Yamada M - Search Results

1

On the role of kerato-epithelin in the pathogenesis of 5q31-linked corneal dystrophies.

Korvatska E, Munier FL, Chaubert P, Wang MX, Mashima Y, Yamada M, Uffer S, Zografos L, Schorderet DF. Korvatska E, et al. Among authors: yamada m. Invest Ophthalmol Vis Sci. 1999 Sep;40(10):2213-9. Invest Ophthalmol Vis Sci. 1999. PMID: 10476785

2

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.

Korvatska E, Henry H, Mashima Y, Yamada M, Bachmann C, Munier FL, Schorderet DF. Korvatska E, et al. Among authors: yamada m. J Biol Chem. 2000 Apr 14;275(15):11465-9. doi: 10.1074/jbc.275.15.11465. J Biol Chem. 2000. PMID: 10753964 Free article.

3

The classic form of granular corneal dystrophy associated with R555W mutation in the BIGH3 gene is rare in Japanese patients.

Konishi M, Mashima Y, Yamada M, Kudoh J, Shimizu N. Konishi M, et al. Among authors: yamada m. Am J Ophthalmol. 1998 Sep;126(3):450-2. doi: 10.1016/s0002-9394(98)00105-6. Am J Ophthalmol. 1998. PMID: 9744382

4

Association of autosomal dominantly inherited corneal dystrophies with BIGH3 gene mutations in Japan.

Mashima Y, Yamamoto S, Inoue Y, Yamada M, Konishi M, Watanabe H, Maeda N, Shimomura Y, Kinoshita S. Mashima Y, et al. Among authors: yamada m. Am J Ophthalmol. 2000 Oct;130(4):516-7. doi: 10.1016/s0002-9394(00)00571-7. Am J Ophthalmol. 2000. PMID: 11024425

5

Immunohistology of kerato-epithelin in corneal stromal dystrophies associated with R124 mutations of the BIGH3 gene.

Konishi M, Yamada M, Nakamura Y, Mashima Y. Konishi M, et al. Among authors: yamada m. Curr Eye Res. 2000 Nov;21(5):891-6. doi: 10.1076/ceyr.21.5.891.5536. Curr Eye Res. 2000. PMID: 11262611

6

[Autosomal dominant inherited corneal dystrophies associated with TGFBI mutation].

Mashima Y, Yamada M, Oguchi Y. Mashima Y, et al. Among authors: yamada m. Nippon Ganka Gakkai Zasshi. 2001 Oct;105(10):659-72. Nippon Ganka Gakkai Zasshi. 2001. PMID: 11692612 Review. Japanese.

7

Corneal electrolysis for recurrence of corneal stromal dystrophy after keratoplasty.

Mashima Y, Kawai M, Yamada M. Mashima Y, et al. Among authors: yamada m. Br J Ophthalmol. 2002 Mar;86(3):273-5. doi: 10.1136/bjo.86.3.273. Br J Ophthalmol. 2002. PMID: 11864880 Free PMC article.

8

Varied appearance of cornea of patients with corneal dystrophy associated with R124H mutation in the BIGH3 gene.

Konishi M, Yamada M, Nakamura Y, Mashima Y. Konishi M, et al. Among authors: yamada m. Cornea. 1999 Jul;18(4):424-9. doi: 10.1097/00003226-199907000-00006. Cornea. 1999. PMID: 10422854

9

Haplotye analysis of Jaanese families with a superficial variant of granular corneal dystrohy: evidence for multiple origins of R124L mutation of keratoepithelin.

Korvatska E, Yamada M, Yamamoto S, Okada M, Munier FL, Schorderet DF, Mashima Y. Korvatska E, et al. Among authors: yamada m. Ophthalmic Genet. 2000 Mar;21(1):63-5. Ophthalmic Genet. 2000. PMID: 10896446 No abstract available.

10

Quantitative analysis of lipid deposits from Schnyder's corneal dystrophy.

Yamada M, Mochizuki H, Kamata Y, Nakamura Y, Mashima Y. Yamada M, et al. Br J Ophthalmol. 1998 Apr;82(4):444-7. doi: 10.1136/bjo.82.4.444. Br J Ophthalmol. 1998. PMID: 9640198 Free PMC article.

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