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Small Case Series Multimodal Fundus Imaging in Foveal Hypoplasia: Combined Scanning Laser Ophthalmoscope Imaging and Spectral-Domain Optical Coherence Tomography
Ophthalmic Molecular Genetics Association of a Novel Mutation in the Retinol Dehydrogenase 12 (RDH12) Gene With Autosomal Dominant Retinitis Pigmentosa
John H. Fingert; Kean Oh; Mina Chung; Todd E. Scheetz; Jeaneen L. Andorf; Rebecca M. Johnson; Val C. Sheffield; Edwin M. Stone
Arch Ophthalmol 2008; 126: 1301-1307.
[Abstract][Full text][PDF]
Small Case Series Familial Retinoblastoma With Unilateral and Unifocal Involvement in 2 Families
Shaden Sarafzadeh; Zélia M. Corrêa; James J. Augsburger
Arch Ophthalmol 2008; 126: 1308-1309.
[Extract][Full text][PDF]
Ophthalmic Molecular Genetics Phenotypic Expression of a PRPF8 Gene Mutation in a Large African American Family
Saloni Walia; Gerald A. Fishman; Jana Zernant-Rajang; Kairi Raime; Rando Allikmets
Arch Ophthalmol 2008; 126: 1127-1132.
[Abstract][Full text][PDF]
Ophthalmic Molecular Genetics Intraocular Pressure Response to Topical β-Blockers Associated With an ADRB2 Single-Nucleotide Polymorphism
Catherine A. McCarty; James K. Burmester; Bickol N. Mukesh; Richard B. Patchett; Russell A. Wilke
Arch Ophthalmol 2008; 126: 959-963.
[Abstract][Full text][PDF]
Clinical Sciences Retinal Morphological Changes of Patients With X-linked Retinoschisis Evaluated by Fourier-Domain Optical Coherence Tomography
Christina Gerth; Robert J. Zawadzki; John S. Werner; Elise Héon
Arch Ophthalmol 2008; 126: 807-811.
[Abstract][Full text][PDF]
Commentaries Adaptive Optics Retinal Imaging: Applications for Studying Retinal Degeneration
