PubMed HealthSearch

PubMed · 2197689

Paperless electroencephalography.

Abstract

"Paperless EEG" incorporates a variety of techniques for recording, storing, reformatting, transmitting, and analyzing EEG records. The general advance in microelectronics has provided the EEG community with this collection of options. Many of these will come to be commonplace in the EEG laboratory of the future, and indeed some of these are making inroads into EEG practice. Storage of EEG may be the simplest area in which these tools can be used at present, and they may be cost-effective for many laboratories even now. Other features offer ways to improve the EEG product, including the ability to change the filters, paper speed, and montage after the recording has been made. In these ways, even reading of the traditional polygraph EEG can be enhanced by paperless tools. Some other tools are still under development or are best used at specialty centers. Methods of artifact removal, event detectors, and spike detectors still are not quite ready for routine use everywhere, but can now enhance EEG techniques in specific settings. As the field of EEG moves toward the 21st century, the impact of modern electronics should continue to encourage advances toward more widespread use of all of these tools. These advances should help to create an EEG that is cost-competitive with existing services while providing a qualitatively better product.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

M R Nuwer. 1990. Paperless electroencephalography.. https://doi.org/10.1055/s-2008-1041267

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Topographical representations of mental images in primary visual cortex.

We report here the use of positron emission tomography (PET) to reveal that the primary visual cortex is activated when subjects close their eyes and visualize objects. The size of the image is systematically related to the location of maximal activity, which is as expected because the earliest visual areas are spatially organized. These results were only evident, however, when imagery conditions were compared to a non-imagery baseline in which the same auditory cues were presented (and hence the stimuli were controlled); when a resting baseline was used (and hence brain activation was uncontrolled), imagery activation was obscured because of activation in visual cortex during the baseline condition. These findings resolve a debate in the literature about whether imagery activates early visual cortex and indicate that visual mental imagery involves 'depictive' representations, not solely language-like descriptions. Moreover, the fact that stored visual information can affect processing in even the earliest visual areas suggests that knowledge can fundamentally bias what one sees.

Brain Mapping

Cognitive potentials: ipsilateral corticocortical interconnections in prefrontal human cortex ablations.

The research deals with the possible role of the essentially monosynaptic bidirectional corticocortical connections between occipito-temporo-parietal association cortical areas and frontal areas in the genesis of some contingent negative variation (CNV) components, especially on the supramodal dorsolateral prefrontal regions. With standard and topographic mapping methods of analysis, the multicomponent CNV complex formation was examined in 7 patients with extensive frontal cortex ablations exactly identified through CT/MRI examinations, and in 10 normal subjects. On the scalp over the ablated frontocortical areas, no consistent post-warning auditory N100 a-b-c, P200, P300, early and late CNV components were recordable. The hypothesis is proposed that the bidirectional ipsilateral long-distance pathways which interconnect uni-polymodal occipito-temporo-parietal cortical areas to prefrontal ones, in particular the arcuate-superior longitudinal and superior/inferior occipito-frontal fasciculi, play an important role in the genesis of several CNV complex components, especially the multicomponent post-S1 auditory N100. The posteroanterior sequential latency differences of these neurocognitive components, roughly measured along the scalp or on MRI imagings, is probably accounted for by the transcortical ipsilateral conduction time of about 1 cm/ms (10 m/s).

Brain Mapping