板橋俊隆 (Toshitaka Itabashi) - 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）眼科感覚器・理学診療科眼科助手

J-GLOBAL ID: 200901069073507608
researchmap会員ID: 5000064702

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
Introduction of the Low Vision Evaluator (LoVE) for children

H Kunikata, O Nakagawa, M Noro, T Itabashi, H Yoshida, R Wakusawa, Y Ban, E Mai, M Nakamura, M Kikuchi …

JOURNAL OF PEDIATRIC OPHTHALMOLOGY & STRABISMUS 42(3) 155-162 2005年5月
Clinical features of Japanese families with a 402delT or a 555-556delAG mutation in choroideremia gene

Toshitaka Itabashi, Yuko Wada, Miyuki Kawamura, Hajime Sato, Makoto Tamai

Retina 24(6) 940-945 2004年12月
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
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
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 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
Autosomal Dominant Macular Degeneration Associated With 208delG Mutation in the FSCN2 Gene

Yuko Wada, Toshiaki Abe, Toshitaka Itabashi, Hajime Sato, Miyuki Kawamura, Makoto 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
Adult-onset foveomacular vitelliform dystrophy with retinal folds.

YAMAGUCHI K, YOSHIDA M, KANO T, ITABASHI T, YOSHIOKA Y, TAMAI M

Jpn J Ophthalmol 45(5) 533-537 2001年
Adult-onset foveomacular vitelliform dystrophy with retinal folds.

Jpn J Ophthalmol 45(5) 533-537 2001年

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