A C Bird

Author PubWeight™ 346.02‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 An international classification and grading system for age-related maculopathy and age-related macular degeneration. The International ARM Epidemiological Study Group. Surv Ophthalmol 1995 10.05
2 Distribution of fundus autofluorescence with a scanning laser ophthalmoscope. Br J Ophthalmol 1995 3.62
3 A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy. Nat Genet 1999 3.32
4 X-linked retinitis pigmentosa. Br J Ophthalmol 1975 3.11
5 Tears of detached retinal pigment epithelium. Br J Ophthalmol 1981 3.08
6 A human homolog of yeast pre-mRNA splicing gene, PRP31, underlies autosomal dominant retinitis pigmentosa on chromosome 19q13.4 (RP11). Mol Cell 2001 3.07
7 A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p. Nat Genet 1993 2.97
8 Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa. Nat Genet 2000 2.82
9 Smoking and age related macular degeneration: the number of pack years of cigarette smoking is a major determinant of risk for both geographic atrophy and choroidal neovascularisation. Br J Ophthalmol 2006 2.67
10 Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28. Nature 1984 2.52
11 Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13). Hum Mol Genet 2001 2.48
12 RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections. J Med Genet 2003 2.45
13 Fundus autofluorescence in age-related macular disease imaged with a laser scanning ophthalmoscope. Invest Ophthalmol Vis Sci 1997 2.31
14 The development of neovascularization of senile disciform macular degeneration. Am J Ophthalmol 1973 2.17
15 Recent advances in the treatment of senile disciform macular degeneration by photocoagulation. Br J Ophthalmol 1974 2.14
16 In vivo fundus autofluorescence in macular dystrophies. Arch Ophthalmol 1997 2.10
17 Senile disciform macular degeneration in the second eye. Br J Ophthalmol 1977 2.07
18 Bilateral acute retinal necrosis. Br J Ophthalmol 1978 2.07
19 Phenotypic subtypes of Stargardt macular dystrophy-fundus flavimaculatus. Arch Ophthalmol 2001 2.04
20 Aging changes in Bruch's membrane. A histochemical and morphologic study. Ophthalmology 1990 1.99
21 Treatment of chronic macular edema with acetazolamide. Arch Ophthalmol 1988 1.90
22 A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa. Am J Hum Genet 1991 1.88
23 A clinical, psychophysical, and electroretinographic survey of patients with autosomal dominant retinitis pigmentosa. Br J Ophthalmol 1985 1.87
24 Mutations in the retinal guanylate cyclase (RETGC-1) gene in dominant cone-rod dystrophy. Hum Mol Genet 1998 1.84
25 A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1. Hum Mol Genet 1998 1.81
26 A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis pigmentosa. Hum Mol Genet 1992 1.80
27 A mutation in NRL is associated with autosomal dominant retinitis pigmentosa. Nat Genet 1999 1.79
28 A clinical study of the vascularity of senile disciform macular degeneration. Am J Ophthalmol 1973 1.77
29 Degenerative changes in a retina affected with autosomal dominant retinitis pigmentosa. Invest Ophthalmol Vis Sci 1989 1.75
30 Retinal pigment epithelial detachments in the elderly: classification and outcome. Br J Ophthalmol 1985 1.74
31 Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity. Br J Ophthalmol 2006 1.74
32 Pigment epithelial detachment in the elderly. Clinical differentiation, natural course and pathogenetic implications. Graefes Arch Clin Exp Ophthalmol 2002 1.74
33 Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19. Hum Mol Genet 1994 1.71
34 Acute zonal occult outer retinopathy: towards a set of diagnostic criteria. Br J Ophthalmol 2005 1.70
35 Functional loss in age-related Bruch's membrane change with choroidal perfusion defect. Invest Ophthalmol Vis Sci 1992 1.69
36 Choroidal perfusion abnormality with age-related Bruch's membrane change. Am J Ophthalmol 1990 1.66
37 Retinal vascular abnormalities in facioscapulohumeral muscular dystrophy. A general association with genetic and therapeutic implications. Brain 1987 1.66
38 Drusen as risk factors in age-related macular disease. Am J Ophthalmol 1990 1.66
39 Autosomal dominant exudative vitreoretinopathy. Br J Ophthalmol 1980 1.65
40 Retinal macroaneurysms. Br J Ophthalmol 1975 1.64
41 Retinopathy in haemoglobin C trait. Eye (Lond) 1996 1.63
42 The role of axoplasmic transport in the pathogenesis of retinal cotton-wool spots. Br J Ophthalmol 1977 1.62
43 Relationship between melatonin rhythms and visual loss in the blind. J Clin Endocrinol Metab 1997 1.58
44 Vitamin A treatment for night blindness in primary biliary cirrhosis. Br Med J (Clin Res Ed) 1984 1.57
45 Analysis of lipid deposits extracted from human macular and peripheral Bruch's membrane. Arch Ophthalmol 1994 1.55
46 Senile disciform macular degeneration: features indicating suitability for photocoagulation. Br J Ophthalmol 1979 1.54
47 Retinal venous sheathing in optic neuritis. Its significance for the pathogenesis of multiple sclerosis. Brain 1987 1.54
48 Symptomatic abnormalities of dark adaptation in patients with age-related Bruch's membrane change. Br J Ophthalmol 1993 1.51
49 On the retinal vasculature of the human fovea. Exp Eye Res 1974 1.50
50 Bilateral macular drusen in age-related macular degeneration. Prognosis and risk factors. Ophthalmology 1994 1.49
51 Low vision services for vision rehabilitation in the United Kingdom. Br J Ophthalmol 2002 1.47
52 Autosomal dominant retinitis pigmentosa: four new mutations in rhodopsin, one of them in the retinal attachment site. Genomics 1991 1.46
53 Long-term management of abetalipoproteinaemia. Possible role for vitamin E. Arch Dis Child 1977 1.44
54 Histopathology of ruby and argon laser lesions in monkey and human retina. A comparative study. Br J Ophthalmol 1975 1.42
55 Histopathology of incipient fundus flavimaculatus. Ophthalmology 1991 1.42
56 Radiotherapy for age-related macular degeneration. Clin Oncol (R Coll Radiol) 1998 1.41
57 Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic study. Br J Ophthalmol 1993 1.41
58 A comparative histopathological study of argon and krypton laser irradiations of the human retina. Br J Ophthalmol 1979 1.41
59 Functional correlates of fundus autofluorescence abnormalities in patients with RPGR or RIMS1 mutations causing cone or cone rod dystrophy. Br J Ophthalmol 2007 1.40
60 The role of molecular genetics in the prenatal diagnosis of retinal dystrophies. Eye (Lond) 1995 1.39
61 A linkage survey of 20 dominant retinitis pigmentosa families: frequencies of the nine known loci and evidence for further heterogeneity. J Med Genet 1998 1.39
62 Sorsby's fundus dystrophy. A light and electron microscopic study. Ophthalmology 1989 1.38
63 Experimental retinal branch vein occlusion in rhesus monkeys. I. Clinical appearances. Br J Ophthalmol 1979 1.37
64 Fruits and vegetables that are sources for lutein and zeaxanthin: the macular pigment in human eyes. Br J Ophthalmol 1998 1.35
65 Visual prognosis of disciform degeneration in myopia. Ophthalmology 1983 1.34
66 Distribution of pigment epithelium autofluorescence in retinal disease state recorded in vivo and its change over time. Graefes Arch Clin Exp Ophthalmol 1999 1.34
67 Confocal imaging of the fundus using a scanning laser ophthalmoscope. Br J Ophthalmol 1992 1.32
68 A fluorescein and indocyanine green angiographic study of choriocapillaris in age-related macular disease. Arch Ophthalmol 1999 1.31
69 Sorsby's fundus dystrophy. A clinical study. Ophthalmology 1989 1.30
70 Quantitative evaluation of fundus autofluorescence imaged "in vivo" in eyes with retinal disease. Br J Ophthalmol 2000 1.29
71 Correlation between lipids extracted from Bruch's membrane and age. Ophthalmology 1993 1.29
72 Acute zonal occult outer retinopathy (AZOOR) associated with multifocal choroidopathy. Eye (Lond) 1994 1.29
73 Mutations in the RP2 gene cause disease in 10% of families with familial X-linked retinitis pigmentosa assessed in this study. Am J Hum Genet 1999 1.28
74 Polypoidal choroidal vasculopathy in exudative and haemorrhagic pigment epithelial detachments. Br J Ophthalmol 2000 1.27
75 Ocular abnormalities in Alagille syndrome. Ophthalmology 1999 1.25
76 Sickle cell retinopathy in Jamaican children: further observations from a cohort study. Br J Ophthalmol 1988 1.25
77 X-linked recessive fundus dystrophies and their carrier states. Trans Ophthalmol Soc U K 1970 1.25
78 Clinical characterisation of a family with retinal dystrophy caused by mutation in the Mertk gene. Br J Ophthalmol 2006 1.24
79 Sickle cell retinopathy in young children in Jamaica. Br J Ophthalmol 1982 1.24
80 Morphology of posterior segment lesions of the eye in patients with onchocerciasis. Br J Ophthalmol 1976 1.24
81 Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1. Arch Ophthalmol 2001 1.24
82 Retinitis pigmentosa and retinal oedema. Br J Ophthalmol 1978 1.23
83 Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1. Arch Ophthalmol 2001 1.22
84 Ocular fundus lesions in divers. Lancet 1988 1.21
85 Geographical choroidopathy. Br J Ophthalmol 1974 1.20
86 Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutation. Br J Ophthalmol 1992 1.20
87 Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another: confirmation of genetic heterogeneity. Am J Hum Genet 1990 1.20
88 Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclase. Ophthalmology 2000 1.20
89 Electrophysiologic studies in birdshot chorioretinopathy. Am J Ophthalmol 1988 1.20
90 Assessment of the phenotypic range seen in Doyne honeycomb retinal dystrophy. Arch Ophthalmol 1997 1.19
91 Abnormal dark adaptation and rhodopsin kinetics in Sorsby's fundus dystrophy. Invest Ophthalmol Vis Sci 1992 1.19
92 Retinal vascular changes in congenital hypertrophy of the retinal pigment epithelium. Br J Ophthalmol 1976 1.18
93 Outcome of cataract surgery in patients with retinitis pigmentosa. Br J Ophthalmol 2001 1.17
94 Correlation between biochemical composition and fluorescein binding of deposits in Bruch's membrane. Ophthalmology 1992 1.17
95 Unruptured aneurysm of the supraclinoid carotid artery. A treatable cause of blindness. Neurology 1970 1.16
96 Evolution of age-related macular degeneration with choroidal perfusion abnormality. Am J Ophthalmol 1992 1.15
97 Recurrent choroidal neovascularization after laser photocoagulation in Sorsby's fundus dystrophy. Retina 1994 1.15
98 The dark choroid in posterior retinal dystrophies. Br J Ophthalmol 1981 1.15
99 ABCA4 mutations and discordant ABCA4 alleles in patients and siblings with bull's-eye maculopathy. Br J Ophthalmol 2007 1.15
100 Accumulation of tissue inhibitor of metalloproteinases-3 in human eyes with Sorsby's fundus dystrophy or retinitis pigmentosa. Br J Ophthalmol 1998 1.14
101 Retinal pattern dystrophy associated with a 4 bp insertion at codon 140 in the RDS-peripherin gene. Hum Mol Genet 1994 1.14
102 Repeated injections of a ciliary neurotrophic factor analogue leading to long-term photoreceptor survival in hereditary retinal degeneration. Invest Ophthalmol Vis Sci 1999 1.14
103 The pathogenesis of tears of the retinal pigment epithelium. Am J Ophthalmol 1988 1.14
104 Adult vitelliform macular dystrophy. Eye (Lond) 1990 1.13
105 Are low inflammatory reactions involved in exudative age-related macular degeneration? Morphological and immunhistochemical analysis of AMD associated with basal deposits. Graefes Arch Clin Exp Ophthalmol 2008 1.13
106 A detailed phenotypic study of "cone dystrophy with supernormal rod ERG". Br J Ophthalmol 2005 1.13
107 Decreasing stromal iris pigmentation as a risk factor for age-related macular degeneration. Am J Ophthalmol 1994 1.12
108 Ocular histoplasmosis syndrome in the United Kingdom. Br J Ophthalmol 1974 1.12
109 Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19q. Br J Ophthalmol 1995 1.12
110 Further refinement of the location for autosomal dominant retinitis pigmentosa on chromosome 7p (RP9). Am J Hum Genet 1994 1.11
111 Intrafamilial variation of phenotype in Stargardt macular dystrophy-Fundus flavimaculatus. Invest Ophthalmol Vis Sci 1999 1.11
112 Age related macular degeneration and sun exposure, iris colour, and skin sensitivity to sunlight. Br J Ophthalmol 2006 1.11
113 Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies. J Med Genet 2001 1.11
114 Internuclear ophthalmoplegia. An electro-oculographic study of peak angular saccadic velocities. Br J Ophthalmol 1976 1.10
115 Ophthalmological screening for von Hippel-Lindau disease. Eye (Lond) 1991 1.10
116 Sickle cell retinopathy in Jamaican children: a search for prognostic factors. Br J Ophthalmol 1983 1.10
117 Ocular findings in a double-blind study of ivermectin versus diethylcarbamazine versus placebo in the treatment of onchocerciasis. Br J Ophthalmol 1987 1.10
118 Visual outcomes in the subfoveal radiotherapy study: a randomized controlled trial of teletherapy for age-related macular degeneration. Arch Ophthalmol 2002 1.10
119 The relationships of age changes in retinal pigment epithelium and Bruch's membrane. Invest Ophthalmol Vis Sci 1999 1.09
120 Repair after tears of the retinal pigment epithelium. Eye (Lond) 1988 1.09
121 Genotype-phenotype correlation in British families with X linked congenital stationary night blindness. Br J Ophthalmol 2003 1.08
122 Sorsby's fundus dystrophy in the British Isles: demonstration of a striking founder effect by microsatellite-generated haplotypes. Genome Res 1996 1.08
123 Aphakic macular edema: incidence and pathogenesis. Invest Ophthalmol 1975 1.08
124 Placoid pigment epitheliopathy. Presenting with bilateral serous retinal detachment. Br J Ophthalmol 1972 1.08
125 Changes in visual function and in the posterior segment of the eye during treatment of onchocerciasis with diethylcarbamazine citrate. Br J Ophthalmol 1980 1.07
126 Functional observations in vitamin A deficiency: diagnosis and time course of recovery. Eye (Lond) 2005 1.07
127 A histopathologic study of a choroideremia carrier. Invest Ophthalmol Vis Sci 1990 1.07
128 Sorsby's pseudoinflammatory macular dystrophy. Br J Ophthalmol 1981 1.06
129 Retinitis pigmentosa and retinal neovascularization. Ophthalmology 1986 1.06
130 Detection of the carrier state of X-linked retinoschisis. Am J Ophthalmol 1988 1.05
131 Intra-retinal absorption of argon laser irradiation in human and monkey retinae. Experientia 1974 1.05
132 RP1 protein truncating mutations predominate at the RP1 adRP locus. Invest Ophthalmol Vis Sci 2000 1.04
133 Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies. J Med Genet 1999 1.04
134 Long-term effect of acetazolamide in a patient with retinitis pigmentosa. Invest Ophthalmol Vis Sci 1990 1.03
135 Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14. Am J Hum Genet 1987 1.03
136 Juxtapapillary choroidal neovascularization in older patients. Am J Ophthalmol 1988 1.03
137 Phenotype of a British North Carolina macular dystrophy family linked to chromosome 6q. Br J Ophthalmol 1998 1.03
138 A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1. Br J Ophthalmol 2005 1.02
139 No evidence for linkage between late onset autosomal dominant retinitis pigmentosa and chromosome 3 locus D3S47 (C17): evidence for genetic heterogeneity. Genomics 1990 1.02
140 Choroidal folds in association with papilloedema. Br J Ophthalmol 1973 1.02
141 Immunological studies in retinitis pigmentosa associated with retinal vascular leakage. Br J Ophthalmol 1978 1.02
142 Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 families. Arch Ophthalmol 1999 1.02
143 Dominantly inherited drusen represent more than one disorder: a historical review. Eye (Lond) 1995 1.01
144 Retinal dysfunction in central serous retinopathy. Eye (Lond) 1987 1.00
145 Sorsby's pseudoinflammatory macula dystrophy--Sorsby's fundus dystrophies. Eye (Lond) 1988 1.00
146 Diagnostic uses of the Pulfrich phenomenon. Lancet 1973 1.00
147 TIMP-3, collagen, and elastin immunohistochemistry and histopathology of Sorsby's fundus dystrophy. Invest Ophthalmol Vis Sci 2000 0.99
148 Treatmenf of optic neuritis by retrobulbar injection of triamcinolone. Br Med J 1977 0.99
149 Photocoagulation of disciform macular lesions with krypton laser. Br J Ophthalmol 1979 0.99
150 Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locus. Hum Genet 1999 0.99
151 Disturbance of sleep in blindness. Am J Ophthalmol 1998 0.98
152 DNA probes in X-linked retinitis pigmentosa. Trans Ophthalmol Soc U K 1983 0.98
153 Spectrum of mutations in USH2A in British patients with Usher syndrome type II. Exp Eye Res 2001 0.98
154 PIgment epithelial diseases with abnormal choroidal perfusion. Am J Ophthalmol 1980 0.97
155 Genetic linkage between X-linked retinitis pigmentosa and DNA probe DXS7 (L1.28): further linkage data, heterogeneity testing, and risk estimation. Hum Genet 1986 0.97
156 Defects in supranuclear control of horizontal eye movements. Trans Ophthalmol Soc U K 1970 0.97
157 Essential blepharospasm. Trans Ophthalmol Soc U K 1975 0.97
158 Supranuclear abnormalities of the vertical ocular motor system. Trans Ophthalmol Soc U K 1970 0.97
159 Localization of a gene (CORD7) for a dominant cone-rod dystrophy to chromosome 6q. Am J Hum Genet 1998 0.97
160 Dominant retinitis pigmentosa associated with two rhodopsin gene mutations. Leu-40-Arg and an insertion disrupting the 5'-splice junction of exon 5. Arch Ophthalmol 1993 0.97
161 Pattern ERG: clinical overview, and some observations on associated fundus autofluorescence imaging in inherited maculopathy. Doc Ophthalmol 2003 0.96
162 Macular pigment in the human retina: histological evaluation of localization and distribution. Eye (Lond) 2007 0.96
163 Choroidal ischemia. Am J Ophthalmol 1982 0.96
164 Age-related Bruch's membrane change: a clinical study of the relative role of heredity and environment. Br J Ophthalmol 1993 0.96
165 Membrane-bound carbonic anhydrase in human retinal pigment epithelium. Invest Ophthalmol Vis Sci 1994 0.96
166 The argon laser-the effect on retinal tissues and its clinical applications. Trans Ophthalmol Soc U K 1973 0.96
167 Familial cavernous hemangioma: An expanding ocular spectrum. Arch Ophthalmol 2000 0.95
168 Macular pigment: quantitative analysis on autofluorescence images. Graefes Arch Clin Exp Ophthalmol 2003 0.95
169 Functional aspects of drusen regression in age-related macular degeneration. Br J Ophthalmol 2009 0.95
170 Founder effect, seen in the British population, of the 172 peripherin/RDS mutation-and further refinement of genetic positioning of the peripherin/RDS gene. Am J Hum Genet 1998 0.94
171 Bilaterality of drusen. Br J Ophthalmol 1990 0.94
172 Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6q. Hum Mol Genet 1995 0.94
173 Localisation of a gene for dominant cone-rod dystrophy (CORD6) to chromosome 17p. Hum Mol Genet 1997 0.93
174 Alternative therapies in exudative age related macular degeneration. Br J Ophthalmol 1998 0.93
175 Relationship between napping and melatonin in the blind. J Biol Rhythms 1997 0.93
176 Ultrastructural changes associated with accumulation of inclusion bodies in rat retinal pigment epithelium. Invest Ophthalmol Vis Sci 2000 0.93
177 Macular disciform response and laser treatment. Trans Ophthalmol Soc U K 1977 0.92
178 Conflict monitoring in early frontotemporal dementia. Neurology 2009 0.92
179 Autosomal dominant pattern dystrophy of the retina associated with a 4-base pair insertion at codon 140 in the peripherin/RDS gene. Arch Ophthalmol 1995 0.92
180 The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16. Hum Mol Genet 1996 0.92
181 Recurrences of acute posterior multifocal placoid pigment epitheliopathy. Am J Ophthalmol 1984 0.92
182 Macular disease in an elderly population. Ger J Ophthalmol 1992 0.92
183 Dark adaptation and scotopic perimetry over 'peau d'orange' in pseudoxanthoma elasticum. Br J Ophthalmol 1994 0.91
184 Bilaterality of tears of the retinal pigment epithelium. Br J Ophthalmol 1988 0.91
185 Laser treatment in subjects with high-risk clinical features of age-related macular degeneration. Posterior pole appearance and retinal function. Arch Ophthalmol 1997 0.91
186 Autosomal dominant optic atrophy with asymptomatic peripheral neuropathy. J Neurol Neurosurg Psychiatry 1996 0.90
187 Fundus autofluorescence imaging compared with different confocal scanning laser ophthalmoscopes. Br J Ophthalmol 2003 0.90
188 Chromosome 19q cone-rod retinal dystrophy. Ocular phenotype. Arch Ophthalmol 1995 0.90
189 Characterisation of the macular dystrophy in patients with the A3243G mitochondrial DNA point mutation with fundus autofluorescence. Br J Ophthalmol 2008 0.90
190 Acute macular neuroretinopathy. Ophthalmology 1989 0.90
191 Novel frameshift mutations in the RP2 gene and polymorphic variants. Hum Mutat 2000 0.89
192 Retinal pigment epithelium translocation and central visual function in age related macular degeneration: preliminary results. Int Ophthalmol 2001 0.89
193 Reproducibility of fundus autofluorescence measurements obtained using a confocal scanning laser ophthalmoscope. Br J Ophthalmol 1999 0.89
194 Paramacular telangiectasis. Trans Ophthalmol Soc U K 1986 0.89
195 Laser treatment of retinal angiomatosis. Eye (Lond) 1989 0.89
196 Polypoidal choroidal vasculopathy and central serous chorioretinopathy. Ophthalmology 2001 0.89
197 [Dynamics of accumulation and degradation of lipofuscin in retinal pigment epithelium in senile macular degeneration]. Klin Monbl Augenheilkd 1998 0.88
198 Optical coherence tomography (OCT): principles of operation, technology, indications in vitreoretinal imaging and interpretation of results. Int Ophthalmol 2001 0.88
199 New classification of peripheral retinal vascular changes in sickle cell disease. Br J Ophthalmol 1994 0.88
200 Progressive retinal dysfunction in diffuse unilateral subacute neuroretinitis. Br J Ophthalmol 2006 0.88
201 Field loss due to lesions at the anterior angle of the chiasm. Proc R Soc Med 1972 0.88
202 Divergence paralysis with raised intracranial pressure. An electro-oculographic study. Br J Ophthalmol 1972 0.87
203 Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindred. J Med Genet 1991 0.87
204 Retinitis pigmentosa and mutations in rhodopsin. Lancet 1991 0.87
205 Nematode optic neuritis. Am J Ophthalmol 1970 0.87
206 [Antiretinal antibodies associated with cystoid macular edema]. Klin Monbl Augenheilkd 2000 0.87
207 Controlled trial of laser photocoagulation of pigment epithelial detachments in the elderly: 4 year review. Br J Ophthalmol 1992 0.87
208 The surgical management of uveal effusion syndrome. Eye (Lond) 1987 0.86
209 Ophthalmological results from a placebo controlled comparative 3-dose ivermectin study in the treatment of onchocerciasis. Trop Med Parasitol 1989 0.86
210 Colour contrast sensitivity in patients with age-related Bruch's membrane changes. Ger J Ophthalmol 1995 0.86
211 Histopathological and biochemical studies on donor eyes affected with retinitis pigmentosa. Prog Clin Biol Res 1987 0.86
212 Recombination between rhodopsin and locus D3S47 (C17) in rhodopsin retinitis pigmentosa families. Am J Hum Genet 1992 0.86
213 Foveal involvement and lack of visual recovery in APMPPE associated with uncommon features. Eye (Lond) 1995 0.86
214 Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits variable expression. Br J Ophthalmol 1995 0.85
215 Segregation of a PRKCG mutation in two RP11 families. Am J Hum Genet 1998 0.85
216 Exclusion of chromosome 6 and 8 locations in nonrhodopsin autosomal dominant retinitis pigmentosa families: further locus heterogeneity in adRP. Genomics 1992 0.85
217 Nine generations of a family with autosomal dominant retinitis pigmentosa and evidence of variable expressivity from census records. J Med Genet 1992 0.85
218 The contribution of USH1C mutations to syndromic and non-syndromic deafness in the UK. Clin Genet 2003 0.85
219 Linkage refinement localises Sorsby fundus dystrophy between markers D22S275 and D22S278. J Med Genet 1995 0.85
220 Treatment of pigment epithelial detachments due to age-related macular degeneration with intra-ocular C3F8 injection. Aust N Z J Ophthalmol 1998 0.84
221 Placoid pigment epitheliopathy and Harada's disease. Br J Ophthalmol 1978 0.84
222 Difference between RP2 and RP3 phenotypes in X linked retinitis pigmentosa. Br J Ophthalmol 1999 0.84
223 Prevention of blindness due to senile disciform macular degeneration. Trans Ophthalmol Soc U K 1978 0.84
224 Management of inherited outer retinal dystrophies: present and future. Br J Ophthalmol 1999 0.84
225 Laser photocoagulation of senile macular degeneration. Br Med J (Clin Res Ed) 1983 0.84
226 Autosomal dominant macular dystrophy simulating North Carolina macular dystrophy. Arch Ophthalmol 1995 0.84
227 Bilateral giant macular schisis in a patient with enhanced S-cone syndrome from a family showing pseudo-dominant inheritance. Br J Ophthalmol 2008 0.83
228 Partial laser ablation of massive peripapillary subretinal neovascularization. Ophthalmology 1996 0.83
229 Molecular genetic heterogeneity in autosomal dominant drusen. J Med Genet 2001 0.83
230 Does smoking influence the type of age related macular degeneration causing visual impairment? Br J Ophthalmol 2006 0.82
231 Treatment of senile disciform macular degeneration. Trans Ophthalmol Soc N Z 1977 0.82
232 Congenital stationary night blindness and a "Schubert-Bornschein" type electrophysiology in a family with dominant inheritance. Br J Ophthalmol 2004 0.82
233 Clinical features of progressive bifocal chorioretinal atrophy: a retinal dystrophy linked to chromosome 6q. Ophthalmology 1996 0.82
234 Novel mutations of the RPGR gene in RP3 families. Hum Mutat 2000 0.82
235 Retinal vessel constriction under hyperbaric conditions. Lancet 1989 0.82
236 Visual loss from retinal oedema in autosomal dominant exudative vitreoretinopathy. Br J Ophthalmol 1982 0.82
237 An immunohistochemical study of an autosomal dominant feline rod/cone dysplasia (Rdy cats). Exp Eye Res 1999 0.82
238 Visual loss during oral diethylcarbamazine treatment for onchocerciasis. Lancet 1979 0.82
239 Cell loss in retinal dystrophies by apoptosis--death by informed consent! Br J Ophthalmol 1995 0.82
240 Refined genetic and physical positioning of the gene for Doyne honeycomb retinal dystrophy (DHRD). Hum Genet 1999 0.82
241 Risk of multisystem disease in isolated ocular angioma (haemangioblastoma) J Med Genet 2000 0.81
242 [Biochemical and histochemical analysis of age related lipid deposits in Bruch's membrane]. Ophthalmologe 1994 0.81
243 Ocular ultrasound in Alagille syndrome: a new sign. Ophthalmology 1997 0.81
244 The genetics of complex ophthalmic disorders. Br J Ophthalmol 1996 0.81
245 Symptomatic abnormalities of dark adaptation in patients with EFEMP1 retinal dystrophy (Malattia Leventinese/Doyne honeycomb retinal dystrophy). Eye (Lond) 2002 0.81
246 Comparison of optical coherence tomography and fluorescein angiography in assessing macular edema in retinal dystrophies: preliminary results. Int Ophthalmol 2001 0.81
247 Long-term drusen study. Retina 1999 0.81
248 Potential diagnostic dilemmas using the multifocal electroretinogram in intermittent exotropia. Br J Ophthalmol 2004 0.81
249 Retinal telangiectasis in facioscapulohumeral muscular dystrophy with deafness. Arch Ophthalmol 1985 0.81
250 A new family linked to the RP13 locus for autosomal dominant retinitis pigmentosa on distal 17p. J Med Genet 1996 0.81
251 Cutaneous melanoma-associated retinopathy. Ophthalmology 1994 0.81
252 The risk of fellow eye visual loss with unilateral retinal pigment epithelial tears. Am J Ophthalmol 1989 0.80
253 Quantification of the ocular reactions to microfilaricides in the chemotherapy of onchocerciasis. Eye (Lond) 1992 0.80
254 Recurrent visual loss in homozygous sickle cell disease. Br J Ophthalmol 1985 0.80
255 The dark choroid in posterior retinal dystrophies. Ophthalmology 1987 0.80
256 Leber's hereditary optic atrophy. Ophthalmic Paediatr Genet 1989 0.80
257 Peripheral retinal vasculature in normal Jamaican children. Br J Ophthalmol 1994 0.80
258 Visual functioning and quality of life in the SubFoveal Radiotherapy Study (SFRADS): SFRADS report 2. Br J Ophthalmol 2005 0.80
259 Ocular manifestations in autosomal dominant retinitis pigmentosa with a Lys-296-Glu rhodopsin mutation at the retinal binding site. Br J Ophthalmol 1994 0.80
260 Adult vitelliform macular degeneration. Br J Ophthalmol 1981 0.79
261 Age-related macular disease in rural southern Italy. Arch Ophthalmol 1997 0.79
262 Natriuretic peptides and their receptors in human neural retina and retinal pigment epithelium. Ger J Ophthalmol 1994 0.79
263 Detection of subpigment epithelial neovascularisation in cases of retinal pigment epithelial detachments: a review of the Moorfields treatment trial. Br J Ophthalmol 1992 0.79
264 Tears of detached retinal pigment epithelium. Trans New Orleans Acad Ophthalmol 1983 0.79
265 Isolated foveal retinoschisis as a cause of visual loss in young females. Br J Ophthalmol 2003 0.78
266 Treatment of acute optic neuritis. Trans Ophthalmol Soc U K 1976 0.78
267 Localization of CSNBX (CSNB4) between the retinitis pigmentosa loci RP2 and RP3 on proximal Xp. Invest Ophthalmol Vis Sci 1997 0.78
268 Fluorescein angiographic abnormalities after prophylactic macular photocoagulation for high-risk age-related maculopathy. Am J Ophthalmol 1999 0.78
269 A clinical and molecular genetic analysis of solitary ocular angioma. Ophthalmology 1999 0.78
270 Severe visual loss associated with retinal telangiectasis and facioscapulohumeral muscular dystrophy. Graefes Arch Clin Exp Ophthalmol 1992 0.78
271 NRL S50T mutation and the importance of 'founder effects' in inherited retinal dystrophies. Eur J Hum Genet 2000 0.78
272 What is the future of research in age-related macular disease? Arch Ophthalmol 1997 0.78
273 Retinitis pigmentosa families showing apparent X linked inheritance but unlinked to the RP2 or RP3 loci. J Med Genet 1994 0.78
274 The evolution of subpigment epithelial neovascularization in senile disciform macular degeneration. Trans Ophthalmol Soc U K 1972 0.78
275 [Serous central chorioretinopathy. Acute autofluorescence of the pigment epithelium of the eye]. Ophthalmologe 1999 0.78
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