Shigeo Yoshida
Department of Ophthalmology
Kyushu University Graduate School of Medicine
Fukuoka
Japan
Name/email consistency: high
- Prognostic DNA testing and counselling for dominant optic atrophy due to a novel OPA1 mutation. Yoshida, S., Yamaji, Y., Yoshida, A., Kuwahara, R., Fujisawa, K., Ishibashi, T. Can. J. Ophthalmol. (2006)
- Novel mutation in ABCC6 gene in a Japanese pedigree with pseudoxanthoma elasticum and retinitis pigmentosa. Yoshida, S., Honda, M., Yoshida, A., Nakao, S., Goto, Y., Nakamura, T., Fujisawa, K., Ishibashi, T. Eye. (Lond) (2005)
- Rapid genotyping for most common TGFBI mutations with real-time polymerase chain reaction. Yoshida, S., Yamaji, Y., Yoshida, A., Noda, Y., Kumano, Y., Ishibashi, T. Hum. Genet. (2005)
- Lattice corneal dystrophy type I without typical lattice lines: role of mutational analysis. Yoshida, S., Yoshida, A., Nakao, S., Emori, A., Nakamura, T., Fujisawa, K., Kumano, Y., Ishibashi, T. Am. J. Ophthalmol. (2004)
- Induction of IL-8, MCP-1, and bFGF by TNF-alpha in retinal glial cells: implications for retinal neovascularization during post-ischemic inflammation. Yoshida, S., Yoshida, A., Ishibashi, T. Graefes Arch. Clin. Exp. Ophthalmol. (2004)
- Novel mutation in FZD4 gene in a Japanese pedigree with familial exudative vitreoretinopathy. Yoshida, S., Arita, R., Yoshida, A., Tada, H., Emori, A., Noda, Y., Nakao, S., Fujisawa, K., Ishibashi, T. Am. J. Ophthalmol. (2004)
