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Karin Ishikawa

Keio University

12

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253

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[Clinical phenotype of a Japanese family with primary open-angle glaucoma caused by a Ala 363 Thr mutation in the MYOC gene].

2006 Japanese Journal of Ophthalmology
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Citations (1)
SNPs and interaction analyses of noelin 2, myocilin, and optineurin genes in Japanese patients with open-angle glaucoma

2006 Investigative Ophthalmology & Visual Science
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Citations (42)
Genetic variants of TP53 and EPHX1 in Leber’s hereditary optic neuropathy and their relationship to age at onset

2005 Japanese Journal of Ophthalmology
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Citations (16)
Association between glaucoma and gene polymorphism of endothelin type A receptor.

2005 Molecular Vision
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Citations (37)
Genetic Polymorphisms in the Angiotensin II Receptor Gene and Their Association with Open-Angle Glaucoma in a Japanese Population

2005 Investigative Ophthalmology & Visual Science
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Citations (35)
Novel myoc Gene Mutation, Phe369leu, in Japanese Patients with Primary Open-angle Glaucoma Detected by Denaturing High-performance Liquid Chromatography

2004 Journal of Glaucoma
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Citations (17)
Variants in optineurin gene and their association with tumor necrosis factor-α polymorphisms in Japanese patients with glaucoma

2004 Investigative Ophthalmology & Visual Science
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Citations (87)
In situ confirmation of retinal blood flow improvement after carotid endarterectomy in a patient with ocular ischemic syndrome

2002 American Journal of Ophthalmology
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Citations (14)
Corneal Stromal Penetration Of Topically Applied Levofloxacin, Norfloxacin, And Lomefloxacin In The Same Human Eyes

2002 Investigative Ophthalmology & Visual Science
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