메뉴 건너뛰기




Volumn 2013, Issue , 2013, Pages

Multimodal imaging in hereditary retinal diseases

Author keywords

[No Author keywords available]

Indexed keywords


EID: 84877958074     PISSN: 2090004X     EISSN: 20900058     Source Type: Journal    
DOI: 10.1155/2013/634351     Document Type: Article
Times cited : (24)

References (37)
  • 2
    • 40449094820 scopus 로고    scopus 로고
    • Fundus autofluorescence imaging: Review and perspectives
    • DOI 10.1097/IAE.0b013e318164a907, PII 0000698220080300000002
    • Schmitz-Valckenberg S., Holz F. G., Bird A. C., Spaide R. F., Fundus autofluorescence imaging: review and perspectives. Retina 2008 28 3 385 409 2-s2.0-40449094820 10.1097/IAE.0b013e318164a907 (Pubitemid 351354940)
    • (2008) Retina , vol.28 , Issue.3 , pp. 385-409
    • Schmitz-Valckenberg, S.1    Holz, F.G.2    Bird, A.C.3    Spaide, R.F.4
  • 3
    • 84862843405 scopus 로고    scopus 로고
    • Perivenular whitening in central vein occlusion described by fundus autofluorescence and spectral domain optical coherence tomography
    • Pichi F., Morara M., Veronese C., Lembo A., Nucci P., Ciardella A. P., Perivenular whitening in central vein occlusion described by fundus autofluorescence and spectral domain optical coherence tomography. Retina 2012 32 7 1438 1439
    • (2012) Retina , vol.32 , Issue.7 , pp. 1438-1439
    • Pichi, F.1    Morara, M.2    Veronese, C.3    Lembo, A.4    Nucci, P.5    Ciardella, A.P.6
  • 4
    • 0029655876 scopus 로고    scopus 로고
    • Infrared imaging of sub-retinal structures in the human ocular fundus
    • Elsner A. E., Burns S. A., Weiter J. J., Delori F. C., Infrared imaging of sub-retinal structures in the human ocular fundus. Vision Research 1996 36 1 191 205 2-s2.0-0029655876 (Pubitemid 126755364)
    • (1996) Vision Research , vol.36 , Issue.1 , pp. 191-205
    • Elsner, A.E.1    Burns, S.A.2    Weiter, J.J.3    Delori, F.C.4
  • 5
    • 84865801444 scopus 로고    scopus 로고
    • Swelling of the arcuate nerve fiber layer after internal limiting membrane peeling
    • Clark A., Balducci N., Pichi F., Veronese C., Morara M., Torrazza C., Ciardella A. P., Swelling of the arcuate nerve fiber layer after internal limiting membrane peeling. Retina 2012 32 8 1608 1613
    • (2012) Retina , vol.32 , Issue.8 , pp. 1608-1613
    • Clark, A.1    Balducci, N.2    Pichi, F.3    Veronese, C.4    Morara, M.5    Torrazza, C.6    Ciardella, A.P.7
  • 6
    • 0029824808 scopus 로고    scopus 로고
    • Pre-injection fluorescence in indocyanine green angiography
    • Piccolino F. C., Borgia L., Zinicola E., Iester M., Torrielli S., Pre-injection fluorescence in indocyanine green angiography. Ophthalmology 1996 103 11 1837 1845 2-s2.0-0029824808 (Pubitemid 26403737)
    • (1996) Ophthalmology , vol.103 , Issue.11 , pp. 1837-1845
    • Piccolino, F.C.1    Borgia, L.2    Zinicola, E.3    Iester, M.4    Torrielli, S.5
  • 7
    • 78649900356 scopus 로고    scopus 로고
    • Clinical evaluation of simultaneous confocal scanning laser ophthalmoscopy imaging combined with high-resolution, spectral-domain optical coherence tomography
    • 2-s2.0-78649900356 10.1111/j.1755-3768.2009.01602.x
    • Helb H. M., Issa P. C., Fleckenstein M., Schmitz-Valckenberg S., Scholl H. P. N., Meyer C. H., Eter N., Holz F. G., Clinical evaluation of simultaneous confocal scanning laser ophthalmoscopy imaging combined with high-resolution, spectral-domain optical coherence tomography. Acta Ophthalmologica 2010 88 8 842 849 2-s2.0-78649900356 10.1111/j.1755-3768.2009.01602.x
    • (2010) Acta Ophthalmologica , vol.88 , Issue.8 , pp. 842-849
    • Helb, H.M.1    Issa, P.C.2    Fleckenstein, M.3    Schmitz-Valckenberg, S.4    Scholl, H.P.N.5    Meyer, C.H.6    Eter, N.7    Holz, F.G.8
  • 8
    • 84859107213 scopus 로고    scopus 로고
    • A spectral-domain optical coherence tomography description of ND: YAG laser hyaloidotomy in premacular subhyaloid hemorrhage
    • Pichi F., Ciardella A. P., Torrazza C., Morara M., Scano G., Mattana G., Nucci P., A spectral-domain optical coherence tomography description of ND: YAG laser hyaloidotomy in premacular subhyaloid hemorrhage. Retina 2012 32 4 861 862
    • (2012) Retina , vol.32 , Issue.4 , pp. 861-862
    • Pichi, F.1    Ciardella, A.P.2    Torrazza, C.3    Morara, M.4    Scano, G.5    Mattana, G.6    Nucci, P.7
  • 10
    • 0021850103 scopus 로고
    • Multilocus linkage analysis in humans: Detection of linkage and estimation of recombination
    • Lathrop G. M., Lalouel J. M., Julier C., Ott J., Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. American Journal of Human Genetics 1985 37 3 482 498 2-s2.0-0021850103 (Pubitemid 15046057)
    • (1985) American Journal of Human Genetics , vol.37 , Issue.3 , pp. 482-498
    • Lathrop, G.M.1    Lalouel, J.M.2    Julier, C.3    Ott, J.4
  • 11
    • 33748472782 scopus 로고    scopus 로고
    • Analysis of retinal flecks in fundus flavimaculatus using optical coherence tomography
    • DOI 10.1136/bjo.2006.094136
    • Querques G., Leveziel N., Benhamou N., Voigt M., Soubrane G., Souied E. H., Analysis of retinal flecks in fundus flavimaculatus using optical coherence tomography. British Journal of Ophthalmology 2006 90 9 1157 1162 2-s2.0-33748472782 10.1136/bjo.2006.094136 (Pubitemid 44351149)
    • (2006) British Journal of Ophthalmology , vol.90 , Issue.9 , pp. 1157-1162
    • Querques, G.1    Leveziel, N.2    Benhamou, N.3    Voigt, M.4    Soubrane, G.5    Souied, E.H.6
  • 13
    • 84907113514 scopus 로고
    • North Carolina macular dystrophy (MCDR1): A review and refined mapping to 6q14-q16.2
    • Small K. W., Weber J., Roses A., Pericak-Vance P., North Carolina macular dystrophy (MCDR1): a review and refined mapping to 6q14-q16.2. Ophthalmic Paediatrics and Genetics 1993 14 4 143 150 2-s2.0-0027842816 (Pubitemid 24116575)
    • (1993) Ophthalmic Paediatrics and Genetics , vol.14 , Issue.4 , pp. 143-150
    • Small, K.W.1    Weber, J.2    Roses, A.3    Pericak-Vance, P.4
  • 14
    • 0026710901 scopus 로고
    • North Carolina macular dystrophy is assigned to chromosome 6
    • 2-s2.0-0026710901 10.1016/0888-7543(92)90141-E
    • Small K. W., Weber J. L., Roses A., Lennon F., Vance J. M., Pericak-Vance M. A., North Carolina macular dystrophy is assigned to chromosome 6. Genomics 1992 13 3 681 685 2-s2.0-0026710901 10.1016/0888-7543(92)90141-E
    • (1992) Genomics , vol.13 , Issue.3 , pp. 681-685
    • Small, K.W.1    Weber, J.L.2    Roses, A.3    Lennon, F.4    Vance, J.M.5    Pericak-Vance, M.A.6
  • 15
    • 70349456645 scopus 로고    scopus 로고
    • A reappraisal of the clinical spectrum of North Carolina macular dystrophy
    • 2-s2.0-70349456645 10.1016/j.ophtha.2009.03.028
    • Khurana R. N., Sun X., Pearson E., Yang Z., Harmon J., Goldberg M. F., Zhang K., A reappraisal of the clinical spectrum of North Carolina macular dystrophy. Ophthalmology 2009 116 10 1976 1983 2-s2.0-70349456645 10.1016/j.ophtha.2009.03.028
    • (2009) Ophthalmology , vol.116 , Issue.10 , pp. 1976-1983
    • Khurana, R.N.1    Sun, X.2    Pearson, E.3    Yang, Z.4    Harmon, J.5    Goldberg, M.F.6    Zhang, K.7
  • 18
    • 84867341462 scopus 로고    scopus 로고
    • Fundus autofluorescence patterns in stargardt disease over time
    • Smith R. T., Fundus autofluorescence patterns in stargardt disease over time. Archives of Ophthalmology 2012 130 10 1354 1355
    • (2012) Archives of Ophthalmology , vol.130 , Issue.10 , pp. 1354-1355
    • Smith, R.T.1
  • 22
    • 84863483494 scopus 로고    scopus 로고
    • Choroideremia: A review of general findings and pathogenesis
    • Coussa R. G., Traboulsi E. I., Choroideremia: a review of general findings and pathogenesis. Ophthalmic Genetics 2012 33 2 57 65
    • (2012) Ophthalmic Genetics , vol.33 , Issue.2 , pp. 57-65
    • Coussa, R.G.1    Traboulsi, E.I.2
  • 23
    • 78649256487 scopus 로고    scopus 로고
    • Microperimetry and OCT findings in female carriers of choroideremia
    • 2-s2.0-78649256487 10.3109/13816810.2010.518578
    • Thobani A., Anastasakis A., Fishman G. A., Microperimetry and OCT findings in female carriers of choroideremia. Ophthalmic Genetics 2010 31 4 235 239 2-s2.0-78649256487 10.3109/13816810.2010.518578
    • (2010) Ophthalmic Genetics , vol.31 , Issue.4 , pp. 235-239
    • Thobani, A.1    Anastasakis, A.2    Fishman, G.A.3
  • 24
    • 67349105082 scopus 로고    scopus 로고
    • Fundus autofluorescence in carriers of choroideremia and correlation with electrophysiologic and psychophysical data
    • 2-s2.0-67349105082 10.1016/j.ophtha.2009.01.016
    • Preising M. N., Wegscheider E., Friedburg C., Poloschek C. M., Wabbels B. K., Lorenz B., Fundus autofluorescence in carriers of choroideremia and correlation with electrophysiologic and psychophysical data. Ophthalmology 2009 116 6 1201.e2 1209.e2 2-s2.0-67349105082 10.1016/j.ophtha.2009.01.016
    • (2009) Ophthalmology , vol.116 , Issue.6
    • Preising, M.N.1    Wegscheider, E.2    Friedburg, C.3    Poloschek, C.M.4    Wabbels, B.K.5    Lorenz, B.6
  • 26
    • 33750991867 scopus 로고    scopus 로고
    • Genotype-phenotype correlation and longitudinal course in ten families with Best vitelliform macular dystrophy
    • DOI 10.1007/s00417-006-0286-6
    • Wabbels B., Preising M. N., Kretschmann U., Demmler A., Lorenz B., Genotype-phenotype correlation and longitudinal course in ten families with Best vitelliform macular dystrophy. Graefe's Archive for Clinical and Experimental Ophthalmology 2006 244 11 1453 1466 2-s2.0-33750991867 10.1007/s00417-006-0286-6 (Pubitemid 44741257)
    • (2006) Graefe's Archive for Clinical and Experimental Ophthalmology , vol.244 , Issue.11 , pp. 1453-1466
    • Wabbels, B.1    Preising, M.N.2    Kretschmann, U.3    Demmler, A.4    Lorenz, B.5
  • 27
    • 33747149304 scopus 로고    scopus 로고
    • Vitelliform macular dystrophy
    • 2-s2.0-33747149304
    • Spaide R. F., Noble K., Morgan A., Freund K. B., Vitelliform macular dystrophy. Ophthalmology 2006 113 8 1392 1400 2-s2.0-33747149304
    • (2006) Ophthalmology , vol.113 , Issue.8 , pp. 1392-1400
    • Spaide, R.F.1    Noble, K.2    Morgan, A.3    Freund, K.B.4
  • 29
    • 0033739625 scopus 로고    scopus 로고
    • Bestrophin, the product of the Best vitelliform macular dystrophy gene (VMD2), localizes to the basolateral plasma membrane of the retinal pigment epithelium
    • 2-s2.0-0033739625 10.1073/pnas.220402097
    • Marmorstein A. D., Marmorstein L. Y., Rayborn M., Wang X., Hollyfield J. G., Petrukhin K., Bestrophin, the product of the Best vitelliform macular dystrophy gene (VMD2), localizes to the basolateral plasma membrane of the retinal pigment epithelium. Proceedings of the National Academy of Sciences of the United States of America 2000 97 23 12758 12763 2-s2.0-0033739625 10.1073/pnas.220402097
    • (2000) Proceedings of the National Academy of Sciences of the United States of America , vol.97 , Issue.23 , pp. 12758-12763
    • Marmorstein, A.D.1    Marmorstein, L.Y.2    Rayborn, M.3    Wang, X.4    Hollyfield, J.G.5    Petrukhin, K.6
  • 30
    • 0028927183 scopus 로고
    • Enhanced S cone syndrome: Svidence for an abnormally large number of S cones
    • 2-s2.0-0028927183 10.1016/0042-6989(95)98727-Q
    • Hood D. C., Cideciyan A. V., Roman A. J., Jacobson S. G., Enhanced S cone syndrome: svidence for an abnormally large number of S cones. Vision Research 1995 35 10 1473 1481 2-s2.0-0028927183 10.1016/0042-6989(95)98727-Q
    • (1995) Vision Research , vol.35 , Issue.10 , pp. 1473-1481
    • Hood, D.C.1    Cideciyan, A.V.2    Roman, A.J.3    Jacobson, S.G.4
  • 31
    • 0027437720 scopus 로고
    • Enhanced S cone sensitivity syndrome: Long-term follow-up, electrophysiological and psychophysical findings
    • Kellner U., Zrenner E., Sadowski B., Foerster M. H., Enhanced S cone sensitivity syndrome: long-term follow-up, electrophysiological and psychophysical findings. Clinical Vision Sciences 1993 8 5 425 434 2-s2.0-0027437720 (Pubitemid 23355721)
    • (1993) Clinical Vision Sciences , vol.8 , Issue.5 , pp. 425-434
    • Kellner, U.1    Zrenner, E.2    Sadowski, B.3    Foerster, M.H.4
  • 33
    • 0033033364 scopus 로고    scopus 로고
    • Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatus
    • DOI 10.1038/9707
    • Yamamoto H., Simon A., Eriksson U., Harris E., Berson E. L., Dryja T. P., Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatus. Nature Genetics 1999 22 2 188 191 2-s2.0-0033033364 10.1038/9707 (Pubitemid 29264816)
    • (1999) Nature Genetics , vol.22 , Issue.2 , pp. 188-191
    • Yamamoto, H.1    Simon, A.2    Eriksson, U.3    Harris, E.4    Berson, E.L.5    Dryja, T.P.6
  • 34
    • 70249134052 scopus 로고    scopus 로고
    • Cellular origin of fundus autofluorescence in patients and mice with a defective NR2E3 gene
    • 2-s2.0-70249134052 10.1136/bjo.2008.153577
    • Wang N. K., Fine H. F., Chang S., Chou C. L., Cella W., Tosi J., Lin C. S., Nagasaki T., Tsang S. H., Cellular origin of fundus autofluorescence in patients and mice with a defective NR2E3 gene. British Journal of Ophthalmology 2009 93 9 1234 1240 2-s2.0-70249134052 10.1136/bjo.2008.153577
    • (2009) British Journal of Ophthalmology , vol.93 , Issue.9 , pp. 1234-1240
    • Wang, N.K.1    Fine, H.F.2    Chang, S.3    Chou, C.L.4    Cella, W.5    Tosi, J.6    Lin, C.S.7    Nagasaki, T.8    Tsang, S.H.9
  • 35
    • 78650178490 scopus 로고    scopus 로고
    • Lack of autofluorescence in fundus albipunctatus associated with mutations in RDH5
    • 2-s2.0-78650178490 10.1097/IAE.0b013e3181dc050a
    • Schatz P., Preising M., Lorenz B., Sander B., Larsen M., Eckstein C., Rosenberg T., Lack of autofluorescence in fundus albipunctatus associated with mutations in RDH5. Retina 2010 30 10 1704 1713 2-s2.0-78650178490 10.1097/IAE.0b013e3181dc050a
    • (2010) Retina , vol.30 , Issue.10 , pp. 1704-1713
    • Schatz, P.1    Preising, M.2    Lorenz, B.3    Sander, B.4    Larsen, M.5    Eckstein, C.6    Rosenberg, T.7
  • 36
    • 77952230956 scopus 로고    scopus 로고
    • Spectral-domain optical coherence tomography and fundus autofluorescence characteristics in patients with fundus albipunctatus and retinitis punctata albescens
    • 2-s2.0-77952230956 10.3109/13816810903584971
    • Genead M. A., Fishman G. A., Lindeman M., Spectral-domain optical coherence tomography and fundus autofluorescence characteristics in patients with fundus albipunctatus and retinitis punctata albescens. Ophthalmic Genetics 2010 31 2 66 72 2-s2.0-77952230956 10.3109/13816810903584971
    • (2010) Ophthalmic Genetics , vol.31 , Issue.2 , pp. 66-72
    • Genead, M.A.1    Fishman, G.A.2    Lindeman, M.3
  • 37
    • 65649105723 scopus 로고    scopus 로고
    • High-definition optical coherence tomographic visualization of photoreceptor layer and retinal flecks in fundus albipunctatus associated with cone dystrophy
    • 2-s2.0-65649105723
    • Querques G., Carrillo P., Querques L., Bux A. V., del Curatolo M. V., delle Noci N., High-definition optical coherence tomographic visualization of photoreceptor layer and retinal flecks in fundus albipunctatus associated with cone dystrophy. Archives of Ophthalmology 2009 127 5 703 706 2-s2.0-65649105723
    • (2009) Archives of Ophthalmology , vol.127 , Issue.5 , pp. 703-706
    • Querques, G.1    Carrillo, P.2    Querques, L.3    Bux, A.V.4    Del Curatolo, M.V.5    Delle Noci, N.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.