User menu

Cerebellar Clustering and Functional Connectivity During Pain Processing.

Bibliographic reference Diano, Matteo ; D'Agata, Federico ; Cauda, Franco ; Costa, Tommaso ; Geda, Elisabetta ; et. al. Cerebellar Clustering and Functional Connectivity During Pain Processing.. In: The Cerebellum : an international journal from neurosciences to clinical perspectives, Vol. 15, no. 3, p. 346-356 (2016)
Permanent URL
  1. STOODLEY C, SCHMAHMANN J, Functional topography in the human cerebellum: A meta-analysis of neuroimaging studies, 10.1016/j.neuroimage.2008.08.039
  2. Saab Carl Y., Willis William D., The cerebellum: organization, functions and its role in nociception, 10.1016/s0165-0173(03)00151-6
  3. Ruscheweyh Ruth, Kühnel Maria, Filippopulos Filipp, Blum Bernhard, Eggert Thomas, Straube Andreas, Altered experimental pain perception after cerebellar infarction : , 10.1016/j.pain.2014.04.006
  4. Duerden Emma G., Albanese Marie-Claire, Localization of pain-related brain activation: A meta-analysis of neuroimaging data, 10.1002/hbm.21416
  5. Mehack R., Torgerson W. S., On the Language of Pain : , 10.1097/00000542-197101000-00017
  6. Ngamkham Srisuda, Vincent Catherine, Finnegan Lorna, Holden Janean E., Wang Zaijie Jim, Wilkie Diana J., The McGill Pain Questionnaire as a Multidimensional Measure in People with Cancer: An Integrative Review, 10.1016/j.pmn.2010.12.003
  7. De Gagné Théo A., Mikail Samuel F., DʼEon Joyce L., Confirmatory factor analysis of a 4-factor model of chronic pain evaluation : , 10.1016/0304-3959(94)00114-t
  8. Melzack Ronald, The McGill Pain Questionnaire: Major properties and scoring methods : , 10.1016/0304-3959(75)90044-5
  9. Moulton Eric A., Schmahmann Jeremy D., Becerra Lino, Borsook David, The cerebellum and pain: Passive integrator or active participator?, 10.1016/j.brainresrev.2010.05.005
  10. Ito Masao, Bases and implications of learning in the cerebellum — adaptive control and internal model mechanism, Progress in Brain Research (2005) ISBN:9780444517548 p.95-109, 10.1016/s0079-6123(04)48009-1
  11. CARRIVE PASCAL, MORGAN MICHAEL M., Periaqueductal Gray, The Human Nervous System (2004) ISBN:9780125476263 p.393-423, 10.1016/b978-012547626-3/50013-2
  12. Benarroch E. E., Periaqueductal gray: An interface for behavioral control, 10.1212/wnl.0b013e31823fcdee
  13. Kong Jian, Loggia Marco L., Zyloney Carolyn, Tu Peichi, LaViolette Peter, Gollub Randy L., Exploring the brain in pain: Activations, deactivations and their relation : , 10.1016/j.pain.2009.11.008
  14. Linnman Clas, Beucke Jan-Carl, Jensen Karin B., Gollub Randy L., Kong Jian, Sex similarities and differences in pain-related periaqueductal gray connectivity : , 10.1016/j.pain.2011.11.006
  15. Sillery Emma, Bittar Richard G., Robson Matthew D., Behrens Timothy E. J., Stein John, Aziz Tipu Z., Johansen-Berg Heidi, Connectivity of the human periventricular—periaqueductal gray region, 10.3171/jns.2005.103.6.1030
  16. Kong Jian, Tu Pei-chi, Zyloney Carolyn, Su Tung-ping, Intrinsic functional connectivity of the periaqueductal gray, a resting fMRI study, 10.1016/j.bbr.2010.03.042
  17. Linnman Clas, Moulton Eric A., Barmettler Gabi, Becerra Lino, Borsook David, Neuroimaging of the periaqueductal gray: State of the field, 10.1016/j.neuroimage.2011.11.095
  18. Cauda Franco, Costa Tommaso, Diano Matteo, Sacco Katiuscia, Duca Sergio, Geminiani Giuliano, Torta Diana M.E., Massive Modulation of Brain Areas After Mechanical Pain Stimulation: A Time-Resolved fMRI Study, 10.1093/cercor/bht153
  19. Mayhew Stephen D., Hylands-White Nicholas, Porcaro Camillo, Derbyshire Stuart W.G., Bagshaw Andrew P., Intrinsic variability in the human response to pain is assembled from multiple, dynamic brain processes, 10.1016/j.neuroimage.2013.02.028
  20. Moulton E. A., Pendse G., Becerra L. R., Borsook D., BOLD Responses in Somatosensory Cortices Better Reflect Heat Sensation than Pain, 10.1523/jneurosci.0006-12.2012
  21. Oldfield R.C., The assessment and analysis of handedness: The Edinburgh inventory, 10.1016/0028-3932(71)90067-4
  22. Baumgartner U., Iannetti G. D., Zambreanu L., Stoeter P., Treede R.-D., Tracey I., Multiple Somatotopic Representations of Heat and Mechanical Pain in the Operculo-Insular Cortex: A High-Resolution fMRI Study, 10.1152/jn.00253.2010
  23. Miezin F.M., Maccotta L., Ollinger J.M., Petersen S.E., Buckner R.L., Characterizing the Hemodynamic Response: Effects of Presentation Rate, Sampling Procedure, and the Possibility of Ordering Brain Activity Based on Relative Timing, 10.1006/nimg.2000.0568
  24. Talairach J, Tournoux P. Co-planar stereotaxic atlas of the human brain: 3-dimensional proportional system: an approach to cerebral imaging. New York: Thieme; 1988.
  25. Smolders Alain, De Martino Federico, Staeren Noël, Scheunders Paul, Sijbers Jan, Goebel Rainer, Formisano Elia, Dissecting cognitive stages with time-resolved fMRI data: a comparison of fuzzy clustering and independent component analysis, 10.1016/j.mri.2007.02.018
  26. Bezdek James C., Ehrlich Robert, Full William, FCM: The fuzzy c-means clustering algorithm, 10.1016/0098-3004(84)90020-7
  27. Fadili M.J., Ruan S., Bloyet D., Mazoyer B., A multistep Unsupervised Fuzzy Clustering Analysis of fMRI time series, 10.1002/1097-0193(200008)10:4<160::aid-hbm20>;2-u
  28. Golay Xavier, Kollias Spyros, Stoll Gautier, Meier Dieter, Valavanis Anton, Boesiger Peter, A new correlation-based fuzzy logic clustering algorithm for FMRI, 10.1002/mrm.1910400211
  29. Esposito Fabrizio, Scarabino Tommaso, Hyvarinen Aapo, Himberg Johan, Formisano Elia, Comani Silvia, Tedeschi Gioacchino, Goebel Rainer, Seifritz Erich, Di Salle Francesco, Independent component analysis of fMRI group studies by self-organizing clustering, 10.1016/j.neuroimage.2004.10.042
  30. Cauda Franco, Geminiani Giuliano, D'Agata Federico, Sacco Katiuscia, Duca Sergio, Bagshaw Andrew P., Cavanna Andrea E., Functional Connectivity of the Posteromedial Cortex, 10.1371/journal.pone.0013107
  31. Goebel Rainer, Esposito Fabrizio, Formisano Elia, Analysis of functional image analysis contest (FIAC) data with brainvoyager QX: From single-subject to cortically aligned group general linear model analysis and self-organizing group independent component analysis, 10.1002/hbm.20249
  32. Forman Steven D., Cohen Jonathan D., Fitzgerald Mark, Eddy William F., Mintun Mark A., Noll Douglas C., Improved Assessment of Significant Activation in Functional Magnetic Resonance Imaging (fMRI): Use of a Cluster-Size Threshold, 10.1002/mrm.1910330508
  33. Cauda Franco, D'Agata Federico, Sacco Katiuscia, Duca Sergio, Geminiani Giuliano, Vercelli Alessandro, Functional connectivity of the insula in the resting brain, 10.1016/j.neuroimage.2010.11.049
  34. Friston K., Statistical parametric mapping, Statistical Parametric Mapping (2007) ISBN:9780123725608 p.10-31, 10.1016/b978-012372560-8/50002-4
  35. Fox Peter T., Lancaster Jack L., OPINIONMapping context and content: the BrainMap model, 10.1038/nrn789
  36. Lancaster Jack L., Laird Angela R., Eickhoff Simon B., Martinez Michael J., Fox P. Mickle, Fox Peter T., Automated regional behavioral analysis for human brain images, 10.3389/fninf.2012.00023
  37. Eickhoff Simon B., Laird Angela R., Grefkes Christian, Wang Ling E., Zilles Karl, Fox Peter T., Coordinate-based activation likelihood estimation meta-analysis of neuroimaging data: A random-effects approach based on empirical estimates of spatial uncertainty, 10.1002/hbm.20718
  38. Fox Peter T., Laird Angela R., Fox Sarabeth P., Fox P. Mickle, Uecker Angela M., Crank Michelle, Koenig Sandra F., Lancaster Jack L., Brainmap taxonomy of experimental design: Description and evaluation, 10.1002/hbm.20141
  39. Eickhoff Simon B., Bzdok Danilo, Laird Angela R., Kurth Florian, Fox Peter T., Activation likelihood estimation meta-analysis revisited, 10.1016/j.neuroimage.2011.09.017
  40. Kochunov P., Lancaster J., Thompson P., Toga A.W., Brewer P., Hardies J., Fox P., An Optimized Individual Target Brain in the Talairach Coordinate System, 10.1006/nimg.2002.1084
  41. Peyron R., Laurent B., García-Larrea L., Functional imaging of brain responses to pain. A review and meta-analysis (2000), 10.1016/s0987-7053(00)00227-6
  42. T�lle Thomas R., Kaufmann Tanja, Siessmeier Thomas, Lautenbacher Stefan, Berthele Achim, Munz Frank, Zieglg�nsberger Walter, Willoch Frode, Schwaiger Markus, Conrad Bastian, Bartenstein Peter, Region-specific encoding of sensory and affective components of pain in the human brain: A positron emission tomography correlation analysis, 10.1002/1531-8249(199901)45:1<40::aid-art8>;2-l
  43. Veldhuijzen Dieuwke S., Nemenov Michael I., Keaser Michael, Zhuo Jiachen, Gullapalli Rao P., Greenspan Joel D., Differential brain activation associated with laser-evoked burning and pricking pain: An event-related fMRI study : , 10.1016/j.pain.2008.10.027
  44. Wager Tor D., Atlas Lauren Y., Lindquist Martin A., Roy Mathieu, Woo Choong-Wan, Kross Ethan, An fMRI-Based Neurologic Signature of Physical Pain, 10.1056/nejmoa1204471
  45. Coghill RC, Sang CN, Maisog JM, Iadarola MJ. Pain intensity processing within the human brain: a bilateral, distributed mechanism. J Neurophysiol. 1999;82:1934–43.
  46. Kong Jian, White Nathan S., Kwong Kenneth K., Vangel Mark G., Rosman Ilana S., Gracely Richard H., Gollub Randy L., Using fMRI to dissociate sensory encoding from cognitive evaluation of heat pain intensity, 10.1002/hbm.20213
  47. Baliki M. N., Geha P. Y., Apkarian A. V., Parsing Pain Perception Between Nociceptive Representation and Magnitude Estimation, 10.1152/jn.91100.2008
  48. Asplund Christopher L, Todd J Jay, Snyder Andy P, Marois René, A central role for the lateral prefrontal cortex in goal-directed and stimulus-driven attention, 10.1038/nn.2509
  49. Fox Michael D., Raichle Marcus E., Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging, 10.1038/nrn2201
  50. Mobbs D., Petrovic P., Marchant J. L., Hassabis D., Weiskopf N., Seymour B., Dolan R. J., Frith C. D., When Fear Is Near: Threat Imminence Elicits Prefrontal-Periaqueductal Gray Shifts in Humans, 10.1126/science.1144298
  51. Bud Craig A. D., Significance of the insula for the evolution of human awareness of feelings from the body : Insula and awareness, 10.1111/j.1749-6632.2011.05990.x
  52. Mesmoudi Salma, Perlbarg Vincent, Rudrauf David, Messe Arnaud, Pinsard Basile, Hasboun Dominique, Cioli Claudia, Marrelec Guillaume, Toro Roberto, Benali Habib, Burnod Yves, Resting State Networks' Corticotopy: The Dual Intertwined Rings Architecture, 10.1371/journal.pone.0067444
  53. Bernard Jessica A., Seidler Rachael D., Hassevoort Kelsey M., Benson Bryan L., Welsh Robert C., Wiggins Jillian Lee, Jaeggi Susanne M., Buschkuehl Martin, Monk Christopher S., Jonides John, Peltier Scott J., Resting state cortico-cerebellar functional connectivity networks: a comparison of anatomical and self-organizing map approaches, 10.3389/fnana.2012.00031
  54. Buckner R. L., Krienen F. M., Castellanos A., Diaz J. C., Yeo B. T. T., The organization of the human cerebellum estimated by intrinsic functional connectivity, 10.1152/jn.00339.2011
  55. Habas C., Kamdar N., Nguyen D., Prater K., Beckmann C. F., Menon V., Greicius M. D., Distinct Cerebellar Contributions to Intrinsic Connectivity Networks, 10.1523/jneurosci.1868-09.2009
  56. Krienen Fenna M., Buckner Randy L., Segregated Fronto-Cerebellar Circuits Revealed by Intrinsic Functional Connectivity, 10.1093/cercor/bhp135
  57. Stoodley CJ, Valera EM, Schmahmann JD. Functional topography of the cerebellum for motor and cognitive tasks: an fMRI study. Neuroimage. 2011;59:1560–70. doi: 10.1016/j.neuroimage.2011.08.065 .
  58. Legrain Valéry, Iannetti Gian Domenico, Plaghki Léon, Mouraux André, The pain matrix reloaded, 10.1016/j.pneurobio.2010.10.005
  59. Simons Laura E., Moulton Eric A., Linnman Clas, Carpino Elizabeth, Becerra Lino, Borsook David, The human amygdala and pain: Evidence from neuroimaging : Human Amygdala and Pain, 10.1002/hbm.22199
  60. Moulton E. A., Elman I., Pendse G., Schmahmann J., Becerra L., Borsook D., Aversion-Related Circuitry in the Cerebellum: Responses to Noxious Heat and Unpleasant Images, 10.1523/jneurosci.6709-10.2011
  61. Baumann Oliver, Mattingley Jason B., Functional topography of primary emotion processing in the human cerebellum, 10.1016/j.neuroimage.2012.03.044
  62. Sacchetti B., Scelfo B., Strata P., Cerebellum and emotional behavior, 10.1016/j.neuroscience.2009.01.064
  63. Schienle A., Scharmüller W., Cerebellar activity and connectivity during the experience of disgust and happiness, 10.1016/j.neuroscience.2013.04.048
  64. Stoodley Catherine J., Valera Eve M., Schmahmann Jeremy D., Functional topography of the cerebellum for motor and cognitive tasks: An fMRI study, 10.1016/j.neuroimage.2011.08.065
  65. Adamaszek M., D’Agata F., Kirkby K. C., Trenner M. U., Sehm B., Steele C. J., Berneiser J., Strecker K., Impairment of Emotional Facial Expression and Prosody Discrimination Due to Ischemic Cerebellar Lesions, 10.1007/s12311-013-0537-0
  66. Damasio A. R., Everitt B. J., Bishop D., The Somatic Marker Hypothesis and the Possible Functions of the Prefrontal Cortex [and Discussion], 10.1098/rstb.1996.0125