Normal and abnormal fMRI activation patterns in the visual cortex after recovery from optic neuritis

NeuroImage

Volumn 33, Issue 4, 2006, Pages 1161-1168

  Levin, Netta ^a,b   Orlov, Tanya ^a   Dotan, Shlomo ^b   Zohary, Ehud ^a  

^a HEBREW UNIVERSITY OF JERUSALEM   (Israel)

^b HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BRAIN CORTEX; CELL STIMULATION; CLINICAL ARTICLE; CLINICAL ASSESSMENT; CONTROLLED STUDY; ELECTROENCEPHALOGRAM; FEMALE; FUNCTIONAL MAGNETIC RESONANCE IMAGING; HUMAN; MALE; OPTIC NEURITIS; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; VISUAL CORTEX;

ADULT; EVOKED POTENTIALS, VISUAL; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; OPTIC NEURITIS; RECOVERY OF FUNCTION; VISUAL CORTEX;

EID: 33750682379     PISSN: 10538119     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuroimage.2006.07.030     Document Type: Article

References (24)

1. Avidan G., Harel M., Hendler T., Ben-Bashat D., Zohary E., and Malach R. Contrast sensitivity in human visual areas and its relationship to object recognition. J. Neurophysiol. 87 (2002) 3102-3116
2. Baker C.I., Peli E., Knouf N., and Kanwisher N.G. Reorganization of visual processing in macular degeneration. J. Neurosci. 19 (2005) 614-648
3. Boynton G.M., Engel S.A., Glover G.H., and Heeger D.J. Linear systems analysis of functional magnetic resonance imaging in human V1. J. Neurosci. 16 (1996) 4207-4221
4. Darian-Smith C., and Gilbert C.D. Topographic reorganization in the striate cortex of the adult cat and monkey is cortically mediated. J. Neurosci. 15 (1995) 1631-1647
5. Durand A.C., and Gould G.M. A method of determining ocular dominance. JAMA 55 (1910) 369-370
6. Engel S.A., Glover G.H., and Wandell B.A. Retinotopic organization in human visual cortex and the spatial precision of functional MRI. Cereb. Cortex 7 (1997) 181-192
7. Forman S.D., Cohen J.D., Fitzgerald M., Eddy W.F., Mintun M.A., and Noll D.C. Improved assessment of significant activation in functional magnetic resonance imaging (fMRI): use of a cluster-size threshold. Magn. Reson. Med. 33 (1995) 636-647
8. Gareau P.J., Gati J.S., Menon R.S., Lee D., Rice G., Mitchell J.R., Mandelfino P., and Karlik S.J. Reduced visual evoked responses in multiple sclerosis patients with optic neuritis: comparison of functional magnetic resonance imaging and visual evoked potentials. Mult. Scler. 5 (1999) 161-164
9. Grill-Spector K., Kushnir T., Hendler T., Edelman S., Itzchak Y., and Malach R. A sequence of object-processing stages revealed by fMRI in the human occipital lobe. Hum. Brain Mapp. 6 (1998) 316-328
10. Grill-Spector K., Kushnir T., Edelman S., Avidan G., Itzchak Y., and Malach R. Differential processing of objects under various viewing conditions in the human lateral occipital complex. Neuron 24 (1999) 187-203
11. Halliday A.M., McDonald W.I., and Mushin J. Delayed visual evoked response in optic neuritis. Lancet 1 (1972) 982-985
12. Hickman S.J., Dalton C.M., Miller D.H., and Plant G.T. Management of acute optic neuritis. Lancet 360 (2002) 1953-1962
13. Langkilde A.R., Frederiksen J.L., Rostrup E., and Larsson H.B. Functional MRI of the visual cortex and visual testing in patients with previous optic neuritis. Eur. J. Neurol. 9 (2002) 277-286
14. Lerner Y., Hendler T., and Malach R. Object-completion effects in the human lateral occipital complex. Cereb. Cortex 12 (2002) 163-177
15. Malach R., Reppas J.B., Benson R.R., Kwong K.K., Jiang H., Kennedy W.A., Ledden P.J., Brady T.J., Rosen B.R., and Tootell R.B. Object-related activity revealed by functional magnetic resonance imaging in human occipital cortex. Proc. Natl. Acad. Sci. U. S. A. 92 (1995) 8135-8139
16. Merzenich M.M., Nelson R.J., Stryker M.P., Cynader M.S., Schoppmann A., and Zook J.M. Somatosensory cortical map changes following digit amputation in adult monkeys. J. Comp. Neurol. 224 (1984) 591-605
17. Pons T.P., Garraghty P.E., Ommaya A.K., Kaas J.H., Taub E., and Mishkin M. Massive cortical reorganization after sensory deafferentation in adult macaques. Science 252 (1991) 1857-1860
18. Rodriguez M., Siva A., Cross S.A., O'Brien P.C., and Kurland L.T. Optic neuritis: a population-based study in Olmsted County, Minnesota. Neurology 45 (1995) 244-250
19. Rombouts S.A., Lazeron R.H., Scheltens P., Uitdehaag B.M., Sprenger M., Valk J., and Barkhof F. Visual activation patterns in patients with optic neuritis: an fMRI pilot study. Neurology 50 (1998) 1896-1899
20. Toosy A.T., Werring D.J., Bullmore E.T., Plant G.T., Barker G.J., Miller D.H., and Thompson A.J. Functional magnetic resonance imaging of the cortical response to photic stimulation in humans following optic neuritis recovery. Neurosci. Lett. 330 (2002) 255-259
21. Toosy A.T., Hickman S.J., Miszkiel K.A., Jones S.J., Plant G.T., Altmann D.R., Barker G.J., Miller D.H., and Thompson A.J. Adaptive cortical plasticity in higher visual areas after acute optic neuritis. Ann. Neurol. 57 (2005) 622-633
22. Van Essen D.C., and Drury H.A. Structural and functional analyses of human cerebral cortex using a surface-based atlas. J. Neurosci. 17 (1997) 7079-7102
23. Wandell B.A. Computational neuroimaging of human visual cortex. Annu. Rev. Neurosci. 22 (1999) 145-173
24. Werring D.J., Bullmore E.T., Toosy A.T., Miller D.H., Barker G.J., MacManus D.G., Brammer M.J., Giampietro V.P., Brusa A., Brex P.A., Moseley I.F., Plant G.T., McDonald W.I., and Thompson A.J. Recovery from optic neuritis is associated with a change in the distribution of cerebral response to visual stimulation: a functional magnetic resonance imaging study. J. Neurol., Neurosurg. Psychiatry 68 (2000) 441-449