Nishida T - Search Results

1

Two brothers with gelatinous drop-like dystrophy at different stages of the disease: role of mutational analysis.

Yoshida S, Kumano Y, Yoshida A, Numa S, Yabe N, Hisatomi T, Nishida T, Ishibashi T, Matsui T. Yoshida S, et al. Among authors: nishida t. Am J Ophthalmol. 2002 Jun;133(6):830-2. doi: 10.1016/s0002-9394(02)01407-1. Am J Ophthalmol. 2002. PMID: 12036680

2

Ocular surface changes after excimer laser phototherapeutic keratectomy.

Dogru M, Katakami C, Miyashita M, Hida E, Uenishi M, Tetsumoto K, Kanno S, Nishida T, Yamanaka A. Dogru M, et al. Among authors: nishida t. Ophthalmology. 2000 Jun;107(6):1144-52. doi: 10.1016/s0161-6420(00)00113-5. Ophthalmology. 2000. PMID: 10857835

3

Corneal sensation after correction of myopia by photorefractive keratectomy and laser in situ keratomileusis.

Matsui H, Kumano Y, Zushi I, Yamada T, Matsui T, Nishida T. Matsui H, et al. Among authors: nishida t. J Cataract Refract Surg. 2001 Mar;27(3):370-3. doi: 10.1016/s0886-3350(00)00756-2. J Cataract Refract Surg. 2001. PMID: 11255047

4

Alteration of the ocular surface with recurrence of granular/avellino corneal dystrophy after phototherapeutic keratectomy: report of five cases and literature review.

Dogru M, Katakami C, Nishida T, Yamanaka A. Dogru M, et al. Among authors: nishida t. Ophthalmology. 2001 Apr;108(4):810-7. doi: 10.1016/s0161-6420(00)00657-6. Ophthalmology. 2001. PMID: 11297503 Review.

5

An analysis of BIGH3 mutations in patients with corneal dystrophies in the Kyushu district of Japan.

Yoshida S, Kumano Y, Yoshida A, Hisatomi T, Matsui H, Nishida T, Ishibashi T, Matsui T. Yoshida S, et al. Among authors: nishida t. Jpn J Ophthalmol. 2002 Jul-Aug;46(4):469-71. doi: 10.1016/s0021-5155(02)00528-2. Jpn J Ophthalmol. 2002. PMID: 12225829

6

Recovery of corneal sensation after myopic correction by laser in situ keratomileusis with a nasal or superior hinge.

Kumano Y, Matsui H, Zushi I, Mawatari A, Matsui T, Nishida T, Miyazaki M. Kumano Y, et al. Among authors: nishida t. J Cataract Refract Surg. 2003 Apr;29(4):757-61. doi: 10.1016/s0886-3350(02)01840-0. J Cataract Refract Surg. 2003. PMID: 12686245

7

Unusual phenotype of an individual with the R124C mutation in the TGFBI gene.

Morishige N, Chikama T, Ishimura Y, Nishida T, Takahashi M, Mashima Y. Morishige N, et al. Among authors: nishida t. Arch Ophthalmol. 2004 Aug;122(8):1224-7. doi: 10.1001/archopht.122.8.1224. Arch Ophthalmol. 2004. PMID: 15302666 No abstract available.

8

Delayed corneal epithelial wound healing after penetrating keratoplasty in individuals with lattice corneal dystrophy.

Kawamoto K, Morishige N, Yamada N, Chikama T, Nishida T. Kawamoto K, et al. Among authors: nishida t. Am J Ophthalmol. 2006 Jul;142(1):173-4. doi: 10.1016/j.ajo.2006.01.077. Am J Ophthalmol. 2006. PMID: 16815275

9

Double mutation (R124H, N544S) of TGFBI in two sisters with combined expression of Avellino and lattice corneal dystrophies.

Yamada N, Kawamoto K, Morishige N, Chikama T, Nishida T, Nishioka M, Okayama N, Hinoda Y. Yamada N, et al. Among authors: nishida t. Mol Vis. 2009 May 15;15:974-9. Mol Vis. 2009. PMID: 19461933 Free PMC article.

10

New mode of treatment for lattice corneal dystrophy type I: corneal epithelial debridement and fibronectin eye drops.

Morita Y, Chikama T, Yamada N, Morishige N, Sonoda KH, Nishida T. Morita Y, et al. Among authors: nishida t. Jpn J Ophthalmol. 2012 Jan;56(1):26-30. doi: 10.1007/s10384-011-0104-5. Epub 2011 Nov 12. Jpn J Ophthalmol. 2012. PMID: 22080335

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