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Artykuły w czasopismach na temat "Evoked potentials, Visual"

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Celesia, G. G. "Evoked visual potentials". Cleveland Clinic Journal of Medicine 52, nr 2 (1.06.1985): 221–22. http://dx.doi.org/10.3949/ccjm.52.2.221.

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Nehamkin, Sheryl, Michael Windom i Tanvir U. Syed. "Visual Evoked Potentials". American Journal of Electroneurodiagnostic Technology 48, nr 4 (grudzień 2008): 233–48. http://dx.doi.org/10.1080/1086508x.2008.11079688.

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Aminoff, Michael J., i Douglas S. Goodin. "Visual Evoked Potentials". Journal of Clinical Neurophysiology 11, nr 5 (wrzesień 1994): 493–99. http://dx.doi.org/10.1097/00004691-199409000-00004.

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Rönnberg, Jerker, Stig Arlinger, Björn Lyxell i Catharina Kinnefors. "Visual Evoked Potentials". Journal of Speech, Language, and Hearing Research 32, nr 4 (grudzień 1989): 725–35. http://dx.doi.org/10.1044/jshr.3204.725.

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This study investigated the putative relationship between visual evoked potentials (VEPs) and specific aspects of speechreading. The nature and constraints of the relationship between VEPs and cognitive functioning was also examined. The original finding of Shepherd, DeLavergne, Frueh, and Clobridge (1977) that visual-neural speed (VN 130) predicts speechreading skill was not replicated. However, the picture is rather complex in that we find significant correlations for some context-free word discrimination and sign-alphabet testing conditions. These correlations occur only for the VN 130/P 200 peak-to-peak amplitude measure, not for neural speed. Nevertheless, visual-neural speed (VN 130 and P 200) was relevant to certain aspects of long-term memory access (i.e., letter matching, Posner & Mitchell, 1967) and to complex short-term memory function (i.e., reading span, Baddeley, Logie, Nimmo-Smith, & Brereton, 1985).
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Anschel, David J. "Intraoperative Visual Evoked Potentials". Journal of Clinical Neurophysiology 35, nr 4 (lipiec 2018): 355. http://dx.doi.org/10.1097/wnp.0000000000000477.

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Millichap, J. Gordon. "Visual Evoked Potentials in Phenylketonuria". Pediatric Neurology Briefs 9, nr 10 (1.10.1995): 75. http://dx.doi.org/10.15844/pedneurbriefs-9-10-4.

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Miltner, Wolfgang, Wolfgang Larbig i Christoph Braun. "Biofeedback of Visual Evoked Potentials". International Journal of Neuroscience 29, nr 3-4 (styczeń 1986): 291–303. http://dx.doi.org/10.3109/00207458608986158.

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Krashenyi, I. E., i A. A. Popov. "Modeling of visual evoked potentials". Electronics and Communications 18, nr 1 (15.05.2013): 45–52. http://dx.doi.org/10.20535/2312-1807.2013.18.1.187030.

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Yilmaz, Hikmet, Esin F. Erkin, Hatice Mavioglu i Ümit Sungurtekin. "Visual evoked potentials in pregnancy". Neuro-Ophthalmology 21, nr 4 (styczeń 1999): 205–10. http://dx.doi.org/10.1076/noph.21.4.205.3891.

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Rosenberg, Michael L., i Bahman Jabbari. "Nystagmus and visual evoked potentials". Neuro-Ophthalmology 7, nr 3 (styczeń 1987): 133–38. http://dx.doi.org/10.3109/01658108709007442.

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Rozprawy doktorskie na temat "Evoked potentials, Visual"

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Bergkvist, Linn. "Visual Evoked Potentials : Referensvärden och könsskillnader". Thesis, Umeå universitet, Biomedicinsk laboratorievetenskap, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-171567.

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O’Toole, Dennis Michael. "Removal of ocular artifact from visual evoked response recordings". Thesis, University of British Columbia, 1985. http://hdl.handle.net/2429/25502.

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Potentials generated by the eye cause unwanted artifact in Visual Evoked Response (VER) recordings. These artifacts often contaminate the data in a systematic way that can lead to spurious experimental results. Although it is widely agreed that ocular artifact must be accounted for, the methods used to deal with this problem are varied. The present study compared four methods used to control ocular artifact; blink rejection, eyes closed, subtraction and regression. Twenty normal, female subjects were tested twice within the same session. Subjects watched light flashes of 4 intensities; 2, 30, 80, and 240 ft lamberts. The lights were presented at 1 hertz, reached maximum brightness in 0.5 msec and lasted for 0.5 sec. During testing the VER, and electroocculographic (EOG) response generated by a blink, were recorded. In the blink rejection method, any VER epoch that contained blink artifact was excluded from the average. The eyes closed method consisted of having subjects watch the stimuli through closed eyelids. The subtraction method corrects blink artifact by digitally subtracting the averaged EOG from the EEG. The proportion of EOG subtracted was determined by the EEG/EOG ratio estimated while subjects blinked spontaneously in a darkened environment. The regression method determines what proportion of EOG is to be subtracted on the basis of the correlation between EOG and EEG within VER epochs. Two correction, factors are calculated, one to correct for vertical movements and one to correct for horizontal movements. The blink rejection method was found to be useful with subjects who had 40% or more blink-free epochs, but was an unreliable method for the majority of subjects. The eyes closed method was also found to produce poor VER data. The eyelids appear to attenuate the light reaching the retina and there may be eyeball movement despite having the eyes closed. Both the subtraction and regression methods substantially reduced the ocular artifact. Horizontal eye movements do not appear to be a significant problem over the short intervals of VER recording because the regression method was not superior to the subtraction method in removing artifact. Although the subtraction and regression methods effectively reduce ocular artifact, both are less effective at posterior electrode placements. The reason for this may be that ocular potential is not propagated across the scalp in a linear fashion, as often assumed. Using spontaneously generated blinks in a darkened environment, it was found that the ocular potential waveform changes shape as it moves towards the back of the head.
Arts, Faculty of
Psychology, Department of
Graduate
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Mackay, Alison. "Assessing children's visual acuity with steady state evoked potentials". Thesis, University of Glasgow, 2003. http://theses.gla.ac.uk/6573/.

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The majority of children attending ophthalmology clinics require a visual acuity assessment. The optimal technique depends on age as well as the ability to cooperate with testing. Most acuity assessments are performed subjectively by an orthoptist. Objective acuity assessment by Visual Evoked Potential (VEP) provides a complementary assessment in those subjects who cannot complete subjective tests. The aim of this study was to develop and evaluate a rapid, objective visual acuity assessment. The technique was named the step_ VEP and is based on the real-time analysis of steady-state VEPs (ssVEP). It presents high contrast checkerboard stimuli of sizes 0.4 to 3.0 LogMAR with a successive approximation algorithm. Speed of response detection, specificity and sensitivity were optimised by investigation of recording montage and analysis techniques in a group of normal children and adults (N=102). The success, duration and outcome of step_ VEP acuity assessment was compared to transient VEP (t-VEP) acuity assessment and subjective acuity assessment in a group of paediatric patients (N=218). I-D Laplacian analysis of three occipital electrodes was significantly faster than conventional recording and analysis (Oz-Fz) at detecting ssVEP responses near visual acuity threshold (3' checks) from three years upwards, and at detecting responses to 6' and 9' checks in the 7-9 year age group. A lateral electrode site at 15% of the half-head circumference was fastest most often in adults. Step_ VEPs were 16% more successful than t-VEPs and 9% more successful than subjective tests in providing a complete acuity assessment. Subjective acuity scores were systematically higher than VEP acuity scores in subjects who successfully completed both assessments. A closer agreement with subjective acuity scores was found for step_ VEPs than t-VEPs. The disparity between step_ VEP acuity score and subjective acuity score was shown to reduce with age.
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Calvert, Julie. "Visual evoked potentials in normal aging and Alzheimer's disease". Thesis, Glasgow Caledonian University, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.395798.

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Khalil, Nofal Mohammed. "Investigations of visual function in migraine by visual evoked potentials and visual psychophysical tests". Thesis, Imperial College London, 1991. http://hdl.handle.net/10044/1/8336.

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Simpson, David Gordon Giles, i dsimpson@swin edu au. "Instrumentation for high spatial resolution of steady state visual evoked potentials". Swinburne University of Technology, 1998. http://adt.lib.swin.edu.au./public/adt-VSWT20060711.123100.

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This thesis reports on several new and innovative instrumentation developments to solve some of the problems of brain activity monitoring, particularly SSVEP (Steady State Visual Evoked Potentials) studies. SSVEP systems generate suitable stimuli and record the resulting brain biopotentials from scalp electrodes. The instrumentation is configured as a 'Neuropsychiatric Workstation', supporting up to 136 scalp electrodes. Operating in the SSVEP mode, the Neuropsychiatric Workstation reported here significantly improves upon the previously reported spatial resolution and accuracy of maps related to the generated stimuli. These maps allows insights to be gained into the cognitive workings of the brain. A significant component of the work reported here covers the development of the multielectrode EEG measurement modules and the associated techniques for minimising interference and cross-talk. The techniques for synchronising recordings from all electrodes with the stimulus, interfacing to a host computer and real-time storage of the very large amounts of data generated to hard disk, are all reported. The SSVEP paradigm uses a sinusoidal-modulated visual stimuli. A novel linearised LED (light emitting diode) head-up display was developed, in addition to more conventional stimuli, such as the alternating checker-board display, all with sinusoidal modulation capability over a range of frequencies. The Neuropsychiatric Workstation described in thesis has been replicated several times and is in regular use at Brain Sciences Institute (BSI) at Swinburne University of Technology, and other collaborative research institutes.
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Matthews, David. "Dissociation of P300 brain potentials evoked by rare visual stimuli". Thesis, University of St Andrews, 1995. http://hdl.handle.net/10023/14732.

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The P300 event related potential (ERP) has consistently been dissociated into separate components on the basis of scalp amplitude distribution within the auditory modality (for instance Squires et al. 1975). A parietally maximum P300 deflection being evoked in response to target stimuli in comparison with a more frontally maximum P300 deflection evoked in response to rare nontarget stimuli. Results obtained within experiment 1 and 6 demonstrated such a dissociation employing auditory stimuli within a three stimulus oddball paradigm. It did not prove possible to obtain such a dissociation of P300 deflections on the basis of scalp amplitude distribution within the visual modality. Across a number of experimental manipulations both target and rare nontarget stimuli evoked P300 deflections with similar amplitude distributions (centro-parietal maximum along the midline). Experiment 5 demonstrated that frequent stimuli similarly evoked a centro-parietal maximum amplitude distribution. It was demonstrated that both stimulus probability (Experiment 4) and the physical characteristics of the stimuli (Experiment 5) affected the mean amplitude of the evoked P300 deflection. However, the scalp amplitude distribution of the evoked deflections remained constant. Within Experiment 6 it was demonstrated that within both auditory and visual modalities P300 deflections, evoked in response to both target and rare nontarget stimuli, demonstrated an equipotential amplitude distribution within an elderly group of subjects. In addition across both modalities amplitude evoked in response to rare nontarget stimuli demonstrated an asymmetric distribution across lateral chains of electrodes. Amplitude evoked along the right chain was significantly reduced in comparison to that evoked along the left chain. It would appear that the same, or a similar combination of, underlying neural generators are responsible for the activity that may be recorded at the scalp as the P300 deflection within the visual modality.
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Marshall, David. "Brain-computer games interfacing with motion-onset visual evoked potentials". Thesis, Ulster University, 2016. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.685554.

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A brain-computer interface (BCI) measures brain activity and translates this activity into commands for a program to execute. BCls enable movement-free communication and interaction with technologies. This thesis evaluates the effectiveness and limitations of motion-onset visual evoked potentials (mVEP) based BCI as a control method for brain-computer games interaction. MVEP incorporates neural activity from the dorsal pathway of the visual system which allows more elegant visual stimuli than other types ofVEP and has yet to be used in computer games. This thesis investigates ifmVEP can be used as a control method in multiple computer games, what genre of game is best for interaction with m VEP and can we correct problems with existing VEP BCI computer games? Before conducting experiments involving games of different genres an evaluation of the present stateof- the-art BCI games was carried out in an extensive literature survey on BCI games categorised by genre. The literature survey shows that 'action' is the most popular genre in BCI games (49% of BC I games) and provides both games developers and BCI experts a set of design and development guidelines for BCI games. The conclusions of the survey led to the development of three BCI games of different genres namely action, puzzle and sports. The testing of different BCI games using a single paradigm enables thorough assessment ofmVEP as a control method. Five mVEP stimuli are presented as buttons to allow the subject to choose from five possible actions in each game. The performance was assessed based on offline and online BCI accuracy and game score. The results indicate that players could control the games with reasonable online accuracy (66% average for 5 class classification, with an average training accuracy of 74%). The next study intended on improving the initial study's results by adding the mVEP to an on screen HUD (Heads up Display), training in the same game environment as the participants are tested within and adding a questionnaire. Results indicate that the players could control the games with an average online accuracy of 71 %, a significant improvement from the previous study. After further analysis of recorded data the ideal setup for mVEP games is defined with key specifications indicating between three and four channels is most economical setup without influencing accuracy whilst averaging over three trials (minimises latency in communication). Finally, through the evaluation of a range o,fthe games related surveys, we found that players enjoyed the m VEP puzzle game most, rating it both the most enjoyable and appropriate game with m VEP control. Overall this thesis shows that m VEP can be used in multiple games genres with good accuracy and provides players with an entertaining and novel control method for computer games.
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Lloyd, Robyn School of Optometry &amp Visual Science UNSW. "Achromatic and chromatic VEPs in adults with down syndrome". Awarded by:University of New South Wales. School of Optometry and Visual Science, 2005. http://handle.unsw.edu.au/1959.4/23957.

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Previous studies have found that spatial processing in children and adults with Down syndrome is different in comparison to the normal population. Some previous studies have also found that there is a high prevalence of colour vision deficiencies in people with Down syndrome. The aim of the present study was to use an objective test, the transient visual evoked potential (VEP), to assess achromatic and chromatic visual processing in adults with Down syndrome. Achromatic VEPs were recorded in response to black-white stimuli presented in patternreversal mode. Chromatic VEPs were recorded in response to two types of colour pattern, presented in pattern onset-offset mode. The two colour types were intended to preferentially stimulate the two principal chromatic pathways of the visual system, the ???redgreen??? and ???blue-yellow??? colour-opponent pathways. These stimuli are here termed the ???LM??? and ???S-(L+M) stimuli, respectively, reflecting the cone types that input to the pathways they are intended to stimulate. Each subject also completed two subjective colour vision tests, the Colour Vision Test Made Easy (CVTME) and the City University Colour Vision Test (CUT). Morphology of the achromatic and chromatic VEPs was found to differ between the group with Down syndrome and an age-matched control group. The latency of the P100 component of the achromatic VEP was found to be significantly later in the group with Down syndrome compared to the control group (the N75 latency was earlier in the group with Down syndrome, but not significantly so). The group-averaged peak-to-peak amplitude of the achromatic VEP was significantly lower in the group with Down syndrome compared to the control group. The major positive component of the VEP in response to the L-M stimulus was of significantly longer latency compared to that of the control group. The major negative component and the peak-to-peak amplitude of this response were not significantly different between the groups. For the response to S-(L+M) stimuli, the latency of the major negativity was significantly earlier in the group with Down syndrome and the major positivity was later, but not significantly so. Amplitude of this response was significantly higher in adults with Down syndrome compared to the control group. Most subjects in both groups passed both the CVTME and CUT. Our findings indicate that chromatic VEPs are abnormal in Down syndrome, and this may reflect abnormal processing of chromatic stimuli in this population. Alternatively, these abnormalities may arise due to abnormal cortical morphology, which may occur with normal or abnormal processing of chromatic signals. These findings further indicate that abnormality of chromatic VEPs may be expected in Down syndrome, and is not necessarily indicative of pathology or other abnormal function that is unrelated to the syndrome.
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Shawkat, Fatima Suham. "Pattern visual evoked potentials : comparison of onset, reversal and offset components". Thesis, University College London (University of London), 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.266482.

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Książki na temat "Evoked potentials, Visual"

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Evoked potential primer: Visual, auditory, and somatosensory evoked potentials in clinical diagnosis. Boston: Butterworth, 1985.

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Chang, Corina Yee-Mei. Analysis of infant visual evoked potentials. Ottawa: National Library of Canada, 1993.

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Spehlmann, Rainer. Evoked potential primer: Visual, auditory, and somatosensory evoked potentials in clinical diagnosis. Boston: Butterworth, 1985.

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1931-, Spehlmann Rainer, red. Spehlmann's evoked potential primer: Visual, auditory, and somatosensory evoked potentials in clinical diagnosis. Wyd. 2. Boston: Butterworth-Heinemann, 1994.

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Flanagan, John Gerard. Automated assessment of visual fields and their inter-relation to evoked potentials in visual disorders. Birmingham: University of Aston. Department of Vision Sciences, 1985.

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Robson, A. G. Blue/yellow visual evoked potentials and the limitations of flat-screen stimulation. Manchester: UMIST, 1995.

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Samuel, Sokol, red. Electrophysiologic testing in disorders of the retina, optic nerve, and visual pathway. San Francisco, CA: American Academy of Ophthalmology, 1990.

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Padhiar, Sanjita. Study of the cholinergic factors affecting the flash and pattern reversal visual evoked potentials. Birmingham: Aston University. Department of Vision Sciences, 1993.

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Morong, Sharon Elizabeth. Sweep visual evoked potentials in children with west syndrome before and during vigabatrin treatment. Ottawa: National Library of Canada, 2003.

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NATO Advanced Research Workshop on Advances in Understanding Visual Processes: Convergence of Neurophysiological and Psychophysical Evidence (1990 Røros, Norway). From pigments to perception: Advances in understanding visual processes. New York: Plenum Press, 1991.

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Części książek na temat "Evoked potentials, Visual"

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Markand, Omkar N. "Visual Evoked Potentials". W Clinical Evoked Potentials, 83–137. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-36955-2_3.

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Hammond, Flora M., i Sheryl Katta-Charles. "Visual Evoked Potentials". W Encyclopedia of Clinical Neuropsychology, 3612. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-57111-9_81.

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Parry, Neil. "Visual Evoked Potentials". W Encyclopedia of Color Science and Technology, 1253–59. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4419-8071-7_107.

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Hammond, Flora, i Lori Grafton. "Visual Evoked Potentials". W Encyclopedia of Clinical Neuropsychology, 2628. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-0-387-79948-3_81.

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Toleikis, Sandra C., i J. Richard Toleikis. "Visual-Evoked Potentials". W Monitoring the Nervous System for Anesthesiologists and Other Health Care Professionals, 51–70. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-46542-5_4.

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Hammond, Flora, i Sheryl Katta-Charles. "Visual Evoked Potentials". W Encyclopedia of Clinical Neuropsychology, 1–2. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-56782-2_81-3.

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Parry, Neil. "Visual Evoked Potentials". W Encyclopedia of Color Science and Technology, 1–8. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-27851-8_107-1.

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Sinatra, M. G., i L. Carenini. "Subclavian Steal: Diagnostic Value of Reactive Hyperemia During Visual and Auditory Evoked Potential Recordings". W Evoked Potentials, 145–51. Vienna: Springer Vienna, 1988. http://dx.doi.org/10.1007/978-3-7091-4431-2_15.

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de Weerd, A. W. "Visual evoked potentials in clinical neurology". W Evoked Potential Manual, 161–204. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-2059-0_5.

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Møller, Aage R. "Monitoring Visual Evoked Potentials". W Intraoperative Neurophysiological Monitoring, 163–65. New York, NY: Springer New York, 2010. http://dx.doi.org/10.1007/978-1-4419-7436-5_8.

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Streszczenia konferencji na temat "Evoked potentials, Visual"

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Hemalatha, G., i B. Anuradha. "Enhancement of visual evoked potentials". W 2016 International Conference on Electrical, Electronics, and Optimization Techniques (ICEEOT). IEEE, 2016. http://dx.doi.org/10.1109/iceeot.2016.7754835.

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Dobrowolski, Andrzej P., i Marta Okon. "Spectral analysis of visual evoked potentials". W 2015 Signal Processing Symposium (SPSympo). IEEE, 2015. http://dx.doi.org/10.1109/sps.2015.7168275.

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Gaume, Antoine, Francois Vialatte i Gerard Dreyfus. "Detection of steady-state visual evoked potentials using simulated trains of transient evoked potentials". W 2014 IEEE Faible Tension Faible Consommation (FTFC). IEEE, 2014. http://dx.doi.org/10.1109/ftfc.2014.6828619.

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Hajipour, Sepideh, Mohammad B. Shamsollahi i Vahid Abootalebi. "Visual Acuity Classification Using Single Trial Visual Evoked Potentials". W 2009 31st Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC). IEEE, 2009. http://dx.doi.org/10.1109/iembs.2009.5334015.

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Marshall, David, Shane Wilson i Damien Coyle. "Motion-Onset Visual Evoked Potentials for Gaming". W Annual International Conference on Computer Games, Multimedia and Allied Technology. Global Science & Technology Forum (GSTF), 2015. http://dx.doi.org/10.5176/2251-1679_cgat15.41.

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Xiao-Ou Li, Xiao-Wei Zhang i Huan-qing Feng. "Real time extraction of Visual Evoked Potentials". W Proceedings of 2003 International Conference on Neural Networks and Signal Processing. IEEE, 2003. http://dx.doi.org/10.1109/icnnsp.2003.1281120.

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Friman, Ola, Thorsten Luth, Ivan Volosyak i Axel Graser. "Spelling with Steady-State Visual Evoked Potentials". W 2007 3rd International IEEE/EMBS Conference on Neural Engineering. IEEE, 2007. http://dx.doi.org/10.1109/cne.2007.369683.

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Cysewska-Sobusiak, A., A. Hulewicz i A. Grzybowski. "Application of visual evoked potentials to objective visual acuity assessment". W 4th IET International Conference on Advances in Medical, Signal and Information Processing (MEDSIP 2008). IEE, 2008. http://dx.doi.org/10.1049/cp:20080448.

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Lehman, D. M., i Joseph M. Harrison. "Flash Visual Evoked Potentials in Hypomyelinated Shiverer Mice". W Vision Science and its Applications. Washington, D.C.: OSA, 1999. http://dx.doi.org/10.1364/vsia.1999.fb4.

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Krusienski, Dean J., i Brendan Z. Allison. "Harmonic coupling of steady-state visual evoked potentials". W 2008 30th Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 2008. http://dx.doi.org/10.1109/iembs.2008.4650345.

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Raporty organizacyjne na temat "Evoked potentials, Visual"

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Nakayama, Ken. Visual Evoked Potentials. Fort Belvoir, VA: Defense Technical Information Center, listopad 1987. http://dx.doi.org/10.21236/ada187942.

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Mermeklieva, Elena. Reference Values of Binocular Pattern Reversal Visual Evoked Potentials in Bulgarian Population. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, listopad 2020. http://dx.doi.org/10.7546/crabs.2020.11.17.

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Harsh, John R. Auditory and Visual Evoked Potentials as a Function of Sleep Deprivation and Irregular Sleep. Fort Belvoir, VA: Defense Technical Information Center, sierpień 1989. http://dx.doi.org/10.21236/ada228488.

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