Rchr

J-GLOBAL ID：200901069073507608 Update date: Dec. 18, 2024

Itabashi Toshitaka

イタバシトシタカ | Itabashi Toshitaka

Affiliation and department：
Job title： Research Associate
Research theme for competitive and other funds (2)：

-
-

MISC (16)：

H Sato, Y Wada, T Itabashi, M Nakamura, M Kawamura, M Tamai. Mutations in the Pre-mRNA splicing gene, PRPF31, in Japanese families with autosomal dominant retinitis pigmentosa. AMERICAN JOURNAL OF OPHTHALMOLOGY. 2005. 140. 3. 537-540
Y Wada, A Tada, T Itabashi, M Kawamura, H Sato, M Tamai. Screening for mutations in the IMPDH1 gene in Japanese patients with autosomal dominant retinitis pigmentosa. AMERICAN JOURNAL OF OPHTHALMOLOGY. 2005. 140. 1. 163-165
Y Wada, T Itabashi, H Sato, M Kawamura, A Tada, M Tamai. Screening for mutations in CYP4V2 gene in Japanese patients with Bietti's crystalline corneoretinal dystrophy. AMERICAN JOURNAL OF OPHTHALMOLOGY. 2005. 139. 5. 894-899
H Kunikata, O Nakagawa, M Noro, T Itabashi, H Yoshida, R Wakusawa, Y Ban, E Mai, M Nakamura, M Kikuchi, et al. Introduction of the Low Vision Evaluator (LoVE) for children. JOURNAL OF PEDIATRIC OPHTHALMOLOGY & STRABISMUS. 2005. 42. 3. 155-162
Toshitaka Itabashi, Yuko Wada, Miyuki Kawamura, Hajime Sato, Makoto Tamai. Clinical features of Japanese families with a 402delT or a 555-556delAG mutation in choroideremia gene. Retina. 2004. 24. 6. 940-945

ｍore...

※ Researcher’s information displayed in J-GLOBAL is based on the information registered in researchmap. For details, see here.

Return to Previous Page

TOP

BOTTOM