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Citation: Sm. Downes et al., Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1, ARCH OPHTH, 119(1), 2001, pp. 96-105
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Citation: Mc. Westcott et al., Response time prolongation for a motion stimulus in patients with glaucomaand its relationship with elevation of the motion threshold, J GLAUCOMA, 9(4), 2000, pp. 289-295
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Citation: Df. Garway-heath et al., Mapping the visual field to the optic disc in normal tension glaucoma eyes, OPHTHALMOL, 107(10), 2000, pp. 1809-1815
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Citation: K. Gregory-evans et al., Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclase, OPHTHALMOL, 107(1), 2000, pp. 55-61
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Citation: Df. Garway-heath et al., Scaling the hill of vision: The physiological relationship between light sensitivity and ganglion cell numbers, INV OPHTH V, 41(7), 2000, pp. 1774-1782
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Citation: Ds. Kamal et al., Use of sequential Heidelberg retina tomograph images to identify changes at the optic disc in ocular hypertensive patients at risk of developing glaucoma, BR J OPHTH, 84(9), 2000, pp. 993-998
Citation: N. Lois et al., Quantitative evaluation of fundus autofluorescence imaged "in vivo" in eyes with retinal disease, BR J OPHTH, 84(7), 2000, pp. 741-745
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Citation: Wl. Membrey et al., Comparison of visual field progression in patients with normal pressure glaucoma between eyes with and without visual field loss that threatens fixation, BR J OPHTH, 84(10), 2000, pp. 1154-1158
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Citation: Xl. Zhang et al., High-titer recombinant adeno-associated virus production from replicating amplicons and herpes vectors deleted for glycoprotein H, HUM GENE TH, 10(15), 1999, pp. 2527-2537
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Citation: A. Von Ruckmann et al., Autofluorescence of the retinal pigment epithelium in patients with central serous chorioretinopathy, OPHTHALMOLO, 96(1), 1999, pp. 6-10
Citation: A. Von Ruckmann et al., Distribution of pigment epithelium autofluorescence in retinal disease state recorded in vivo and its change over time, GR ARCH CL, 237(1), 1999, pp. 1-9
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Lois, N
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Citation: N. Lois et al., Intrafamilial variation of phenotype in Stargardt macular dystrophy-Fundusflavimaculatus, INV OPHTH V, 40(11), 1999, pp. 2668-2675
Authors:
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Citation: Mc. Westcott et al., Characteristics of frequency-of-seeing curves for a motion stimulus in glaucoma eyes, glaucoma suspect eyes, and normal eyes, VISION RES, 39(3), 1999, pp. 631-639
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Citation: N. Lois et al., Reproducibility of fundus autofluorescence measurements obtained using a confocal scanning laser ophthalmoscope, BR J OPHTH, 83(3), 1999, pp. 276-279
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Citation: Ac. Viswanathan et al., Severity and stability of glaucoma - Patient perception compared with objective measurement, ARCH OPHTH, 117(4), 1999, pp. 450-454
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Citation: Sm. Downes et al., Clinical features of codon 172 RDS macular dystrophy - Similar phenotype in 12 families, ARCH OPHTH, 117(10), 1999, pp. 1373-1383