Tsujikawa K - Search Results

1

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

2

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

3

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

4

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

5

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

6

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

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 in Avellino corneal dystrophy due to a founder effect.

Tsujikawa K, Tsujikawa M, Watanabe H, Maeda N, Inoue Y, Fujikado T, Tano Y. Tsujikawa K, et al. Among authors: tsujikawa m. J Hum Genet. 2007;52(1):92-97. doi: 10.1007/s10038-006-0083-4. Epub 2006 Nov 10. J Hum Genet. 2007. PMID: 17096061

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

336 results

Search Page

Filters