D. Oh

Description of a new mutation in rhodopsin, Pro23Ala, and comparison with electroretinographic and clinical characteristics of the Pro23His mutation.

E. Stone, A. Lotery, K. T. Oh, 2000, Archives of ophthalmology.

LONG-TERM FOLLOW-UP OF PATIENTS WITH SERPINGINOUS CHOROIDITIS

J. Folk, D. Oh, K. Oh, 2002, Retina.

CLINICAL PHENOTYPE AS A PROGNOSTIC FACTOR IN STARGARDT DISEASE

E. Stone, R. Weleber, D. Oh, 2004, Retina.

Optic disc vasculitis

S. Hayreh, D. Oh, K. Oh, 2000, Graefe's Archive for Clinical and Experimental Ophthalmology.

Corneal thickness in Fuchs' dystrophy with and without epithelial oedema

D. Oh, W. Mathers, K. Oh, 1998, Eye.

ELECTRORETINOGRAPHIC FINDINGS IN PATIENTS WITH STARGARDT DISEASE AND FUNDUS FLAVIMACULATUS

E. Stone, R. Weleber, D. Oh, 2002, Retina.

Genotype-phenotype correlation in a family with Arg135Leu rhodopsin retinitis pigmentosa

R G Weleber, E. Stone, R. Weleber, 2004, British Journal of Ophthalmology.

Comparison of the clinical expression of retinitis pigmentosa associated with rhodopsin mutations at codon 347 and codon 23.

G. Fishman, E. Stone, K. Gehrs, 2003, American journal of ophthalmology.