A PREFRONTAL ERP INVOLVED IN DECISION MAKING DURING VISUAL DURATION AND SIZE DISCRIMINATION TASKS

REFERENCES

• Basso G., Nichelli P., Wharton C. M., Peterson M., Grafman J. Distributed neural systems for temporal production: A functional MRI study. Brain Research Bulletin 2003; 59: 405–411
   PubMed Web of Science ®Google Scholar
• Bertrand O., Perrin F., Pernier J. A theoretical justification of the average reference in topographic evoked potential studies. Electroencephalography and Clinical Neurophysiology 1985; 62: 462–464
   PubMedGoogle Scholar
• Brown S. W. Attentional resources in timing: Interference effects in concurrent temporal and non-temporal working memory tasks. Perception and Psychophysics 1997; 59: 1118–1129
   PubMed Web of Science ®Google Scholar
• Casini L., Macar F. Multiples approaches to investigate the existence of an internal clock using attentional resources. Behavioural Processes 1999; 45: 73–85
   PubMed Web of Science ®Google Scholar
• Constantinidis C., Williams G. V., Goldman-Rakic P. S. A role for inhibition in shaping the temporal flow of information in prefrontal cortex. Nature Neuroscience 2002; 5: 175–180
   PubMed Web of Science ®Google Scholar
• Elbert T., Ulrich R., Rockstroh B., Lutzenberger W. The processing of temporal intervals reflected by CNV-like brain potentials. Psychophysiology 1991; 28: 648–655
   PubMed Web of Science ®Google Scholar
• Fraisse P. Perception and estimation of time. Annual Review of Psychology 1984; 35: 1–36
   PubMed Web of Science ®Google Scholar
• Gibbon J., Church R. M., Meck W. Scalar timing in memory. Annals of the New York Academy of Sciences 1984; 423: 52–77
   PubMed Web of Science ®Google Scholar
• Gruber O., Kleinschmidt A., Binkofski F., Steinmetz H., von Cramon D. Y. Cerebral correlates of working memory for temporal information. Neuroreport 2000; 11: 1689–1693
   PubMed Web of Science ®Google Scholar
• Harrington D. L., Boyd L. A., Mayer A. R., Sheltraw D. M., Lee R. R., Huang M., Rao S. M. Neural representation of interval encoding and decision making. Cognitive Brain Research 2004; 21: 193–205
   PubMedGoogle Scholar
• Harrington D. L., Haaland K. Y. Neural underpinnings of temporal processing: A review of focal lesion, pharmacological, and functional imaging research. Neuroscience 1999; 10: 91–116
   Web of Science ®Google Scholar
• Harrington D. L., Haaland K. Y., Knight R. T. Cortical networks underlying mechanisms of time perception. The Journal of Neuroscience 1998; 18: 1085–1095
   PubMed Web of Science ®Google Scholar
• Hicks R. E., Miller G. W., Kinsbourne M. Prospective and retrospective judgements of time as a function of amount of information processed. The American Journal of Psychology 1976; 89: 719–730
   PubMed Web of Science ®Google Scholar
• Kagerer F. A., Wittman M., Szelag E., von Steinbüchel N. Cortical involvement in temporal reproduction: Evidence for differential roles of the hemispheres. Neuropsychologia 2002; 40: 357–366
   PubMed Web of Science ®Google Scholar
• Krawczyk D. C. Contributions of the prefrontal cortex to the neural basis of human decision making. Neuroscience and Biobehavioral Reviews 2002; 26: 631–664
   PubMed Web of Science ®Google Scholar
• Lalonde R., Hannequin D. The neurobiological basis of time estimation and temporal order. Reviews in the Neurosciences 1999; 10: 151–173
   PubMed Web of Science ®Google Scholar
• Macar F. Temporal judgments on intervals containing stimuli of varying quantity, complexity and periodicity. Acta Psychologica 1996; 92: 297–308
   Web of Science ®Google Scholar
• Macar F., Grondin S., Casini L. Controlled attention sharing influences time estimation. Memory and Cognition 1994; 22: 673–686
   PubMed Web of Science ®Google Scholar
• Macar F., Lejeune H., Bonnet M., Ferrara A., Pouthas V., Vidal F., Maquet P. Activation of the supplementary motor area and of attentional networks during temporal processing. Experimental Brain Research 2002; 142: 475–485
   PubMed Web of Science ®Google Scholar
• Mangels J., Ivry R., Shimizu N. Dissociable contribution to the prefrontal and neocerebellar cortex to time perception. Cognitive Brain Research 1998; 7: 15–39
   PubMedGoogle Scholar
• Maquet P., Lejeune H., Pouthas V., Bonnet M., Casini L., Macar F., Timsit-Berthier M., Vidal F., Ferrara A., Degueldre C., Quaglia L., Delfiore G., Luxan A., Woods R., Mazziotta J. C., Comar D. Brain activation induced by estimation of duration: A PET study. Neuroimage 1996; 3: 119–126
   PubMed Web of Science ®Google Scholar
• Meck W. Attentional bias between modalities: Effect on the internal clock, memory and decision stages used in animal time discrimination. Annals of the New York Academy of Sciences 1984; 423: 528–541
   PubMed Web of Science ®Google Scholar
• Michon J. A. The making of the present. Attention and performance (pp. 90–111; Vol. 7), J. Requin. Lawrence Erlbaum Associates, Hillsdale, NJ 1985
   Google Scholar
• Mishkin M., Ungerleider L. G., Macko K. A. Object vision and spatial vision: Two cortical pathways. Trends in Neurosciences 1983; 6: 414–417
   Web of Science ®Google Scholar
• Nolde S. F., Johnson M. K., Ray C. The role of prefrontal cortex during tests of episodic memory. Trends in Cognitive Sciences 1998; 2(10)399–406
   PubMed Web of Science ®Google Scholar
• Oldfield R. C. The assessment of analysis of handeness: The Edinburg Inventory. Neuropsychologia 1971; 9: 97–113
   PubMed Web of Science ®Google Scholar
• Paul I., Le Dantec C., Bernard C., Lalonde R., Rebaï M. Frontal lobe event-related potentials in a visual duration discrimination task. Journal of Clinical Neurophysiology 2003; 20: 351–360
   PubMed Web of Science ®Google Scholar
• Picton T. W., Bentin S., Berg P., Donchin E., Hillyard S. A., Johnson R., Miller G. A., Ritter W., Ruchkin D. S., Rugg M. D., Taylor M. J. Guidelines for using human event-related potentials to study cognition: Recording standards and publication criteria. Psychophysiology 2000; 37: 127–152
   PubMed Web of Science ®Google Scholar
• Pouthas V., Garnero L., Ferrandez A. M., Renault B. ERPs and PET analysis of time perception: Spatial and temporal brain mapping during visual discrimination tasks. Human Brain Mapping 2000; 10: 49–60
   PubMed Web of Science ®Google Scholar
• Pouthas V., Perbal S. Time perception does not only depend on accurate clock mechanisms but also on unimpaired attention and memory processes. Acta Neurobiologiae Experimentalis 2004; 64: 367–385
   PubMed Web of Science ®Google Scholar
• Rao S. M., Mayer A. R., Harrington D. L. The evolution of brain activation during temporal processing. Nature Neuroscience 2001; 4: 317–323
   PubMed Web of Science ®Google Scholar
• Rockstroh B., Elbert T., Lutzenberger W., Birbaumer N. The effects of slow cortical potentials on response speed. Psychophysiology 1982; 19: 211–217
   PubMed Web of Science ®Google Scholar
• Rubia K., Smith A. The neural correlates of cognitive time management: A review. Acta Neurobiologiae Experimentalis 2004; 64: 329–340
   PubMed Web of Science ®Google Scholar
• Smith A., Lidzba K., Taylor E., Rubia K. A right hemispheric fronto-striatal network for temporal discrimination. Neuroimage 2003; 20: 344–350
   PubMed Web of Science ®Google Scholar
• Timsit-Berthier M., Gérono A. Manuel d’interprétation des potentiels évoqués endogènes (P300 et VCN). Sprimont, Mardaga 1998
   Google Scholar
• Van Essen D C., Maunsell J. H. R. Hierarchical organization and functional streams in the visual cortex. Trends in Neurosciences 1983; 6: 370–375
   Web of Science ®Google Scholar
• Zakay D. Subjective time and attentional resource allocation: An integrated model of time estimation. Time and human cognition: A life-span perspective, I. Levin, D. Zakay. Elsevier, Amsterdam 1989; 365–397
   Google Scholar
• Zakay D., Block R. A. Prospective and retrospective duration judgments: An executive-control perspective. Acta Neurobiologiae Experimentalis 2004; 64: 319–328
   PubMed Web of Science ®Google Scholar