“…This is primarily caused by the fact that the use of traditional neuroimaging modalities (for an overview, see Friston, ) such as electroencephalography (EEG), magnetoencephalography (MEG), positron emission tomography (PET), or functional magnetic resonance imaging (fMRI) is restricted. In addition to questions of cost and accessibility (McLane et al, ) or the use of ionizing radiation (limited repeatability), these modalities also include contraindications due to electrical artefact's (Gilley et al, ; Viola, Thorne, Bleeck, Eyles, & Debener, ; Viola et al, ) or ferromagnetic components (Teissl, Kremser, Hochmair, & Hochmair‐Desoyer, ; Teissl, Kremser, Hochmair, & Hochmair‐Desoyer, ) of the implant. Thus, another reliable method for verification, which is frequently applicable, and bedside usable, is required.…”