Search Results - "Fishman, G A"

Effects of chronic exposure to hydroxychloroquine or chloroquine on inner retinal structures by Pasadhika, S, Fishman, G A

“…Purpose To evaluate peripapillary retinal nerve fibre layer (RNFL) thickness and macular inner and outer retinal thickness using spectral domain optical…”
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The prevalence of cystoid macular oedema in retinitis pigmentosa patients determined by optical coherence tomography by Hajali, M, Fishman, G A, Anderson, R J

“…To determine the prevalence of cystoid macular oedema (CMO) in retinitis pigmentosa (RP) patients of various genetic subtypes using optical coherence…”
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The prevalence of cystoid macular oedema on optical coherence tomography in retinitis pigmentosa patients without cystic changes on fundus examination by Hajali, M, Fishman, G A

“…Purpose To determine the prevalence of cystoid macular oedema (CME) by optical coherence tomography (OCT) in retinitis pigmentosa (RP) patients with no…”
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Cystic macular oedema on spectral-domain optical coherence tomography in choroideremia patients without cystic changes on fundus examination by Genead, M A, Fishman, G A

“…Purpose To determine the prevalence of cystic macular oedema (CME) in patients with choroideremia (CHM) by using spectral-domain optical coherence tomography…”
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Selective thinning of the perifoveal inner retina as an early sign of hydroxychloroquine retinal toxicity by Pasadhika, S, Fishman, G A, Choi, D, Shahidi, M

“…Purpose To evaluate macular thickness profiles using spectral-domain optical coherence tomography (SDOCT) and image segmentation in patients with chronic…”
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Clinical value, normative retinal sensitivity values, and intrasession repeatability using a combined spectral domain optical coherence tomography scanning laser ophthalmoscope microperimeter by Anastasakis, A, McAnany, J J, Fishman, G A, Seiple, W H

“…Purpose To establish normative values for macular light sensitivity and to determine the intrasession fluctuation of perimetric responses using the OPKO/OTI…”
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Prevalence of cystic macular lesions in patients with Usher II syndrome by Walia, S, Fishman, G A, Hajali, M

“…Purpose To evaluate the prevalence of cystic macular lesions in patients with Usher II syndrome. Methods All Usher type II patients seen in the inherited eye…”
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Mutation of a nuclear receptor gene, NR2E3 , causes enhanced S cone syndrome, a disorder of retinal cell fate by Sheffield, Val C, Carmi, Rivka, Hockey, Robin, Haider, Neena B, Searby, Charles, Cideciyan, Artur V, Gorman, Susan, Streb, Luan M, Stone, Edwin M, Wright, Alan F, Hanna, David B, Swiderski, Ruth, Jacobson, Samuel G, Fishman, Gerald A, Bennett, Jean, Duhl, David, Beck, Gretel, Weleber, Richard G

“…Hereditary human retinal degenerative diseases usually affect the mature photoreceptor topography by reducing the number of cells through apoptosis, resulting…”
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Retinal nerve fibre layer thickness analysis in X-linked retinoschisis using Fourier-domain OCT by Genead, M A, Pasadhika, S, Fishman, G A

“…Purpose To evaluate the presence of retinal nerve fibre layer (RNFL) defects in patients with X-linked retinoschisis (XLRS) using high-speed, high-resolution,…”
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An Analysis of Allelic Variation in the ABCA4 Gene by Webster, Andrew R, Heon, Elise, Lotery, Andrew J, Vandenburgh, Kimberlie, Casavant, Thomas L, Oh, Kean T, Beck, Gretel, Fishman, Gerald A, Lam, Byron L, Levin, Alex, Heckenlively, John R, Jacobson, Samuel G, Weleber, Richard G, Sheffield, Val C, Stone, Edwin M

“…To assess the allelic variation of the ATP-binding transporter protein (ABCA4). A combination of single-strand conformation polymorphism (SSCP) and automated…”
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Retrospective, longitudinal, and cross sectional study of visual acuity impairment in choroideraemia by Roberts, M Flynn, Fishman, G A, Roberts, D K, Heckenlively, J R, Weleber, R G, Anderson, R J, Grover, S

“…Background/aims: Few studies have reported on the change in visual acuity (VA) in patients with choroideraemia. In order to determine the degree and rate of VA…”
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Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or older by Grover, S, Fishman, G A, Anderson, R J, Tozatti, M S, Heckenlively, J R, Weleber, R G, Edwards, A O, Brown, Jr, J

“…To determine the severity of visual acuity impairment in patients, age 45 years or older, with either isolated or identifiable genetic subtypes of retinitis…”
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Attainment of educational levels in patients with Leber's congenital amaurosis by Apushkin, M A, Fishman, G A

“…To assess the educational level attained by patients legally blind with Leber's congenital amaurosis (LCA). Cross-sectional assessment. None. Highest…”
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Allelic Variation in the VMD2 Gene in Best Disease and Age-Related Macular Degeneration by Lotery, Andrew J, Munier, Francis L, Fishman, Gerald A, Weleber, Richard G, Jacobson, Samuel G, Affatigato, Louisa M, Nichols, Brian E, Schorderet, Daniel F, Sheffield, Val C, Stone, Edwin M

“…To assess the allelic variation of the VMD2 gene in patients with Best disease and age-related macular degeneration (AMD). Three hundred twenty-one AMD…”
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Rate of visual field loss in retinitis pigmentosa by Grover, S, Fishman, G A, Anderson, R J, Alexander, K R, Derlacki, D J

“…The authors quantitate the rate of visual field loss in patients with retinitis pigmentosa as it relates to different clinical field phenotypes. Goldmann…”
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Disease Expression of RP1 Mutations Causing Autosomal Dominant Retinitis Pigmentosa by Jacobson, Samuel G, Cideciyan, Artur V, Iannaccone, Alessandro, Weleber, Richard G, Fishman, Gerald A, Maguire, Albert M, Affatigato, Louisa M, Bennett, Jean, Pierce, Eric A, Danciger, Michael, Farber, Debora B, Stone, Edwin M

“…To determine the disease expression in heterozygotes for mutations in the RP1 gene, a newly identified cause of autosomal dominant retinitis pigmentosa (adRP)…”
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Patterns of visual field progression in patients with retinitis pigmentosa by Grover, S, Fishman, G A, Brown, Jr, J

“…The purpose of the study was to determine whether distinct patterns of visual field progression are present in patients with retinitis pigmentosa (RP) and to…”
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Interocular amplitude differences of the full field electroretinogram in normal subjects by Rotenstreich, Y, Fishman, G A, Anderson, R J, Birch, D G

“…Aims: To determine the interocular amplitude response difference of the electroretinogram (ERG) in normal subjects. Methods: 79 subjects, without retinal…”
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Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population by Billingsley, Gail, Bin, Jenea, Fieggen, Karen J, Duncan, Jacque L, Gerth, Christina, Ogata, Koji, Wodak, Shoshana S, Traboulsi, Elias I, Fishman, Gerald A, Paterson, Andrew, Chitayat, David, Knueppel, Tanja, Millán, José M, Mitchell, Grant A, Deveault, Catherine, Héon, Elise

“…Bardet-Biedl syndrome is a pleiotropic disorder with 14 BBS genes identified. BBS1, BBS2, BBS4, BBS5, BBS7, BBS8, and BBS9 form a complex called the BBSome,…”
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Frequency of optic disc or parapapillary nerve fiber layer drusen in retinitis pigmentosa by Grover, S, Fishman, G A, Brown, Jr, J

“…To determine the frequency and characteristics of optic disc and parapapillary nerve fiber layer drusen in patients with retinitis pigmentosa and to attempt to…”
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