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Biomedical subjects

M H Giard

Publications and source records attributed to M H Giard.

35 records · Page 2Linked to original sources
PubMed1988

Electrophysiological evidence for a shared representational medium for visual images and visual percepts.

Does mental imagery involve the activation of representations in the visual system? Systematic effects of imagery on visual signal detection performance have been used to argue that imagery and the perceptual processing of stimuli interact at some common locus of activity (Farah, 1985). However, such a result is neutral with respect to the question of whether the interaction occurs during modality-specific visual processing of the stimulus. If imagery affects stimulus processing at early, modality-specific stages of stimulus representation, this implies that the shared stimulus representations are visual, whereas if imagery affects stimulus processing only at later, amodal stages of stimulus representation, this implies that imagery involves more abstract, postvisual stimulus representations. To distinguish between these two possibilities, we repeated the earlier imagery-perception interaction experiment while recording event-related potentials (ERPs) to stimuli from 16 scalp electrodes. By observing the time course and scalp distribution of the effect of imagery on the ERP to stimuli, we can put constraints on the locus of the shared representations for imagery and perception. An effect of imagery was seen within 200 ms following stimulus presentation, at the latency of the first negative component of the visual ERP, localized at the occipital and posterior temporal regions of the scalp, that is, directly over visual cortex. This finding provides support for the claim that mental images interact with percepts in the visual system proper and hence that mental images are themselves visual representations.

Adult↗
PubMed1987

Mapping of scalp potentials by surface spline interpolation.

Evoked potentials and EEGs record punctate electrical activity at electrode sites. To represent the overall potential distribution on the entire scalp it is necessary to interpolate between these sampled values. Surface splines are mathematical tools for interpolating functions of two variables. In comparison to the classical methods of interpolation, based on linear combination of the potentials of the 4 nearest electrodes, spline methods are smoother, give more precisely located extrema and converge faster toward the 'true' potential surface when the number of recording electrodes is increased. These advantages are at the expense of lengthier computation time.

Brain Mapping↗
PubMed1986

Separate generators with distinct orientations for N20 and P22 somatosensory evoked potentials to finger stimulation?

Sequential spatial maps of scalp potentials, obtained with a 16-channel montage, were used in 12 healthy subjects in order to assess the temporal and spatial distribution of early cortical SEPs to single finger stimulation. It was found that when the contralateral parietal N20 negativity peaks there is a synchronous frontal P20 positivity, supporting the view of a tangentially orientated dipolar generator for this couple of scalp SEPs components. It was not possible to show a distribution of N20 peak on the scalp that would parallel the somatotopic finger representations in area S1; however, the orientation of the putative dipolar source of the N20/P20 complex was found to change according to the finger stimulated. A central P22 component was also constantly obtained without any synchronous negativity on the scalp surface corresponding to the electrode array; a clear somatotopic organisation was found for P22. These features favour the hypothesis that this latter component has a radially orientated generator situated in the prerolandic motor cortex, close to the scalp surface. Because of overlapping between the P20 and P22 components, the determination of P22 onset latency was hazardous in some cases, and spatial mapping was then essential to identify this component. The conclusion that the contralateral parietal N20 and central P22 could be generated by separate dipolar generators with distinct orientations is supported by recent data from combined electrical and magnetic field recording.

Adult↗
PubMed1985

Sequential colour mapping system of brain potentials.

We present a colour mapping system for the visualization of both the spatial scalp distribution and the temporal evolution of brain potentials. The system is applicable to recordings of auditory, visual and somatosensory potentials. It uses a Tektronix 4113 colour terminal connected to a Solar 16 (SEMS) mini-computer. The brain potentials are recorded on up to 16 scalp electrodes. The gain and the baseline are corrected separately on each channel. At each point of the scalp the potential is reconstructed by a linear interpolation of the measured potentials of the four nearest electrodes. Simultaneously n2 (1 less than n less than 8) colour maps can be presented on the screen. This allows the study of the temporal evolution of full scalp evoked potentials. The user chooses the two extreme latencies defining the time window to be explored and the latencies of the maps are regularly time-spaced within this window. In a typical case, in which four maps are desired, the latencies of the maps can be chosen independently. The 16-colour palette is predetermined but the user has three possibilities to establish the correspondence between the electrical potential and the colours. Examples are shown in the visual and somatosensory stimulation modalities. The advantages and limitations of such a representation are discussed.

Brain↗
PubMed1985

[Sequential spatial maps of visual potentials evoked by checkerboard-pattern reversal: effect of the retinal field stimulated on response topography].

Sequential color maps of visual potentials evoked by the reversal of various checkerboard patterns were recorded in 10 young adults using a 16 channel montage. It was found that each of the components of the N75-P100-N145 occipital complex had a specific spatial distribution on the scalp and was selectively influenced by the size, the spatial frequency, the luminance and possibly the wave length of the stimulus. Component N75 was found to be elicited by the more peripheral area of the TV stimulus (12 degrees X 16 degrees). Component P100 was associated with a frontal negativity of similar latency favoring the hypothesis of a dipolar occipital generator. With half-field stimulations the dipole orientation was modified, leading to a 'paradoxical' lateralization of P100 in most cases. However the reverse situation (P100 contralateral to the stimulated half-field) was observed in 4 and 3 subjects out of 10 with left and right half-field stimulations respectively. Thus VEP to full-field TV pattern reversal cannot be recommended to investigate hemianopic patients. Component N145 was of maximal amplitude when elicited by the reversal of small foveal patterns (2.18 degrees), especially red light emitting diodes.

Adult↗
PubMed1985

[Rare cause of myoclonus with giant SEP's: methyl bromide poisoning. Apropos of a case with unilateral predominance].

Giant and asymmetric SEPs were recorded in a patient with predominantly unilateral, spontaneous and intention myoclonus due to voluntary intoxication with methyl bromide as soon as day 3 after intoxication. The N10 Erb's point potential, cervical N13 and scalp recorded P15 potentials were found to be normal in latency, morphology and amplitude. The somesthetic informations could be considered as normally processed up to the subcortical levels of the somatosensory pathways. The parietal cortical potentials N20 and P25 and the frontal cortical potentials P22 and N30, contralateral to myoclonus, were abnormally large. This suggests that myoclonus could be related with an abnormal reactivity of somatomotor and somatosensory cortices to the afferent volleys triggered by voluntary movements. The prerolandic components P22 and N30 were found to be relatively more enhanced than the parietal N20 and P15.

Cerebral Cortex↗
PubMed1984

The temporal component of the auditory evoked potential: a reinterpretation.

The auditory evoked potentials in man cannot be explained by a single source even though a strong influence of the primary areas in the supra-temporal plane has been pointed out in different works. In 26 normal adults we mathematically extracted the greater part of the experimental AEPs explicable by such an origin. The residual part obtained by subtracting this first component from the experimental data is in agreement with an origin in the precentral motor cortex.

Brain Mapping↗
PubMed1979

[Original method of multivariate analysis, adapted for comparison of mean evoked potentials: E2 test].

This paper describes a multivariate statistical method of analysis for the comparison of 2 paired series. For such paired series, this test, called E2, is analogous to the generalized Hotteling T2 test, as epsilon test (pairing method) is analogous to Student's t test. Here we give an example of its application to a comparison of curves, in this particular case average auditory evoked potentials, picked up at symmetrical points on the scalp.

Acoustic Stimulation↗