Authors:
Ogawa, Y
Okamoto, S
Kuwana, M
Mori, T
Watanabe, R
Nakajima, T
Yamada, M
Mashima, Y
Tsubota, K
Oguchi, Y
Citation: Y. Ogawa et al., Successful treatment of dry eye in two patients with chronic graft-versus-host disease with systemic administration of FK506 and corticosteroids, CORNEA, 20(4), 2001, pp. 430-434
Authors:
Mashima, Y
Suzuki, Y
Sergeev, Y
Ohtake, Y
Tanino, T
Kimura, I
Miyata, H
Aihara, M
Tanihara, H
Inatani, M
Azuma, N
Iwata, T
Araie, A
Citation: Y. Mashima et al., Novel cytochrome P4501B1 (CYP1B1) gene mutations in Japanese patients withprimary congenital glaucoma, INV OPHTH V, 42(10), 2001, pp. 2211-2216
Authors:
Ogawa, Y
Yamazaki, K
Kuwana, M
Mashima, Y
Nakamura, Y
Ishida, S
Toda, I
Oguchi, Y
Tsubota, K
Okamoto, SJ
Kawakami, Y
Citation: Y. Ogawa et al., A significant role of stromal fibroblasts in rapidly progressive dry eye in patients with chronic GVHD, INV OPHTH V, 42(1), 2001, pp. 111-119
Authors:
Yamada, M
Shinoda, K
Hatakeyama, A
Nishina, S
Mashima, Y
Citation: M. Yamada et al., Fat adherence syndrome after retinal surgery treated with amniotic membrane transplantation, AM J OPHTH, 132(2), 2001, pp. 280-282
Authors:
Shinoda, K
Ohde, H
Mashima, Y
Inoue, R
Ishida, S
Inoue, M
Kawashima, S
Oguchi, Y
Citation: K. Shinoda et al., On- and off-responses of the photopic electroretinograms in X-linked juvenile retinoschisis, AM J OPHTH, 131(4), 2001, pp. 489-494
Authors:
Mashima, Y
Kigasawa, K
Wakakura, M
Oguchi, Y
Citation: Y. Mashima et al., Do idebenone and vitamin therapy shorten the time to achieve visual recovery in Leber hereditary optic neuropathy?, J NEURO-OPH, 20(3), 2000, pp. 166-170
Authors:
Ma, CL
Kasama, A
Tanaka, H
Tan, Y
Tanaka, R
Mashima, Y
Hanada, S
Citation: Cl. Ma et al., Microstructures and mechanical properties of Nb/Nb-silicide in-situ composites synthesized by reactive hot pressing of ball milled powders, MATER T JIM, 41(3), 2000, pp. 444-451
Authors:
Konishi, M
Yamada, M
Nakamura, Y
Mashima, Y
Citation: M. Konishi et al., Immunohistology of kerato-epithelin in corneal stromal dystrophies associated with R124 mutations of the BIGH3 gene, CURR EYE R, 21(5), 2000, pp. 891-896
Authors:
Oshima, T
Kurosaka, D
Kato, K
Kurosaka, H
Mashima, Y
Tanaka, Y
Tajima, S
Citation: T. Oshima et al., Tranilast inhibits cell proliferation and collagen synthesis by rabbit corneal and Tenon's capsule fibroblasts, CURR EYE R, 20(4), 2000, pp. 283-286
Authors:
Korvatska, E
Henry, H
Mashima, Y
Yamada, M
Bachmann, C
Munier, FL
Schorderet, DF
Citation: E. Korvatska et al., Amyloid and non-amyloid forms of 5q31-linked corneal dystrophy resulting from kerato-epithelin mutations at Arg-124 are associated with abnormal turnover of the protein, J BIOL CHEM, 275(15), 2000, pp. 11465-11469
Authors:
Mashima, Y
Yamamoto, S
Inoue, Y
Yamada, M
Konishi, M
Watanabe, H
Maeda, N
Shimomura, Y
Kinoshita, S
Citation: Y. Mashima et al., Association of autosomal dominantly inherited corneal dystrophies with BIGH3 gene mutations in Japan, AM J OPHTH, 130(4), 2000, pp. 516-517
Authors:
Mashima, Y
Saga, M
Hiida, Y
Imamura, Y
Kudoh, J
Shimizu, N
Citation: Y. Mashima et al., Novel mutation in RP2 gene in two brothers with X-linked retinitis pigmentosa and mtDNA mutation of Leber hereditary optic neuropathy who showed marked differences in clinical severity, AM J OPHTH, 130(3), 2000, pp. 357-359
Citation: M. Yamada et al., Decreased substance P concentrations in tears from patients with corneal hypesthesia, AM J OPHTH, 129(5), 2000, pp. 671-672
Authors:
Ohtake, Y
Chen, JB
Gamou, S
Takayanagi, A
Mashima, Y
Oguchi, Y
Shimizu, N
Citation: Y. Ohtake et al., Ex vivo delivery of suicide genes into melanoma cells using epidermal growth factor receptor-specific Fab immunogene, JPN J CANC, 90(4), 1999, pp. 460-468
Authors:
Nagasawa, A
Kudoh, J
Noda, S
Mashima, Y
Wright, A
Oguchi, Y
Shimizu, N
Citation: A. Nagasawa et al., Human and mouse ISLR (immunoglobulin superfamily containing leucine-rich repeat) genes: Genomic structure and tissue expression, GENOMICS, 61(1), 1999, pp. 37-43
Authors:
Fujiki, K
Hotta, Y
Hayakawa, M
Saito, A
Mashima, Y
Mori, M
Yoshii, M
Murakami, A
Matsumoto, M
Hayasaka, S
Tagami, N
Isashiki, Y
Ohba, N
Kanai, A
Citation: K. Fujiki et al., REP-1 gene mutations in Japanese patients with choroideremia, GR ARCH CL, 237(9), 1999, pp. 735-740
Authors:
Konishi, M
Yamada, M
Nakamura, Y
Mashima, Y
Citation: M. Konishi et al., Varied appearance of cornea of patients with corneal dystrophy associated with R124H mutation in the BIGH3 gene, CORNEA, 18(4), 1999, pp. 424-429
Authors:
Yamada, K
Oguchi, Y
Hotta, Y
Nakamura, M
Isashiki, Y
Mashima, Y
Citation: K. Yamada et al., Multicenter study on the frequency of three primary mutations of mitochondrial DNA in Japanese pedigrees with Leber's hereditary optic neuropathy: comparison with American and British counterparts, NEURO-OPHTH, 22(3), 1999, pp. 187-193
Authors:
Korvatska, E
Munier, FL
Chaubert, P
Wang, MX
Mashima, Y
Yamada, M
Uffer, S
Zografos, L
Schorderet, DF
Citation: E. Korvatska et al., On the role of kerato-epithelin in the pathogenesis of 5q31-linked cornealdystrophies, INV OPHTH V, 40(10), 1999, pp. 2213-2219