Non-invasive single-trial EEG detection of evoked human neocortical population spikes

NeuroImage ◽  
2015 ◽  
Vol 105 ◽  
pp. 13-20 ◽  
Author(s):  
Gunnar Waterstraat ◽  
Martin Burghoff ◽  
Tommaso Fedele ◽  
Vadim Nikulin ◽  
Hans Jürgen Scheer ◽  
...  
2014 ◽  
Vol 125 ◽  
pp. S32
Author(s):  
G. Waterstraat ◽  
M. Burghoff ◽  
T. Fedele ◽  
H.J. Scheer ◽  
G. Curio

2013 ◽  
Vol 333 ◽  
pp. e699
Author(s):  
T. Fedele ◽  
H.-J. Scheer ◽  
M. Burghoff ◽  
G. Waterstraat ◽  
V. Nikulin ◽  
...  

2015 ◽  
Vol 126 (8) ◽  
pp. e158
Author(s):  
G. Waterstraat ◽  
M. Scheuermann ◽  
M. Burghoff ◽  
T. Fedele ◽  
G. Curio

2013 ◽  
Vol 44 (01) ◽  
Author(s):  
T Fedele ◽  
HJ Scheer ◽  
M Burghoff ◽  
G Waterstraat ◽  
V Nikulin ◽  
...  

Neuroreport ◽  
2001 ◽  
Vol 12 (8) ◽  
pp. 1689-1692 ◽  
Author(s):  
Bruno-Marcel Mackert ◽  
Gerd Wübbeler ◽  
Stefanie Leistner ◽  
Lutz Trahms ◽  
Gabriel Curio

2021 ◽  
Vol 118 (11) ◽  
pp. e2017401118
Author(s):  
Gunnar Waterstraat ◽  
Rainer Körber ◽  
Jan-Hendrik Storm ◽  
Gabriel Curio

Neuronal spiking is commonly recorded by invasive sharp microelectrodes, whereas standard noninvasive macroapproaches (e.g., electroencephalography [EEG] and magnetoencephalography [MEG]) predominantly represent mass postsynaptic potentials. A notable exception are low-amplitude high-frequency (∼600 Hz) somatosensory EEG/MEG responses that can represent population spikes when averaged over hundreds of trials to raise the signal-to-noise ratio. Here, a recent leap in MEG technology—featuring a factor 10 reduction in white noise level compared with standard systems—is leveraged to establish an effective single-trial portrayal of evoked cortical population spike bursts in healthy human subjects. This time-resolved approach proved instrumental in revealing a significant trial-to-trial variability of burst amplitudes as well as time-correlated (∼10 s) fluctuations of burst response latencies. Thus, ultralow-noise MEG enables noninvasive single-trial analyses of human cortical population spikes concurrent with low-frequency mass postsynaptic activity and thereby could comprehensively characterize cortical processing, potentially also in diseases not amenable to invasive microelectrode recordings.


Author(s):  
H.W. Deckman ◽  
B.F. Flannery ◽  
J.H. Dunsmuir ◽  
K.D' Amico

We have developed a new X-ray microscope which produces complete three dimensional images of samples. The microscope operates by performing X-ray tomography with unprecedented resolution. Tomography is a non-invasive imaging technique that creates maps of the internal structure of samples from measurement of the attenuation of penetrating radiation. As conventionally practiced in medical Computed Tomography (CT), radiologists produce maps of bone and tissue structure in several planar sections that reveal features with 1mm resolution and 1% contrast. Microtomography extends the capability of CT in several ways. First, the resolution which approaches one micron, is one thousand times higher than that of the medical CT. Second, our approach acquires and analyses the data in a panoramic imaging format that directly produces three-dimensional maps in a series of contiguous stacked planes. Typical maps available today consist of three hundred planar sections each containing 512x512 pixels. Finally, and perhaps of most import scientifically, microtomography using a synchrotron X-ray source, allows us to generate maps of individual element.


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