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Results: 1-13 |
Results: 13
Pattern electroretinography (PERG) and an integrated approach to visual pathway diagnosis
Authors: Holder, GE
Citation: Ge. Holder, Pattern electroretinography (PERG) and an integrated approach to visual pathway diagnosis, PROG RET EY, 20(4), 2001, pp. 531-561
Optical coherence tomography and electrophysiology in X-linked juvenile retinoschisis associated with a novel mutation in the XLRS1 gene
Authors: Stanga, PE Chong, NHV Reck, AC Hardcastle, AJ Holder, GE
Citation: Pe. Stanga et al., Optical coherence tomography and electrophysiology in X-linked juvenile retinoschisis associated with a novel mutation in the XLRS1 gene, RETINA, 21(1), 2001, pp. 78-80
Electrophysiological abnormalities following intravitreal vitravene (ISIS 2922) in two patients with CMV retinitis
Authors: Zambarakji, HJ Mitchell, SM Lightman, S Holder, GE
Citation: Hj. Zambarakji et al., Electrophysiological abnormalities following intravitreal vitravene (ISIS 2922) in two patients with CMV retinitis, BR J OPHTH, 85(9), 2001, pp. 1142-1142
Phenotypic subtypes of Stargardt macular dystrophy-fundus flavimaculatus
Authors: Lois, N Holder, GE Bunce, C Fitzke, FW Bird, AC
Citation: N. Lois et al., Phenotypic subtypes of Stargardt macular dystrophy-fundus flavimaculatus, ARCH OPHTH, 119(3), 2001, pp. 359-369
Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1
Authors: Downes, SM Payne, AM Kelsell, RE Fitzke, FW Holder, GE Hunt, DM Moore, AT Bird, AC
Citation: Sm. Downes et al., Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1, ARCH OPHTH, 119(11), 2001, pp. 1667-1673
Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1
Authors: Downes, SM Holder, GE Fitzke, FW Payne, AM Warren, MJ Bhattacharya, SS Bird, AC
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
Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclase
Authors: Gregory-Evans, K Kelsell, RE Gregory-Evans, CY Downes, SM Fitzke, FW Holder, GE Simunovic, M Mollon, JD Taylor, R Hunt, DM Bird, AC Moore, AT
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
Visual prognostic value of the pattern electroretinogram in chiasmal compression
Authors: Parmar, DN Sofat, A Bowman, R Bartlett, JR Holder, GE
Citation: Dn. Parmar et al., Visual prognostic value of the pattern electroretinogram in chiasmal compression, BR J OPHTH, 84(9), 2000, pp. 1024-1026
Intrafamilial variation of phenotype in Stargardt macular dystrophy-Fundusflavimaculatus
Authors: Lois, N Holder, GE Fitzke, FW Plant, C Bird, AC
Citation: N. Lois et al., Intrafamilial variation of phenotype in Stargardt macular dystrophy-Fundusflavimaculatus, INV OPHTH V, 40(11), 1999, pp. 2668-2675
S-cone ERGs elicited by a simple technique in normals and in tritanopes
Authors: Arden, G Wolf, J Berninger, T Hogg, CR Tzekov, R Holder, GE
Citation: G. Arden et al., S-cone ERGs elicited by a simple technique in normals and in tritanopes, VISION RES, 39(3), 1999, pp. 641-650
Clinical features of codon 172 RDS macular dystrophy - Similar phenotype in 12 families
Authors: Downes, SM Fitzke, FW Holder, GE Payne, AM Bessant, DAR Bhattacharya, SS Bird, AC
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
Duane's retraction syndrome and juvenile Batten's disease: A new association?
Authors: Marshman, WE Lee, JP Jones, B Schalit, G Holder, GE
Citation: We. Marshman et al., Duane's retraction syndrome and juvenile Batten's disease: A new association?, AUS NZ J OP, 26(3), 1998, pp. 251-254
Electrophysiological findings in dominant optic atrophy (DOA) linking to the OPA1 locus on chromosome 3q 28-qter
Authors: Holder, GE Votruba, M Carter, AC Bhattacharya, SS Fitzke, FW Moore, AT
Citation: Ge. Holder et al., Electrophysiological findings in dominant optic atrophy (DOA) linking to the OPA1 locus on chromosome 3q 28-qter, DOC OPHTHAL, 95(3-4), 1998, pp. 217-228
Risultati: 1-13 |