extrastriate visual cortex: connectional basis for multisensory processing in 'unimodal' visual neurons,” Experimental Brain Research, vol. 191, no. 1, pp. 37–47, 2008. View at Publisher · View at Google Scholar · View at Scopus
  156. A. Falchier, C. E. Schroeder, T. A. Hackett et al., “Projection from visual areas V2 and prostriata to caudal auditory cortex in the monkey,” Cerebral Cortex, vol. 20, no. 7, pp. 1529–1538, 2010. View at Publisher · View at Google Scholar · View at Scopus
  157. S. Clavagnier, A. Falchier, and H. Kennedy, “Long-distance feedback projections to area V1: implications for multisensory integration, spatial awareness, and visual consciousness,” Cognitive, Affective and Behavioral Neuroscience, vol. 4, no. 2, pp. 117–126, 2004. View at Google Scholar · View at Scopus
  158. A. L. Beer, T. Plank, and M. W. Greenlee, “Diffusion tensor imaging shows white matter tracts between human auditory and visual cortex,” Experimental Brain Research, vol. 213, no. 2-3, pp. 299–308, 2011. View at Publisher · View at Google Scholar · View at Scopus
  159. J. Driver and T. Noesselt, “Multisensory interplay reveals crossmodal influences on “sensory-specific” brain regions, neural responses, and judgments,” Neuron, vol. 57, no. 1, pp. 11–23, 2008. View at Publisher · View at Google Scholar · View at Scopus
  160. J. W. Lewis and D. C. Van Essen, “Corticocortical connections of visual, sensorimotor, and multimodal processing areas in the parietal lobe of the macaque monkey,” Journal of Comparative Neurology, vol. 428, no. 1, pp. 112–137, 2000. View at Google Scholar
  161. M. S. Beauchamp, S. Pasalar, and T. Ro, “Neural substrates of reliability-weighted visual-tactile multisensory integration,” Frontiers in Systems Neuroscience, vol. 4, article 25, 2010. View at Publisher · View at Google Scholar · View at Scopus
  162. G. A. Calvert, P. C. Hansen, S. D. Iversen, and M. J. Brammer, “Detection of audio-visual integration sites in humans by application of electrophysiological criteria to the BOLD effect,” NeuroImage, vol. 14, no. 2, pp. 427–438, 2001. View at Publisher · View at Google Scholar · View at Scopus
  163. J. F. Smiley and A. Falchier, “Multisensory connections of monkey auditory cerebral cortex,” Hearing Research, vol. 258, no. 1-2, pp. 37–46, 2009. View at Publisher · View at Google Scholar · View at Scopus
  164. T. Noesselt, J. W. Rieger, M. A. Schoenfeld et al., “Audiovisual temporal correspondence modulates human multisensory superior temporal sulcus plus primary sensory cortices,” Journal of Neuroscience, vol. 27, no. 42, pp. 11431–11441, 2007. View at Publisher · View at Google Scholar · View at Scopus
  165. S. Werner and U. Noppeney, “Distinct functional contributions of primary sensory and association areas to audiovisual integration in object categorization,” Journal of Neuroscience, vol. 30, no. 7, pp. 2662–2675, 2010. View at Publisher · View at Google Scholar · View at Scopus
  166. T. Sugihara, M. D. Diltz, B. B. Averbeck, and L. M. Romanski, “Integration of auditory and visual communication information in the primate ventrolateral prefrontal cortex,” Journal of Neuroscience, vol. 26, no. 43, pp. 11138–11147, 2006. View at Publisher · View at Google Scholar · View at Scopus
  167. L. M. Romanski, “Representation and integration of auditory and visual stimuli in the primate ventral lateral prefrontal cortex,” Cerebral Cortex, vol. 17, supplement, pp. i61–69, 2007. View at Publisher · View at Google Scholar · View at Scopus
  168. K. S. Rockland and H. Ojima, “Multisensory convergence in calcarine visual areas in macaque monkey,” International Journal of Psychophysiology, vol. 50, no. 1-2, pp. 19–26, 2003. View at Publisher · View at Google Scholar · View at Scopus
  169. M. E. Laramée, T. Kurotani, K. S. Rockland, G. Bronchti, and D. Boire, “Indirect pathway between the primary auditory and visual cortices through layer V pyramidal neurons in V2L in mouse and the effects of bilateral enucleation,” European Journal of Neuroscience, vol. 34, no. 1, pp. 65–78, 2011. View at Publisher · View at Google Scholar · View at Scopus
  170. J. D. Schmahmann and D. N. Pandya, “The complex history of the fronto-occipital fasciculus,” Journal of the History of the Neurosciences, vol. 16, no. 4, pp. 362–377, 2007. View at Publisher · View at Google Scholar · View at Scopus
  171. J. D. Schmahmann, D. N. Pandya, R. Wang et al., “Association fibre pathways of the brain: parallel observations from diffusion spectrum imaging and autoradiography,” Brain, vol. 130, no. 3, pp. 630–653, 2007. View at Publisher · View at Google Scholar · View at Scopus
  172. H. E. M. Den Ouden, K. J. Friston, N. D. Daw, A. R. McIntosh, and K. E. Stephan, “A dual role for prediction error in associative learning,” Cerebral Cortex, vol. 19, no. 5, pp. 1175–1185, 2009. View at Publisher · View at Google Scholar · View at Scopus
  173. M. A. Eckert, N. V. Kamdar, C. E. Chang, C. F. Beckmann, M. D. Greicius, and V. Menon, “A cross-modal system linking primary auditory and visual cortices: evidence from intrinsic fMRI connectivity analysis,” Human Brain Mapping, vol. 29, no. 7, pp. 848–857, 2008. View at Publisher · View at Google Scholar · View at Scopus
  174. C. Klinge, F. Eippert, B. Röder, and C. Büchel, “Corticocortical connections mediate primary visual cortex responses to auditory stimulation in the blind,” Journal of Neuroscience, vol. 30, no. 38, pp. 12798–12805, 2010. View at Publisher · View at Google Scholar · View at Scopus
  175. G. F. Wittenberg, K. J. Werhahn, E. M. Wassermann, P. Herscovitch, and L. G. Cohen, “Functional connectivity between somatosensory and visual cortex in early blind humans,” European Journal of Neuroscience, vol. 20, no. 7, pp. 1923–1927, 2004. View at Publisher · View at Google Scholar · View at Scopus
  176. M. Ptito, A. Fumal, A. M. De Noordhout, J. Schoenen, A. Gjedde, and R. Kupers, “TMS of the occipital cortex induces tactile sensations in the fingers of blind Braille readers,” Experimental Brain Research, vol. 184, no. 2, pp. 193–200, 2008. View at Publisher · View at Google Scholar · View at Scopus
  177. L. A. de la Mothe, S. Blumell, Y. Kajikawa, and T. A. Hackett, “Thalamic connections of auditory cortex in marmoset monkeys: lateral belt and parabelt regions,” Anatomical Record, vol. 295, no. 5, pp. 822–836, 2012. View at Publisher · View at Google Scholar · View at Scopus
  178. M. Ptito, J.-F. Giguère, D. Boire, D. O. Frost, and C. Casanova, “When the auditory cortex turns visual,” Progress in Brain Research, vol. 134, pp. 447–458, 2001. View at Publisher · View at Google Scholar · View at Scopus
  179. M. Ptito and R. Kupers, “Cross-modal plasticity in early blindness,” Journal of Integrative Neuroscience, vol. 4, no. 4, pp. 479–488, 2005. View at Publisher · View at Google Scholar · View at Scopus
  180. E. Macaluso, C. D. Frith, and J. Driver, “Modulation of human visual cortex by crossmodal spatial attention,” Science, vol. 289, no. 5482, pp. 1206–1208, 2000. View at Publisher · View at Google Scholar · View at Scopus
  181. S. Facchini and S. M. Aglioti, “Short term light deprivation increases tactile spatial acuity in humans,” Neurology, vol. 60, no. 12, pp. 1998–1999, 2003. View at Google Scholar · View at Scopus
  182. B. Boroojerdi, K. O. Bushara, B. Corwell et al., “Enhanced excitability of the human visual cortex induced by short-term light deprivation,” Cerebral Cortex, vol. 10, no. 5, pp. 529–534, 2000. View at Google Scholar · View at Scopus
  183. L. B. Merabet, R. Hamilton, G. Schlaug et al., “Rapid and reversible recruitment of early visual cortex for touch,” PLoS ONE, vol. 3, no. 8, Article ID e3046, 2008. View at Publisher · View at Google Scholar · View at Scopus
  184. A. Pascual-Leone and R. Hamilton, “The metamodal organization of the brain,” Progress in Brain Research, vol. 134, pp. 427–445, 2001. View at Publisher · View at Google Scholar · View at Scopus
  185. J. Lewald, “More accurate sound localization induced by short-term light deprivation,” Neuropsychologia, vol. 45, no. 6, pp. 1215–1222, 2007. View at Publisher · View at Google Scholar · View at Scopus
  186. A. Amedi, N. Raz, H. Azulay, R. Malach, and E. Zohary, “Cortical activity during tactile exploration of objects in blind and sighted humans,” Restorative Neurology and Neuroscience, vol. 28, no. 2, pp. 143–156, 2010. View at Publisher · View at Google Scholar · View at Scopus
  187. J. N. Lucan, J. J. Foxe, M. Gomez-Ramirez, K. Sathian, and S. Molholm, “Tactile shape discrimination recruits human lateral occipital complex during early perceptual processing,” Human Brain Mapping, vol. 31, no. 11, pp. 1813–1821, 2010. View at Publisher · View at Google Scholar · View at Scopus
  188. A. F. Rossi, N. P. Bichot, R. Desimone, and L. G. Ungerleider, “Top-down attentional deficits in Macaques with lesions of lateral prefrontal cortex,” Journal of Neuroscience, vol. 27, no. 42, pp. 11306–11314, 2007. View at Publisher · View at Google Scholar · View at Scopus
  189. S. R. Friedman-Hill, L. C. Robertson, R. Desimone, and L. G. Ungerleider, “Posterior parietal cortex and the filtering of distractors,” Proceedings of the National Academy of Sciences of the United States of America, vol. 100, no. 7, pp. 4263–4268, 2003. View at Publisher · View at Google Scholar · View at Scopus
  190. M. Rosanova, A. Casali, V. Bellina, F. Resta, M. Mariotti, and M. Massimini, “Natural frequencies of human corticothalamic circuits,” Journal of Neuroscience, vol. 29, no. 24, pp. 7679–7685, 2009. View at Publisher · View at Google Scholar · View at Scopus
  191. K. McAlonan, J. Cavanaugh, and R. H. Wurtz, “Guarding the gateway to cortex with attention in visual thalamus,” Nature, vol. 456, no. 7220, pp. 391–394, 2008. View at Publisher · View at Google Scholar · View at Scopus
  192. I. Melzer, E. Damry, A. Landau, and R. Yagev, “The influence of an auditory-memory attention-demanding task on postural control in blind persons,” Clinical Biomechanics, vol. 26, no. 4, pp. 358–362, 2011. View at Publisher · View at Google Scholar · View at Scopus
  193. H. Burton, R. J. Sinclair, and S. Dixit, “Working memory for vibrotactile frequencies: comparison of cortical activity in blind and sighted individuals,” Human Brain Mapping, vol. 31, no. 11, pp. 1686–1701, 2010. View at Publisher · View at Google Scholar · View at Scopus
  194. A. Garg, D. Schwartz, and A. A. Stevens, “Orienting auditory spatial attention engages frontal eye fields and medial occipital cortex in congenitally blind humans,” Neuropsychologia, vol. 45, no. 10, pp. 2307–2321, 2007. View at Publisher · View at Google Scholar · View at Scopus
  195. O. Després, V. Candas, and A. Dufour, “Spatial auditory compensation in early-blind humans: involvement of eye movements and/or attention orienting?” Neuropsychologia, vol. 43, no. 13, pp. 1955–1962, 2005. View at Publisher · View at Google Scholar · View at Scopus
  196. A. H. Neuhaus, C. Urbanek, C. Opgen-Rhein et al., “Event-related potentials associated with Attention Network Test,” International Hournal of Psychophysiology, vol. 76, no. 2, pp. 72–79, 2010. View at Google Scholar
  197. A. Zani and A. M. Proverbio, “Is that a belt or a snake? Object attentional selection affects the early stages of visual sensory processing,” Behavioral and Brain Functions, vol. 8, article 6, 2012. View at Publisher · View at Google Scholar · View at Scopus
  198. M. Stokes, R. Thompson, R. Cusack, and J. Duncan, “Top-down activation of shape-specific population codes in visual cortex during mental imagery,” Journal of Neuroscience, vol. 29, no. 5, pp. 1565–1572, 2009. View at Publisher · View at Google Scholar · View at Scopus
  199. M. Stokes, A. Saraiva, G. Rohenkohl, and A. C. Nobre, “Imagery for shapes activates position-invariant representations in human visual cortex,” NeuroImage, vol. 56, no. 3, pp. 1540–1545, 2011. View at Publisher · View at Google Scholar · View at Scopus
  200. A. G. De Volder, H. Toyama, Y. Kimura et al., “Auditory triggered mental imagery of shape involves visual association areas in early blind humans,” NeuroImage, vol. 14, no. 1 I, pp. 129–139, 2001. View at Publisher · View at Google Scholar · View at Scopus
  201. S. D. Slotnick, W. L. Thompson, and S. M. Kosslyn, “Visual mental imagery induces retinotopically organized activation of early visual areas,” Cerebral Cortex, vol. 15, no. 10, pp. 1570–1583, 2005. View at Publisher · View at Google Scholar · View at Scopus
  202. A. Vanlierde, A. G. De Volder, M. Wanet-Defalque, and C. Veraart, “Occipito-parietal cortex activation during visuo-spatial imagery in early blind humans,” NeuroImage, vol. 19, no. 3, pp. 698–709, 2003. View at Publisher · View at Google Scholar · View at Scopus
  203. E. Mellet, N. Tzourio, F. Crivello, M. Joliot, M. Denis, and B. Mazoyer, “Functional anatomy of spatial mental imagery generated from verbal instructions,” Journal of Neuroscience, vol. 16, no. 20, pp. 6504–6512, 1996. View at Google Scholar · View at Scopus
  204. R. B. H. Tootell, N. Hadjikhani, E. K. Hall et al., “The retinotopy of visual spatial attention,” Neuron, vol. 21, no. 6, pp. 1409–1422, 1998. View at Publisher · View at Google Scholar · View at Scopus
  205. J. B. Hopfinger, M. H. Buonocore, and G. R. Mangun, “The neural mechanisms of top-down attentional control,” Nature Neuroscience, vol. 3, no. 3, pp. 284–291, 2000. View at Publisher · View at Google Scholar · View at Scopus
  206. H. Zhou and R. Desimone, “Feature-based attention in the frontal eye field and area V4 during visual search,” Neuron, vol. 70, no. 6, pp. 1205–1217, 2011. View at Publisher · View at Google Scholar · View at Scopus
  207. A. D. Cate, T. J. Herron, E. W. Yund et al., “Auditory attention activates peripheral visual cortex,” PLoS ONE, vol. 4, no. 2, article e4645, 2009. View at Publisher · View at Google Scholar · View at Scopus
  208. N. Kanwisher and E. Wojciulik, “Visual attention: insights from brain imaging,” Nature Reviews Neuroscience, vol. 1, no. 2, pp. 91–100, 2000. View at Google Scholar · View at Scopus
  209. C.-T. Wu, D. H. Weissman, K. C. Roberts, and M. G. Woldorff, “The neural circuitry underlying the executive control of auditory spatial attention,” Brain Research, vol. 1134, no. 1, pp. 187–198, 2007. View at Publisher · View at Google Scholar · View at Scopus
  210. D. N. Saito, K. Yoshimura, T. Kochiyama, T. Okada, M. Honda, and N. Sadato, “Cross-modal binding and activated attentional networks during audio-visual speech integration: a functional MRI study,” Cerebral Cortex, vol. 15, no. 11, pp. 1750–1760, 2005. View at Publisher · View at Google Scholar · View at Scopus
  211. A. Degerman, T. Rinne, J. Salmi, O. Salonen, and K. Alho, “Selective attention to sound location or pitch studied with fMRI,” Brain Research, vol. 1077, no. 1, pp. 123–134, 2006. View at Publisher · View at Google Scholar · View at Scopus
  212. C. E. Wakefield, J. Homewood, and A. J. Taylor, “Cognitive compensations for blindness in children: an investigation using odour naming,” Perception, vol. 33, no. 4, pp. 429–442, 2004. View at Publisher · View at Google Scholar · View at Scopus
  213. Q. Chen, M. Zhang, and X. Zhou, “Spatial and nonspatial peripheral auditory processing in congenitally blind people,” NeuroReport, vol. 17, no. 13, pp. 1449–1452, 2006. View at Publisher · View at Google Scholar · View at Scopus
  214. B. Forster, A. F. Eardley, and M. Eimer, “Altered tactile spatial attention in the early blind,” Brain Research, vol. 1131, no. 1, pp. 149–154, 2007. View at Publisher · View at Google Scholar · View at Scopus
  215. B. Röder, U. M. Krämer, and K. Lange, “Congenitally blind humans use different stimulus selection strategies in hearing: an ERP study of spatial and temporal attention,” Restorative Neurology and Neuroscience, vol. 25, no. 3-4, pp. 311–322, 2007. View at Google Scholar · View at Scopus
  216. K. E. Weaver and A. A. Stevens, “Attention and sensory interactions within the occipital cortex in the early blind: an fMRI study,” Journal of Cognitive Neuroscience, vol. 19, no. 2, pp. 315–330, 2007. View at Publisher · View at Google Scholar · View at Scopus
  217. H. Burton, “Visual cortex activity in early and late blind people,” Journal of Neuroscience, vol. 23, no. 10, pp. 4005–4011, 2003. View at Google Scholar · View at Scopus
  218. A. P. Saygin and M. I. Sereno, “Retinotopy and attention in human occipital, temporal, parietal, and frontal cortex,” Cerebral Cortex, vol. 18, no. 9, pp. 2158–2168, 2008. View at Publisher · View at Google Scholar · View at Scopus
  219. F. Moradi, G. T. Buračas, and R. B. Buxton, “Attention strongly increases oxygen metabolic response to stimulus in primary visual cortex,” NeuroImage, vol. 59, no. 1, pp. 601–607, 2012. View at Publisher · View at Google Scholar · View at Scopus
  220. J. A. Brefczynski and E. A. DeYoe, “A physiological correlate of the “spotlight” of visual attention,” Nature Neuroscience, vol. 2, no. 4, pp. 370–374, 1999. View at Publisher · View at Google Scholar · View at Scopus
  221. G. Deshpande, S. LaConte, G. A. James, S. Peltier, and X. Hu, “Multivariate granger causality analysis of fMRI data,” Human Brain Mapping, vol. 30, no. 4, pp. 1361–1373, 2009. View at Publisher · View at Google Scholar · View at Scopus
  222. S. Peltier, R. Stilla, E. Mariola, S. LaConte, X. Hu, and K. Sathian, “Activity and effective connectivity of parietal and occipital cortical regions during haptic shape perception,” Neuropsychologia, vol. 45, no. 3, pp. 476–483, 2007. View at Publisher · View at Google Scholar · View at Scopus
  223. G. Deshpande, X. Hu, S. Lacey, R. Stilla, and K. Sathian, “Object familiarity modulates effective connectivity during haptic shape perception,” NeuroImage, vol. 49, no. 3, pp. 1991–2000, 2010. View at Publisher · View at Google Scholar · View at Scopus