6 Diagnostic Capability of Optical Coherence Tomography …
157
8. D.J. Browning, C.M. Fraser, Intraobserver variability in optical coherence tomography. Am.
J. Ophthalmol. 138, 477–479 (2004)
9. A. Polito, M. Del Borrello, M. Isola, N. Zemella, F. Bandello, Repeatability and reproducibility
of fast macular thickness mapping with stratus optical coherence tomography. Arch. Ophthalmol. 123, 1330–1337 (2005)
10. M.G. Krzystolik, S.F. Strauber, L.P. Aiello, R.W. Beck, B.B. Berger, N.M. Bressler, D.J.
Browning, R.B. Chambers, R.P. Danis, M.D. Davis, A.R. Glassman, V.H. Gonzalez, P.B.
Greenberg, J.G. Gross, J.E. Kim, C. Kollman, Diabetic Retinopathy Clinical Research Network. Reproducibility of macular thickness and volume using Zeiss optical coherence tomography in patients with diabetic macular edema. Ophthalmology 114, 1520–1525 (2007)
11. P.F. Stetson, Z. Yehoshua, C.A. Garcia Filho, R. Portella Nunes, G. Gregori, P.J. Rosenfeld,
OCT minimum intensity as a predictor of geographic atrophy enlargement. Invest. Ophthalmol. Vis. Sci. 55(2), 792–800 (2014). https://doi.org/10.1167/iovs.13-13199
12. N.S. Abdelfattah, H. Zhang, D.S. Boyer, P.J. Rosenfeld, W.J. Feuer, G. Gregori, S.R. Sadda,
Drusen volume as a predictor of disease progression in patients with late age-related macular
degeneration in the fellow eye. Invest. Ophthalmol. Vis. Sci. 57(4), 1839–1846 (2016). https://
doi.org/10.1167/iovs.15-18572
13. E. Tatrai, M. Simo, A. Iljicsov, J. Nemeth, D. Cabrera Debuc, G.M. Somfai, In vivo evaluation
of retinal neurodegeneration in patients with multiple sclerosis. PLoS ONE 7(1), e30922
(2012). https://doi.org/10.1371/journal.pone.0030922
14. B.C. Chauhan, V.M. Danthurebandara, G.P. Sharpe, S. Demirel, C.A. Girkin, C.Y. Mardin,
A.F. Scheuerle, C.F. Burgoyne, Bruch’s membrane opening minimum rim width and retinal
nerve fiber layer thickness in a normal white population: a multicenter study. Ophthalmology
122(9), 1786–1794 (2015). https://doi.org/10.1016/j.ophtha.2015.06.001
15. H. Laviers, H. Zambarakji, Enhanced depth imaging-OCT of the choroid: a review of the
current literature. Graefes Arch. Clin. Exp. Ophthalmol. 252(12), 1871–1883 (2014). https://
doi.org/10.1007/s00417-014-2840-y. Epub 4 Nov 2014
16. B.E. Varga, W. Gao, K.L. Laurik, E. Tátrai, M. Simó, G.M. Somfai, D. Cabrera DeBuc,
Investigating tissue optical properties and texture descriptors of the retina in patients with
multiple sclerosis. PLoS One 30; 10(11), e0143711 (2015). https://doi.org/10.1371/journal.p
one.0143711. eCollection 2015
17. G.M. Somfai, E. Tátrai, L. Laurik, B.E. Varga, V. Ölvedy, W.E. Smiddy, R. Tchitnga, A.
Somogyi, D. Cabrera DeBuc, Fractal-based analysis of optical coherence tomography data to
quantify retinal tissue damage. BMC Bioinform. 15, 295 (2014)
18. D. Cabrera Fernández, H. Salinas, C.A. Puliafito, Automated detection of retinal layer structures on optical coherence tomography images. Opt. Express 13(25), 10200–10216 (2005)
19. N.R. Kim, S. Hong, J.H. Kim, S.S. Rho, G.J. Seong et al., Comparison of macular ganglion
cell complex thickness by Fourier-domain OCT in normal tension glaucoma and primary
open-angle glaucoma. J. Glaucoma 22(2), 133–139 (2013)
20. D. Cabrera DeBuc, G.M. Somfai, Early detection of retinal thickness changes in diabetes
using Optical Coherence Tomography. Med. Sci. Monit. 16, MT15–MT21 (2010)
21. H.W. van Dijk, F.D. Verbraak, P.H. Kok et al., Decreased retinal ganglion cell layer thickness
in patients with type 1 diabetes. Invest. Ophthalmol. Vis. Sci. 51, 3660–3665 (2010)
22. H.W. van Dijk, F.D. Verbraak, P.H.B. Kok et al., Early neurodegeneration in the retina of type
2 diabetic patients. Invest. Ophthalmol. Vis. Sci. 53, 2715–2719 (2012)
23. Z.Z. Nagy, M. Ecsedy, I. Kovács, Á. Takács, E. Tátrai, G.M. Somfai, D. Cabrera, DeBuc,
Macular morphology assessed by optical coherence tomography image segmentation after
femtosecond laser-assisted and standard cataract surgery. J. Cataract Refract. Surg. 38(6),
941–946 (2012). https://doi.org/10.1016/j.jcrs.2012.02.031.d
24. O. Altintas, P. Iseri, B. Ozkan, Y. Caglar, Correlation between retinal morphological and functional findings and clinical severity in Parkinson’s disease. Doc. Ophthalmol. 116, 137–146
(2008)
25. M.E. Hajee, W.F. March, D.R. Lazzaro, A.H. Wolintz, E.M. Shrier et al., Inner retinal layer
thinning in Parkinson disease. Arch. Ophthalmol. 127, 737–741 (2009)
157
8. D.J. Browning, C.M. Fraser, Intraobserver variability in optical coherence tomography. Am.
J. Ophthalmol. 138, 477–479 (2004)
9. A. Polito, M. Del Borrello, M. Isola, N. Zemella, F. Bandello, Repeatability and reproducibility
of fast macular thickness mapping with stratus optical coherence tomography. Arch. Ophthalmol. 123, 1330–1337 (2005)
10. M.G. Krzystolik, S.F. Strauber, L.P. Aiello, R.W. Beck, B.B. Berger, N.M. Bressler, D.J.
Browning, R.B. Chambers, R.P. Danis, M.D. Davis, A.R. Glassman, V.H. Gonzalez, P.B.
Greenberg, J.G. Gross, J.E. Kim, C. Kollman, Diabetic Retinopathy Clinical Research Network. Reproducibility of macular thickness and volume using Zeiss optical coherence tomography in patients with diabetic macular edema. Ophthalmology 114, 1520–1525 (2007)
11. P.F. Stetson, Z. Yehoshua, C.A. Garcia Filho, R. Portella Nunes, G. Gregori, P.J. Rosenfeld,
OCT minimum intensity as a predictor of geographic atrophy enlargement. Invest. Ophthalmol. Vis. Sci. 55(2), 792–800 (2014). https://doi.org/10.1167/iovs.13-13199
12. N.S. Abdelfattah, H. Zhang, D.S. Boyer, P.J. Rosenfeld, W.J. Feuer, G. Gregori, S.R. Sadda,
Drusen volume as a predictor of disease progression in patients with late age-related macular
degeneration in the fellow eye. Invest. Ophthalmol. Vis. Sci. 57(4), 1839–1846 (2016). https://
doi.org/10.1167/iovs.15-18572
13. E. Tatrai, M. Simo, A. Iljicsov, J. Nemeth, D. Cabrera Debuc, G.M. Somfai, In vivo evaluation
of retinal neurodegeneration in patients with multiple sclerosis. PLoS ONE 7(1), e30922
(2012). https://doi.org/10.1371/journal.pone.0030922
14. B.C. Chauhan, V.M. Danthurebandara, G.P. Sharpe, S. Demirel, C.A. Girkin, C.Y. Mardin,
A.F. Scheuerle, C.F. Burgoyne, Bruch’s membrane opening minimum rim width and retinal
nerve fiber layer thickness in a normal white population: a multicenter study. Ophthalmology
122(9), 1786–1794 (2015). https://doi.org/10.1016/j.ophtha.2015.06.001
15. H. Laviers, H. Zambarakji, Enhanced depth imaging-OCT of the choroid: a review of the
current literature. Graefes Arch. Clin. Exp. Ophthalmol. 252(12), 1871–1883 (2014). https://
doi.org/10.1007/s00417-014-2840-y. Epub 4 Nov 2014
16. B.E. Varga, W. Gao, K.L. Laurik, E. Tátrai, M. Simó, G.M. Somfai, D. Cabrera DeBuc,
Investigating tissue optical properties and texture descriptors of the retina in patients with
multiple sclerosis. PLoS One 30; 10(11), e0143711 (2015). https://doi.org/10.1371/journal.p
one.0143711. eCollection 2015
17. G.M. Somfai, E. Tátrai, L. Laurik, B.E. Varga, V. Ölvedy, W.E. Smiddy, R. Tchitnga, A.
Somogyi, D. Cabrera DeBuc, Fractal-based analysis of optical coherence tomography data to
quantify retinal tissue damage. BMC Bioinform. 15, 295 (2014)
18. D. Cabrera Fernández, H. Salinas, C.A. Puliafito, Automated detection of retinal layer structures on optical coherence tomography images. Opt. Express 13(25), 10200–10216 (2005)
19. N.R. Kim, S. Hong, J.H. Kim, S.S. Rho, G.J. Seong et al., Comparison of macular ganglion
cell complex thickness by Fourier-domain OCT in normal tension glaucoma and primary
open-angle glaucoma. J. Glaucoma 22(2), 133–139 (2013)
20. D. Cabrera DeBuc, G.M. Somfai, Early detection of retinal thickness changes in diabetes
using Optical Coherence Tomography. Med. Sci. Monit. 16, MT15–MT21 (2010)
21. H.W. van Dijk, F.D. Verbraak, P.H. Kok et al., Decreased retinal ganglion cell layer thickness
in patients with type 1 diabetes. Invest. Ophthalmol. Vis. Sci. 51, 3660–3665 (2010)
22. H.W. van Dijk, F.D. Verbraak, P.H.B. Kok et al., Early neurodegeneration in the retina of type
2 diabetic patients. Invest. Ophthalmol. Vis. Sci. 53, 2715–2719 (2012)
23. Z.Z. Nagy, M. Ecsedy, I. Kovács, Á. Takács, E. Tátrai, G.M. Somfai, D. Cabrera, DeBuc,
Macular morphology assessed by optical coherence tomography image segmentation after
femtosecond laser-assisted and standard cataract surgery. J. Cataract Refract. Surg. 38(6),
941–946 (2012). https://doi.org/10.1016/j.jcrs.2012.02.031.d
24. O. Altintas, P. Iseri, B. Ozkan, Y. Caglar, Correlation between retinal morphological and functional findings and clinical severity in Parkinson’s disease. Doc. Ophthalmol. 116, 137–146
(2008)
25. M.E. Hajee, W.F. March, D.R. Lazzaro, A.H. Wolintz, E.M. Shrier et al., Inner retinal layer
thinning in Parkinson disease. Arch. Ophthalmol. 127, 737–741 (2009)