Published in Br J Ophthalmol on February 01, 1973
Retinal and Choroidal Folds in Papilledema. Invest Ophthalmol Vis Sci (2015) 2.32
Macular changes resulting from papilloedema. Br J Ophthalmol (1980) 0.89
Choroidal folds and papilloedema. Br J Ophthalmol (1999) 0.83
Acquired choroidal folds: a sign of idiopathic intracranial hypertension. Graefes Arch Clin Exp Ophthalmol (2006) 0.81
Causes and Prognosis of Visual Acuity Loss at the Time of Initial Presentation in Idiopathic Intracranial Hypertension. Invest Ophthalmol Vis Sci (2015) 0.78
Acute visual loss in papilloedema: the diagnostic pitfalls. Int Ophthalmol (2013) 0.75
Optic nerve sheath decompression for relief of chronic monocular choked disc. Am J Ophthalmol (1969) 1.84
Parallel retinal folds; their significance in orbital space-taking lesions. Arch Ophthalmol (1959) 1.48
Virus infections of the upper respiratory tract (abridged). Proc R Soc Med (1969) 1.24
Benign chorioretinal folds. Am J Ophthalmol (1970) 0.96
[Formation of retinal folds following tumor pressure on bulbus]. Klin Monbl Augenheilkd Augenarztl Fortbild (1957) 0.92
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
Distribution of fundus autofluorescence with a scanning laser ophthalmoscope. Br J Ophthalmol (1995) 3.62
Ischaemic papillopathy. Clinical and fluorescein aniographic review of forty cases. Br J Ophthalmol (1974) 3.56
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy. Nat Genet (1999) 3.32
X-linked retinitis pigmentosa. Br J Ophthalmol (1975) 3.11
Tears of detached retinal pigment epithelium. Br J Ophthalmol (1981) 3.08
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
A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p. Nat Genet (1993) 2.97
The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation. Brain (1995) 2.94
Visual capacity in the hemianopic field following a restricted occipital ablation. Brain (1974) 2.92
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa. Nat Genet (2000) 2.82
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
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
Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13). Hum Mol Genet (2001) 2.48
RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections. J Med Genet (2003) 2.45
Benign retinal vasculitis. Clinical and fluorescein angiographic study. Br J Ophthalmol (1971) 2.32
Fundus autofluorescence in age-related macular disease imaged with a laser scanning ophthalmoscope. Invest Ophthalmol Vis Sci (1997) 2.31
The development of neovascularization of senile disciform macular degeneration. Am J Ophthalmol (1973) 2.17
Recent advances in the treatment of senile disciform macular degeneration by photocoagulation. Br J Ophthalmol (1974) 2.14
Viscosity and retinal vein thrombosis. Br J Ophthalmol (1976) 2.12
Fluorescein fundus photography in the detection of early papilloedema and its differentiation from pseudo-papilloedema. Lancet (1965) 2.12
Hypoxic ocular sequelae of carotid-cavernous fistulae. Study of the caues of visual failure before and after neurosurgical treatment in a series of 25 cases. Br J Ophthalmol (1969) 2.11
In vivo fundus autofluorescence in macular dystrophies. Arch Ophthalmol (1997) 2.10
Senile disciform macular degeneration in the second eye. Br J Ophthalmol (1977) 2.07
Bilateral acute retinal necrosis. Br J Ophthalmol (1978) 2.07
Phenotypic subtypes of Stargardt macular dystrophy-fundus flavimaculatus. Arch Ophthalmol (2001) 2.04
Aging changes in Bruch's membrane. A histochemical and morphologic study. Ophthalmology (1990) 1.99
A neurovisceral storage disease with vertical supranuclear ophthalmoplegia, and its relationship to Niemann-Pick disease. A report of nine patients. Brain (1973) 1.94
Treatment of chronic macular edema with acetazolamide. Arch Ophthalmol (1988) 1.90
Factors affecting visual loss in benign intracranial hypertension. Ophthalmology (1984) 1.89
A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa. Am J Hum Genet (1991) 1.88
A clinical, psychophysical, and electroretinographic survey of patients with autosomal dominant retinitis pigmentosa. Br J Ophthalmol (1985) 1.87
Mutations in the retinal guanylate cyclase (RETGC-1) gene in dominant cone-rod dystrophy. Hum Mol Genet (1998) 1.84
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
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
Ophthalmologic findings in 70 patients with evidence of retinal embolism. Ophthalmology (1982) 1.79
A mutation in NRL is associated with autosomal dominant retinitis pigmentosa. Nat Genet (1999) 1.79
Computer assisted tomography in orbital disease. Br J Ophthalmol (1974) 1.79
Ischaemic papillopathy. Trans Ophthalmol Soc U K (1971) 1.79
A clinical study of the vascularity of senile disciform macular degeneration. Am J Ophthalmol (1973) 1.77
Degenerative changes in a retina affected with autosomal dominant retinitis pigmentosa. Invest Ophthalmol Vis Sci (1989) 1.75
Retinal pigment epithelial detachments in the elderly: classification and outcome. Br J Ophthalmol (1985) 1.74
Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity. Br J Ophthalmol (2006) 1.74
Pigment epithelial detachment in the elderly. Clinical differentiation, natural course and pathogenetic implications. Graefes Arch Clin Exp Ophthalmol (2002) 1.74
Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19. Hum Mol Genet (1994) 1.71
Acute zonal occult outer retinopathy: towards a set of diagnostic criteria. Br J Ophthalmol (2005) 1.70
Functional loss in age-related Bruch's membrane change with choroidal perfusion defect. Invest Ophthalmol Vis Sci (1992) 1.69
Anti-retinal autoimmunity and circulating immune complexes in patients with retinal vasculitis. Lancet (1982) 1.68
Choroidal perfusion abnormality with age-related Bruch's membrane change. Am J Ophthalmol (1990) 1.66
Retinal vascular abnormalities in facioscapulohumeral muscular dystrophy. A general association with genetic and therapeutic implications. Brain (1987) 1.66
Drusen as risk factors in age-related macular disease. Am J Ophthalmol (1990) 1.66
Autosomal dominant exudative vitreoretinopathy. Br J Ophthalmol (1980) 1.65
Retinal macroaneurysms. Br J Ophthalmol (1975) 1.64
Retinopathy in haemoglobin C trait. Eye (Lond) (1996) 1.63
The role of axoplasmic transport in the pathogenesis of retinal cotton-wool spots. Br J Ophthalmol (1977) 1.62
Fluorescein angiography in the diagnosis of drusen of the disc. Trans Ophthalmol Soc U K (1967) 1.62
Relationship between melatonin rhythms and visual loss in the blind. J Clin Endocrinol Metab (1997) 1.58
Vitamin A treatment for night blindness in primary biliary cirrhosis. Br Med J (Clin Res Ed) (1984) 1.57
Analysis of lipid deposits extracted from human macular and peripheral Bruch's membrane. Arch Ophthalmol (1994) 1.55
Retinal venous sheathing in optic neuritis. Its significance for the pathogenesis of multiple sclerosis. Brain (1987) 1.54
Senile disciform macular degeneration: features indicating suitability for photocoagulation. Br J Ophthalmol (1979) 1.54
Fundus changes in histologically confirmed sarcoidosis. Br J Ophthalmol (1981) 1.52
Symptomatic abnormalities of dark adaptation in patients with age-related Bruch's membrane change. Br J Ophthalmol (1993) 1.51
On the retinal vasculature of the human fovea. Exp Eye Res (1974) 1.50
Bilateral macular drusen in age-related macular degeneration. Prognosis and risk factors. Ophthalmology (1994) 1.49
Low vision services for vision rehabilitation in the United Kingdom. Br J Ophthalmol (2002) 1.47
Autosomal dominant retinitis pigmentosa: four new mutations in rhodopsin, one of them in the retinal attachment site. Genomics (1991) 1.46
Long-term management of abetalipoproteinaemia. Possible role for vitamin E. Arch Dis Child (1977) 1.44
Ophthalmoplegia in carotid cavernous sinus fistula. Br J Ophthalmol (1984) 1.43
Histopathology of ruby and argon laser lesions in monkey and human retina. A comparative study. Br J Ophthalmol (1975) 1.42
Histopathology of incipient fundus flavimaculatus. Ophthalmology (1991) 1.42
Radiotherapy for age-related macular degeneration. Clin Oncol (R Coll Radiol) (1998) 1.41
Retinal vasculitis: a review. J R Soc Med (1979) 1.41
Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic study. Br J Ophthalmol (1993) 1.41
Retinal, choroidal, and optic disc involvement in sarcoidosis. Trans Ophthalmol Soc U K (1976) 1.41
A comparative histopathological study of argon and krypton laser irradiations of the human retina. Br J Ophthalmol (1979) 1.41
Bilateral sudden visual loss due to sphenoid mucocele in Albright's syndrome. Br J Ophthalmol (1995) 1.40
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
The role of molecular genetics in the prenatal diagnosis of retinal dystrophies. Eye (Lond) (1995) 1.39
Ocular changes in limited forms of Wegener's granulomatosis. Br J Ophthalmol (1981) 1.39
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
Sorsby's fundus dystrophy. A light and electron microscopic study. Ophthalmology (1989) 1.38
Experimental retinal branch vein occlusion in rhesus monkeys. I. Clinical appearances. Br J Ophthalmol (1979) 1.37
Fruits and vegetables that are sources for lutein and zeaxanthin: the macular pigment in human eyes. Br J Ophthalmol (1998) 1.35
Migraine complicated by ischaemic papillopathy. Lancet (1971) 1.35
Visual prognosis of disciform degeneration in myopia. Ophthalmology (1983) 1.34
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
"Blindsight": Vision in a field defect. Lancet (1974) 1.32
Confocal imaging of the fundus using a scanning laser ophthalmoscope. Br J Ophthalmol (1992) 1.32
A fluorescein and indocyanine green angiographic study of choriocapillaris in age-related macular disease. Arch Ophthalmol (1999) 1.31
Sorsby's fundus dystrophy. A clinical study. Ophthalmology (1989) 1.30
Quantitative evaluation of fundus autofluorescence imaged "in vivo" in eyes with retinal disease. Br J Ophthalmol (2000) 1.29
Correlation between lipids extracted from Bruch's membrane and age. Ophthalmology (1993) 1.29
Papilledema and asymptomatic intracranial hypertension in systemic lupus erythematosus. A fluorescein angiographic study of resolving papilledema. Arch Ophthalmol (1968) 1.29
Acute zonal occult outer retinopathy (AZOOR) associated with multifocal choroidopathy. Eye (Lond) (1994) 1.29
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
Polypoidal choroidal vasculopathy in exudative and haemorrhagic pigment epithelial detachments. Br J Ophthalmol (2000) 1.27
Ocular abnormalities in Alagille syndrome. Ophthalmology (1999) 1.25
X-linked recessive fundus dystrophies and their carrier states. Trans Ophthalmol Soc U K (1970) 1.25
Sickle cell retinopathy in Jamaican children: further observations from a cohort study. Br J Ophthalmol (1988) 1.25