Clinical sectionNeural generators of N18 and P14 far-field somatosensory evoked potentials studied in patients with lesion of thalamus or thalamo-cortical radiationsGénérateurs des composantes far field P14 et N18 des potentiels évoqués somesthésiques: malades avec lésion du thalamus ou des radiations thalamo-corticales☆
References (39)
- et al.
Short latency somatosensory evoked potentials: studies in patients with focal neurological disease
Electroenceph. clin. Neurophysiol.
(1980) - et al.
Topography and intracranial sources of somatosensory evoked potentials in the monkey: early components
Electroenceph. clin. Neurophysiol.
(1979) - et al.
Somatosensory evoked potentials in man: far-field potentials
Electroenceph. clin. Neurophysiol.
(1976) - et al.
Central somatosensory conduction in man: neural generators and interpeak latencies of the far-field components recorded from neck and right or left scalp and earlobes
Electroenceph. clin. Neurophysiol.
(1980) - et al.
Somatosensory evoked potentials to finger stimulation in healthy octogenarians and in young adults: wave forms, scalp topography and transit times of parietal and frontal components
Electroenceph. clin. Neurophysiol.
(1980) - et al.
Prevertebral (oesophageal) recording of subcortical somatosensory evoked potentials in man: the spinal P13 component and the dual nature of the spinal generators
Electroenceph. clin. Neurophysiol.
(1981) - et al.
Non-cephalic reference recording of early somatosensory potentials to finger stimulation in adult or aging man: differentiation of widespread N18 and contralateral N20 from the prerolandic P22 and N30 components
Electroenceph. clin. Neurophysiol.
(1981) - et al.
Somatosensory evoked potentials of the normal human neonate in REM sleep, in slow wave sleep and in waking
Electroenceph. clin. Neurophysiol.
(1970) - et al.
Thalamic evoked potentials to somatosensory stimulation in man
Electroenceph. clin. Neurophysiol.
(1976) - et al.
Conduction time in central somatosensory pathways in man
Electroenceph. clin. Neurophysiol.
(1978)
Re-analysis of the antidromic cortical response. On the contribution of cell discharge and PSPs to the evoked potentials
Electroenceph. clin. Neurophysiol.
The initial positive component of scalp-recorded somatosensory evoked potentials in normal subjects and in patients with neurological disorders
Electroenceph. clin. Neurophysiol.
Somatosensory evoked potentials in cervical spondylosis and herniated disc
Electroenceph. clin. Neurophysiol.
Projections of the ascending somesthetic pathways to the cat superior colliculus visualized by the HRP technique
Exp. Brain Res.
The termination of secondary somatosensory neurons within the thalamus of Macaca mulatta: an experimental degeneration study
J. comp. Neurol.
Evoked potentials in clinical medicine
New Engl. J. Med.
Short-latency somatosensory evoked potentials following median nerve stimulation in patients with neurological lesions
Somatosensory evoked responses in controlled A-alpha sensory fiber disease
J. Neurol.
Somatosensory cerebral evoked potentials in man
Cited by (187)
Reconstructing subcortical and cortical somatosensory activity via the RAMUS inverse source analysis technique using median nerve SEP data
2021, NeuroImageCitation Excerpt :In Tsuji et al. (1984), N16 is suggested to reflect the subcortical activity onto the fronto-central areas. At 18 ms, the far-field activity is a relatively widespread bilateral distribution and involved with multiple generators from the brainstem (Mauguière et al., 1983; Noël et al., 1996) to the upper midbrain and the thalamus, where the negative peak, N18, is detectable (Mauguière and Desmedt, 1989; Nuwer, 1998; Passmore et al., 2014). In Urasaki et al. (1990), the N18 peak is suggested to be generated between the upper pons and midbrain, excluding the thalamus as an active area.
Contribution of different somatosensory afferent input to subcortical somatosensory evoked potentials in humans
2021, Clinical NeurophysiologyCitation Excerpt :The origin of the scalp N18 potential has been debated for a long time. Early studies suggested that this widely distributed response could be originated from the thalamus, but some clinical and experimental elements led to localize its generator in the brainstem (Desmedt and Cheron, 1981; Mauguière et al., 1983). N18 origin in the midbrain and/or pons was suggested by Uraski et al. (1992), on the base of absent N18 potential in patients with pontine and mesencephalic lesions, and Philips et al. (1998), who recorded intracranial brainstem SEPs during surgery.
Somatosensory evoked potentials
2019, Handbook of Clinical NeurologyValidation of connectivity-based thalamic segmentation with direct electrophysiologic recordings from human sensory thalamus
2012, NeuroImageCitation Excerpt :In both cases, the site of phase reversal of the thalamic signal corresponding to N18 (Case 1:RTL5 and Case 2:LTL2) spatially corresponded to the thalamic region with the highest probability of connectivity with primary sensory cortex (postcentral gyrus) corresponding to the VPL nucleus of the thalamus (Table 1). Using three independent methods of localizing the VPL nucleus of the thalamus, we not only confirm prior reports which inferred the subcortical, thalamic potential (N18) of the MN-SSEP waveform (Mauguiere and Courjon, 1981; Mauguiere et al., 1983; Noel and Desmedt, 1980), but also provide direct within-subject electrophysiologic confirmation of the accuracy, functional specificity, validity, and reliability of DTI-based segmentation of subcortical anatomy. Because of its non-invasive nature and its wide-spread availability and accessibility, MR-based approaches to studying brain connectivity, including diffusion tensor-based tractography to study anatomic connectivity and resting-state MRI to study functional connectivity, have emerged as the primary means of studying human brain connectivity in the laboratory and in the clinical setting (Mars et al., 2011).
Frontal phasic and oscillatory generators of the N30 somatosensory evoked potential
2011, NeuroImageCitation Excerpt :The identification of distinct somatosensory evoked potentials (SEP) components represents an asset for accurate neurological diagnosis in patients with focal brain disorders (Amantini et al., 2005; Logi et al., 2003; Mauguiere et al., 1983a, b).
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This research has been supported by grants from the Fonds de la Recherche Scientifique Médicale, Belgium