Journal articles on the topic 'Cortex'

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1

SELEMON, LYNN D., PATRICIA S. GOLDMAN-RAKIC, and CAROL A. TAMMINGA. "Corex, III; Prefrontal Cortex." American Journal of Psychiatry 152, no. 1 (January 1995): 5. http://dx.doi.org/10.1176/ajp.152.1.5.

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2

Kaufman, K. J. "The Cerebral Cortex: Visual Cortex." Archives of Ophthalmology 104, no. 8 (August 1, 1986): 1141. http://dx.doi.org/10.1001/archopht.1986.01050200047040.

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3

Bohn Stafleu van Loghum. "Cortex." Sociaal Bestek 79, no. 5 (October 2017): 2. http://dx.doi.org/10.1007/s41196-017-0100-5.

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4

Cowey, A. "Cerebral Cortex, Vol. 3, Visual Cortex." Neuroscience 19, no. 3 (November 1986): 1023. http://dx.doi.org/10.1016/0306-4522(86)90314-3.

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5

Hughes, John R. "Cerebral cortex. Vol. 3. Visual cortex." Electroencephalography and Clinical Neurophysiology 63, no. 4 (April 1986): 392. http://dx.doi.org/10.1016/0013-4694(86)90029-5.

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6

Kennedy, Philip R. "Cursor Cortex." Science News 156, no. 15 (October 9, 1999): 227. http://dx.doi.org/10.2307/4011902.

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7

Sasano, Hironobu, and Yuto Yamazaki. "Adrenal Cortex." AJSP: Reviews and Reports 22, no. 4 (July 2017): 217–24. http://dx.doi.org/10.1097/pcr.0000000000000181.

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8

Cui, Hongchang, and Philip N. Benfey. "Cortex proliferation." Plant Signaling & Behavior 4, no. 6 (June 2009): 551–53. http://dx.doi.org/10.4161/psb.4.6.8731.

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9

LeBrasseur, Nicole. "Cortex construction." Journal of Cell Biology 175, no. 3 (November 6, 2006): 365b. http://dx.doi.org/10.1083/jcb.1753iti2.

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10

Dluhy, Robert G. "Adrenal cortex." Current Opinion in Endocrinology, Diabetes and Obesity 14, no. 3 (June 2007): 209. http://dx.doi.org/10.1097/med.0b013e328169eeee.

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11

Espiner, Eric A. "Adrenal cortex." Current Opinion in Endocrinology and Diabetes 1, no. 1 (January 1994): 107–8. http://dx.doi.org/10.1097/00060793-199400010-00020.

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12

Espiner, Eric A. "Adrenal cortex." Current Opinion in Endocrinology and Diabetes 2, no. 3 (June 1995): 191–93. http://dx.doi.org/10.1097/00060793-199506000-00001.

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13

&NA;. "Adrenal cortex." Current Opinion in Endocrinology and Diabetes 4, no. 3 (June 1997): B97–110. http://dx.doi.org/10.1097/00060793-199706000-00012.

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14

&NA;. "Adrenal Cortex." Current Opinion in Endocrinology and Diabetes 5, no. 3 (June 1998): B81–97. http://dx.doi.org/10.1097/00060793-199806000-00015.

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15

Stewart, Paul M. "Adrenal cortex." Current Opinion in Endocrinology & Diabetes 6, no. 3 (June 1999): 177. http://dx.doi.org/10.1097/00060793-199906000-00001.

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16

Stewart, Paul M. "Adrenal cortex." Current Opinion in Endocrinology & Diabetes 7, no. 3 (June 2000): 107–8. http://dx.doi.org/10.1097/00060793-200006000-00001.

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17

Stewart, Paul M. "Adrenal cortex." Current Opinion in Endocrinology & Diabetes 8, no. 3 (June 2001): 111. http://dx.doi.org/10.1097/00060793-200106000-00001.

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18

Miller, K. D. "= Visual Cortex." Science 330, no. 6007 (November 18, 2010): 1059–60. http://dx.doi.org/10.1126/science.1198857.

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19

Benarroch, Eduardo E. "Insular cortex." Neurology 93, no. 21 (October 23, 2019): 932–38. http://dx.doi.org/10.1212/wnl.0000000000008525.

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20

Stewart, Paul M. "Adrenal cortex." Current Opinion in Endocrinology & Diabetes 7, no. 3 (June 2000): 107–8. http://dx.doi.org/10.1097/00075197-200006000-00001.

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21

Wlesel, Torsten N., and Charles D. Gilbert. "Visual cortex." Trends in Neurosciences 9 (January 1986): 509–12. http://dx.doi.org/10.1016/0166-2236(86)90161-x.

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22

Innocenti, Giorgio M., and Jon H. Kaas. "The cortex." Trends in Neurosciences 18, no. 9 (September 1995): 371–72. http://dx.doi.org/10.1016/0166-2236(95)93931-m.

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23

Witter, Menno. "Entorhinal cortex." Scholarpedia 6, no. 10 (2011): 4380. http://dx.doi.org/10.4249/scholarpedia.4380.

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24

Kertesz, Andrew. "Language cortex." Aphasiology 5, no. 3 (May 1991): 207–34. http://dx.doi.org/10.1080/02687039108248525.

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25

Della Sala, Sergio, and Jordan Grafman. "Cortex covers." Cortex 45, no. 5 (May 2009): 565. http://dx.doi.org/10.1016/j.cortex.2009.02.003.

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26

Della Sala, Sergio. "Cortex Prize." Cortex 46, no. 3 (March 2010): 281. http://dx.doi.org/10.1016/j.cortex.2009.12.005.

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27

Ehret, G., and H. Scheich. "Auditory cortex." Journal of Comparative Physiology A: Sensory, Neural, and Behavioral Physiology 181, no. 6 (December 11, 1997): 545. http://dx.doi.org/10.1007/s003590050138.

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28

Ricci, Stefano. "Double Cortex." Archives of Neurology 49, no. 1 (January 1, 1992): 61. http://dx.doi.org/10.1001/archneur.1992.00530250065017.

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29

Rudebeck, Peter H., and Erin L. Rich. "Orbitofrontal cortex." Current Biology 28, no. 18 (September 2018): R1083—R1088. http://dx.doi.org/10.1016/j.cub.2018.07.018.

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30

Buchanan, Robert W., and Godfrey Pearlson. "Prefrontal Cortex, Structural Analysis: Segmenting the Prefrontal Cortex." American Journal of Psychiatry 161, no. 11 (November 2004): 1978. http://dx.doi.org/10.1176/appi.ajp.161.11.1978.

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31

Kaas, Jon H. "The transformation of association cortex into sensory cortex." Brain Research Bulletin 50, no. 5-6 (November 1999): 425. http://dx.doi.org/10.1016/s0361-9230(99)00176-8.

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32

Huxlin, Krystel R. "Cerebral Cortex: Extrastriate Cortex in Primates (Vol. 12)." Trends in Neurosciences 21, no. 11 (November 1998): 499. http://dx.doi.org/10.1016/s0166-2236(98)01321-6.

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33

Cowey, A. "Cerebral cortex, functional properties of the cerebral cortex." Neuroscience 17, no. 4 (April 1986): 1297–98. http://dx.doi.org/10.1016/0306-4522(86)90096-5.

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34

Kawasaki, Akihiro, Yutaka Matsuzaki, and Taku Kawada. "Neuroregulatory Effects of Microcone Patch Stimulation on the Auricular Branch of the Vagus Nerve and the Prefrontal Cortex: A Feasibility Study." Journal of Clinical Medicine 13, no. 8 (April 20, 2024): 2399. http://dx.doi.org/10.3390/jcm13082399.

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Background: The primary purpose of this study was to preliminarily examine the effects of autonomic nervous system activity on the dorsolateral prefrontal cortex. Recent studies have examined approaches to modulating autonomic activity using invasive and non-invasive methods, but the effects of changes in autonomic activity during cognitive tasks on the dorsolateral prefrontal cortex have not been fully investigated. The purpose of this preliminary investigation was to examine changes in autonomic activity and blood oxygen saturation in the dorsolateral prefrontal cortex during reading tasks induced by vagus nerve stimulation using a microcone patch. Methods: A cohort of 40 typically developing adults was enrolled in this study. We carefully examined changes in autonomic nervous system activity and blood oxygen saturation in the dorsolateral prefrontal cortex during a reading task in two conditions: with and without microcone patch stimulation. Results: Significant changes in brain activation in the dorsolateral prefrontal cortext due to microcone patch stimulation were confirmed. In addition, hierarchical multiple regression analysis revealed specific changes in reading task-related blood oxygen saturation in the dorsolateral prefrontal region during microcone patch stimulation. Conclusions: It should be recognized that this study is a preliminary investigation and does not have immediate clinical applications. However, our results suggest that changes in autonomic nervous system activity induced by external vagal stimulation may affect activity in specific reading-related regions of the dorsolateral prefrontal cortex. Further research and evaluation are needed to fully understand the implications and potential applications of these findings.
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35

Livingstone, Margaret S., Michael J. Arcaro, and Peter F. Schade. "Cortex Is Cortex: Ubiquitous Principles Drive Face-Domain Development." Trends in Cognitive Sciences 23, no. 1 (January 2019): 3–4. http://dx.doi.org/10.1016/j.tics.2018.10.009.

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36

Freund, H. J. "Contributions of the cortex other than the motor cortex." Electroencephalography and Clinical Neurophysiology 87, no. 2 (August 1993): S6. http://dx.doi.org/10.1016/0013-4694(93)90874-u.

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37

Swindale, Nicholas V. "Cerebral Cortex: The Singular Precision of Visual Cortex Maps." Current Biology 16, no. 23 (December 2006): R991—R994. http://dx.doi.org/10.1016/j.cub.2006.10.039.

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38

Muhammad, Rahmat, Jonathan D. Wallis, and Earl K. Miller. "A Comparison of Abstract Rules in the Prefrontal Cortex, Premotor Cortex, Inferior Temporal Cortex, and Striatum." Journal of Cognitive Neuroscience 18, no. 6 (June 2006): 974–89. http://dx.doi.org/10.1162/jocn.2006.18.6.974.

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The ability to use abstract rules or principles allows behavior to generalize from specific circumstances. We have previously shown that such rules are encoded in the lateral prefrontal cortex (PFC) and premotor cortex (PMC). Here, we extend these investigations to two other areas directly connected with the PFC and the PMC, the inferior temporal cortex (ITC) and the dorsal striatum (STR). Monkeys were trained to use two abstract rules: “same” or “different”. They had to either hold or release a lever, depending on whether two successively presented pictures were the same or different, and depending on which rule was in effect. The rules and the behavioral responses were reflected most strongly and, on average, tended to be earlier in the PMC followed by the PFC and then the STR; few neurons in the ITC reflected the rules or the actions. By contrast, perceptual information (the identity of the pictures used as sample and test stimuli) was encoded more strongly and earlier in the ITC, followed by the PFC; they had weak, if any, effects on neural activity in the PMC and STR. These findings are discussed in the context of the anatomy and posited functions of these areas.
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39

Taira, Masato, and Narumi Katsuyama. "Visual association cortex." Journal of Japan Society for Fuzzy Theory and Intelligent Informatics 18, no. 3 (2006): 377–82. http://dx.doi.org/10.3156/jsoft.18.3_377.

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40

Brown, Jeffrey A. "Motor cortex stimulation." Neurosurgical Focus 11, no. 3 (September 2001): 1–5. http://dx.doi.org/10.3171/foc.2001.11.3.6.

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In 1991 Tsubokawa and colleagues first published their landmark results from a series in which epidural motor cortex stimulation (MCS) was used in the treatment of eight patients with central and neuropathic pain. In ensuing studies authors have elaborated on the indications, technique, hypotheical mechanisms, and beneficial results of this treatment. Epidural MCS is effective for trigeminal neuropathy, lateral medullary and thalamic infarction, anesthesia dolorosa, postherpetic neuralgia, spinal cord injury, and limb stump pain. Postoperative outcomes are better when patients present with only mild or absent motor weakness in the region of pain and when there is pain in the trigeminal region. It is hypothesized that MCS is effective because it increases regional cerebral blood flow in the ipsilateral ventrolateral thalamus in which corticothalamic connections from the motor and premotor areas predominate. The extent of pain alleviation also correlates with the increase of blood flow in the cingulate gyrus. This suggests that stimulation reduces the suffering experienced by a patient with chronic pain. Procedure-related morbidity has included epidural hematoma, subdural effusion, gradual diminution of benefit, and painful stimulation. Although of concern, treatment-induced chronic seizure disorders have not occurred as a complication or in animal models of chronic cortical stimulation. Stimulation-induced pain relief occurs within minutes. There are no associated paresthesias or muscle contractions that confirm function. Pain relief may last for hours after electrical stimulation is discontinued. Motor cortex stimulation is an established therapy for the treatment of complex central and neuropathic pain syndromes that have proved refractory to medical treatment.
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41

Millichap, J. Gordon. "Double Cortex Syndrome." Pediatric Neurology Briefs 13, no. 3 (March 1, 1999): 17. http://dx.doi.org/10.15844/pedneurbriefs-13-3-1.

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42

Reiss, George R., David M. Dulaney, and Jill Ness. "BIMANUAL CORTEX REMOVAL." Ophthalmic Surgery, Lasers and Imaging Retina 25, no. 9 (September 1994): 659–60. http://dx.doi.org/10.3928/1542-8877-19940901-22.

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43

Nieder, Andreas. "Consciousness without cortex." Current Opinion in Neurobiology 71 (December 2021): 69–76. http://dx.doi.org/10.1016/j.conb.2021.09.010.

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44

Naito, Yasushi. "Human vestibular cortex." Rinsho Shinkeigaku 51, no. 11 (2011): 1096. http://dx.doi.org/10.5692/clinicalneurol.51.1096.

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45

Nishiike, Suetaka, and Yoshiharu Sakata. "The Vestibular Cortex." Equilibrium Research 61, no. 2 (2002): 71–77. http://dx.doi.org/10.3757/jser.61.71.

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46

Swash, M. "The Motor Cortex." Journal of Neurology, Neurosurgery & Psychiatry 53, no. 7 (July 1, 1990): 627. http://dx.doi.org/10.1136/jnnp.53.7.627-a.

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47

Albin, R. L. "The Motor Cortex." Neurology 40, no. 5 (May 1, 1990): 869. http://dx.doi.org/10.1212/wnl.40.5.869-a.

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48

Buchsbaum, Monte S. "Frontal Cortex Function." American Journal of Psychiatry 161, no. 12 (December 2004): 2178. http://dx.doi.org/10.1176/appi.ajp.161.12.2178.

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49

Janeš, Ivona. "Insular Cortex - Review." Gyrus 3, no. 2 (2015): 108–14. http://dx.doi.org/10.17486/gyr.3.1023.

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50

Markus, Annette. "Folding the cortex." Nature Neuroscience 6, no. 12 (December 2003): 1249. http://dx.doi.org/10.1038/nn1203-1249.

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