Published in Ophthalmology on June 01, 1990
A comprehensive survey of sequence variation in the ABCA4 (ABCR) gene in Stargardt disease and age-related macular degeneration. Am J Hum Genet (2000) 2.18
Cone photoreceptor abnormalities correlate with vision loss in patients with Stargardt disease. Invest Ophthalmol Vis Sci (2011) 1.37
Quantitative evaluation of fundus autofluorescence imaged "in vivo" in eyes with retinal disease. Br J Ophthalmol (2000) 1.29
A YAC contig encompassing the recessive Stargardt disease gene (STGD) on chromosome 1p. Am J Hum Genet (1995) 1.19
A new locus for autosomal dominant stargardt-like disease maps to chromosome 4. Am J Hum Genet (1999) 1.15
Keypathophysiologic pathways in age-related macular disease. Graefes Arch Clin Exp Ophthalmol (2004) 1.13
Multifocal electroretinography in patients with Stargardt's macular dystrophy. Br J Ophthalmol (1998) 1.11
Therapy for macular degeneration: insights from acne. Proc Natl Acad Sci U S A (2003) 1.01
Defective lipid transport and biosynthesis in recessive and dominant Stargardt macular degeneration. Prog Lipid Res (2010) 0.99
Genetics and molecular pathology of Stargardt-like macular degeneration. Prog Retin Eye Res (2010) 0.95
Retinal photodamage mediated by all-trans-retinal. Photochem Photobiol (2012) 0.93
Correlations among near-infrared and short-wavelength autofluorescence and spectral-domain optical coherence tomography in recessive Stargardt disease. Invest Ophthalmol Vis Sci (2014) 0.90
Reproducibility of fundus autofluorescence measurements obtained using a confocal scanning laser ophthalmoscope. Br J Ophthalmol (1999) 0.89
Flecks in Recessive Stargardt Disease: Short-Wavelength Autofluorescence, Near-Infrared Autofluorescence, and Optical Coherence Tomography. Invest Ophthalmol Vis Sci (2015) 0.85
Dark adaptation in patients with Best vitelliform macular dystrophy. Br J Ophthalmol (1994) 0.79
Genotype-phenotype correlations and differential diagnosis in autosomal dominant macular disease. Doc Ophthalmol (2001) 0.78
Genetic basis of inherited macular dystrophies and implications for stem cell therapy. Stem Cells (2009) 0.78
North Carolina macular dystrophy: clinicopathologic correlation. Trans Am Ophthalmol Soc (2001) 0.77
Age-related changes in the basement membrane of the retinal pigment epithelium of Rpe65 -/- and wild-type mice. Graefes Arch Clin Exp Ophthalmol (2004) 0.77
Three-dimensional spectral domain optical coherence tomography in Stargardt disease and fundus flavimaculatus. J Ocul Biol Dis Infor (2012) 0.76
Dark adaptation in retinal abnormalities. Br J Ophthalmol (1994) 0.76
Molecular genetics of macular dystrophies. Br J Ophthalmol (1996) 0.75
Retinal ganglion cell atrophy correlated with automated perimetry in human eyes with glaucoma. Am J Ophthalmol (1989) 6.53
Optic nerve damage in human glaucoma. III. Quantitative correlation of nerve fiber loss and visual field defect in glaucoma, ischemic neuropathy, papilledema, and toxic neuropathy. Arch Ophthalmol (1982) 6.39
Optic nerve damage in human glaucoma. II. The site of injury and susceptibility to damage. Arch Ophthalmol (1981) 5.09
Rhodopsin mutations in autosomal dominant retinitis pigmentosa. Proc Natl Acad Sci U S A (1991) 4.10
Ocular explosion after peribulbar anesthesia: case report and experimental study. Ophthalmology (1997) 3.59
Morphologic changes in the lamina cribrosa correlated with neural loss in open-angle glaucoma. Am J Ophthalmol (1983) 3.42
Ocular explosions from periocular anesthetic injections: a clinical, histopathologic, experimental, and biophysical study. Ophthalmology (1999) 3.35
Molecular genetics of human blue cone monochromacy. Science (1989) 2.92
Characterization of a human ovarian carcinoma cell line (NIH:OVCAR-3) with androgen and estrogen receptors. Cancer Res (1983) 2.90
Pathologic features of senile macular degeneration. Ophthalmology (1985) 2.73
Assessment of neonatal conjunctivitis with a direct immunofluorescent monoclonal antibody stain for Chlamydia. JAMA (1986) 2.69
Autosomal dominant cerulean cataract is associated with a chain termination mutation in the human beta-crystallin gene CRYBB2. Hum Mol Genet (1997) 2.69
Birdshot retinochoroidopathy associated with HLA-A29 antigen and immune responsiveness to retinal S-antigen. Am J Ophthalmol (1982) 2.61
Chronic human glaucoma causing selectively greater loss of large optic nerve fibers. Ophthalmology (1988) 2.59
Brief report: uveitis caused by Tropheryma whippelii (Whipple's bacillus) N Engl J Med (1995) 2.47
Conjunctival lesions in adults. A clinical and histopathologic review. Cornea (1987) 2.43
Unilateral Duane's retraction syndrome (Type 1). Arch Ophthalmol (1982) 2.40
Epiretinal and vitreous membranes. Comparative study of 56 cases. Arch Ophthalmol (1981) 2.34
A histopathologic study of Best's macular dystrophy. Arch Ophthalmol (1982) 2.27
Ocular and orbital involvement in leukemia. Surv Ophthalmol (1983) 2.26
Senile macular degeneration: a histopathologic study. Trans Am Ophthalmol Soc (1977) 2.20
Histologic characteristics of filtering blebs in glaucomatous eyes. Arch Ophthalmol (1983) 2.19
Efficacy of unilateral versus bilateral temporal artery biopsies for the diagnosis of giant cell arteritis. Am J Ophthalmol (1999) 2.18
Genetic basis of total colourblindness among the Pingelapese islanders. Nat Genet (2000) 2.18
Clinicopathologic correlation of a macular hole treated by cortical vitreous peeling and gas tamponade. Ophthalmology (1994) 2.16
Pathologic findings in pathologic myopia. Retina (1992) 2.14
Ectopia lentis. Surv Ophthalmol (1983) 2.12
The Stickler syndrome: evidence for close linkage to the structural gene for type II collagen. Genomics (1987) 2.11
Lesions of the caruncle: a clinicohistopathologic study. Surv Ophthalmol (1979) 2.08
Prevalence of AIPL1 mutations in inherited retinal degenerative disease. Mol Genet Metab (2000) 2.07
Bilateral Duane's retraction syndrome. A clinical-pathologic case report. Arch Ophthalmol (1980) 2.01
The histology of human glaucoma cupping and optic nerve damage: clinicopathologic correlation in 21 eyes. Ophthalmology (1979) 1.97
Histologic studies of the vasculature of the anterior optic nerve. Am J Ophthalmol (1976) 1.96
X-linked ocular albinism. An oculocutaneous macromelanosomal disorder. Arch Ophthalmol (1976) 1.94
Primary adenocarcinoma of the lacrimal gland. A retrospective study. Ophthalmology (1993) 1.93
A histopathologic review of 168 cases of preretinal membrane. Am J Ophthalmol (1977) 1.93
Clinicopathologic study of bilateral macular holes treated with pars plana vitrectomy and gas tamponade. Retina (1992) 1.91
Upregulation of vascular endothelial growth factor in ischemic and non-ischemic human and experimental retinal disease. Histol Histopathol (1997) 1.90
Detection of herpes simplex viral DNA in the iridocorneal endothelial syndrome. Arch Ophthalmol (1994) 1.88
White centered hemorrhages: their significance. Ophthalmology (1980) 1.88
Epibulbar tumors in childhood. Am J Ophthalmol (1975) 1.88
The eye in the Marfan syndrome. Trans Am Ophthalmol Soc (1981) 1.86
Sebaceous gland carcinoma. Review of 40 cases. Arch Ophthalmol (1984) 1.83
Neurotoxic effects of cisplatin therapy. Arch Neurol (1982) 1.83
Ocular manifestations of acquired immune deficiency syndrome. Ophthalmology (1989) 1.76
Bardet-Biedl syndrome and related disorders. Arch Ophthalmol (1982) 1.74
Leber hereditary optic neuropathy. Electron microscopy and molecular genetic analysis of a case. Ophthalmology (1995) 1.74
Senile disciform degeneration of the macula. Retinal arterialization of the fibrous plaque demonstrated clinically and histopathologically. Arch Ophthalmol (1971) 1.74
Clinicopathologic correlation of drusen and retinal pigment epithelial abnormalities in age-related macular degeneration. Retina (1994) 1.72
Transforming growth factor beta. A biologic chorioretinal glue. Arch Ophthalmol (1989) 1.71
Retinal pathologic changes in multiple sclerosis. Retina (1994) 1.71
Posterior capsule opacification in pseudophakic eyes. Ophthalmology (1983) 1.66
Mutational analysis and clinical correlation in Leber congenital amaurosis. Ophthalmic Genet (2000) 1.65
Toxicity of intravitreous ceftazidime in primate retina. Arch Ophthalmol (1992) 1.63
Histopathology of commotio retinae. Retina (1992) 1.62
CD3+ CD8+ CTL activity within the human female reproductive tract: influence of stage of the menstrual cycle and menopause. J Immunol (1997) 1.62
Asperillosis of the orbit. Report of ten cases and review of the literature. Arch Ophthalmol (1969) 1.56
The role of apoptosis in the pathogenesis of Fuchs endothelial dystrophy of the cornea. Arch Ophthalmol (2001) 1.56
Clinicopathologic correlation of surgically removed macular hole opercula. Am J Ophthalmol (1995) 1.55
Detection of human papillomavirus type 6/11 DNA in conjunctival papillomas by in situ hybridization with radioactive probes. Hum Pathol (1987) 1.54
Central retinal vein occlusion: a prospective histopathologic study of 29 eyes in 28 cases. Trans Am Ophthalmol Soc (1981) 1.52
The eye in bone marrow transplantation. VI. Retinal complications. Arch Ophthalmol (1994) 1.51
Bietti's crystalline dystrophy. A clinicopathologic correlative study. Arch Ophthalmol (1989) 1.51
The eye in bone marrow transplantation. I. Clinical study. Arch Ophthalmol (1983) 1.51
Ocular manifestations of graft-vs-host disease. Ophthalmology (1983) 1.50
Histopathologic study of nine branch retinal vein occlusions. Arch Ophthalmol (1982) 1.48
Endophthalmitis due to Propionibacterium acnes sequestered between IOL optic and posterior capsule. Ophthalmic Surg (1989) 1.48
Genetic heterogeneity among blue-cone monochromats. Am J Hum Genet (1993) 1.47
Frequency of ocular metastases in patients dying of cancer in eye bank populations. Br J Ophthalmol (1996) 1.46
Clinical features, laboratory investigations, and survival in ocular reticulum cell sarcoma. Ophthalmology (1987) 1.46
Granulomatous reaction to Bruch's membrane in age-related macular degeneration. Arch Ophthalmol (1994) 1.46
Identification of novel rhodopsin mutations responsible for retinitis pigmentosa: implications for the structure and function of rhodopsin. Am J Hum Genet (1993) 1.45
Congenital motor nystagmus linked to Xq26-q27. Am J Hum Genet (1999) 1.45
Idiopathic epiretinal membranes. Ultrastructural characteristics and clinicopathologic correlation. Ophthalmology (1989) 1.45
Oxidative damage in age-related macular degeneration. Histol Histopathol (2007) 1.44
Immunohistochemical localization of fibrillin in human ocular tissues. Relevance to the Marfan syndrome. Arch Ophthalmol (1995) 1.44
Brown tumor of the orbit associated with primary hyperparathyroidism. Am J Ophthalmol (1980) 1.44
Massive hemorrhage complicating age-related macular degeneration. Clinicopathologic correlation and role of anticoagulants. Ophthalmology (1986) 1.44
Histopathologic features of idiopathic macular holes and cysts. Ophthalmology (1990) 1.43
The Lenz microphthalmia syndrome. Am J Ophthalmol (1988) 1.43
Autosomal recessive pericentral pigmentary retinopathy. Am J Ophthalmol (1988) 1.42
Histopathologic studies of ischemic optic neuropathy. Trans Am Ophthalmol Soc (2000) 1.41
Antibody to the ligand of CD40, gp39, blocks the occurrence of the acute and chronic forms of graft-vs-host disease. J Clin Invest (1994) 1.41
Elevated intraocular pressure, pigment dispersion and dark hypopyon in endogenous endophthalmitis from Listeria monocytogenes. Surv Ophthalmol (1992) 1.41
Provision of anesthesia with single application of lidocaine 2% gel. J Cataract Refract Surg (1999) 1.40
Morphology, pathology, and surgery of idiopathic vitreoretinal macular disorders. A review. Retina (1990) 1.40
Visual prognosis in autosomal dominant optic atrophy (Kjer type). Am J Ophthalmol (1993) 1.38
Immunohistochemical localization of blood-retinal barrier breakdown in human diabetics. Am J Pathol (1989) 1.38
A histopathologic study of macular cysts and holes. Retina (1981) 1.36
Vitreoretinal degeneration as a sign of generalized connective tissue diseases. Am J Ophthalmol (1979) 1.36
Ophthalmologic manifestations of carotid occlusive disease. Eye (Lond) (1991) 1.34
Temporal arteritis. A clinicopathologic study. Ophthalmology (1986) 1.34
The eye in bone marrow transplantation. III. Conjunctival graft-vs-host disease. Arch Ophthalmol (1989) 1.34
Autosomal recessively inherited ocular albinism. A new form of ocular albinism affecting females as severely as males. Arch Ophthalmol (1978) 1.33
Endogenous Serratia marcescens endophthalmitis with dark hypopyon: case report and review. Surv Ophthalmol (2001) 1.33
Detection of CX3CR1 single nucleotide polymorphism and expression on archived eyes with age-related macular degeneration. Histol Histopathol (2005) 1.32
Ocular clinicopathologic study of gyrate atrophy. Am J Ophthalmol (1991) 1.32