Search | IOVS | ARVO Journals

Access Provided By:
MIT Libraries

Forgot password?

Create an Account

View

Showing 1 – 13 of 13

SORT: Best Match Most Recent Oldest

VIEW: Basic | Expanded

ARVO Annual Meeting Abstract April 2011

Dominant Mutations In RP1L1 Are Responsible For Occult Macular Dystrophy

Masakazu Akahori; Kazushige Tsunoda; Yozo Miyake; Shoji Tsuji; Tomoaki Usui; Makoto Nakamura; Hisao Ohde; Takeshi Itabashi; Takeshi Iwata

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):5385.

ARVO Annual Meeting Abstract May 2006

Mutation Analysis of ROM1 Gene in Japanese Patients with Autosomal Dominant Retinitis Pigmentosa

H. Sato; Y. Wada; T. Itabashi; A. Tada; E. Imai; K. Nishida

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):1032.

ARVO Annual Meeting Abstract May 2006

A Novel Gly222Glu Mutation in VMD2 Causes Best Macular Dystrophy in Japanese Population

S. Yokokura; Y. Wada; T. Itabashi; H. Sato; K. Nishida

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):1051.

ARVO Annual Meeting Abstract May 2006

Mutation Survey and Clinical Characteristics of Japanese Patients With X–Linked Juvenile Retinoschisis

T. Itabashi; Y. Wada; A. Tada; H. Sato; E. Imai; M. Sukegawa; K. Nishida

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):4611.

ARVO Annual Meeting Abstract May 2006

Screening for Mutations in CYP4V2 Gene in Japanese Patients With Bietti's Crystalline Corneoretinal Dystrophy

M. Sukegawa; Y. Wada; T. Itabashi; A. Tada; H. Sato; E. Imai; K. Nishida

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):4633.

ARVO Annual Meeting Abstract May 2006

Prevalence of Mutations in Seven Candidate Genes in Japanese Patients With Leber`s Congenital Amaurosis

Y. Wada; T. Itabashi; M. Sukegawa; A. Tada; H. Sato; E. Imai; K. Nishida

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):1691.

ARVO Annual Meeting Abstract May 2006

Mutation Survey of the ABCA4 Gene in Japanese Patients With Stargardt Disease, Cone Rod Dystrophy and Autosomal Recessive Retinitis Pigmentosa

A. Tada; Y. Wada; T. Itabashi; M. Sukegawa; H. Sato; E. Imai; K. Nishida

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):1695.

ARVO Annual Meeting Abstract May 2004

Autosomal Dominant Retinitis Pigmentosa Associated with 1142delG, 1155–1159delGGACG/insAGGGATT and IVS6 –3 to –45del Mutations in PRPF31 Gene.

H. Sato; Y. Wada; T. Itabashi; M. Nakamura; M. Kawamura; M. Tamai

Invest. Ophthalmol. Vis. Sci.. 2004; 45(13):2455.

ARVO Annual Meeting Abstract May 2004

Prevalence of Mutations in Nine Candidate Genes in Japanese Patients with Autosomal Dominant Retinitis Pigmentosa

Y. Wada; H. Sato; T. Itabashi; M. Kawamura; Y. Noda; M. Nakamura; T. Ishibashi; M. Tamai

Invest. Ophthalmol. Vis. Sci.. 2004; 45(13):2456.

ARVO Annual Meeting Abstract May 2004

Three Novel Mutations in the RPGR Gene in Three Japanese Families with X–linked Retinitis Pigmentosa.

T. Itabashi; Y. Wada; H. Sato; M. Kawamura; A. Tada; M. Tamai

Invest. Ophthalmol. Vis. Sci.. 2004; 45(13):2468.

ARVO Annual Meeting Abstract May 2003

Clinical Features of Japanese Families Associated with 402 delT and 555-556 delAG Mutations in the CHM Gene

T. Itabashi; Y. Wada; M. Kawamura; H. Sato; M. Tamai

Invest. Ophthalmol. Vis. Sci.. 2003; 44(13):1487.

ARVO Annual Meeting Abstract May 2003

Two Novel ARG825X and 2336-2337delCT Mutations in the RP1 Gene in Japanese Families With Autosomal Dominant Retinitis Pigmentosa

M. Kawamura; Y. Wada; T. Itabashi; S. Ogawa; H. Sato; T. Abe; Y. Noda; T. Ishibashi; M. Tamai

Invest. Ophthalmol. Vis. Sci.. 2003; 44(13):2304.

ARVO Annual Meeting Abstract May 2003

Low Vision Evaluator (LoVE) in Children with Ocular Diseases

H. Kunikata; Y. Nakagawa; T. Itabashi; M. Noro; M. Tamai

Invest. Ophthalmol. Vis. Sci.. 2003; 44(13):2768.

Advertisement