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Results: 1-22 |
Results: 22
Origin of deficits in the flicker electroretinogram of the cone system in X-linked retinoschisis as derived from response nonlinearities
Authors: Alexander, KR Barnes, CS Fishman, GA
Citation: Kr. Alexander et al., Origin of deficits in the flicker electroretinogram of the cone system in X-linked retinoschisis as derived from response nonlinearities, J OPT SOC A, 18(4), 2001, pp. 747-754
Perceived and actual performance of daily tasks: Relationship to visual function tests in individuals with retinitis pigmentosa
Authors: Szlyk, JP Seiple, W Fishman, GA Alexander, KR Grover, S Mahler, CL
Citation: Jp. Szlyk et al., Perceived and actual performance of daily tasks: Relationship to visual function tests in individuals with retinitis pigmentosa, OPHTHALMOL, 108(1), 2001, pp. 65-75
High-frequency attenuation of the cone ERG and ON-response deficits in X-linked retinoschisis
Authors: Alexander, KR Barnes, CS Fishman, GA
Citation: Kr. Alexander et al., High-frequency attenuation of the cone ERG and ON-response deficits in X-linked retinoschisis, INV OPHTH V, 42(9), 2001, pp. 2094-2101
An analysis of allelic variation in the ABCA4 gene
Authors: Webster, AR Heon, E Lotery, AJ Vandenburgh, K Casavant, TL Oh, KT Beck, G Fishman, GA Lam, BL Levin, A Heckenlively, JR Jacobson, SG Weleber, RG Sheffield, VC Stone, EM
Citation: Ar. Webster et al., An analysis of allelic variation in the ABCA4 gene, INV OPHTH V, 42(6), 2001, pp. 1179-1189
ON-response deficit in the electroretinogram of the cone system in X-linked retinoschisis
Authors: Alexander, KR Fishman, GA Barnes, CS Grover, S
Citation: Kr. Alexander et al., ON-response deficit in the electroretinogram of the cone system in X-linked retinoschisis, INV OPHTH V, 42(2), 2001, pp. 453-459
CORD9 a new locus for arCRD: Mapping to 8p11, estimation of frequency, evaluation of a candidate gene
Authors: Danciger, M Hendrickson, J Lyon, J Toomes, C McHale, JC Fishman, GA Inglehearn, CF Jacobson, SG Farber, DB
Citation: M. Danciger et al., CORD9 a new locus for arCRD: Mapping to 8p11, estimation of frequency, evaluation of a candidate gene, INV OPHTH V, 42(11), 2001, pp. 2458-2465
Contrast discrimination deficits in retinitis pigmentosa are greater for stimuli that favor the magnocellular pathway
Authors: Alexander, KR Pokorny, J Smith, VC Fishman, GA Barnes, CS
Citation: Kr. Alexander et al., Contrast discrimination deficits in retinitis pigmentosa are greater for stimuli that favor the magnocellular pathway, VISION RES, 41(5), 2001, pp. 671-683
Mutations in the CRB1 gene cause Leber congenital amaurosis
Authors: Lotery, AJ Jacobson, SG Fishman, GA Weleber, RG Fulton, AB Namperumalsamy, P Heon, E Levin, AV Grover, S Rosenow, JR Kopp, KK Sheffield, VC Stone, EM
Citation: Aj. Lotery et al., Mutations in the CRB1 gene cause Leber congenital amaurosis, ARCH OPHTH, 119(3), 2001, pp. 415-420
Retinal findings in melanoma-associated retinopathy
Authors: Borkowski, LM Grover, S Fishman, GA Jampol, LM
Citation: Lm. Borkowski et al., Retinal findings in melanoma-associated retinopathy, AM J OPHTH, 132(2), 2001, pp. 273-275
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate
Authors: Haider, NB Jacobson, SG Cideciyan, AV Swiderski, R Streb, LM Searby, C Beck, G Hockey, R Hanna, DB Gorman, S Duhl, D Carmi, R Bennett, J Weleber, RG Fishman, GA Wright, AF Stone, EM Sheffield, VC
Citation: Nb. Haider et al., Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate, NAT GENET, 24(2), 2000, pp. 127-131
A longitudinal study of visual function in carriers of X-linked recessive retinitis pigmentosa
Authors: Grover, S Fishman, GA Anderson, RJ Lindeman, M
Citation: S. Grover et al., A longitudinal study of visual function in carriers of X-linked recessive retinitis pigmentosa, OPHTHALMOL, 107(2), 2000, pp. 386-396
Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosa
Authors: Jacobson, SG Cideciyan, AV Iannaccone, A Weleber, RG Fishman, GA Maguire, AM Affatigato, LM Bennett, J Pierce, EA Danciger, M Farber, DB Stone, EM
Citation: Sg. Jacobson et al., Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosa, INV OPHTH V, 41(7), 2000, pp. 1898-1908
Allelic variation in the VMD2 gene in best disease and age-related maculardegeneration
Authors: Lotery, AJ Munier, FL Fishman, GA Weleber, RG Jacobson, SG Affatigato, LM Nichols, BE Schorderet, DF Sheffield, VC Stone, EM
Citation: Aj. Lotery et al., Allelic variation in the VMD2 gene in best disease and age-related maculardegeneration, INV OPHTH V, 41(6), 2000, pp. 1291-1296
Psychological profiles of patients with central vision loss
Authors: Szlyk, JP Becker, JE Fishman, GA Seiple, W
Citation: Jp. Szlyk et al., Psychological profiles of patients with central vision loss, J VIS IMP B, 94(12), 2000, pp. 781-786
Temporal frequency deficits in the electroretinogram of the cone system inX-linked retinoschisis
Authors: Alexander, KR Fishman, GA Grover, S
Citation: Kr. Alexander et al., Temporal frequency deficits in the electroretinogram of the cone system inX-linked retinoschisis, VISION RES, 40(20), 2000, pp. 2861-2868
Mutation analysis of 3 genes in patients with leber congenital amaurosis
Authors: Lotery, AJ Namperumalsamy, P Jacobson, SG Weleber, RG Fishman, GA Musarella, MA Hoyt, CS Heon, E Levin, A Jan, J Lam, B Carr, RE Franklin, A Radha, S Andorf, JL Sheffield, VC Stone, EM
Citation: Aj. Lotery et al., Mutation analysis of 3 genes in patients with leber congenital amaurosis, ARCH OPHTH, 118(4), 2000, pp. 538-543
Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or older
Authors: Grover, S Fishman, GA Anderson, RJ Tozatti, MSV Heckenlively, JR Weleber, RG Edwards, AO Brown, J
Citation: S. Grover et al., Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or older, OPHTHALMOL, 106(9), 1999, pp. 1780-1785
Screening of the gene encoding the alpha '-subunit of cone cGMP-PDE in patients with retinal degenerations
Authors: Gao, YQ Danciger, M Longmuir, R Piriev, NI Zhao, DY Heckenlively, JR Fishman, GA Weleber, RG Jacobson, SG Stone, EM Farber, DB
Citation: Yq. Gao et al., Screening of the gene encoding the alpha '-subunit of cone cGMP-PDE in patients with retinal degenerations, INV OPHTH V, 40(8), 1999, pp. 1818-1822
Coherence and the judgment of spatial displacements in retinitis pigmentosa
Authors: Alexander, KR Derlacki, DJ Fishman, GA
Citation: Kr. Alexander et al., Coherence and the judgment of spatial displacements in retinitis pigmentosa, VISION RES, 39(13), 1999, pp. 2267-2274
Variation of clinical expression in patients with Stargardt dystrophy and sequence variations in the ABCR gene
Authors: Fishman, GA Stone, EM Grover, S Derlacki, DJ Haines, HL Hockey, RR
Citation: Ga. Fishman et al., Variation of clinical expression in patients with Stargardt dystrophy and sequence variations in the ABCR gene, ARCH OPHTH, 117(4), 1999, pp. 504-510
X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60
Authors: Fishman, GA Grover, S Jacobson, SG Alexander, KR Derlacki, DJ Wu, WP Buraczynska, M Swaroop, A
Citation: Ga. Fishman et al., X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60, OPHTHALMOL, 105(12), 1998, pp. 2286-2296
Difficulty in performing everyday activities in patients with juvenile macular dystrophies: comparison with patients with retinitis pigmentosa
Authors: Szlyk, JP Fishman, GA Grover, S Revelins, BI Derlacki, DJ
Citation: Jp. Szlyk et al., Difficulty in performing everyday activities in patients with juvenile macular dystrophies: comparison with patients with retinitis pigmentosa, BR J OPHTH, 82(12), 1998, pp. 1372-1376
Risultati: 1-22 |