Нейропсихологический анализ патологии мозолистого тела - Мария Ковязина

Sowell E. R., Mattson S. N., Thompson P. M., Jernigan T. L., Riley E. P., Toga A. W. Mapping Corpus Callosum Morphology and its Neurocognitive Correlates: The Effects of Prenatal Alcohol Exposure // Neurology. 2001. V. 57. № 2. P. 235–244.

Sperry R. W. The great cerebral commissure // Scientific American. 1964. V. 210. № 1. P. 42–52.

Sperry R. W. Brain bisection and mechanisms of consciousness // Brain and Conscious Experience / J. C. Eccles (Ed.). – Heidelberg: Springer-Verlag, 1966. P. 298–313.

Stein B. E., Price D. D., Gazzaniga M. S. Pain perception in a man with total corpus callosum transaction // Pain. 1989. V. 38. № 1. P. 51–56.

Stickles J. L., Schilmoeller G. L., Schilmoeller, K.J. A 23-year review of communication development in an individual with agenesis of the corpus callosum // International Journal of Disability, Development, and Education. 2002. V. 49. № 4. P. 367–383.

Suls J. M. A two-stage model for the appreciation of jokes and cartoons: an information processing analysis // The Psychology of Humor: Theoretical Perspectives and Empirical Issues / J. H. Goldstein, P. E. McGhee (Eds.). – N. Y. Academic Press, 1972. P. 81– 100.

Tabibnia G., Zaidel E. Alexithymia, interhemispheric transfer, and right hemispheric specialization: a critical review // Psychotherapy and Psychosomatics. 2005. V. 74. № 2. P. 81–92.

Taylor M., David A. S. Agenesis of the corpus callosum: a United Kingdom series of 56 cases // Journal of Neurology, Neurosurgery, and Psychiatry. 1998. V. 64. № 1. P. 131–134.

Temple C. M., Jeeves M. A., Vilarroya O. Reading in callosal agenesis // Brain and Language. 1990. V. 39. № 2. P. 235–253.

TenHouten W. D., Walter D. O., Hoppe K. D., Bogen J. E. Alexithymia and the split brain: V. EEG alpha-band interhemispheric coherence analysis // Psychotherapy and Psychosomatics. 1987. V. 47. № 1. P. 1–10.

Thatcher R. W., Walker R. A., Guidice S. Human cerebral hemispheres develop at different rates and ages // Science. 1987. V. 236. № 4805. P. 1110–1113.

Thompson P. M., Giedd J. N., Woods R. P., MacDonald D., Evans A. S., Toga A. W. Growth patterns in the developing brain detected by using continuum – mechanical tensor maps // Nature. 2000. V. 404. № 6774. P. 190–193.

Thut G., Halsband U., Regard M., Mayer E., Leenders K. L., Landis T. What is the role of the corpus callosum in intermanual transfer of motor skills? A study of three cases with callosal pathology // Experimental Brain Research. 1997.V. 113. № 2. P. 365–370.

Tibbo P., Nopoulos P., Arndt S., Andreasen N. Corpus callosum shape and size in male patients with schizophrenia // Biological Psychiatry. 1998. V. 44. №.6. P. 405–412.

Tovar-Moll F., Moll J., de Oliveira-Souza R, Bramati I. E., Andreiuolo P. A., Lent R. Neuroplasticity in human callosal dysgenesis: a diffusion tensor imaging study // Cerebral Cortex. 2007. V. 17. № 3. P. 531–541.

Trevarthen C. B. Two mechanisms of vision in primates // Psychologische Forschung. 1968. V. 31. № 2. P. 299–337.

Tulving E., Kapur S., Craik F.I.M., Moscovitch M., Houle S. Hemispheric encoding/retrieval asymmetry in episodic memory: Positron emission tomography findings // Proceedings of the National Academy of Sciences of the United States of America. 1994. V. 91. № 6. P. 2016–2020.

Velichkovsky B. M. Heterarchy of cognition: The depths and the highs of a framework for memory research // Memory. 2002. V. 10. № 5–6. P. 405–419.

Vergani P., Ghidini A., Strobelt N., Locatelli A., Mariani S., Bertalero C., Cavallone M. Prognostic indicators in the prenatal diagnosis of agenesis of the corpus callosum // American Journal of Obstetrics and Gynecology. 1994. V. 170. № 3. P. 753–758.

Vidal C. N., Nicolson R., DeVito T., Hayashi K. M., Drost D. J., Williamson P. C. et al. Mapping corpus callosum deficits in autism: an index of aberrant cortical connectivity // Biological Psychiatry. 2006. V. 60. № 3. P. 218–225.

Voneida T. J. Performance of a visual conditioned response in split-brain cats // Experimental Neurology. 1963. V. 8. № 6. P. 493–504.

Van Wagenen W. P., Herren R. Y. Surgical division of the commissural pathways in the corpus callosum. Relation to spread of an epileptic attack // Archives of Neurology and Psychiatry. 1940. V. 44. № 4. P. 740–759.

Walterfang M., Wood A. G., Reutens D. C., Wood S. J., Chen J., Velakoulis D., McGorry P. D., Pantelis C. Corpus callosum size and shape in first-episode affective and schizophrenia-spectrum psychosis // Psychiatry Research. 2009. V. 173. № 1. P. 77–82.

Wapner W., Hamby S., Gardner H. The role of the right hemisphere in the apprehension of complex linguistic materials // Brain and Language. 1981. Sep. 14(1). P. 15–33.

Watson R. T., Heilman K. M. Callosal apraxia // Brain. 1983 V. 106. № 2. P. 391–403.

Westerhausen R., Kreuder F., Dos Santos Sequeira S., Walter C., Woerner W., Wittling R. A., Schweiger E., Wittling W. Effects of handedness and gender on macro– and microstructure of the corpus callosum and its subregions: a combined high-resolution and diffusion-tensor MRI study // Brain Research Cognitive Brain Research. 2004. V. 21. № 3. P. 418–426.

Wilkemeyer M. F., Chen S., Menkari C. E., Brenneman D. E., Sulik K. K., Charness M. E. Differential effects of ethanol antagonism and neuroprotection in peptide fragment NAPVSIPQ prevention of ethanol-induced developmental toxicity // Proceedings of the National Academy of Sciences of the United States of America. 2003. V. 100. № 14. P. 8543–8548.

Wisniewski A. B. Sexually-dimorphic patterns of cortical asymmetry, and the role for sex steroid hormones in determining cortical patterns of lateralization // Psychoneuroendocrinology. 1998. V. 23. № 5. P. 519–547.

Wisniewski K. E., Jeret J. S. Callosal agenesis: A review of the clinical, pathological and cytogenetic features // Callosal Agenesis: A natural split brain? / M. Lassonde, M. A. Jeeves (Eds.). – N.Y.: Plenum Press, 1994. P. 1–6.

Witelson S. F. The brain connection: the corpus callosum is larger in left-handers // Science. 1985. V. 229. № 4714. P. 665–668.

Witelson S. F. Hand and sex differences in the isthmus and genu of the human corpus callosum. A postmortem morphological study // Brain. 1989. V. 112. № 3. P. 799–835.

Witelson SF. Neural sexual mosaicism: sexual differentiation of the human temporo-parietal region for functional asymmetry // Psychoneuroendocrinology. 1991. V. 16. № 1–3. P. 131–153.

Witelson S. F., Goldsmith C. H. The relationship of hand preference to anatomy of the corpus callosum in men // Brain Research. 1991. V. 545. № 1–2. P. 175–182.