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R W Hintze

Publications and source records attributed to R W Hintze.

3 recordsLinked to original sources

Cortical and subcortical components of the pattern VEP.

Studies in the past have shown that wavelength related VEPs can be recorded from both cortical and noncortical sites. Elements of pattern-specific VEPs for both transient and pattern-reversal stimuli are also obtained from these sites. From the noncortical montage consistent responses are obtained with a major component at about 100 msec, which has been found for both the wavelength related and pattern related VEP. In contrast, the cortical VEP to both types of stimuli include two major components, at around 100 and 200 msec. In pattern reversal these components react quite differently to changes in spatial frequency. The component around 100 msec reacts strongly to a wide range of spatial frequencies when recorded from either cortical or noncortical sites. In contrast, the component around 200 msec, obtained with cortical recording, reacts very strongly to high spatial frequencies and very weakly to low spatial frequencies. This finding corresponds to recent results of single-cell studies in the macaque LGN and striate cortex.

Adult↗

Pattern component ratio in pattern-reversal VEP: normative data and clinical applications.

It has been well established that there is a reliable implicit time to the VEP positive component (ca 100 msec) in response to pattern reversal. This has become a valuable test of the status of the visual system. Recent data suggest that activity around 200 msec is another useful measure of the cortical response to pattern alternation. We have carried out a normative study of the relative amplitudes of the two components. Among adults with normal visual acuity activity around 200 msec is directly related to the spatial frequency of the stimulus, peaking markedly in amplitude at a narrow range of spatial frequencies. This is in sharp contrast to the earlier component, which does not exhibit such sensitive size differentiation. Recently we have used the ratio between the late and early component amplitudes as a quantitative indicator of the efficiency of higher-level processing of pattern information. We present our normative data and illustrate the effects of decreased visual responses not related to known peripheral optical problems. The results of this work are also interpreted as showing basic characteristics of information processing in the visual system, in that higher spatial frequencies are processed by a continuum of rather sharply tuned cortical processes, with the higher spatial frequencies being processed later in time.

Evoked Potentials, Visual↗

Effect of altered central and peripheral visual field stimulation on correct recognition and visual evoked response.

Hemispheric asymmetry was assessed using combined electrophysiological (visual evoked response) and behavioral (percentage-correct-recognition) techniques. Right-handed, right-eyed, male undergraduates who viewed tachistoscopically exposed CVCs and random shapes in both central and peripheral visual fields were scored for their ability to recognize the stimuli correctly. Latency and amplitude of visual evoked responses were compared with correct recognition. Central and peripheral stimuli produced significant results. Superiority of the left hemisphere for verbal stimulus processing was supported. Small but consistent positive peak latencies of visual evoked responses also indicated language specialization of the left lobe. Results were interpreted as supporting hemispheric functional asymmetry. Additional findings of "cognitive masking" and marked reduction in intersubject variance in postive peak latencies of visual evoked responses by a central stimulus occurring at approximately 300 msec were also obtained. Mechanisms of iconic image storage, neuropsychological attentional theories, and differential hemispheric structural organization were discussed in interpreting results.

Adolescent↗