1989
DOI: 10.1016/0168-5597(89)90058-0
|View full text |Cite
|
Sign up to set email alerts
|

Abnormalities of short-latency somatosensory evoked potentials in parkinsonian patients

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

6
71
1

Year Published

1996
1996
2014
2014

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 185 publications
(78 citation statements)
references
References 32 publications
6
71
1
Order By: Relevance
“…The physiological meaning of the frontal N30 somatosensory evoked potential (SEP) is still a matter of debate. [1][2][3]5,8,10,17,32,43,44,46,51 Indirect elements for solving this problem might be found by analyzing the modifications of the N30 component that occur in response to different physiological stimuli. Cortical SEPs can be elicited by stimulation of cutaneous as well as proprioceptive afferents.…”
mentioning
confidence: 99%
“…The physiological meaning of the frontal N30 somatosensory evoked potential (SEP) is still a matter of debate. [1][2][3]5,8,10,17,32,43,44,46,51 Indirect elements for solving this problem might be found by analyzing the modifications of the N30 component that occur in response to different physiological stimuli. Cortical SEPs can be elicited by stimulation of cutaneous as well as proprioceptive afferents.…”
mentioning
confidence: 99%
“…Scalp mapping studies and recordings from patients with cerebral lesions like Huntington's disease and from focal infarctions suggested area 4 as generator (Abbruzzese et al 1990;Desmedt and Ozaki 1991;Desmedt et al 1987;Mauguiere and Desmedt 1991;Rossini et al 1989;Töpper et al 1993). In a recent study using electroencephalographic (EEG) dipole source analysis, Jung et al (2008) localized the P22 dipole source in area 4 but could not rule out area 1, which also contributed to the signal.…”
Section: Introductionmentioning
confidence: 99%
“…In PD, tactile localization 2 and spatial acuity 3 are impaired. Deficiencies in tactile processing may relate to a loss of epidermal nerve fibers and Meissner corpuscles 4 , alterations in cortical circuitry targeted by nigro-striatal output 5 , changes in somatosensory afferent transmission 6 or mutation of the PINK1 gene 7 . In PD, tactile acuity in the time domain has been studied using temporal discrimination threshold (TDT), which refers to the minimum time interval between two sequential stimuli to be perceived as distinct.…”
mentioning
confidence: 99%