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Ophthalmological Disorders, Other
Contributing journals to this collection:
JAMA & Archives Journals
Citations 401-410 of 461 total displayed.
- Clinical Sciences
Classification of Visual Field Abnormalities in the Ocular Hypertension Treatment Study
- John L. Keltner; Chris A. Johnson; Kimberly E. Cello; Mary A. Edwards; Shannan E. Bandermann; Michael A. Kass; Mae O. Gordon
Arch Ophthalmol 2003; 121: 643-650.
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- Clinical Sciences
Retinal Microvascular Abnormalities in Patients Treated With External Radiation for Graves Ophthalmopathy
- Dennis M. Robertson; Helmut Buettner; Colum A. Gorman; James A. Garrity; Vahab Fatourechi; Rebecca S. Bahn; Ivy A. Petersen; Scott L. Stafford; John D. Earle; Glenn S. Forbes; Robert W. Kline; Erik J. Bergstralh; Kenneth P. Offord; Diana M. Rademacher; Nancy M. Stanley; George B. Bartley
Arch Ophthalmol 2003; 121: 652-657.
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- Clinical Sciences
Idiopathic Orbital Inflammation: Distribution, Clinical Features, and Treatment Outcome
- Sonia J. Ahn Yuen; Peter A. D. Rubin
Arch Ophthalmol 2003; 121: 491-499.
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- Clinicopathologic Reports, Case Reports, and Small Case Series
Chiasmal Enlargement and Optic Nerve Enhancement on Magnetic Resonance Imaging in Leber Hereditary Optic Neuropathy
- Paul H. Phillips; Michael Vaphiades; Charles M. Glasier; Lawrence G. Gray; Andrew G. Lee
Arch Ophthalmol 2003; 121: 577-579.
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- Clinical Sciences
Using the Arteriolar Pressure Attenuation Index to Predict Ocular Hypertension Progression to Open-angle Glaucoma
- Shawn L. Cohen; Paul P. Lee; Leon W. Herndon; Pratap Challa; Olga Overbury; R. Rand Allingham
Arch Ophthalmol 2003; 121: 33-38.
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- Ophthalmic Molecular Genetics
Paternal Uniparental Heterodisomy With Partial Isodisomy of Chromosome 1 in a Patient With Retinitis Pigmentosa Without Hearing Loss and a Missense Mutation in the Usher Syndrome Type II Gene USH2A
- Carlo Rivolta; Eliot L. Berson; Thaddeus P. Dryja
Arch Ophthalmol 2002; 120: 1566-1571.
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- Clinical Sciences
One-Year, Randomized Study Comparing Bimatoprost and Timolol in Glaucoma and Ocular Hypertension
- Eve J. Higginbotham; Joel S. Schuman; Ivan Goldberg; Ronald L. Gross; Amanda M. VanDenburgh; Kuankuan Chen; Scott M. Whitcup; for the Bimatoprost Study Groups 1 and 2
Arch Ophthalmol 2002; 120: 1286-1293.
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- Clinical Sciences
Electroretinographic Abnormalities in Parents of Patients With Leber Congenital Amaurosis Who Have Heterozygous GUCY2D Mutations
- Robert K. Koenekoop; Gerald A. Fishman; Alessandro Iannaccone; Hany Ezzeldin; Maria L. Ciccarelli; Alfonso Baldi; Janet S. Sunness; Andrew J. Lotery; Monica M. Jablonski; Steven J. Pittler; Irene Maumenee
Arch Ophthalmol 2002; 120: 1325-1330.
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- Ophthalmic Molecular Genetics
The Phenotype in Norwegian Patients With Bardet-Biedl Syndrome With Mutations in the BBS4 Gene
- Ruth Riise; Kristina Tornqvist; Alan F. Wright; Kirk Mykytyn; Val C. Sheffield
Arch Ophthalmol 2002; 120: 1364-1367.
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- Clinical Sciences
Quantitative Electroretinogram Measures of Phototransduction in Cone and Rod Photoreceptors: Normal Aging, Progression With Disease, and Test-Retest Variability
- David G. Birch; Donald C. Hood; Kirsten G. Locke; Dennis R. Hoffman; Radoul T. Tzekov
Arch Ophthalmol 2002; 120: 1045-1051.
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