Phase-encoded retinotopy as an evaluation of diffuse optical neuroimaging

NeuroImage

Volumn 49, Issue 1, 2010, Pages 568-577

  White, Brian R ^a,b   Culver, Joseph P ^a,b  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b WASHINGTON UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BRAIN DEPTH STIMULATION; BRAIN FUNCTION; CONTRAST ENHANCEMENT; DECISION MAKING; FEMALE; FUNCTIONAL MAGNETIC RESONANCE IMAGING; HEMISPHERE; HUMAN; HUMAN EXPERIMENT; IMAGE PROCESSING; IMAGE RECONSTRUCTION; MALE; NEUROIMAGING; NON INVASIVE MEASUREMENT; NORMAL HUMAN; OPTICAL TOMOGRAPHY; POSITRON EMISSION TOMOGRAPHY; PRIORITY JOURNAL; RETINOSCOPY; SIGNAL NOISE RATIO; VISUAL CORTEX;

ADULT; ALGORITHMS; BRAIN MAPPING; FEMALE; FOURIER ANALYSIS; FUNCTIONAL LATERALITY; HUMANS; IMAGE PROCESSING, COMPUTER-ASSISTED; INDIVIDUALITY; MAGNETIC RESONANCE IMAGING; MALE; PHOTIC STIMULATION; RETINA; TOMOGRAPHY, OPTICAL; VISUAL CORTEX; VISUAL FIELDS; YOUNG ADULT;

EID: 70349976069     PISSN: 10538119     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuroimage.2009.07.023     Document Type: Article

References (39)

1. Benaron D.A., Hintz S.R., et al. Noninvasive functional imaging of human brain using light. J. Cereb. Blood Flow. Metab. 20 (2000) 469-477
2. Bluestone A.Y., Abdoulaev G., et al. Three-dimensional optical tomography of hemodynamics in the human head. Opt. Express 9 (2001) 272-286
3. Boas D.A., Chen K., et al. Improving the diffuse optical imaging spatial resolution of the cerebral hemodynamic response to brain activation in humans. Opt. Lett. 29 (2004) 1506-1508
4. Colier W., Quaresima V., et al. Simultaneous near-infrared spectroscopy monitoring of left and right occipital areas reveals contra-lateral hemodynamic changes upon hemi-field paradigm. Vision Res. 41 (2001) 97-102
5. Dehghani H., Pogue B.W., et al. Multiwavelength three-dimensional near-infrared tomography of the breast: initial simulation, phantom, and clinical results. Appl. Opt. 42 (2003) 135-145
6. Dehghani H., White B.R., et al. Depth sensitivity and image reconstruction analysis of dense imaging arrays for mapping brain function with diffuse optical tomography. Appl. Opt. 48 (2009) D137-D143
7. DeYoe E.A., Bandettini P., et al. Functional magnetic resonance imaging (FMRI) of the human brain. J. Neurosci. Methods 54 (1994) 171-187
8. DeYoe E.A., Carman G.J., et al. Mapping striate and extrastriate visual areas in human cerebral cortex. Proc. Natl. Acad. Sci. U. S. A. 93 (1996) 2382-2386
9. Dougherty R.F., Koch V.M., et al. Visual field representations and locations of visual areas V1/2/3 in human visual cortex. J. Vision 3 (2003) 586-598
10. Engel S.A., Rumelhart D.E., et al. fMRI of human visual cortex. Nature 369 (1994) 525
11. Engel S.A., Glover G.H., et al. Retinotopic organization in human visual cortex and the spatial precision of functional MRI. Cereb. Cortex 7 (1997) 181-192
12. Fox P.T., Miezin F.M., et al. Retinotopic organization of human visual cortex mapped with positron-emission tomography. J. Neurosci. 7 (1987) 913-922
13. Gratton G., Corballis P.M., et al. Shades of gray matter: noninvasive optical images of human brain responses during visual stimulation. Psychophysiology 32 (1995) 505-509
14. Hebden J.C., Gibson A., et al. Three-dimensional optical tomography of the premature infant brain. Phys. Med. Biol. 47 (2002) 4155-4166
15. Heiskala J., Hiltunen P., et al. Significance of background optical properties, time-resolved information and optode arrangement in diffuse optical imaging of term neonates. Phys. Med. Biol. 54 (2009) 535-554
16. Joseph D.K., Huppert T.J., et al. Diffuse optical tomography system to image brain activation with improved spatial resolution and validation with functional magnetic resonance imaging. Appl. Opt. 45 (2006) 8142-8151
17. Kang H.C., Burgund E.D., et al. Comparison of functional activation foci in children and adults using a common stereotactic space. Neuroimage 19 (2003) 16-28
18. Karen T., Morren G., et al. Hemodynamic response to visual stimulation in newborn infants using functional near-infrared spectroscopy. Hum. Brain Mapp. 29 (2008) 453-460
19. Plichta M.M., and Herrmann M.J. Event-related functional near-infrared spectroscopy (fNIRS): are the measurements reliable?. Neuroimage 31 (2006) 116-124
20. Saager R., and Berger A. Measurement of layer-like hemodynamic trends in scalp and cortex: implications for physiological baseline suppression in functional near-infrared spectroscopy. J. Biomed. Opt. 13 (2008) 034017
21. Saager R.B., and Berger A.J. Direct characterization and removal of interfering absorption trends in two-layer turbid media. J. Opt. Soc. Am. A 22 (2005) 1874-1882
22. Schroeter M.L., Bucheler M.M., et al. Towards a standard analysis for functional near-infrared imaging. Neuroimage 21 (2004) 283-290
23. Selb J., Franceschini M.A., et al. Improved sensitivity to cerebral hemodynamics during brain activation with a time-gated optical system: analytical model and experimental validation. J. Biomed. Opt. 10 (2005) 011013
24. Sereno M.I., McDonald C.T., et al. Analysis of retinotopic maps in extrastriate cortex. Cereb. Cortex 6 (1994) 601-620
25. Sereno M.I., Dale A.M., et al. Borders of multiple visual areas in humans revealed by functional magnetic-resonance-imaging. Science 268 (1995) 889-893
26. Steinbrink J., Wabnitz H., et al. Determining changes in NIR absorption using a layered model of the human head. Phys. Med. Biol. 46 (2001) 879-896
27. Stensaas S.S., Eddington D.K., et al. The topography and variability of the primary visual cortex in man. J. Neurosurg. 40 (1974) 747-755
28. Taga G., Asakawa K., et al. Brain imaging in awake infants by near-infrared optical topography. Proc. Natl. Acad. Sci. U. S. A. 100 (2003) 10722-10727
29. Tootell R.B.H., Mendola J.D., et al. Functional analysis of V3A and related areas in human visual cortex. J. Neurosci. 17 (1997) 7060-7078
30. Tootell R.B.H., Hadjikhani N.K., et al. Functional analysis of primary visual cortex (V1) in humans. Proc. Natl. Acad. Sci. U. S. A. 95 (1998) 811-817
31. Tootell R.B.H., and Hadjikhani N.K. Where is 'Dorsal V4' in human visual cortex? Retinotopic, topographic and functional evidence. Cereb. Cortex 11 (2001) 298-311
32. Toronov V.Y., Zhang X., et al. A spatial and temporal comparison of hemodynamic signals measured using optical and functional magnetic resonance imaging during activation in the human primary visual cortex. Neuroimage 34 (2007) 1136-1148
33. Van Essen D.C., Anderson C.H., et al. Information processing in the primate visual system: an integrated systems perspective. Science 255 (1992) 419-423
34. Wandell B.A., and Wade A.R. Functional imaging of the visual pathways. Neurol. Clin. N. Am. 21 (2003) 417-443
35. Wandell B.A., Brewer A.A., et al. Visual field map clusters in human cortex. Phil. Trans. R. Soc. B. 360 (2005) 693-707
36. Warnking J., Dojat M., et al. fMRI retinotopic mapping-step by step. Neuroimage 17 (2002) 1665-1683
37. Wylie G.R., Graber H., et al. Using co-variation in the Hb signal to detect visual activation: a near infrared spectroscopy study. Neuroimage 47 (2009) 473-481
38. Yodh A.G., and Boas D.A. Functional imaging with diffusing light. In: Vo-Dinh T. (Ed). Biomedical Photonics (2003), CRC Press, Boca Raton 21-1-21-45
39. Zeff B.W., White B.R., et al. Retinotopic mapping of adult human visual cortex with high-density diffuse optical tomography. Proc. Natl. Acad. Sci. U. S. A. 104 (2007) 12169-12174