Abstract
The temporal lobes are usually associated with the processing of auditory stimuli; indeed, the primary and association auditory areas are localized within the superior temporal gyms. Nevertheless, the temporal lobe also receives extensive projections from the somesthetic and visual association areas 18 and 19 (Jones & Powell, 1970; Seltzer and Pandya, 1978); receives and processes gustatory, visceral, and olfactory sensations; harbors the amygdala and hippocampus within its inferior depths; and contains a considerable number of neurons that are heavily involved in the performance of complex visual integrative activities, including visual closure and the recognition of specific meaningful forms. Indeed, it has been argued that the temporal lobe evolved from visual cortex (Diamond, 1943), and it is apparent based on a variety of neurophysiological, neuroanatomical, and behavioral studies that the middle, inferior, and posterior—superior temporal lobe are indeed cortical visual areas.
Keywords
Temporal Lobe Temporal Lobe Epilepsy Environmental Sound Left Temporal Lobe Arcuate FasciculusPreview
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References
- Abraham, A., and Mathai, K. V. (1983). The effect of right temporal lesions on matching of smells. Neuropsychologia, 21, 277–282.PubMedGoogle Scholar
- Abrams, R., and Taylor, M. A. (1980). Psychopathology and the electroencephalogram. Biological Psychiatry, 15, 871–878.PubMedGoogle Scholar
- Albert, M. L., and Bear, D. (1974). Time to understand. A case study of word deafness with reference to the role of time in auditory comprehension. Brain, 97, 383–394.Google Scholar
- Albert, M. L., Sparks, R., von Strockert, T., and Sax, D. (1972). A case of auditory agnosia. Linguistic and nonlinlguistic processing. Cortex, 8, 427–443.PubMedGoogle Scholar
- Albright, T. D., Desimone, R., and Gross, C. G. (1984). Columnar organization of directionally selective cells in visual area MT of the macaque. Journal of Neurophysiology, 51, 16–31.PubMedGoogle Scholar
- Anel, R. N., Golden, C. J., Berg, R. A., et al. (1983). Regional blood flow in schizophrenia. Archives of General Psychiatry, 40, 258–263.Google Scholar
- Auerbach, S. H., Allard, T., Naeser, M., et al. (1982). Pure word deafness. Brain, 105, 271–300.Google Scholar
- Baldwin, M., Lewis, S. A., and Bach, S. A. (1959). The effects of lysergic after cerebral ablation. Neurology (New York), 9, 469–474.Google Scholar
- Bartlet, J. E. A. (1951). A case of organized visual halluciantion in an old man with cataract, and their relation to the phenomena of the phantom limb. Brain, 84, 363–373.Google Scholar
- Bear, D. (1977). The significance of behavior change in temporal lobe epilepsy. McLean Hospital Journal, 9, 11–23.Google Scholar
- Bear, D. M. (1979). Temporal lobe epilepsy: A syndrome of sensory-limbic hyperconnexion. Cortex, 15, 357–384.PubMedGoogle Scholar
- Bear, D. M., Levin, K., Blumer, D., et al. (1982). Interictal behaviour in hospitalized temporal lobe epileptics. Journal of Neurology, Neurosurgery and psychiatry, 45, 481–488.Google Scholar
- Beaumont, J. G., and Dimond, S. J. (1973). Brain disconnection and schizophrenia. British Journal of Psychiatry, 23, 661–662.Google Scholar
- Berman, K. F., Weinberger, D. R., Shelton, R. C., and Zec, R. F. (1987). A relationship between anatomical and physiological brain pathology in schizophrenia. American Journal of Psychiatry, 144, 1277–1282.PubMedGoogle Scholar
- Berman, K. F., Zek, R. F., and Weinberger, D. R. (1986). Physiological dysfucntion of dorsolateral prefrontal cortex in schizophrenia. Archives of General Psychiatry, 43, 126–143.PubMedGoogle Scholar
- Blumstein, S., and Cooper, W. E. (1974). Hemispheric processing of intonational contours, Cortex, 10, 146158.Google Scholar
- Bogerts, B., Meertz, E., and Schonfeldt-Bausch, R. (1985). Basal ganglia and limbic system pathology in schizophrenia. Archives of General Psychiatry, 42, 784–791.PubMedGoogle Scholar
- Bradshaw, J. L., Taylor, M. J., Patterson, K., and Nettleton, N. (1980). Upright and inverted faces, and housefronts, in the two visual fields: A right and a left hemisphere contribution. Journal of Clinical Neuropsychologj’, 2, 245–257.Google Scholar
- Brodai, A. (1981). Neurological anatomy. New York: Oxford University Press.Google Scholar
- Brown, J. W. (1972). Aphasia, apraxia and agnosia. Springfield, IL: Charles Thomas.Google Scholar
- Brown, R., Colter, N., Corsellis, J. A. N., et al. (1986). Postmortem evidence of structural brain changes in schizophrenia. Archives of General Psychiatry, 43, 36–42.Google Scholar
- Bryden, M. P. (1967). A model for the sequential organization of behaviour. Canadian Journal of Psychology, 21, 36–56.Google Scholar
- Carr, S. A. (1980). Interhmispheric transfer of stereognostic information in chronic schizophrenics. British Journal of Psychiatry, 136, 53–58.PubMedGoogle Scholar
- Chapman, L. F., and Walter, R. D. (1965). Actions of lysergic acid dienthalamid on averaged human cortical evoked rsposnes to light flash. Recent Advances in Biological Psychiatry, 7, 23–36.Google Scholar
- Chapman, L. F., Walter, R. D., Ross, W. (1963). Altered electrical activity of human hippocampus and amygdala induced by LSD-25. Physiologist, 5, 118.Google Scholar
- Chase, R. A. (1967). Discussion. In F. L. Darley (Ed.), Brain mechanisms underlying speech and language (pp. 136–139 ). New York: Grune and Stratton.Google Scholar
- Chaika, E. (1982). A unified explanation for the diverse structural deviations reported for adult schizophrenics with disrupted speech. Journal of Communication Disorders, 15, 167–189.PubMedGoogle Scholar
- Chen, R., and Forster, F. M. (1973). Cursive and gelastic epilepsy. Neurology (New York), 23, 1019–1029.Google Scholar
- Chow, K. L. (1950). A retrograde cell degeneration study of the cortical projection field of the pulvinar of the monkey. Journal of Comparative Neurology, 93, 313–340.PubMedGoogle Scholar
- Corkin, S. (1965). Tactually guided maze learning in man. Neuropsychologia, 3, 339–352.Google Scholar
- Critchley, M. (1939). Neurological aspect of visual and auditory hallucinations. British Medical Journal, 33, 634–639.Google Scholar
- Cutting, J. E. (1974). Two left hemisphere mechanisms in speech perception. Perception and Psychophysics, 16, 601–612.Google Scholar
- Damasio, A. R., and Damsio, H. (1983). Localization of lesions in achromatopsia and prosopagnosia. In A. Kertesz (Ed.), Localization in neuropsychology (pp. 182–197 ). Orlando, FL: Academic Press.Google Scholar
- Delaney, R. C., Rosen, A. J., Mattson, R. H., and Novelly, R. A. (1980). Memory function in focal epilepsy: A comparison of non-surgical unilateral temporal lobe and frontal lobe samples. Cortex, 16, 103–117.PubMedGoogle Scholar
- DeRenzi, E. (1982). Disorder of space exploration and cognition. Chichester: John Wiley and Sons.Google Scholar
- DeRenzi, E. (1986). Prosopagnosia in two patients with CT-scan evidence of damage confined to the right hemisphere. Neuropsychologia, 24, 385–389.Google Scholar
- DeRenzi, E., Faglioni, P., and Spinnler, H. (1968). The performance of patients with unilateral brain damage on face recognition tasks. Cortex, 4, 17–34.Google Scholar
- DeRenzi, E., and Spinnler, H. (1966). Facial recognition in brain-damaged patients. An experimental approach. Neurology (New York), 16, 145–152.Google Scholar
- Desimone, R., and Gross, C. G. (1979). Visual areas in the temporal cortex of the macaque. Brain Research, 178, 363–380.PubMedGoogle Scholar
- Desimone, R., and Schein, S. J. (1987). Visual properties iof neruons in area V4 of the Macaque: Sensitivity to stimulus form. Journal of Neurophysiology, 57, 835–867.PubMedGoogle Scholar
- Dewson, J. H., Pribram, K., and Lynch, J. C. (1969). Effects of ablations of temporal cortex upon speech sound discrimination in the monkey. Experimental Neurology, 24, 579–591.PubMedGoogle Scholar
- Diamond, I. T. (1973). The evolution of the tectal-pulvinar system in mammals: Structural and behavioural studies of the visual system. Symposium of the Zoological Society of London, 33, 205–233.Google Scholar
- Earnest, M. P., Monroe, P. A., and Yarnell, P. R. (1977). Cortical deafness. Neurology (New York), 27, 1172–1175.Google Scholar
- Faber, R., Abrams, R., Taylor, M., Kasprisin, A., Morris, C., and Weisz, R. (1983). Comparison of schizophrenic patients with formal thought disorder and neurologically impaired patients with aphasia. American Journal of Psychiatry, 140, 1348–1351.PubMedGoogle Scholar
- Felleman, D. J., and Kaas, J. H. (1974). Receptive field properties of neruons in middle temporal visual area (MT) of owl monkeys. Journal of Neurophysiology, 52, 488–513.Google Scholar
- Flor-Henry, P. (1969). Psychosis and temporal lobe epilepsy. Epilepsia, 10, 363–395.PubMedGoogle Scholar
- Flor-Henry, P. (1983). Cerebral basis of psychopathology. Boston: John Wright.Google Scholar
- Flournoy, H. (1923). Hallucinations. Encephale, 2, 566–572.Google Scholar
- Foulkes, W. D. (1962). Dream reports from different stages of sleep. Journal of Abnormal and Social Psychology, 65, 14–25.PubMedGoogle Scholar
- Freedman, S. J. (1961). Perceptual changes in sensory deprivation. Journal of Nervous and Mental Disease, 132, 17–21.PubMedGoogle Scholar
- Fried, I., Mateer, C., Ojemann, G., Wohns, R., and Fedio, P. (1982). Organization of visuospatial functions in human cortex. Brain, 105, 349–371.PubMedGoogle Scholar
- Geffen, G., and Bradshaw, J. L., and Wallace, G. (1971). Interhemispheric effects on reaction time to verbal and nonverbal visual stimuli. Journal of Experimental Psychology, 87, 415–422.PubMedGoogle Scholar
- Geschwind, N., and Levitsky, W. (1968). Human brain: Left-right asymmetries in temporal speech regions. Science, 161, 186–187.PubMedGoogle Scholar
- Gibbs, A. F. (1951). Ictal and non-ictal psychiatric disorders in temporal lobe epilepsy. Journal of Nervous and Mental Disease, 113, 522–528.PubMedGoogle Scholar
- Gloor, P. (1972). Temporal lobe epilepsy. In B. E. Elftheriou (Ed.), The neurobiology of the amygdala (pp. 212–275 ). New York: Plenum.Google Scholar
- Gloor, P., Olivier, A., Quesney, L. F., et al: (1982). The role of the limbic system in experimental phenomena of temporal lobe epilepsy. Annals of Neurology, 12, 129–144.PubMedGoogle Scholar
- Goldstein, L., Stoltzfus, N. W., and Gardocki, J. F. (1972). Changes in interhemispheric amplitude relationships in the EEG during sleep. Physiology and Behavior, 8, 811–815.PubMedGoogle Scholar
- Goodenough, D. R., Shapiro, A., Holden, M., and Steinschriber, R. (1959). Comparison of “dreamers” and “non-dreamers”. Journal of Nervous and Mental Disease, 59, 295–302.Google Scholar
- Gorelick, P. B., and Ross, E. D. (1987). Journal of Neurology, Neurosurgery and Psychiatry, 37, 727–737.Google Scholar
- Green, G. L., and Lessel, S. (1977). Acquired cerebral dyschromatopsia. Archives of Ophthamology, 95, 12 1128.Google Scholar
- Gross, C. G., and Mishkin, M. (1977). The neural basis of stimulus equivalence across retinal translation. In S. Hamad, et al. (Eds.), Lateralization in the nervous system. New York: Academic Press.Google Scholar
- Gross, C. G., Rocha-Miranda, C. E., and Bender, D. B. (1972). Visual properties of neurons in inferotemporal cortex of the macaque. Journal of Neurophysiology, 35, 96–111.PubMedGoogle Scholar
- Halgren, E., Babb, T. L., and Crandall, P. H. (1978). Activity of human hippocampal formation and amygdala neurons during memory tests. Electroencephalography and Clinical Neurophysiology, 45, 585–601.PubMedGoogle Scholar
- Heath, R. (1954). Studies in schizophrenia. Cambridge, MA: Harvard University Press.Google Scholar
- Heath, R. (1964). Pleasure response of human subjects to direct stimulation of the brain. In R. G. Heath (Ed.), The role of pleasure in behavior (pp. 121–170 ). New York: Harper and Row.Google Scholar
- Hecaen, H., and Albert, M. L. (1978). Human neuropsychology. New York, John Wiley and Sons.Google Scholar
- Hecaen, H., and Angelergues, R. (1962). Agnosia for faces (prospagnosia). Archives of Neurology, 7, 92–100.PubMedGoogle Scholar
- Hermann, B. P., and Chambria, S. (1980). Interictal psychopathology in patients with ictal fear. Archives of Neurology, 37, 667–668.PubMedGoogle Scholar
- Hillbom, E. (1951). Schizophrenia-like psychoses after brain trauma. Acta Psychiatrica, 60, 36–47.Google Scholar
- Hillbom, E. (1960). After-effects of brain injuries. Acta Psychiatrica Scandinavica (Suppl.) 142, 1–183.Google Scholar
- Hodoba, D. (1986). Paradoxic sleep facilitation by interictal epileptic activity of right temporal origin. Biological Psychiatry, 21, 1267–1278.PubMedGoogle Scholar
- Hoffman, R. E. (1986). Verbal hallucinations and language production processes in schizophrenia. Behavioral and Brain Sciences, 9, 503–548.Google Scholar
- Hoffman, R., Stopek, S., and Andreasen, N. (1986). A discourse analysis comparing manic versus schizophrenic speech disorganization. Archives of General Psychiatry, 43, 831–838.PubMedGoogle Scholar
- Horowitz, M. J., Adams, J. E., and Rutkin, B. B. (1968). Visual imagery on brain stimulation. Archives of General Psychiatry, 19, 469–486.PubMedGoogle Scholar
- Hubel, D. H., Calvin, O. H., Rupert, A., and Galambos, R. (1959). Attention units in the auditory cortex. Science, 129, 1279–1280.PubMedGoogle Scholar
- Ingvar, D. H., and Franzen, G. (1974). Abnormalities of cerebral blood flow distribution in patients with chronic schizophrenia. Acta Psychiatrica Scandinavica, 50, 425–462.PubMedGoogle Scholar
- Jensen, I., and Larsen, J. K. (1979). Psychoses in drug-resistant temporal lobe epilepsy. Journal of Neurology, Neurosurgery and Psychiatry, 42, 948–954.Google Scholar
- Jones, E. G., and Powell, T. P. S. (1970). An antomical study of converging sensory pathways within the cerebral cortex of the monkey. Brain, 93, 793–820.PubMedGoogle Scholar
- Joseph, R. (1982). The neuropsychology of development: Limbic language, hemispheric laterality, and the origin of thought. Journal of Clinical Psychology, 38, 4–33.PubMedGoogle Scholar
- Joseph, R. (1986). Reversal of cerebral dominance for language and emotion in a corpus callostomy patient. Journal of Neurology, Neurosurgery and Psychiatry, 49, 628–634.Google Scholar
- Joseph, R. (1988). The right cerebral hemisphere. Journal of Clinical Psychology, 44, 630–673.PubMedGoogle Scholar
- Joseph, R. (1989). The limbic system. Emotion, laterality, unconscious mind. Psychoanalytic Review Google Scholar
- Kimura, D. (1961). Cerebral dominance and the perception of verbal stimuli. Canadian Journal of Psychology, 15, 156–171.PubMedGoogle Scholar
- Kimura, D. (1963). Right temporal lobe damage: Perception of unfamiliar stimuli after damage. Archives of Neurology, 18, 264–271.Google Scholar
- Kimura, D., and Folb, S. (1968). Neural processing of backward speech sounds. Science, 161, 395–396.PubMedGoogle Scholar
- Kuypers, H. G. J. M., Szwarcbart, M. K., Mishkin, M., and Rosvold, H. E. (1965). Occipitotemporal corticocortical connections in the Rhesus monkey. Experimental Neurology, 11, 245–262.PubMedGoogle Scholar
- Landis, T., Cummings, J. L., Christen, L., Bogen, J. E., and Imhof, H-G (1986). Are unilateral right posterior cerebral lesions sufficient to cause prosopagnosia? Clinical and radiological findings in six additional patients. Cortex, 22, 243–252.PubMedGoogle Scholar
- Lansdell, H. (1968). Extent of temporal lobe albations on two lateralized deficits. Physiology and Behavior, 3, 271–273.Google Scholar
- Lansdell, H. (1970). Relation of extent of temporal removal to closure and visuomotor factors. Perceptual and Motor Skills, 31, 491–498.PubMedGoogle Scholar
- Levine, D. N. (1978). Prosopagnosia and visual object agnosia: A behavioral study. Brain and Language, 5, 341–365.PubMedGoogle Scholar
- Levy, J. (1974). Psychological implications of bilateral asymmetry. In S. Diamond and J. G. Beaumont (Eds.), Hemisphere function in the human brain (pp. 127–183 ). London: Paul Elek.Google Scholar
- Levy, J., Trevarthen, C., and Sperry, R. W. (1972). Perception of bilateral chimeric figures following hemispheric deconnection. Brain, 95, 61–78.PubMedGoogle Scholar
- Ley, R. G., and Bryden, M. P. (1979). Hemispheric differences in processing emotions and faces. Brain and Language, 7, 127–138.PubMedGoogle Scholar
- Lilly, J. C. (1956). Mental effects of reduction of ordinary levels of physical stimuli on intact, healthy persons. Psychiatric Research Reports, 5, 1–9.PubMedGoogle Scholar
- Lilly, J. C. (1972). The center of the cyclone. New York: Julian Press.Google Scholar
- Lindsley, D. (1961). Common factors in sensory deprivation. In P. Solomon (Ed.), Sensory deprivation (pp. 27–52 ). Cambridge, MA: Harvard University Press.Google Scholar
- Luria, A. (1973). The working brain. New York: Basic Books.Google Scholar
- Luria, A. (1980). Higher cortical functions in man. New York: Basic Books.Google Scholar
- Malh, G. F., Rothenberg, A., Delgado, J. M. R., and Hamlin, H. (1964). Psychological resposne in the human to intracerebral electrical stimulation. Psychosomatic Medicine, 26, 337–368.Google Scholar
- Marzi, I. A., and Berlucchi, G. (1977). Right visual field superiority for accuracy of recognition of famous faces in normals. Neuropsychologia, 15, 751–756.PubMedGoogle Scholar
- Matthews, W. S., Barbas, G., and Ferrari, M. (1982). Emotional concomitants of childhood epilepsy. Epilepsia, 23, 671–681.PubMedGoogle Scholar
- Maunsell, J. H. R., and Van Essen, D. C. (1983). Functional properties of neurons in middle temporal visual area of the macaque. Journal of Neurophysiology, 49, 1127–1165.PubMedGoogle Scholar
- Meadows, J. C. (1974). The anatomical basis of prosopagnosia. Journal of Neurology, Neurosurgery and Psychiatry, 37, 489–501.Google Scholar
- Mendez, M. F., and Geehand, G. R. (1988). Journal of Neurology, Neurosurgery and Psychiatry, 51, 1–9.Google Scholar
- Merzenich, M. M., and Brugge, J. F. (1973). Representation of the cochlear partition of the superior temporal plan of teh macaque monkey. Brain Research, 50, 275–296.PubMedGoogle Scholar
- Meyer, J. S., Ishikawa, Y., Hata, T., and Karacan, I. (1987). Cerebral blood flow in normal and abnormal sleep and dreaming. Brain and Cognition, 6, 266–294.PubMedGoogle Scholar
- Meyer, V., and Yates, A. (1955). Intellectual changes following temporal lobecotomy for pschomotor epilepsy. Journal of Neurology, Neurosurgery and Psychiatry, 18, 44–52.Google Scholar
- Mills, L., and Rollman, G. B. (1980). Hemispheric asymmetry for auditory perception of temporal order. Neuropsychologia, 18, 41–47.PubMedGoogle Scholar
- Milner, B. (1958). Psychological defects produced by temporal lobe excisions. Research Publication of the Association for Research in Nervous and Mental Disease, 36, 244–257.Google Scholar
- Milner, B. (1962). Laterality effect in audition. In V. Mountcastle (Ed.), Interhemispheric relations and cerebral dominance (pp. 44–82 ). Baltimore: John Hopkins University Press.Google Scholar
- Milner, B. (1968). Visual recognition and recall after right temporal lobe excision in man. Neuropsychologia, 6, 191–209.Google Scholar
- Milner, B. (1974). Hemispheric specialization: Scope and limits. In F. E. Schmitt and F. G. Worden (Eds.), The neurosciences. Third study program (pp. 215–231 ). Cambridge, MA: MIT Press.Google Scholar
- Milner, B., and Teuber, H. L. (1968). Alteration of perception and memory in man. In L. Weiskrantz (Ed.), Analysis of behavioral changes (pp. 107–130 ). New York: Harper and Row.Google Scholar
- Mishkin, M. (1972). Cortical visual areas and their interaction. In A. G. Karczman and J. C. Eccles (Eds.), Brain and human behavior (pp. 57–93 ). Berlin: Springer-Verlag.Google Scholar
- Mishkin, M. (1978). Memory in monkeys severely impaired by combined but not by separate removal of amygdala and hippocampus. Nature (London) 273, 297–299.Google Scholar
- Morihisa, A., Duffy, F. H., and Wyatt, R. J. (1983). Brain electrical activity mapping (BEAM) in schizophrenic patients. Archives of General Psychiatry, 40, 719–728.PubMedGoogle Scholar
- Monroe, B., Rechtschaffen, A., Foulkes, D., and Jensen, J. (1965). Discriminability of REM and NREM reports. Personality and Social Psychology, 2, 456–460.Google Scholar
- Morstyn, R., Duffy, F. H., and McCarley, R. (1983). Altered topography of EEG spectral content in schizophrenia. Electroenecephalograpy and Clinical Neurophysiology, 56, 263–271.Google Scholar
- Mullan, S., and Penfield, W. (1959). Epilepsy and visual hallucinations. Archives of Neurology and Psychiatry, 81, 269–281.PubMedGoogle Scholar
- Myers, R. E. (1959). Interhemispheric communication through the corpus callosum: Limitations under conditions of conflict. Journal of Comparative and Physiological Psychology, 52, 6–9.PubMedGoogle Scholar
- Novelly, R. J., and Joseph, R. (1983). Complex partial epilepsy of early development: Gender specific effects on IQ with right hemisphere speech, In 15th Annual Epilepsy International Symposium, September (p. 53 ).Google Scholar
- Offen, M. L., Davidoff, R. A. Troost, B. T., and Richey, E. T. (1976). Dacrystic epilepsy. Journal of Neurology, Neurosurgery and Psychiatry, 39, 829–834.Google Scholar
- Ojemann, G. A., Blick, K. I., and Ward, A. A. (1971). Improvement and disturbance of short-term verbal memory with human ventrolateral stimulation. Brain, 94, 225–240.PubMedGoogle Scholar
- Ojemann, G. A. Fedio, P., and van Buren, J. (1968). Anomia from pulvinar and subcortical parietal stimulation. Brain, 91, 99–116.PubMedGoogle Scholar
- Ojemann, G. A., and Fedio, P. (1968). Effect of stimulation of the human thalamus, parietal, and temporal white matter on short-term memory. Journal of Neurosurgery, 29, 51–59.PubMedGoogle Scholar
- Pandya, D. N., and Kuypers, H. G. J. M. (1969). Corticocortical connections in the rhesus monkey. Brain Research, 13, 13–36.PubMedGoogle Scholar
- Papcun, G., Krashen, S., Terbeek, D. (1974). Is the left hemisphere specialized for speech, language and/or something else. Journal of the Acoustical Society of America, 55, 319–327.PubMedGoogle Scholar
- Penfield, W., and Evans, J. (1934). Functional defects produced by cerebral lobectomies. Publication of the Association for Research in Nervous and Mental Disease, 13, 352–377.Google Scholar
- Penfield, W., and Jasper, H. (1954). Epilepsy and the functional anatomy of the human brain. Boston: Little, Brown.Google Scholar
- Penfield, W., and Perot, P. (1963). The brain’s record of auditory and visual experience. Brain, 86, 595–696.PubMedGoogle Scholar
- Penfield, W., and Rasmussen, T. (1950). The cerebral cortex of man: A clinical study of localization of function. New York: Macmillan.Google Scholar
- Perez, M. M., and Trimble, M. R. (1980). Epileptic psychosis-Diagnostic comparison with process schizophrenia. British Journal of Psychiatry, 137, 245–249.PubMedGoogle Scholar
- Pesme, P. (1939). Auditory hallucinations in a deaf person. Review of Neuropathology and Ophthamalogy, 17, 280–291.Google Scholar
- Redlich, F. C., and Dorsey, J. E. (1945). Denial of blindness by patients with cerebral disease. Archives of Neurology and Psychiatry, 53, 407–417.Google Scholar
- Reinhold, M. (1950). A case of pure auditory agnosia. Brain, 73, 203–223.PubMedGoogle Scholar
- Rhein, J. H. W. (1913). Hallucinations of hearing and diseases of the ear. New York Medical Journal, 97, 1236–1238.Google Scholar
- Richmond, B. J., Optican, L. M., Podel, M., and Spitzer, H. (1987). Temporal encoding of two-dimensional patterns by single units in primate inferior temporal cortex. Journal of Neurophysiology, 57, 132–162.PubMedGoogle Scholar
- Richmond, B. J., Wurtz, R. H., and Sato, T. (1983). Visual responses of inferior temporal neurons in awake rhesus monkey. Journal of Neurophysiology, 50, 1415–1432.PubMedGoogle Scholar
- Rocha-Miranda, C. E. Bender, D. B., Gross, C. G., and Mishkin, M. (1975). Visual activation of neruons in the inferior-temporal cortex depends on striate cortex and forebrain commissures. Journal of Neurophysiology, 38, 475–491.Google Scholar
- Ross, E. (1981). The aprosodias: Functional-anatomic organization of the affective components of language in the right hemisphere. Archives of Neurology, 38, 561–589.PubMedGoogle Scholar
- Ross, E. D., Jossman, P. B., Bell, B. et al. (1975). Musical halucinations in deafness. Journal of the American Medical Association, 231, 620–622.PubMedGoogle Scholar
- Rozanski, J., and Rosen, H. (1952). Musical hallucinosis in otosclerosis. Cinfina Neurologica, 12, 49–54.Google Scholar
- Rutter, D. (1979). The reconstruction of schizophrenic speech. British Journal of Psychiatry, 134, 356–359.PubMedGoogle Scholar
- Sanchez-Longo, L. P., and Forster, F. M. (1958). Clinical significance of impairment of sound localization. Neurology (New York), 8, 119–125.Google Scholar
- Schiff, H. B., Sabin, T. D., Geller, A., et al. (1982). Lithium in aggressive behaivor. American Journal of Psychiatry, 139, 1346–1348.Google Scholar
- Seltzer, B., and Pandya, D. N. (1978). Afferent cortical connections and architectonics of the superior temproal sulcus and surrounding cortex in the rhesus monkey. Brain Research, 149, 1–24.PubMedGoogle Scholar
- Semrad, E. V. (1938). Study of the auditory apparatus in patients experiencing auditory hallucinations. American Journal of Psychiatry, 95, 53–63.Google Scholar
- Serafetinides, E. A. (1965). The significance of the temporal lobes and of hemisphere dominance in the production of the LSD-25 symptomology in man. Neuropsychologia, 3, 69–79.Google Scholar
- Sethi, P. K., and Rao, S. T. (1976). Gelastic, quiritarian, and cursive epilepsy. Journal of Neurology, Neurosurgery and Psychiatry, 39, 823–828.Google Scholar
- Shankweiler, D. (1961). Performance of brain-damaged patients on two tests of sound localization. Journal of Comparative and Physiological Psychology, 54, 375–381.Google Scholar
- Shankweiler, D. (1966). Effects of temporal lobe damage on the perception of dichotically prsented melodies. Journal of Comparative and Physiological Psychology, 62, 115–122.PubMedGoogle Scholar
- Shankweiler, D., and Studdert-Kennedy, M. (1966). Lateral differences in perception of dichotically presented synthetic consonant-vowel syllables and steady-state vowels. Journal of the Acoustic Society of America, 39, 1256A.Google Scholar
- Shankweiler, D., and Studdert-Kennedy, M. (1967). Identification of consonants and vowels presented to left and right ears. Quarterly Journal of Experimental Psychology, 19, 59–63.PubMedGoogle Scholar
- Sherwin, I. (1977). Clinical and EEG aspects of temporal lobe epilepsy with behavior disorder. McLean Hospital Journal, 12, 40–50.Google Scholar
- Sherwin, I. (1981). Psychosis associated with epilepsy. Journal of Neurology, Neurosurgery and Psychiatry, 44, 83–85.Google Scholar
- Sherwin, I., Peron-Magnana, P., Bancard, J. (1982). Prevalence of psychosis in epilepsy as a function of the laterality of the epileptogenic lesion. Archives of Neurology, 39, 621–625.PubMedGoogle Scholar
- Shurley, J. (1960). Profound experimental sensory isolation. American Journal of Psychiatry, 117, 539–545.Google Scholar
- Squire, L. (1987). Memory and brain. New York: Oxford University Press.Google Scholar
- Stevens, J. R., Bigelow, L., Denney, D. (1979). TeleMetered EEG in schizophrenia. Journal of Neurology, Neurosurgery and Psychiatry, 36, 251–262.Google Scholar
- Strauss, E., Risser, A., and Jones, M. W. (1982). Fear responses in patients with epilepsy. Archives of Neurology, 39, 626–630.PubMedGoogle Scholar
- Studdert-Kennedy, M., and Shankweiler, D. (1970). Hemispheric specialization for speech perception. Journal of the Acoustical Society of America, 48, 579–594.PubMedGoogle Scholar
- Swerdlow, N. R., and Koob, G. F. (1987). Dopamine, schizophrenia, mania, and depression. Behavioral and Brain Sciences, 10, 197–245.Google Scholar
- Tarachow, S. (1941). The clinical value of hallucinations in localizing brain tumors. American Journal of Psychiatry, 99, 1434–1442.Google Scholar
- Taylor, D. C. (1969). Aggression and epilepsy. Journal of Psychosomatic Research, 13, 229–236.PubMedGoogle Scholar
- Taylor, D. C. (1972). Mental state and temporal lobe epilepsy. Epilepsia, 13, 727–765.PubMedGoogle Scholar
- Taylor, D. C. (1975). Factors influencing the occurrence of schizophrenia-like psychosis in patients with temporal lobe epilepsy. Psychological Medicine, 5, 429–254.Google Scholar
- Tigges, J., Tigges, M., Anschell, S. (1981). Areal and laminar distribution of neurons interconnecting the central visual cortical areas, 17, 18, 19 and MT. Journal of Comparative Neurology, 202, 539–560.PubMedGoogle Scholar
- Wada, J., Clarke, R., and Hamm, A. (1975). Cerebral hemispheric asymmetry in humans. Cortical speech zones in 100 adults and 100 infant brains. Archives of Neurology, 32, 239–246.PubMedGoogle Scholar
- Wall, J. T., Symonds, L. L., and Kaas, J. H. (1982). Cortical and subcortical projections of the middle temporal area (MT) and adjacent cortex in galagos. Journal of Comparative Neurology, 211, 193–214.PubMedGoogle Scholar
- Weil, A. A. (1956). Ictal depression and anxiety in temporal lobe disorders. American Journal of Psychiatry, 113, 149–157.PubMedGoogle Scholar
- Weinberger, D. R., Berman, K. F., and Zek, R. F. (1986). Physiological dysfunction of dorsolateral prefrontal cortex in schizophrenia. Archives of General Psychiatry, 114, 114–125.Google Scholar
- Weingartner, H. (1968). Verbal learning in patients with temporal lobe lesions. Journal of Verbal Learning and Verbal Behavior, 7, 520–526.Google Scholar
- Weiskrantz, L., and Mishkin, M. (1958). Effect of temporal and frontal cortical lesions on auditory functions in monkey. Brain, 81, 233–275.Google Scholar
- Whiteley A. M., and Warrington, E K. (1977). Prosopagnosia: A clinical, psychological and anatomical study of three patients. Journal of Neurology, Neurosurgery and Psychiatry, 40, 395–403.Google Scholar
- Williams, D. (1956). The structure of emotions reflected in epileptic experience. Brain, 79, 29–67.PubMedGoogle Scholar
- Wollberg, Z., and Newman, V. D. (1972). Auditory cortex of squirrel monkey. Science, 175, 212–214.PubMedGoogle Scholar
- Woolsey, C. N., and Fairman, D. (1946). Contralteral, ipsilateral, and bilateral representation of cutaneous receptors in somatic areas I and II of the cerebral cortex. Surgery, 19, 684–702.PubMedGoogle Scholar
- Wolpert E. A., and Trosman, H. (1958). Studies in psychophysiology of dreams. I. Experimental evocation of sequential dream episodes. Archives of Neurology, 79, 603–606.Google Scholar
- Zeki, S. M. (1978b). The cortical projections of fovea] striate cortex in the rhesus monkey. Journal of Physiology, 277, 227–244.PubMedGoogle Scholar
- Zuckerman, M., and Cohen, N. (1964). Sources of reports of visual and auditory sensations in perceptual-isolation experiments. Psychological Bulletin, 62, 1034–1956.Google Scholar