Tsujikawa M - Search Results

1

Angiographic lesion of polypoidal choroidal vasculopathy on indocyanine green and fluorescein angiography.

Gomi F, Sawa M, Mitarai K, Tsujikawa M, Tano Y. Gomi F, et al. Among authors: tsujikawa m. Graefes Arch Clin Exp Ophthalmol. 2007 Oct;245(10):1421-7. doi: 10.1007/s00417-007-0564-y. Epub 2007 Mar 9. Graefes Arch Clin Exp Ophthalmol. 2007. PMID: 17347808

2

Differentiating full thickness macular holes from impending macular holes and macular pseudoholes.

Tsujikawa M, Ohji M, Fujikado T, Saito Y, Motokura M, Ishimoto I, Tano Y. Tsujikawa M, et al. Br J Ophthalmol. 1997 Feb;81(2):117-22. doi: 10.1136/bjo.81.2.117. Br J Ophthalmol. 1997. PMID: 9059244 Free PMC article. Clinical Trial.

3

Secondary vitrectomy for the treatment of macular holes occurring after vitrectomy.

Tsujikawa M, Saito Y, Lewis JM, Tano Y. Tsujikawa M, et al. Ophthalmic Surg Lasers. 1997 Apr;28(4):336-7. Ophthalmic Surg Lasers. 1997. PMID: 9101578

4

Granular corneal dystrophy with homozygous mutations in the kerato-epithelin gene.

Okada M, Yamamoto S, Watanabe H, Inoue Y, Tsujikawa M, Maeda N, Shimomura Y, Nishida K, Kinoshita S, Tano Y. Okada M, et al. Among authors: tsujikawa m. Am J Ophthalmol. 1998 Aug;126(2):169-76. doi: 10.1016/s0002-9394(98)00075-0. Am J Ophthalmol. 1998. PMID: 9727509

5

Chorioretinal damage caused by the excision of choroidal neovascularization.

Tsujikawa M, Sawa M, Lewis JM, Motokura M, Tsujikawa K, Ohji M, Saito Y, Tano Y. Tsujikawa M, et al. Among authors: tsujikawa k. Am J Ophthalmol. 1998 Sep;126(3):348-57. doi: 10.1016/s0002-9394(98)00089-0. Am J Ophthalmol. 1998. PMID: 9744367

6

Novel polymorphisms in the beta ig-h3 gene.

Tsujikawa M, Shimomura Y, Okada M, Yamamoto S, Tano Y, Kurahashi H. Tsujikawa M, et al. J Hum Genet. 1998;43(3):214-5. doi: 10.1007/s100380050075. J Hum Genet. 1998. PMID: 9747041

7

Homozygosity mapping of a gene responsible for gelatinous drop-like corneal dystrophy to chromosome 1p.

Tsujikawa M, Kurahashi H, Tanaka T, Okada M, Yamamoto S, Maeda N, Watanabe H, Inoue Y, Kiridoshi A, Matsumoto K, Ohashi Y, Kinoshita S, Shimomura Y, Nakamura Y, Tano Y. Tsujikawa M, et al. Am J Hum Genet. 1998 Oct;63(4):1073-7. doi: 10.1086/302071. Am J Hum Genet. 1998. PMID: 9758629 Free PMC article.

8

Two distinct kerato-epithelin mutations in Reis-Bücklers corneal dystrophy.

Okada M, Yamamoto S, Tsujikawa M, Watanabe H, Inoue Y, Maeda N, Shimomura Y, Nishida K, Quantock AJ, Kinoshita S, Tano Y. Okada M, et al. Among authors: tsujikawa m. Am J Ophthalmol. 1998 Oct;126(4):535-42. doi: 10.1016/s0002-9394(98)00135-4. Am J Ophthalmol. 1998. PMID: 9780098

9

Identification of the gene responsible for gelatinous drop-like corneal dystrophy.

Tsujikawa M, Kurahashi H, Tanaka T, Nishida K, Shimomura Y, Tano Y, Nakamura Y. Tsujikawa M, et al. Nat Genet. 1999 Apr;21(4):420-3. doi: 10.1038/7759. Nat Genet. 1999. PMID: 10192395

10

Change in retinal sensitivity due to excision of choroidal neovascularization and its influence on visual acuity outcome.

Tsujikawa M, Tsujikawa K, Lewis JM, Tano Y. Tsujikawa M, et al. Among authors: tsujikawa k. Retina. 1999;19(2):135-40. doi: 10.1097/00006982-199902000-00009. Retina. 1999. PMID: 10213240

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