Andrej Stančák
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Andrej Stančák has a total of 26 co-authors. Here are the top co-authors by number of shared publications:
Hubert Poláček
Clinic of Nuclear Medicine, Jessenius Faculty of Medicine, Kollarova 2, 036 01 Martin, Slovak Republic
4 shared publicationsJiří Vrána
Charles University Prague, Department of Normal, Pathological and Clinical Physiology, Third Faculty of Medicine, Ke Karlovu 4, 120 00 Prague 2, Czech Republic
3 shared publicationsCarl H Lücking
2 shared publicationsJaroslav Tintera
Institute of Clinical and Experimental Medicine, Vıdenská 800, 140 00 Prague 4, Czech Republic
2 shared publicationsKarsten Hoechstetter
2 shared publicationsMichael Scherg
2 shared publications
Latest Publications
- 1 March 2010
- Published by Elsevier in Brain Research
- Vol. 1317, 69-79
Bursts of 15–30 Hz oscillations following noxious laser stimulus originate in posterior cingulate cortex
- 1 March 2010
- Published by Elsevier in Brain Research
- Vol. 1317, 69-79
Bursts of 15–30 Hz oscillations following noxious laser stimulus originate in posterior cingulate cortex
- 1 February 2008
- Published by Wiley in European journal of pain
- Vol. 12 (2) , 137-148
Functional magnetic resonance imaging of cerebral activation during spinal cord stimulation in failed back surgery syndrome patients
Spinal cord stimulation (SCS) consisting of electrical stimulation of the dorsal spinal cord using epidural electrodes has been shown to relieve chronic neuropathic pain. To analyze the cerebral activation patterns related to SCS, and to evaluate the effects of SCS on the processing of acute experimental pain, we performed functional magnetic resonance imaging (fMRI) on eight patients suffering from failed back surgery syndrome who were also being treated with SCS for severe pain in their legs and lower back. Three types of stimulation were used, each lasting 36s: (i) SCS, (ii) heat pain (HP) applied to the leg affected by neuropathic pain, and (iii) simultaneous HP and SCS.During SCS, we found increased activation of the medial primary sensorimotor cortex somatotopically corresponding to the foot and/or perineal region, contralateral posterior insula, and the ipsilateral secondary somatosensory cortex (S2). Decreased activation was seen in the bilateral primary motor cortices and the ipsilateral primary somatosensory cortex corresponding to the shoulder, elbow and hand. Compared to separately presented HP and SCS, simultaneous HP and SCS showed statistically significant activation of the bilateral inferior temporal cortex and the ipsilateral cerebellar cortex.The activation of the primary motor cortex, insula and S2 during SCS may directly interfere with the processing of neuropathic pain. When SCS is associated with heat pain, the paralimbic association cortex and cerebellum show activation exceeding the sum of activations resulting from separate SCS and heat pain stimulation. The explanation of this could possibly rest with the continuous comparisons of simultaneous pain and somatosensory sensations occurring in a single dermatome.
- 1 February 2008
- Published by Wiley in European journal of pain
- Vol. 12 (2) , 137-148
Functional magnetic resonance imaging of cerebral activation during spinal cord stimulation in failed back surgery syndrome patients
Spinal cord stimulation (SCS) consisting of electrical stimulation of the dorsal spinal cord using epidural electrodes has been shown to relieve chronic neuropathic pain. To analyze the cerebral activation patterns related to SCS, and to evaluate the effects of SCS on the processing of acute experimental pain, we performed functional magnetic resonance imaging (fMRI) on eight patients suffering from failed back surgery syndrome who were also being treated with SCS for severe pain in their legs and lower back. Three types of stimulation were used, each lasting 36s: (i) SCS, (ii) heat pain (HP) applied to the leg affected by neuropathic pain, and (iii) simultaneous HP and SCS.During SCS, we found increased activation of the medial primary sensorimotor cortex somatotopically corresponding to the foot and/or perineal region, contralateral posterior insula, and the ipsilateral secondary somatosensory cortex (S2). Decreased activation was seen in the bilateral primary motor cortices and the ipsilateral primary somatosensory cortex corresponding to the shoulder, elbow and hand. Compared to separately presented HP and SCS, simultaneous HP and SCS showed statistically significant activation of the bilateral inferior temporal cortex and the ipsilateral cerebellar cortex.The activation of the primary motor cortex, insula and S2 during SCS may directly interfere with the processing of neuropathic pain. When SCS is associated with heat pain, the paralimbic association cortex and cerebellum show activation exceeding the sum of activations resulting from separate SCS and heat pain stimulation. The explanation of this could possibly rest with the continuous comparisons of simultaneous pain and somatosensory sensations occurring in a single dermatome.
- 1 November 2006
- Published by Elsevier in NeuroImage
- Vol. 33 (2) , 660-671
Source imaging of the cortical 10 Hz oscillations during cooling and warming in humans
- 1 November 2006
- Published by Elsevier in NeuroImage
- Vol. 33 (2) , 660-671
Source imaging of the cortical 10 Hz oscillations during cooling and warming in humans
- 1 January 2006
- Published by Elsevier
- Vol. 159, 237-252
Cortical oscillatory changes occurring during somatosensory and thermal stimulation
- 1 January 2006
- Published by Elsevier
- Vol. 159, 237-252
Cortical oscillatory changes occurring during somatosensory and thermal stimulation
- 1 July 2005
- Published by Elsevier in NeuroImage
- Vol. 26 (3) , 793-800
Oscillatory motor cortex–muscle coupling during painful laser and nonpainful tactile stimulation
- 1 July 2005
- Published by Elsevier in NeuroImage
- Vol. 26 (3) , 793-800
Oscillatory motor cortex–muscle coupling during painful laser and nonpainful tactile stimulation
- 1 March 2005
- Published by Elsevier in NeuroImage
- Vol. 25 (1) , 8-20
EEG source analysis and fMRI reveal two electrical sources in the fronto-parietal operculum during subepidermal finger stimulation
- 1 March 2005
- Published by Elsevier in NeuroImage
- Vol. 25 (1) , 8-20
EEG source analysis and fMRI reveal two electrical sources in the fronto-parietal operculum during subepidermal finger stimulation
- 1 October 2003
- Published by Elsevier in Clinical Neurophysiology
- Vol. 114 (10) , 1936-1947
Desynchronization of cortical rhythms following cutaneous stimulation: effects of stimulus repetition and intensity, and of the size of corpus callosum
- 1 October 2003
- Published by Elsevier in Clinical Neurophysiology
- Vol. 114 (10) , 1936-1947
Desynchronization of cortical rhythms following cutaneous stimulation: effects of stimulus repetition and intensity, and of the size of corpus callosum
- 1 May 2002
- Published by Elsevier in Brain Research
- Vol. 936 (1-2) , 47-57
Source activity in the human secondary somatosensory cortex depends on the size of corpus callosum
- 1 May 2002
- Published by Elsevier in Brain Research
- Vol. 936 (1-2) , 47-57
Source activity in the human secondary somatosensory cortex depends on the size of corpus callosum
- 1 February 2002
- Published by Elsevier in Cognitive Brain Research
- Vol. 13 (1) , 61-74
The size of corpus callosum and functional connectivities of cortical regions in finger and shoulder movements
- 1 February 2002
- Published by Elsevier in Cognitive Brain Research
- Vol. 13 (1) , 61-74
The size of corpus callosum and functional connectivities of cortical regions in finger and shoulder movements
- 1 April 2000
- Published by Elsevier in Clinical Neurophysiology
- Vol. 111 (4) , 636-650
Oscillatory cortical activity and movement-related potentials in proximal and distal movements
- 1 April 2000
- Published by Elsevier in Clinical Neurophysiology
- Vol. 111 (4) , 636-650
Oscillatory cortical activity and movement-related potentials in proximal and distal movements