Fundus autofluorescence imaging of retinal dystrophies
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Thomas Theelen | Carel B. Hoyng | B. J. Klevering | J. Keunen | C. Hoyng | T. Theelen | C. Boon | Camiel J.F. Boon | B. Jeroen Klevering | Jan E.E. Keunen
[1] J. Kobrin,et al. Histopathology of Best's macular dystrophy. , 1982, Archives of ophthalmology.
[2] B. Wissinger,et al. MORPHOLOGY AND FUNCTIONAL CHARACTERISTICS IN ADULT VITELLIFORM MACULAR DYSTROPHY , 2004, Retina.
[3] H. Gin,et al. Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness. GEDIAM Group. , 1999, Ophthalmology.
[4] A. Bird,et al. Fundus autofluorescence in Stargardt macular dystrophy-fundus flavimaculatus. , 2004, American journal of ophthalmology.
[5] M. Kiyosawa,et al. Ciliary and retinal changes in myotonic dystrophy. , 1984, Archives of ophthalmology.
[6] B. Lorenz,et al. Phenotypes of 16 Stargardt macular dystrophy/fundus flavimaculatus patients with known ABCA4 mutations and evaluation of genotype–phenotype correlation , 2002, Graefe's Archive for Clinical and Experimental Ophthalmology.
[7] Jean Bennett,et al. Mutations in ABCA4 result in accumulation of lipofuscin before slowing of the retinoid cycle: a reappraisal of the human disease sequence. , 2004, Human molecular genetics.
[8] C K Dorey,et al. In vivo fluorescence of the ocular fundus exhibits retinal pigment epithelium lipofuscin characteristics. , 1995, Investigative ophthalmology & visual science.
[9] F W Fitzke,et al. In vivo fundus autofluorescence in macular dystrophies. , 1997, Archives of ophthalmology.
[10] Club Jules Gonin,et al. Graefe's archive for clinical and experimental ophthalmology , 1982 .
[11] T. Meigen,et al. Clinical findings in a multigeneration family with autosomal dominant central areolar choroidal dystrophy associated with an Arg195Leu mutation in the peripherin/RDS gene. , 2006, Archives of ophthalmology.
[12] M. Lavail,et al. Light and inherited retinal degeneration , 2006, British Journal of Ophthalmology.
[13] C. Wadelius,et al. Enhanced accumulation of A2E in individuals homozygous or heterozygous for mutations in BEST1 (VMD2). , 2007, Experimental eye research.
[14] E. R. Büchi,et al. Genetic heterogeneity in autosomal dominant pattern dystrophy of the retina. , 1996, Molecular vision.
[15] M. Boulton,et al. RPE lipofuscin and its role in retinal pathobiology. , 2005, Experimental eye research.
[16] A. Deutman,et al. The development of central areolar choroidal dystrophy , 1996, Graefe's Archive for Clinical and Experimental Ophthalmology.
[17] M. Małecki. Genetics of type 2 diabetes mellitus. , 2005, Diabetes research and clinical practice.
[18] B. J. Klevering,et al. Clinical and genetic heterogeneity in multifocal vitelliform dystrophy. , 2007, Archives of ophthalmology.
[19] A. Deutman,et al. Butterfly-shaped pigment dystrophy of the fovea. , 1970, Archives of ophthalmology.
[20] E. Rodriguez-Boulan,et al. The lipofuscin fluorophore A2E perturbs cholesterol metabolism in retinal pigment epithelial cells , 2007, Proceedings of the National Academy of Sciences.
[21] K. Nakanishi,et al. A2E, a fluorophore of RPE lipofuscin, can destabilize membrane. , 2006, Advances in experimental medicine and biology.
[22] J. Sparrow,et al. Blue light-induced apoptosis of A2E-containing RPE: involvement of caspase-3 and protection by Bcl-2. , 2001, Investigative ophthalmology & visual science.
[23] M. Metzker,et al. Identification of the gene responsible for Best macular dystrophy , 1998, Nature Genetics.
[24] G. Silvestri,et al. Fine localisation of the gene for central areolar choroidal dystrophy on chromosome 17p. , 1998, Journal of medical genetics.
[25] Sander R. Dubovy,et al. ADULT‐ONSET FOVEOMACULAR PIGMENT EPITHELIAL DYSTROPHY: Clinicopathologic Correlation of Three Cases , 2000, Retina.
[26] K. Nakanishi,et al. The lipofuscin fluorophore A2E mediates blue light-induced damage to retinal pigmented epithelial cells. , 2000, Investigative ophthalmology & visual science.
[27] J. Lupski,et al. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Starqardt macular dystrophy , 1997, Nature Genetics.
[28] B. Lorenz,et al. Fundus autofluorescence in children and teenagers with hereditary retinal diseases , 2005, Graefe's Archive for Clinical and Experimental Ophthalmology.
[29] J. Weiter,et al. Retinal pigment epithelial lipofuscin and melanin and choroidal melanin in human eyes. , 1986, Investigative ophthalmology & visual science.
[30] M. Nakagawa,et al. Retinal manifestations in mitochondrial diseases associated with mitochondrial DNA mutation. , 1998, Acta ophthalmologica Scandinavica.
[31] K. Freund,et al. Vitelliform macular dystrophy. , 2014, JAMA ophthalmology.
[32] D. Zack,et al. Butterfly-shaped pattern dystrophy: a genetic, clinical, and histopathological report. , 2002, Archives of ophthalmology.
[33] A. Bird,et al. Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 families. , 1999, Archives of ophthalmology.
[34] A. Deutman,et al. Autosomal dominant central areolar choroidal dystrophy caused by a mutation in codon 142 in the peripherin/RDS gene. , 1996, American journal of ophthalmology.
[35] S. Jockusch,et al. A2E-epoxides Damage DNA in Retinal Pigment Epithelial Cells , 2003, The Journal of Biological Chemistry.
[36] G. Travis,et al. Biosynthesis of a major lipofuscin fluorophore in mice and humans with ABCR-mediated retinal and macular degeneration. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[37] E. Stone,et al. Differential macular and peripheral expression of bestrophin in human eyes and its implication for best disease. , 2007, Investigative ophthalmology & visual science.
[38] Alexander Sumaroka,et al. In vivo dynamics of retinal injury and repair in the rhodopsin mutant dog model of human retinitis pigmentosa. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[39] K. Nakanishi,et al. A2E, a byproduct of the visual cycle , 2003, Vision Research.
[40] A. Bird,et al. Pattern ERG correlates of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity. , 2003, Investigative ophthalmology & visual science.
[41] B. S. Fine,et al. Patterned dystrophies of the retinal pigment epithelium. , 1977, Archives of ophthalmology.
[42] Hendrik P N Scholl,et al. Localized retinal electrophysiological and fundus autofluorescence imaging abnormalities in maternal inherited diabetes and deafness. , 2004, Investigative ophthalmology & visual science.
[43] U. Kellner,et al. Late onset is common in best macular dystrophy associated with VMD2 gene mutations. , 2005, Ophthalmology.
[44] Y. Jang,et al. Complement activation by photooxidation products of A2E, a lipofuscin constituent of the retinal pigment epithelium , 2006, Proceedings of the National Academy of Sciences.
[45] H. Burian,et al. Ocular changes in myotonic dystrophy. , 1967, American journal of ophthalmology.
[46] Vision Research , 1961, Nature.
[47] A. Bird,et al. Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity , 2006, British Journal of Ophthalmology.
[48] A. Deutman,et al. Pigment dispersion syndrome and pigmented pattern dystrophy of retinal pigment epithelium. , 1983, The British journal of ophthalmology.
[49] J. Weiter,et al. In vivo measurement of lipofuscin in Stargardt's disease--Fundus flavimaculatus. , 1995, Investigative ophthalmology & visual science.
[50] R. Radu,et al. Characterization of Native Retinal Fluorophores Involved in Biosynthesis of A2E and Lipofuscin-associated Retinopathies* , 2006, Journal of Biological Chemistry.
[51] M. Hawlina,et al. Fundus Autofluorescence Imaging in Best's Vitelliform Dystrophy , 2003, Klinische Monatsblatter fur Augenheilkunde.
[52] A. Pinckers. Patterned dystrophies of the retinal pigment epithelium. A review. , 1988, Ophthalmic paediatrics and genetics.
[53] J. Ott,et al. Genetic and phenotypic heterogeneity in pattern dystrophy , 2005, British Journal of Ophthalmology.
[54] S. Fine,et al. A histopathologic study of Best's macular dystrophy. , 1982, Archives of ophthalmology.
[55] A. Deutman,et al. Genetic heterogeneity of butterfly-shaped pigment dystrophy of the fovea. , 2003, Molecular vision.
[56] R. Fagan,et al. PATTERN DYSTROPHY OF THE PIGMENT EPITHELIUM , 1981, Retina.
[57] K. Nakanishi,et al. A2E, a fluorophore of RPE lipofuscin: can it cause RPE degeneration? , 2003, Advances in experimental medicine and biology.
[58] B. J. Klevering,et al. Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy simulating STGD1/fundus flavimaculatus , 2007, British Journal of Ophthalmology.
[59] R. L. Font,et al. Foveomacular vitelliform dystrophy, adult type. A clinicopathologic study including electron microscopic observations. , 1985, Ophthalmology.
[60] M. Katz,et al. Fluorophores of the human retinal pigment epithelium: separation and spectral characterization. , 1988, Experimental eye research.
[61] B. Lorenz,et al. Genotype-phenotype correlation and longitudinal course in ten families with Best vitelliform macular dystrophy , 2006, Graefe's Archive for Clinical and Experimental Ophthalmology.
[62] D. Birch,et al. Insights into the Function of Rim Protein in Photoreceptors and Etiology of Stargardt's Disease from the Phenotype in abcr Knockout Mice , 1999, Cell.
[63] E. Stone,et al. Late development of vitelliform lesions and flecks in a patient with best disease: clinicopathologic correlation. , 2005, Archives of ophthalmology.
[64] T. Aleman,et al. ABCA4-associated retinal degenerations spare structure and function of the human parapapillary retina. , 2005, Investigative ophthalmology & visual science.
[65] G. Fishman,et al. Histopathologic findings in Best's vitelliform macular dystrophy. , 1988, Archives of ophthalmology.
[66] A. Bird,et al. Distribution of pigment epithelium autofluorescence in retinal disease state recorded in vivo and its change over time , 1999, Graefe's Archive for Clinical and Experimental Ophthalmology.
[67] A. Edwards,et al. Peripherin/RDS and VMD2 mutations in macular dystrophies with adult-onset vitelliform lesion. , 2006, Molecular vision.
[68] P. Liao,et al. Stereoscopic Atlas of Macular Diseases. Diagnosis and Treatment , 1987, The Yale Journal of Biology and Medicine.
[69] T. Aleman,et al. Reduced-illuminance autofluorescence imaging in ABCA4-associated retinal degenerations. , 2007, Journal of the Optical Society of America. A, Optics, image science, and vision.
[70] C K Dorey,et al. Age-related accumulation and spatial distribution of lipofuscin in RPE of normal subjects. , 2001, Investigative ophthalmology & visual science.