和田裕子 (Yuko Wada) - マイポータル

基本情報

所属: 旧所属東北大学病院（医科部門）眼科講師

J-GLOBAL ID: 200901052976982299
researchmap会員ID: 5000030952

MISC

Mutations in the Pre-mRNA splicing gene, PRPF31, in Japanese families with autosomal dominant retinitis pigmentosa

H Sato, Y Wada, T Itabashi, M Nakamura, M Kawamura, M Tamai

AMERICAN JOURNAL OF OPHTHALMOLOGY 140(3) 537-540 2005年9月
Screening for mutations in the IMPDH1 gene in Japanese patients with autosomal dominant retinitis pigmentosa.

Y Wada, A Tada, T Itabashi, M Kawamura, H Sato, M Tamai

AMERICAN JOURNAL OF OPHTHALMOLOGY 140(1) 163-165 2005年7月
Screening for mutations in CYP4V2 gene in Japanese patients with Bietti's crystalline corneoretinal dystrophy

Y Wada, T Itabashi, H Sato, M Kawamura, A Tada, M Tamai

AMERICAN JOURNAL OF OPHTHALMOLOGY 139(5) 894-899 2005年5月
Screen of the IMPDH1 gene among patients with dominant retinitis pigmentosa and clinical features associated with the most common mutation, Asp226Asn

Y Wada, MA Sandberg, TL McGee, MA Stillberger, EL Berson, TP Dryja

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 46(5) 1735-1741 2005年5月
Targeted disruption of FSCN2 gene induces retinopathy in mice.

Invest Ophthalmol Vis Sci 46(8) 2905-2915 2005年
Targeted disruption of FSCN2 gene induces retinopathy in mice.

Invest Ophthalmol Vis Sci 46(8) 2905-2915 2005年
Clinical features of Japanese families with a 402delT or a 555-556delAG mutation in choroideremia gene

T Itabashi, Y Wada, M Kawamura, J Sato, M Tamai

RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES 24(6) 940-945 2004年12月
Clinical features of a Japanese family with autosomal dominant retinitis pigmentosa associated with a Thr494Met mutation in the HPRP3 gene

Yuko Wada, Toshitaka Itabashi, Hajime Sato, Makoto Tamai

Graefe's Archive for Clinical and Experimental Ophthalmology 242(11) 956-961 2004年11月
Clinical features of a Japanese family with autosomal dominant retinitis pigmentosa associated with a Thr494Met mutation in the HPRP3 gene

Y Wada, T Itabashi, H Sato, M Tamai

GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY 242(11) 956-961 2004年11月
Novel 615delC mutation in the CRX gene in a Japanese family with cone-rod dystrophy

T Itabashi, Y Wada, H Sato, M Kawamura, T Shiono, M Tamai

AMERICAN JOURNAL OF OPHTHALMOLOGY 138(5) 876-877 2004年11月
Novel 2336-2337 delCT mutation in RP1 gene in a Japanese family with autosomal dominant retinitis pigmentosa

M Kawamura, Y Wada, Y Noda, T Itabashi, SI Ogawa, H Sato, K Tanaka, T Ishibashi, M Tamai

AMERICAN JOURNAL OF OPHTHALMOLOGY 137(6) 1137-1139 2004年6月
An instrument capable of grading visual function: results from patients with retinitis pigmentosa.

TAMAI M, KUNIKATA H, ITABASHI T, KAWAMURA M, SAIGO Y, SATO H, WADA Y, NAKAGAWA Y

Tohoku J Exp Med 203(4) 305-312 2004年
An instrument capable of grading visual function: results from patients with retinitis pigmentosa.

Tohoku J Exp Med 203(4) 305-312 2004年
Autosomal dominant macular degeneration associated with 208delG mutation in the FSCN2 gene

Y Wada, T Abe, T Itabashi, H Sato, M Kawamura, M Tamai

ARCHIVES OF OPHTHALMOLOGY 121(11) 1613-1620 2003年11月
Ocular findings in a Japanese family with an Arg41Trp mutation of the CRX gene

T Itabashi, Y Wada, H Sato, H Kunikata, M Kawamura, M Tamai

GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY 241(7) 535-540 2003年7月
[Molecular genetic analysis for Japanese patients with autosomal dominant retinitis pigmentosa] (Nippon Ganka Gakkai Zasshi)

Nippon Ganka Gakkai Zasshi 107(11) 687-694 2003年
Retinitis pigmentosa associated with ectopia lentis

H Sato, Y Wada, T Abe, M Kawamura, R Wakusawa, M Tamai

ARCHIVES OF OPHTHALMOLOGY 120(6) 852-854 2002年6月
A novel (Pro79Thr) mutation in the FKHL7 gene in a Japanese family with Axenfeld-Rieger syndrome

T Suzuki, K Takahashi, S Kuwahara, Y Wada, T Abe, M Tamai

AMERICAN JOURNAL OF OPHTHALMOLOGY 132(4) 572-575 2001年10月
Mutation of human retinal fascin gene (FSCN2) causes autosomal dominant retinitis pigmentosa

Y Wada, T Abe, T Takeshita, H Sato, K Yanashima, M Tamai

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 42(10) 2395-2400 2001年9月
A novel Gly35Ser mutation in the RDH5 gene in a Japanese family with fundus albipunctatus associated with cone dystrophy

Y Wada, T Abe, H Sato, M Tamai

ARCHIVES OF OPHTHALMOLOGY 119(7) 1059-1063 2001年7月

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