Tsujikawa K - Search Results

1

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

2

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

3

Effect of simultaneous oblique muscle surgery in foveal translocation by 360 degrees retinotomy.

Fujikado T, Shimojyo H, Hosohata J, Tsujikawa K, Fukui T, Ohji M, Tano Y. Fujikado T, et al. Among authors: tsujikawa k. Graefes Arch Clin Exp Ophthalmol. 2002 Jan;240(1):21-30. doi: 10.1007/s00417-001-0401-7. Graefes Arch Clin Exp Ophthalmol. 2002. PMID: 11954777

4

A novel missense mutation in a Japanese patient with gelatinous droplike corneal dystrophy.

Taniguchi Y, Tsujikawa M, Hibino S, Tsujikawa K, Tanaka T, Kiridoushi A, Tano Y. Taniguchi Y, et al. Among authors: tsujikawa k, tsujikawa m. Am J Ophthalmol. 2005 Jan;139(1):186-8. doi: 10.1016/j.ajo.2004.06.090. Am J Ophthalmol. 2005. PMID: 15652848

5

Micro serial analysis of gene expression in normal human choroid and retinal pigment epithelial transcriptomes.

Kobashi-Hashida M, Ohguro N, Tsujikawa M, Furukawa T, Furukawa A, Hashida N, Tsujikawa K, Nakai K, Tano Y. Kobashi-Hashida M, et al. Among authors: tsujikawa k, tsujikawa m. Jpn J Ophthalmol. 2005 Jan-Feb;49(1):15-22. doi: 10.1007/s10384-004-0133-4. Jpn J Ophthalmol. 2005. PMID: 15692769

6

Vitrectomy for rhegmatogenous or tractional retinal detachment with familial exudative vitreoretinopathy.

Ikeda T, Fujikado T, Tano Y, Tsujikawa K, Koizumi K, Sawa H, Yasuhara T, Maeda K, Kinoshita S. Ikeda T, et al. Among authors: tsujikawa k. Ophthalmology. 1999 Jun;106(6):1081-5. doi: 10.1016/S0161-6420(99)90268-3. Ophthalmology. 1999. PMID: 10366074

7

Rapid detection of M1S1 mutations by the protein truncation test.

Tsujikawa M, Tsujikawa K, Maeda N, Watanabe H, Inoue Y, Mashima Y, Shimomura Y, Tano Y. Tsujikawa M, et al. Among authors: tsujikawa k. Invest Ophthalmol Vis Sci. 2000 Aug;41(9):2466-8. Invest Ophthalmol Vis Sci. 2000. PMID: 10937555

8

Two patterns of opacity in corneal dystrophy caused by the homozygous BIG-H3 R124H mutation.

Watanabe H, Hashida Y, Tsujikawa K, Tsujikawa M, Maeda N, Inoue Y, Yamamoto S, Tano Y. Watanabe H, et al. Among authors: tsujikawa k, tsujikawa m. Am J Ophthalmol. 2001 Aug;132(2):211-6. doi: 10.1016/s0002-9394(01)00962-x. Am J Ophthalmol. 2001. PMID: 11476681

9

Allelic homogeneity due to a founder mutation in Japanese patients with lattice corneal dystrophy type IIIA.

Tsujikawa K, Tsujikawa M, Yamamoto S, Fujikado T, Tano Y. Tsujikawa K, et al. Among authors: tsujikawa m. Am J Med Genet. 2002 Nov 15;113(1):20-2. doi: 10.1002/ajmg.10709. Am J Med Genet. 2002. PMID: 12400061

10

Chromosomal sharing in atypical cases of gelatinous drop-like corneal dystrophy.

Tsujikawa M, Maeda N, Tsujikawa K, Hori Y, Inoue T, Nishida K. Tsujikawa M, et al. Among authors: tsujikawa k. Jpn J Ophthalmol. 2010 Sep;54(5):494-8. doi: 10.1007/s10384-010-0861-6. Epub 2010 Nov 5. Jpn J Ophthalmol. 2010. PMID: 21052915

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