A. Kimura

发表

RDS gene mutations causing retinitis pigmentosa or macular degeneration lead to the same abnormality in photoreceptor function.

C. M. Kemp, V. Sheffield, A. Cideciyan, 1994, Investigative ophthalmology & visual science.

Identification of novel rhodopsin mutations associated with retinitis pigmentosa by GC-clamped denaturing gradient gel electrophoresis.

V. Sheffield, G. Fishman, E. Stone, 1991, American journal of human genetics.

Clinical and electroretinographic findings of female carriers and affected males in a progressive X-linked cone-rod dystrophy (COD-1) pedigree.

M. Gorin, Jeremiah Brown, A. Kimura, 2000, Ophthalmology.

VISUAL OUTCOME FOLLOWING SUBRETINAL HEMORRHAGE IN BEST DISEASE

E. Stone, M. Chung, K. Oh, 2001, Retina.

Common variant in VEGFA and response to anti-VEGF therapy for neovascular age-related macular degeneration.

R. Avery, D. Pieramici, I. Kozák, 2013, Current molecular medicine.

Visual prognosis of multifocal choroiditis, punctate inner choroidopathy, and the diffuse subretinal fibrosis syndrome.

J. Folk, C. Reddy, A. Kimura, 1996, Ophthalmology.

Laser treatment for subfoveal neovascular membranes in ocular histoplasmosis syndrome: results of a pilot randomized clinical trial.

N. Bressler, G. Fish, M. Maguire, 1993, Archives of ophthalmology.

A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea.

V. Sheffield, E. Stone, B. Nichols, 1993, Human molecular genetics.

Procollagen II gene mutation in Stickler syndrome.

V. Sheffield, E. Stone, T. Weingeist, 1992, Archives of ophthalmology.

Erosive vitreoretinopathy. A new clinical entity.

E. Stone, T. Weingeist, A. Kimura, 1994, Ophthalmology.

Central retinal artery occlusion. Retinal survival time.

S. Hayreh, M. Zimmerman, A. Kimura, 2004, Experimental eye research.

Retinitis Pigmentosa and Associated Disorders

A. Drack, A. Kimura, 2006 .

Acute promyelocytic infiltration of the optic nerve treated by oral trans-retinoic acid.

K. Ossoinig, G. Weiner, A. Kimura, 1992, Ophthalmology.

Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13.

V. Sheffield, J. Folk, E. Stone, 1992, Human molecular genetics.

Enlarged blind spots in chorioretinal inflammatory disorders.

S. Gupta, J. Folk, C. Reddy, 1996, Ophthalmology.

Differentiation of ischemic from non-ischemic central retinal vein occlusion during the early acute phase

S. Hayreh, P. Podhajsky, A. Kimura, 2004, Graefe's Archive for Clinical and Experimental Ophthalmology.

Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q.

V. Sheffield, E. Stone, T. Weingeist, 1994, Archives of ophthalmology.

Ocular findings associated with rhodopsin gene codon 17 and codon 182 transition mutations in dominant retinitis pigmentosa.

V. Sheffield, G. Fishman, E. Stone, 1992, Archives of ophthalmology.

Genetic linkage of Wagner disease and erosive vitreoretinopathy to chromosome 5q13-14.

A. Schinzel, T. Weingeist, E. Messmer, 1995, Archives of ophthalmology.

Acetazolamide for treatment of chronic macular edema in retinitis pigmentosa.

G. Fishman, L. Jampol, R. Fiscella, 1989, Archives of ophthalmology.

Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13

V. Sheffield, E. Stone, B. Nichols, 1992, Nature Genetics.

Intraocular lens placement behind the posterior capsule.

A. Mansour, A. Kimura, R. A. Yannis, 1990, Ophthalmic surgery.

INTRAVITREAL DEXAMETHASONE IMPLANT IN RETINITIS PIGMENTOSA–RELATED CYSTOID MACULAR EDEMA

A. Mansour, M. Moschos, M. Maia, 2017, Retina.

Autosomal dominant neovascular inflammatory vitreoretinopathy.

J. Folk, S. Russell, E. Stone, 1990, Ophthalmology.

Butterfly–shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene

V. Sheffield, E. Stone, B. Nichols, 1993, Nature Genetics.

Regional distribution of retinal degeneration in patients with the proline to histidine mutation in codon 23 of the rhodopsin gene.

V. Sheffield, G. Fishman, E. Stone, 1991, Ophthalmology.

Linkage analysis of X-linked cone-rod dystrophy: localization to Xp11.4 and definition of a locus distinct from RP2 and RP3.

J. O’Connell, R. Ferrell, A. Seymour, 1998, American Journal of Human Genetics.

Sustained elevation of intraocular pressure after intravitreal injections of anti-VEGF agents

M. Kahook, N. Mandava, A. Kimura, 2010, British Journal of Ophthalmology.

Sustained elevation in intraocular pressure associated with intravitreal bevacizumab injections.

M. Kahook, N. Mandava, D. Ammar, 2009, Ophthalmic surgery, lasers & imaging : the official journal of the International Society for Imaging in the Eye.

Autoimmune retinopathy in the absence of cancer.

J. B. Mizener, R. Kardon, G. Adamus, 1997, American journal of ophthalmology.

The treatment of serous macular detachment secondary to choroidal melanomas and nevi.

R. Folberg, J. Folk, T. Weingeist, 1989, Ophthalmology.

Removal of subretinal hemorrhage facilitated by preoperative intravitreal tissue plasminogen activator.

J. Folk, C. Reddy, A. Kimura, 1994, Retina.

Subretinal fluid associated with membranoproliferative glomerulonephritis type 2.

J. Gass, D. Park, A. Kimura, 1997, A M A Archives of Ophthalmology.

Diabetic retinopathy screening and the use of telemedicine

Sunil Gupta, I. Zimmer-Galler, A. Kimura, 2015, Current opinion in ophthalmology.

A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea.

V. Sheffield, E. Stone, B. Nichols, 1993, Human molecular genetics.

THE USE OF INTRAVTTREAL TISSUE PLASMINOGEN ACTIVATOR IN THE TREATMENT OF EXPERIMENTAL SUBRETINAL HEMORRHAGE IN THE PIG MODEL

J. Folk, A. Kimura, H. Boldt, 1996, Retina.

Ocular findings associated with a Cys39Arg mutation in the Norrie disease gene.

E. Stone, K. Joos, K. Vandenburgh, 1994, Archives of ophthalmology.